Customer Service Agent Location: Caerphilly (Office based) Duration: 12 months Pay rate: £13 per hour PAYE Hours: 37.5 hours per week (From 8-10am to 4-6pm flex) The company are seeking a highly skilled and dedicated Customer Service Agent to join our dynamic team. As a Customer Service Agent, you will play a crucial role in ensuring exceptional customer experiences and satisfaction. You will be responsible for handling customer inquiries, resolving issues, and providing accurate and timely information. The ideal candidate will possess excellent communication skills, a strong customer service orientation, and the ability to handle challenging situations with professionalism and empathy. Key Responsibilities: - Respond promptly and professionally to customer inquiries via various channels. - Provide accurate and comprehensive information to customers regarding products, services, policies, and procedures. - Identify and assess customer needs, effectively troubleshoot problems, and provide appropriate solutions or escalate issues to the appropriate department. - Process customer orders, returns, exchanges, and refunds in accordance with company policies and guidelines. - Maintain accurate and detailed records of customer interactions, transactions, inquiries, and complaints in the customer relationship management (CRM) system. - Collaborate with cross-functional teams to resolve complex customer issues and ensure timely resolution. - Proactively identify opportunities to improve customer satisfaction and provide feedback to the management team. - Stay up to date with product knowledge, industry trends, and company updates to effectively address customer inquiries and provide accurate information. - Adhere to established service level agreements (SLAs) and maintain a high level of professionalism, empathy, and courtesy in all customer interactions. - Contribute to a positive and collaborative team environment by actively participating in meetings, training sessions, and sharing knowledge and best practices with colleagues. Minimum Qualifications: - High school qualifications or equivalent -At least 1 year customer service experience - Proficient with Microsoft Office Suite software (Excel, Word, Access, and Outlook) - Experience using Customer Service software Preferred Qualifications: - Ability to interact professionally with others and work independently in a fast-paced environment - Prior experience utilizing a multi-line telephone system - Strong problem solving and interpersonal skills - Excellent verbal and written communication skills - Highly dependable team player - Ability to prioritize workload and complete responsibilities on time
Jun 16, 2025
Full time
Customer Service Agent Location: Caerphilly (Office based) Duration: 12 months Pay rate: £13 per hour PAYE Hours: 37.5 hours per week (From 8-10am to 4-6pm flex) The company are seeking a highly skilled and dedicated Customer Service Agent to join our dynamic team. As a Customer Service Agent, you will play a crucial role in ensuring exceptional customer experiences and satisfaction. You will be responsible for handling customer inquiries, resolving issues, and providing accurate and timely information. The ideal candidate will possess excellent communication skills, a strong customer service orientation, and the ability to handle challenging situations with professionalism and empathy. Key Responsibilities: - Respond promptly and professionally to customer inquiries via various channels. - Provide accurate and comprehensive information to customers regarding products, services, policies, and procedures. - Identify and assess customer needs, effectively troubleshoot problems, and provide appropriate solutions or escalate issues to the appropriate department. - Process customer orders, returns, exchanges, and refunds in accordance with company policies and guidelines. - Maintain accurate and detailed records of customer interactions, transactions, inquiries, and complaints in the customer relationship management (CRM) system. - Collaborate with cross-functional teams to resolve complex customer issues and ensure timely resolution. - Proactively identify opportunities to improve customer satisfaction and provide feedback to the management team. - Stay up to date with product knowledge, industry trends, and company updates to effectively address customer inquiries and provide accurate information. - Adhere to established service level agreements (SLAs) and maintain a high level of professionalism, empathy, and courtesy in all customer interactions. - Contribute to a positive and collaborative team environment by actively participating in meetings, training sessions, and sharing knowledge and best practices with colleagues. Minimum Qualifications: - High school qualifications or equivalent -At least 1 year customer service experience - Proficient with Microsoft Office Suite software (Excel, Word, Access, and Outlook) - Experience using Customer Service software Preferred Qualifications: - Ability to interact professionally with others and work independently in a fast-paced environment - Prior experience utilizing a multi-line telephone system - Strong problem solving and interpersonal skills - Excellent verbal and written communication skills - Highly dependable team player - Ability to prioritize workload and complete responsibilities on time
Data Centre Engineering Operations Technician 6 month contract £200 per day Onsite: Hemel Hempstead Key Skills: Operate and maintain mechanical and electrical equipment This engineering operations technician position serves as the on-site maintenance technician and operator for an AWS data centre. The Data Centre Engineering Operations Technician (EOT) is responsible for operating and maintaining all electrical, mechanical, emergency generator, and fire/life safety equipment within the data centre. The EOT serves as a technical resource to support within its data centres. Data centre equipment that supports mission-critical servers must maintain better than 99.999% uptime. EOT's are also tasked with driving innovation while reducing operational costs in the facilities. Key job responsibilities Responsibilities: - Operate and maintain mechanical and electrical equipment - Troubleshooting of facility and rack-level events within internal SLAs - Perform limited maintenance tasks to include: filter changes, HVAC PMs, rack power installs, rack PDU, and rack ATS replacements - Provide support to Data Centre Operations technicians - Perform root cause analysis of equipment failures - Ensure all safety procedures are adhered to while performing work - Take daily operational readings of all mechanical and electrical equipment through routine rounds/log taking (temperatures, voltages, currents, etc.) - Utilise internal CMMS to manage building workflows and spare part inventory - Supervise contractors who perform servicing or preventive maintenance - Respond to off hour emergency calls per on call rotation for any one of the region's sites - Fully comply with all physical security procedures and policies If you are interested please apply or send your CV to
Jun 16, 2025
Full time
Data Centre Engineering Operations Technician 6 month contract £200 per day Onsite: Hemel Hempstead Key Skills: Operate and maintain mechanical and electrical equipment This engineering operations technician position serves as the on-site maintenance technician and operator for an AWS data centre. The Data Centre Engineering Operations Technician (EOT) is responsible for operating and maintaining all electrical, mechanical, emergency generator, and fire/life safety equipment within the data centre. The EOT serves as a technical resource to support within its data centres. Data centre equipment that supports mission-critical servers must maintain better than 99.999% uptime. EOT's are also tasked with driving innovation while reducing operational costs in the facilities. Key job responsibilities Responsibilities: - Operate and maintain mechanical and electrical equipment - Troubleshooting of facility and rack-level events within internal SLAs - Perform limited maintenance tasks to include: filter changes, HVAC PMs, rack power installs, rack PDU, and rack ATS replacements - Provide support to Data Centre Operations technicians - Perform root cause analysis of equipment failures - Ensure all safety procedures are adhered to while performing work - Take daily operational readings of all mechanical and electrical equipment through routine rounds/log taking (temperatures, voltages, currents, etc.) - Utilise internal CMMS to manage building workflows and spare part inventory - Supervise contractors who perform servicing or preventive maintenance - Respond to off hour emergency calls per on call rotation for any one of the region's sites - Fully comply with all physical security procedures and policies If you are interested please apply or send your CV to
