Pharmacy Accuracy Checking Technician - Northampton Opportunity: Are you currently working as a Pharmacy Accuracy Checking Technician looking for a new role? Are you a registered Pharmacy Technician with the GPhC? Do you have an appropriate Accuracy Checking qualification? Want to work for a global pharmaceutical company? If yes then please read on. Your role as a Pharmacy Accuracy Checking Technician based in Northampton will involve: Providing accurate final checking of all Renal orders (PD, HHD) that contain POM & P (Prescription Only Medicines & Pharmacy medicines) and ancillary items before their dispatch from NDC to patients. Ensuring that pharmacy patient dispensing processes are compliant with regulations such as the General Pharmaceutical Council, Royal Pharmaceutical Society, Companies Pharmacy Standard Operating Procedures, Good Documentation Practices and Good Warehousing Practices. Ensuring all Standards and Guidelines issued by the GPhC and the RPS are met and are implemented. Providing technical assistance in the registered pharmacy. Supporting the Responsible Pharmacist (RP) as required. Ensuring all medication is managed in compliance with the company and Royal Pharmaceutical Society of Great Britain processes. Site based role. The hours of work are Monday to Friday 2.00 pm to 10.00 pm. This is a full time permanent job opportunity based in Northampton paying an excellent salary of £33,000 - £37,295.80 per annum with great benefits such as 25 days holiday plus bank holidays on top, Pension, Life insurance, Childcare vouchers and much more. Skills: To apply for the role of Pharmacy Accuracy Checking Technician you will have the following: Appropriate pharmaceutical qualification i.e. BTEC, NVQ Level 3 or equivalent. UK recognised or GPhC accredited Pharmacy Accuracy Checking qualification. Registered as a Pharmacy Technician with the GPhC. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Aug 18, 2025
Full time
Pharmacy Accuracy Checking Technician - Northampton Opportunity: Are you currently working as a Pharmacy Accuracy Checking Technician looking for a new role? Are you a registered Pharmacy Technician with the GPhC? Do you have an appropriate Accuracy Checking qualification? Want to work for a global pharmaceutical company? If yes then please read on. Your role as a Pharmacy Accuracy Checking Technician based in Northampton will involve: Providing accurate final checking of all Renal orders (PD, HHD) that contain POM & P (Prescription Only Medicines & Pharmacy medicines) and ancillary items before their dispatch from NDC to patients. Ensuring that pharmacy patient dispensing processes are compliant with regulations such as the General Pharmaceutical Council, Royal Pharmaceutical Society, Companies Pharmacy Standard Operating Procedures, Good Documentation Practices and Good Warehousing Practices. Ensuring all Standards and Guidelines issued by the GPhC and the RPS are met and are implemented. Providing technical assistance in the registered pharmacy. Supporting the Responsible Pharmacist (RP) as required. Ensuring all medication is managed in compliance with the company and Royal Pharmaceutical Society of Great Britain processes. Site based role. The hours of work are Monday to Friday 2.00 pm to 10.00 pm. This is a full time permanent job opportunity based in Northampton paying an excellent salary of £33,000 - £37,295.80 per annum with great benefits such as 25 days holiday plus bank holidays on top, Pension, Life insurance, Childcare vouchers and much more. Skills: To apply for the role of Pharmacy Accuracy Checking Technician you will have the following: Appropriate pharmaceutical qualification i.e. BTEC, NVQ Level 3 or equivalent. UK recognised or GPhC accredited Pharmacy Accuracy Checking qualification. Registered as a Pharmacy Technician with the GPhC. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Assurance and Regulatory Engineer Homebased Opportunity: Do you have experience in quality assurance and regulatory affairs for medical devices? Do you have experience of working to ISO 13485, ISO 14971 and UK MDR, Regulation (EU) 2017/745, MDSAP, ISO 9001 standards? Want to work for an innovative medical device manufacturing company? If yes then this is the role for you. Your role as a Quality Assurance and Regulatory Engineer will involve: Supplier & Purchasing: Reviewing the supplier onboarding, supplier revaluation and purchasing processes to ensure compliance with specific country regulations. Creating new documents to support the supplier and purchasing processes. Establishing controls for critical suppliers. Creating supplier quality agreements. Labelling Reviewing product and software labelling and conducting a gap analysis to ensure labels meet all regulatory and compliance standards. Risk Management Supporting product risk management activities according to current procedures. Reviewing all processes within the quality management system and document process risks in accordance with ISO 14971. Trend Analysis Establishing a process to collect, analyse and report on quality data to identify trends and areas for improvement. Training Creating training material on relevant regulations, standards, and guidance (e.g. UK MDR, Regulation (EU) 2017/745, MDSAP, ISO9001). Regulatory: Supporting the QARA team in: Creating a documentation pack aligned to the IMDRF table of contents to support registration of medical devices within Europe, Canada, Australia and the rest of the world. Maintaining and archiving technical documentation and regulatory files, including the regular review and updates required to ensure ongoing compliance with current standards and legal requirements. Preparing and compiling reports necessary for regulatory compliance, including monthly quality reports. This is a 6 Months Contract role based working from home. You will attend the office at Walsall, West Midlands approx. 