Senior Performance Analyst Location: Ealing, London Salary: £49,083 -£51,093 per annum inclusive - Grade 12 The Role The Council Plan 2022-26 sets out our ambitions for a borough where every family has a decent living income and can reside in a genuinely affordable home, where everyone can live a long and healthy life in communities full of pride and identity. We are on a journey to transform the way we work to achieve the council's ambitions using the best data and insight. Contribute significantly to embed the development of an insight and intelligence culture throughout the council. This role will form part of a wider Corporate Performance Team with specific responsibility for supporting the Adult Social Care Directorate. The role would: Manage the delivery of the Performance function in Adult Social Care and the provision of data necessary for the Department to make timely, relevant and strategic decisions and fully support national and local reporting requirements for Adult Social Care. Develop, plan and deliver business intelligence products such as dashboards and bespoke performance analysis to drive operational decision making and service improvement Key Accountabilities To be responsible for the delivery of the performance framework for Adult Social Care ensuring the framework reflects Central Government reporting requirements. To be responsible for the accurate completion and submission of all statutory returns, being the main point of contact and liaising with all relevant outside bodies, and to ensure the maintenance of accurate and robust auditable records of performance data. To have overall responsibility for co-ordination, production and delivery of performance monitoring data to a variety of internal and external sources, to inform strategic service planning and budget, procurement and commissioning decisions in relation to Adult Social Care. To lead on the coordination of data to support the council's preparation for CQC Assurance. To lead on Data Quality for the Department, managing and promoting data quality and implementing assurance and audits systems to ensure accurate data. To work with auditors and ensure smooth running of audits and any follow up work. To work with a range of stakeholders across adult social care to ensure that business processes are developed to capture accurately the data required to support the production of statutory returns and management and commissioning information. To lead on the development and management of reporting tools, business intelligence systems, applications and dashboards. To advise and support senior managers on relevant service and operational matters regarding performance data. To work with the ICS and other NHS partners to develop and implement integrated performance management systems and monitoring which supports national and local policy initiatives. To ensure all Member queries and FOIs are dealt with promptly and effectively. To provide effective management of staff, including recruitment, training, development and appropriate application of policies on staffing matters. To contribute towards the development of good working relations and collaborative arrangements with relevant third-party organisations including 3 private, voluntary and other public organisations and to forge effective partnership working. Skills and Experience Knowledge and experience of using information systems and reporting tools in Adult Social Care to generate performance data Expert knowledge and understanding of performance frameworks and national policy including national performance indicators affecting services for adults Knowledge of current legislation for adult social care Experience of using SQL or web-based business intelligence applications such as Business Objects to a high level Experience of managing the development of business intelligence systems and applications in line with changing national and local reporting requirements. Experience of developing and implementing performance management frameworks Experience of implementing systems and processes to ensure data quality and integrity, including business process reviews and design Educated to degree standard in a relevant field or equivalent by work experience To Apply If you feel you are a suitable candidate and would like to work for this reputable Council, then please click apply to be redirected to their website to complete your application.
Apr 16, 2024
Full time
Senior Performance Analyst Location: Ealing, London Salary: £49,083 -£51,093 per annum inclusive - Grade 12 The Role The Council Plan 2022-26 sets out our ambitions for a borough where every family has a decent living income and can reside in a genuinely affordable home, where everyone can live a long and healthy life in communities full of pride and identity. We are on a journey to transform the way we work to achieve the council's ambitions using the best data and insight. Contribute significantly to embed the development of an insight and intelligence culture throughout the council. This role will form part of a wider Corporate Performance Team with specific responsibility for supporting the Adult Social Care Directorate. The role would: Manage the delivery of the Performance function in Adult Social Care and the provision of data necessary for the Department to make timely, relevant and strategic decisions and fully support national and local reporting requirements for Adult Social Care. Develop, plan and deliver business intelligence products such as dashboards and bespoke performance analysis to drive operational decision making and service improvement Key Accountabilities To be responsible for the delivery of the performance framework for Adult Social Care ensuring the framework reflects Central Government reporting requirements. To be responsible for the accurate completion and submission of all statutory returns, being the main point of contact and liaising with all relevant outside bodies, and to ensure the maintenance of accurate and robust auditable records of performance data. To have overall responsibility for co-ordination, production and delivery of performance monitoring data to a variety of internal and external sources, to inform strategic service planning and budget, procurement and commissioning decisions in relation to Adult Social Care. To lead on the coordination of data to support the council's preparation for CQC Assurance. To lead on Data Quality for the Department, managing and promoting data quality and implementing assurance and audits systems to ensure accurate data. To work with auditors and ensure smooth running of audits and any follow up work. To work with a range of stakeholders across adult social care to ensure that business processes are developed to capture accurately the data required to support the production of statutory returns and management and commissioning information. To lead on the development and management of reporting tools, business intelligence systems, applications and dashboards. To advise and support senior managers on relevant service and operational matters regarding performance data. To work with the ICS and other NHS partners to develop and implement integrated performance management systems and monitoring which supports national and local policy initiatives. To ensure all Member queries and FOIs are dealt with promptly and effectively. To provide effective management of staff, including recruitment, training, development and appropriate application of policies on staffing matters. To contribute towards the development of good working relations and collaborative arrangements with relevant third-party organisations including 3 private, voluntary and other public organisations and to forge effective partnership working. Skills and Experience Knowledge and experience of using information systems and reporting tools in Adult Social Care to generate performance data Expert knowledge and understanding of performance frameworks and national policy including national performance indicators affecting services for adults Knowledge of current legislation for adult social care Experience of using SQL or web-based business intelligence applications such as Business Objects to a high level Experience of managing the development of business intelligence systems and applications in line with changing national and local reporting requirements. Experience of developing and implementing performance management frameworks Experience of implementing systems and processes to ensure data quality and integrity, including business process reviews and design Educated to degree standard in a relevant field or equivalent by work experience To Apply If you feel you are a suitable candidate and would like to work for this reputable Council, then please click apply to be redirected to their website to complete your application.
Care Quality Commission
Newcastle Upon Tyne, Tyne And Wear
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework - if you are London office based or homebased and live within the boundary of the M25) - There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We're the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary.One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network.Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England.We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days' annual leave, rising with service to 32.5 days, plus 8 Bank Holidays- NHS pension scheme, with around a 14% employer contribution- Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers- Cycle to work scheme- Internal reward scheme where you could win a voucher or two!- Equipment for homeworking Why this could be a great role for you If you're experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation.You'll play a pivotal role at the forefront of overseeing optimal healthcare across the nation.What's more, you'll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need:- Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations- Experience of handling confidential matters- Experience of keeping accurate document management logs- Experience of the liaison and co-ordination of requests as they arise- Experience of building effective relationships- The ability to work and deliver under pressure What you'll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations.Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews.You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst.Additionally, you will: - Support individual witnesses, alongside Engagement colleagues- Co-ordinate our agreed corporate position for statements- Liaise with the Director of Legal Services for legal support- Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management- Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application.We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation.So, if you'd like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Apr 14, 2024
Full time
