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We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

• Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
• Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
• Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
• Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
• Raising and overseeing the implementation of Change Controls and CAPA's when required
• Participating in site inspections by Regulatory Authorities
• Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
• Writing, reviewing and contributing to Risk Assessments

Benefits:

• Discretionary Bonus
• Healthcare & More

About You:

• Experience within a pharmaceutical environment
• A strong Quality Assurance background (2 to 3 years experience)
• Experience within sterile manufacturing environments (desirable)
• Good working knowledge of GMP requirements and quality systems
• Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
• Strong communicator and team player
• Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

• Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
• Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
• Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
• Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
• Raising and overseeing the implementation of Change Controls and CAPA's when required
• Participating in site inspections by Regulatory Authorities
• Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
• Writing, reviewing and contributing to Risk Assessments

Benefits:

• Discretionary Bonus
• Healthcare & More

About You:

• Experience within a pharmaceutical environment
• A strong Quality Assurance background (2 to 3 years experience)
• Experience within sterile manufacturing environments (desirable)
• Good working knowledge of GMP requirements and quality systems
• Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
• Strong communicator and team player
• Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

Our client is a leading Pharmaceutical Manufacturer going through a period of successful expansion to cater for their ever growing production requirements.

They are a well regarded GMP site, producing products that fall under the "Liquids, Orals and Creams" definition of Pharmaceutical Products.

As part of their expansion, they are looking for a Quality Assurance Officer (x2) for their site near Liverpool.

This role is 100% site based, and is offering a competative salary and benefits package, and the opportunity to work within a very exciting Life Science company.

Requirements

- Previous experience as a QA officer (preferably in a GMP environent)

- A degree in Life Sciences

- The ability to be on site 5 days per week

- Strong communication skills and a high attention to detail

We are working with an established pharmaceutical company who are looking to employ a QA Officer, permanently in the Sandwich area.

PLEASE DO NOT APPLY IF YOU DON'T LIVE LOCALLY TO SANDWICH, KENT AND HAVE A FULL RIGHT TO WORK WITH NO RESTRICTIONS (NO GRADUATE VISAS/SPONSORSHIP/RELOCATIONS PLEASE)

This is an exciting full-time permanent position with a salary of up to 35,000/annum and a host of great benefits.

Responsibilities:

• To provide QA support to all departments.
• Maintain and develop the Quality Management System.
• Ensure all pre & post-production documentation is submitted to QA, checked and approved prior to use of any materials, and batch release.
• Ensure all materials meet required specifications.
• Complete QA review and approval of deviations, C.A.P.A's, change controls, complaints, out of specifications and other documentation such as SOP's and forms.
• Assist with internal and external audits.
• Assist with product recalls.
• Ensure quality agreements and quality questionnaires are in place with external companies.
• Manage and develop the company training matrix and complete quarterly reviews on employee training records.
• Participate in weekly QA meetings.
• Ensure investigations are carried out in a timely manner.
• Develop and update logbooks as and when required.

About You:

• Minimum 3 years' Quality Assurance experience within a GMP pharmaceutical manufacturing environment
• Strong understanding of GMP and wider GxP requirements
• Experience of QMS, CAPAs, Deviations, Change Controls and batch record review
• Excellent investigation and problem-solving skills
• Ability to write clear technical reports and quality documentation
• Strong organisational skills with the ability to prioritise multiple activities
• Excellent communication skills and confidence working across all departments

Local candidates need only apply and those with no restrictions on their right to work.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975.

If this role isn't for you, please check out our website for other opportunities that may be suitable, or send us your CV, we'd still like to hear from you. You can find us on our website or on LinkedIn, Facebook, Instagram and

We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. New Appointments Group acts as an Employment Agency for permanent roles and as an Employment Business for temporary roles.

Sterility Assurance Specialist
Burton upon Trent On-site Pharmaceutical Manufacturing

Talentmark is partnering with an established pharmaceutical manufacturer to recruit a Sterility Assurance Specialist. This is an excellent opportunity for an experienced microbiologist or sterility assurance professional with aseptic production experience to play a key role in safeguarding product quality and patient safety within a GMP-regulated aseptic manufacturing environment.

Working as the site's sterility assurance expert, you'll help strengthen quality systems, lead microbiological initiatives, and support the development of a growing microbiology function.

Key Responsibilities

• Lead and maintain sterility assurance and environmental monitoring programmes in line with GMP requirements.
• Act as the site subject matter expert for microbiology and sterility assurance.
• Investigate deviations, non-conformances, environmental monitoring excursions and complaints.
• Analyse and trend microbiological and environmental monitoring data to identify risks and opportunities for improvement.
• Support validation activities, including microbiological methods and sanitisation processes.
• Manage external laboratory relationships and oversee testing programmes.
• Develop and maintain quality documentation, SOPs and technical procedures.
• Deliver microbiology and aseptic technique training across the business.
• Drive continuous improvement initiatives to strengthen quality and compliance.

• A degree in Microbiology or a related scientific discipline (or equivalent experience).
• Strong operational experience in sterility assurance within a GMP-regulated aseptic environment.
• Strong knowledge of environmental monitoring programmes and microbiological quality systems.
• Experience investigating deviations, out-of-specification or out-of-limit results.
• A good understanding of GMP and pharmaceutical regulatory requirements.

