Executive - Reagent Quality

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