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Today's latest Regulatory And Drug Safety job vacancies include:

Job FieldDisciplineRegionActions
Regulatory And Drug SafetyQAAny Location (Belgium)Details
QA Release Manager - New Product Introduction manager needed for a new Sterile & Vaccine team within one of the Top 5 Pharma Companies in the world. Requirements: Good knowledge of cGMP, GMP and GDP. Industrial Pharmacist with Belgium QP number Minimum 5 to 7 years' experience in QA Operation role Technical knowledge of manufacturing, quality and regulations and quidelines Ability... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAAny Location (Belgium)Details
Senior Commercial Quality Assurance Manager (QC GMP) My client, one the Top 5 Pharmaceutical Companies in the world, have expanded their Vaccines department and are recruiting for a Senior Manager (director level) to lead 4 to 6 QC release laboratories. With progression and growth as the heart of this company, it is important that candidates are willing to progress and become a solid... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAAny Location (Belgium)Details
My client, one the Top 5 Pharmaceutical Companies in the world, have expanded their Vaccines department and are recruiting for a Senior QA Sterility Specialist With progression and growth as the heart of this company, it is important that candidates are willing to progress and become a solid foundation for the organisation. What could you bring to the team? Why would you be the right... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAEast Sussex (United Kingdom)Details
•Qualified person •Global Pharmaceutical company •Permanent position JOB BACKGROUND The source department of Chiltern International acts in a similar way to that of a staffing solutions provider. The department is currently recruiting for a Qualified Person to work for our client a global Pharmaceutical company. The position is a full time permanent role based at their... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (France)Details
My client is a leading pharmaceutical company based in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases, including 20 phase 1 and 2 studies on going in France and 10 Phase 3 trials in over twenty countries.... [Full Details]
Salary: Negotiable (45000 - 55000 £)
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (United Kingdom)Details
My client, a very large Pharmaceutical company based in the East of England, are currently searching for a Senior Regulatory Affairs Officer to join their team on a permanent basis. Within this role you will be responsible for the EU licence Hospital products portfolio and line manage one or more team members. This role will offer excellent progression within a fast moving team. It is... [Full Details]
Salary: Negotiable (35000 - 45000 £)
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Hertfordshire (United Kingdom)Details
An excellent opportunity has arisen for a Regulatory Executive with 1-2 years of regulatory experience to join a fast joining pharmaceutical company based in the Hertfordshire area. Within this role you will be responsible for assisting with UK and EU submissions; MAAs, Variations and Renewals, labelling, PILs, SmPCs and user testing. The team are currently growing at a fast rate and they... [Full Details]
Salary: 30000 - 35000 £
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (France)Details
My client is a leading pharmaceutical company based in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases, including 20 phase 1 and 2 studies on going in France and 10 Phase 3 trials in over twenty countries.... [Full Details]
Salary: Negotiable (45000 - 55000 £)
Regulatory And Drug SafetyQAAny Location (United Kingdom)Details
Senior QA Officer - Management opportunities at entry level Hard-working, Charismatic individual needed for a steadily growing Pharmaceutical Company Requirements: A fantastic opportunity to join a growing Pharmaceutical Company in preparing for expansion and development of a team. Management potential and leadership will be the focus of the company, so this is a great opportunity... [Full Details]
Salary: Negotiable (20000 - 29000 £)
Regulatory And Drug SafetyClinical Project Manager,...Buckinghamshire (United Kingdom)Details
The main purpose of the job is as follows; To manage the case processing team of Pharmacovigilance (PV) Officers and Principal PV Officers Manages case management activities for the companies products for the UK Affiliate Responsible for reviewing daily work flow and, when needed, adjusting day-to-day PV operations work / resources to meet individual case safety reports (ICSR)... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAAny Location (Germany)Details
My client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They active in over 45 countries across the globe and continue to steadily grow and are looking to add to their team! Their European activities are growing rapidly, and are currently seeking a full-time, office-based GCP Auditor to join our Quality Assurance team. This... [Full Details]
Salary: Negotiable (35000 - 55000 €)
Regulatory And Drug SafetyQAAny Location (Germany)Details
My client is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. They active in over 45 countries across the globe and continue to steadily grow and are looking to add to their team! Their European activities are growing rapidly, and are currently seeking a full-time, office-based GCP Auditor to join our Quality Assurance team. This... [Full Details]
Salary: Negotiable (25000 - 45000 €)
Regulatory And Drug SafetyQA, Regulatory AffairsAny Location (United Kingdom)Details
Calling all Executive Quality Assurance Associates! Interested in working for a cutting edge drug development biotech? Could you bring fresh and dynamic skills to their quality systems? My exclusive client is urgently seeking a consultant for a 3-6 month contract based in the North of England with a proven track record in leading GXP programmes. As the Quality Assurance Specialist you will... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyRegulatory AffairsEast Sussex, London, Surrey, West Sussex (United...Details
