Proclinical are recruiting a Clinical Data Manager for a biotech organisation. This role is on a permanent basis and is located in London. The client is focused on producing innovative treatments for cancer. Responsibilities: Handle external service suppliers for the delivery of DM milestones to scope, quality, budget, time, resource planning and risk management. Supervise data transfers with CROs and third-party data sources, SAE/AE data reconciliation and MedDRA and WHODrug coding. Responsible for core data management deliverables which involves eCRF and database design, data quality, data review, and reporting of database / data quality status. Guarantee programs meet all GXP/ICH regulations and remain prompt for inspection. Assist in database transfer, locking, and filing of clinical study databases. Contribute to the development as well as the optimisation of data management SOPs, procedures and initiatives. You will assist with cross-functional process definition, novelty and optimisation. Other duties may be assigned to this role. Skills & Requirements: At least 5 years of experience in clinical data management within a pharmaceutical organisation or similar science, ideally a small to midsize biotech. Know-how of clinical trial data notions, procedures and processes, as well as clinical trial guidelines, industry guidance, conventions and standards. Competence in using CDISC standards, SAS, a variety of eDC planforms, systems integrations such as eDC IRT), MedDRA and WHODrug coding. Acquaintance with oncology clinical development / drug development in multiple phases of development which involves early phase development. Familiarity with efficient external supplier establishments. Deliberation, interpersonal and communication skills both verbally and in writing. Able to work well with others in a team. Know-how of GCP regulations and any other guidelines applicable to clinical trial management. An organised individual with the ability to manage priorities and work efficiently while under pressure to meet deadlines. Educated to a degree level in a science, medical or pharmacy discipline. A driven individual who is focused on business objectives. Able to work well independently. Solution oriented who is flexible to change. Outcomes oriented with a high attention to detail. Comprehension of cell and gene therapy. Past involvement in regulatory inspections is ideal. A fast learner. If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 24, 2022
Full time
Proclinical are recruiting a Clinical Data Manager for a biotech organisation. This role is on a permanent basis and is located in London. The client is focused on producing innovative treatments for cancer. Responsibilities: Handle external service suppliers for the delivery of DM milestones to scope, quality, budget, time, resource planning and risk management. Supervise data transfers with CROs and third-party data sources, SAE/AE data reconciliation and MedDRA and WHODrug coding. Responsible for core data management deliverables which involves eCRF and database design, data quality, data review, and reporting of database / data quality status. Guarantee programs meet all GXP/ICH regulations and remain prompt for inspection. Assist in database transfer, locking, and filing of clinical study databases. Contribute to the development as well as the optimisation of data management SOPs, procedures and initiatives. You will assist with cross-functional process definition, novelty and optimisation. Other duties may be assigned to this role. Skills & Requirements: At least 5 years of experience in clinical data management within a pharmaceutical organisation or similar science, ideally a small to midsize biotech. Know-how of clinical trial data notions, procedures and processes, as well as clinical trial guidelines, industry guidance, conventions and standards. Competence in using CDISC standards, SAS, a variety of eDC planforms, systems integrations such as eDC IRT), MedDRA and WHODrug coding. Acquaintance with oncology clinical development / drug development in multiple phases of development which involves early phase development. Familiarity with efficient external supplier establishments. Deliberation, interpersonal and communication skills both verbally and in writing. Able to work well with others in a team. Know-how of GCP regulations and any other guidelines applicable to clinical trial management. An organised individual with the ability to manage priorities and work efficiently while under pressure to meet deadlines. Educated to a degree level in a science, medical or pharmacy discipline. A driven individual who is focused on business objectives. Able to work well independently. Solution oriented who is flexible to change. Outcomes oriented with a high attention to detail. Comprehension of cell and gene therapy. Past involvement in regulatory inspections is ideal. A fast learner. If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical Staffing are looking for a Senior Clinical Project Manager to join a small Biotech company of 40 people in London on a permanent basis to develop their drug/ digital healthcare study portfolio. As well as managing studies, you'll be involved with formulating the strategy of their future study portfolio and will play a key role with responsibilities such as Clinical Study concepts and Study Planning. This opportunity is open for an intelligent, passionate and enthusiastic individual who would not need to be motivated by solely managing a conveyer belt of clinical studies as this a role which is more varied than this - a truly unique opportunity where you can be impactful and bring your ideas forward to the table. This is a broad Project Management position where you'll have the opporutnity to manage a team from the beginning of joining even if you don't have prior line management experience. A great opporutnity for someone who is looking to take that next step in their career. Our client is open to candidates who have an academia background too so this could be a perfect role for someone who is looking to transition into the commercial side of the industry. You'll be required to come into their office in central London as little as 1 to 2 times per month if you wished, but also you'll have the chance to come in much more than that if you'd prefer - they're flexible around you! Key requirements: 3 or more years Clinical Project Management experience in an Academia, Pharma or Biotech setting. Open to UK, EU or global experience. Phases I-III. Oncology or adv. Some exposure with managing vendors/ CROs. Budget management experience ideally but not essential. A personable, approachable, and dynamic individual who has the 'roll your sleeves up' approach - knows what is needed to work a small company environment. BSc, MSc or PhD background. The company offers a negotiable basic salary + discretionary bonus + stock options + 8% pension. If you are having difficulty in applying or if you have any questions, please contact Jack O'Neill at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 24, 2022
Full time
Proclinical Staffing are looking for a Senior Clinical Project Manager to join a small Biotech company of 40 people in London on a permanent basis to develop their drug/ digital healthcare study portfolio. As well as managing studies, you'll be involved with formulating the strategy of their future study portfolio and will play a key role with responsibilities such as Clinical Study concepts and Study Planning. This opportunity is open for an intelligent, passionate and enthusiastic individual who would not need to be motivated by solely managing a conveyer belt of clinical studies as this a role which is more varied than this - a truly unique opportunity where you can be impactful and bring your ideas forward to the table. This is a broad Project Management position where you'll have the opporutnity to manage a team from the beginning of joining even if you don't have prior line management experience. A great opporutnity for someone who is looking to take that next step in their career. Our client is open to candidates who have an academia background too so this could be a perfect role for someone who is looking to transition into the commercial side of the industry. You'll be required to come into their office in central London as little as 1 to 2 times per month if you wished, but also you'll have the chance to come in much more than that if you'd prefer - they're flexible around you! Key requirements: 3 or more years Clinical Project Management experience in an Academia, Pharma or Biotech setting. Open to UK, EU or global experience. Phases I-III. Oncology or adv. Some exposure with managing vendors/ CROs. Budget management experience ideally but not essential. A personable, approachable, and dynamic individual who has the 'roll your sleeves up' approach - knows what is needed to work a small company environment. BSc, MSc or PhD background. The company offers a negotiable basic salary + discretionary bonus + stock options + 8% pension. If you are having difficulty in applying or if you have any questions, please contact Jack O'Neill at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Laboratory Instrument Support Engineer for a pharmaceutical organisation. This role is on a contract basis. The client is focused on modernising to make the world a healthier place every day. Check out the role overview below If you are confident you have got the right skills and experience, apply today. Responsibilities: Supervise TSA email and logging calls, producing and allocating work requests to pertinent queues in EAMS, escalating Ariba purchase order and resolving those matters. Offer performance certification, calibration, qualification services for lab equipment. Handle and guide the actions of vendors and contract personnel. Manage calibration and upkeep of organised instrument events, which involves instruments calibrated and preserved by external suppliers, and those sent away for calibration. Provide test equipment, evaluating and archiving of calibration 7 maintenance documents, and accomplishment of affiliated EAMS work orders and upkeep of the EAMS database instrument list. The ideal candidate will conduct tasks rendering to affiliated processes and regulatory standards. You will manage the documentation of instrumentation calibrations such as upkeep of logbooks, evaluating and archiving calibration and maintenance documents, etc. Accomplish any electronic notifications in the EAMS system to confirm accomplishment of calibration work orders. