Total 14 job vacancies by SRG

Title: QA Officer (Shifts) - 8-month Contract

Location: West Yorkshire

Salary: £32,000 - £36,500

SRG are recruiting for a Quality Assurance Officer to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS.

This position will join the QA Operations team and will supporting the QMS teams & shop floor, playing a vital role in ensuring ongoing quality & compliance.

The role

As the QA Officer, you will be responsible for:

• Supporting the Deviation systems and investigations.
• Assisting with the Implementation & review of CAPAs.
• Supporting Customer Compliant investigations.
• Supporting product quality reports & Batch review activities of licensed medicines & Medical devices.
• Ensure all activities, changes to equipment and working practices are made in line with regulations and guidelines for products including licensed medicines, medical devices, cosmetics, food, and biocides.
• Ensure all improvement opportunities are in line with ISO and all manufacturing operations are defined and documented to ensure optimum performance.

Requirements:

• A degree or similar qualification or experience in a relevant subject.
• Proven professional experience in a similar QA position & systems.
• Experienced in the use of SAP, MasterControl, QPulse or other eQMS/eDMS systems.
• A keen eye for detail, with the ability to identify & resolve issues as required.
• An effective communicator, able to effectively engage with people at all levels.
• Available to work rotation / night shifts.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Senior QA Officer (Shifts)

Location: West Yorkshire

Salary: £42,000 - £49,500

SRG are recruiting for a Senior Quality Assurance Officer to be based with a rapidly growing pharmaceutical producer in West Yorkshire. Manufacturing numerous household brands found in homes across the country, they also produce specialist prescription products for the NHS.

This position will take on a senior role within the QA Operations team and will support colleagues in QA and the shop floor, playing a vital role in preparing & reviewing critical documentation and coordinating batch release priorities.

The role

As the Senior QA Officer, you will be responsible for:

• Supporting the Deviation systems and investigations.
• Implementing & reviewing the effectiveness of CAPAs.
• Managing the Customer Compliant systems and related investigations.
• Producing & managing product quality reports & batch certificates.
• Batch review activities of licensed medicines & Medical devices
• Quality release of cosmetic and food products.
• Ensure all activities, changes to equipment and working practices are made in line with regulations and guidelines for products including licensed medicines, medical devices, cosmetics, food, and biocides.
• Ensure all improvement opportunities are in line with ISO and all manufacturing operations are defined and documented to ensure optimum performance.

Requirements:

• A degree or similar qualification or experience in a relevant subject.
• Proven professional experience in all aspects of quality management and management systems.
• Experienced in the use of SAP, MasterControl, QPulse or other eQMS/eDMS systems.
• A keen eye for detail, with the ability to identify & resolve issues as required.
• An effective communicator, able to effectively engage with people at all levels.
• Available to work rotation / night shifts.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: QC Validation Analyst

Location: West Yorkshire

Salary: £27,500 - £29,000

SRG are working with a pharmaceuticals company who develop & manufacture novel medicines to improve the outcomes & wellbeing of patients, unable to take traditional does forms. Based in West Yorkshire, we are looking to recruit a QC Validation Analyst on a 12-month initial contract to aid the team during a key period of growth.

This would be a great opportunity to join a highly experienced team, in a cGMP environment that can also offer flexible working hours.

The Role:

As the QC Validation Analyst, you will be responsible for ensuring the quality & compliance of raw materials & finished products by performing analysis on sample relevant to the release of products.

Key responsibilities will include:

• Conducting validation activities in accordance with cGMP regulations.
• Writing & reviewing validation documents.
• Performing QC analysis of raw materials, in - process & Finished products.
• Participate in out-of-specification / failure investigations and corrective actions.
• Reviewing external testing data to ensure accuracy & regulatory compliance

The Person:

• A degree or similar qualification in Chemistry or a relevant field.
• Previous method or cleaning validation experience within a GMP environment.
• Prior experience of HPLC would be advantageous, but not essential.
• Keen eye for detail and accuracy - with the ability to understand, review and write documents & procedures.