2 days every fortnight. The client will review the contract towards the end date with a view of extending it or making the role permanent however this is all dependent on the individual and business performance. The PAYE rate is between £28.00 - £41.19 per hour. This is purely dependent on skills and experience. Skills: To apply for the role of Quality Assurance and Regulatory Engineer you will have the following: Proven experience in quality assurance and regulatory affairs within the medical device sector. Strong analytical and problem-solving skills. Confident, professional, and comfortable working in a close-knit team environment. Working knowledge of international medical device regulations, standards, and guidance documents including MDSAP, Regulation (EU) 2017/745, ISO 13485, ISO 9001 and ISO 14971. Competence in the use of QMS and IT tools, including MS Office, SharePoint, MS Teams, Word, Excel and Outlook. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Aug 12, 2025
Contractor
Quality Assurance and Regulatory Engineer Homebased Opportunity: Do you have experience in quality assurance and regulatory affairs for medical devices? Do you have experience of working to ISO 13485, ISO 14971 and UK MDR, Regulation (EU) 2017/745, MDSAP, ISO 9001 standards? Want to work for an innovative medical device manufacturing company? If yes then this is the role for you. Your role as a Quality Assurance and Regulatory Engineer will involve: Supplier & Purchasing: Reviewing the supplier onboarding, supplier revaluation and purchasing processes to ensure compliance with specific country regulations. Creating new documents to support the supplier and purchasing processes. Establishing controls for critical suppliers. Creating supplier quality agreements. Labelling Reviewing product and software labelling and conducting a gap analysis to ensure labels meet all regulatory and compliance standards. Risk Management Supporting product risk management activities according to current procedures. Reviewing all processes within the quality management system and document process risks in accordance with ISO 14971. Trend Analysis Establishing a process to collect, analyse and report on quality data to identify trends and areas for improvement. Training Creating training material on relevant regulations, standards, and guidance (e.g. UK MDR, Regulation (EU) 2017/745, MDSAP, ISO9001). Regulatory: Supporting the QARA team in: Creating a documentation pack aligned to the IMDRF table of contents to support registration of medical devices within Europe, Canada, Australia and the rest of the world. Maintaining and archiving technical documentation and regulatory files, including the regular review and updates required to ensure ongoing compliance with current standards and legal requirements. Preparing and compiling reports necessary for regulatory compliance, including monthly quality reports. This is a 6 Months Contract role based working from home. You will attend the office at Walsall, West Midlands approx. 2 days every fortnight. The client will review the contract towards the end date with a view of extending it or making the role permanent however this is all dependent on the individual and business performance. The PAYE rate is between £28.00 - £41.19 per hour. This is purely dependent on skills and experience. Skills: To apply for the role of Quality Assurance and Regulatory Engineer you will have the following: Proven experience in quality assurance and regulatory affairs within the medical device sector. Strong analytical and problem-solving skills. Confident, professional, and comfortable working in a close-knit team environment. Working knowledge of international medical device regulations, standards, and guidance documents including MDSAP, Regulation (EU) 2017/745, ISO 13485, ISO 9001 and ISO 14971. Competence in the use of QMS and IT tools, including MS Office, SharePoint, MS Teams, Word, Excel and Outlook. