- Quality Control Systems Manager (QC Systems Manager), Harrogate, North Yorkshire
COVANCE - one of the top 5 global Contract Research Organizations is currently looking for a Quality Control Systems Manager for its BioCMC solutions Division located in Harrogate, North Yorkshire.
- PW 6360 Interim Regulatory Manager, Neuroscience
Our global pharmaceutical client is looking for an interim Regulatory Manager to support a major, key neuroscience project in their global regulatory affairs group. This has numerous maintenance activities with major milestones in 2015 which require a regulatory professional experienced in life cycle management, including Type 1A/B variations, Type II variation (CMC), PSUR submission, Management of Linguistic review & PIP annual reports
- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging MarketsThe CompanyMy client, a leading Biotech company, with a global presence and highly reputable market presence, is looking for a Manager within their Regulatory Team. This company is rapidly growing year on year and producing products that are changing the world. With more and more MA applications happening each year, their expansion is set to continue exponentially. ...
- PW 6362 Manager, Growth markets, Global Regulatory
Our global pharmaceutical client is looking for a regulatory professional to utilise their broad experience working across a range of products in their Growth Markets for its products to the drug development process, including promulgation of health authority marketing authorisation dossiers to enable efficient and effective registration of medicinal products consistent with the supported regions commercial objectives.
- Regulatory Affairs Manager
Medpace is seeking a Regulatory Affairs Manager in either our London, United Kingdom or Munich, Germany office.
- Regulatory Affairs Senior Global CMC Specialist / Switzerland – Global Projects – Excellent Salary – Fantastic Company…!!!
This Global CMC department provides leadership for commercialized products and your role will be to operate as the Regulatory project lead for interactions with all major global regulatory agencies. If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
- Principal Regulatory Services Associate
We are currently looking for Principal Associate (Regulatory Affairs) to join our team in Uxbridge or as a home-based
- Regulatory Affairs Managers wanted in Basle Switzerland- Global CMC roles covering EU/US/Japan/Emg/Japan/LatAm – Salary to 150,000CHF + Bonus
These exciting opportunities will allow you to take the strategic lead for marketed products, managing the generation of high quality regulatory submissions required for the filing of technical changes to health authorities globally. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380
- Principal Associate
The Principal Associate, Regulatory Operations is responsible for the production of submissions and delivery of regulatory services in accordance with defined agency guidelines while balancing the quality and timeliness of customer deliverables.
- Regulatory Affairs Strategist CMC
A business critical role with direct responsibility for linking Genpact Pharmalink and the Client in a true outsourcing partnership.