- Location
- France - Cassagne - rue de Bouque de lens
- Workplace
- Onsite
- Type
- Full-time
- Department
- Engineering
- Education
- Bachelor
- Source
- Workday
Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific’s Mazères‑sur‑Salat site, we design, assemble, and qualify measurement instruments and components for laboratory analysis and process control. Here, industrial excellence meets metrological rigor: our teams develop, test, and calibrate reliable solutions for pharmaceuticals, food and beverage, environmental monitoring, and research. From production to maintenance—plus logistics for parts and consumables—we deliver performance, traceability, and high‑level technical support, helping our customers make the world healthier, cleaner, and safer.
DESCRIPTION:
As a Quality Engineer II, you will ensure compliance with quality standards and regulatory requirements across our manufacturing operations. You'll collaborate with cross-functional teams to drive continuous improvement initiatives, lead investigations, and implement corrective actions to maintain our high standards of product quality. This role offers exposure to innovative technologies and the opportunity to directly impact patient care through quality oversight of critical products.
REQUIREMENTS:
• Advanced Degree with no prior experience, or Bachelor's Degree plus 2 years of quality assurance experience in GMP/ISO regulated environments, preferably in medical devices, pharmaceuticals or biotechnology
• Preferred Fields of Study: Life Sciences, Engineering, Chemistry or related scientific/technical field
• Strong knowledge of quality systems, cGMP regulations, and standards including ISO 9001 version 2015
• Expertise in quality tools and methodologies including risk management, root cause analysis, CAPA, and documentation management.
• Demonstrated experience leading investigations, analyzing quality data, and implementing effective corrective actions
• Excellent documentation and technical writing skills for developing SOPs, protocols and reports
• Strong proficiency in quality management software (GED, SAP QM, etc.) and Microsoft Office suite
• Experience conducting internal audits and supporting external audits.
• Demonstrated ability to build consensus and collaborate across functions
• Strong verbal and written communication skills - In French and English.
• Ability to work independently while contributing effectively in team environments
• Strong attention to detail with analytical and problem-solving capabilities
• Experience with statistical analysis tools and quality metrics reporting
• Project management skills and ability to prioritize effectively
• Foreign language skills beneficial (English)