Quality Control Analyst

1 week ago

Singapore PharmEng Technology Pte Ltd Full time $60,000 - $80,000 per year

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking for a Quality Control Analyst with experience in pharmaceutical industry for a role in Singapore.
**Job Summary:
Support the Microbiology Laboratory in SGBO Singapore QC for the establishing and maintaining
of Utilities Monitoring of the SGBO Singapore Facility in Singapore. Perform sampling and testing
under supervision, following written procedures and specifications, and in accordance with
Local/international regulations.
**Key Accountabilities**:
- Supports activities to establish and maintain a Microbiology lab in full cGMP-compliance.
- Supports activities to conduct/perform necessary sampling/test methods or compendia
methods in the lab and site under cGMP
- Follows existing procedures and methods, and perform sampling/testing following routine activities:
- HVAC Viable and Non -viable particle sampling and surface sampling
- Pharmaceutical Water and Clean Steam Condensate sampling for Biological and
- Chemical tests
- Compressed Gases; Biological Chemical and Physical sampling and testing
- Data compilation
- Data evaluation and trending support
- Receives training and analyst qualification to perform sampling/testing under cGMPs.
- Follows the priorities for sampling/testing provided by lab management.
- Ensures sampling/testing is performed in a timely manner.
- Participates in Laboratory investigations.
- (after sample testing) Compiles test documents in a complete, accurate and consistent manner to ensure that samples, materials or products and intermediates have been tested, or inspected according to specification and cGMPs.
- Suggests optimizations of test procedures to improve efficiency whenever possible.
- Be able to explain, his/her area of work, in health authorities inspections and internal audits
**Performance Indicator**:
- Delivery of results on time and with quality (e.g. timely testing)
- Adherence to established KPI targets related to QC activities
- Open communication; Concise and clear communication skills
**Why PharmEng Technology?
Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone's unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.
**EEOC Statement
At PharmEng Technology, we don't just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.

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