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a metrology or engineering discipline with pertinent work experience. Acquaintance with commercial/industrial settings. Familiarity with operating in a pharmaceutical setting. Know-how of regulatory needs for cGMP and GLP. Prior involvement in planning and timetabling team actions. Know-how of GRP work management. Computer literacy in accomplishing emails and documentation. Know-how of the company's computerised maintenance management systems. Comprehension of policies and SOPs for use of computerised maintenance management systems. Able to write, read and comprehend calibration SOPs. Partake in the evaluation and providing updates to calibration SOPs. Capable of cooperating with international workplace solutions co-workers, crucial clients/shareholders to fulfil function. Exhibits honesty and an ethical manner. A good listener and responds suitably. A committed individual who is able to meet and comprehend the clients' requirements. A high attention to detail with the ability to assume ownership. Works towards a consistent performance. Adaptable across the organisation. An open individual to new concepts and working techniques. Capable of pursuing prospects to improve systems. Assists and motivated others. Able to embrace diversity, agility in fostering new technology. Know-how and use of suitable influencing abilities. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 23, 2022
Full time
Proclinical are recruiting a Laboratory Instrument Support Engineer for a pharmaceutical organisation. This role is on a contract basis. The client is focused on modernising to make the world a healthier place every day. Check out the role overview below If you are confident you have got the right skills and experience, apply today. Responsibilities: Supervise TSA email and logging calls, producing and allocating work requests to pertinent queues in EAMS, escalating Ariba purchase order and resolving those matters. Offer performance certification, calibration, qualification services for lab equipment. Handle and guide the actions of vendors and contract personnel. Manage calibration and upkeep of organised instrument events, which involves instruments calibrated and preserved by external suppliers, and those sent away for calibration. Provide test equipment, evaluating and archiving of calibration 7 maintenance documents, and accomplishment of affiliated EAMS work orders and upkeep of the EAMS database instrument list. The ideal candidate will conduct tasks rendering to affiliated processes and regulatory standards. You will manage the documentation of instrumentation calibrations such as upkeep of logbooks, evaluating and archiving calibration and maintenance documents, etc. Accomplish any electronic notifications in the EAMS system to confirm accomplishment of calibration work orders. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a metrology or engineering discipline with pertinent work experience. Acquaintance with commercial/industrial settings. Familiarity with operating in a pharmaceutical setting. Know-how of regulatory needs for cGMP and GLP. Prior involvement in planning and timetabling team actions. Know-how of GRP work management. Computer literacy in accomplishing emails and documentation. Know-how of the company's computerised maintenance management systems. Comprehension of policies and SOPs for use of computerised maintenance management systems. Able to write, read and comprehend calibration SOPs. Partake in the evaluation and providing updates to calibration SOPs. Capable of cooperating with international workplace solutions co-workers, crucial clients/shareholders to fulfil function. Exhibits honesty and an ethical manner. A good listener and responds suitably. A committed individual who is able to meet and comprehend the clients' requirements. A high attention to detail with the ability to assume ownership. Works towards a consistent performance. Adaptable across the organisation. An open individual to new concepts and working techniques. Capable of pursuing prospects to improve systems. Assists and motivated others. Able to embrace diversity, agility in fostering new technology. Know-how and use of suitable influencing abilities. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a QC Scientist (Stability) for a biotech establishment. This role is on a permanent basis and is located in Abingdon. The client is focused on revolutionising solutions for cancer. All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description. Responsibilities: Accountable for the protocol and document production of assays transfers linked to QC tests using practices such as ELISA, gel electrophoresis, bioassay's spectroscopy, PCR, etc. Uphold QC systems linked to in-process, final drug product and stability sample. Evaluate testing data of other analysts. Supervise sampling and storage of QC samples and uphold retain inventory. Conduct QC testing of raw resources, in-process, water and product samples adhering to SOPs. You will engage within internal as well as cross functionally to communicate QC needs. Organise shipping samples to Milton Park and contract testing labs. Form, review and uphold processes for QC testing. Support the upkeep of QC lab and equipment. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a chemistry/biochemistry/microbiology or a similar science discipline. At least 3 - 5 years of experience with GLP/GMP within a pertinent work setting. Computer literacy in MS Word, Excel, etc. Works well within a team setting. Communication skills both verbally and in writing. An organised individual. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 23, 2022
Full time
Proclinical are recruiting a QC Scientist (Stability) for a biotech establishment. This role is on a permanent basis and is located in Abingdon. The client is focused on revolutionising solutions for cancer. All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description. Responsibilities: Accountable for the protocol and document production of assays transfers linked to QC tests using practices such as ELISA, gel electrophoresis, bioassay's spectroscopy, PCR, etc. Uphold QC systems linked to in-process, final drug product and stability sample. Evaluate testing data of other analysts. Supervise sampling and storage of QC samples and uphold retain inventory. Conduct QC testing of raw resources, in-process, water and product samples adhering to SOPs. You will engage within internal as well as cross functionally to communicate QC needs. Organise shipping samples to Milton Park and contract testing labs. Form, review and uphold processes for QC testing. Support the upkeep of QC lab and equipment. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a chemistry/biochemistry/microbiology or a similar science discipline. At least 3 - 5 years of experience with GLP/GMP within a pertinent work setting. Computer literacy in MS Word, Excel, etc. Works well within a team setting. Communication skills both verbally and in writing. An organised individual. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Service Desk Analyst for a pharmaceutical corporation. This role is on a contract basis and is located in the United Kingdom. The client is focused on finding, developing and supplying novel remedies that aid people in overcoming serious illnesses. Responsibilities: When required, you will contribute to application testing, upgrades and deployments, as well as internal service desk projects. Conduct troubleshooting to solve or raise to the suitable tier 2 teams. The ideal candidate will research and solve more multifaceted field/scientific application and business process problems. You will accept incoming calls, chats, tickets, redirect calls/tickets if needed, to suitable support groups for resolution while setting end user expectations throughout the initial interaction. Produce tickets and report all actions within the company's ticket system aligned with the company's quality standards. Offer application and process training to others as well as serve as a SME/POC for other team members. Other duties may be assigned to the role. Skills & Requirements: Educated to a high school diploma level, ideally to a university degree level in a pertinent discipline. Comprehension of ITIL Framework and ITSM. Familiarity within a technical support setting, and/or service desk setting, ideally involved with tools, processes, methodologies, telephony systems and servicenow, etc. Computer literacy with Microsoft office, application support and Microsoft windows. Acquaintance with assisting the life sciences. Fluency in the Italian and English languages with knowledge in Spanish. Communication skills both verbally and in writing. Customer service abilities. Capable of troubleshooting and research application problems. Able to explain technical information to end users. Ability to set priorities and manage various tasks simultaneously. Capable of resolving issues. Able to adhere to service desk procedures and processes. A positive, efficient and agile individual with the ability to partake in completing team goals and objectives. Works well in a team environment. Keen to learn new skills as well as open to ideas. To optimise service delivery, you will be able to drive quality, process improvement and novelty. Capable of conducting documentation translation. Willing to work flexible days and hours. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 23, 2022
