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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | QA | Hampshire (United Kingdom) | Details |
| Our client is a leader is development of surgical equipment as well as playing a central role in the development of products that are used in various sugery operations. They are looking for a Regulatory Affairs and Quality Assurance Coordinator with experience working with the FDA, MHRA, Technical Dossiers, ISO13485 and ISO9001.
This position will require you to work to ensure compliance with... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | London - Central (United Kingdom) | Details |
| Our client is a Contract Research Organisation specialising in Phase 1 of Clinical Trials based in the Greater London area offering excellent facilities and an attractive client base. As a QA GCP Manager you will be at the forefront of leading the auditing team as well as ensuring a good standard of service is offered to the clients in the bid for further business development.
As the QA... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | London - Central (United Kingdom) | Details |
| As the QA Manager you will be responsible for planning, preparing and reporting on clinical audits to ensure trials conform to applicable regulations, GMP guidelines, ICH-GCP and the relevant Standard Operating Procedures (SOPs). This includes responsibilities for arranging and conducting procedural audits on individual studies and/or specific areas of Unit's operations, as determined by... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | London - Central (United Kingdom) | Details |
| As the QA Manager you will be responsible for planning, preparing and reporting on clinical audits to ensure trials conform to applicable regulations, GMP guidelines, ICH-GCP and the relevant Standard Operating Procedures (SOPs). This includes responsibilities for arranging and conducting procedural audits on individual studies and/or specific areas of Unit's operations, as determined by... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Surrey, London - South (United Kingdom) | Details |
| ----Company:
Our Client is a large Contract Research Organisation (CRO) dealing in early phase clinical trials. They are looking for a Quality Assurance Manager to join their team in Croyden.
----Role:
The Quality Assurance Manager will report to the Research director and will be responsible for clinical audits ensuring the trials conform to the appropriate regulations, ICH-GCP, GMP... [Full Details] |
| Salary: Negotiable (35000 - 40000 £) |
| Regulatory And Drug Safety | QA | East Midlands (United Kingdom) | Details |
| ----Company:
Our client is a major Pharmaceutical and Medical Device company based in East-Midlands/North UK. They are dedicated to providing cost-effective products to meet the growing needs of the healthcare industry in the UK. The company is currently looking for QA professionals to join their team.
----Role:
•To analyse and report results of raw materials and products
•To... [Full Details] |
| Salary: Negotiable (18000 - 25000 £) |
| Regulatory And Drug Safety | QA | London - Central, London - North, London - East, London -... | Details |
| Clinical Quality Assurance Officer
A rare opportunity to work for a leading global pharmaceutical company in a Quality Assurance Officer ( QA) role, this position offers the very highest level of professional’s development focusing on CNS trials.
Clinical Quality Assurance Officer
To ensure that systems with procedures that assure the quality of every aspect of clinical trials... [Full Details] |
| Salary: Negotiable (Up to 50000 £) |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, Surrey (United Kingdom) | Details |
| International Quality Assurance Manager
We have an excellent opportunity that has arisen with a TOP global pharmaceutical company working to provide QA support and ensure that products are manufactured in accordance with Marketing/Manufacturing Authorisations and GMP guidelines. This role will report in to the Director of QA and is offering a competitive salary and benefits package. This is a... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Bedfordshire, Buckinghamshire, Essex, Hertfordshire... | Details |
| Manager, Regulatory Affairs, Submissions Compliance (QC)
An excellent opportunity to work with a top global Pharmaceutical company who are currently developing a number of diverse and exciting products. Working within this large company will be an fantastic opportunity to broaden your experience, enabling you to take your next step up the career ladder!
The position will be responsible... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, Surrey, London - South (United... | Details |
| Interested in oncology/haematology? looking for a new challenge in a young global company based in Berkshire?
To assist the Clinical Quality Assurance Manager in ensuring the full compliance with GCP and the constant improvement in standards of development within the I.C.T.R.
Work to be performed:
1.To assist the Clinical Quality Assurance Manager to ensure the implementation of and... [Full Details] |
| Salary: 40000 £ |
| Regulatory And Drug Safety | QA | Bedfordshire, Buckinghamshire, Cambridgeshire, Essex,... | Details |
| Senior Manager Clinical QA
Our client a TOP GLOBAL Pharmaceutical company are now looking to recruit again due to expansion; as a large Pharmaceutical company our client provides excellent career progression with exciting and diverse products. An excellent company to take the next step up your career ladder!
Main purpose of the job:
To support the Associate Director, Clinical QA in the... [Full Details] |
| Salary: 45000 £ |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, London - Central, Surrey, London -... | Details |
| Are you are looking to move to a Director level role? An excellent opportunity for a Quality Assurance specialist to join a growing pharmaceutical company based in Berkshire. In this role you will be responsible for ensuring quality awareness throughout the company, you will also deliver the company's R&D Audit Programme, and ensure that Clinical Trials supplies production and subsequent... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, London - Central, Surrey, London -... | Details |
| Primary Purposes of Position:
This progressive and innovative company is now looking for a Senior Quality Assurance Officer, to perform audits and to assist in the development of a quality system, in order to support and promote the overall quality improvement of company drug development activities and therefore to help achieving clinical excellence.