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srgtalent.com to view our other vacancies.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: QC Tech Transfer Scientist

Location: Leeds

Employment Type: 12 month FTC

Salary: Competitive with flexible hours and generous package

We are currently working with a global leader in medicinal manufacturing who are looking for a QC Tech Transfer Scientist to join the Tech Transfer team. As the QC Tech Transfer Scientist, you will be responsible for successfully ensuring the Quality and Compliance of raw materials and products by performing analytical testing on samples relative to the release of company materials and product, according to cGMP requirements.

The main duties and responsibilities will include:

• Ensuring lab cleanliness and safety standards are maintained
• Performing analytical testing of finished products using validated methods at a high RFT.
• Performing analytical testing and Micro/PET to USP, EP, BP monographs at a high RFT
• Participate in out-of-specification and failure investigations and recommend corrective actions.

Experience required:

• A degree in a relevant scientific subject with a basic understanding of cGMP.
• At least 2 years of relevant work experience is required.

Interested? Or know someone who will be?

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you are interested in this role and require more information, please contact Elliott Howells on 0161 526 1903 or email

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: Assistant QC Analyst

Location: Leeds

Employment Type: Permanent

Salary: Competitive with flexible hours and generous package

We are currently working with a global leader in medicinal manufacturing who are looking for an Assistant QC Analyst to join their raw materials team. As the Assistant QC Analyst, you will be responsible for successfully ensuring the Quality and Compliance of raw materials and products by performing analytical testing on samples relative to the release of company materials and product, according to cGMP requirements

The main duties and responsibilities will include:

• Ensuring lab cleanliness and safety standards are maintained
• Performs analytical testing of Finished or Stability batches using validated HPLC methods
• Ability to perform physicals testing of finished products, raw materials & Components
• Ability to document all Chemistry, Micro or packaging analysis following good data documentation practice with minimal supervision

Experience required:

• A degree in a relevant scientific subject with a basic understanding of cGMP.
• Any prior experience within industrial pharmaceutical Quality Control will naturally be beneficial.

Interested? Or know someone who will be?

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you are interested in this role and require more information, please contact Elliott Howells on 0161 526 1903 or email

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job title: QC Analyst

Location: Worthing, West Sussex

Contract: 12- month FTC.

Pay rate: £14.45p/h

SRG are looking for an QC analyst to join a global pharmaceutical company based in Worthing. As a QC analyst you would be responsible for carrying out physical and chemical analytical test methods on oral, stability and sterile products., using SOPs and accurately document the results as part of the QXC process to ensure products are of satisfactory quality for market release.

This role would be perfect for anyone with analytical chemistry testing experience, either from industry or an academic lab, whether you are coming from a QC lab, or looking for your first role out of university we would like to hear from you!

Key Responsibilities will include:

• To test routine production and stability samples supplied from the site value streams and meet testing lead-time targets.
• Calibrate and maintain analytical equipment.
• Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions ect)
• To carry our OOS investigations and discuss outcomes with other team members.
• Perform validation of equipment and methods as required.
• To adhere to and help maintain the highest levels of GLP within the section and ensure training records are kept up to date.

Candidate Requirements:

• Degree or HNC in chemistry or related discipline
• Hands on experience with HPLC, UV-Vis or other analytical testing methods.
• Experience working to GMP standards would be an advantage.
• Experience with following SOPs would be an advantage.

To apply click the link or send your CV

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Title: 2x Method Qualification Scientist (Bioanalysis)
Vacancy Type: 4 Month Temp (potential to extend to rolling contract)
Area: North East
Salary: Competitive

SRG is working on an exclusive partnership with a highly innovative biopharmaceutical partner.

They are looking for a short-term temp/contractor to come in and support the recombinant protein drug delivery programme, in the effort to develop recombinant protein-based vaccines. This role is looking for someone with solid experience working with qPCR, SEC-HPLC, ELISA and Western blot, and SDS PAGE assays.

The role is a critical part of the project and is looking for people to start as soon as possible. If you have developed assays in the above techniques and would like to work in a highly innovative company, get in touch.

Responsibilities include, but are not limited to:

• To perform laboratory analyses and data analysis on starting materials, intermediates and finished products.
• Perform all Quality Control duties and tasks in accordance with relevant GMP guidelines.
• Perform method development and method qualification activities.
• Calibration and routine monitoring/maintenance of analytical equipment.
• Support the site Quality Management System including input into investigations and/or CAPAs.
• Utilise a range of techniques such as UV Absorption Spectrophotometry, SDS-PAGE, RP HPLC, SEC-HPLC, qPCR, ELISA etc.