Full time
Proclinical are recruiting a Service Desk Analyst for a pharmaceutical corporation. This role is on a contract basis and is located in the United Kingdom. The client is focused on finding, developing and supplying novel remedies that aid people in overcoming serious illnesses. Responsibilities: When required, you will contribute to application testing, upgrades and deployments, as well as internal service desk projects. Conduct troubleshooting to solve or raise to the suitable tier 2 teams. The ideal candidate will research and solve more multifaceted field/scientific application and business process problems. You will accept incoming calls, chats, tickets, redirect calls/tickets if needed, to suitable support groups for resolution while setting end user expectations throughout the initial interaction. Produce tickets and report all actions within the company's ticket system aligned with the company's quality standards. Offer application and process training to others as well as serve as a SME/POC for other team members. Other duties may be assigned to the role. Skills & Requirements: Educated to a high school diploma level, ideally to a university degree level in a pertinent discipline. Comprehension of ITIL Framework and ITSM. Familiarity within a technical support setting, and/or service desk setting, ideally involved with tools, processes, methodologies, telephony systems and servicenow, etc. Computer literacy with Microsoft office, application support and Microsoft windows. Acquaintance with assisting the life sciences. Fluency in the Italian and English languages with knowledge in Spanish. Communication skills both verbally and in writing. Customer service abilities. Capable of troubleshooting and research application problems. Able to explain technical information to end users. Ability to set priorities and manage various tasks simultaneously. Capable of resolving issues. Able to adhere to service desk procedures and processes. A positive, efficient and agile individual with the ability to partake in completing team goals and objectives. Works well in a team environment. Keen to learn new skills as well as open to ideas. To optimise service delivery, you will be able to drive quality, process improvement and novelty. Capable of conducting documentation translation. Willing to work flexible days and hours. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting for a Junior / Project Manager to join an exciting start up Biotech that specialise within Inflammation & Oncology for permanent position on a home working model. This is an amazing and rare opportunity to step away from a CRO environment and work directly with a Sponsor which will open so many career opportunities for you in the future. This is an opportunity to work directly with a Biotech at a very exciting stage of their growth where you will be a key hire into their UK Clinical Operations team, which means there will be ample opportunity for you to progress and develop within the company as they continue to grow. Job Description A fully homebased position with the opportunity to have office presence in their Scottish based hub. Exposure to working in a small team, start up feel. Liaise and support the Associate / Director of Clinical Operations. Working on budget oversight and extensive vendor management. Presenting updates to the board and investors. Key Requirements Three+ years' experience in CRO oversight and Vendor management. 5+ years' experience working in a CRO, Pharma or Biotech environment. Strong experience and knowledge in Inflammation and Oncology therapeutic areas preferred. Familiar with working with short lines of communications as you will be working closely with the CEO, CFO, Director of Clinical Operations. Exposure with Preclinical data and transitioning to early phase is extremely beneficial. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting for a Junior / Project Manager to join an exciting start up Biotech that specialise within Inflammation & Oncology for permanent position on a home working model. This is an amazing and rare opportunity to step away from a CRO environment and work directly with a Sponsor which will open so many career opportunities for you in the future. This is an opportunity to work directly with a Biotech at a very exciting stage of their growth where you will be a key hire into their UK Clinical Operations team, which means there will be ample opportunity for you to progress and develop within the company as they continue to grow. Job Description A fully homebased position with the opportunity to have office presence in their Scottish based hub. Exposure to working in a small team, start up feel. Liaise and support the Associate / Director of Clinical Operations. Working on budget oversight and extensive vendor management. Presenting updates to the board and investors. Key Requirements Three+ years' experience in CRO oversight and Vendor management. 5+ years' experience working in a CRO, Pharma or Biotech environment. Strong experience and knowledge in Inflammation and Oncology therapeutic areas preferred. Familiar with working with short lines of communications as you will be working closely with the CEO, CFO, Director of Clinical Operations. Exposure with Preclinical data and transitioning to early phase is extremely beneficial. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Risk Management Operations Specialist for a pharmaceutical organisation. This role is on a contract basis and is located in the UK. The client is focused on finding, evolving and providing novel remedies that assist people in overcoming serious illnesses. Responsibilities: Assist the associate manager risk management by offering supervised support to a third-part provider of the risk management operations team for eRMP data processing actions. Supply client assistance to healthcare professionals for the operational UK PPP. You will investigate prospects for compliance growth working alongside the associate manager. To recognise and execute prospects to grow customer experience and satisfaction, you will assist the associate manager. To guarantee that the third-party suppliers are compliantly conducting eRMP data processing actions, you will be assisting the associate manager. Accountable for meeting outlines productivity metrics for quality and productivity KPIs for both RMO and the third-party provider. Serve as a delegate of the Associate Manager in attending meetings when the Associate Manager is unable to. Other duties may be assigned to the role. Skills & Requirements: An organised individual with a high attention to detail and precision. Process outlook along with process development/documentation abilities. Works well in a team environment. Know-how of medical vocabulary. Communication skills both verbally and in writing. Fluency in the English language. Capable of handling self in a pressurised setting. An enthusiastic, self-motivated individual with the ability to take the initiative. Computer literacy in Word, Outlook, Excel, etc. Educated to a degree level in a life science discipline. Past involvement within a pharmaceutical organisation handling responsibilities which include things such as drug safety, risk management, medical, quality & compliance, regulatory or audit. Operations and client service experience would be ideal. Comprehension of database systems and linked IT terminology. Presentation abilities. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a Risk Management Operations Specialist for a pharmaceutical organisation. This role is on a contract basis and is located in the UK. The client is focused on finding, evolving and providing novel remedies that assist people in overcoming serious illnesses. Responsibilities: Assist the associate manager risk management by offering supervised support to a third-part provider of the risk management operations team for eRMP data processing actions. Supply client assistance to healthcare professionals for the operational UK PPP. You will investigate prospects for compliance growth working alongside the associate manager. To recognise and execute prospects to grow customer experience and satisfaction, you will assist the associate manager. To guarantee that the third-party suppliers are compliantly conducting eRMP data processing actions, you will be assisting the associate manager. Accountable for meeting outlines productivity metrics for quality and productivity KPIs for both RMO and the third-party provider. Serve as a delegate of the Associate Manager in attending meetings when the Associate Manager is unable to. Other duties may be assigned to the role. Skills & Requirements: An organised individual with a high attention to detail and precision. Process outlook along with process development/documentation abilities. Works well in a team environment. Know-how of medical vocabulary. Communication skills both verbally and in writing. Fluency in the English language. Capable of handling self in a pressurised setting. An enthusiastic, self-motivated individual with the ability to take the initiative. Computer literacy in Word, Outlook, Excel, etc. Educated to a degree level in a life science discipline. Past involvement within a pharmaceutical organisation handling responsibilities which include things such as drug safety, risk management, medical, quality & compliance, regulatory or audit. Operations and client service experience would be ideal. Comprehension of database systems and linked IT terminology. Presentation abilities. