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Clinigen

Quality Control / Quality Assurance Associate

1w

Clinigen

Singapore, SG · Full-time · S$42,000 – S$66,000

About this role

Clinigen is at the forefront of delivering critical medicines and support to healthcare professionals and patients. We are seeking a Quality Control / Quality Assurance Associate to join our team in Singapore. You will uphold quality management standards as we expand operations in the Southeast Asia region.

In this role, you will oversee documentation processes for our Quality Management System (QMS)/electronic QMS (eQMS). You will facilitate product releases to ensure compliance with quality standards and conduct vendor and customer approvals and validations. Additionally, you will provide support for secondary packaging processes and assist with validation activities.

You will collaborate with warehouse and cleanroom facilities to ensure adherence to quality parameters. This involves working cross-functionally to maintain operational efficacy in healthcare and pharmaceutical environments. Your efforts will support our commitment to excellence in quality practices.

We offer ongoing professional development opportunities, including training programs and workshops. A performance bonus rewards exceptional achievements. These benefits support career advancement within our organization.

Requirements

  • Tertiary qualification in Science, Pharmacy, or a relevant technical discipline, or equivalent professional experience
  • Minimum of 2 years of experience in a quality assurance or quality control role; experience within a warehouse and cleanroom environment in the Healthcare, Pharmaceutical, or Food industries is highly desirable
  • Familiarity with Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP) quality management systems
  • Exceptional communication skills, both verbal and written
  • Ability to cultivate collaborative relationships with cross-functional team members
  • Strong organizational and time management skills, with a focus on detail-oriented execution
  • Commitment to excellence in administrative and documentation practices

Responsibilities

  • Oversee documentation processes for Quality Management System (QMS)/electronic QMS (eQMS)
  • Facilitate product releases to ensure compliance with established quality standards
  • Conduct vendor and customer approvals and validations
  • Provide support for secondary packaging processes
  • Assist with validation activities to maintain operational efficacy
  • Collaborate with warehouse and cleanroom facilities to ensure adherence to quality parameters

Benefits

  • Performance bonus designed to reward exceptional performance and achievements
  • Ongoing professional development opportunities, including training programs, workshops, and access to resources
  • Monthly salary that reflects experience, skills, and industry standards