In addition to viewing our QA jobs, you may also wish to register now for other specialist medical recruitment services including Jobs by Email.
| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | QA | Any Location (Wales) | Details |
| Job Description:
• Responsible for the day-to-day management of the Quality Assurance function
• Acting as a Qualified Person on behalf of the company – responsible for the review (& release) of the packing records
• Responsibility for the management of the Deviation Control System, ensuring deviations that may occur during packing are recorded, discussed via regular scheduled... [Full Details] |
| Salary: Negotiable (50000 - 55000 £) |
| Regulatory And Drug Safety | QA | Cambridgeshire, Hertfordshire (United Kingdom) | Details |
| You will be someone who has experience of document management or archiving within an electronic environment, our ideal person would have worked in drug development and be familiar with tools used in electronic regulatory submissions.
Tasks include:
Preparation, dispatch and tracking of electronic and paper media for regulatory submissions
Addition of bookmarks and hyperlinks to pdf... [Full Details] |
| Salary: Negotiable (23000 - 28000 £) |
| Regulatory And Drug Safety | QA | Any Location (Germany) | Details |
| Chiltern wurde 1982 gegründet und ist eine führende, weltweit agierende Contract Research Organisation mit umfassender Erfahrung in der Durchführung globaler Phase I bis IV Studien, welche ein breites therapeutisches Einsatzgebiet umfassen.
Wir bieten Produktentwicklungsdienstleistungen für pharmazeutische und biotechnologische Unternehmen sowie für Medizinproduktehersteller an. Diese... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Italy) | Details |
| We are looking for a Head of Development QA for an international Pharmaceutical company. Based in Italy you will lead cGMP strategy and compliance in development.
You will:
• Have experience in development GMP
• Ensure products and processes handling, manufacturing and distribution of investigational medicinal products are cGMP compliant
• Provide Quality oversight over the entire... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| QA Officer / Quality Assurance Officer – International Manufacturing – Northwest
SUMMARY
There is now the opportunity for an experienced Quality Assurance Officer to join this international organisation in a senior position that will see you in a small team of experienced QA Officers reporting directly to the Head of Quality. This is an exciting and progressive company offering training... [Full Details] |
| Salary: Negotiable (26000 - 28000 £) |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| Sterile Engineer – International Pharmaceutical Manufacturing – Northwest
SUMMARY
There is now the opportunity for an experienced Cell Engineer to join this truly international pharmaceutical manufacturing company. You will be working in a senior position and very much responsible for the progression of the department through your expertise.
JOB TITLE: Cell Engineer / Sterile... [Full Details] |
| Salary: Negotiable (35000 - 45000 £) |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| Packaging Technologist – International Pharmaceutical Manufacturing Organisation – Northwest England – £30,000
SUMMARY
There is now an excellent opportunity for an experienced PACKAGING TECHNOLOGIST to join this organisation in an exciting position and at an exciting time. You will be a senior member within the team, responsible for a number of key duties and a lead point of knowledge... [Full Details] |
| Salary: Negotiable (25000 - 35000 £) |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| Pre-Filled Syringe Operator (Sterile Manufacturing) – International Pharmaceutical Company – North West – Salary Negotiable
SUMMARY
There is now the opportunity for an experienced pre-Filled Syringe Operator to join this rapidly expanding international pharmaceutical company. Working in a state or the art manufacturing environment and one of the most friendly and supportive... [Full Details] |
| Salary: Negotiable (25000 - 30000 £) |
| Regulatory And Drug Safety | QA | Any Location (United Kingdom) | Details |
| Senior Regulatory Affairs Officer – National Biotechnology Organisation – Scotland - £35,000-40,000
SUMMARY
There is now an exciting opportunity for an experienced Regulatory Affairs professional to join this hugely success and expanding company. You will be joining an established and extremely friendly team and be responsible for really driving the improvements for the site. This is... [Full Details] |
| Salary: Negotiable (35000 - 45000 £) |
| Regulatory And Drug Safety | QA | Cambridgeshire (United Kingdom) | Details |
| An excellent opportunity has arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company.
As a Pharmacovigilance and GCP QA Auditor within the multi-disciplined company QA team you will utilise your expert regulatory knowledge and excellent communication skills to assist with the design and implementation of the audit programme for the... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Germany) | Details |
| Chiltern wurde 1982 gegründet und ist eine führende, weltweit agierende Contract Research Organisation mit umfassender Erfahrung in der Durchführung globaler Phase I bis IV Studien, welche ein breites therapeutisches Einsatzgebiet umfassen.