QC Microbiology - Sterility 6 month contract - £18 per hour Liverpool Cpl Life Sciences are recruiting for a QC Microbiologist to join a global pharmaceutical company that focusses on the development of vaccines, this is an excellent opportunity contributing to helping protect the lives of millions of people across the world. The main purpose of the Microbiologist is to perform sterility testing and method validation on microbiology assays. Experience; 1-2 years Microbiology experience in the pharmaceutical industry Sterility testing, method validation experience Prior use of Celsis instrument desirable Quality experience For more information please contact
Feb 01, 2024
Full time
QC Microbiology - Sterility 6 month contract - £18 per hour Liverpool Cpl Life Sciences are recruiting for a QC Microbiologist to join a global pharmaceutical company that focusses on the development of vaccines, this is an excellent opportunity contributing to helping protect the lives of millions of people across the world. The main purpose of the Microbiologist is to perform sterility testing and method validation on microbiology assays. Experience; 1-2 years Microbiology experience in the pharmaceutical industry Sterility testing, method validation experience Prior use of Celsis instrument desirable Quality experience For more information please contact
Clinical Scientific Expert Contract length: 6 months Rate : £15 - £19 p/h PAYE Location : Fully remote Do you have experience interpreting clinical data? Well, one of our pharma clients is looking for a candidate with an analytical mindset and great attention to detail to analyse and review data sets. Ideal candidates should be comfortable and confident assessing whether data is plausibly consistent and familiar with EDC systems and data visualisation tools. Responsibilities: Interpreting data and assessing data to check if it's plausibly consistent across an entire data set Checking clinical data is scientifically plausible Strong excel skills to check data sets Interpretation of clinical data Checking for inconsistencies or errors within large data sets Help contribute to the development of the data review plan, data review strategy & case report form Produce training materials Required : Familiarity with advanced functionality in excel, EDC systems & data visualisation tools Ability to appraise and review data from clinical perspective Analytical skills If you think you would be a suitable candidate, please reach out with your up to date CV to
Dec 15, 2022
Full time
Clinical Scientific Expert Contract length: 6 months Rate : £15 - £19 p/h PAYE Location : Fully remote Do you have experience interpreting clinical data? Well, one of our pharma clients is looking for a candidate with an analytical mindset and great attention to detail to analyse and review data sets. Ideal candidates should be comfortable and confident assessing whether data is plausibly consistent and familiar with EDC systems and data visualisation tools. Responsibilities: Interpreting data and assessing data to check if it's plausibly consistent across an entire data set Checking clinical data is scientifically plausible Strong excel skills to check data sets Interpretation of clinical data Checking for inconsistencies or errors within large data sets Help contribute to the development of the data review plan, data review strategy & case report form Produce training materials Required : Familiarity with advanced functionality in excel, EDC systems & data visualisation tools Ability to appraise and review data from clinical perspective Analytical skills If you think you would be a suitable candidate, please reach out with your up to date CV to
Senior Associate (part qualified) - Manchester - Hybrid working Salary £32,000 - £38,000 plus benefits Senior Associate required by a top accounting firm based in Manchester We have partnered with a team of finance professionals who deliver bespoke and standard finance solutions to clients on an insourced, outsourced or co-sourced basis. Skills and Experience Part qualified individuals who are progressing towards completion of ACA, ACCA, CIMA, CIPFA or other relevant qualification Operational finance experience including knowledge of finance processes e.g. OTC, PTP, OTC etc Financial management experience including forecasting, budgeting, management accounting, Financial reporting, statutory reporting Reporting to clients and/ or senior stakeholders with agility and ability to build relationships and rapport within a diverse team, collaborating, coaching and supporting others Good analytical skills, commercial aptitude and professionally sceptical mindset (ability to identify issues, understand complex problems, draw sound conclusions) Proven ability to manage time, prioritise tasks and work under pressure and to tight deadlines Proficiency in the use of spreadsheets and other finance tools About the role Finance Solutions consists of a team of accounting professionals at all levels providing operational delivery expertise for large execution programmes, such as finance transformation programmes, Accounts Payable/Accounts Receivable management, budgeting and forecasting, P&L review and KPI Development. Key responsibilities: Operational finance including: accounts payable, receivable management, bank reconciliations, general ledger accounting Management accounting - actuals, budgets and rolling forecasts Financial controlling including preparation, reconciliation and presentation of balance sheet reviews Assisting with period/ year end close processes Financial accounting - preparing financial statements under applicable Reporting Standards Collaborating with the client delivery teams in tasks and activities that span across operational finance and financial reporting Managing and coaching trainee accountants, finance assistants in their roles in delivery
Dec 12, 2022
Full time
Senior Associate (part qualified) - Manchester - Hybrid working Salary £32,000 - £38,000 plus benefits Senior Associate required by a top accounting firm based in Manchester We have partnered with a team of finance professionals who deliver bespoke and standard finance solutions to clients on an insourced, outsourced or co-sourced basis. Skills and Experience Part qualified individuals who are progressing towards completion of ACA, ACCA, CIMA, CIPFA or other relevant qualification Operational finance experience including knowledge of finance processes e.g. OTC, PTP, OTC etc Financial management experience including forecasting, budgeting, management accounting, Financial reporting, statutory reporting Reporting to clients and/ or senior stakeholders with agility and ability to build relationships and rapport within a diverse team, collaborating, coaching and supporting others Good analytical skills, commercial aptitude and professionally sceptical mindset (ability to identify issues, understand complex problems, draw sound conclusions) Proven ability to manage time, prioritise tasks and work under pressure and to tight deadlines Proficiency in the use of spreadsheets and other finance tools About the role Finance Solutions consists of a team of accounting professionals at all levels providing operational delivery expertise for large execution programmes, such as finance transformation programmes, Accounts Payable/Accounts Receivable management, budgeting and forecasting, P&L review and KPI Development. Key responsibilities: Operational finance including: accounts payable, receivable management, bank reconciliations, general ledger accounting Management accounting - actuals, budgets and rolling forecasts Financial controlling including preparation, reconciliation and presentation of balance sheet reviews Assisting with period/ year end close processes Financial accounting - preparing financial statements under applicable Reporting Standards Collaborating with the client delivery teams in tasks and activities that span across operational finance and financial reporting Managing and coaching trainee accountants, finance assistants in their roles in delivery