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Assurance and Regulatory Engineer Homebased Opportunity: Do you have experience in quality assurance and regulatory affairs for medical devices? Do you have experience of working to ISO 13485, ISO 14971 and UK MDR, Regulation (EU) 2017/745, MDSAP, ISO 9001 standards? Want to work for an innovative medical device manufacturing company? If yes then this is the role for you. Your role as a Quality Assurance and Regulatory Engineer will involve: Supplier & Purchasing: Reviewing the supplier onboarding, supplier revaluation and purchasing processes to ensure compliance with specific country regulations. Creating new documents to support the supplier and purchasing processes. Establishing controls for critical suppliers. Creating supplier quality agreements. Labelling Reviewing product and software labelling and conducting a gap analysis to ensure labels meet all regulatory and compliance standards. Risk Management Supporting product risk management activities according to current procedures. Reviewing all processes within the quality management system and document process risks in accordance with ISO 14971. Trend Analysis Establishing a process to collect, analyse and report on quality data to identify trends and areas for improvement. Training Creating training material on relevant regulations, standards, and guidance (e.g. UK MDR, Regulation (EU) 2017/745, MDSAP, ISO9001). Regulatory: Supporting the QARA team in: Creating a documentation pack aligned to the IMDRF table of contents to support registration of medical devices within Europe, Canada, Australia and the rest of the world. Maintaining and archiving technical documentation and regulatory files, including the regular review and updates required to ensure ongoing compliance with current standards and legal requirements. Preparing and compiling reports necessary for regulatory compliance, including monthly quality reports. This is a 6 Months Contract role based working from home. You will attend the office at Walsall, West Midlands approx. 2 days every fortnight. The client will review the contract towards the end date with a view of extending it or making the role permanent however this is all dependent on the individual and business performance. The PAYE rate is between £28.00 - £41.19 per hour. This is purely dependent on skills and experience. Skills: To apply for the role of Quality Assurance and Regulatory Engineer you will have the following: Proven experience in quality assurance and regulatory affairs within the medical device sector. Strong analytical and problem-solving skills. Confident, professional, and comfortable working in a close-knit team environment. Working knowledge of international medical device regulations, standards, and guidance documents including MDSAP, Regulation (EU) 2017/745, ISO 13485, ISO 9001 and ISO 14971. Competence in the use of QMS and IT tools, including MS Office, SharePoint, MS Teams, Word, Excel and Outlook. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Aug 12, 2025
Contractor
Quality Assurance and Regulatory Engineer Homebased Opportunity: Do you have experience in quality assurance and regulatory affairs for medical devices? Do you have experience of working to ISO 13485, ISO 14971 and UK MDR, Regulation (EU) 2017/745, MDSAP, ISO 9001 standards? Want to work for an innovative medical device manufacturing company? If yes then this is the role for you. Your role as a Quality Assurance and Regulatory Engineer will involve: Supplier & Purchasing: Reviewing the supplier onboarding, supplier revaluation and purchasing processes to ensure compliance with specific country regulations. Creating new documents to support the supplier and purchasing processes. Establishing controls for critical suppliers. Creating supplier quality agreements. Labelling Reviewing product and software labelling and conducting a gap analysis to ensure labels meet all regulatory and compliance standards. Risk Management Supporting product risk management activities according to current procedures. Reviewing all processes within the quality management system and document process risks in accordance with ISO 14971. Trend Analysis Establishing a process to collect, analyse and report on quality data to identify trends and areas for improvement. Training Creating training material on relevant regulations, standards, and guidance (e.g. UK MDR, Regulation (EU) 2017/745, MDSAP, ISO9001). Regulatory: Supporting the QARA team in: Creating a documentation pack aligned to the IMDRF table of contents to support registration of medical devices within Europe, Canada, Australia and the rest of the world. Maintaining and archiving technical documentation and regulatory files, including the regular review and updates required to ensure ongoing compliance with current standards and legal requirements. Preparing and compiling reports necessary for regulatory compliance, including monthly quality reports. This is a 6 Months Contract role based working from home. You will attend the office at Walsall, West Midlands approx. 2 days every fortnight. The client will review the contract towards the end date with a view of extending it or making the role permanent however this is all dependent on the individual and business performance. The PAYE rate is between £28.00 - £41.19 per hour. This is purely dependent on skills and experience. Skills: To apply for the role of Quality Assurance and Regulatory Engineer you will have the following: Proven experience in quality assurance and regulatory affairs within the medical device sector. Strong analytical and problem-solving skills. Confident, professional, and comfortable working in a close-knit team environment. Working knowledge of international medical device regulations, standards, and guidance documents including MDSAP, Regulation (EU) 2017/745, ISO 13485, ISO 9001 and ISO 14971. Competence in the use of QMS and IT tools, including MS Office, SharePoint, MS Teams, Word, Excel and Outlook. