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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | QA | Berkshire, Hertfordshire, London, Surrey,... | Details |
| We are currently seeking a Senior Drug Safety Specialist for an exciting new role, based in London. This occupation entails handling global Regulatory Affairs including the planning, management and maintenance on established, licenced products.
At Meet we ensure that we provide all of our candidates with 100% confidentiality at all times. If you are interested in this role please do not... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Hertfordshire, London, Middlesex (United Kingdom) | Details |
| We are currently seeking a Senior Drug Safety Specialist for an exciting new role, based in London. This occupation entails handling global Regulatory Affairs including the planning, management and maintenance on established, licenced products.
At Meet we ensure that we provide all of our candidates with 100% confidentiality at all times. If you are interested in this role please do not... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
A Senior Analytical Development Analyst is needed to join the team of a growing London based pharmaceutical company. Offering industry beating training that could see you moving up the career ladder quickly. £24-27k
You will be working with a dynamic team dealing with a constantly increasing number of products in development, in a variety of formulations. As an Analytical... [Full Details] |
| Salary: Negotiable (24 - 27 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| My client is actively recruiting for a Quality Assurance Auditor/Executive to join them on a permanent contract.
Requirements:
Quality Assurance Auditor/Executive - UK Home Based
Role Purpose
Provide Clinical Quality Assurance support and services to ensure regulatory compliance and adherence to company procedures.
Key Accountabilities
• Undertake GCP compliance audits in all... [Full Details] |
| Salary: Negotiable (31500 - 39000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| As a Senior Clinical Quality Assurance Auditor within a multi-disciplined company, you will utilise your GCP auditing expertise, regulatory knowledge and excellent communication skills to support the audit programme for the clinical development and pharmacovigilance functions. You will also be expected to plan, conduct and follow-up investigator site audits, process audits, vendor audits and... [Full Details] |
| Salary: Negotiable (42000 - 46000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| Job Summary:
SENIOR QA ROLE!. Must have experience of auditing to GCP.
Principal responsibilities of QA Associate Director role will include:
• Leads and manages the Clinical Quality Assurance strategies and activities for ensuring that the appropriate processes and quality metrics are established in accordance with regulatory requirements and CRO/client industry standards.
•... [Full Details] |
| Salary: Negotiable (60000 - 80000 £) |
| Regulatory And Drug Safety | QA | Any Location (Germany) | Details |
An ambitious, growing international pharmaceutical company wants to add a junior Qualified/Sachkundige person to their well paid, well supported team, based near Munich.
While experiencing substantial growth, this Germany based pharma company has a stable background with considerable depth to their products and formulations, giving them a solid platform for growth. Due to this Growth... [Full Details] |
| Salary: Negotiable (90 - 91 £) |
| Regulatory And Drug Safety | QA | Wiltshire (United Kingdom) | Details |
| Senior Clinical Quality Assurance Auditor – 2-Year Contract
An excellent opportunity has arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company.
As a Senior Clinical Quality Assurance Auditor within a multi-disciplined company, you will utilise your GCP auditing expertise, regulatory knowledge and excellent communication skills... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Holland) | Details |
| Due to continued growth we are looking for an experienced validation expert to join a global pharmaceutical company working in a permanent position site based in Amsterdam.
The successful person will have an in-depth understanding of Validation, GMP guidelines and speak fluent Dutch.
Position Overview:
• You will be responsible for the preparation of validation programs and advising... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| LCRA/ Lead Clinical Research Associate MIDLANDs
We are currently recruiting for an experienced SCRA/ LCRA( Lead Clinical Research Associate) to join our successful organisation. This is an excellent opportunity to join a small Pharmaceutical Company and work directly with the Sponsor. Office based role
You will have both LCRA (lead clinical research associate) and team leadership... [Full Details] |
| Salary: Negotiable (45000 - 55000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| Senior Drug Safety Specialist – Junior Drug Safety Manager – Hertfordshire/Middlesex/London – Up to £40,000
Ideal for - Senior Drug Safety Specialist / Senior Pharmacovigilance Specialist / Senior Drug Safety Officer / Senior Pharmacovigilance Officer/ Drug Safety Specialist/ Drug Safety Officer/ Pharmacovigilance Specialist
Please contact Zoe Benningfield on +44 (0)7896 693960 or... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | QA | Dublin (Ireland) | Details |
A major Global Pharma are looking to hire a Quality Assurance/Change Control Specialist due to their continued success and expansion.
The successful Quality Specialist will take responsibility over Deviations, Change Controls and APR. You help to develop Quality Systems (QMS) and will monitor QA trends and provide senior management with input for process improvement.
