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2 years

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On-site

Job Type

Full Time

Job Description

Position Title: Quality Assurance (QA) Manager – Enzyme Manufacturing

Department: Quality Assurance

Location: [Company Location]

Reporting To: Head – Operations / Managing Director

Job Purpose:

The QA Manager will be responsible for implementing, monitoring, and continuously improving the quality management systems (QMS) for enzyme production. The role will ensure that all products meet regulatory, customer, and internal quality standards from raw material procurement to final product dispatch.

Key Responsibilities:

1. Quality Management System (QMS) Implementation:

Establish and maintain ISO, FSSC, GMP, and other regulatory standards applicable to enzyme manufacturing.

Develop, review, and implement SOPs (Standard Operating Procedures) across departments.

2. Product Quality Assurance:

Oversee incoming raw material inspections, in-process quality checks, and final product release.

Ensure adherence to defined product specifications, batch records, and quality protocols.

3. Regulatory Compliance:

Ensure compliance with national and international quality standards (e.g., FSSAI, ISO, Kosher, Halal, etc.).

Coordinate with external auditors, certification bodies, and regulatory agencies.

4. Customer Complaint Handling:

Investigate customer complaints related to quality issues.

Conduct root cause analysis (RCA) and implement Corrective and Preventive Actions (CAPA).

Maintain a Customer Complaint Log.

5. Internal Audits and Continuous Improvement:

Plan and conduct internal quality audits.

Lead continuous improvement projects to minimize deviations, defects, and non-conformities.

Monitor KPIs like rejection rate, customer complaints, and process deviations.

6. Supplier Quality Management:

Evaluate and audit critical suppliers and raw material vendors.

Maintain supplier quality records.

7. Documentation and Reporting:

Maintain all QA-related documentation including batch records, COAs (Certificates of Analysis), and deviation reports.

Submit monthly QA performance reports to management.

8. Team Management:

Lead and mentor QA officers, QC analysts, and lab assistants.

Provide regular training on GMP, SOP adherence, and safety protocols.

Qualification & Experience:

Education: B.Sc. / M.Sc. in Microbiology, Biotechnology, Biochemistry, Chemistry, or related fields.

Experience: Preffered with 2 years of experience in QA/QC, preferably in enzyme manufacturing, biotech, or specialty chemicals.

Skills Required:

Strong knowledge of quality standards (ISO, FSSC, GMP, etc.).

Expertise in regulatory documentation and internal auditing.

Problem-solving and decision-making ability.

Good understanding of enzyme production processes and application requirements.

Excellent leadership and team management skills.

Strong communication and reporting skills.

Job Type: Full-time

Pay: ₹30,000.00 - ₹40,000.00 per month

Schedule:

  • Day shift

Supplemental Pay:

  • Yearly bonus

Work Location: In person

Speak with the employer
+91 9978178140Expected Start Date: 01/08/2025

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