Wir bieten Produktentwicklungsdienstleistungen für pharmazeutische und biotechnologische Unternehmen sowie für Medizinproduktehersteller an. Diese... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| Packaging Technologist – International Pharmaceutical Manufacturing Organisation – Northwest England – £30,000
SUMMARY
There is now an excellent opportunity for an experienced PACKAGING TECHNOLOGIST to join this organisation in an exciting position and at an exciting time. You will be a senior member within the team, responsible for a number of key duties and a lead point of knowledge... [Full Details] |
| Salary: Negotiable (25000 - 30000 £) |
| Regulatory And Drug Safety | QA | East Sussex (United Kingdom) | Details |
| Qualified Person QP – International Pharmaceutical Company – South East - £50,000
Join this forward thinking international pharmaceutical company as a key player within their quality department as a Qualified Person. You will of course be responsible for the management of the release of a variety of dosage formats, but also acting as an integral part of the quality system and a... [Full Details] |
| Salary: Negotiable (50000 - 55000 £) |
| Regulatory And Drug Safety | QA | Any Location (Scotland) | Details |
| Senior Regulatory Affairs Officer – National Biotechnology Organisation – Scotland - £35,000-40,000
SUMMARY
There is now an exciting opportunity for an experienced Regulatory Affairs professional to join this hugely success and expanding company. You will be joining an established and extremely friendly team and be responsible for really driving the improvements for the site. This is... [Full Details] |
| Salary: Negotiable (35000 - 40000 £) |
| Regulatory And Drug Safety | QA | Buckinghamshire (United Kingdom) | Details |
| Senior Quality Compliance Associate / Senior GLP Auditor - Buckinghamshire or Home based or Any EU Location
Introduction
Our client is seeking to appoint a Senior Quality Compliance Associate / Senior GLP Auditor. The Senior Quality Compliance Associate / Senior GLP Auditor will conduct GLP audits of investigator sites, vendors, databases and study reports.
Client Profile
The... [Full Details] |
| Salary: Negotiable (34000 - 35000 £) |
| Regulatory And Drug Safety | QA | Hampshire (United Kingdom) | Details |
| Senior Quality Assurance Associate – Hampshire
Introduction
Our client is seeking to appoint a new Senior Quality Assurance Associate. The Senior Quality Assurance Associate will be responsible for working with vendors supporting regulatory inspections, GMP support / compliance and ensuring technical agreements are in place with vendors and reviewing them on a regular basis. GMP auditing... [Full Details] |
| Salary: Negotiable (41000 - 48000 £) |
| Regulatory And Drug Safety | QA | Buckinghamshire (United Kingdom) | Details |
| Quality Assurance Auditor (GCP) – Buckinghamshire
Introduction
Our client is seeking to appoint a Quality Assurance Auditor (GCP). The Quality Assurance Auditor (GCP) is responsible for the independent planning and conduct of audits of the clinical research activities of the company, business partners and vendors. These audits provide an independent quality assessment to ensure... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | QA | Hertfordshire (United Kingdom) | Details |
| Qualified Person (QP) - Hertfordshire
Introduction
Our client is seeking to appoint a new Qualified Person (QP). The Qualified Person’s (QP’s) primary accountability will be to ensure that all GMP/GDP activities are compliant, in addition to providing Quality Assurance expertise to both the sales and development divisions.
Client Profile
The client is a globally leading research... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Middlesex (United Kingdom) | Details |
| As an international pharmaceutical company with offices in the UK and India, my client is looking to recruit a Regulatory Affairs and Compliance Officer to be based at their UK headquarters in Middlesex.
You will be responsible for the compilation, administration and submission of European Marketing Variations in accordance with both National and European legislation, whilst ensuring the... [Full Details] |
| Salary: Negotiable (22000 - 26000 £) |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| Pre-Filled Syringe Operator (Sterile Manufacturing) – International Pharmaceutical Company – North West – Salary Negotiable
SUMMARY
There is now the opportunity for an experienced pre-Filled Syringe Operator to join this rapidly expanding international pharmaceutical company. Working in a state or the art manufacturing environment and one of the most friendly and supportive... [Full Details] |
| Salary: Negotiable (20000 - 25000 £) |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| QA Officer / Quality Assurance Officer – International Manufacturing – Northwest
SUMMARY
There is now the opportunity for an experienced Quality Assurance Officer to join this international organisation in a senior position that will see you in a small team of experienced QA Officers reporting directly to the Head of Quality. This is an exciting and progressive company offering training... [Full Details] |
| Salary: 26000 - 30000 £ |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| Mechanical (Sterile) Engineer – International Pharmaceutical Manufacturing – Northwest
SUMMARY
There is now the opportunity for an experienced Cell Engineer to join this truly international pharmaceutical manufacturing company. You will be working in a senior position and very much responsible for the progression of the department through your expertise.
JOB TITLE: Cell Engineer /... [Full Details] |
| Salary: Negotiable (30000 - 35000 £) |
| Regulatory And Drug Safety | QA | Any Location (Switzerland) | Details |
| Our client, is seeking a Clinical QA GCP Manager for Switzerland.
PRINCIPAL RESPONSIBILITIES include:
• Driving the establishment of quality objectives associated with clinical development
• Responsible for providing quality GCP oversight, in collaboration with local GCP quality
• Providing oversight, expertise and direction in the implementation/execution of quality standards... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Any Location (Switzerland) | Details |
| I am currently working with an Internation pharmaceutical company, who are seeking contract Regulatory Affairs associates (CMC) to be based in Switzerland.
For more information, please contact Stuart Gill on 01293 776 644.
Barrington James is a professional recruitment consultancy who specialises in the placement of high calibre candidates within the Pharmaceutical Industry.
With well... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Manchester (United Kingdom) | Details |
| My client is an international Medical Device company with a well recognised portfolio of products. Their portfolio specialises in Critical Care, Surgery and post operative care.
Due to their success in 2010 they are now looking to expand their Quality team in their Manchester branch.
Responsibilities
Head the branches Quality Management system
Must lead internal Audits and coach... [Full Details] |
| Salary: Negotiable (48000 - 52000 €) |
Site by Redder