Quality Control Manager ( AMV | GLP) - Toa Payoh
The Supreme HR Advisory Toa Payoh Full-time
Position title: Quality Control Supervisor/ Manager
Location: Redhill
Working days: 5 days [ Mon - Fri ]
Working hours: 8:30am - 6pm
Location: Redhill
Working days: 5 days [ Mon - Fri ]
Working hours: 8:30am - 6pm
Salary : $3,500 - $4,500
Job Duties and Responsibilities:
Quality Functions:
- Responsible for the operations of the Quality Control Lab.
- Ensure that all lab analyses (starting materials, packaging materials, intermediates and finished products, stability samples etc.) are done in a timely manner, according to established test method and to provide accurate results.
- Prepare or revise Standard Operating Procedures (SOPs) relevant to product quality.
- Prepare or revise Specifications, Test Methods and Quality Control Procedures for all starting materials, intermediates and finished products.
- Ensure the maintenance of reference and retention samples
- Ensure that on-going stability studies are conducted for finished products as per cGMP requirements
- Perform sampling and testing of Starting Materials (Packaging) in accordance with Standard Operating Procedures (SOPs) in a timely manner.
- Perform Product testing in accordance with Standard Operating Procedures (SOPs) in a timely manner.
- Perform Analytical Method Validation and Cleaning Method Validation
- Assist in validation or revalidation of manufacturing processes
- Handle installation, operation, calibration and maintenance of lab instruments.
- Maintain good lab practice, lab safety, inventories and housekeeping programs.
- Participate in the investigation of product complaint in evaluation of returned goods relating to product quality.
- Perform supplier qualification.
- Conduct and coordinate Out-Of-Specification/Deviations/atypical results investigation.
- Review Changes, Deviations, Corrective and /or Preventive Actions as Area/Process Owner.
- Ensure that the required initial and continued training is carried out to quality control personnel.
- Maintain all Quality Control documents and records.
Requirements:
- Candidate must possess a Degree in a relevant Science field or related discipline
- Lab experience in a Chemistry related field
- Hands-on experience in GC
- Must have experience in Analytical Method Validation (AMV)
- Knowledge of GLP
LIEW ONN KEE REG NO : R22108518
THE SUPREME HR ADVISORY EA NO:14C7279
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