QC Technician
QC Technician
Posted on :
12-09-2025
Employer Active
1 Vacancy
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Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Strong Odors (chemical lubricants biological products etc.) Will work with hazardous/toxic materialsJob Description
Position Summary
Oversee daily maintenance and management of laboratory facilities equipment and materials to ensure safe compliant and stable operation. Independently conduct release testing for raw materials in-process samples and finished products (per quality standards). Assist in product/process equipment/facility Validation & Verification (V&V); support quality engineers and production lines in addressing quality defects/customer feedback; and participate in Corrective & Preventive Actions (CAPA). Enforce to company EHS (Environmental Health Safety) rules.
Crucial Job Functions and Accountabilities
1. Laboratory Operation & Maintenance
- Manage daily cleaning maintenance upkeep and status labeling of lab facilities/instruments.
- Operate and maintain inspection equipment (including daily checks of measuring tools and calibration coordination).
- Control lab reagents/consumables (procurement receipt storage registration distribution expiration monitoring).
- Ensure lab environment (temperature humidity cleanliness) meets requirements; conduct monitoring and documentation.
- Maintain lab safety (wear PPE keep work area organized per 5S); assist EHS in hazard identification assessment and risk control.
2. Inspection Execution
- Follow company quality/environmental policies SOPs inspection methods and WIs.
- Monitor key production control points to meet quality and environmental standards.
- Independently perform IQC (raw materials) IPQC (in-process) and finished product release testing; ensure accurate timely results.
3. Record & Document Management
- Comply with Good Documentation Practices (GDP) to fill out inspection records equipment logs and environmental data in real time accurately and completely.
- Store and archive inspection records and raw data accurately.
4. Quality Support & Issue Handling
- Assist in V&V for products process equipment and facilities.
- Support quality engineers in investigating defects deviations and customer feedback; help develop and implement CAPA.
- Report abnormalities/non-conformities/major quality issues promptly to production technology and quality teams.
5. Teamwork & Task Delivery
- Communicate and collaborate with production warehouse and facilities teams for smooth workflow.
- Complete superior-assigned tasks timely and efficiently; participate in safety quality and skill training.
Educational Qualifications
- College diploma or above.
- Preferred: Background in Biotechnology Medical Laboratory Science Molecular Biology Immunology Pharmacy Analytical Chemistry or related life sciences.
Experience and Other Qualifications
- Preferred: Laboratory work experience (especially in medical devices or IVD reagents).
- Familiarity with ISO9001/ISO13485; GMP/cGMP experience a plus.
- Basic English reading/writing (understand English SOPs handle work emails).
- Proficiency in Microsoft Office (Word Excel).
- Strong communication responsibility teamwork attention to detail hands-on ability and problem-solving skills.
Required Experience:
IC
Employment Type
Full-Time
Key Skills
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