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework - if you are London office based or homebased and live within the boundary of the M25) - There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We're the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary.One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network.Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England.We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days' annual leave, rising with service to 32.5 days, plus 8 Bank Holidays- NHS pension scheme, with around a 14% employer contribution- Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers- Cycle to work scheme- Internal reward scheme where you could win a voucher or two!- Equipment for homeworking Why this could be a great role for you If you're experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation.You'll play a pivotal role at the forefront of overseeing optimal healthcare across the nation.What's more, you'll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need:- Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations- Experience of handling confidential matters- Experience of keeping accurate document management logs- Experience of the liaison and co-ordination of requests as they arise- Experience of building effective relationships- The ability to work and deliver under pressure What you'll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations.Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews.You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst.Additionally, you will: - Support individual witnesses, alongside Engagement colleagues- Co-ordinate our agreed corporate position for statements- Liaise with the Director of Legal Services for legal support- Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management- Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application.We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation.So, if you'd like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework if you are London office based or homebased and live within the boundary of the M25) There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We re the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary. One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network. Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England. We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days annual leave, rising with service to 32.5 days, plus 8 Bank Holidays - NHS pension scheme, with around a 14% employer contribution - Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers - Cycle to work scheme - Internal reward scheme where you could win a voucher or two! - Equipment for homeworking Why this could be a great role for you If you re experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation. You ll play a pivotal role at the forefront of overseeing optimal healthcare across the nation. What s more, you ll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need: - Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations - Experience of handling confidential matters - Experience of keeping accurate document management logs - Experience of the liaison and co-ordination of requests as they arise - Experience of building effective relationships - The ability to work and deliver under pressure What you ll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations. Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews. You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst. Additionally, you will: - Support individual witnesses, alongside Engagement colleagues - Co-ordinate our agreed corporate position for statements - Liaise with the Director of Legal Services for legal support - Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management - Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application. We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation. So, if you d like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Apr 10, 2024
Contractor
Senior Public Inquiries Advisor Salary: Grade B - £39,390 (National Framework) or £44,792 (London Framework if you are London office based or homebased and live within the boundary of the M25) There is also an additional homeworking allowance of £553 per annum for those working from home Contracted Hours: Full time 37 hours per week Contract Type: 12 Month Fixed Term or Secondment Opportunity Location: Home or office based Closing date: Thursday 18th April 2024 at 11.59pm About Us We re the Care Quality Commission (CQC) and we work to improve health and adult social care in England. Through the dedication of our expert team, we monitor health and social care services to provide England with a safe and compassionate care system, recognising when services perform well as well as encouraging improvements and taking action over poorer care, where necessary. One of our main commitments is to become a truly inclusive organisation and to role model a diverse and representative culture. To do so, we work with a variety of networks, including the Disability Equality Network, Race Equality Network and LGBT+ Equality Network. Our Governance and Legal Services Teams provide us with essential legal support and advice, enabling us to accomplish our duties and focus on achieving our aims of ensuring the best health and social care is provided across England. We are now looking for a Senior Public Inquiries Advisor to join us on a full-time basis for a twelve-month fixed-term contract. The Benefits - 27 days annual leave, rising with service to 32.5 days, plus 8 Bank Holidays - NHS pension scheme, with around a 14% employer contribution - Free employee assistance service 24 hours a day - Discounts to supermarkets, high street stores, electronics and fleet cars - Discounted gym vouchers - Cycle to work scheme - Internal reward scheme where you could win a voucher or two! - Equipment for homeworking Why this could be a great role for you If you re experienced in providing advice and robust solutions and handling confidential information, this is the perfect opportunity to join our vital organisation. You ll play a pivotal role at the forefront of overseeing optimal healthcare across the nation. What s more, you ll be able to develop upon your advisory and investigative skillset, honing your expertise and adding our reputable organisation to your portfolio of experience. What you will bring To be considered as a Senior Public Inquiries Advisor, you will need: - Experience of providing advice, taking into account extensive evidence and legal requirements, and making robust recommendations - Experience of handling confidential matters - Experience of keeping accurate document management logs - Experience of the liaison and co-ordination of requests as they arise - Experience of building effective relationships - The ability to work and deliver under pressure What you ll be doing As the Senior Public Inquiries Advisor, you will deputise for the Public Inquiries Manager in relation to the Covid-19 Public Inquiry, Thirlwall Inquiry and other independent inquiries, reviews and investigations. Acting as a contact point for Public Inquiry secretariats, you will manage our relationships with investigators and reviewers, as well as our response to investigations and reviews. You will also handle our disclosure to investigation panels, identifying and locating relevant documentation and effectively managing our documentation to ensure full and frank disclosure, with the support of a Senior Records Analyst. Additionally, you will: - Support individual witnesses, alongside Engagement colleagues - Co-ordinate our agreed corporate position for statements - Liaise with the Director of Legal Services for legal support - Arrange liaison with paralegal and administrative support - Provide coaching, support, supervision, and line management - Review transcripts and provide summaries of key points Next steps If you require any support or assistance with the recruitment process, please get in touch with our team or include a note in your application. We know diverse teams allow for a more creative and productive environment and therefore encourage applications from everyone regardless of age, gender/sex, gender identity or expression, religion or belief, disability, ethnicity or sexual orientation. So, if you d like to join us as a Senior Public Inquiries Advisor, please apply via the button shown. Other organisations may call this role Senior External Affairs Advisor, Public Enquiries Consultant, Head of Public Affairs, Senior Public Enquiries Associate, Head of Public Investigations, or Public Investigations Leader.
Organic Analyst & Senior Analyst, GC/MS Location: Cambridge Salary:£26,000 - £28,000 Dependant on experience Role: Conducting regular/ daily GC test work (GC FID & GC/MS), whilst maintaining and calibrating the instruments. Assistance in the generation of accurate and timely sample and QC data in line with client expectations and our clients Quality Systems click apply for full job details
Apr 04, 2024
Full time
Organic Analyst & Senior Analyst, GC/MS Location: Cambridge Salary:£26,000 - £28,000 Dependant on experience Role: Conducting regular/ daily GC test work (GC FID & GC/MS), whilst maintaining and calibrating the instruments. Assistance in the generation of accurate and timely sample and QC data in line with client expectations and our clients Quality Systems click apply for full job details
Salary 80,000 - 85,000 GBP per year Requirements: - Senior Business Analyst with Understanding of investments, lending, and equity. Must be able to Write a clear business requirement document (BRD).in the form of user stories in Jira Ability to raise a defect, and experience in Agile methodologies Waterfall model Interaction with all stakeholders, analysis, and requirement documentation, creating test case scenario, Acceptance Criteria, documentation in QC, test execution and test result documentation. Must acquire business knowledge, understand business analyst process, and perform testing of the new requirement in the system Responsibilities: - Performs and coordinates the analysis and design of business systems. Develops and maintains a thorough understanding of the needs of the assigned customer group from the business and technical perspective. Works closely with clients and with other system groups to capture business requirements and see them through implementation. Develops and executes systems testing. Acts as a liaison between the business user groups and the technical systems groups. This resource type provides analytical, technical, business and management expertise to the group and completes assignments which require this expertise. The resource may be required to lead teams of up to 10 professionals or operations personnel. This resource will respond and resolve issues beyond standard management requests as well as using independent judgment to make decisions where no clear precedents exist and should typically be used for a senior or lead level resource Technologies: - JIRA More: Strong analytical skills Ability to collaborate Adaptability Excellent communication skills Innovation, Inquisitive mind, endless curiosity, and passion for learning about customers, industries, and new approaches to doing things, how end users perform their jobs, industry challenges and solutions. Strong self-starter with the ability to effectively build, develop and manage relationships with internal and client stakeholders.
Nov 24, 2022
Full time
Salary 80,000 - 85,000 GBP per year Requirements: - Senior Business Analyst with Understanding of investments, lending, and equity. Must be able to Write a clear business requirement document (BRD).in the form of user stories in Jira Ability to raise a defect, and experience in Agile methodologies Waterfall model Interaction with all stakeholders, analysis, and requirement documentation, creating test case scenario, Acceptance Criteria, documentation in QC, test execution and test result documentation. Must acquire business knowledge, understand business analyst process, and perform testing of the new requirement in the system Responsibilities: - Performs and coordinates the analysis and design of business systems. Develops and maintains a thorough understanding of the needs of the assigned customer group from the business and technical perspective. Works closely with clients and with other system groups to capture business requirements and see them through implementation. Develops and executes systems testing. Acts as a liaison between the business user groups and the technical systems groups. This resource type provides analytical, technical, business and management expertise to the group and completes assignments which require this expertise. The resource may be required to lead teams of up to 10 professionals or operations personnel. This resource will respond and resolve issues beyond standard management requests as well as using independent judgment to make decisions where no clear precedents exist and should typically be used for a senior or lead level resource Technologies: - JIRA More: Strong analytical skills Ability to collaborate Adaptability Excellent communication skills Innovation, Inquisitive mind, endless curiosity, and passion for learning about customers, industries, and new approaches to doing things, how end users perform their jobs, industry challenges and solutions. Strong self-starter with the ability to effectively build, develop and manage relationships with internal and client stakeholders.