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical Staffing are representing a top 5 CRO who are looking for 10 x CRA IIs / Senior CRAs to join their team in the UK on a permanent basis. These are amazing opportunities to work with a top British Pharmaceutical company in the industry, where you'll perform industry standard site visits per month as well as being offered the chance to develop quickly in your career - this is due to our client's renowned training and development training program for CRAs who are looking to step up into Line Management or Project Management. The preferred candidates will have a strong oncology background, however they are very flexible on candidates with all types of therapy area experience. For these positions, 12-18 months independent monitoring experience is needed as a minimum to be considered. Site visits will vary from being regional based as much as possible to being nationwide visits, so they would need candidates who are open minded to this. What's on offer? Highly flexible basic salary + 6k car allowance + sign on bonus + standard benefits. The chance to develop down an FSP model or multi -sponsor route. Regional and National site visits, dependant on location. Key requirements: Valid UK driver licence. British / permanent residency. Nursing, BSc, MSc or PHD qualifications. 12 months independent monitoring experience. If you are having difficulty in applying or if you have any questions, please contact James Hassan on . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical Staffing are representing a top 5 CRO who are looking for 10 x CRA IIs / Senior CRAs to join their team in the UK on a permanent basis. These are amazing opportunities to work with a top British Pharmaceutical company in the industry, where you'll perform industry standard site visits per month as well as being offered the chance to develop quickly in your career - this is due to our client's renowned training and development training program for CRAs who are looking to step up into Line Management or Project Management. The preferred candidates will have a strong oncology background, however they are very flexible on candidates with all types of therapy area experience. For these positions, 12-18 months independent monitoring experience is needed as a minimum to be considered. Site visits will vary from being regional based as much as possible to being nationwide visits, so they would need candidates who are open minded to this. What's on offer? Highly flexible basic salary + 6k car allowance + sign on bonus + standard benefits. The chance to develop down an FSP model or multi -sponsor route. Regional and National site visits, dependant on location. Key requirements: Valid UK driver licence. British / permanent residency. Nursing, BSc, MSc or PHD qualifications. 12 months independent monitoring experience. If you are having difficulty in applying or if you have any questions, please contact James Hassan on . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Scientist for a pharmaceutical organisation. This role is on a contract basis. The client is focused on providing remedies. Responsibilities: Produce and uphold clear electronic experimental records. The ideal candidate will deliver high quality in vitro data rendering to the study plan as approved with the team leader or project supervisor. Uphold a consciousness of present developments in the literature to assist projects, bring forward new target concepts or new technologies/assay strategies. You will drive personal development within Oncology bioscience, independently recognising prospects where pertinent. Offer expert interpretation of experimental data, recognising novel solutions to issues and putting forward plans for further experiments. Discuss experimental data and crucial discoveries in a clear and concise way towards project teams. Skills & Requirements: Educated to a degree level in a cell biology, biochemistry, pharmacology or a similar discipline with a PhD or at least 2 - 3 years of experience in a pertinent lab environment. Demonstrated ability to deliver data from the lab. Knowledge in mammalian cell line tissue culture practices which involves cell line maintenance, transfection, transduction, etc. Knowledge in a variety of in vitro cell based & mechanistic practices and assays which involves cellular proliferation and survival assays, flow cytometry and high-content imaging. Know-how in a variety of molecular biological practices which involves molecular cloning, isolation and analysis of nucleic acids and proteins. Presentation and communication skills both verbally and in writing. A positive individual who works well in a team environment. Eager to improve and develop new abilities. A passionate individual regarding experimental work with an eagerness to pursue a career from the lab. Comprehension of cancer cell biology. Familiarity with lab-based drug discovery within an academic or a pharmaceutical company environment. Knowledge of CRISPR gene editing and stable cell line production. Comprehension of the drug discovery procedure. Acquaintance with analysing large data sets. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a Scientist for a pharmaceutical organisation. This role is on a contract basis. The client is focused on providing remedies. Responsibilities: Produce and uphold clear electronic experimental records. The ideal candidate will deliver high quality in vitro data rendering to the study plan as approved with the team leader or project supervisor. Uphold a consciousness of present developments in the literature to assist projects, bring forward new target concepts or new technologies/assay strategies. You will drive personal development within Oncology bioscience, independently recognising prospects where pertinent. Offer expert interpretation of experimental data, recognising novel solutions to issues and putting forward plans for further experiments. Discuss experimental data and crucial discoveries in a clear and concise way towards project teams. Skills & Requirements: Educated to a degree level in a cell biology, biochemistry, pharmacology or a similar discipline with a PhD or at least 2 - 3 years of experience in a pertinent lab environment. Demonstrated ability to deliver data from the lab. Knowledge in mammalian cell line tissue culture practices which involves cell line maintenance, transfection, transduction, etc. Knowledge in a variety of in vitro cell based & mechanistic practices and assays which involves cellular proliferation and survival assays, flow cytometry and high-content imaging. Know-how in a variety of molecular biological practices which involves molecular cloning, isolation and analysis of nucleic acids and proteins. Presentation and communication skills both verbally and in writing. A positive individual who works well in a team environment. Eager to improve and develop new abilities. A passionate individual regarding experimental work with an eagerness to pursue a career from the lab. Comprehension of cancer cell biology. Familiarity with lab-based drug discovery within an academic or a pharmaceutical company environment. Knowledge of CRISPR gene editing and stable cell line production. Comprehension of the drug discovery procedure. Acquaintance with analysing large data sets. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Senior Regulatory Executive for a biotech corporation. This role is on a contract basis and is located in Surrey. The client is focused on improving people's everyday health. Responsibilities: Handle country labelling variations and assist the CLS process rendering to approved standards. Evolve replies to regulatory authorities with regional regulatory affairs assistance and crucial shareholders. You will update the GDS aligned with the formed processes and systems. Offer labelling knowledge for RA actions such as renewal, PBRERs. Guarantee compliance of their activities by adhering to forms procedures, policies, SOPs and working instructions. Produce and review the assisted documentation needed for GDS sanction at CHSLC. The deal candidate might serve as a representative to external groups on specific task forces with labelling knowledge, such as digital e-leaflet, etc. Other duties may be assigned to this role. If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a Senior Regulatory Executive for a biotech corporation. This role is on a contract basis and is located in Surrey. The client is focused on improving people's everyday health. Responsibilities: Handle country labelling variations and assist the CLS process rendering to approved standards. Evolve replies to regulatory authorities with regional regulatory affairs assistance and crucial shareholders. You will update the GDS aligned with the formed processes and systems. Offer labelling knowledge for RA actions such as renewal, PBRERs. Guarantee compliance of their activities by adhering to forms procedures, policies, SOPs and working instructions. Produce and review the assisted documentation needed for GDS sanction at CHSLC. The deal candidate might serve as a representative to external groups on specific task forces with labelling knowledge, such as digital e-leaflet, etc. Other duties may be assigned to this role. If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a QC Scientist (Stability) for a biotech establishment. This role is on a permanent basis and is located in Abingdon. The client is focused on revolutionising solutions for cancer. Responsibilities: Accountable for the protocol and document production of assays transfers linked to QC tests using practices such as ELISA, gel electrophoresis, bioassay's spectroscopy, PCR, etc. Uphold QC systems linked to in-process, final drug product and stability sample. Evaluate testing data of other analysts. Supervise sampling and storage of QC samples and uphold retain inventory. Conduct QC testing of raw resources, in-process, water and product samples adhering to SOPs. You will engage within internal as well as cross functionally to communicate QC needs. Organise shipping samples to Milton Park and contract testing labs. Form, review and uphold processes for QC testing. Support the upkeep of QC lab and equipment. