QA Manager

8 hours ago

Gwalior, Madhya Pradesh, India Amrutam Full time ₹ 2,00,000 - ₹ 6,00,000 per year

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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