Our client a world leader in their imaging products, is currently looking to appoint an experienced Materials Administrator to join the team. As the Materials Administrator you will ensure the timely purchase and supply of parts predominantly driven by demand from the production schedule and place orders for any other goods required and approved by department/senior managers. To ensure that all core areas of the business adhere to the requirements of ISO9001:2015, the QMS, internal processes and procedures and address the needs of internal and external interested parties (customers, regulators and internal stakeholders). To identify possible improvements to the quality management system (QMS). Be aware of the Quality Policy, Quality Objectives and contribute towards the effectiveness of the Quality Management System and the implications of not conforming with the Quality Management System requirements. Role Dimensions The Materials Administrator carries out a regular review of the master production schedule and other general planner order requests acting on the recommendations as appropriate The role involves close working with the Supply Chain Manager, Production Manager, production supervisors and Sales Team. The role involves an understanding of MPS/MRP methods The role is a part-time role working within office hours onsite at the company's premises. Key Responsibilities Purchasing Implement and maintain a matrix of lead-times for products and minimum order levels for materials + overs for waste and yield A key liaison with the Suppliers Review Sales/Customer requirements and plan appropriate quotes and purchases to ensure parts are available to meet on-time delivery Gather approvals, then raise and issue purchase orders to suppliers in good time Maintain appropriate call-off schedules for high quantity, regular parts to manage stock inventory and cash flow. Maintain oversight on consumables stock and ensure replenishment orders are placed in a timely manner. Maintain and develop a good working relationship with our suppliers, working with the Supply Chain Manager to foster continuous improvement in their performance. Highlight poor supplier performance to the Supply Chain Manager and Quality Manager so that appropriate remedial action may be taken. Manage the process for items being returned to suppliers due to poor quality, raising returns and new orders on MRP system as appropriate. Complete purchase order acknowledgments and work with suppliers to minimise late deliveries, looking at purchase order priorities with the Supply Chain Manager as necessary. Monitor pricing changes from Suppliers and advise finance team of material fluctuations in prices of key inputs when applicable Coordination with Sales and Finance teams for import clearance procedures where required Works orders Co-ordinate with Sales Team to create work orders in response to the sales orders and demand from clients Co-ordinate with Production Manager and Supervisors to ensure proper flow of work orders onto shop floor. Completion of work orders into MRP system Inventory Control Assisting the Supply Chain Manager with the coordination of stock counts, post stock adjustments and stock reconciliations. Assisting the Supply Chain Manager with the MRP stock control computerised record system is maintained. Support Warehouse in issuing the picking/packing lists to allow the packing and booking of shipments to customers. Support Warehouse in processing the despatch paperwork required for the shipping and finance staff to complete the customer shipment process. Health and Safety Promote and maintain awareness and compliance of H&S in accordance with best practice and legal requirements. Human Resources Promote and uphold company performance standards and ideology (quality, continuous improvement, housekeeping & work ethic). Participate in internal and external training where provided as necessary for the job and the individual to ensure continuous professional development. To ensure the role holders training file is current Other Other reasonable duties which may be assigned related to the role dimensions. This is a part-time role, based at our Cambridge office.
Dec 02, 2022
Full time
Our client a world leader in their imaging products, is currently looking to appoint an experienced Materials Administrator to join the team. As the Materials Administrator you will ensure the timely purchase and supply of parts predominantly driven by demand from the production schedule and place orders for any other goods required and approved by department/senior managers. To ensure that all core areas of the business adhere to the requirements of ISO9001:2015, the QMS, internal processes and procedures and address the needs of internal and external interested parties (customers, regulators and internal stakeholders). To identify possible improvements to the quality management system (QMS). Be aware of the Quality Policy, Quality Objectives and contribute towards the effectiveness of the Quality Management System and the implications of not conforming with the Quality Management System requirements. Role Dimensions The Materials Administrator carries out a regular review of the master production schedule and other general planner order requests acting on the recommendations as appropriate The role involves close working with the Supply Chain Manager, Production Manager, production supervisors and Sales Team. The role involves an understanding of MPS/MRP methods The role is a part-time role working within office hours onsite at the company's premises. Key Responsibilities Purchasing Implement and maintain a matrix of lead-times for products and minimum order levels for materials + overs for waste and yield A key liaison with the Suppliers Review Sales/Customer requirements and plan appropriate quotes and purchases to ensure parts are available to meet on-time delivery Gather approvals, then raise and issue purchase orders to suppliers in good time Maintain appropriate call-off schedules for high quantity, regular parts to manage stock inventory and cash flow. Maintain oversight on consumables stock and ensure replenishment orders are placed in a timely manner. Maintain and develop a good working relationship with our suppliers, working with the Supply Chain Manager to foster continuous improvement in their performance. Highlight poor supplier performance to the Supply Chain Manager and Quality Manager so that appropriate remedial action may be taken. Manage the process for items being returned to suppliers due to poor quality, raising returns and new orders on MRP system as appropriate. Complete purchase order acknowledgments and work with suppliers to minimise late deliveries, looking at purchase order priorities with the Supply Chain Manager as necessary. Monitor pricing changes from Suppliers and advise finance team of material fluctuations in prices of key inputs when applicable Coordination with Sales and Finance teams for import clearance procedures where required Works orders Co-ordinate with Sales Team to create work orders in response to the sales orders and demand from clients Co-ordinate with Production Manager and Supervisors to ensure proper flow of work orders onto shop floor. Completion of work orders into MRP system Inventory Control Assisting the Supply Chain Manager with the coordination of stock counts, post stock adjustments and stock reconciliations. Assisting the Supply Chain Manager with the MRP stock control computerised record system is maintained. Support Warehouse in issuing the picking/packing lists to allow the packing and booking of shipments to customers. Support Warehouse in processing the despatch paperwork required for the shipping and finance staff to complete the customer shipment process. Health and Safety Promote and maintain awareness and compliance of H&S in accordance with best practice and legal requirements. Human Resources Promote and uphold company performance standards and ideology (quality, continuous improvement, housekeeping & work ethic). Participate in internal and external training where provided as necessary for the job and the individual to ensure continuous professional development. To ensure the role holders training file is current Other Other reasonable duties which may be assigned related to the role dimensions. This is a part-time role, based at our Cambridge office.
