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Production Control Specialist

Zuellig Pharma · Singapour

New
Mid 🇬🇧 English
GMP GDP GSDP CAPA Quality Control Quality Assurance

Job description

About the role

Zuellig Pharma, a leading healthcare solutions company in Asia, is hiring a Production Control Specialist. The specialist ensures that repackaging, operational and compliance activities follow approved standards, regulatory requirements, GMP, GDP and GSDP, safeguarding product quality and supporting process improvement and a strong quality culture.

Key responsibilities

  • Ensure all repackaging complies with authorised specifications, GMP, GDP and regulatory requirements.
  • Investigate near misses and process deviations and support the implementation of corrective and preventive actions (CAPA).
  • Verify that repackaging operations are carried out correctly against approved procedures and work instructions.
  • Perform routine quality checks and record inspection results accurately.
  • Work with cross-functional teams to maintain quality throughout operations.
  • Support quality culture initiatives, internal audits and ad-hoc projects.
  • Deliver internal training to team members and carry out administrative duties as required.
  • Be flexible to support flexi-shifts or overtime when needed to meet production timelines.

Required profile

  • Diploma in a relevant discipline, or equivalent practical knowledge of quality/compliance in a packaging or manufacturing environment.
  • Proven QC or QA experience in manufacturing, production or assembly settings.
  • Strong interpersonal and communication skills with a high commitment to quality assurance.

Required skills

  • Good working knowledge of GMP and quality-related regulatory requirements.
  • Advantageous: familiarity with ISO and GSDP standards, and experience in repackaging oversight or QC inspection.

Questions fréquentes

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Published 2 hours ago

Expires 1 month from now

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Zuellig Pharma

Singapour