QC Senior Sponsor Contracts Manager Summary: Manages Quality Control of all client deliverables within the Global Deal and Contract Management (GDCM) group. Guarantees high quality of departmental output through detailed review of both contract documentation and study budgets. Ensures all deliverables conform to both client expectations and audit requirements. Provides detailed and constructive feedback to internal stakeholders and works with them to refine contractual materials. Tracks adherence to company processes and provides regular performance feedback. Why Syneos Health • means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference. • We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job responsibilities : Analytically reviews the more complex budget tools and contractual materials from a Syneos Health, client and audit perspective to ensure the highest possible quality of output. Proactively works with contract analysts to refine deliverables in accordance with existing QC checklists and company policies. Evaluates all budget commentary to ensure a clear, concise and robust narrative. Assesses validity of study pricing and suitability of budgets prior to client delivery. Ensures consistency between pricing tools, budget grids, payment schedules and all contractual documentation. Utilizes QC checklists to perform a thorough review of Change Order, Change Notification Form and Ballpark documentation to ensure quality and consistency. Ensures all legal entities and defined terms are correct, appropriate and applied consistently throughout documents. Validates the presence and accuracy of inflation language if applicable. Maintains a high level of flexibility and adaptability. Proactively creates and revises priorities as the need arises whilst working toward standard cycle times of review. Supports the Change Order process through expeditious reviews and the provision of concise feedback. Identifies and raises issues before they become critical and adjusts quickly to the changes of a dynamic organization. Ensures adherence to Contract Management systems by reviewing records during the QC process. Reviews these systems to drive compliance with both GDCM and Syneos Health reporting processes and approval policies. Evaluates the performance of analysts within the GDCM group by assessing the quality of materials submitted for QC and providing performance feedback on a monthly basis. Assists with ownership of this performance report as needed. Updates and maintains departmental template and process documents. Leads QC training for the Client Contracting Solutions group as needed. Assists with audit inquiries as needed. Mentors members of the QC team as needed. Performs other duties as assigned. What we're looking for: BA/BS degree in a Business Administration or Finance with a minimum of 7 years' experience preferably in budgeting, finance, proposal development and/or contracts management within a clinical research/pharmaceutical environment; or equivalent combination of education, training and experience. Flexibility in responding to job demands. Have excellent problems solving skills and outstanding attention to detail. Ability to perform several tasks simultaneously to meet critical deadlines and possess strong analytical skills. Knowledge of Microsoft Excel, Word and understanding of costing models. Ability to review and interpret budgets. Ability to work successfully in a team environment and maintain effective working relationships with colleagues and manager. Demonstrates effective time management skills. Ability to prioritize multiple tasks with management guidance and oversight. Excellent interpersonal, verbal and written communication skills. Demonstrates a positive and flexible attitude toward new and/or unconventional work assignments. Ability to consistently perform and deliver a high quality work product. Excellent organizational skills. Ability to work well under pressure and adapt to changing priorities. Knowledge of clinical trial proposal process and budget management. Professional ability to interact with individuals at all levels and different personalities. Proficiency in mathematics, written language and ability to work with both budgets and text. Good interpersonal skills and ability to work well with others. Disclaimer: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
Sep 24, 2022
Full time
QC Senior Sponsor Contracts Manager Summary: Manages Quality Control of all client deliverables within the Global Deal and Contract Management (GDCM) group. Guarantees high quality of departmental output through detailed review of both contract documentation and study budgets. Ensures all deliverables conform to both client expectations and audit requirements. Provides detailed and constructive feedback to internal stakeholders and works with them to refine contractual materials. Tracks adherence to company processes and provides regular performance feedback. Why Syneos Health • means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference. • We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job responsibilities : Analytically reviews the more complex budget tools and contractual materials from a Syneos Health, client and audit perspective to ensure the highest possible quality of output. Proactively works with contract analysts to refine deliverables in accordance with existing QC checklists and company policies. Evaluates all budget commentary to ensure a clear, concise and robust narrative. Assesses validity of study pricing and suitability of budgets prior to client delivery. Ensures consistency between pricing tools, budget grids, payment schedules and all contractual documentation. Utilizes QC checklists to perform a thorough review of Change Order, Change Notification Form and Ballpark documentation to ensure quality and consistency. Ensures all legal entities and defined terms are correct, appropriate and applied consistently throughout documents. Validates the presence and accuracy of inflation language if applicable. Maintains a high level of flexibility and adaptability. Proactively creates and revises priorities as the need arises whilst working toward standard cycle times of review. Supports the Change Order process through expeditious reviews and the provision of concise feedback. Identifies and raises issues before they become critical and adjusts quickly to the changes of a dynamic organization. Ensures adherence to Contract Management systems by reviewing records during the QC process. Reviews these systems to drive compliance with both GDCM and Syneos Health reporting processes and approval policies. Evaluates the performance of analysts within the GDCM group by assessing the quality of materials submitted for QC and providing performance feedback on a monthly basis. Assists with ownership of this performance report as needed. Updates and maintains departmental template and process documents. Leads QC training for the Client Contracting Solutions group as needed. Assists with audit inquiries as needed. Mentors members of the QC team as needed. Performs other duties as assigned. What we're looking for: BA/BS degree in a Business Administration or Finance with a minimum of 7 years' experience preferably in budgeting, finance, proposal development and/or contracts management within a clinical research/pharmaceutical environment; or equivalent combination of education, training and experience. Flexibility in responding to job demands. Have excellent problems solving skills and outstanding attention to detail. Ability to perform several tasks simultaneously to meet critical deadlines and possess strong analytical skills. Knowledge of Microsoft Excel, Word and understanding of costing models. Ability to review and interpret budgets. Ability to work successfully in a team environment and maintain effective working relationships with colleagues and manager. Demonstrates effective time management skills. Ability to prioritize multiple tasks with management guidance and oversight. Excellent interpersonal, verbal and written communication skills. Demonstrates a positive and flexible attitude toward new and/or unconventional work assignments. Ability to consistently perform and deliver a high quality work product. Excellent organizational skills. Ability to work well under pressure and adapt to changing priorities. Knowledge of clinical trial proposal process and budget management. Professional ability to interact with individuals at all levels and different personalities. Proficiency in mathematics, written language and ability to work with both budgets and text. Good interpersonal skills and ability to work well with others. Disclaimer: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
What you will do: The Senior Clinical Data Analyst (SCDA) shall independently perform all clinical data cleaning activities on assigned FSP projects, commensurate with experience and/or project role. Further responsibilities shall include support on data processing activities and study level documents e.g. Protocol Deviation Specification, Data Validation specification, etc. The SCDA may act as a Data Management Lead where required. Key Accountabilities: Assume the ability to meet the requirements of a CDA III roIe with a high degree of proficiency and autonomy. Lead/Responsible for data cleaning and data review activities e.g. query management. Management of project timelines (including creation, review and tracking of plans). Review of protocols and EDC Screens if required. Support data processing activities from database setup to database lock, e.g. SAE reconciliation. Perform user acceptance testing on study database setups. Perform medical coding on small studies. Track and review CRFs. Support data entry where required. Perform and or support the setup of DM documents and ensure proper documentation e.g. CRF Completion Guidelines (CCG) Perform/lead functional QC activities and testing. Mentor project team members. Be a subject matter expert when needed. Ideal candidate will possess: Bachelor's degree and / or other medical qualifications. Understanding of Global Data Operations tasks, specifically within Data Management and Database Programming and relevant data standards. Sound awareness of relevant regulations, including ICH-GCP, 21CRF11. Experience in clinical research. Good interpersonal, verbal and written communication skills. Knowledge of medical terminology and awareness of coding dictionaries (e.g.MedDRA & WHODRUG). Good knowledge of EDC systems (e.g. DataLabs, Rave.) Good knowledge of electronic source data capture systems (e.g. ClinBase). Good knowledge of all DB set-up activities including but not limited to Database Configuration. Specifications, Data Validation. Ability to work in team environment. Good analytical skills and attention to detail. Effective time management to meet daily metrics or team objectives, completion of assigned tasks in a timely manner. Basic knowledge of SAS.
Sep 22, 2022
Full time
What you will do: The Senior Clinical Data Analyst (SCDA) shall independently perform all clinical data cleaning activities on assigned FSP projects, commensurate with experience and/or project role. Further responsibilities shall include support on data processing activities and study level documents e.g. Protocol Deviation Specification, Data Validation specification, etc. The SCDA may act as a Data Management Lead where required. Key Accountabilities: Assume the ability to meet the requirements of a CDA III roIe with a high degree of proficiency and autonomy. Lead/Responsible for data cleaning and data review activities e.g. query management. Management of project timelines (including creation, review and tracking of plans). Review of protocols and EDC Screens if required. Support data processing activities from database setup to database lock, e.g. SAE reconciliation. Perform user acceptance testing on study database setups. Perform medical coding on small studies. Track and review CRFs. Support data entry where required. Perform and or support the setup of DM documents and ensure proper documentation e.g. CRF Completion Guidelines (CCG) Perform/lead functional QC activities and testing. Mentor project team members. Be a subject matter expert when needed. Ideal candidate will possess: Bachelor's degree and / or other medical qualifications. Understanding of Global Data Operations tasks, specifically within Data Management and Database Programming and relevant data standards. Sound awareness of relevant regulations, including ICH-GCP, 21CRF11. Experience in clinical research. Good interpersonal, verbal and written communication skills. Knowledge of medical terminology and awareness of coding dictionaries (e.g.MedDRA & WHODRUG). Good knowledge of EDC systems (e.g. DataLabs, Rave.) Good knowledge of electronic source data capture systems (e.g. ClinBase). Good knowledge of all DB set-up activities including but not limited to Database Configuration. Specifications, Data Validation. Ability to work in team environment. Good analytical skills and attention to detail. Effective time management to meet daily metrics or team objectives, completion of assigned tasks in a timely manner. Basic knowledge of SAS.
Are you an experienced senior analyst with a passion for Quality Control? Do you want to become part of an expanding company with limitless possibilities? If so, we may just have the ideal role for you! We are hiring for the position of Analytical Development Chemist for our highly-skilled Quality Control Team. We want you to be a key player in some of the most exciting projects we've had, to date. We're in the process of developing our CDMO business and want you involved in both this and our ongoing Omega-3 business needs. Become part of a this Global Leader and not only excel professionally but develop world-class skills while working with highly-astute experts in your field. The main purpose for this role is to support the business directly in both the validation and development of robust analytical test methods of various raw materials, finished product samples and intermediates. This is to be done with a focus on ensuring that the delivery is in accordance with not only project timescales but also the deadlines, while working with multiple departments such as R&D, Production and of course the Quality Assurance Teams! Responsibilities: The method development and also qualification of various analytical techniques to be used in respect to the structural classification of product such as UV-Vis, chromatography methods etc Development and validation of analytical test methods in regards to the testing of pharma products in line with both cGMP and ICH Q2 requirements Development and validation test methods for cleaning validation in line with cGMP and ICH Q7 requirements Preparation of analytical method development, validation and analytical investigation reports Transferring new analytical techniques to the Quality Control (QC) laboratory Manage multiple projects to completion working closely with various departments Controlling laboratory chemicals Provide input for technical assessment of quotations Participate in the documentation of laboratory systems and processes including the updating of existing documentation as required Train QC Analysts/Technicians Review and evaluate data and ensure all activities are carried out to cGMP standards Complying with the technical, operational, SHE and cGMP guidelines to generate high quality, relevant, accurate and timely data Generation of Laboratory KPI's and seeking to improve laboratory processes Potential external customer interfacing on development activities. Qualifications and Experience: Degree in Chemistry, Pharmaceutical Science, analytical or related, but preferably PhD. Proven experience of 5+ years in pharmaceutical method development, qualification, technology transfer and cleaning validation, from first principles Proven track record of undertaking testing, analysis, troubleshooting using instrumentational analysis such as; GC, HPLC, MS, UV, in a regulated environment. Experience of regulatory guideline, GMP, ICH guidelines, BP/EP/USP methods with a strong understanding of QA processes and methodologies. Experience in equipment qualification, calibration and servicing, including writing associated validation documentation. Write, review and revise SOPs etc, as required Supervisory experience and the ability to support and motivate team members.
