Global Regulatory Lead, Biologics

Global Compliance Lead - Contract - 12+ Months - Remote - Pharma - Jan StartAre you ready to take the lead in driving compliance and validation excellence across cutting-edge digital solutions? This is your chance to step into a pivotal role where you’ll define global strategies, ensure regulatory integrity, and champion digital transformation across...

Global Compliance Lead - Contract - 12+ Months - Remote - Pharma Are you ready to take the lead in driving compliance and validation excellence across cutting-edge digital solutions? This is your chance to step into a pivotal role where you’ll define global strategies, ensure regulatory integrity, and champion digital transformation across manufacturing,...

Global Compliance Lead - Contract - 12+ Months - Remote - Pharma - Jan StartAre you ready to take the lead in driving compliance and validation excellence across cutting-edge digital solutions? This is your chance to step into a pivotal role where you'll define global strategies, ensure regulatory integrity, and champion digital transformation across...

Senior Director Business Development Central Europe Job Summary: Partner with new biotech and pharma companies, to drive top line services growth in Central Europe Continue to deepen relationships with existing client base to enable their success Work closely with the business development and CMC teams to develop the right strategies and tactics to meet the...

A leading global Biologics CDMO is looking for a Vice President of Business Development to drive commercial growth across Europe. The ideal candidate will have 10+ years of experience in business development within biologics, a strong track record in leading successful teams, and the ability to cultivate strategic partnerships. Responsibilities include...

Job Title Regulatory Consultant (EMEA) Contract 12-Month Contract, 0.5 FTE Location Remote (EU-based) About Us Our client is a specialist consultancy supporting emerging and established biotechnology companies in navigating complex regulatory pathways. We work across a diverse range of innovative therapeutic products, helping clients build robust regulatory...

**QA Contract Manufacturing Senior Manager**: **Mission**: Ensure excellence in Quality Assurance (QA) management of Contract Manufacturing Organizations (CMOs) and the associated Quality Management System (QMS) for commercial Pharmaceutical and Biopharmaceutical drug products manufactured and supplied by external sites. **Functions and key aspects of the...

Mantell Associates is partnered with a leading global Biologics CDMO who is seeking a strategic, high-impact Vice President of Business Development to drive commercial growth across Europe and beyond. This executive role is perfect for a seasoned commercial leader with deep biologics expertise and a strong track record of cultivating strategic partnerships,...

Title : RAQA Lead - Spain and Portugal Location : Barcelona, Spain ✉️ Contact : The company Are you someone who has Iberia-wide regulatory experiences and are looking for the next step in your medical devices career at the EMEA level? Are you someone who likes to think creatively and prioritizes medical devices that are always accessible to patients and...

Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Mantell Associates Head of Validation & Automation - Mantell Associates | CDMO | Cell & Gene Therapy | Validation, Automation & Engineering Mantell Associates is partnered with a globally leading Cell & Gene Therapy CDMO, who is seeking a forward-thinking and...