QA Compliance Expert – French, GMP vacancy for our Neuchatel based client in the Manufacturing sector.

Your tasks:

• Act as representative for the GMP Self-Inspection programmer, ensuring compliance with internal standards and regulatory requirements
• The QA Compliance Expert reports to the Head of Quality Compliance and Systems and is specifically responsible for the Quality System related to GMP Self-Inspection activities, data integrity, and other quality projects deployment.
• In this role, the QA Compliance Expert acts as the representative for routine GMP Self-Inspection activities, ensuring compliance with internal standards and regulatory expectations.
• The QA Compliance Expert collaborates closely with all the departments (Production Unit Team, Quality Control laboratories, Warehouse, and Engineering/Maintenance departments etc) for the self-inspection program.
• Coordinate, plan, and execute self-inspection schedules, using a risk-based approach and collaborating with all departments
• Deliver coaching sessions to subject matter experts and audit teams to ensure inspection readiness
• Support the preparation and follow-up of internal and external audits, acting as part of the audit support team
• Champion local data integrity activities, collaborating with Global Teams and other facilities
• Ensuring the quality and accuracy of documentation and information within systems, in alignment with current guidelines, compliance requirements, and regulatory expectations, is a core responsibility.
• Participation in GMP audits, inspections.
• The QA Compliance Expert is expected to promote and actively contribute to Continuous Improvement initiatives.
• Promote and participate in continuous improvement initiatives and quality projects

Your experience/knowledge:

• University degree in technical/ scientific discipline such as biochemistry, chemistry, engineering or equivalent
• At least 7 years of experience in the biotechnology and/or pharmaceutical industry, preferably both
• Strong knowledge of a GMP environment
• Good understanding of manufacturing, laboratory testing and warehousing operations applicable to biological products.
• Good understanding of Good Data and Documentation Practices (GDDP) and Data Integrity principles.
• Experience in creating, reviewing, and revising Standard Operating Procedures (SOPs) and technical documents.
  Experience supporting regulatory inspections and audits.

• Familiarity with risk management tools and methodologies (e.g., FMEA, root cause analysis).
• Proficiency in French and English (minimum B2 level or equivalent).
• Proficiency in using electronic quality management (e.g., Veeva Vault, TrackWise).
• Proficiency in Microsoft Office tools, including Word, Excel, Power Point and SharePoint.
• Proficiency with data analysis and reporting tools, including Power BI.

Location: Neuchatel, Switzerland
Work setting: Hybrid
Sector: Manufacturing
Start: ASAP
Duration: 3+ months 
Workload: 100%
Ref.Nr.: BH 24010

Take the next step and send us your resume along with a daytime phone number where we can reach you.

Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current work-permit holders for Switzerland.

We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application.

As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.