Skills Required:

• Educated to a BSc, MSc or PhD level in a Scientific or Engineering related discipline.
• Possess technical expertise with SDS-PAGE, RP HPLC, SEC-HPLC, qPCR, ELISA and Western Blotting. Need at least 3 techniques from this list.
• Experience with DNA and RNA purification and scale up is essential.
• Method Development experience highly desired.
• GMP experience highly desired.
• Happy to hear from QC Scientists with the above experience.

Interested? Or know someone who will be?
SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary,

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

QC Analyst required, based in Teesside on a 6-month contract. Requiring proven industrial experience of analytical chemistry including HPLC or GC amongst other techniques.

Title: QC Analyst

Location: Teesside

Salary: £27,000 - £32,000 (dependent on experience, pro-rata)

Employment Term: 6-month contract

SRG are working with an international company who specialise in the creation of speciality chemicals for a range of markets. They are now looking to add a QC Analyst to their analytical team on a 6-month contract at their site in Teesside. This temporary role will be supporting with an ongoing project, and will involve analysis of samples using a range of analytical techniques including HPLC, GC, GC-MS, FT-IR amongst others. Experienced analysts who are between roles, or recent graduates who have completed an analytical placement year in industry are encouraged to apply.

Benefits: 28 days holiday plus bank holidays (pro-rata). Monday - Friday, 9am-5pm (with flexibility).

Role / Description

• Perform QC analysis of unknown samples using a range of techniques including HPLC and GC, amongst others.
• Provide results and data to maintain QC records in accordance with site requirements.
• Carry out calibration of equipment and method development of techniques and maintenance of calibration records to the appropriate standard.
• Communicate internally in a timely manner to appropriate departments.
• Monitor and maintain stock levels of reagents and consumables

Requirements

• Degree in Chemistry (or similar)
• Proven industrial experience of analysis including HPLC or GC in a busy, fast-paced laboratory setting
• Positive, pro-active attitude
• Team player work a strong work ethic

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to For more information regarding this position or any others, please call Chris on 0161 526 1898.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srgtalent.co.uk to view our other vacancies.

Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products, chromatography.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

QC Analyst required, based in Teesside on a permanent basis. Requiring proven industrial experience of analytical chemistry including HPLC or GC.

Title: QC Analyst

Location: Teesside

Salary: £27,000 - £29,000 (dependent on experience)

Employment Term: Permanent

SRG are working with an international company who specialise in the creation of speciality chemicals for a range of markets. They are now looking to add a QC analyst to their analytical team on a full-time basis at their site in Teesside. This role will be supporting a recent increased workload and sample volumes, and will primarily involve analysing finished product samples using a range of techniques including HPLC and GC. Candidates that have proven industrial experience of these techniques in a busy, fast-paced laboratory setting are encouraged to apply. GMP is desirable but not essential for this position.

Benefits: 28 days holiday plus bank holidays. Monday - Friday, 9am-5pm (with flexibility).

Role / Description

• Perform QC analysis of raw materials, in-process and finished product samples in support of production using a range of techniques including HPLC and GC.
• Provide results and data to maintain QC records in accordance with site requirements.
• Carry out calibration of equipment and method development of techniques and maintenance of calibration records to the appropriate standard.
• Communicate internally in a timely manner to appropriate departments.
• Monitor and maintain stock levels of reagents and consumables

Requirements

• Degree in Chemistry (or similar)
• Proven industrial experience of analysis includingHPLC orGC in a busy, fast-paced laboratory setting
  • GMP experience is desirable but not essential
• Positive, pro-active attitude
• Team player work a strong work ethic

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to For more information regarding this position or any others, please call Chris on 0161 526 1898.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srgtalent.co.uk to view our other vacancies.

Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products, chromatography.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

2 x QC Analysts required, based in Teesside on a permanent basis. Requiring proven industrial experience of analytical chemistry including HPLC or GC.