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a chemistry/biochemistry/microbiology or a similar science discipline. At least 3 - 5 years of experience with GLP/GMP within a pertinent work setting. Computer literacy in MS Word, Excel, etc. Works well within a team setting. Communication skills both verbally and in writing. An organised individual. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a QC Scientist (Stability) for a biotech establishment. This role is on a permanent basis and is located in Abingdon. The client is focused on revolutionising solutions for cancer. Responsibilities: Accountable for the protocol and document production of assays transfers linked to QC tests using practices such as ELISA, gel electrophoresis, bioassay's spectroscopy, PCR, etc. Uphold QC systems linked to in-process, final drug product and stability sample. Evaluate testing data of other analysts. Supervise sampling and storage of QC samples and uphold retain inventory. Conduct QC testing of raw resources, in-process, water and product samples adhering to SOPs. You will engage within internal as well as cross functionally to communicate QC needs. Organise shipping samples to Milton Park and contract testing labs. Form, review and uphold processes for QC testing. Support the upkeep of QC lab and equipment. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a chemistry/biochemistry/microbiology or a similar science discipline. At least 3 - 5 years of experience with GLP/GMP within a pertinent work setting. Computer literacy in MS Word, Excel, etc. Works well within a team setting. Communication skills both verbally and in writing. An organised individual. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a QC Operations Manager for a pharmaceutical organisation. This role is on a permanent basis and is located in Hatfield. The client is focused on enhancing the advantages that healthcare supplies to patients. Responsibilities: Handle the analysis and documenting of any analytical data from third-party contractors. Organise and assist in testing for EU importation, guaranteeing a solid relationship is upheld with the contract labs and resolve any problems/aberrations. Partake in the QC lab consistent improvement programme. Sanction QC testing performed on bulk product, stability and finished product rendering to GMP. You will guarantee that all lab processes and equipment are covered by SOPs. Assist in the upkeep of lab quality systems and quality management systems in compliance, rendering agreed protocols. Train personnel for the QC functions and follow systems and processes to assist in their development. Other duties may be assigned to this role. Skills & Requirements: Capable of forming and upholding efficient working relations within EML, associated establishments and any other clients. Know-how of quality control, quality systems, GMP, regulatory compliance and manufacture and packaging of pharmaceutical products. Solid scientific and technical judgement. Able to comprehend multifaceted data and display crucial discoveries. Computer literacy in Word, PowerPoint, Excel, etc. Know-how, comprehension and implementation of GMP regulations and guidelines. Leadership capabilities with the ability to people manage. Able to resolve issues and make decisions. Presents self in a professional, diplomatic manner. Self-conscious. Capable of motivating and influencing others. Presentation and communication skills both verbally and in writing. Able to manage time efficiently. If you are having difficulty in applying or if you have any questions, please contact Ieuan Philips on . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a QC Operations Manager for a pharmaceutical organisation. This role is on a permanent basis and is located in Hatfield. The client is focused on enhancing the advantages that healthcare supplies to patients. Responsibilities: Handle the analysis and documenting of any analytical data from third-party contractors. Organise and assist in testing for EU importation, guaranteeing a solid relationship is upheld with the contract labs and resolve any problems/aberrations. Partake in the QC lab consistent improvement programme. Sanction QC testing performed on bulk product, stability and finished product rendering to GMP. You will guarantee that all lab processes and equipment are covered by SOPs. Assist in the upkeep of lab quality systems and quality management systems in compliance, rendering agreed protocols. Train personnel for the QC functions and follow systems and processes to assist in their development. Other duties may be assigned to this role. Skills & Requirements: Capable of forming and upholding efficient working relations within EML, associated establishments and any other clients. Know-how of quality control, quality systems, GMP, regulatory compliance and manufacture and packaging of pharmaceutical products. Solid scientific and technical judgement. Able to comprehend multifaceted data and display crucial discoveries. Computer literacy in Word, PowerPoint, Excel, etc. Know-how, comprehension and implementation of GMP regulations and guidelines. Leadership capabilities with the ability to people manage. Able to resolve issues and make decisions. Presents self in a professional, diplomatic manner. Self-conscious. Capable of motivating and influencing others. Presentation and communication skills both verbally and in writing. Able to manage time efficiently. If you are having difficulty in applying or if you have any questions, please contact Ieuan Philips on . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Maintenance Controls Technician for a pharmaceutical organisation. This role is on a permanent basis. The client is focused on developing life-changing remedies within various therapeutic areas. Responsibilities: Offer technical hardware, software and coding assistance to guarantee systems and equipment are upheld to meet performance needs. Be involved in reliability processes, for example: RCM, RCA, FMEA, etc. Produce, uphold, and implement automation maintenance processes for equipment/computerised systems, which involves use of suitable personal protective equipment and safety processes. You will be responsive to change as well as to the requirements of the company when needed. The ideal candidate will carry out planned, corrective and breakdown maintenance. Assist in the reduction of automation maintenance plans through data driven equipment performance as well as FMEA examinations. You will be a part of the quality processes, for example: CAPA, UE, change control and internal auditing. Actively look for reliability/improvement prospects and guarantee their accomplishment. Other duties may be assigned to this role. Skills & Requirements: An HNC in automation or linked engineering discipline and eager to be educated to a degree level in a linked engineering discipline. At least 2+ years of experience in configuring and upholding programmable electronic systems used for process control, ideally in a cGMP regulated setting such as GAMP5, FDA 21 CFR11, EU ANNEX 11. Acquaintance with Siemens PLC/HMI and SCADA configuration and maintenance. Knowledgeable in regulatory expectations together with the latest developments and automation matters within the international pharmaceutical industry such as GAMP5, FDA 21 CFR11, EU ANNEX 11. Familiarity with successful pre-approval inspection or corresponding regulatory audit including Programmable Electronic Systems. Competent with Siemens S7 software and applications. Able to think analytically and technically with the ability to resolve issues. An organised individual. Works well in a team environment. Skilled in the programming, maintenance, specification and validation of automation systems. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 22, 2022
Full time
Proclinical are recruiting a Maintenance Controls Technician for a pharmaceutical organisation. This role is on a permanent basis. The client is focused on developing life-changing remedies within various therapeutic areas. Responsibilities: Offer technical hardware, software and coding assistance to guarantee systems and equipment are upheld to meet performance needs. Be involved in reliability processes, for example: RCM, RCA, FMEA, etc. Produce, uphold, and implement automation maintenance processes for equipment/computerised systems, which involves use of suitable personal protective equipment and safety processes. You will be responsive to change as well as to the requirements of the company when needed. The ideal candidate will carry out planned, corrective and breakdown maintenance. Assist in the reduction of automation maintenance plans through data driven equipment performance as well as FMEA examinations. You will be a part of the quality processes, for example: CAPA, UE, change control and internal auditing. Actively look for reliability/improvement prospects and guarantee their accomplishment. Other duties may be assigned to this role. Skills & Requirements: An HNC in automation or linked engineering discipline and eager to be educated to a degree level in a linked engineering discipline. At least 2+ years of experience in configuring and upholding programmable electronic systems used for process control, ideally in a cGMP regulated setting such as GAMP5, FDA 21 CFR11, EU ANNEX 11. Acquaintance with Siemens PLC/HMI and SCADA configuration and maintenance. Knowledgeable in regulatory expectations together with the latest developments and automation matters within the international pharmaceutical industry such as GAMP5, FDA 21 CFR11, EU ANNEX 11. Familiarity with successful pre-approval inspection or corresponding regulatory audit including Programmable Electronic Systems. Competent with Siemens S7 software and applications. Able to think analytically and technically with the ability to resolve issues. An organised individual. Works well in a team environment. Skilled in the programming, maintenance, specification and validation of automation systems. