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Senior Principal Scientist - Parenteral ExM MS&T

AlbedisBoudry, Neuchâtel, Switzerland, Neuchâtel

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.Serve as... Mehr anzeigen

TECHNICIEN QUALITÉ (H/F)

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Senior Manager, Regional Sales

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Director, Global Clinical Physician

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Ordonnanceur H/F

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French Speaker – Would you like to live in Athens? (Relocation Included)

CbtalentsLa Chaux-de-Fonds, Switzerland

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Senior Principal Scientist - Parenteral ExM MS&T

Interiman group - AlbedisBoudry, Neuchâtel, Switzerland

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Senior Principal Scientist - Parenteral ExM MS&T

AlbedisBoudry, Neuchâtel, Switzerland, Neuchâtel

Vor 7 Tagen

Stellenbeschreibung

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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.