Location: Bulle, Switzerland ...
Dettagli di lavoro
Riepilogo
Pubblicato il 15. maggio 2026
- Riferimento
- 209836-298
contattaci
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L
Laetitia Stirer
randstad operational
We bring diverse and pre qualified professional talent and businesses together to connect the right people with the right roles. By building specialized teams, we help individuals flourish in their careers and businesses succeed.
Dettagli di lavoro
Activity rate : 100%
Type of contract: Temporary contract (until 31.12.2026 with a potential extension)
Start Date: ASAP
In this role, you will act as the bridge between development and production, ensuring the successful transfer and implementation of analytical methods within a strictly regulated pharmaceutical cGMP environment. You will focus on coordination, documentation, and technical expertise without performing routine laboratory testing.
Your key responsibilities:
- Coordinate the transfer, validation, and verification of physicochemical methods (HPLC, GC, UV, KF, dissolution) in compliance with cGMP and regulatory standards.
- Draft and review all lifecycle documentation, including validation plans, protocols, risk assessments, and final reports.
- Act as the technical SME for investigations, Change Controls, and continuous improvement projects.
- Lead the global transfer strategy and manage post-transfer activities until the full commissioning of methods in the QC laboratory.
- Present and defend analytical validation and transfer documentation during health authority inspections and partner audits.
- Transfer technical knowledge to QC teams through dedicated coaching and training on new analytical methods.
- Serve as a Key User for the Chromatography Data System (CDS) and support laboratory software administration.
- Oversee the acquisition of new laboratory equipment, including procedure writing and user training.
- Provide expert troubleshooting support for new equipment and ensure the general smooth running of laboratory operations.
Location: Bulle, Switzerland
Activity rate : 100%
Type of contract: Temporary contract (until 31.12.2026 with a potential extension)
Start Date: ASAP
In this role, you will act as the bridge between development and production, ensuring the successful transfer and implementation of analytical methods within a strictly regulated pharmaceutical cGMP environment. You will focus on coordination, documentation, and technical expertise without performing routine laboratory testing.
Your key responsibilities:
- Coordinate the transfer, validation, and verification of physicochemical methods (HPLC, GC, UV, KF, dissolution) in compliance with cGMP and regulatory standards.
- Draft and review all lifecycle documentation, including validation plans, protocols, risk assessments, and final reports.
- Act as the technical SME for investigations, Change Controls, and continuous improvement projects.
- Lead the global transfer strategy and manage post-transfer activities until the full commissioning of methods in the QC laboratory.
- Present and defend analytical validation and transfer documentation during health authority inspections and partner audits.
- Transfer technical knowledge to QC teams through dedicated coaching and training on new analytical methods.
- Serve as a Key User for the Chromatography Data System (CDS) and support laboratory software administration.
- Oversee the acquisition of new laboratory equipment, including procedure writing and user training.
- Provide expert troubleshooting support for new equipment and ensure the general smooth running of laboratory operations.
Qualifiche
What will make you successful:
- Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific field.
- Significant hands-on laboratory experience.
- Solid expertise in cGMP and pharmaceutical regulatory environments, with a focus on compliance and quality standards.
- Strong technical background in physicochemical analysis (HPLC, GC, dissolution, etc.) and Chromatography Data Systems.
- Proven ability to coordinate complex projects and manage cross-functional stakeholders between R&D and QC.
- Fluency in French (mandatory) with a strong command of English for technical writing and international documentation.
- Highly organized and solution-oriented, with a structured communication style and a proactive approach to troubleshooting.
We can offer you a new challenge in a diverse and innovative environment that gives temporary contrats the opportunity to step aside for a long period.
Have we sparked your interest? Then we look forward to receiving your online application.