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Laboratory Instrument Support Engineer for a pharmaceutical organisation. This role is on a contract basis. The client is focused on modernising to make the world a healthier place every day. Responsibilities: Supervise TSA email and logging calls, producing and allocating work requests to pertinent queues in EAMS, escalating Ariba purchase order and resolving those matters. Offer performance certification, calibration, qualification services for lab equipment. Handle and guide the actions of vendors and contract personnel. Manage calibration and upkeep of organised instrument events, which involves instruments calibrated and preserved by external suppliers, and those sent away for calibration. Provide test equipment, evaluating and archiving of calibration 7 maintenance documents, and accomplishment of affiliated EAMS work orders and upkeep of the EAMS database instrument list. The ideal candidate will conduct tasks rendering to affiliated processes and regulatory standards. You will manage the documentation of instrumentation calibrations such as upkeep of logbooks, evaluating and archiving calibration and maintenance documents, etc. Accomplish any electronic notifications in the EAMS system to confirm accomplishment of calibration work orders. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a metrology or engineering discipline with pertinent work experience. Acquaintance with commercial/industrial settings. Familiarity with operating in a pharmaceutical setting. Know-how of regulatory needs for cGMP and GLP. Prior involvement in planning and timetabling team actions. Know-how of GRP work management. Computer literacy in accomplishing emails and documentation. Know-how of the company's computerised maintenance management systems. Comprehension of policies and SOPs for use of computerised maintenance management systems. Able to write, read and comprehend calibration SOPs. Partake in the evaluation and providing updates to calibration SOPs. Capable of cooperating with international workplace solutions co-workers, crucial clients/shareholders to fulfil function. Exhibits honesty and an ethical manner. A good listener and responds suitably. A committed individual who is able to meet and comprehend the clients' requirements. A high attention to detail with the ability to assume ownership. Works towards a consistent performance. Adaptable across the organisation. An open individual to new concepts and working techniques. Capable of pursuing prospects to improve systems. Assists and motivated others. Able to embrace diversity, agility in fostering new technology. Know-how and use of suitable influencing abilities. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Sep 20, 2022
Full time
Proclinical are recruiting a Laboratory Instrument Support Engineer for a pharmaceutical organisation. This role is on a contract basis. The client is focused on modernising to make the world a healthier place every day. Responsibilities: Supervise TSA email and logging calls, producing and allocating work requests to pertinent queues in EAMS, escalating Ariba purchase order and resolving those matters. Offer performance certification, calibration, qualification services for lab equipment. Handle and guide the actions of vendors and contract personnel. Manage calibration and upkeep of organised instrument events, which involves instruments calibrated and preserved by external suppliers, and those sent away for calibration. Provide test equipment, evaluating and archiving of calibration 7 maintenance documents, and accomplishment of affiliated EAMS work orders and upkeep of the EAMS database instrument list. The ideal candidate will conduct tasks rendering to affiliated processes and regulatory standards. You will manage the documentation of instrumentation calibrations such as upkeep of logbooks, evaluating and archiving calibration and maintenance documents, etc. Accomplish any electronic notifications in the EAMS system to confirm accomplishment of calibration work orders. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a metrology or engineering discipline with pertinent work experience. Acquaintance with commercial/industrial settings. Familiarity with operating in a pharmaceutical setting. Know-how of regulatory needs for cGMP and GLP. Prior involvement in planning and timetabling team actions. Know-how of GRP work management. Computer literacy in accomplishing emails and documentation. Know-how of the company's computerised maintenance management systems. Comprehension of policies and SOPs for use of computerised maintenance management systems. Able to write, read and comprehend calibration SOPs. Partake in the evaluation and providing updates to calibration SOPs. Capable of cooperating with international workplace solutions co-workers, crucial clients/shareholders to fulfil function. Exhibits honesty and an ethical manner. A good listener and responds suitably. A committed individual who is able to meet and comprehend the clients' requirements. A high attention to detail with the ability to assume ownership. Works towards a consistent performance. Adaptable across the organisation. An open individual to new concepts and working techniques. Capable of pursuing prospects to improve systems. Assists and motivated others. Able to embrace diversity, agility in fostering new technology. Know-how and use of suitable influencing abilities. If you are having difficulty in applying or if you have any questions, please contact Mohammed Alli at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Proclinical are recruiting a Quality Manager, GLP for a laboratory. This role is on a permanent basis and is located in Manchester. The client is focused on providing services to their clients on a variety of products, materials and processes for a varied set of end markets. Responsibilities: Uphold and execute the company's quality management system. Encourage constant advancement action in the company's quality management system. Form a positive and active quality culture that drives employee engagement and makes the company a great place to work and be a part of. You will handle QA materials to assist both commercial and operational actions. The ideal candidate will host client, accreditation and regulatory assessments and inspections. Evolve and sustain the company's quality management system to meet all particular GLP, cGMP and UKAS regulatory needs. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a life science field, with familiarity in a pharmaceutical testing or pertinent setting such as manufacturing. Acquaintance with team leadership and management. Past involvement in quality assurance, ideally within a fast-paced analytical laboratory or similar setting; preferably with involvement in setting up/upholding a quality system. Familiarity with working within a GLP regulated setting as a member of a GLP monitoring authority programme. Prior involvement with GMP would be advantageous for the role. An acquaintance with leading/evaluating/sanctioning quality investigations, assuming responsibility of root cause analysis, evolving corrective activity plans and guaranteeing the efficiency of activities assumed. Keep updated with the modifications in the quality landscape and uphold personal professional development. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Jul 22, 2022
Full time
Proclinical are recruiting a Quality Manager, GLP for a laboratory. This role is on a permanent basis and is located in Manchester. The client is focused on providing services to their clients on a variety of products, materials and processes for a varied set of end markets. Responsibilities: Uphold and execute the company's quality management system. Encourage constant advancement action in the company's quality management system. Form a positive and active quality culture that drives employee engagement and makes the company a great place to work and be a part of. You will handle QA materials to assist both commercial and operational actions. The ideal candidate will host client, accreditation and regulatory assessments and inspections. Evolve and sustain the company's quality management system to meet all particular GLP, cGMP and UKAS regulatory needs. Other duties may be assigned to this role. Skills & Requirements: Educated to a degree level in a life science field, with familiarity in a pharmaceutical testing or pertinent setting such as manufacturing. Acquaintance with team leadership and management. Past involvement in quality assurance, ideally within a fast-paced analytical laboratory or similar setting; preferably with involvement in setting up/upholding a quality system. Familiarity with working within a GLP regulated setting as a member of a GLP monitoring authority programme. Prior involvement with GMP would be advantageous for the role. An acquaintance with leading/evaluating/sanctioning quality investigations, assuming responsibility of root cause analysis, evolving corrective activity plans and guaranteeing the efficiency of activities assumed. Keep updated with the modifications in the quality landscape and uphold personal professional development. If you are having difficulty in applying or if you have any questions, please contact Robert Scott at . Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.
