Head of QC

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. And with over $1 billion invested annually in R&D, we empower our teams to put science into meaningful action and give our R&D colleagues the autonomy, resources and tools they need to take science a step beyond.

Lead a Quality Control team responsible for ensuring product excellence and regulatory compliance at Thermo Fisher Scientific. Implement analytical testing, method validation, and quality systems while supporting a culture of continuous improvement. Collaborate with cross-functional teams to deliver high-quality products that help make the world healthier, cleaner, and safer. Oversee testing operations including raw materials, in-process controls, environmental monitoring, and finished product release. Support data integrity and Good Manufacturing Practices (GMP) while developing team members through mentoring and training. Ensure laboratory readiness for regulatory inspections and customer audits while improving operational efficiency through quality metrics and process improvements.

REQUIREMENTS:
• Advanced degree plus 8 years of experience in regulated pharmaceutical/biotech industry quality control
• Preferred Fields of Study: Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related scientific field
• 3+ years of people management experience

- Experience in leading QC laboratory teams
• Extensive knowledge of cGMP regulations, quality systems, and regulatory requirements
• Strong understanding of analytical testing methods and laboratory operations
• Experience managing laboratory investigations, deviations, and CAPA processes
• Demonstrated success implementing and improving quality systems and processes
• Experience with laboratory information management systems (LIMS) and data integrity requirements
• Experience within the CDMO industry is a plus
• Project management and organizational skills
• Clear written and verbal communication skills, both in French and English
• Experience supporting regulatory inspections and customer audits
• Proficiency with standard business software (MS Office) and quality systems
• Ability to adapt to changing priorities
• Problem-solving skills and scientific decision-making abilities
• Commitment to workplace safety and compliance

• Fluency in French and English is a must