1. Position OverviewThe QC Manager is responsible for overseeing daily Quality Control operations, ensuring timely testing and release of materials and products, maintaining laboratory compliance, and supporting continuous improvement in quality standards. This role is ideal for a candidate with3+ years of QC experiencewho is ready to manage a team and lead analytical operations in a nutraceutical or softgel manufacturing setup.
2. Key ResponsibilitiesA. QC Operations Management- Supervise testing of raw materials, packing materials, bulk, and finished products.
- Ensure testing is carried out as per approved specifications, STPs, and regulatory standards.
- Review and approve analytical results, worksheets, and COAs.
- Ensure timely sample management and batch release coordination with QA.
B. Laboratory Management- Oversee daily functioning of the chemical and instrumental labs.
- Ensure proper calibration, qualification, and maintenance of instruments (HPLC, UV, GC, dissolution testers, etc.).
- Implement Good Laboratory Practices (GLP) and maintain lab safety standards.
- Ensure availability of reagents, chemicals, and reference standards.
C. Compliance & Documentation- Ensure adherence to GMP, GLP, FSSAI, WHO-GMP, and other applicable quality standards.
- Review and maintain documentation including STPs, specifications, logbooks, and records.
- Support QA in deviations, OOS/OOT investigations, and CAPA implementation.
- Maintain data integrity and secure documentation practices.
D. Audit & Regulatory Readiness- Prepare and support QC-related activities during internal and external audits.
- Ensure closure of audit observations within agreed timelines.
- Maintain audit-ready documentation at all times.
E. Cross-Functional Coordination- Work closely with QA, Production, Stores, and Procurement to ensure smooth operations.
- Provide analytical support for process improvements, validations, and troubleshooting.
3. Skills & Competencies- Strong knowledge of analytical instruments (HPLC, UV, GC, etc.).
- Good understanding of GMP, GLP, and data integrity principles.
- Ability to manage QC documentation and compliance.
- Strong leadership, communication, and problem-solving skills.
- Experience handling OOS/OOT and deviations.
- Familiarity with nutraceutical/softgel analytical requirements preferred.
4. Qualifications & Experience- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field.
- Minimum 3 years of QC experience, preferably in nutraceutical or pharmaceutical manufacturing.
- Hands-on experience with analytical methods and lab instruments.
- Experience facing audits or inspections is an advantage.
