- Regulatory Affairs Associate -CMC - International
To apply for this regulatory affairs associate CMC please call Julie Cooper on 07951 082482
Alternatively please send your to me at :firstname.lastname@example.org
- Senior Regulatory Affairs Associate CMC
Our client a leading biopharmaceutical company now have a vacancy for a Senior Regulatory Affairs Associate.
This role will involve the coordination, preparation and maintaining a variety of regulatory CMC submissions to support both development and commercial products.
- Associate Director/Director, Regulatory Affairs – CMC Team Head-126127
PPD has an exciting new vacancy for a Head of CMC Team, within Global Regulatory Affairs. This is a fantastic opportunity to take your Regulatory Affairs career to the next level.
In this role, you will provide innovative solutions and CMC expertise for provision of technical guidance and leadership as part of the Global Regulatory Affairs leadership team. ...
- Senior Regulatory Affairs Associate
Responsibilities * Preparation and review of high quality, Chemistry Manufacturing and Control (CMC) detailed regulatory documents for dossier submission * Liaising and working closely with other company personnel (R&D, Quality, Business Development and Licensing) to ensure accuracy of such documents Submission of MAAs (generic/bibliographical) in the EU via national, MRP, DCP routes * Provide regulatory support for out-licensing activities in EU and non-EU territories Auditing registration ...
- Regulatory Affairs Associate Director - Netherlands - EU & International strategic leadership role - Excellent Portfolio - Expanding Pharma Company
This will be a results orientated strategic leadership role where your strategy and regulatory knowledge will carve a path for product submissions and registrations ion the EU and other major RoW/International territories.If you wish to apply for this role send your CV to email@example.com or call Theo Moore on Matt Grieg on +44 (0)207 801 3380
- PW 6423 Interim CMC Regulatory Affairs Team Leader / Director
Our Client, a Global pharmaceutical company, requires an exceptional leader to manage the CMC team and function. You’ll require proven experience in leading teams and CMC operations and demonstrate drive, passion and professionalism to achieve continued improvement for this department. Office based role in Cambridge.
- PW 6424 CMC Regulatory Affairs Team Leader / Director
Our Client, a Global pharmaceutical company, requires an exceptional leader to manage the CMC team and function. You’ll require proven experience in leading teams and CMC operations whilst demonstrating drive, passion and professionalism to achieve continued improvement for this department. Office based role in Cambridge.
- Senior Manager/Associate Director – CMC – Ireland Office or Home Based-126125
PPD has a new opportunity for a Senior Manager/Associate Director, Regulatory Affairs, based in Ireland. This position sits within the CMC team in Global Regulatory Affairs department.
Major responsibilities include:
Management and input for GMP/GDP/GLP licensing aspects and provision of technical guidance related to licensing requirements for varying environments in order to support the business. ...
- Associate Director CMC - Small Molecules
An experienced CMC professional with a background in small molecules is wanted to join my client, one of the leading pharmaceutical companies in Switzerland.
- Associate Director CMC Cell Therapy, Switzerland
An experienced CMC professional with a background in both Cell Therapies and Biologics is wanted to join my client, one of the Top 5 Pharmaceutical Companies in the world.