Laboratory Technician Slough 12 months Contract £10.67 - £12.55 PAYE Cpl Life Sciences are partnering with a leading contract manufacturer for Pharma and Biotech companies recruiting a Laboratory technician to work as part of a team providing support services to laboratory-based scientists. Core activities are to ensure equipment is in calibration and ready to use, consumables and buffers are always stocked and the high standards of the lab are maintained at all times. Key Accountabilities: Completion of routine (daily and weekly equipment calibration checks. Generation of simple analytical buffers for laboratory methods and processes. Technical review of simple buffers prepared within the team. Laboratory consumables stock management - checking laboratory stock locations and points of use and listing items to be ordered. Ordering consumables from internal stores using the Warehouse Management System (WMS). Glassware and plastic ware cleaning, maintaining high levels of cleanliness and tidiness in the washroom environment. Processing of laboratory deliveries, receipt, storage and notifications Dispensing of buffers as part of buffer preparation. Autoclaving of laboratory equipment and fermentation feeds. Generation of large-scale buffers for laboratory methods and processes. Preparation and cleaning of bioreactor fermentation equipment. Completing housekeeping activities to maintain workplace standards. Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind. Assisting in all activities in laboratories supported by Site Laboratory Services. For more information please apply within or send your CV to
Dec 02, 2022
Full time
Laboratory Technician Slough 12 months Contract £10.67 - £12.55 PAYE Cpl Life Sciences are partnering with a leading contract manufacturer for Pharma and Biotech companies recruiting a Laboratory technician to work as part of a team providing support services to laboratory-based scientists. Core activities are to ensure equipment is in calibration and ready to use, consumables and buffers are always stocked and the high standards of the lab are maintained at all times. Key Accountabilities: Completion of routine (daily and weekly equipment calibration checks. Generation of simple analytical buffers for laboratory methods and processes. Technical review of simple buffers prepared within the team. Laboratory consumables stock management - checking laboratory stock locations and points of use and listing items to be ordered. Ordering consumables from internal stores using the Warehouse Management System (WMS). Glassware and plastic ware cleaning, maintaining high levels of cleanliness and tidiness in the washroom environment. Processing of laboratory deliveries, receipt, storage and notifications Dispensing of buffers as part of buffer preparation. Autoclaving of laboratory equipment and fermentation feeds. Generation of large-scale buffers for laboratory methods and processes. Preparation and cleaning of bioreactor fermentation equipment. Completing housekeeping activities to maintain workplace standards. Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind. Assisting in all activities in laboratories supported by Site Laboratory Services. For more information please apply within or send your CV to
Senior Statistician Location: Fully Remote 6 month contract Day Rate: Negotiable Start Date: ASAP Skills: Stata Skills Cpl Life Sciences are partnering with our large client to source a senior Statistician with experience in Stata data for a 6 month contract position. We are looking for an enthusiastic communicator of sound statistical approaches to join a flourishing Clinical Trials Unit supporting high quality clinical trials and other research studies in primary care, psychiatry, women's health, surgery, orthopaedics and beyond. The Pragmatic Clinical Trials Unit (PCTU) is a UKCRC-registered Clinical Trials Unit with particular expertise in pragmatic trials - clinical trials of interventions as they would be delivered in practice. You will be joining a team of statisticians and health economists currently working within the unit on a wide variety of trials, systematic reviews and observational studies at different stages of their development and completion. The unit also conducts methodological research, and has an international reputation for its work on cluster-randomised trials and trials of complex interventions. The post will involve contributing to trial protocols, developing statistical analysis plans, conducting statistical analyses, and liaising with other researchers and health professionals. In addition, the post-holder will be expected to do a small amount of teaching. About You You should have a PhD or MSc in statistics, epidemiology or closely related field, or equivalent professional experience. Experience in providing statistical input in research or healthcare, as well as detailed and up-to-date knowledge of clinical trial designs in applied health research. You must be able to work as part of a team and to organise and prioritise your own work. Good understanding of current regulatory framework in relation to clinical trials would be an advantage. If you're interested please apply or send your CV to
Dec 01, 2022
Full time
Senior Statistician Location: Fully Remote 6 month contract Day Rate: Negotiable Start Date: ASAP Skills: Stata Skills Cpl Life Sciences are partnering with our large client to source a senior Statistician with experience in Stata data for a 6 month contract position. We are looking for an enthusiastic communicator of sound statistical approaches to join a flourishing Clinical Trials Unit supporting high quality clinical trials and other research studies in primary care, psychiatry, women's health, surgery, orthopaedics and beyond. The Pragmatic Clinical Trials Unit (PCTU) is a UKCRC-registered Clinical Trials Unit with particular expertise in pragmatic trials - clinical trials of interventions as they would be delivered in practice. You will be joining a team of statisticians and health economists currently working within the unit on a wide variety of trials, systematic reviews and observational studies at different stages of their development and completion. The unit also conducts methodological research, and has an international reputation for its work on cluster-randomised trials and trials of complex interventions. The post will involve contributing to trial protocols, developing statistical analysis plans, conducting statistical analyses, and liaising with other researchers and health professionals. In addition, the post-holder will be expected to do a small amount of teaching. About You You should have a PhD or MSc in statistics, epidemiology or closely related field, or equivalent professional experience. Experience in providing statistical input in research or healthcare, as well as detailed and up-to-date knowledge of clinical trial designs in applied health research. You must be able to work as part of a team and to organise and prioritise your own work. Good understanding of current regulatory framework in relation to clinical trials would be an advantage. If you're interested please apply or send your CV to
Clinical Operations Manager required by leading Pharmaceutical firm based near Welwyn A leading Pharmaceutical company, based near Welwyn, currently requires a Clinical Operations Manager to join the team managing clinical studies in Oncology. Upon joining, the Clinical Operations Manager will ensure that study deliverables are met according to the agreed quality standards and timelines. The Clinical Operations Manager will also ensure that studies are executing according to ICH/GCP guidelines as well as any other regulatory requirements. The Clinical Operations Manager will also mentor more junior members of the team. In terms of skills, we are looking for Clinical Operations Managers who have solid experience within Clinical Operations as well as a track record of coordinating EMEA regional activities, including managing CRO/Vendor collaborations. Any previous Oncology experience would also be very good to have. This opportunity would suit a Clinical Operations Manager who is looking to work at a highly successful Pharmaceutical company who have had some very interesting results of late - if you want to be a part of that journey, please apply within.
Dec 01, 2022
Full time
Clinical Operations Manager required by leading Pharmaceutical firm based near Welwyn A leading Pharmaceutical company, based near Welwyn, currently requires a Clinical Operations Manager to join the team managing clinical studies in Oncology. Upon joining, the Clinical Operations Manager will ensure that study deliverables are met according to the agreed quality standards and timelines. The Clinical Operations Manager will also ensure that studies are executing according to ICH/GCP guidelines as well as any other regulatory requirements. The Clinical Operations Manager will also mentor more junior members of the team. In terms of skills, we are looking for Clinical Operations Managers who have solid experience within Clinical Operations as well as a track record of coordinating EMEA regional activities, including managing CRO/Vendor collaborations. Any previous Oncology experience would also be very good to have. This opportunity would suit a Clinical Operations Manager who is looking to work at a highly successful Pharmaceutical company who have had some very interesting results of late - if you want to be a part of that journey, please apply within.
