Supervisor 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:

You will lead a Quality Control team while ensuring compliance with cGMP standards and regulatory requirements. As a QC Supervisor you'll provide technical leadership and oversight for laboratory operations supporting pharmaceutical manufacturing, from raw materials to finished products. Support operational excellence through mentoring staff, optimizing workflows, and implementing continuous improvement initiatives while maintaining high quality standards.

REQUIREMENTS:

Bachelor's Degree plus 5 years of experience preferred in pharmaceutical/biotech quality control, with 2+ years in a leadership role

Preferred Fields of Study: Chemistry, Biology, Biochemistry, Microbiology or related scientific field

Additional certifications in quality systems, regulatory compliance, or project management beneficial

Strong knowledge of cGMP, FDA regulations, ICH guidelines and quality systems

Experience with analytical testing methods and instrumentation (HPLC, GC, dissolution testing, etc.)

Proven ability to lead and develop teams while fostering a quality-focused culture

Strong technical writing skills for SOPs, investigations, and regulatory documentation

Experience managing laboratory operations, including scheduling, resource planning and process improvements

Proficiency with laboratory information management systems (LIMS) and quality management software

Excellent project management and organizational skills

Strong interpersonal and communication abilities to interact with all levels of the organization, where fluency in Dutch language is an advantage

Experience supporting regulatory audits and inspections

Demonstrated problem-solving skills and ability to lead investigations

Working knowledge of data integrity principles and documentation requirements

Ability to prioritize multiple responsibilities while maintaining high quality standards

Experience with risk assessment and root cause analysis

Proficiency with Microsoft Office applications

Flexibility to adjust schedules as needed to support manufacturing operations