Title: 2 x QC Analysts

Location: Teesside

Salary: £27,000 - £28,000 (dependent on experience)

Employment Term: Permanent

SRG are working with an international company who specialise in the creation of speciality chemicals for a range of markets. They are now looking to add 2 QC Analysts to their analytical team on a full-time basis at their site in Teesside. These permanent roles will be supporting a recent increased workload and sample volumes, and will primarily involve analysing finished product samples using a range of techniques including HPLC and GC. Candidates that have proven industrial experience of these techniques in a busy, fast-paced laboratory setting are encouraged to apply. GMP is desirable but not essential for this position.

Benefits: 28 days holiday plus bank holidays. Monday - Friday, 9am-5pm (with flexibility).

Role / Description

• Perform QC analysis of raw materials, in-process and finished product samples in support of production using a range of techniques including HPLC and GC.
• Provide results and data to maintain QC records in accordance with site requirements.
• Carry out calibration of equipment and method development of techniques and maintenance of calibration records to the appropriate standard.
• Communicate internally in a timely manner to appropriate departments.
• Monitor and maintain stock levels of reagents and consumables

Requirements

• Degree in Chemistry (or similar)
• Proven industrial experience ofanalysisincludingHPLCorGC in a busy, fast-paced laboratory setting
  • GMP experience is desirable but not essential
• Positive, pro-active attitude
• Team player work a strong work ethic

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to For more information regarding this position or any others, please call Chris on 0161 526 1898.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srgtalent.co.uk to view our other vacancies.

Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products, chromatography.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

2 x QC Analysts required, based in Teesside on a permanent basis. Requiring proven industrial experience of analytical chemistry including HPLC or GC.

Title: 2 x QC Analysts

Location: Teesside

Salary: £27,000 - £28,000 (dependent on experience)

Employment Term: Permanent

SRG are working with an international company who specialise in the creation of speciality chemicals for a range of markets. They are now looking to add 2 QC Analysts to their analytical team on a full-time basis at their site in Teesside. These permanent roles will be supporting a recent increased workload and sample volumes, and will primarily involve analysing finished product samples using a range of techniques including HPLC and GC. Candidates that have proven industrial experience of these techniques in a busy, fast-paced laboratory setting are encouraged to apply. GMP is desirable but not essential for this position.

Benefits: 28 days holiday plus bank holidays. Monday - Friday, 9am-5pm (with flexibility).

Role / Description

• Perform QC analysis of raw materials, in-process and finished product samples in support of production using a range of techniques including HPLC and GC.
• Provide results and data to maintain QC records in accordance with site requirements.
• Carry out calibration of equipment and method development of techniques and maintenance of calibration records to the appropriate standard.
• Communicate internally in a timely manner to appropriate departments.
• Monitor and maintain stock levels of reagents and consumables

Requirements

• Degree in Chemistry (or similar)
• Proven industrial experience of analysisincludingHPLCorGC in a busy, fast-paced laboratory setting
  • GMP experience is desirable but not essential
• Positive, pro-active attitude
• Team player work a strong work ethic

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to For more information regarding this position or any others, please call Chris on 0161 526 1898.

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit www.srgtalent.co.uk to view our other vacancies.

Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products, chromatography.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job: Title: Associate Director of Quality Assurance (GCP)

Salary: Competitive

Location: York (Hybrid role)

SRG are supporting a global clinical lab services company in their search for an Associate Director of Quality Assurance.

The successful Quality Assurance Lead will be responsible for implementing strategies to allow successful delivery of high-quality Clinical Trials studies; by driving effective, efficient, global processes across the various aspects of our Quality and Operations.

Responsibilities:

• Work closely with the global QA leadership team to provide regional oversight of the quality assurance team.
• Promote and uphold a high performing culture through effective talent planning, selection, onboarding and continuing education. Curate and deliver comprehensive training plans and materials to foster successful onboarding and employee performance.
• Identify and implement strategies to maintain a culture of quality. Develop and execute holistic audit program, including internal audits, vendor audits, client audits and regulatory inspections, to ensure compliance.
• Leverage industry knowledge to refine our strategies and processes for delivering high quality clinical trials. Maintain working knowledge of industry and regulatory standards and requirements.
• Provide guidance and leadership as it relates to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), MHRA, FDA, data privacy and other regulatory standards as needed or directed. Serve as a responsive escalation point for Clinical Trials quality issues and concerns.
• Oversee and manage vendor management program to ensure supply compliance, computer systems validation program, and data privacy program regionally to ensure compliance.

