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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | QA | Berkshire, Buckinghamshire, Hertfordshire, Middlesex... | Details |
| Summary:
QA Officer role within the area of Clinical Trial Supplies at a Global Pharma Company. This great opportunity would suits a graduate (ideally in Pharmacy) who already has some exposure to QA / compliance within a Clinical Trial / Supplies setting and has a GENUINE interest to follow a Quality Assurance career path. Salary range £25k - £28k, office based in... [Full Details] |
| Salary: Negotiable (25000 - 28000 £) |
| Regulatory And Drug Safety | QA | Cambridgeshire, Norfolk, Suffolk (United Kingdom) | Details |
| Experienced Quality Assurance (QA) Manager required by niche CRO. The successful candidate will develop and improve Quality Systems, manage QA activities and collate and report quality metrics to the management team.
A QA Manager is required by our client, one of the largest niche clinical data management and statistics CROs in Europe. They are seeking an individual who is passionate about... [Full Details] |
| Salary: Negotiable (35000 - 37000 £) |
| Regulatory And Drug Safety | QA | Hertfordshire (United Kingdom) | Details |
| Urgent Requirement for a GMP Quality Auditor to work for a major pharmaceutical company based in Hertfordshire. This role is initially a 3-4 month rolling contract with the possibility of extension. Equivalent salary of around 33K.
Role
To perform Quality Compliance review/release of Investigational Medicinal Products for use in Clinical Trials.
To audit and approve procedures and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| The Specialist will be responsible for providing a service to improve compliance of the Technical Files and Design Dossiers required for CE Marking product. The role will involve ensuring that relevant data is identified, supplied and incorporated into the Technical Documentation. The Specialist will maintain up to date knowledge of the related procedures and assist with any improvements... [Full Details] |
| Salary: Negotiable (23 - 25 £) |
| Regulatory And Drug Safety | QA | Dublin (Ireland) | Details |
| Our client is a leading global biopharmaceutical company. They are currently seeking a full time Senior QA Specialist (GMP) within their Supplies/Manufacturing division to be based on site in Dublin, Ireland.
JOB ROLE:
To ensure that all appropriate batch related documents and finished product packs are available from the contractors/suppliers to enable the release of products for sale or... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire (United Kingdom) | Details |
| Quality / Compliance Officer - GMP, Cambridgeshire, Neg Salary + bens.
We are looking for a quality assurance / regulatory compliance specialist to take responsibility for GMP compliance within a biologics analytical facility that supports product development and IMP and commercial manufacture in the fast expanding biotech market. You will be responsible for the operation of GMP systems and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire, Northamptonshire (United Kingdom) | Details |
| GMP Compliance Specialist, Cambridgeshire, £35,000 Region + bens.
An excellent opportunity for a GMP Quality Management Systems Specialist to join an established and fast expanding biopharmaceutical development company. This department provides specialist analytical support for the biological products in clinical and late stage development; your role will be to run the GMP Quality Management... [Full Details] |
| Salary: 30000 - 35000 £ |
| Regulatory And Drug Safety | QA | Cambridgeshire, Northamptonshire (United Kingdom) | Details |
| GMP Data Reviewer - Contract, Cambridgeshire, Negotiable Rate.
A fast expanding Biologics CMC / QC support laboratory has an opportunity for two GMP Data Reviewers to help them audit their facilities and review GMP compliance. The company’s continuous improvement policy requires high quality, efficient procedures that are ahead of current GMP standards – your role will be to review QC... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire, Northamptonshire (United Kingdom) | Details |
| Team Leader - Biologics Quality Testing, Cambridgeshire, Negotiable Rate.
An excellent opportunity for a Biopharmaceutical Analysis Specialist to join a fast expanding biological products support company. You will play a pivotal role in the development of services to companies producing products such as recombinant proteins, monoclonal antibodies and protein and DNA vaccines.
