- Regulatory Affairs Senior CMC Manager – Biologicals – Close to Lausanne – Develop your expertise in MAbs & Global development projects
My rapidly expanding, and hugely successful Bio/pharmaceutical is expanding its global Biologicals CMC team which is based in Switzerland, close to Lausanne. If you wish to apply for this role send your CV with a covering note to firstname.lastname@example.org quoting reference number noted above call Matt Grieg or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
- 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
- Regulatory Affairs Manager – Relocation Assistance – Austria
As Regulatory Affairs Manager you will be responsible for the quality part, mainly module 2.3 and 3, for international submissions. You will be working in life cycle development but also life cycle maintenance. In addition to working on submissions, renewals, and variations, you will be working on CMC strategies and how to improve the regulatory process. Another aspect to you work is the communication with regulatory agencies, including EMA and AGES.
- 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.
- Regulatory Affairs Associate
With 5 commercial products, 7 more in the pipeline and over half a billion dollars of revenue, a global footprint in 40 countries, and a personal connection to our patients, BioMarin is the recognized industry leader in rare disease development. Come work in an entrepreneurial environment where you’ll have the resources and infrastructure combined with visibility and opportunity to tangibly impact patent’s lives and the future of our company. This is your chance to be part of something amazing!
- Regulatory Affairs Associate - Contract - Large Pharma - UK
This is a fantastic opportunity for an experienced CMC contractor to join one of the world’s leading Pharmaceutical companies.
- Head of Project Management