The... [Full Details] |
| Salary: Negotiable (45000 - 60000 £) |
| Regulatory And Drug Safety | QA | Any Location (Germany) | Details |
Currently a leader in the German Generics market, my client is offering an ideal position for a Qualified Person to join their expanding team. You will have the opportunity to gain hands on experience and work closely with other QPs and become more seasoned in this profession.
As the QP, you will have a few years experience as a QP and will have a strong QA... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Austria) | Details |
Our client is a global manufacturer of consumable products and automated solutions for Research, diagnostic laboratories, and biotechnology companies. We have an exceptional opportunity available for a Quality Manager to... [Full Details] |
| Salary: Negotiable (Up to 90000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| Senior Regulatory Affairs Associate - Lifecycle Management
Business type: Large Pharmaceutical Company
Location: Buckinghamshire, Berkshire, England, UK
Salary: Up to £43,000 + Bonus + Benefits
Working within this large, very stable and successful company you will be responsible for the lifecycle management activities of some of the companies most successful products currently... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| As a Senior GCP Quality Assurance Auditor within a multi-disciplined company, you will utilise your GCP auditing expertise, regulatory knowledge and excellent communication skills to support the audit programme for the clinical development and Pharmacovigilance functions.
You will also be expected to plan, conduct and follow-up investigator site audits, process audits, vendor audits and... [Full Details] |
| Salary: Negotiable (42000 - 49000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| JOB ROLE:
Our client requires someone with GMP expertise to lead the audit program, planning and executing and following up site, process, vendor and documentation audits.
You will also be expected to plan, conduct and follow-up investigator site audits, process audits, vendor audits and documentation audits. In addition, you will provide support, advice, education and training to other... [Full Details] |
| Salary: Negotiable (42000 - 46000 £) |
| Regulatory And Drug Safety | QA | Any Location (Netherlands, The) | Details |
| Due to continued growth we are looking for an experienced validation expert to join a global pharmaceutical company working in a permanent position site based in Amsterdam.
The successful person will have an in-depth understanding of Validation, GMP guidelines and speak fluent Dutch.
Position Overview:
• You will be responsible for the preparation of validation programs and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Switzerland) | Details |
| Job Title: Regulatory Associate, Operations and System Management
Location: Bern, Switzerland
Package: Flexible according to experience
Start Date: Suitable to your needs
This position involves:
Compilation and publishing of regulatory dossiers for submission in all markets
Responsible for the management of source documents needed for the compilation and creation of the... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| A fantastic and exciting new opportunity has become available for a Quality Assurance professional to join a leading Pharmaceutical company as a Quality Assurance Representative.
My client is seeking an individual with excellent communication, organisation and decision making skills. You will be responsible for ensuring compliance to Quality Agreements, reviewing batch documentation and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | West Sussex (United Kingdom) | Details |
| I am currently working with a Speciality pharmaceutical company based in West Sussex, looking for a Regulatory Medical Writer to join their expanding team in their offices near Brighton.
We are searching for a candidate with approx 2 years experience within writing specifically Module 3, CMC sections of the CTD, experience writing preclinical documentation would be beneficial.... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| My client is seeking a candidate with a QA background who wishes to expand their QA skills and experience. Reporting to the QA Projects Manager the main purpose of this role will be to manage the Controlled Changes systems and act as the QA contact with all current and new export markets ensuring that the client is compliant with all regulatory requirements.
Responsibilities
Undertake... [Full Details] |
| Salary: Negotiable (24000 - 35000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| As a Senior Clinical Quality Assurance Auditor within a multi-disciplined company, you will utilise your GCP auditing expertise, regulatory knowledge and excellent communication skills to support the audit programme for the clinical development and pharmacovigilance functions. You will also be expected to plan, conduct and follow-up investigator site audits, process audits, vendor audits and... [Full Details] |
| Salary: Negotiable (40000 - 45000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| My client is currently recruiting for a GCP Compliance Manager to join a successful and growing global Biotech. You will be responsible for the compliance and QA activities within Europe. This is an excellent opportunity to join a company that offers excellent rewards to its employees and as great working environment.
Perfect opening for those with strong regulatory compliance and GCP quality... [Full Details] |
| Salary: Negotiable (60000 - 80000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| My client is currently recruiting for a GCP Compliance Manager to join a successful and growing global Biotech. You will be responsible for the compliance and QA activities within Europe. This is an excellent opportunity to join a company that offers excellent rewards to its employees and as great working environment.
Perfect opening for those with strong regulatory compliance and GCP quality... [Full Details] |
| Salary: Negotiable (60000 - 80000 £) |
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