SP

Scientist I, Project QA

Sta Pharmaceutical Singapore Pte. Ltd.

D07 Middle Road, Golden MilePermanentS$4,500 – S$6,000/mo

Posted 7 Jul 2026

About this role

Working Location: Tuas, Singapore Responsibilities: Participate in the review of technical documents related to technology transfer, ensuring the transfer process meets quality requirements and is implemented smoothly. Responsible for master batch record review to ensure related documents, processes, and procedures comply with company policies and regulatory requirements. Execute batch record review, verifying production records for completeness, accuracy, and compliance. Review quality standards and analytical methods to ensure their scientific validity and compliance with regulatory requirements. Review process validation master plans (VMP),validation protocols, and validation reports to ensure validation activities comply with company and regulatory standards. Lead change control and deviation management related to projects, driving deviation investigations, corrective actions, and preventive measures. Responsible for product release, strictly controlling quality standards to ensure timely release of compliant products. Host customer audits by preparing relevant documentation, coordinating onsite audit activities, and responding to audit inquiries to ensure successful audit outcomes. Attend customer meetings to communicate project quality matters promptly, provide feedback on issues and improvements, and maintain good customer relationships. Review deviation and investigation reports, ensuring reports are logically structured, data is detailed, and conclusions are clear. Perform any other ad hoc duties as required by the Department. Responsible for other tasks temporarily assigned. Qualifications: Master’s degree or above in Organic Chemistry, Pharmaceutical Engineering, or related fields. Fresh graduates are welcome to apply Relevant work experience is preferred; familiarity with pharmaceutical manufacturing and quality management regulations (e.g., GMP) is essential. Clear thinking and rigorous logical reasoning skills, with proficiency in problem analysis and investigation report writing. Strong communication and coordination skills, capable of effectively collaborating across departments to drive issue resolution. Strong sense of responsibility, attention to detail, and good team spirit. Fluent in both Chinese and English, capable of professional bilingual communication and report writing.

What they're looking for

Quality StandardsUSPCGMP manufacturingrelationships with internal clients

About Sta Pharmaceutical Singapore Pte. Ltd.

Industry: Manufacturing

Frequently asked questions

What does a Scientist I, Project QA at Sta Pharmaceutical Singapore Pte. Ltd. do?

Working Location: Tuas, Singapore Responsibilities: Participate in the review of technical documents related to technology transfer, ensuring the transfer process meets quality requirements and is implemented smoothly. Responsible for master batch record review to ensure related documents, processes…

What skills does this Scientist I, Project QA role need?

Key skills for this role include Quality Standards, USP, CGMP manufacturing, relationships with internal clients.

How much does a Scientist I, Project QA at Sta Pharmaceutical Singapore Pte. Ltd. pay?

This role lists a salary of S$4,500 – S$6,000 per month.

Is this Scientist I, Project QA role remote, hybrid, or on-site?

The listing is based in D07 Middle Road, Golden Mile. Check the posting for remote or hybrid options.

How do I apply for this Scientist I, Project QA role?

You can apply directly on Sta Pharmaceutical Singapore Pte. Ltd.'s careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.