Job description
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
Required Skill Profession
Operations Specialties Managers