Aug 03, 2022
Full time
Are you an experienced senior analyst with a passion for Quality Control? Do you want to become part of an expanding company with limitless possibilities? If so, we may just have the ideal role for you! We are hiring for the position of Analytical Development Chemist for our highly-skilled Quality Control Team. We want you to be a key player in some of the most exciting projects we've had, to date. We're in the process of developing our CDMO business and want you involved in both this and our ongoing Omega-3 business needs. Become part of a this Global Leader and not only excel professionally but develop world-class skills while working with highly-astute experts in your field. The main purpose for this role is to support the business directly in both the validation and development of robust analytical test methods of various raw materials, finished product samples and intermediates. This is to be done with a focus on ensuring that the delivery is in accordance with not only project timescales but also the deadlines, while working with multiple departments such as R&D, Production and of course the Quality Assurance Teams! Responsibilities: The method development and also qualification of various analytical techniques to be used in respect to the structural classification of product such as UV-Vis, chromatography methods etc Development and validation of analytical test methods in regards to the testing of pharma products in line with both cGMP and ICH Q2 requirements Development and validation test methods for cleaning validation in line with cGMP and ICH Q7 requirements Preparation of analytical method development, validation and analytical investigation reports Transferring new analytical techniques to the Quality Control (QC) laboratory Manage multiple projects to completion working closely with various departments Controlling laboratory chemicals Provide input for technical assessment of quotations Participate in the documentation of laboratory systems and processes including the updating of existing documentation as required Train QC Analysts/Technicians Review and evaluate data and ensure all activities are carried out to cGMP standards Complying with the technical, operational, SHE and cGMP guidelines to generate high quality, relevant, accurate and timely data Generation of Laboratory KPI's and seeking to improve laboratory processes Potential external customer interfacing on development activities. Qualifications and Experience: Degree in Chemistry, Pharmaceutical Science, analytical or related, but preferably PhD. Proven experience of 5+ years in pharmaceutical method development, qualification, technology transfer and cleaning validation, from first principles Proven track record of undertaking testing, analysis, troubleshooting using instrumentational analysis such as; GC, HPLC, MS, UV, in a regulated environment. Experience of regulatory guideline, GMP, ICH guidelines, BP/EP/USP methods with a strong understanding of QA processes and methodologies. Experience in equipment qualification, calibration and servicing, including writing associated validation documentation. Write, review and revise SOPs etc, as required Supervisory experience and the ability to support and motivate team members.
About LabCorp Drug Development: As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role: Our UK site in Harrogate, is currently recruiting for a QC Scientist to join the Bioassay CMC team. The CMC business unit; provides dedicated release and stability testing from preclinical phases through the commercial life of a product. The CMC team support method development, transfer, phase appropriate validation & assay establishment of large molecules. We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role within the CMC department is a senior scientist position. You will provide technical and regulatory oversight for stability and batch release testing; executed by the laboratory QC Analyst team in a GMP environment. Alternative terminology for the QC Scientist include Study Manager and Lead Scientist Job Responsibilities: Acting as the scientific lead in one or more of the following analytical techniques: ELISA & Cell Based Assays. Supporting client projects for Stability and Batch Release for Large Molecule products including Monoclonal Antibodies and Vaccines. Designing method development and validation strategies. Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. Perform regulatory compliance checks and maintain regulatory oversight during study execution. Lead technical or regulatory investigations when required throughout the conduct of a project. Training, mentoring and coaching of laboratory analysts and other team members. What Labcorp Drug Development can offer you: A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information: Position includes a 6-month onboarding & probationary period during which working hours are 8:45am - 5pm. The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. Prerequisites: Required: Scientific degree (BSc / MSc / PhD or equivalent). Required: Able to communicate effectively at all levels with internal employees and external clients, with theability to get things done by influencing others. Required: Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes. Either: Technical expertise in at least one of the following scientific disciplines: ELISA, or Cell Based Assays. Either: Experience within industry or similar, with study management and client management. Preferred: An in-depth understanding of health and safety policies and a good understanding of GMP regulatory guidelines. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
Aug 03, 2022
Full time
About LabCorp Drug Development: As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role: Our UK site in Harrogate, is currently recruiting for a QC Scientist to join the Bioassay CMC team. The CMC business unit; provides dedicated release and stability testing from preclinical phases through the commercial life of a product. The CMC team support method development, transfer, phase appropriate validation & assay establishment of large molecules. We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role within the CMC department is a senior scientist position. You will provide technical and regulatory oversight for stability and batch release testing; executed by the laboratory QC Analyst team in a GMP environment. Alternative terminology for the QC Scientist include Study Manager and Lead Scientist Job Responsibilities: Acting as the scientific lead in one or more of the following analytical techniques: ELISA & Cell Based Assays. Supporting client projects for Stability and Batch Release for Large Molecule products including Monoclonal Antibodies and Vaccines. Designing method development and validation strategies. Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. Perform regulatory compliance checks and maintain regulatory oversight during study execution. Lead technical or regulatory investigations when required throughout the conduct of a project. Training, mentoring and coaching of laboratory analysts and other team members. What Labcorp Drug Development can offer you: A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information: Position includes a 6-month onboarding & probationary period during which working hours are 8:45am - 5pm. The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. Prerequisites: Required: Scientific degree (BSc / MSc / PhD or equivalent). Required: Able to communicate effectively at all levels with internal employees and external clients, with theability to get things done by influencing others. Required: Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes. Either: Technical expertise in at least one of the following scientific disciplines: ELISA, or Cell Based Assays. Either: Experience within industry or similar, with study management and client management. Preferred: An in-depth understanding of health and safety policies and a good understanding of GMP regulatory guidelines. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
About LabCorp Drug Development: As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role: Our largest UK site in Harrogate, is currently recruiting for a QC Scientist to join the Molecular Biology CMC team. Within the CMC business unit; the Molecular Biology department is dedicated to the development, validation and execution of molecular techniques, such as QPCR, RTqPCR and Digital PCR to support Cell Therapies, Gene Therapies and Vaccines . We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role within the Molecular Biology department is a senior scientist position. You will provide technical and regulatory oversight for clinical and pre-clinical studies; executed by the laboratory QC Analyst team in a GLP & GCP environment. Alternative terminologies for QC Scientist include Study Manager, Principal Investigator, Contributing Scientist and Study Director . Job Responsibilities: Acting as the scientific lead in one or more of the following analytical techniques: qPCR, RTqPCR, Digital PCR,and Nucleic Acid Extractions. Supporting client projects including biodistribution, persistence & shedding studies and clinical trials for Cell Therapies, Gene Therapies and Vaccines. Designing method development and validation strategies. Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. Perform regulatory compliance checks and maintain regulatory oversight during study execution. Lead technical or regulatory investigations when required throughout the conduct of a project. Training, mentoring and coaching of laboratory analysts and other team members. What Labcorp Drug Development can offer you: A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information: Position includes a 6-month onboarding & probationary period during which working hours are 8:45am - 5pm, based at our site in Harrogate. Following the initial onboarding period; you will move to one of the following shift patterns 6:00am - 2:15pm or 8:45am - 5:00pm. Currently we are recruiting for 6:00am - 2:15pm shift. The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. Education/Qualifications: Required: Scientific degree (BSc / MSc / PhD or equivalent). Experience: Required: Able to communicate effectively at all levels with internal employees and external clients, with theability to get things done by influencing others. Required: Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes. Either: Technical expertise in at least one of the following scientific disciplines: qPCR or DNA extraction within Molecular Biology or Gene Therapy OR Either: Experience within industry or similar, with study management and client management. Preferred: An in-depth understanding of health and safety policies and a good understanding of GLP/GCP regulatory guidelines. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
Aug 02, 2022
Full time
About LabCorp Drug Development: As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role: Our largest UK site in Harrogate, is currently recruiting for a QC Scientist to join the Molecular Biology CMC team. Within the CMC business unit; the Molecular Biology department is dedicated to the development, validation and execution of molecular techniques, such as QPCR, RTqPCR and Digital PCR to support Cell Therapies, Gene Therapies and Vaccines . We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role within the Molecular Biology department is a senior scientist position. You will provide technical and regulatory oversight for clinical and pre-clinical studies; executed by the laboratory QC Analyst team in a GLP & GCP environment. Alternative terminologies for QC Scientist include Study Manager, Principal Investigator, Contributing Scientist and Study Director . Job Responsibilities: Acting as the scientific lead in one or more of the following analytical techniques: qPCR, RTqPCR, Digital PCR,and Nucleic Acid Extractions. Supporting client projects including biodistribution, persistence & shedding studies and clinical trials for Cell Therapies, Gene Therapies and Vaccines. Designing method development and validation strategies. Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. Perform regulatory compliance checks and maintain regulatory oversight during study execution. Lead technical or regulatory investigations when required throughout the conduct of a project. Training, mentoring and coaching of laboratory analysts and other team members. What Labcorp Drug Development can offer you: A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information: Position includes a 6-month onboarding & probationary period during which working hours are 8:45am - 5pm, based at our site in Harrogate. Following the initial onboarding period; you will move to one of the following shift patterns 6:00am - 2:15pm or 8:45am - 5:00pm. Currently we are recruiting for 6:00am - 2:15pm shift. The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. Education/Qualifications: Required: Scientific degree (BSc / MSc / PhD or equivalent). Experience: Required: Able to communicate effectively at all levels with internal employees and external clients, with theability to get things done by influencing others. Required: Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes. Either: Technical expertise in at least one of the following scientific disciplines: qPCR or DNA extraction within Molecular Biology or Gene Therapy OR Either: Experience within industry or similar, with study management and client management. Preferred: An in-depth understanding of health and safety policies and a good understanding of GLP/GCP regulatory guidelines. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
