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Harman Finochem Hiring For Production Department

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Harman Finochem Limited Hiring 2026: QMS Documentation – API Production Experts

Harman Finochem Limited is looking for dedicated and experienced professionals to join their API Production team specializing in Quality Management System (QMS) documentation. This is a brilliant opportunity for seasoned pharma professionals to excel in a high-compliance manufacturing environment.

Job Vacancy Details

Department: Production – API Pharma

Designation: Officer / Senior Officer / Executive

Experience: 5 to 10 Years

Qualification: M.Sc. Chemistry / B.E. Chemical




Key Skill or Job Description

  • Preparation, review, and control of QMS documents related to API Production.
  • Handling of SOPs, BMR/BPR, Formats, Logbooks, and Protocols.
  • Documentation compliance as per GMP, cGMP, and regulatory requirements.
  • Coordination with QA, Production, and other departments for document management.
  • Preparation and review of deviation, change control, CAPA, and incident documentation.
  • Ensure proper archival and retrieval of production documents.
  • Support during internal audits, customer audits, and regulatory inspections.
  • Review and issuance of controlled documents.
  • Maintain documentation records and ensure data integrity compliance.
  • Training production personnel on documentation practices and GMP requirements.

Who Can Apply

  • Candidates with 5 to 10 years of solid experience in the pharma industry.
  • Professionals with an M.Sc. in Chemistry or B.E. in Chemical Engineering.
  • Individuals with a strong understanding of GMP/cGMP and regulatory guidelines.
  • Those proficient in MS Office and documentation management systems.

Why Harman Finochem is a Great Choice

Harman Finochem Limited is a leading manufacturer of Active Pharmaceutical Ingredients (APIs). The company is known for its commitment to quality and regulatory excellence, exporting products to over 35 countries. Working here offers a professional atmosphere where you can handle complex regulatory documentation, gain experience with global audits, and grow within a structured corporate framework dedicated to “Healthcare through Quality.”




How To Apply

Interested and eligible candidates can share their updated CV/Resume on the following email ID:

Email: atull@harmanfinochem.com

Frequently Asked Questions (FAQ)

1. What is the experience requirement for the QMS Documentation role at Harman Finochem?

Applicants must have between 5 and 10 years of experience, specifically within the API Pharma manufacturing industry.


2. Which educational qualifications are accepted?

The company is looking for candidates with an M.Sc. in Chemistry or a B.E. in Chemical Engineering.


3. What are the key responsibilities for this position?

The role focuses on the preparation and review of QMS documents like SOPs, BMR/BPR, CAPA, and ensuring compliance with GMP/cGMP standards.


4. How do I apply for this vacancy?

You should send your latest CV directly to the recruitment email: atull@harmanfinochem.com.


5. Is this a fresher-friendly role?

No, this specific vacancy requires significant experience (minimum 5 years) in QMS documentation and API production.



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