Job Description

Key Responsibilities

Update Value Sheets and ensure accurate version control. Maintain and update the production share folder with all required QC value sheets/ values based on the packing plan. Ensure documentation complies with internal SOPs, ISO standards, and regulatory requirements. Update product Value Sheets, COA, and any QC-related documents on the Agappe website. Coordinate with the IT/Marketing team for smooth publishing and version control. Ensure uploaded information is accurate, up-to-date, and consistent with production and QC records. Perform daily QC log sheet entries for all assigned QC instruments/ QC area Report any deviations, instrument errors, or abnormal QC results to the QC Manager. Assist in internal and external audits by providing required QC documents. Participate in CAPA, change control, and deviation reporting as needed.

Required Qualifications

B.Sc./M.Sc. in Chemistry, Biochemistry, Microbiology, Biotechnology, or related Life Sciences field. Male candidates are preferred due to job-specific requirements.

Experience:

1-3 years of experience in QC documentation or Medical laboratory, pharma, or related industry (preferred).

Skills:

Proficiency in MS Office (Excel, Word, PDF tools). Basic understanding of website content updating (training can be provided). Ability to follow SOPs and regulatory compliance requirements.
Job Types: Full-time, Permanent

Pay: From ?20,000.00 per month

Benefits:

Cell phone reimbursement Food provided Health insurance Provident Fund
Work Location: In person