About LabCorp Drug Development: As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role: Our largest UK site in Harrogate, is currently recruiting for a QC Scientist to join the Molecular Biology CMC team. Within the CMC business unit; the Molecular Biology department is dedicated to the development, validation and execution of molecular techniques, such as QPCR, RTqPCR and Digital PCR to support Cell Therapies, Gene Therapies and Vaccines . We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role within the Molecular Biology department is a senior scientist position. You will provide technical and regulatory oversight for clinical and pre-clinical studies; executed by the laboratory QC Analyst team in a GLP & GCP environment. Alternative terminologies for QC Scientist include Study Manager, Principal Investigator, Contributing Scientist and Study Director . Job Responsibilities: Acting as the scientific lead in one or more of the following analytical techniques: qPCR, RTqPCR, Digital PCR,and Nucleic Acid Extractions. Supporting client projects including biodistribution, persistence & shedding studies and clinical trials for Cell Therapies, Gene Therapies and Vaccines. Designing method development and validation strategies. Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. Perform regulatory compliance checks and maintain regulatory oversight during study execution. Lead technical or regulatory investigations when required throughout the conduct of a project. Training, mentoring and coaching of laboratory analysts and other team members. What Labcorp Drug Development can offer you: A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information: Position includes a 6-month onboarding & probationary period during which working hours are 8:45am - 5pm, based at our site in Harrogate. Following the initial onboarding period; you will move to one of the following shift patterns 6:00am - 2:15pm or 8:45am - 5:00pm. The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. Education/Experience: Required: Scientific degree (BSc / MSc / PhD or equivalent). Required: Able to communicate effectively at all levels with internal employees and external clients, with theability to get things done by influencing others. Required: Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes. Either: Technical expertise in at least one of the following scientific disciplines: qPCR or DNA extraction within Molecular Biology or Gene Therapy Either: Experience within industry or similar, with study management and client management. Preferred: An in-depth understanding of health and safety policies and a good understanding of GLP/GCP regulatory guidelines. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
Aug 02, 2022
Full time
About LabCorp Drug Development: As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. The Role: Our largest UK site in Harrogate, is currently recruiting for a QC Scientist to join the Molecular Biology CMC team. Within the CMC business unit; the Molecular Biology department is dedicated to the development, validation and execution of molecular techniques, such as QPCR, RTqPCR and Digital PCR to support Cell Therapies, Gene Therapies and Vaccines . We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market. The QC Scientist role within the Molecular Biology department is a senior scientist position. You will provide technical and regulatory oversight for clinical and pre-clinical studies; executed by the laboratory QC Analyst team in a GLP & GCP environment. Alternative terminologies for QC Scientist include Study Manager, Principal Investigator, Contributing Scientist and Study Director . Job Responsibilities: Acting as the scientific lead in one or more of the following analytical techniques: qPCR, RTqPCR, Digital PCR,and Nucleic Acid Extractions. Supporting client projects including biodistribution, persistence & shedding studies and clinical trials for Cell Therapies, Gene Therapies and Vaccines. Designing method development and validation strategies. Performing technical appraisal of analytical data against acceptance criteria and study parameters for reporting to the client. Perform regulatory compliance checks and maintain regulatory oversight during study execution. Lead technical or regulatory investigations when required throughout the conduct of a project. Training, mentoring and coaching of laboratory analysts and other team members. What Labcorp Drug Development can offer you: A comprehensive onboarding training plan covering laboratory, technical and regulatory training packages. Unsurpassed career development opportunities, with the ability to develop your technical and managerial skills. Ability to work with a variety of different clients on wide ranging projects. Competitive salaries and a comprehensive benefits package including health cover and contributory pension. Key Information: Position includes a 6-month onboarding & probationary period during which working hours are 8:45am - 5pm, based at our site in Harrogate. Following the initial onboarding period; you will move to one of the following shift patterns 6:00am - 2:15pm or 8:45am - 5:00pm. The role incorporates both office working and laboratory based activities, with the flexibility to work both on site and at home. Education/Experience: Required: Scientific degree (BSc / MSc / PhD or equivalent). Required: Able to communicate effectively at all levels with internal employees and external clients, with theability to get things done by influencing others. Required: Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes. Either: Technical expertise in at least one of the following scientific disciplines: qPCR or DNA extraction within Molecular Biology or Gene Therapy Either: Experience within industry or similar, with study management and client management. Preferred: An in-depth understanding of health and safety policies and a good understanding of GLP/GCP regulatory guidelines. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
Randstad Construction, Property and Engineering
Queenborough, Kent
Are you an experienced Quality Control Analyst? Are you looking for your next position in an exciting Pharma development company? My client, a leading Pharma development business has an exciting opportunity for a Senior QC Analyst to join their team in Kent. As Senior QC Analyst, you will: Testing raw materials, in-process, finished product and stability samples Ensure that the production schedules are met. Liaise with production management, quality, planning and technical to ensure that the needs of customers are identified and satisfied to high standards Ensure all activities are performed in compliance with customer and ICH procedures To be considered for the role of Senior QC Analyst, you'll: Educated to degree level in a scientific field Significant experience in a pharmaceutical laboratory environment and cGMP requirements Proven experience/ skill with HPLC, GV, UV, FTIR and Dissolution Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Dec 08, 2021
Full time
Are you an experienced Quality Control Analyst? Are you looking for your next position in an exciting Pharma development company? My client, a leading Pharma development business has an exciting opportunity for a Senior QC Analyst to join their team in Kent. As Senior QC Analyst, you will: Testing raw materials, in-process, finished product and stability samples Ensure that the production schedules are met. Liaise with production management, quality, planning and technical to ensure that the needs of customers are identified and satisfied to high standards Ensure all activities are performed in compliance with customer and ICH procedures To be considered for the role of Senior QC Analyst, you'll: Educated to degree level in a scientific field Significant experience in a pharmaceutical laboratory environment and cGMP requirements Proven experience/ skill with HPLC, GV, UV, FTIR and Dissolution Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Job Title: Quality Control Officer Location: Lytham, Salary: £19,000 - £23,000 D.O.E Job type: Full time VetPlus is a privately held company based in Lytham. Within the group are ten limited companies, each operating as stand-alone entities. We specialise in the manufacture and sales of animal health and nutrition products for farm and companion animals, including veterinary and equine products. We are currently the 2nd biggest manufacturer of Veterinary Nutraceuticals in the world. In addition, we currently distribute to 40 countries in the world and looking to increase this to 80 in the next 5 years. A great opportunity to join a successful quality team within a global company that distributes to over 40 countries worldwide has arisen due to an internal promotion. The Role As the QC Officer you will provide quality control support to the production team and assist with the maintenance of quality documentation and GMP compliance. Main duties (but not limited to): Sample raw materials, submit samples to the lab for analysis, review results reports and release stock in accordance with written procedures. Sample, check and release packaging for use in production in accordance with written procedures. Provide production personnel with all required manufacturing documentation, batch numbers, expiry dates and fill weights, and ensure production documentation is accurately completed. Perform documented systematic production checks (start-up, on-line, release and cleaning) to ensure compliance to manufacturing processes, specifications, procedures and GMP. Submit samples of bulk, intermediate and/or finished product to the lab for analysis, review results reports and release stock in accordance with written procedures. Inform the Group Quality Manager when raw materials, bulk, intermediate or finished products fail to meet specification and provide assistance with investigations and rejections. Complete daily transfer sheets for bulk, intermediate and finished products. Input batch details on artwork and print the associated labels for production. * Perform pallet checking for palletised finished product orders. Provide assistance with generating the batch record packs for QP licensed product release. Ensure retains of raw materials, bulk and finished products are appropriately logged and retained. Perform batch reconciliation for each completed batch of finished product. Assist the Senior Quality Officer with validation and stability study requirements. Assist the QA Officer in the review and assessment of returned products. Assist with the submission of analytical test requests such as retesting or micro surveillance. The Candidate: Either a Science degree or 2 years quality control experience. Good interpersonal skills. Excellent time management. High attention to detail. Ideally we are looking for someone with relevant QC experience that is looking to develop their career within a dedicated and successful quality team. Please click on the APPLY button to send your CV and Cover Letter for this role. Candidates with the relevant experience or job titles of; Lab Assistant, Laboratory Assistant, Scientific Assistant, Science Assistant, Lab Administrator, Administrative Support, Laboratory Support, Lab Support, Administrator, Laboratory Engineer, Lab Technician, Laboratory Tech, Lab Tech, Lab Analyst, Graduate Science Technician, Team Leader, Quality Supervisor, Supervisor, Coordinator, Stock Controller, Inventory Management, Stock Movement Coordinator, Inventory Controller, Quality Controller, Stock Preparation Supervisor, Stock Control Supervisor, Senior Stock Controller may also be considered for this role.