Senior Manager Regulatory Affairs 12 month contract Remote only need to commit to going to site on occasion Rates PAYE - 54.80, Umbrella - 65.30 (Inside of IR35) Job Description: This role will support one or more products from a regional regulatory perspective. As a member of the Global Regulatory Team (GRT), you will achieve the desired labelling by developing and executing regional regulatory strategies and managing effective agency interactions. The purpose of this role is: To ensure that the client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as well as to market approved medicinal products to ensure timely regulatory compliance with above approvals, this role may provide management and leadership by supervising one or more other regional regulatory leads and/or support staff. This role is responsible for: Advising the GRT on regional considerations in developing strategy ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders May manage one or more regional leads or support roles Strategy and Execution Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products within the client's portfolio in compliance with global filing plans and local regulatory requirements. Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Leads development of regional regulatory documents and meetings in accordance with GRT strategy Provide regulatory direction on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, conditional/accelerated approvals, compassionate use and paediatric plan) Direct the development of the regional product label by collaborating with the Labelling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent. Manages regional label negotiation activities with minimal supervision, participate in the development and execution of regional regulatory product strategies, including precedence, risk management and contingency planning Consistent with GRT strategy, advise GDT on regulatory implications and requirements related to global clinical development plans and objectives Co-ordinates company responses to requests from regulatory authorities, e.g Response to Questions (RTQs) Communicates regulatory strategies as appropriate such that expectations are understood. Estimate the likelihood of regulatory success based on proposed strategies and discuss with GRT and line Management Develop predictions for expectations and risks associated with outcomes by regulatory agencies Ensure regulatory product compliance for product (e.g. IMR, PMCs, paediatric and other agency commitments) Collaboration Share regulatory information and implications with the GRT colleagues on an ongoing basis and provide advice on regional considerations Communicate and ensure alignment of regional management before GRT strategy decisions Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to the clients products. Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement. Evaluates and communicate impact of relevant regional regulations, guidances, current regulatory environment and competitor labelling Health Authority Interactions Act as contact and create relationships with agency staff on specific product assignment Document and communicate details and outcomes of regulatory agency interactions to GRT and relevant sr. management Manage core regulatory activities to ensure effective regional agency interactions consistent with the Global Regulatory strategy, includes contingency regulatory planning/risk assessment Management Supports communication/collaboration between direct reports who are regional leads and regional head for program issues requiring next level engagement Knowledge and Skills Regulatory knowledge in regional legislation Working with policies, procedures and SOPs Experience with national legislation and regulations relating to medicinal products Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals. Understanding of drug development Scientific / Technical Excellence Strong knowledge of and experience in regional regulatory environment in relevant product area and development stage Comprehensive understanding of regulatory activities, touch points and how they affect projects and processes Cultural awareness and sensitivity to achieve results across both regional country and International borders. Please apply within or for more information contact
Feb 02, 2022
Full time
Senior Manager Regulatory Affairs 12 month contract Remote only need to commit to going to site on occasion Rates PAYE - 54.80, Umbrella - 65.30 (Inside of IR35) Job Description: This role will support one or more products from a regional regulatory perspective. As a member of the Global Regulatory Team (GRT), you will achieve the desired labelling by developing and executing regional regulatory strategies and managing effective agency interactions. The purpose of this role is: To ensure that the client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as well as to market approved medicinal products to ensure timely regulatory compliance with above approvals, this role may provide management and leadership by supervising one or more other regional regulatory leads and/or support staff. This role is responsible for: Advising the GRT on regional considerations in developing strategy ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders May manage one or more regional leads or support roles Strategy and Execution Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products within the client's portfolio in compliance with global filing plans and local regulatory requirements. Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Leads development of regional regulatory documents and meetings in accordance with GRT strategy Provide regulatory direction on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, conditional/accelerated approvals, compassionate use and paediatric plan) Direct the development of the regional product label by collaborating with the Labelling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent. Manages regional label negotiation activities with minimal supervision, participate in the development and execution of regional regulatory product strategies, including precedence, risk management and contingency planning Consistent with GRT strategy, advise GDT on regulatory implications and requirements related to global clinical development plans and objectives Co-ordinates company responses to requests from regulatory authorities, e.g Response to Questions (RTQs) Communicates regulatory strategies as appropriate such that expectations are understood. Estimate the likelihood of regulatory success based on proposed strategies and discuss with GRT and line Management Develop predictions for expectations and risks associated with outcomes by regulatory agencies Ensure regulatory product compliance for product (e.g. IMR, PMCs, paediatric and other agency commitments) Collaboration Share regulatory information and implications with the GRT colleagues on an ongoing basis and provide advice on regional considerations Communicate and ensure alignment of regional management before GRT strategy decisions Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to the clients products. Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement. Evaluates and communicate impact of relevant regional regulations, guidances, current regulatory environment and competitor labelling Health Authority Interactions Act as contact and create relationships with agency staff on specific product assignment Document and communicate details and outcomes of regulatory agency interactions to GRT and relevant sr. management Manage core regulatory activities to ensure effective regional agency interactions consistent with the Global Regulatory strategy, includes contingency regulatory planning/risk assessment Management Supports communication/collaboration between direct reports who are regional leads and regional head for program issues requiring next level engagement Knowledge and Skills Regulatory knowledge in regional legislation Working with policies, procedures and SOPs Experience with national legislation and regulations relating to medicinal products Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals. Understanding of drug development Scientific / Technical Excellence Strong knowledge of and experience in regional regulatory environment in relevant product area and development stage Comprehensive understanding of regulatory activities, touch points and how they affect projects and processes Cultural awareness and sensitivity to achieve results across both regional country and International borders. Please apply within or for more information contact
Senior Legal Counsel Want to get closer to the action? As Senior Legal Counsel, youll be at the heart of the decisions that impact a leading global business. This is a unique opportunity to join a dynamic and entrepreneurial team in the company's fastest growing global business unit. Inspired by our purpose to protect, heal and nurture in the relentless pursuit of a cleaner and healthier world thr...... click apply for full job details
Jan 12, 2022
Contractor
Senior Legal Counsel Want to get closer to the action? As Senior Legal Counsel, youll be at the heart of the decisions that impact a leading global business. This is a unique opportunity to join a dynamic and entrepreneurial team in the company's fastest growing global business unit. Inspired by our purpose to protect, heal and nurture in the relentless pursuit of a cleaner and healthier world thr...... click apply for full job details
Marketing Events Coordinator Contract: 9 months 20 per hour (paye) Remote/Berkshire based Start date: January Cpl have partnered with a global pharmaceutical company who are in urgent need of a Marketing Events Coordinator to join their business on an interim basis. This role will focus on event management and supporting the customer facing events and marketing team. The successful individual will also be fundamental in ensuring that the company is fully compliant with local and regional rules and regulations. Essential Skills and Experience Required: Partnership with commercial and medical teams to assist with the arrangement on specific events Create and manage contracts required for relevant events Support the compliance and administration tasks including copy approval documents Experience in testing marketing materials Raising PO numbers when requested Strong spoken and written communication and team work ethic Attend key meetings when required, including providing reports and progress If you are interested in this position and have the relevant marketing experience then please apply here or email your CV to [](mailto:).
