We’re seeking a qualified individual to join our team in a QC role. You’ll assist in audits, manage testing, train staff, ensure compliance with GMP/GDPMD, and oversee lab safety. Ideal candidates must have 2+ years in the pharmaceutical industry, with experience in QMS, stability testing, and inventory management.
Key Duties and Responsibilities:
- Participate in internal GMP/GDPMD audits.
- Assist in monitoring OOS, OOT, non-conformance, deviations, and change control.
- Train and supervise lab analysts, technicians, and inspectors, overseeing testing and analytical activities according to established procedures.
- Perform Qualified Personnel duties, including reviewing, verifying, and signing off on testing/analytical reports and batch manufacturing documents. Release or reject materials for production and finished product sales, as delegated by the Head of Department.
- Review and verify testing/analytical reports and batch manufacturing documents via the SAP system.
- Update specifications, analytical protocols, and QA/QC documents.
- Monitor stability programs and environmental control programs.
- Assist in process validation and quality refinement.
- Recommend the purchase of instruments, chemicals, and consumables.
- Handle the installation, operation, calibration, maintenance, and repair of instruments.
- Maintain laboratory safety and housekeeping programs.
- Prepare and review the quality portion of dossiers for regulatory submissions.
- Perform labeling checks and highlight discrepancies against stipulated label requirements for export and import.
- Undertake any other projects or assignments as directed by the supervisor.
Job Requirements:
- 2-3 years relevant working experience in the pharmaceutical industry / GMP facility is a requirement.
- Possess positive attitude, self-motivated and self-disciplined.
- Able to work independently and work under pressure.
- Team player with good analytical skills and experience in QC laboratory.
- Experience in managing or performing testing for stability samples is an advantage.
- Experience in handling QMS (OOS, OOT, Laboratory Incident, Change Control, Deviation, etc.).
- Experience in handling QC inventory, procurement, and calibration of instruments such as GC, HPLC, Karl-Fischer would be advantageous.
How do your skills match this job?
How do your skills match this job?
Your application will include the following questions:
- Which of the following statements best describes your right to work in Malaysia?
- What’s your expected monthly basic salary?
- Which of the following types of qualifications do you have?
- How many years' experience do you have as a Quality Control Executive?
- How many years' experience do you have planning and executing performance tests?
Pharmaceuticals, Biotechnology & Medical 51-100 employees
TIGER BALM (M) SDN BHD is an established company that manufactures, markets, and distributes high-quality OTC pharmaceutical products. Nearly 100 years ago, a Chinese herbalist prepared an effective, fast-acting balm under a secret formula with all natural ingredients. Tiger Balm is a brand leader in many overseas markets and is famous worldwide. The production base moved from Burma to Singapore in 1926. From here, the product was aggressively marketed and sold into many neighboring countries. Today, Tiger Balm is sold in over 100 countries across 5 continents. Why join us? Attractive remuneration package, excellent career advancement opportunities, and a good learning environment. We advocate a safe working environment for all our employees.