Associate Recruitment Consultant- Dutch Speaker (Entry Level or Experienced Recruiter Life Sciences preferred but not essential) Location: London (2 minute walk from London Liverpool Street Station or a 3 minute walk from Moorgate Station) Salary: £24,000+ Basic (Negotiable dependent on experience + Uncapped commission & luxurious incentives including holidays, directors lunch and much more!) Start Date: As soon as you're available! We Offer You: · Quick Career Progression - At least one promotion a year with multiple tailored career paths including 360 Perm and/or Contract, Client Services, MSP, Delivery based teams, Executive search, Leadership and International Opportunities amongst others. Across the business we have a lot of roles to work on so there isn't as much a need to do BD like there is in most recruitment companies. · High Earning Potential and Uncapped Commission - Average OTE £27-35K+ YR1, up to £60K+ YR2, up to £100K+ YR3 and a salary increase with each promotion · 9 - 6 working hours and an earlier finish on Friday with dress down · Not KPI driven, realistic targets you can achieve as we believe in a positive environment · Promote international moves - Los Angeles, New York, San Francisco, Philadelphia, Boston, Basel, Frankfurt, Switzerland, Singapore, Sydney, Melbourne, Beijing, Tokyo, Shanghai and more offices to start up within the next 2 years · Access to a large international client base · Annual incentive trips away to Cape Town, Cancun, Singapore, Vegas, New York, Skiing etc. · Multiple Services to offer clients which makes you more appealing when winning business · Incentives include trips to the theatre, horse racing, go karting and Michelin star restaurants. · Continuous Support and Training with both your mentor and our Learning and Development team regardless of your level · Dynamic and Inclusive Culture · Fun Office space located by London Liverpool Street · Company Benefits - Pru Vitality healthcare, Subsidised Virgin Active gym membership, Extended gym lunches, Season ticket travel loan, Contributory pension scheme, Childcare vouchers, Cycle to work scheme · Hire into roles/projects that have a moral purpose Your Role and Responsibilities: With the initial job title of Associate Consultant, you will be fully trained in all aspects of recruitment by one of the senior members of the company and our Learning and Development team. During your time in this role, you will be working with a Senior / Principal Consultant and tasked with finding suitable candidates for open job vacancies across Europe. Responsibilities include: · Advertising jobs on social media sites · Searching for resumes via the database · Head-hunting candidates and networking on social media platforms · Taking referrals and adding CVs to the database · Introducing yourself to and briefing candidates about job opportunities · Discussing financial packages, timing and travel etc Working against many competing firms and their candidates, you will have some successes and some disappointments. You will be rewarded with commission for every placement that you make during your time as a Resourcer and if successful then you can be rewarded with a promotion and will be introduced to client management and business development (Consultant). What you need to have: · Fluent in Dutch · Fluent or professional level in English · Life Science Recruitment experience or in another industry is not essential but would be a plus · A Motivated attitude · Drive and ambition · A strong work ethic · An entrepreneurial spirit · Strong business acumen · Resilience · Scientific knowledge and sales experience is preferable; however it is not essential · Eager to learn *To Apply* Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. #LI-SR1
Dec 01, 2021
Full time
Associate Recruitment Consultant- Dutch Speaker (Entry Level or Experienced Recruiter Life Sciences preferred but not essential) Location: London (2 minute walk from London Liverpool Street Station or a 3 minute walk from Moorgate Station) Salary: £24,000+ Basic (Negotiable dependent on experience + Uncapped commission & luxurious incentives including holidays, directors lunch and much more!) Start Date: As soon as you're available! We Offer You: · Quick Career Progression - At least one promotion a year with multiple tailored career paths including 360 Perm and/or Contract, Client Services, MSP, Delivery based teams, Executive search, Leadership and International Opportunities amongst others. Across the business we have a lot of roles to work on so there isn't as much a need to do BD like there is in most recruitment companies. · High Earning Potential and Uncapped Commission - Average OTE £27-35K+ YR1, up to £60K+ YR2, up to £100K+ YR3 and a salary increase with each promotion · 9 - 6 working hours and an earlier finish on Friday with dress down · Not KPI driven, realistic targets you can achieve as we believe in a positive environment · Promote international moves - Los Angeles, New York, San Francisco, Philadelphia, Boston, Basel, Frankfurt, Switzerland, Singapore, Sydney, Melbourne, Beijing, Tokyo, Shanghai and more offices to start up within the next 2 years · Access to a large international client base · Annual incentive trips away to Cape Town, Cancun, Singapore, Vegas, New York, Skiing etc. · Multiple Services to offer clients which makes you more appealing when winning business · Incentives include trips to the theatre, horse racing, go karting and Michelin star restaurants. · Continuous Support and Training with both your mentor and our Learning and Development team regardless of your level · Dynamic and Inclusive Culture · Fun Office space located by London Liverpool Street · Company Benefits - Pru Vitality healthcare, Subsidised Virgin Active gym membership, Extended gym lunches, Season ticket travel loan, Contributory pension scheme, Childcare vouchers, Cycle to work scheme · Hire into roles/projects that have a moral purpose Your Role and Responsibilities: With the initial job title of Associate Consultant, you will be fully trained in all aspects of recruitment by one of the senior members of the company and our Learning and Development team. During your time in this role, you will be working with a Senior / Principal Consultant and tasked with finding suitable candidates for open job vacancies across Europe. Responsibilities include: · Advertising jobs on social media sites · Searching for resumes via the database · Head-hunting candidates and networking on social media platforms · Taking referrals and adding CVs to the database · Introducing yourself to and briefing candidates about job opportunities · Discussing financial packages, timing and travel etc Working against many competing firms and their candidates, you will have some successes and some disappointments. You will be rewarded with commission for every placement that you make during your time as a Resourcer and if successful then you can be rewarded with a promotion and will be introduced to client management and business development (Consultant). What you need to have: · Fluent in Dutch · Fluent or professional level in English · Life Science Recruitment experience or in another industry is not essential but would be a plus · A Motivated attitude · Drive and ambition · A strong work ethic · An entrepreneurial spirit · Strong business acumen · Resilience · Scientific knowledge and sales experience is preferable; however it is not essential · Eager to learn *To Apply* Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. #LI-SR1
