Production Control Specialist

Zuellig Pharma; Singapore; On-site; SGD 39,000 - 78,000; Full time

Benefits offered by this job

Inclusive environment

Diversity & inclusion

Regional healthcare industry knowledge

Work-life balance

Total Rewards program

Job summary

Zuellig Pharma in Singapore is seeking a Production Control Specialist to ensure repackaging, operations and compliance meet GMP, GDP and GSDP requirements, safeguarding product quality and supporting continuous improvement.

You will perform routine quality checks, investigate deviations, train team members, and collaborate with cross-functional groups to uphold a strong quality culture and regulatory compliance within Production.

Qualifications

• Diploma in a relevant discipline, or equivalent practical knowledge of Quality/Compliance within a packaging or manufacturing environment.
• Proven experience in Quality Control (QC) or Quality Assurance (QA) within manufacturing, production, or assembly settings.
• Good working knowledge of GMP and quality-related regulatory requirements.
• Strong interpersonal and communication skills, with a high commitment to quality assurance.

Responsibilities

• Ensure all repackaging activities comply with authorized specifications, GMP, GDP, and regulatory requirements.
• Investigate near misses and process deviations; support the implementation of CAPA.
• Verify correct execution of repackaging operations against approved procedures and work instructions.
• Perform routine quality checks and accurately record inspection results.
• Work closely with cross-functional teams to maintain and champion quality throughout operations.
• Support quality culture initiatives, internal audits, and ad-hoc projects.
• Deliver internal training to team members and perform administrative duties as required.
• Maintain flexibility to support flexi-shifts or overtime when operationally necessary to meet production timelines.

Skills

Quality control

Quality assurance

GMP knowledge

Communication skills

Education

Diploma in a relevant discipline

Job description

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Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.

Production Control Specialist

Requisition ID: 2234

Posting Start Date: 23 Sept 2026

Location: Singapore

Zuellig Pharmais a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region.

The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.

Purpose of The Role:

The Production Control Specialist ensures that all repackaging, operational, and compliance activities adhere to approved standards, regulatory requirements, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and Good Storage and Distribution Practices (GSDP). This role safeguards product quality, supports process improvement initiatives, and contributes to maintaining a strong organizational quality culture and regulatory compliance within Production.

What You'll Do:

• Ensure all repackaging activities comply with authorized specifications, GMP, GDP, and regulatory requirements.
• Investigate near misses and process deviations; support the implementation of appropriate Corrective and Preventive Actions (CAPA).
• Verify correct execution of repackaging operations against approved procedures and work instructions.
• Perform routine quality checks and accurately record inspection results.
• Work closely with cross-functional teams to maintain and champion quality throughout operations.
• Support quality culture initiatives, internal audits, and ad-hoc projects.
• Deliver internal training to team members and perform administrative duties as required.
• Maintain flexibility to support flexi-shifts or overtime when operationally necessary to meet production timelines.

Must-Have:

• Diploma in a relevant discipline, or equivalent practical knowledge of Quality/Compliance within a packaging or manufacturing environment.
• Proven experience in Quality Control (QC) or Quality Assurance (QA) within manufacturing, production, or assembly settings.
• Good working knowledge of GMP (Good Manufacturing Practices) and quality-related regulatory requirements.
• Strong interpersonal and communication skills, with a high commitment to quality assurance.

Advantage to Have:

• Familiarity with ISO and GSDP (Good Storage and Distribution Practices) standards.
• Experience in repackaging production oversight or Quality Control (QC) inspection operations.
• Strong organizational skills with the ability to prioritize and adapt to changing operational needs.

What We Offer:

• We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
• We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
• As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
• Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
• Our Total Rewards program is designed to support your overall well-being in every aspect.

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Zuellig Pharma promotes an inclusive, fair workplace by ensuring equitable employment and compensation based on merit, regardless of background.