Cmed is looking for a clinical research expert to manage all aspects of regulatory work for our trials and marketing authorisations, on a fixed term contract for 3 months. This includes preparing and approving regulatory packages at a local and EC level, performing intelligence activities and supporting study teams... The successful applicant will have experience in a similar role and an... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyRegulatory AffairsAvon, Bedfordshire, Berkshire, Buckinghamshire,...Details
Senior Regulatory Affairs Officer, Europe. Chiltern is looking to recruit a Senior Regulatory Affairs Officer on a permanent basis. This role will ideally be office based in Slough, Berkshire. We may also consider field based options. We will consider applications from candidates with CRO Regulatory Affairs background and offer those coming from a Pharmaceutical company background the... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyDrug Safety, Pharmacovigilance, Drug...Any Location (Switzerland)Details
Senior Pharmacovigilance Consultant, Basel, Switzerland My exclusive client is seeking to employ a number of experienced Pharmacovigilance professionals on a permanent basis. For the first 3 months these roles will initially be based from Basel but, thereafter, can be based from home anywhere in Europe. Responsibilities may include: PV Quality and Compliance: • Manage PV SOPs and... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAEast Sussex (United Kingdom)Details
JOB BACKGROUND The source department of Chiltern International acts in a similar way to that of a staffing solutions provider. The department is currently recruiting for a Qualified Person to work for our client a global Pharmaceutical company. The position is a full time permanent role based at their Eastbourne site... SUMMARY Reporting to the Head of Quality, you will ensure that... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (Spain)Details
New role for a Senior Regulatory Affairs Manager. I am looking for an international regulatory CMC professional who will be responsible for human pharmaceutical products, involving both small and large molecules, injectable devices, investigational and marketed products. In this great position you will be responsible for independently planning and executing regulatory submission for compounds... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (France)Details
New role for a Senior Regulatory Affairs Manager. I am looking for an international regulatory CMC professional who will be responsible for human pharmaceutical products, involving both small and large molecules, injectable devices, investigational and marketed products. In this great position you will be responsible for independently planning and executing regulatory submission for compounds... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (Portugal)Details
New role for a Senior Regulatory Affairs Manager. I am looking for an international regulatory CMC professional who will be responsible for human pharmaceutical products, involving both small and large molecules, injectable devices, investigational and marketed products. In this great position you will be responsible for independently planning and executing regulatory submission for compounds... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyRegulatory AffairsBerkshire (United Kingdom)Details
Entrust Clinical People are actively resourcing for their Global CRO client for a Regulatory Affairs Manager or Associate Director, Regulatory Affairs. This is an exciting time to join a newly created team and work on a range of key projects within Regulatory Affairs, specifically on Product Life Cycle maintenance, Regulatory CMC and Labelling. These are permanent opportunities, full time... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAScotland (United Kingdom)Details
Entrust Clinical People are actively resourcing for an experienced Quality Assurance Specialist for their Global Pharmaceutical client in Dundee.. This is a temporary contract running until Dec 2015. Applicants must demonstrate Quality Assurance experience in a regulated industry, preferably pharmaceuticals and have good knowledge of understanding of GMP, quality systems and quality... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyQAScotland (United Kingdom)Details
Entrust Clinical People are actively resourcing for an experienced Quality Assurance Specialist for their Global Pharmaceutical client in Dundee, Scotland.. This is a permanent position, full time and site based. Applicants must demonstrate Quality Assurance experience in a regulated industry, preferably pharmaceuticals and have good knowledge of understanding of GMP, quality systems and... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyClinical Project Manager, Regulatory...Any Location (Switzerland)Details
An experienced CMC professional with a background in Biologics is wanted to join my client, one of the leading pharmaceutical companies in Switzerland. With an impressive product portfolio and pipeline this is an opportunity to join a market leader in a senior and strategic position as Associate Director within biologics You will be responsible for the successful implementation of... [Full Details]
Salary: Negotiable
Regulatory And Drug SafetyClinical Project Manager, Regulatory...California (United States Of America)Details
A fantastic opportunity has arisen for a Global Medical Affairs Director to join one of the top 20 pharmaceutical companies in the world. This exciting role based in the USA, sits within the Global Medical Affairs Division. This is a highly visible position and will play a critical role in ensuring a successful launch. In addition, this position will offer the opportunity to shape the future... [Full Details]
Salary: Negotiable

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