Associate Recruitment Consultant- French Speakers (Entry Level or Experienced Recruiter Life Sciences preferred but not essential) Location: London (2 minute walk from London Liverpool Street Station or a 3 minute walk from Moorgate Station) Salary: £24,000+ Basic (Negotiable dependent on experience + Uncapped & luxurious incentives including holidays, directors lunch and much more!) Start Date: As soon as you're available! We Offer You: · Quick Career Progression - At least one promotion a year with multiple tailored career paths including 360 Perm and/or Contract, Client Services, MSP, Delivery based teams, Executive search, Leadership and International Opportunities amongst others. Across the business we have a lot of roles to work on so there isn't as much a need to do BD like there is in most recruitment companies. · High Earning Potential and Uncapped Commission - Average OTE £27-35K+ YR1, £40-60K+ YR2, £60K - £100K+ YR3 and a salary increase with each promotion · 9 - 6 working hours and an earlier finish on Friday with dress down · Not KPI driven, realistic targets you can achieve as we believe in a positive environment · Promote international moves - Los Angeles, New York, San Francisco, Philadelphia, Boston, Basel, Frankfurt, Switzerland, Singapore, Sydney, Melbourne, Beijing, Tokyo, Shanghai and more offices to start up within the next 2 years · Access to a large international client base · Annual incentive trips away to Cape Town, Cancun, Singapore, Vegas, New York, Skiing etc. · Multiple Services to offer clients which makes you more appealing when winning business · Incentives include trips to the theatre, horse racing, go karting and Michelin star restaurants. · Continuous Support and Training with both your mentor and our Learning and Development team regardless of your level · Dynamic and Inclusive Culture · Fun Office space located by London Liverpool Street · Company Benefits - Pru Vitality healthcare, Subsidised Virgin Active gym membership, Extended gym lunches, Season ticket travel loan, Contributory pension scheme, Childcare vouchers, Cycle to work scheme · Hire into roles/projects that have a moral purpose Your Role and Responsibilities: With the initial job title of Associate Consultant, you will be fully trained in all aspects of recruitment by one of the senior members of the company and our Learning and Development team. During your time in this role, you will be working with a Senior / Principal Consultant and tasked with finding suitable candidates for open job vacancies across Europe. Responsibilities include: · Advertising jobs on social media sites · Searching for resumes via the database · Head-hunting candidates and networking on social media platforms · Taking referrals and adding CVs to the database · Introducing yourself to and briefing candidates about job opportunities · Discussing financial packages, timing and travel etc Working against many competing firms and their candidates, you will have some successes and some disappointments. You will be rewarded with commission for every placement that you make during your time as a Resourcer and if successful then you can be rewarded with a promotion and will be introduced to client management and business development (Consultant). What you need to have: · Fluent in French · Must be a Professional or Fluent level in English · Life Science Recruitment experience or in another industry is not essential but would be a plus · A Motivated attitude · Drive and ambition · A strong work ethic · An entrepreneurial spirit · Strong business acumen · Resilience · Scientific knowledge and sales experience is preferable; however it is not essential · Eager to learn *To Apply* Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. #LI-SR1
Dec 01, 2021
Full time
Associate Recruitment Consultant- French Speakers (Entry Level or Experienced Recruiter Life Sciences preferred but not essential) Location: London (2 minute walk from London Liverpool Street Station or a 3 minute walk from Moorgate Station) Salary: £24,000+ Basic (Negotiable dependent on experience + Uncapped & luxurious incentives including holidays, directors lunch and much more!) Start Date: As soon as you're available! We Offer You: · Quick Career Progression - At least one promotion a year with multiple tailored career paths including 360 Perm and/or Contract, Client Services, MSP, Delivery based teams, Executive search, Leadership and International Opportunities amongst others. Across the business we have a lot of roles to work on so there isn't as much a need to do BD like there is in most recruitment companies. · High Earning Potential and Uncapped Commission - Average OTE £27-35K+ YR1, £40-60K+ YR2, £60K - £100K+ YR3 and a salary increase with each promotion · 9 - 6 working hours and an earlier finish on Friday with dress down · Not KPI driven, realistic targets you can achieve as we believe in a positive environment · Promote international moves - Los Angeles, New York, San Francisco, Philadelphia, Boston, Basel, Frankfurt, Switzerland, Singapore, Sydney, Melbourne, Beijing, Tokyo, Shanghai and more offices to start up within the next 2 years · Access to a large international client base · Annual incentive trips away to Cape Town, Cancun, Singapore, Vegas, New York, Skiing etc. · Multiple Services to offer clients which makes you more appealing when winning business · Incentives include trips to the theatre, horse racing, go karting and Michelin star restaurants. · Continuous Support and Training with both your mentor and our Learning and Development team regardless of your level · Dynamic and Inclusive Culture · Fun Office space located by London Liverpool Street · Company Benefits - Pru Vitality healthcare, Subsidised Virgin Active gym membership, Extended gym lunches, Season ticket travel loan, Contributory pension scheme, Childcare vouchers, Cycle to work scheme · Hire into roles/projects that have a moral purpose Your Role and Responsibilities: With the initial job title of Associate Consultant, you will be fully trained in all aspects of recruitment by one of the senior members of the company and our Learning and Development team. During your time in this role, you will be working with a Senior / Principal Consultant and tasked with finding suitable candidates for open job vacancies across Europe. Responsibilities include: · Advertising jobs on social media sites · Searching for resumes via the database · Head-hunting candidates and networking on social media platforms · Taking referrals and adding CVs to the database · Introducing yourself to and briefing candidates about job opportunities · Discussing financial packages, timing and travel etc Working against many competing firms and their candidates, you will have some successes and some disappointments. You will be rewarded with commission for every placement that you make during your time as a Resourcer and if successful then you can be rewarded with a promotion and will be introduced to client management and business development (Consultant). What you need to have: · Fluent in French · Must be a Professional or Fluent level in English · Life Science Recruitment experience or in another industry is not essential but would be a plus · A Motivated attitude · Drive and ambition · A strong work ethic · An entrepreneurial spirit · Strong business acumen · Resilience · Scientific knowledge and sales experience is preferable; however it is not essential · Eager to learn *To Apply* Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. #LI-SR1