▷ (19/10/2025) Qa Manager

7 hours ago


Gwalior, India Amrutam Full time

About Us Amrutam is a pioneering Ayurvedic lifestyle and wellness platform that blends the ancient wisdom of Ayurveda with the convenience of modern technology. Founded with a vision to make holistic health accessible and trustworthy, Amrutam offers a range of authentic Ayurvedic products and services – from doctor consultations to wellness content – all in one place. Job Details Base Location :- Gwalior Department:- Q.A. Manager Working Mode:- In Office Experience:- 3 years (mandatory) Qualification:- Bachelor's degree in B. Pharma & M. Pharma or related field Reporting:- Head – Q.A. AND Q.C. CTC:- As per market standard Leve:- Entry Key Responsibilities 1. Ensuring GMP Compliance (Ayurveda-Specific) - Ensure compliance with Schedule T of the Drugs and Cosmetics Act, which governs GMP for Ayurvedic, Siddha, and Unani medicines. - Monitor hygienic conditions of raw material handling, processing, packaging, and storage. - Verify adherence to SOPs for traditional methods like churna, chyawanprash /Avleh, bhasma,, oil etc. 2. Raw Material Quality Assurance - Ensure proper identification and authentication of raw herbs and minerals. - Check source and documentation (e.G., COA – Certificate of Analysis) for each ingredient. - Conduct tests for adulteration, pesticide residues, heavy metals, and microbial load as per AYUSH or pharmacopoeia standards. 3. In-Process Quality Checks - Monitor critical stages in preparation such as: - Shodhana (purification of metals/minerals) - Bhavana (trituration) - Mardana (grinding) - Putapaka (incineration for bhasmas) - Ensure each step follows documented traditional and regulatory methods. 4. Batch Manufacturing Record (BMR) Review - Verify and review Batch Manufacturing Records for each Ayurvedic product. - Ensure proper documentation of each process step and material used. - Approve or reject batches based on compliance. 5. Packaging and Labeling Verification - Check packaging material quality (e.G., bottles, cap, packs, labels). - Ensure labels comply with Ayurvedic Drug Labeling Rules, including: - Manufacturer details - Composition (with Latin/botanical names) - Dosage - Indications - License number 6. Finished Product Quality Assurance - Review test results for finished products: - Organoleptic properties (color, odor, taste) - Physico-chemical parameters (pH, ash value, etc.) - Microbial testing - Shelf-life study - Approve or reject batches accordingly. 7. Deviation, CAPA & Complaint Handling - Handle deviations during production or packaging. - Initiate CAPA for quality issues. - Address customer complaints and conduct root cause analysis. 8. Training & SOP Management - Conduct GMP and SOP training for production and warehouse staff. - Prepare and update SOPs for all quality-critical activities. 9. Regulatory Compliance & Audits - Ensure adherence to AYUSH, State FDA, and Pharmacopoeial guidelines. - Prepare for and assist in regulatory inspections. - Coordinate documentation for product license, renewals, and audit responses. Key Skills and Knowledge Areas: - Understanding of Ayurvedic raw materials, formulations, and processing techniques. - Familiarity with AYUSH regulations, Schedule T, and Pharmacopoeia of India (API). - Basic knowledge of microbiology and herbal quality testing. - Good documentation and audit readiness practices - Daily checklist or a QA SOP format for an Ayurvedic manufacturing unit? Skill Requirements All working According to GMP (Ayurveda – specific) BMR and BPR with all documents with control



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