ROLE AND RESPONSIBILITIES:

1. Perform analytical equipment lifecycle management as per current regulatory requirements / SOP.

2. Support and / or perform maintenance / calibration of laboratory equipment in compliance with established schedules.

3. Liaise with vendors/service providers for PM / Calibration in a timely manner.

4. Responsible for maintenance / calibration planning of equipment within QC Department.

5. Ensure real time documentation, maintain data integrity and appropriate traceability.

6. Responsible for the accurate, timely and compliant execution of assigned projects and related documentation.

7. Conduct QC Department equipment operation and maintenance training to QC staff as required.

8. Perform and / or support in maintaining the asset register for equipment in the QC Department.

9. Responsible for QC lab and equipment/instrument cleanliness.

10. Any other activities as and when assigned by the Superior.

EDUCATION & EXPERIENCE:

EDUCATION: Diploma in science related discipline (e.g. Chemistry, Chemical Engineering, Biotechnology).

EXPERIENCE: Minimum 1 years of quality control experience in pharmaceutical manufacturing industry.

KNOWLEDGE & SKILLS:

1. Possess working knowledge of GMP in the pharmaceutical industry.

2. A good team player with positive learning attitude.

3. Excellent interpersonal and analytical skills, good verbal and written communication skills.