Quality Control Executive - Ayurvedic Division
About the Role
Why This Role Matters
The Quality Control Executive – Ayurvedic Division plays a vital role in ensuring the safety, purity, and consistency of Ayurvedic and herbal products. This position ensures that raw materials, in-process samples, and finished goods meet regulatory and quality standards before release.
By maintaining laboratory accuracy, ensuring compliance with AYUSH and GMP regulations, and supporting audit readiness, the role directly contributes to product integrity and consumer trust in herbal healthcare solutions.
Job Description
Sunrise Remedies Pvt. Ltd. is hiring a Quality Control Executive – Ayurvedic for its Santej, Ahmedabad facility. The selected candidate will be responsible for routine testing, laboratory instrument handling, documentation control, and regulatory compliance within the Ayurvedic manufacturing unit.
The role requires hands-on experience in quality testing of herbal products, microbiological analysis, stability studies, and collaboration with Production and QA teams for quality investigations.
Key Features of the Role
• Position: Quality Control Executive – Ayurvedic
• Department: Quality Control – Ayurvedic
• Location: Santej, Ahmedabad (Gujarat)
• Experience Required: 1–2 years (Ayurvedic / Herbal QC)
• Qualification: B.Sc | M.Sc | B.Pharm (Ayu) | M.Pharm (Ayu) (Preferred)
• Industry: Ayurvedic / Herbal Pharmaceutical Manufacturing
Additional Benefits:
• Transportation facility (as per company route coverage)
• Mediclaim facility
• Company-provided food facility
Key Responsibilities
• Conduct routine quality checks of Raw Materials (RM), Packaging Materials (PM), in-process samples, and Finished Goods (FG)
• Ensure compliance with AYUSH regulations, GMP, ISO standards, and applicable guidelines
• Operate and calibrate laboratory instruments such as HPTLC, UV-Vis Spectrophotometer, and pH meters
• Prepare and maintain SOPs, test reports, Certificates of Analysis (COAs), and product specifications
• Conduct microbiological testing and stability studies
• Collaborate with Production and QA teams for troubleshooting and quality investigations
• Handle Non-Conformance Reports (NCRs) and support CAPA implementation
• Review Batch Manufacturing Records (BMRs) for compliance
• Support regulatory audits (AYUSH, FSSAI, WHO-GMP) and third-party inspections
Required Qualifications
Educational Background:
• B.Sc
• M.Sc
• B.Pharm (Ayu)
• M.Pharm (Ayu) (Preferred)
Experience:
• 1–2 years of experience in Quality Control within Ayurvedic or herbal manufacturing
Technical Skills:
• Knowledge of herbal quality testing procedures
• Familiarity with AYUSH and GMP compliance requirements
• Experience in handling laboratory analytical instruments
• Understanding of microbiological testing and stability studies
• Knowledge of documentation practices and regulatory audits
Soft Skills:
• Strong analytical and documentation skills
• High attention to detail
• Problem-solving ability
• Team coordination and communication skills
Company Overview
Sunrise Remedies Pvt. Ltd. is a Gujarat-based pharmaceutical manufacturing company known for maintaining high-quality standards across conventional and Ayurvedic product segments. The company continues to expand its operations while adhering to strong regulatory and quality frameworks.
FAQs
Q1. Is Ayurvedic qualification mandatory?
Ayurvedic qualification is preferred, but relevant QC experience in herbal manufacturing is essential.
Q2. Is microbiological testing experience required?
Yes, basic knowledge or exposure to microbiological testing is required.
Q3. Are freshers eligible?
No, 1–2 years of relevant QC experience is required.
Q4. Does the role involve audit participation?
Yes, the role includes supporting AYUSH and other regulatory audits.
Q5. Is instrument handling experience necessary?
Yes, experience with HPTLC, UV-Vis, and related instruments is expected.
Application Tip
• Highlight experience with herbal product testing
• Mention instrument handling expertise clearly
• Include exposure to AYUSH/GMP audits
• Specify stability study and microbiology experience
• Showcase documentation and CAPA handling experience
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