Senior Principal Scientist - Parenteral ExM MS&T

ALBEDIS est un partenaire de recrutement suisse de premier plan, spécialisé d
Senior Principal Scientist - Parenteral ExM MS&T
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).
Senior Principal Scientist - Parenteral ExM MS&T
Description de l'entreprise
For an important international pharmaceutical company based in Neauchâtel area, we are looking for a
Senior Principal Scientist - Parenteral ExM MS&T H/F - 100%
Temporary 6 month assignment
Description du poste
Serve as the primary technical lead for external Contract Manufacturing Organizations (CMOs) producing sterile injectable products.
Lead technology transfer, process validation, and commercial manufacturing activities across global manufacturing sites.
Ensure process robustness, product quality, regulatory compliance, and continuity of supply throughout the product lifecycle.
Drive technical investigations, root cause analysis, CAPAs, and change control activities.
Monitor process performance using data analysis and continuous process verification to identify improvement opportunities.
Collaborate closely with Quality, Supply Chain, Procurement, Product Development, Regulatory Affairs, and external manufacturing partners.
Lead cross-functional technical projects and support regulatory inspections and CMC documentation.
Promote Operational Excellence (OpEx) initiatives to improve manufacturing efficiency and process reliability.
Provide technical leadership, mentoring, and guidance to junior MS&T scientists.
Travel to CMO sites as required to support technology transfers and manufacturing activities.
Profil recherché
Bachelor's degree in Engineering or Life Sciences (Master's or PhD preferred) with solid experience in sterile pharmaceutical manufacturing.
Proven expertise in technology transfer, process validation, commercial manufacturing, and cGMP regulations.
Strong project management, technical problem-solving, and risk assessment skills (FMEA, Ishikawa, CAPA).
Experience working with CMOs and leading cross-functional, international teams.
Proficiency in statistical data analysis tools (Minitab/JMP) and Quality by Design (QbD)/DoE methodologies.
Excellent communication, stakeholder management, and influencing skills in a global environment.
Willingness to travel internationally (10-20%) with occasional temporary on-site assignments at CMO facilities. jid9628015aen jit0833aen jpiy26aen