QA/QC Assistant

- Permanent

- $3,000 - $3,500

- Mon–Fri, 9am - 6.30pm

- Woodlands

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):

***email_hidden*** (Reg No: R25128591)

Please ensure that applications sent through email are no bigger than 1Mb.

We thank all applicants for your interest but regret to inform that only shortlisted candidates would be notified.

Success Resource Centre Pte Ltd (EA License Number: 04C3201)

160 Robinson Road, #13-07/08/09 SBF Center, Singapore 068914

T: 6337 3183 | W: www.successhrc.com.sg