• Private Healthcare cover.
• Company Pension Scheme.
• Life Assurance.
• Gym Discount.
• Access to Wellness platforms.
• Yearly Pay Reviews

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

• Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
• Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
• Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
• Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
• Raising and overseeing the implementation of Change Controls and CAPA's when required
• Participating in site inspections by Regulatory Authorities
• Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
• Writing, reviewing and contributing to Risk Assessments

Benefits:

• Discretionary Bonus
• Healthcare & More

About You:

• Experience within a pharmaceutical environment
• A strong Quality Assurance background (2 to 3 years experience)
• Experience within sterile manufacturing environments (desirable)
• Good working knowledge of GMP requirements and quality systems
• Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
• Strong communicator and team player
• Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

• Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
• Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
• Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
• Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
• Raising and overseeing the implementation of Change Controls and CAPA's when required
• Participating in site inspections by Regulatory Authorities
• Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
• Writing, reviewing and contributing to Risk Assessments

Benefits:

• Discretionary Bonus
• Healthcare & More

About You:

• Experience within a pharmaceutical environment
• A strong Quality Assurance background (2 to 3 years experience)
• Experience within sterile manufacturing environments (desirable)
• Good working knowledge of GMP requirements and quality systems
• Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
• Strong communicator and team player
• Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

QA Microbiologist Irvine, Ayrshire 27,000 - 29,000 + Benefits

Escape Recruitment is working with a well-established manufacturing business in Ayrshire that is investing heavily in its laboratory and quality capabilities. As part of this growth, they are looking to appoint a QA Microbiologist to support the introduction of in-house microbiological testing.

This is an excellent opportunity for someone with commercial microbiology laboratory experience who enjoys a varied, hands-on role within a manufacturing environment. Graduates with a relevant industrial placement are also encouraged to apply.

Reporting into the Quality team, you'll be responsible for carrying out microbiological testing across raw materials, environmental samples and finished products, helping to ensure products meet the highest quality and regulatory standards.

Duties will include:

• Microbiological testing of raw materials, environmental and finished product samples
• Identifying bacteria, yeast and mould contamination
• Environmental monitoring and hygiene testing
• Preparing media and laboratory reagents
• Recording, analysing and reporting test results
• Investigating out of specification results
• Supporting laboratory validation activities
• Maintaining laboratory equipment and consumable stocks
• Working closely with the wider Quality and Laboratory teams
• Supporting continuous improvement within the laboratory

We're interested in candidates who have:

• A degree in Microbiology, Biological Sciences or a related discipline
• Commercial laboratory experience within a manufacturing environment
• Experience of microbiological testing techniques
• Good laboratory documentation and reporting skills
• Strong attention to detail and organisational skills
• The ability to work both independently and as part of a team
• The right to work in the UK without sponsorship

Graduates who have completed a substantial industrial placement within a commercial laboratory are also encouraged to apply.

• Salary of 27,000 - 29,000
• Opportunity to join a growing manufacturing business
• Modern laboratory environment
• Excellent opportunity to develop within Quality and Microbiology
• Full-time permanent position based in Irvine

If you're looking for your next opportunity within microbiology and quality, we'd love to hear from you.

Walker Cole International is supporting a growing pharmaceutical organisation in the search for a Quality Assurance Officer to join their Quality team on a 12-month fixed-term contract. This is an excellent opportunity to join a rapidly expanding business that has experienced significant growth in recent years, offering exposure to a diverse portfolio of pharmaceutical products and medical devices supplied across European markets.

Operating within a virtual pharmaceutical model, the company works closely with Contract Manufacturing Organisations (CMOs), providing broad exposure to external manufacturing and quality assurance activities. This role offers a hybrid working pattern and the opportunity to develop within a collaborative and supportive Quality team.

You will be responsible for:

• Reviewing batch manufacturing and packaging records to ensure compliance with GMP requirements prior to product release.

• Performing batch release activities, ensuring products meet the required quality standards before distribution.

• Working closely with external manufacturing partners and internal stakeholders to support day-to-day quality assurance activities.

• Maintaining accurate quality documentation while supporting compliance with GMP and the Quality Management System.

The successful candidate will have:

• Previous Quality Assurance experience within a GMP-regulated pharmaceutical, biotechnology or medical device environment.

• Experience reviewing batch records and/or supporting batch release activities.

• A strong understanding of GMP principles and pharmaceutical quality systems.

• Excellent attention to detail, communication skills and the ability to work effectively with both internal teams and external manufacturing partners.

Quality Assurance QA Quality Assurance Officer GMP Good Manufacturing Practice Batch Record Review Batch Release QMS Quality Management System Pharmaceutical Medical Devices CMO Contract Manufacturing Organisation Compliance GDP Hybrid

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

• Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
• Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
• Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
• Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
• Raising and overseeing the implementation of Change Controls and CAPA's when required
• Participating in site inspections by Regulatory Authorities
• Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
• Writing, reviewing and contributing to Risk Assessments

Benefits:

• Discretionary Bonus
• Healthcare & More

About You:

• Experience within a pharmaceutical environment
• A strong Quality Assurance background (2 to 3 years experience)
• Experience within sterile manufacturing environments (desirable)
• Good working knowledge of GMP requirements and quality systems
• Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
• Strong communicator and team player
• Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW