External Manufacturing MS&T
- Entreprise
- Albedis Lausanne
- Lieu
- Boudry
- Date de publication
- 23.07.2026
- Référence
- 5307483
Description
ALBEDIS est un partenaire de recrutement suisse de premier plan, spécialisé d
External Manufacturing MS\&T (Drug Substance)
ALBEDIS est un partenaire de recrutement suisse de premier plan, spécialisé dans la mise en relation entre talents et entreprises à travers un large éventail de secteurs, des postes de support jusqu'aux fonctions de direction. Membre d'Interiman Group, ALBEDIS s'appuie sur l'expertise combinée de ses marques partenaires pour couvrir des domaines tels que l'architecture et l'immobilier, la finance, l'IT, les sciences de la vie, le juridique ou encore les ressources humaines, avec une présence dans toute la Suisse (Berne, Genève, Lausanne, Zurich).
External Manufacturing MS\&T (Drug Substance)
Description de l'entreprise
Our client, a leading international biopharmaceutical company, is looking for a :
Senior Scientist - External Manufacturing MS\&T (Drug Substance) 100% H/F
Temporary contract for 5 month with possible extension (2027)
to support its commercial manufacturing and technology transfer activities.
Description du poste
Provide technical support for commercial manufacturing of biologic drug substances at external manufacturing sites (CMOs).
Support technology transfer activities between manufacturing sites and external partners.
Troubleshoot process-related issues, support deviation investigations, change controls, and process optimization.
Monitor manufacturing activities, identify operational risks, and ensure timely resolution of technical issues.
Collaborate closely with Manufacturing, Quality, Supply Chain, and cross-functional technical teams.
Ensure effective communication with internal stakeholders and external manufacturing partners.
Maintain GMP compliance and support high-quality commercial manufacturing operations.
Profil recherché
MSc or BSc in Biotechnology, Biochemistry, Chemical Engineering, or a related scientific discipline.
Proven experience in GMP biopharmaceutical manufacturing, ideally within the biologics industry.
Strong knowledge of mammalian cell culture, downstream purification, and manufacturing processes.
Experience in technology transfer, process support, déviation management, and continuous improvement.
Excellent problem-solving, communication, and stakeholder management skills.
Ability to work independently in a dynamic, cross-functional, and international environment. jpid7bcd6cdjm jpit0730jm jpiy26jm