Quality Control Laboratory Expert

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