Dec 05, 2021
Full time
Job Title: Quality Control Officer Location: Lytham, Salary: £19,000 - £23,000 D.O.E Job type: Full time VetPlus is a privately held company based in Lytham. Within the group are ten limited companies, each operating as stand-alone entities. We specialise in the manufacture and sales of animal health and nutrition products for farm and companion animals, including veterinary and equine products. We are currently the 2nd biggest manufacturer of Veterinary Nutraceuticals in the world. In addition, we currently distribute to 40 countries in the world and looking to increase this to 80 in the next 5 years. A great opportunity to join a successful quality team within a global company that distributes to over 40 countries worldwide has arisen due to an internal promotion. The Role As the QC Officer you will provide quality control support to the production team and assist with the maintenance of quality documentation and GMP compliance. Main duties (but not limited to): Sample raw materials, submit samples to the lab for analysis, review results reports and release stock in accordance with written procedures. Sample, check and release packaging for use in production in accordance with written procedures. Provide production personnel with all required manufacturing documentation, batch numbers, expiry dates and fill weights, and ensure production documentation is accurately completed. Perform documented systematic production checks (start-up, on-line, release and cleaning) to ensure compliance to manufacturing processes, specifications, procedures and GMP. Submit samples of bulk, intermediate and/or finished product to the lab for analysis, review results reports and release stock in accordance with written procedures. Inform the Group Quality Manager when raw materials, bulk, intermediate or finished products fail to meet specification and provide assistance with investigations and rejections. Complete daily transfer sheets for bulk, intermediate and finished products. Input batch details on artwork and print the associated labels for production. * Perform pallet checking for palletised finished product orders. Provide assistance with generating the batch record packs for QP licensed product release. Ensure retains of raw materials, bulk and finished products are appropriately logged and retained. Perform batch reconciliation for each completed batch of finished product. Assist the Senior Quality Officer with validation and stability study requirements. Assist the QA Officer in the review and assessment of returned products. Assist with the submission of analytical test requests such as retesting or micro surveillance. The Candidate: Either a Science degree or 2 years quality control experience. Good interpersonal skills. Excellent time management. High attention to detail. Ideally we are looking for someone with relevant QC experience that is looking to develop their career within a dedicated and successful quality team. Please click on the APPLY button to send your CV and Cover Letter for this role. Candidates with the relevant experience or job titles of; Lab Assistant, Laboratory Assistant, Scientific Assistant, Science Assistant, Lab Administrator, Administrative Support, Laboratory Support, Lab Support, Administrator, Laboratory Engineer, Lab Technician, Laboratory Tech, Lab Tech, Lab Analyst, Graduate Science Technician, Team Leader, Quality Supervisor, Supervisor, Coordinator, Stock Controller, Inventory Management, Stock Movement Coordinator, Inventory Controller, Quality Controller, Stock Preparation Supervisor, Stock Control Supervisor, Senior Stock Controller may also be considered for this role.
Scientist I - Ethical Testing Lab - Fixed-Term and Permanent Contracts available Daresbury, Cheshire If you have experience of working in a regulatory laboratory environment, this is an incredible opportunity to help accelerate the world's transition to 100% animal-free testing. About Us We're XCellR8, an award-winning organisation that is dedicated to developing animal-free testing solutions for the cosmetics and chemical industries. We're committed to Xcellence, being Xtraordinary, Xemplary and going the Xtra mile to achieve outstanding results. We are now seeking a Scientist I to join us at the prestigious National Innovation Campus at Sci-Tech Daresbury and support the day-to-day scientific activities of our laboratory. The Benefits - 25 days' holiday per year - Company pension - Personal development plans and regular appraisals - Access to high-quality training and development - Time devoted to supporting corporate charity efforts - Team nights out and celebrations - Wellbeing initiatives including free fruit in the office Born from a great idea and a passion for animal welfare, XCellR8 has become a world leader in our field and we're constantly pushing boundaries to find animal-free, cutting-edge testing solutions. We provide the ideal environment in which to progress your scientific career. With a reputation for our innovative approach, we have a Good Laboratory Practice certification, as well as a number of awards for our pioneering work. Here, you will have the chance to help develop exciting new scientific techniques, work with some of the world's top cosmetic brands and help to protect human safety. So, if you want to contribute to important work that's providing a more ethical and scientifically advanced alternative to animal testing, we want to hear from you. The Role As a Scientist I, you will carry out animal-free studies in order to demonstrate the safety and efficacy of test items. Working closely with Senior Scientists, QA and other team members, you'll contribute to the research and development of new test methods and provide routine maintenance of both human cell cultures and the XCellR8 lab. You will also: - Process, analyse and communicate the results and data from experiments conducted - Perform QC checks on reports - Work within the GLP regulatory framework - Undertake ongoing training in the appropriate theoretical and practical skills to support the role - Contribute to the review, update and creation of controlled documents, including SOPs, IPs and Forms - Keep up to date with the work of other scientists both internally and externally through regular reading/research and conference attendance in order to support innovation at XCellR8 About You To join us as a Scientist I, you will need: - A degree (or equivalent) in a Life Science subject, with additional prior laboratory experience - To be committed to the development and implementation of in vitro alternatives to animal testing - To work to the requirements of Good Laboratory Practice (GLP) and Good Documentation Practice (GDP) - Proficiency in MS Office applications including Microsoft Excel - To be an analytical thinker who can manage priorities, problem-solve and deliver actions - To be highly detail oriented, able to work autonomously and able to manage multiple tasks and tight deadlines with confidence and ease Although not essential, experience in cell culture, flow cytometry, High Performance Liquid Chromatography (HPLC), and/or assays would be beneficial to your application. Other organisations may call this role Laboratory Scientist, Lab Scientist, Lab Technician, Life Scientist, Life Science Technician, Laboratory Analyst, or Human Cell Culture Scientist. Webrecruit and XCellR8 are equal opportunities employers, value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be. So, if you're seeking your next challenge as a Scientist I, please apply via the button shown. This vacancy is being advertised by Webrecruit. The services advertised by Webrecruit are those of an Employment Agency.
Dec 05, 2021
Full time
Scientist I - Ethical Testing Lab - Fixed-Term and Permanent Contracts available Daresbury, Cheshire If you have experience of working in a regulatory laboratory environment, this is an incredible opportunity to help accelerate the world's transition to 100% animal-free testing. About Us We're XCellR8, an award-winning organisation that is dedicated to developing animal-free testing solutions for the cosmetics and chemical industries. We're committed to Xcellence, being Xtraordinary, Xemplary and going the Xtra mile to achieve outstanding results. We are now seeking a Scientist I to join us at the prestigious National Innovation Campus at Sci-Tech Daresbury and support the day-to-day scientific activities of our laboratory. The Benefits - 25 days' holiday per year - Company pension - Personal development plans and regular appraisals - Access to high-quality training and development - Time devoted to supporting corporate charity efforts - Team nights out and celebrations - Wellbeing initiatives including free fruit in the office Born from a great idea and a passion for animal welfare, XCellR8 has become a world leader in our field and we're constantly pushing boundaries to find animal-free, cutting-edge testing solutions. We provide the ideal environment in which to progress your scientific career. With a reputation for our innovative approach, we have a Good Laboratory Practice certification, as well as a number of awards for our pioneering work. Here, you will have the chance to help develop exciting new scientific techniques, work with some of the world's top cosmetic brands and help to protect human safety. So, if you want to contribute to important work that's providing a more ethical and scientifically advanced alternative to animal testing, we want to hear from you. The Role As a Scientist I, you will carry out animal-free studies in order to demonstrate the safety and efficacy of test items. Working closely with Senior Scientists, QA and other team members, you'll contribute to the research and development of new test methods and provide routine maintenance of both human cell cultures and the XCellR8 lab. You will also: - Process, analyse and communicate the results and data from experiments conducted - Perform QC checks on reports - Work within the GLP regulatory framework - Undertake ongoing training in the appropriate theoretical and practical skills to support the role - Contribute to the review, update and creation of controlled documents, including SOPs, IPs and Forms - Keep up to date with the work of other scientists both internally and externally through regular reading/research and conference attendance in order to support innovation at XCellR8 About You To join us as a Scientist I, you will need: - A degree (or equivalent) in a Life Science subject, with additional prior laboratory experience - To be committed to the development and implementation of in vitro alternatives to animal testing - To work to the requirements of Good Laboratory Practice (GLP) and Good Documentation Practice (GDP) - Proficiency in MS Office applications including Microsoft Excel - To be an analytical thinker who can manage priorities, problem-solve and deliver actions - To be highly detail oriented, able to work autonomously and able to manage multiple tasks and tight deadlines with confidence and ease Although not essential, experience in cell culture, flow cytometry, High Performance Liquid Chromatography (HPLC), and/or assays would be beneficial to your application. Other organisations may call this role Laboratory Scientist, Lab Scientist, Lab Technician, Life Scientist, Life Science Technician, Laboratory Analyst, or Human Cell Culture Scientist. Webrecruit and XCellR8 are equal opportunities employers, value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be. So, if you're seeking your next challenge as a Scientist I, please apply via the button shown. This vacancy is being advertised by Webrecruit. The services advertised by Webrecruit are those of an Employment Agency.
