Production Control

Zuellig Pharma Pte Ltd; Singapore; On-site; SGD 42,000 - 66,000; Full time

Benefits offered by this job

Inclusive environment for learning and

growth

Diversity, equity, and inclusion

Knowledge of healthcare industry

Work-life balance and career growth

Total Rewards program

Job summary

Zuellig Pharma is seeking a Production Control Specialist to safeguard product quality across repackaging and distribution. You will ensure GMP, GDP, and regulatory requirements are met and collaborate with cross-functional teams to maintain quality throughout operations.

A Diploma in Quality/Compliance and QA/QC experience in manufacturing are preferred, along with strong communication skills. The role includes audits, CAPA involvement, and training, with flexibility for overtime to meet

Qualifications

• Diploma in a relevant discipline, or equivalent practical knowledge of Quality/Compliance within a packaging or manufacturing environment.
• Proven experience in QC or 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 repackaging activities comply with GMP, GDP, and regulatory requirements.
• Investigate near misses and deviations; support CAPA implementation.
• Verify repackaging operations against approved procedures and work instructions.
• Perform routine quality checks and record inspection results.
• Work closely with cross-functional teams to maintain and champion quality.
• 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 necessary to meet production timelines.

Skills

Interpersonal & communication skills

Attention to detail

Quality mindset

Education

Diploma or equivalent in Quality/Compliance

Job description

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.

Job Purpose:

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.

Expectations of the Role:

• 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.

Requirements (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.

Advantageous 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 asp