Requirements:

• Bachelor's Degree required; Master's Degree preferred
• Extensive industrial experience in Quality Assurance, Regulatory Affairs, Laboratory Operations or a related field required.
• Experience of progressive leadership in QA required.
• Experience managing quality/regulatory department of regional responsibility.
• Experience with data privacy regulations preferred.
• Experience with Medicines & Healthcare products Regulatory Agency (MHRA), Food & Drug Administration (FDA); knowledge of Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) strongly preferred.

If you are interested in finding out more, please apply using the provided link or send a copy of your CV directly to Alex Sheridan on or contact Alex directly on 0203 854 5418 for a confidential conversation.

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit www.srg.co.uk to view our other vacancies.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job: Title: Associate Director of Quality Assurance (GCP)

Salary: Competitive

Location: York (Hybrid role)

SRG are supporting a global clinical lab services company in their search for an Associate Director of Quality Assurance.

The successful Quality Assurance Lead will be responsible for implementing strategies to allow successful delivery of high-quality Clinical Trials studies; by driving effective, efficient, global processes across the various aspects of our Quality and Operations.

Responsibilities:

• Work closely with the global QA leadership team to provide regional oversight of the quality assurance team.
• Promote and uphold a high performing culture through effective talent planning, selection, onboarding and continuing education. Curate and deliver comprehensive training plans and materials to foster successful onboarding and employee performance.
• Identify and implement strategies to maintain a culture of quality. Develop and execute holistic audit program, including internal audits, vendor audits, client audits and regulatory inspections, to ensure compliance.
• Leverage industry knowledge to refine our strategies and processes for delivering high quality clinical trials. Maintain working knowledge of industry and regulatory standards and requirements.
• Provide guidance and leadership as it relates to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), MHRA, FDA, data privacy and other regulatory standards as needed or directed. Serve as a responsive escalation point for Clinical Trials quality issues and concerns.
• Oversee and manage vendor management program to ensure supply compliance, computer systems validation program, and data privacy program regionally to ensure compliance.

Requirements:

• Bachelor's Degree required; Master's Degree preferred
• Extensive industrial experience in Quality Assurance, Regulatory Affairs, Laboratory Operations or a related field required.
• Significant experience of progressive leadership experience required.
• Experience managing quality/regulatory department of regional responsibility.
• Experience with data privacy regulations preferred.
• Experience with Medicines & Healthcare products Regulatory Agency (MHRA), Food & Drug Administration (FDA); knowledge of Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) strongly preferred.

If you are interested in finding out more, please apply using the provided link or send a copy of your CV directly to Alex Sheridan on or contact Alex directly on 0203 854 5418 for a confidential conversation.

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit www.srg.co.uk to view our other vacancies.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Quality Assurance Manager

Location: York (hybrid working options available)

Salary: £57K per annum

Contract: Permanent, full time (37.5 hours per week)

We are recruiting for a Quality Assurance Manager to join our client, an established environmental services agency striving to improve food and crop security globally.

The purpose of this role is to ensure GLP requirements are being met, providing advice, guidance and recommendations to internal stakeholders on the requirements of quality and operating standards. You will be accountable for ensuring these requirements are implemented, monitored and expanded in line with business objectives.

Key responsibilities:

• Managing the GLP QA function to ensure regulatory auditing is scheduled and maintained, some auditing will be required
• Working with the Test Facility Management Team to ensure regulatory requirements are met and new requirements are implemented
• Offer advice and guidance on the requirements of GLP compliance
• Produce and deliver GLP training
• Liaise with assessing bodies and customers
• Management of all team members, being the first point of contact for any issues they may have and supporting them in finding solutions, including proactive identification of performance issues, providing feedback and coaching
• Effective management of staff resource through line management and liaising with resource planners
• Support and encourage innovation to improve current service delivery, driving improvements and development of the service provided.
• Ensure all team members are trained in and adhere to the relevant H&S and quality standard requirements

Our ideal candidate will have the following skills/experience:

• Extensive experience working in GLP Quality Assurance / GxP environment
• Experience in scheduling audits and managing audit schedules
• Experience in instrumental system validations for the generation of electronic data
• Production and delivery of training material relevant to GLP regulations and requirements
• Experience of hosting inspection visits by regulatory bodies and/or customers
• People and resource management skills

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.