Description

Your main tasks

• Support Compliance in accordance with global cGMP regulations and internal policies
• Support regulatory inspections and internal audits and assist implementation of associated actions
• Coordinate & support change control assessment and related activities
• Support Risk assessment and Data integrity initiatives for QC processes
• Act as QC representative for Projects or support implementation
• Bring technical & process knowledge to ensure proper project implementation
• Communicate and escalate main information or issues highlighted
• Participate in cross functional meetings and execute specific tasks according to Projects needs
• Support Continuous Improvement initiatives within laboratories
• Maintain QC performance data and implement actions defined as part of performance data analysis
• Support implementation of LEAN programs through QC improvement initiatives
• Facilitate System usage for Laboratory teams (LIMS, ERP, etc.)
• Act as an experience collaborator for the Lab
• Report all incidents to EHS immediately, participate in investigations and identify measures to prevent similar accidents in the future

Your profile

• Laboratory Technician or similar education in Microbiology, Biology, Chemistry, Pharmacy, etc.
• Minimum of 2 years of QC or related cGMP lab experience in the pharmaceutical industry
• Knowledge of QC Lab processes
• Knowledge of Lean principles and tools
• Good proficiency in common office software
• Fluent in French and at least basic English skills both verbal and written
• Abilities in organizing, planning, priority setting and time management
• Ability to work collaboratively and cross-functionally with peers

Sebastian Pal is looking forward to receiving your application documents via job portal (CV, diploma, reference letters; no motivational letter necessary).
Full discretion is guaranteed and we will gladly answer any additional questions.