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Pharmaceutical Packaging Technician Opportunity - Oxford Opportunity: My client a global pharmaceutical manufacturing company is looking to recruit a Packaging Technician based in Oxford where you will be packing drugs for shipment to hospitals and homecare patients working to cGMP and ISO standards. This hours of work are Monday to Friday 1.00 pm-9.00 pm with flexibility. Duties and Responsibilities include: Timely picking and packing of drug orders for dispatch in accordance with run sheets. Tracking drug orders across different departments for timely dispatch. Communicating with drivers and customer services on ETA's. Maintaining a safe and clean working environment of the dispensary/warehouse. This is a 3 months contract job opportunity based in Oxford paying an hourly rate of £12.82. There is a possibility that the contract might get extended or go permanent but this is dependent on the individual and business performance. Skills: To apply for the role of Packaging Technician you will have the following: GCSEs in English, Maths, Science (A-C). Excellent attention to detail. IT literate (Shipping software, Excel). A track record in demonstrating an excellent attention to detail and being highly organised. Ideally a stores background in a GMP environment. Physical lifting (15kgmax) will be needed, so manual handling experience would be preferred. Excellent communication skills. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Dec 09, 2022
Full time
Pharmaceutical Packaging Technician Opportunity - Oxford Opportunity: My client a global pharmaceutical manufacturing company is looking to recruit a Packaging Technician based in Oxford where you will be packing drugs for shipment to hospitals and homecare patients working to cGMP and ISO standards. This hours of work are Monday to Friday 1.00 pm-9.00 pm with flexibility. Duties and Responsibilities include: Timely picking and packing of drug orders for dispatch in accordance with run sheets. Tracking drug orders across different departments for timely dispatch. Communicating with drivers and customer services on ETA's. Maintaining a safe and clean working environment of the dispensary/warehouse. This is a 3 months contract job opportunity based in Oxford paying an hourly rate of £12.82. There is a possibility that the contract might get extended or go permanent but this is dependent on the individual and business performance. Skills: To apply for the role of Packaging Technician you will have the following: GCSEs in English, Maths, Science (A-C). Excellent attention to detail. IT literate (Shipping software, Excel). A track record in demonstrating an excellent attention to detail and being highly organised. Ideally a stores background in a GMP environment. Physical lifting (15kgmax) will be needed, so manual handling experience would be preferred. Excellent communication skills. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Locum Pharmacy Accuracy Checking Technician - Northampton Opportunity: Are you currently working as a Pharmacy Accuracy Checking Technician looking for a new contract role? Are you registered with the GPhC? Do you have an appropriate Accuracy Checking qualification? Want to work for a global pharmaceutical company? If yes then please read on. Your role as a Pharmacy Accuracy Checking Technician based in Northampton will involve: Providing accurate final checking of all Renal orders (PD, HHD) that contain POM & P (Prescription Only Medicines & Pharmacy medicines) and ancillary items before their dispatch from NDC to patients. Ensuring that pharmacy patient dispensing processes are compliant with : oGPhC (General Pharmaceutical Council) oRPS (Royal Pharmaceutical Society) o Companies Pharmacy Standard Operating Procedures (SOP) o Good Documentation Practices (GDocP) o Good Warehousing Practices (GWP) Ensuring all Standards and Guidelines issued by the GPhC and the RPS are met and are implemented as part of their practice. Providing technical assistance in the registered pharmacy. Supporting the Responsible Pharmacist (RP) as required. Ensuring all medication is managed in compliance with the company and Royal Pharmaceutical Society of Great Britain processes. This is a 12 months contract working Monday to Friday 2.00 pm to 10.00 pm. There is a possibility that this role will get extended or go permanent full time but this is all dependent on the individual and business performance. The PAYE hourly rate is £22.37. Skills: To apply for the role of Locum Pharmacy Accuracy Checking Technician you will have the following: Appropriate pharmaceutical qualification -i.e. BTEC, NVQ Level 3 or equivalent. Appropriate Accuracy Checking qualification. Registered with the GPhC. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Dec 08, 2022
