Quality Control Manager ( AMV | GLP) - Toa Payoh

apartmentThe Supreme HR Advisory placeToa Payoh scheduleFull-time calendar_month 
Position title: Quality Control Supervisor/ Manager
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

#SCR-angel-liew

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