The QA/QC Assistant supports both Quality Assurance (QA) and Quality Control (QC) functions to ensure compliance with internal procedures and Good Manufacturing Practice (GMP) standards. This role plays a critical part in maintaining product quality, regulatory compliance, and efficient laboratory and production operations. Document Control Management
Manage and administer Document Control System to ensure compliance to applicable internal procedures and GMP requirements
Provide QA support as required, including participation in investigation, validation activities and documentation review
Change Control Management
Support change control processes to ensure all changes to products, processes, or systems are properly evaluated, documents and implemented.
Risk Management
Support risk assessment activities (e.g., deviation, change control, CAPA) to identify, evaluate, and mitigate quality and compliance risks.
Quality Control
Perform sampling and testing of incoming starting materials, intermediate and finished products in accordance with established procedures
Conduct environmental monitoring in controlled areas in compliance with GMP requirements
Generate, review, and maintain accurate test records and reports in compliance with GMP documentation standards
Investigate, resolve, and follow up on quality issues, including deviations, out-of-specification (OOS) results, and product complaints
Lab Operation
Organise and maintain daily laboratory operations to ensure efficiency and compliance
Ensuring lab equipment is qualified, calibrated and maintained at defined intervals according to the procedure
Perform periodic inventory checks for chemical and consumables to ensure availability and control
Maintain good housekeeping and safe workplace
Period:
Permanent
Salary:
$3,000 - $3,500
Working hours:
Mon–Fri, 9am - 6.30pm
Location:
Woodlands
Requirements:
Minimum Diploma in a Science discipline (Microbiology / Chemistry, or related field)
Minimum 1–3 years of experience in a GMP-regulated environment (pharmaceutical, biotechnology, medical device, or related industry)
Familiarity with laboratory operations, including equipment qualification, calibration, and maintenance practices
Strong attention to detail with good documentation, data integrity and record-keeping skills
Ability to work independently as well as collaboratively in a cross-functional team
Good organizational and time management skills to handle multiple tasks and priorities
Interested applicants, kindly email your detailed resume (MS Word format is preferred):
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