Qa manager

4 weeks ago


Gwalior, India Amrutam Full time

About UsAmrutam 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 DetailsBase Location :- GwaliorDepartment:- Q. A. ManagerWorking Mode:- In OfficeExperience:- 3 years (mandatory)Qualification:- Bachelor's degree in B. Pharma & M. Pharma or related fieldReporting:- Head – Q. A. AND Q. C.CTC:- As per market standardLeve:- EntryKey Responsibilities1. 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 number6. Finished Product Quality Assurance- Review test results for finished products:- Organoleptic properties (color, odor, taste)- Physico-chemical parameters (p H, 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 RequirementsAll working According to GMP (Ayurveda – specific) BMR and BPR with all documents with control


  • QA Manager

    4 weeks 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...

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