QC Incoming Lab Supervisor Quality System and AQL, null

il y a 2 semaines


Bruxelles, Région de Bruxelles, Belgique TN Belgium Temps plein

Social network you want to login/join with:

QC Incoming Lab Supervisor Quality System and AQLClient:

Catalent

Location:

Brussels (Neder-Over-Heembeek)

Job Category:

Other

EU work permit required:

Yes

Job Reference:

2d15f6f05670

Job Views:

2

Posted:

06.03.2025

Expiry Date:

20.04.2025

Job Description:

Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics, and consumer health products. With over 80 years serving the industry, Catalent has proven expertise in providing development, production, and packaging services for pharmaceutical and biotech companies.

For our production site in Brussels, specializing in sterile technologies, we are currently looking for a QC Supervisor AQL. The QC Supervisor AQL is in charge of organizing the quality control operation activities in the packaging area.

They lead and manage the QC team responsible for AQL activities in the packaging area, ensuring compliance with GMP, safety regulations, and driving daily quality control operations. They collaborate and develop technician expertise and play an important role in continuous improvement efforts to enhance quality control processes and documentation.

The Role

  • Management and supervision of the QC team in charge of QC AQL activities in the packaging area in close collaboration with the QC AQL team leader.
  • Lead the QC AQL team in the proficient oversight and resolution of daily quality operations ensuring timely and compliant outcomes.
  • Evaluate and anticipate resource needs for planning follow-up.
  • Oversee the training program of QC AQL technicians and develop their expertise.
  • Foster strong relationships with other teams and departments to ensure cohesive operational efficiency and alignment on quality standards.
  • Lead continuous improvement initiatives within the QC department, identifying opportunities for process optimization and quality enhancement.
  • Manage GMP documentation such as SOP's, formulary, training records, investigation records, etc.
  • Collaborate and support the quality investigations (deviations, complaints, etc.), and related quality activities such as CAPA and Change Controls.

The Candidate

  • Good management skills and equivalent proven experience of team management.
  • Minimum Bachelor's in a scientific topic or equivalent through experience.
  • Relevant experience in one or more of the following activities: production, engineering, QC/QA within a pharmaceutical company.
  • Fluent in French and English (reading and written).
  • Experience managing mid-sized teams (10 and more) is an asset.
  • Knowledge of AQL is an asset.
  • Experience in Quality system activities management such as deviations, CAPAs, and Change Controls in the pharmaceutical industry.
  • Good communication skills, able to interact with different levels and across functions.
  • Good stress management, proactive, reactive, and problem solver.
  • What we offer is an exciting role, a chance to grow and learn new skills in a global company, and in the most challenging quality environment within the pharma industry – a sterile business.
  • Potential for personal development within an international company.
  • Contributory pension and benefits package all offered from day one of employment.
  • Competitive salary + company car.
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