Dec 08, 2021
Full time
Marketing Events Coordinator Contract: 9 months 20 per hour (paye) Remote/Berkshire based Start date: January Cpl have partnered with a global pharmaceutical company who are in urgent need of a Marketing Events Coordinator to join their business on an interim basis. This role will focus on event management and supporting the customer facing events and marketing team. The successful individual will also be fundamental in ensuring that the company is fully compliant with local and regional rules and regulations. Essential Skills and Experience Required: Partnership with commercial and medical teams to assist with the arrangement on specific events Create and manage contracts required for relevant events Support the compliance and administration tasks including copy approval documents Experience in testing marketing materials Raising PO numbers when requested Strong spoken and written communication and team work ethic Attend key meetings when required, including providing reports and progress If you are interested in this position and have the relevant marketing experience then please apply here or email your CV to [](mailto:).
Marketing Assistant Contract: 7 months Remote/London based 370 per day (PAYE) Start date: January Cpl have partnered with a global pharmaceutical company who are in urgent need of a Marketing Assistant to join their business to support their marketing needs across the UK over the next 7 months. This role will focus on completing administrative marketing tasks within project timelines and assist with the streamlining of internal processes. Essential Skills and Experience Required: Experience in media planning and online marketing material Experience supporting online and email based campaigns Experience of working on process improvement Experience in testing marketing materials Experience of reporting on marketing campaigns Strong spoken and written communication and team work ethic Comfortable in analysing data and insights If you are interested in this position and have the relevant marketing experience then please apply here or email your CV to [](mailto:).
Dec 08, 2021
Full time
Marketing Assistant Contract: 7 months Remote/London based 370 per day (PAYE) Start date: January Cpl have partnered with a global pharmaceutical company who are in urgent need of a Marketing Assistant to join their business to support their marketing needs across the UK over the next 7 months. This role will focus on completing administrative marketing tasks within project timelines and assist with the streamlining of internal processes. Essential Skills and Experience Required: Experience in media planning and online marketing material Experience supporting online and email based campaigns Experience of working on process improvement Experience in testing marketing materials Experience of reporting on marketing campaigns Strong spoken and written communication and team work ethic Comfortable in analysing data and insights If you are interested in this position and have the relevant marketing experience then please apply here or email your CV to [](mailto:).
*Senior Legal Counsel * Want to get closer to the action? As Senior Legal Counsel, youll be at the heart of the decisions that impact a leading global business. This is a unique opportunity to join a dynamic and entrepreneurial team in the company's fastest growing global business unit. Inspired by our purpose to protect, heal and nurture in the relentless pursuit of a cleaner and healthier world through our products, the ambition of the eRB global business unit is to democratize access to the highest quality Hygiene, Health & Nutrition products through our amazing, globally recognised brands. *Senior Privacy and Digital Legal Counsel * *Slough, Berkshire* *Competitive Salary * Working closely with eRBs Legal Director, you will help deliver the advice and support the company's needs to grow its e-commerce business and develop exciting new online offerings.You will work with senior stakeholders across the business, advising on topics as broad as our product portfolio everything from advertising, marketing, competition law, data protection, privacy, consumer and commercial contracts, intellectual property, and much more. Youll tackle complex issues that cross organisational and geographical boundaries. *Youll succeed because* You are a UK or EU-qualified lawyer with a strong track record of providing e-commerce legal advice.Prior in-house experience and significant exposure to tech and data protection-related issues in the context of an e-commerce business are preferable. You have a strong academic record with a minimum of a 2:1 honors degree (or an overseas qualification equivalent to a 2:1). You have a background of drafting and negotiating a wide range of commercial agreements, including software licenses, digital platform agreements, marketing and advertising agreements, data processing agreements and professional services contracts.You can proficiently identify anti-trust issues. You can advise on consumer law and e-commerce related topics and can advise on the continutally evolving e-commerce regulatory landscape and how it applies practically.You have experience of drafting consumer-facing website disclosures and advising on customer care issues. You have demonstrable experience in supporting CRM and data insights teams and working with businesses to achieve their objectives. You have a strong working knowledge of UK and international data protection and privacy laws and their application to online retail. You can advise on marketing and advertising claims. Youre comfortable with ambiguity, working at speed and collaborating within a global multinational environment including different stakeholders, functions and business units as well as demonstrating a high degree of cultural awareness and sensitivity.You are experienced with working with stakeholders across the organisation including tax, finance, corporate legal services, supply chain, SQRC, compliance and brand protection. You have M&A experience. You can step up to deputising for the Legal Director when needed. Youre an impactful business partner with a high EQ and excellent presentation skills.You know how to effectively communicate your expertise in a way that others can absorb and act on. You are analytical and commercially-minded, able to weigh up legal risk against business aims to give pragmatic advice. You can provide end-to-end advice your internal clients, supporting projects from inception to completion.You compliment your legal advice with guidance on navigating business process, bringing in other Reckitt support functions where necessary. Youre a self-starter, willing to challenge the status quo by identifying bottlenecks and suggesting process improvements that will help eRB move quickly as the business continues to grow. Youre a team-player, willing to pitch in to help others and contribute to developing the skill sets of junior team members. You stay ahead of impactful industry and legal updates.You are willing to develop your network of industry and legal contacts, both within and outside Reckitt. *Youll love it because* Youre fearless and pro-active with a strong sense of urgency and a bias for action. Youll have the freedom to make a difference. Youll put your own ideas into practice whilst being a leader in championing our corporate compliance policies and procedures, particularly around the topics of sustainability and the environment. The products you help us get out there will allow people to live healthier lives and have happier homes and youll thrive on the front line of our mission, our purpose and our fight. Our dynamic, achievement/ownership-driven culture will bring the very best out of you, every day.
