Offre d'emploi Lead Investigator & Quality Control à Neuchâtel

Lead Investigator & Quality Control H/F

Pharmaceutique / Biotechnologies / Chimie
  • Temporaire - Temps plein
  • Référence : INT-040408
  • Partager:


  • Région Neuchâtel
  • Type de contrat Temporaire - Temps plein
  • Secteur d'activité Pharmaceutique / Biotechnologies / Chimie


For our client, a leading international Pharma company, we are searching for a :

Lead Investigator & Quality Control H/F - 100% - 15 months temporary contract

This position is primarily responsible for managing QC deviations, performing formal root cause analysis, and defining effective corrective and preventive actions

Description de la mission

  • Act as Deviation Owner and Lead Investigator for deviations requiring a formal root cause analysis
  • Work cross-functionally with impacted areas to define appropriate and effective corrective and preventive actions
  • Ensure timely and compliant closure of laboratory root cause investigations, QC deviations, corrective and preventive action
  • Timely and appropriately escalate issues requiring management decision and impacting resource allocation. Fill and maintain dashboards, KPIs
  • Communicate effectively with management, quality management and cross-functional teams such as Manufacturing Science and Technology, Analytical Science and technology, Quality Assurance
  • Present deviations and investigation findings at Quality governance forums and in audits conducted by regulatory agency representatives
  • Authors, reviews, and approves complex GMP documentation such as standard procedures, work practices, training plans, protocols, and reports
  • Perform other tasks as assignedQC

Profil attendu

  • BSc degree in Life Sciences, Chemistry, or relevant technical discipline
  • 3 years of work experience in a QC environment in the pharmaceutical industry
  • Ability to take a structured and analytical approach to problem solving. Experienced with root cause analysis tools and methodologies
  • Excellent scientific knowledge and hands-on experience of analytical techniques such as liquid and gas chromatography, dissolution, spectrometry, and Karl Fisher
  • Good knowledge and interpretation of cGMP and Pharmacopeia requirements
  • Experience of analytical testing according to European Pharmacopeia and United States Pharmacopeia
  • General computer literacy including MS Office (Word, Excel, PowerPoint, Outlook, Visio)
  • Effective verbal communication skills, ability to interact with different levels of the organization: manager, peers, lab analysts, and other departments
  • Effective technical writing skills, experience writing GMP documents (procedures, protocols, plans and reports) as well as deviations and investigations
  • Ability to work collaboratively and cross-functionally
  • Capability to work with short deadlines and simultaneous activities
  • Fluent in English or French and professional command of the second language (written and verbal)


  • Publié le 20 février 2023
  • ConsultantBernadette KEHL