Kenton Black Science & Engineering
Bury St. Edmunds, Suffolk
Analytical Specialist (AH046) Location: Bury St Edmunds, Suffolk £28K - £45K Basic (dependent upon experience) + 25 Days Holiday + Pension + Benefits We are currently partnering with an incredibly successful environmental testing company who pride themselves on providing outstanding customer service. Part of a huge group, they are a global business who operate in many countries and, as such, are incredibly well respected in their sector. A multi-million pound turnover business with multiple laboratories across the UK, they are now looking to recruit an Analytical Specialist into their Technical team to be a subject matter expert for chromatography instrumentation - namely GC-MS(/MS), GC-FID and/or HPLC. Role Responsibilities: As an Analytical Specialist, you will be responsible for: • Maintaining a multitude of instrumentation in the lab including GC-MS(/MS), GC-FID and HPLC • Advanced preventative maintenance and troubleshooting of instrumentation • Training and developing Analysts in analysis and equipment troubleshooting • Developing analytical methods from scratch for new sample types • Method troubleshooting and optimisation for existing methods • Method validation to UKAS guidelines • Troubleshooting of chromatograms (split peaks, missing peaks, ghost peaks etc) • Providing technical expertise to senior management. Role Requirements: To be considered for this role, candidates will be degree-level qualified in Chemistry or a closely related subject, with proven significant industrial experience with GC, GC-FID, GC-MS(/MS) or HPLC. You will need to have experience in method development, optimisation and validation; with prior experience training Analysts being a bonus. You must be organised to manage multiple projects, with the desire and motivation to develop the careers of those working in your team. Keywords: GC, Gas Chromatography, GC-MS, GC-MS/MS, GC-FID, HPLC, Liquid Chromatography, UKAS, ISO17025, ISO9001, Method Development, Method Optimisation, Method Troubleshooting, Method Validation, Instrument Troubleshooting, Instrument Maintenance, Senior Analyst, QC, Quality Control, Chemist, QC Analyst, Quality Control Analyst, Lab Analyst, Laboratory Analyst, QC Chemist, Quality Control Chemist, Analytical Chemist, QC Analyst, Lab Analyst, Laboratory Analyst, Analytical Chemist, Analytical Testing, Environmental Testing, Environmental Services, Organic Chemistry, Organic Testing, Soils, Waters, Chemistry.
Dec 04, 2021
Full time
Analytical Specialist (AH046) Location: Bury St Edmunds, Suffolk £28K - £45K Basic (dependent upon experience) + 25 Days Holiday + Pension + Benefits We are currently partnering with an incredibly successful environmental testing company who pride themselves on providing outstanding customer service. Part of a huge group, they are a global business who operate in many countries and, as such, are incredibly well respected in their sector. A multi-million pound turnover business with multiple laboratories across the UK, they are now looking to recruit an Analytical Specialist into their Technical team to be a subject matter expert for chromatography instrumentation - namely GC-MS(/MS), GC-FID and/or HPLC. Role Responsibilities: As an Analytical Specialist, you will be responsible for: • Maintaining a multitude of instrumentation in the lab including GC-MS(/MS), GC-FID and HPLC • Advanced preventative maintenance and troubleshooting of instrumentation • Training and developing Analysts in analysis and equipment troubleshooting • Developing analytical methods from scratch for new sample types • Method troubleshooting and optimisation for existing methods • Method validation to UKAS guidelines • Troubleshooting of chromatograms (split peaks, missing peaks, ghost peaks etc) • Providing technical expertise to senior management. Role Requirements: To be considered for this role, candidates will be degree-level qualified in Chemistry or a closely related subject, with proven significant industrial experience with GC, GC-FID, GC-MS(/MS) or HPLC. You will need to have experience in method development, optimisation and validation; with prior experience training Analysts being a bonus. You must be organised to manage multiple projects, with the desire and motivation to develop the careers of those working in your team. Keywords: GC, Gas Chromatography, GC-MS, GC-MS/MS, GC-FID, HPLC, Liquid Chromatography, UKAS, ISO17025, ISO9001, Method Development, Method Optimisation, Method Troubleshooting, Method Validation, Instrument Troubleshooting, Instrument Maintenance, Senior Analyst, QC, Quality Control, Chemist, QC Analyst, Quality Control Analyst, Lab Analyst, Laboratory Analyst, QC Chemist, Quality Control Chemist, Analytical Chemist, QC Analyst, Lab Analyst, Laboratory Analyst, Analytical Chemist, Analytical Testing, Environmental Testing, Environmental Services, Organic Chemistry, Organic Testing, Soils, Waters, Chemistry.
Senior Development Analyst - Pharmaceuticals A pharmaceutical contract testing company are recruiting for various positions from entry level lab technician through to Senior Development Analyst to join their fast paced lab in West Yorkshire Working in the Analytical Laboratory you will be responsible for processing of pharmaceutical samples and testing using a wide range of analytical techniques in a GMP regulated environment Responsibilities Analytical testing of raw materials and finished products using UV-vis, FTIR, particle size Raising any none-conformances, out of trend or out of spec results and assist with any subsequent investigations Develop Analytical methods from scratch in accordance with ICH guidelines Ensure the laboratory is kept to a GMP standard, ensuring any equipment is calibrated and operating correctly Requirements BSc or equivalent in Chemistry or a related field Demonstrable experience of HPLC, GC, UV-Vis and other analytical techniques Prior experience working in GMP conditions is an advantage Interviews for this Senior QC Analyst position are imminent so please apply now or contact Gareth Gooley at Science Solutions for further information.
Dec 04, 2021
Full time
Senior Development Analyst - Pharmaceuticals A pharmaceutical contract testing company are recruiting for various positions from entry level lab technician through to Senior Development Analyst to join their fast paced lab in West Yorkshire Working in the Analytical Laboratory you will be responsible for processing of pharmaceutical samples and testing using a wide range of analytical techniques in a GMP regulated environment Responsibilities Analytical testing of raw materials and finished products using UV-vis, FTIR, particle size Raising any none-conformances, out of trend or out of spec results and assist with any subsequent investigations Develop Analytical methods from scratch in accordance with ICH guidelines Ensure the laboratory is kept to a GMP standard, ensuring any equipment is calibrated and operating correctly Requirements BSc or equivalent in Chemistry or a related field Demonstrable experience of HPLC, GC, UV-Vis and other analytical techniques Prior experience working in GMP conditions is an advantage Interviews for this Senior QC Analyst position are imminent so please apply now or contact Gareth Gooley at Science Solutions for further information.
Senior QC Analyst - Pharmaceuticals A pharmaceutical CDMO in the North East are currently looking for a Senior QC Analyst to join their team, you will be responsible for testing raw materials and finished products using HPLC, GC and other analytical techniques offering a valuable opportunity to either start or continue a career within Pharmaceuticals. As a Senior QC Analyst you will have experience with analytical techniques including HPLC, GC, UV-Vis and more, you will also need to be familiar with GMP conditions and how a pharmaceutical QC lab operates. Responsibilities Analytical testing of raw materials and finished products using HPLC, GC and more Raising any none-conformances, out of trend or out of spec results and assist with any subsequent investigations Ensure the laboratory is kept to a GMP standard, ensuring any equipment is calibrated and operating correctly Requirements BSc or equivalent in Chemistry or a related field Demonstrable experience of HPLC, GC, UV-Vis and other analytical techniques Prior experience working in GMP conditions is an advantage Interviews for this Senior QC Analyst position are imminent so please apply now or contact Gareth Gooley at Science Solutions for further information.
Dec 04, 2021
Full time
Senior QC Analyst - Pharmaceuticals A pharmaceutical CDMO in the North East are currently looking for a Senior QC Analyst to join their team, you will be responsible for testing raw materials and finished products using HPLC, GC and other analytical techniques offering a valuable opportunity to either start or continue a career within Pharmaceuticals. As a Senior QC Analyst you will have experience with analytical techniques including HPLC, GC, UV-Vis and more, you will also need to be familiar with GMP conditions and how a pharmaceutical QC lab operates. Responsibilities Analytical testing of raw materials and finished products using HPLC, GC and more Raising any none-conformances, out of trend or out of spec results and assist with any subsequent investigations Ensure the laboratory is kept to a GMP standard, ensuring any equipment is calibrated and operating correctly Requirements BSc or equivalent in Chemistry or a related field Demonstrable experience of HPLC, GC, UV-Vis and other analytical techniques Prior experience working in GMP conditions is an advantage Interviews for this Senior QC Analyst position are imminent so please apply now or contact Gareth Gooley at Science Solutions for further information.