Main Duties to be performed:
Audits... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, Surrey (United Kingdom) | Details |
| Working as a core member of the central regulatory team, you will input into the commercial products of this TOP GLOBAL Pharmaceutical company. The portfolio includes a mix of development projects and post approval activity.The department, which has a proven track record of leading switch activity on multi million pound brands, is fast paced delivering innovative self-medication products to the... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire, East Sussex (Bulgaria, Czech Republic, France,... | Details |
| There are outstanding opportunities available around Europe for QA Auditors with GCP experience in clinical trials working for a global CRO that manages all aspects of clinical development programmes for pharmaceutical and biotechnology companies. They have vacancies for QA GCP Auditors in various countries to provide on-going assessment of the status of the compliance of the company's European... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Switzerland) | Details |
| This is an outstanding opportunity for an experienced Clinical Auditor to work for one of the global giant in the pharmaceutical world at their office in Switzerland. An expert in GCP auditing is required for this role by a company that is known as a leading name in the discovery, development and marketing of innovative pharmaceutical products which cure diseases, ease suffering and enhance the... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire (United Kingdom) | Details |
| ----Company:
Our client is one of the world’s leading pharmaceutical companies. Being voted one of the top 100 companies to work for in the UK they are a great company work for and take pride in their staff. They are looking for someone to lead their Quality Assurance team, to maintain high Quality standards and successfully implement quality processes and procedures.
----Role:... [Full Details] |
| Salary: Negotiable (45000 - 55000 £) |
| Regulatory And Drug Safety | QA | Surrey (United Kingdom) | Details |
| Company:
Our Client is a global Pharmaceutical company based in Surrey, UK. They have been voted in the top 100 companies to work for in the UK by the Times and provide great scope for career progression and personal development. The company specialises in a majority of prescription medicines and are looking to expand their Quality team. This role would prove to be an ideal next step in your... [Full Details] |
| Salary: Negotiable (40000 - 50000 £) |
| Regulatory And Drug Safety | QA | Hertfordshire (United Kingdom) | Details |
| Our client is an API subsidary of a rapidly growing pharmaceutical company with a product portfolio range that is within the hundreds. This small subisdary is part of a large chain. The vacancy as a Quality Compliance officer will involve all aspects of document control including issue archiving, review of batch documentation, deviation and change control.
Although our client has not stated... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Spain) | Details |
| The main purpose of the CQA Auditor is to plan, lead and conduct audits of clinical trials across Europe. In addition you will provide compliance advice and will support regulatory authority inspections as necessary.
• Leading or supporting global, regional and local audits according to plans and standards
• Performing scientific misconduct investigations
• Providing GCP and compliance... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Hertfordshire (United Kingdom) | Details |
| Working for a Validation Officer for a API subsidary of a large pharmaceutical company with over 200 products of the market, you will be involved in assisting in the validation of production facilities, equipment, processes and provide QA assistance as necessary. There wil be responsibility for maintaining the validation documentation system and internal/external GMP inspections.
This vacancy... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire (United Kingdom) | Details |
| QA / Quality Assurance Associate
Cambridgeshire
Competitive Salary + bens
We are looking for a Quality Assurance Auditor to join the QA / Quality Assurance department at a world-class research organisation. The company has highly impressive analytical chemistry facilities utilising the latest instrumental techniques. The QA department provides and essential Audit function to ensure all... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire (United Kingdom) | Details |
| Responsibilities:
- Support, plan, conduct and report routine / directed compliance audits
- Report compliance concerns to Global Clinical Quality Assurance Management
- Participate in Global Clinical Quality Assurance projects
- Respond and recommend solutions to compliance concerns
- Maintain knowledge of current regulatory / GCP requirements
- Support Regulatory inspections... [Full Details] |
| Salary: 42000 - 47000 £ |
| Regulatory And Drug Safety | QA | Cambridgeshire, Middlesex, London - West (Germany, Italy,... | Details |
| This is an exciting opportunity and a key CQA role for an experienced GCP Auditor to participate in audits for global clinical trials across Europe. Our client is a world leading independent biotechnology company that discovers and develops important therapeutics, bringing meaningful improvement to the lives of people all over the world. They are seeking a QA Auditor to be based in one of the... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Oxfordshire (United Kingdom) | Details |
| Site Quality Assurance Manager
Company:
Our client is based in Oxfordshire, UK. They are leading designers and manufacturers of a wide range of medical devices and disposables which are used by healthcare professionals and consumers worldwide. They are dedicated to maintaining high quality standards and innovative healthcare solutions for the management of a variety of medical... [Full Details] |
| Salary: Negotiable (40000 - 50000 £) |
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