Senior MS&T Engineer – Pharma Tech Transfer & Manufacturing
5 days ago Be among the first 25 applicants
Eligibility Requirement: Candidates must have the right to work in Switzerland without sponsorship. Fluency in both English and French is essential.
Are you an experienced pharmaceutical professional ready to take your expertise to the next level? BioTalent has partnered with a global leader in pharmaceutical manufacturing services to find an MS&T Engineer for their cutting-edge facility in Neuchâtel, Switzerland. This is an exciting opportunity to lead innovative projects, collaborate with cross-functional teams, and drive the development of life-changing treatments.
Your Impact in This Role
1. Lead the introduction of oral solid dosage forms (capsules & tablets), ensuring seamless technology transfer and regulatory compliance.
2. Conduct risk assessments, perform gap analyses, and provide technical leadership to improve manufacturing processes.
3. Act as a key liaison between QA, packaging, and production operations, ensuring smooth project execution.
4. Define and implement Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs) to uphold the highest industry standards.
5. Drive process optimization, resolve manufacturing challenges, and champion best practices in production.
6. Oversee CAPA implementation and ensure adherence to international EU-GMP, Annex 11, and 21 CFR regulatory frameworks.
7. Guide and mentor junior colleagues, fostering a collaborative and high-performance environment.
8. Work closely with clients to deliver high-quality outcomes within tight timelines.
9. Leverage your English and French fluency to support international teams in a multicultural environment.
10. Be part of an organization poised for expansion, with plans to double capacity and venture into injectable manufacturing & lipid nanoparticle technologies.
What We’re Looking For
Education: BS/MS in Engineering or a related technical field.
Experience: 10–15 years in the pharmaceutical industry, specializing in new product introductions & solid dosage form validation.
Skills: Strong expertise in project management, problem-solving, and electronic documentation systems.
Languages: Fluent in English & French, with excellent communication and stakeholder management abilities.
This role offers a unique opportunity to be part of a high-growth, cutting-edge facility, working on pioneering pharmaceutical solutions that improve patients' lives worldwide.
Ready to make an impact? Apply today!
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance
Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Engineering Services
#J-18808-Ljbffr