Kenton Black Science & Engineering
Canterbury, Kent
Senior Analyst (AH041) Location: Canterbury, Kent £30K - £34K (dependent upon experience) + Share Incentives + Bonus + 25 Days Holiday + Bank Holidays The Company: Our client is an incredibly successful contract research organisation (CRO) based near Canterbury who develop and manufacture a huge range of products, spanning from additives to petrochemicals to APIs. Part of a bigger group, they are a global business who operate in many countries and, as such, are incredibly well respected in their sector. A multi-million pound turnover business with multiple sites across the UK and internationally, they are now looking to recruit a Senior Analyst into the team to support projects across both the GLP contract research and GMP API manufacturing facilities. There are clear, defined progression paths for Senior Analysts in this company with opportunities to move into management opportunities - with >50% of their Senior Managers coming from internal promotions! The Role: As a Senior Analyst, you will be responsible for: • Developing new, optimising existing and validating chromatographic methods • Changing columns or troubleshooting the HPLC instrumentation to clear blockages etc • Interpreting HPLC chromatograms to identify any issues, and ascertaining where the error lies to remedy the issue • Performing quality control testing of a variety of raw materials, chemical intermediates and finished products • Using a wide range of testing techniques including HPLC, UPLC, NMR, GC and wet chemistry • Ensuring that strict cGMP/GLP compliance is adhered to in the laboratory • Completing analytical reports and other subsequent documentation. The Person: To be considered for this role, candidates will be degree-level qualified in Chemistry or a closely related subject, with proven analytical experience in a cGMP regulated environment. You must possess significant experience in method development/optimisation and troubleshooting issues with HPLC instrumentation. You must be self-motivated and highly organised to manage multiple projects, with a keen desire to obtain a role in a leading specialist organisation. Keywords: Method Development, Developing Methods, Method Optimisation, Optimising Methods, Method Troubleshooting, Troubleshooting Methods, Method Validation, Validating Methods, API, Active Pharmaceutical Ingredient, Raw Materials, Chemical Intermediates, Finished Products, UPLC, HPLC, GC-MS, HPLC Troubleshooting, Chromatogram Analysis, GMP, GLP, Senior Analyst, Senior Analytical Chemist, QC, Quality Control, Chemist, QC Analyst, QC Chemist, Pharmaceuticals.
Dec 04, 2021
Full time
Senior Analyst (AH041) Location: Canterbury, Kent £30K - £34K (dependent upon experience) + Share Incentives + Bonus + 25 Days Holiday + Bank Holidays The Company: Our client is an incredibly successful contract research organisation (CRO) based near Canterbury who develop and manufacture a huge range of products, spanning from additives to petrochemicals to APIs. Part of a bigger group, they are a global business who operate in many countries and, as such, are incredibly well respected in their sector. A multi-million pound turnover business with multiple sites across the UK and internationally, they are now looking to recruit a Senior Analyst into the team to support projects across both the GLP contract research and GMP API manufacturing facilities. There are clear, defined progression paths for Senior Analysts in this company with opportunities to move into management opportunities - with >50% of their Senior Managers coming from internal promotions! The Role: As a Senior Analyst, you will be responsible for: • Developing new, optimising existing and validating chromatographic methods • Changing columns or troubleshooting the HPLC instrumentation to clear blockages etc • Interpreting HPLC chromatograms to identify any issues, and ascertaining where the error lies to remedy the issue • Performing quality control testing of a variety of raw materials, chemical intermediates and finished products • Using a wide range of testing techniques including HPLC, UPLC, NMR, GC and wet chemistry • Ensuring that strict cGMP/GLP compliance is adhered to in the laboratory • Completing analytical reports and other subsequent documentation. The Person: To be considered for this role, candidates will be degree-level qualified in Chemistry or a closely related subject, with proven analytical experience in a cGMP regulated environment. You must possess significant experience in method development/optimisation and troubleshooting issues with HPLC instrumentation. You must be self-motivated and highly organised to manage multiple projects, with a keen desire to obtain a role in a leading specialist organisation. Keywords: Method Development, Developing Methods, Method Optimisation, Optimising Methods, Method Troubleshooting, Troubleshooting Methods, Method Validation, Validating Methods, API, Active Pharmaceutical Ingredient, Raw Materials, Chemical Intermediates, Finished Products, UPLC, HPLC, GC-MS, HPLC Troubleshooting, Chromatogram Analysis, GMP, GLP, Senior Analyst, Senior Analytical Chemist, QC, Quality Control, Chemist, QC Analyst, QC Chemist, Pharmaceuticals.
A Biopharmaceutical company who develop and manufacture life saving biopharmaceutical therapeutics and vaccines on a global basis are looking to strengthen their Quality Control department based in the South West of England and are recruiting a Senior QC Analyst. Responsibilities of the role:- You will have responsibility to undertake and supervise chemical and biochemical analyses to support the manufacture of the clients licensed products. You will be responsible for writing SOPs and their associated risk assessments, writing quality records such as non-conformances, investigations, CAPAs and change controls. You will supervise and train QC staff and monitor compliance within QC Analytical and develop strategies to continually improve systems. The interviews for the role are imminent so please apply or contact Natalie for a further discussion on the role.
Dec 03, 2021
Full time
A Biopharmaceutical company who develop and manufacture life saving biopharmaceutical therapeutics and vaccines on a global basis are looking to strengthen their Quality Control department based in the South West of England and are recruiting a Senior QC Analyst. Responsibilities of the role:- You will have responsibility to undertake and supervise chemical and biochemical analyses to support the manufacture of the clients licensed products. You will be responsible for writing SOPs and their associated risk assessments, writing quality records such as non-conformances, investigations, CAPAs and change controls. You will supervise and train QC staff and monitor compliance within QC Analytical and develop strategies to continually improve systems. The interviews for the role are imminent so please apply or contact Natalie for a further discussion on the role.
As a Senior QC Analyst you will be responsible for supervising a team of analysts performing QC analysis for the business. You will be involved in escalation processes along with additional supporting QC related functions. *Client Details* As a Senior QC Analyst you will be responsible for supervising a team of analysts performing QC analysis for the business. You will be involved in escalation processes along with additional supporting QC related functions. *Description* As a Senior QC Analyst you will be responsible for: * Conforming to GMP to ensure compliance to UK, EU and other appropriate regulations * To coordinate with the QC Manager and other Senior Analysts * Prepare method transfer protocol, stability protocol and report * Leading a team of analysts and to plan daily and weekly workloads, ensuring production and testing schedules are met * Prepare and review of SOPs, validation protocols & reports * To check analytically reports, notebooks and documents to ensure that all testing has been performed correctly and that data has been reported correctly and accurately * To provide technical support, guidance and training to QC team members regarding Chemical and Instrument analysis * To perform trouble shooting as appropriate to ensure all equipment is functioning and working as necessary * To investigate any OOS or OOC results to ensure appropriate root cause * To ensure that training has been provided and approved prior to any analyst performs formal analysis on raw materials, intermediates, finished products and stability samples *Profile* As the successful candidate you will have experience with: * Operation of instruments such HPLC (essential) GC, UV, IR Dissolution or other in a pharmaceutical GMP environment * Significant experience of raw material testing, finished product testing, in process testing, packaging material sampling and testing * Minimum 5 years working in Quality Control and/or Analytical Development department in industry * Experience of working in the pharmaceutical industry for approximately 10 years (desirable) *Job Offer* The company are offering a fantastic package in an exciting and dynamic environment, with opportunities to develop moving forward as they continue on their ambitious growth plan.
Dec 03, 2021
Full time
As a Senior QC Analyst you will be responsible for supervising a team of analysts performing QC analysis for the business. You will be involved in escalation processes along with additional supporting QC related functions. *Client Details* As a Senior QC Analyst you will be responsible for supervising a team of analysts performing QC analysis for the business. You will be involved in escalation processes along with additional supporting QC related functions. *Description* As a Senior QC Analyst you will be responsible for: * Conforming to GMP to ensure compliance to UK, EU and other appropriate regulations * To coordinate with the QC Manager and other Senior Analysts * Prepare method transfer protocol, stability protocol and report * Leading a team of analysts and to plan daily and weekly workloads, ensuring production and testing schedules are met * Prepare and review of SOPs, validation protocols & reports * To check analytically reports, notebooks and documents to ensure that all testing has been performed correctly and that data has been reported correctly and accurately * To provide technical support, guidance and training to QC team members regarding Chemical and Instrument analysis * To perform trouble shooting as appropriate to ensure all equipment is functioning and working as necessary * To investigate any OOS or OOC results to ensure appropriate root cause * To ensure that training has been provided and approved prior to any analyst performs formal analysis on raw materials, intermediates, finished products and stability samples *Profile* As the successful candidate you will have experience with: * Operation of instruments such HPLC (essential) GC, UV, IR Dissolution or other in a pharmaceutical GMP environment * Significant experience of raw material testing, finished product testing, in process testing, packaging material sampling and testing * Minimum 5 years working in Quality Control and/or Analytical Development department in industry * Experience of working in the pharmaceutical industry for approximately 10 years (desirable) *Job Offer* The company are offering a fantastic package in an exciting and dynamic environment, with opportunities to develop moving forward as they continue on their ambitious growth plan.