As Team... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cheshire (United Kingdom) | Details |
| Clinical QA Auditor Quality Assurance Adviser, Global R&D, North West
Excellent Rate, Fabulous Company
Role
Immediate openings for experienced GCP Auditors who can work within a global matrix and support audit of clinical trails, Computer system validation (CSV) and pharmaco-vigilance. In this role you will provide compliance advice to global teams and executes routine and complex global... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Hampshire, Surrey (United Kingdom) | Details |
| Quality Manager – Quality – South East 45-50K
You will take a leading role in development and implementation of quality management systems and change control activities. Ideally you will have good experience within a steriles manufacturing environment and in particular have experience conducting internal and external audits. this role will involve a degree of travel to international... [Full Details] |
| Salary: Negotiable (45000 - 55000 £) |
| Regulatory And Drug Safety | QA | Cambridgeshire, Hertfordshire (United Kingdom) | Details |
| Clinical QA Manager – Cambridge – GCP Quality
Clinical QA Manager needed by specialist pharmaceutical company In Cambridge. Clinical Quality Manager is a broad role leading the Clinical Quality group covering GCP standards and compliance for early to late phase studies. Role will include management of existing Clinical QA staff, design and implementation of audit programmes, host... [Full Details] |
| Salary: Negotiable (40000 - 60000 £) |
| Regulatory And Drug Safety | QA | Any Location (Belgium) | Details |
| Job Background
The RS (Resourcing Solutions) department of Chiltern International acts in a similar way to that of a staffing solutions provider. The department is currently seeking a Quality and Compliance R&D Specialist to work for our client, a global pharmaceutical company in Belgium. The role is office based in Rixensart. Candidates can be employed through Chiltern International Belgium... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Hertfordshire (United Kingdom) | Details |
| PRINCIPAL RESPONSIBILITIES :
• Perform Quality Compliance review/release of Investigational Medicinal Products for use in Clinical Trials
• Audit and approve procedures and documents from manufacturing, analytical and service groups
• Assist with ensuring compliance to cGMP of all activities related to the development of pharmaceutical products for use in Clinical Trials, including... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Pennsylvania (United States Of America) | Details |
| Job Category Biopharmaceuticals
Primary Location North America-United States-Pennsylvania-Wayne
Description
The basic purpose of this position is to assure the quality of laboratory data and reports. This is accomplished by audits of data and reports as specified by Standard Operating Procedures and by conducting inspections of laboratory procedures. Written reports are prepared for all... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Wisconsin (United States Of America) | Details |
| Job Category Global Quality and Compliance
Primary Location North America-United States-Wisconsin-Middleton - Research Way
Description
QA Auditor - GMP assures the quality of laboratory data and reports. This is accomplished by audits of data and reports as specified by Standard Operating Procedures and by conducting inspections of laboratory procedures. Written reports are prepared for... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Switzerland) | Details |
| Local Safety Specialist- Switzerland
Description:
A Swiss subsidiary of a leading internationally Pharma company are looking for a motivated person to take up the position of Local Safety Specialist.
The Local Safety Officer is responsible for pharmacovigilance but additionally responsible for quality assurance, complaint handling and preparation of SOPs; training responsibilities and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Buckinghamshire (United Kingdom) | Details |
| QA Officer, Global Pharma
QA Officer required for a global Pharmaceutical company based in Buckinghamshire. Exciting opportunity for a Graduate who has some relevant work experience from within the Pharmaceutical industry. 12 months fixed term contract.
JOB TITLE
QA Officer / QA Associate / Quality Assurance Officer
LOCATION
UK / England /... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire (United Kingdom) | Details |
| Quality Systems Manager, East Anglia, Global Pharmaceutical Company
Quality Systems Manager required for a leading Pharmaceutical manufacturing site. You will be responsible for the implementation of quality improvement programs and will work closely with QA and plant management teams to assure systems are effectively implemented and maintained to ensure compliance with regulatory... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cheshire (United Kingdom) | Details |
| Our global Pharmacetical client is looking for a CQA Auditor to join their team on a contract role which is to start immediately right through to the end of the year. The role is paying an excellent daily rate.
Accountabilities/Responsibilities:
Provides compliance advice and conducts audits (studies, routine systems and compliance areas), in line with the global CQM strategic direction... [Full Details] |
| Salary: Negotiable (450 - 500 £) |
| Regulatory And Drug Safety | QA | Buckinghamshire (United Kingdom) | Details |
| QA Officer, Global Pharma
QA Officer required for a global Pharmaceutical company based in Buckinghamshire. Exciting opportunity for a Graduate who has some relevant work experience from within the Pharmaceutical industry. 12 months fixed term contract.
JOB TITLE
QA Officer / QA Associate / Quality Assurance Officer
LOCATION
UK / England /... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| Job description
• Ensure compliance with cGMP of all activities related to the development of pharmaceutical products for use in Clinical trials, including Quality management System (complaints etc.)
• Approve and audit procedures and documents from manufacturing, analytical and service group
• Perform Quality compliance release and/or review of investigational Medicinal Products... [Full Details] |
| Salary: Negotiable (25000 - 30000 £) |
| Regulatory And Drug Safety | QA | Virginia (United States Of America) | Details |
| Job Category Global Quality and Compliance
Primary Location North America-United States-Virginia-Richmond
Description
Title: QA Auditor
Location: Richmond, VA
The basic purpose of the Quality Assurance (QA) Auditor is to assure the quality and integrity of laboratory data and reports . This is accomplished by reviewing data and reports as specified by SOP's (Standard Operating... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Wisconsin (United States Of America) | Details |
| Job Category Global Quality and Compliance
Primary Location North America-United States-Wisconsin-Middleton - Research Way
Description
This is an entry level position for the Quality Assurance Auditor - GMP. The QA Auditor - GMP assures the quality of laboratory data and reports. This is accomplished by audits of data and reports as specified by Standard Operating Procedures and by... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, Surrey (United Kingdom) | Details |
| QA Quality Senior Auditor– Quality – South East 45-50K
You will take a leading role in development and implementation of quality management systems and change control activities. Ideally you will have good experience within a steriles manufacturing environment and in particular have experience conducting internal and external audits. this role will involve a degree of travel to... [Full Details] |
| Salary: Negotiable (40000 - 50000 £) |
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