Job Description:

• Upholds and ensures GMP compliance in the laboratory.

• Ensures that unauthorized personnel are prohibited/ restricted from entering the laboratory.

• Ensures that SOPs and WIs are made available to authorized personnel and the quality of work carried out in the laboratory is in accordance to SOPs and WIs.

• Ensures that the necessary testing is carried out and batch records are evaluated.

• Ensures that maintenance and calibration of equipment and laboratory apparatus in the QC Laboratory is carried out according to schedule.

• Monitors the inspection and testing of raw materials, packaging materials, in-process bulk and finished products to ensure adherence to established quality standards.

• Investigates the failed products/ materials including raw materials, packaging materials, in-process bulk and finished products.

• Manages work allocation and proper working discipline amongst QC personnel.

• Assists the QC Manager to check all QC related document, SOPs and WIs if any amendments and/ or changes are required.

• Works closely with the QC Manager, Senior QA and QC Inspector to establish QC procedures that meet quality standards and requirements.

• Trains QC personnel to ensure that individuals are able to carry out tasks, testing and inspection according to established procedures stated in SOPs and WIs.

• Recommends and purchases necessary and/or required laboratory equipment, chemicals, and consumables to ensure smooth operation for testing in the laboratory.

• Co-audits internal quality audits to verify effectiveness within the system.

• Co-monitors follow-up corrective actions for non-conformances found within the organization including environmental and hygiene issues.

• Monitors any upgrading and/ or renovation works carried out in the laboratory and testing facilities.

• Covers the role of the QC Manager in his/ her absence.

• Other projects and assignments instructed or delegated by management and director

Job Requirements:

• Minimum qualification with Diploma in Science will be advantage

• At least 3-5 years' in relevant experience

• Preferably with knowledge on cGMP, ISO9001, ISO14001 and ISO45001

• Independent thinker who acts and decides objectively and with integrity

• Willing to learn new things and hands on

• Computer literate

Other information:

• AWS & Variable Bonus

• Medical and dental benefits

• Working location: Ang Mo Kio area (3 bus stops from Yio Chu Kang Interchange)

• Working days: 5 days work week

• Working hours: Monday to Friday 9am to 6pm