QA Manager

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 :-

Department:-

Working Mode:-

Experience:-

Qualification:-

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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