Quality Control Leader – GMP Bioprocessing

Sartorius Stedim North America, Inc.; Herstal; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

Sartorius is seeking a Quality Control Manager based in Herstal to lead QC analytical activities and in-process controls, ensuring consistent product quality across our manufacturing environment.

You will drive continuous improvement of analytical methods, ensure GMP/QMS/regulatory compliance, and collaborate closely with Manufacturing, QA and cross-functional teams while guiding staff and preparing detailed quality reports for audits and CAPA activities.

Qualifications

• Academic degree in Life Sciences or related field.
• Extensive QC management experience in a regulated environment.
• GMP/QMS knowledge preferred.
• Strong data analysis and statistics knowledge.

Responsabilités

• Lead QC analytical activities and in-process product controls.
• Drive continuous improvement of analytical methods and lab processes.
• Ensure compliance with GMP, QMS, and regulatory requirements.
• Review customer requirements and translate them into QC processes.
• Evaluate analytical systems and procedures and identify improvement opportunities.
• Coordinate and develop QC inspectors, technicians, and lab staff with guidance and training.
• Collaborate with Manufacturing, QA and cross-functional stakeholders.
• Prepare detailed quality reports for management and support audits, investigations, and CAPA activities.

Connaissances

QC management

Analytical methods

Regulatory compliance

Team leadership

GMP/QMS knowledge

Data analysis

Problem-solving

English proficiency

Formation

Bachelor's degree in Life Sciences

Outils

Analytical instruments

Quality management software

Description du poste

Sartorius is seeking a Quality Control Manager based in Herstal to lead QC analytical activities and in-process controls, ensuring consistent product quality across our manufacturing environment.

You will drive continuous improvement of analytical methods, ensure GMP/QMS/regulatory compliance, and collaborate closely with Manufacturing, QA and cross-functional teams while guiding staff and preparing detailed quality reports for audits and CAPA activities.