Full time
Locum Pharmacy Accuracy Checking Technician - Northampton Opportunity: Are you currently working as a Pharmacy Accuracy Checking Technician looking for a new contract role? Are you registered with the GPhC? Do you have an appropriate Accuracy Checking qualification? Want to work for a global pharmaceutical company? If yes then please read on. Your role as a Pharmacy Accuracy Checking Technician based in Northampton will involve: Providing accurate final checking of all Renal orders (PD, HHD) that contain POM & P (Prescription Only Medicines & Pharmacy medicines) and ancillary items before their dispatch from NDC to patients. Ensuring that pharmacy patient dispensing processes are compliant with : oGPhC (General Pharmaceutical Council) oRPS (Royal Pharmaceutical Society) o Companies Pharmacy Standard Operating Procedures (SOP) o Good Documentation Practices (GDocP) o Good Warehousing Practices (GWP) Ensuring all Standards and Guidelines issued by the GPhC and the RPS are met and are implemented as part of their practice. Providing technical assistance in the registered pharmacy. Supporting the Responsible Pharmacist (RP) as required. Ensuring all medication is managed in compliance with the company and Royal Pharmaceutical Society of Great Britain processes. This is a 12 months contract working Monday to Friday 2.00 pm to 10.00 pm. There is a possibility that this role will get extended or go permanent full time but this is all dependent on the individual and business performance. The PAYE hourly rate is £22.37. Skills: To apply for the role of Locum Pharmacy Accuracy Checking Technician you will have the following: Appropriate pharmaceutical qualification -i.e. BTEC, NVQ Level 3 or equivalent. Appropriate Accuracy Checking qualification. Registered with the GPhC. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Assurance Associate - Oxford Opportunity: My client a global pharmaceutical manufacturing company are looking to recruit an experienced Quality Assurance Associate based in Oxford where you will be releasing and inspecting compounded drugs as well as maintain the quality system working to relevant GMP / GDP and EH&S standards. Duties and responsibilities include: Review, inspect and release compounded drugs to patients. Dealing with deviations, change controls and customer complaints. Reviewing, approving and leading investigations in the cause of exceptions and reports. CAPA owner and leader. Managing the site Validation Master Plan and equipment validation. Environmental monitoring. Maintaining and continues improvement of the quality management system for the site. Responsible for all quality documents and data management. The hours of work are: Monday to Friday 7.00 am - 3.00 pm and then 10.00 am - 6.00 pm alternating on a weekly basis. This is a 12 months contract which will be reviewed for a possible extension or go permanent but everything is dependent on the candidate and business performance. The PAYE rate is £25.18 per hour. Skills: To apply for the role of Quality Assurance Associate you will have the following: Quality assurance experience ideally within a sterile / aseptic manufacturing environment. Quality systems experience. Environmental / microbiological control experience (preferred). Validation. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on our website. If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Dec 07, 2021
Contractor
Quality Assurance Associate - Oxford Opportunity: My client a global pharmaceutical manufacturing company are looking to recruit an experienced Quality Assurance Associate based in Oxford where you will be releasing and inspecting compounded drugs as well as maintain the quality system working to relevant GMP / GDP and EH&S standards. Duties and responsibilities include: Review, inspect and release compounded drugs to patients. Dealing with deviations, change controls and customer complaints. Reviewing, approving and leading investigations in the cause of exceptions and reports. CAPA owner and leader. Managing the site Validation Master Plan and equipment validation. Environmental monitoring. Maintaining and continues improvement of the quality management system for the site. Responsible for all quality documents and data management. The hours of work are: Monday to Friday 7.00 am - 3.00 pm and then 10.00 am - 6.00 pm alternating on a weekly basis. This is a 12 months contract which will be reviewed for a possible extension or go permanent but everything is dependent on the candidate and business performance. The PAYE rate is £25.18 per hour. Skills: To apply for the role of Quality Assurance Associate you will have the following: Quality assurance experience ideally within a sterile / aseptic manufacturing environment. Quality systems experience. Environmental / microbiological control experience (preferred). Validation. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on our website. If this sounds like the role for you or a colleague then please don't hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