Dec 08, 2021
Full time
*Senior Legal Counsel * Want to get closer to the action? As Senior Legal Counsel, youll be at the heart of the decisions that impact a leading global business. This is a unique opportunity to join a dynamic and entrepreneurial team in the company's fastest growing global business unit. Inspired by our purpose to protect, heal and nurture in the relentless pursuit of a cleaner and healthier world through our products, the ambition of the eRB global business unit is to democratize access to the highest quality Hygiene, Health & Nutrition products through our amazing, globally recognised brands. *Senior Privacy and Digital Legal Counsel * *Slough, Berkshire* *Competitive Salary * Working closely with eRBs Legal Director, you will help deliver the advice and support the company's needs to grow its e-commerce business and develop exciting new online offerings.You will work with senior stakeholders across the business, advising on topics as broad as our product portfolio everything from advertising, marketing, competition law, data protection, privacy, consumer and commercial contracts, intellectual property, and much more. Youll tackle complex issues that cross organisational and geographical boundaries. *Youll succeed because* You are a UK or EU-qualified lawyer with a strong track record of providing e-commerce legal advice.Prior in-house experience and significant exposure to tech and data protection-related issues in the context of an e-commerce business are preferable. You have a strong academic record with a minimum of a 2:1 honors degree (or an overseas qualification equivalent to a 2:1). You have a background of drafting and negotiating a wide range of commercial agreements, including software licenses, digital platform agreements, marketing and advertising agreements, data processing agreements and professional services contracts.You can proficiently identify anti-trust issues. You can advise on consumer law and e-commerce related topics and can advise on the continutally evolving e-commerce regulatory landscape and how it applies practically.You have experience of drafting consumer-facing website disclosures and advising on customer care issues. You have demonstrable experience in supporting CRM and data insights teams and working with businesses to achieve their objectives. You have a strong working knowledge of UK and international data protection and privacy laws and their application to online retail. You can advise on marketing and advertising claims. Youre comfortable with ambiguity, working at speed and collaborating within a global multinational environment including different stakeholders, functions and business units as well as demonstrating a high degree of cultural awareness and sensitivity.You are experienced with working with stakeholders across the organisation including tax, finance, corporate legal services, supply chain, SQRC, compliance and brand protection. You have M&A experience. You can step up to deputising for the Legal Director when needed. Youre an impactful business partner with a high EQ and excellent presentation skills.You know how to effectively communicate your expertise in a way that others can absorb and act on. You are analytical and commercially-minded, able to weigh up legal risk against business aims to give pragmatic advice. You can provide end-to-end advice your internal clients, supporting projects from inception to completion.You compliment your legal advice with guidance on navigating business process, bringing in other Reckitt support functions where necessary. Youre a self-starter, willing to challenge the status quo by identifying bottlenecks and suggesting process improvements that will help eRB move quickly as the business continues to grow. Youre a team-player, willing to pitch in to help others and contribute to developing the skill sets of junior team members. You stay ahead of impactful industry and legal updates.You are willing to develop your network of industry and legal contacts, both within and outside Reckitt. *Youll love it because* Youre fearless and pro-active with a strong sense of urgency and a bias for action. Youll have the freedom to make a difference. Youll put your own ideas into practice whilst being a leader in championing our corporate compliance policies and procedures, particularly around the topics of sustainability and the environment. The products you help us get out there will allow people to live healthier lives and have happier homes and youll thrive on the front line of our mission, our purpose and our fight. Our dynamic, achievement/ownership-driven culture will bring the very best out of you, every day.
Marketing Research Specialist 4 month contract 50 per hour (PAYE) Fully remote Inside IR35 Cpl are working directly with a global pharmaceutical company who are seeking an experience Marketing Research Specialist to support with project management and budget responsibilities as well as market research and reporting. This role will focus on budget oversight and managing external agencies who will be supporting on several marketing projects. It is imperative to have strong knowledge of UK compliance marketing regulations. Essential Skills and Experience Required: Project management of a range of marketing projects Management of internal projects and external agencies that will support with the marketing tasks Analyse market research and intelligence Provide relevant reports based on current market trends Support the brand management plans and coordinate the relevant budgets in correspondence to these Business analysis and consolidation of relevant data sources Attend key meetings when required, including providing reports and progress If you are interested in this position and have the relevant marketing experience then please apply here or email your CV to [](mailto:).
Dec 07, 2021
Full time
Marketing Research Specialist 4 month contract 50 per hour (PAYE) Fully remote Inside IR35 Cpl are working directly with a global pharmaceutical company who are seeking an experience Marketing Research Specialist to support with project management and budget responsibilities as well as market research and reporting. This role will focus on budget oversight and managing external agencies who will be supporting on several marketing projects. It is imperative to have strong knowledge of UK compliance marketing regulations. Essential Skills and Experience Required: Project management of a range of marketing projects Management of internal projects and external agencies that will support with the marketing tasks Analyse market research and intelligence Provide relevant reports based on current market trends Support the brand management plans and coordinate the relevant budgets in correspondence to these Business analysis and consolidation of relevant data sources Attend key meetings when required, including providing reports and progress If you are interested in this position and have the relevant marketing experience then please apply here or email your CV to [](mailto:).
We are looking for a Quality System Associate on behalf of our client based in Hertfordshire The ideal candidate would have experience in: * Change Controls * Qualification and Validation documentation * Knowledge of control of Regulatory Information Details of responsibilities: * To support the Product Quality Review process for company. * To support the process of generation of Quality Agreements. * To support the process for approving suppliers and the maintenance of the Approved Suppliers List. * To support the maintenance of a list of Parallel Importers/Distributors of Eisai products as compiled from notifications and samples received by CompnayRegulatory Affairs. * To support the generation of the Quality Management Systems Indicator reports. * To support the ongoing operation, maintenance, and implementation of improvements to TrackWise processes and systems to meet companyneeds. * To supportTraining Management System. * To maintain copies of Corporate Policies, Guideline, Standards and Procedures. * To write and review all SOPs associated with the Electronic TrackWise QMS * To support the company SOP System. * To support the internal and external audit process and audit schedules * To participate in Audits * To support Quality Systems training ofstaff, as required. * To coordinate and support GMP Training * To support the Deviations System * To support theRisk Management System * To provide day to day support to other members of the Quality Systems team, as appropriate. * Identify and implement continuous improvement opportunities that result in cost savings and more efficient and compliant ways of working * To perform any appropriate duties at the request of the Quality Systems Manager.
Dec 07, 2021
Full time
We are looking for a Quality System Associate on behalf of our client based in Hertfordshire The ideal candidate would have experience in: * Change Controls * Qualification and Validation documentation * Knowledge of control of Regulatory Information Details of responsibilities: * To support the Product Quality Review process for company. * To support the process of generation of Quality Agreements. * To support the process for approving suppliers and the maintenance of the Approved Suppliers List. * To support the maintenance of a list of Parallel Importers/Distributors of Eisai products as compiled from notifications and samples received by CompnayRegulatory Affairs. * To support the generation of the Quality Management Systems Indicator reports. * To support the ongoing operation, maintenance, and implementation of improvements to TrackWise processes and systems to meet companyneeds. * To supportTraining Management System. * To maintain copies of Corporate Policies, Guideline, Standards and Procedures. * To write and review all SOPs associated with the Electronic TrackWise QMS * To support the company SOP System. * To support the internal and external audit process and audit schedules * To participate in Audits * To support Quality Systems training ofstaff, as required. * To coordinate and support GMP Training * To support the Deviations System * To support theRisk Management System * To provide day to day support to other members of the Quality Systems team, as appropriate. * Identify and implement continuous improvement opportunities that result in cost savings and more efficient and compliant ways of working * To perform any appropriate duties at the request of the Quality Systems Manager.
