)
)
Quality Control Laboratory Expert (M/F/D)
Key Responsibilities
Independently perform complex analytical testing activities using LC-MS and FT-IR technologies, including routine, non-routine, and project-related analyses
Act as a technical expert within the QC laboratory, supporting troubleshooting, method optimization, and analytical problem-solving
Ensure proper equipment operation, readiness, calibration status, and maintenance compliance
Provide technical support and guidance to laboratory colleagues regarding analytical methods and instrumentation
Support equipment qualification activities, including URS, qualification protocols, PQ execution, and SOP implementation
Lead or support analytical method feasibility studies, validation activities, and qualification processes
Generate, review, and interpret analytical data to ensure method robustness and reliability
Support the transfer and implementation of analytical methods into routine QC operations
Prepare and review GMP-compliant documentation, including analytical protocols, validation reports, investigation records, and SOP updates
Ensure accurate and complete documentation in accordance with GDP and ALCOA+ principles
Support investigations related to OOS, OOT, and OOL results, including root cause analysis and corrective actions
Ensure compliance with GMP, EHS, and internal quality standards
Identify opportunities for improvement within analytical processes, laboratory workflows, and QC practices
Contribute to continuous improvement initiatives to increase efficiency, robustness, and compliance
Support inspection readiness activities and maintain a high standard of laboratory quality
Provide informal mentoring and technical guidance to QC analysts and laboratory technicians
Qualification
Scientific education such as CFC Laboratory Technician, BTS/DUT, Bachelor’s or Master’s degree in Chemistry, Analytical Sciences, Biotechnology, or equivalent scientific discipline
Strong professional experience in a GMP-regulated Quality Control laboratory environment
Hands-on expertise with LC-MS and/or HPLC analytical techniques
Experience with FT-IR is considered an advantage
Experience with analytical method validation, qualification, and implementation activities
Ability to independently execute laboratory activities while applying strong scientific judgement
Good understanding of GMP requirements, laboratory documentation standards, and regulatory expectations
Strong problem-solving skills with experience in analytical troubleshooting
Ability to collaborate effectively with QC Scientists, Analytical Development, and cross-functional stakeholders
Fluent in French with professional working proficiency in English
Previous experience within the pharmaceutical or life sciences industry
Experience supporting regulatory inspections or audit readiness activities
Experience with raw material testing and analytical method lifecycle management
Knowledge of continuous improvement methodologies (e.g., Lean, 5S)
Experience providing technical leadership or mentoring within a laboratory environment
Requirements
Start: 15.09.2026
Duration: 18 months
Capacity: 5 days per week
Location: Neuchâtel, Switzerland
)