Marketing Research Specialist 4 month contract 50 per hour (PAYE) Fully remote Inside IR35 Cpl are working directly with a global pharmaceutical company who are seeking an experience Marketing Research Specialist to support with project management and budget responsibilities as well as market research and reporting...... click apply for full job details
Dec 07, 2021
Contractor
Marketing Research Specialist 4 month contract 50 per hour (PAYE) Fully remote Inside IR35 Cpl are working directly with a global pharmaceutical company who are seeking an experience Marketing Research Specialist to support with project management and budget responsibilities as well as market research and reporting...... click apply for full job details
Our client is a manufacturer of specialised imaging detectors and systems covering a diverse range of industries from aerospace to biomedical, currently employing approximately 60 people. Applications for such detectors include the detection of single photons and ultrafast cameras capable of sub nanosecond exposure times. The other side of the business a fast-growing specialist imaging equipment m...... click apply for full job details
Dec 07, 2021
Full time
Our client is a manufacturer of specialised imaging detectors and systems covering a diverse range of industries from aerospace to biomedical, currently employing approximately 60 people. Applications for such detectors include the detection of single photons and ultrafast cameras capable of sub nanosecond exposure times. The other side of the business a fast-growing specialist imaging equipment m...... click apply for full job details
QA Associate 12- 18 month contract 24.30 per hour PAYE Liverpool On site We have a long-term contract available for a QA Associate to join a global pharmaceutical company that focusses on vaccines, this is an excellent opportunity contributing to helping protect the lives of millions of people across the world. The main purpose of the QA Associate it to provide frontline/ shop floor QA support to the secondary operations. This role will involve working 11/12 hour shifts, 2 days on, 2 nights on and 4 days off. Key Responsibilities include; Be responsible for QA review and approval of procedures, batch production records (master and executed), and any other relevant cGMP documentation Support and perform tasks as required by the Quality Manager To ensure cGMP behaviours are compliant Safeguard product quality and sterility assurance Provide support for deviation investigations, ensuring effecting root cause analysis investigations are performed Identify repeat deviations To ensure that deviations, CAPAs, protocols/reports and other applicable documents are reviewed and approved within the designated timelines To provide Quality oversight for manufacturing and support functions ensuring that appropriate standards of cGMP, housekeeping, Health, Safety and Environment are applied in the team and site areas of responsibility, in accordance with current regulations and procedures Experience; Educated to graduate level Have an understanding of cGMP requirements Experience working in a pharmaceutical environment For more information please contact
Dec 07, 2021
Full time
QA Associate 12- 18 month contract 24.30 per hour PAYE Liverpool On site We have a long-term contract available for a QA Associate to join a global pharmaceutical company that focusses on vaccines, this is an excellent opportunity contributing to helping protect the lives of millions of people across the world. The main purpose of the QA Associate it to provide frontline/ shop floor QA support to the secondary operations. This role will involve working 11/12 hour shifts, 2 days on, 2 nights on and 4 days off. Key Responsibilities include; Be responsible for QA review and approval of procedures, batch production records (master and executed), and any other relevant cGMP documentation Support and perform tasks as required by the Quality Manager To ensure cGMP behaviours are compliant Safeguard product quality and sterility assurance Provide support for deviation investigations, ensuring effecting root cause analysis investigations are performed Identify repeat deviations To ensure that deviations, CAPAs, protocols/reports and other applicable documents are reviewed and approved within the designated timelines To provide Quality oversight for manufacturing and support functions ensuring that appropriate standards of cGMP, housekeeping, Health, Safety and Environment are applied in the team and site areas of responsibility, in accordance with current regulations and procedures Experience; Educated to graduate level Have an understanding of cGMP requirements Experience working in a pharmaceutical environment For more information please contact
Research Contract Officer *3-month contract* *Salary: *20-24 per hour *Location:* Remote with occasional site visits to London New Research Contract Officer roles have come to light. In this position, you would undertake a specialist paralegal function, within an established academic institute, supporting the Contract and Research team. The role will require you to support internal and external parties, ensuring the timely delivery and tracking of agreements, on behalf of the Contracts Team.The ideal candidate will have strong interpersonal, verbal and written communication skills as well as operational excellence. *Key responsibilities include:* Preparing standard agreements for internal and external parties Organising the signature of required documents General administrative tasks relating to new and existing contractual agreements Highlight when documents require updates and extensions Copy, scan and locate research documents into the correct system and database Assist with drafting and negotiating research agreements Build relationships with internal staff, including monitoring and chasing outstanding requests Escalating matters to the head of research when required Maintain agreement records and databases Experience within academic administration and contract management is required Must be able to commute to London on occasion *Requirements*: Law degree OR significant experience in an equivalent role/job Demonstrated experience of drafting, negotiating, and concluding a wide range and high volume of research contracts, preferably within or related to the Higher Education sector In-depth knowledge and understanding of key research contract topics (e.g., intellectual property, performance, publication, confidentiality, VAT, warranties, and indemnities) Experience of identifying and addressing potential down-side risks in conducting research and with the negotiation and performance of associated research contracts If you would like more information on this role or think you would be a great fit, please do not hesitate to get in contact via email to [](mailto:)
Dec 07, 2021
Full time
Research Contract Officer *3-month contract* *Salary: *20-24 per hour *Location:* Remote with occasional site visits to London New Research Contract Officer roles have come to light. In this position, you would undertake a specialist paralegal function, within an established academic institute, supporting the Contract and Research team. The role will require you to support internal and external parties, ensuring the timely delivery and tracking of agreements, on behalf of the Contracts Team.The ideal candidate will have strong interpersonal, verbal and written communication skills as well as operational excellence. *Key responsibilities include:* Preparing standard agreements for internal and external parties Organising the signature of required documents General administrative tasks relating to new and existing contractual agreements Highlight when documents require updates and extensions Copy, scan and locate research documents into the correct system and database Assist with drafting and negotiating research agreements Build relationships with internal staff, including monitoring and chasing outstanding requests Escalating matters to the head of research when required Maintain agreement records and databases Experience within academic administration and contract management is required Must be able to commute to London on occasion *Requirements*: Law degree OR significant experience in an equivalent role/job Demonstrated experience of drafting, negotiating, and concluding a wide range and high volume of research contracts, preferably within or related to the Higher Education sector In-depth knowledge and understanding of key research contract topics (e.g., intellectual property, performance, publication, confidentiality, VAT, warranties, and indemnities) Experience of identifying and addressing potential down-side risks in conducting research and with the negotiation and performance of associated research contracts If you would like more information on this role or think you would be a great fit, please do not hesitate to get in contact via email to [](mailto:)
