Quality Assurance Jobs in Pharma at Harman Finochem Limited for FDF plant in Aurangabad. Apply for pharma quality jobs with 3–10 years experience now.
Introduction
Harman Finochem Limited has announced new career openings for experienced professionals in the Quality Assurance domain. This hiring is focused on candidates who have prior exposure to pharmaceutical formulation and regulatory compliance, especially in finished dosage forms.
If you are looking to advance your career in QA within a structured and compliance-driven pharmaceutical organization, this opportunity offers strong growth potential and industry exposure.
Company Overview
Harman Finochem Limited is a well-established pharmaceutical company known for its expertise in manufacturing Active Pharmaceutical Ingredients (APIs) and Finished Dosage Forms (FDF). The company operates with a strong focus on quality, regulatory compliance, and international standards.
With its manufacturing facility located in Maharashtra, Harman Finochem serves global markets and maintains strict adherence to GMP and other regulatory guidelines, making it a preferred workplace for quality professionals.
Job Overview
| Job Title | Quality Assurance (QA) Professionals |
|---|---|
| Company Name | Harman Finochem Limited |
| Location | Chhatrapati Sambhajinagar, Maharashtra |
| Employment Type | Full-Time |
| Qualification | B.Pharm / M.Pharm / M.Sc |
| Experience | 3–10 Years |
| Salary | ₹3.5 LPA – ₹10 LPA |
| Application Mode |
Job Location & Employment Type
The job location is Shendra MIDC, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra. This is a full-time, on-site role within the company’s Finished Dosage Form (FDF) manufacturing unit.
Open Positions / Department Details
Harman Finochem Limited is hiring for multiple roles within the Quality Assurance department:
- IPQA Officer (3–5 years experience)
- Lab QA – Junior Executive (4–7 years experience)
- CQA Executive / Senior Executive (7–10 years experience)
These roles are designed for professionals with experience in OSD formulation and pharmaceutical quality systems.
Key Roles & Responsibilities
IPQA Officer:
- Perform in-process quality assurance checks during manufacturing
- Conduct line clearance and monitor production activities
- Review batch manufacturing and packaging records
- Handle sampling procedures and AQL checks
- Ensure adherence to GMP standards
Lab QA – Junior Executive:
- Provide analytical QA support in laboratory operations
- Work with instruments such as HPLC and GC
- Monitor stability studies and maintain records
- Ensure data integrity and audit trail compliance
- Follow GLP guidelines in all lab activities
CQA Executive / Senior Executive:
- Manage audits and regulatory inspections
- Handle quality management systems including CAPA and change control
- Review SOPs, documents, and compliance records
- Ensure audit readiness and regulatory alignment
- Maintain strong documentation practices
Eligibility Criteria
Education:
- B.Pharm, M.Pharm, or M.Sc in relevant specialization
Experience:
- Minimum 3 years and up to 10 years of experience in Quality Assurance roles
- Experience in FDF or OSD manufacturing is highly preferred
Skills Required:
Technical Skills:
- Strong knowledge of GMP, GLP, and regulatory requirements
- Experience in QA systems, documentation, and compliance
- Familiarity with OSD formulation processes
- Understanding of audit handling and quality management systems
- Exposure to instruments like HPLC and GC for QA roles
Soft Skills:
- Attention to detail and accuracy
- Strong documentation and organizational skills
- Effective communication abilities
- Problem-solving and decision-making skills
- Ability to work under regulatory pressure
Salary & Benefits
- Salary range: ₹3.5 LPA to ₹10 LPA depending on experience and role
- Opportunity to work in a regulated pharmaceutical environment
- Exposure to international quality standards and audits
- Career growth in QA and regulatory functions
- Learning opportunities in QMS, CAPA, and compliance systems
- Stable and professional work environment
Selection Process
The selection process may include:
- Resume screening based on relevant experience
- Technical interview focusing on QA knowledge and practical exposure
- HR discussion for final selection and compensation details
Shortlisted candidates will be contacted for further steps.
How to Apply
Interested candidates should send their updated CV to the following email addresses:
amoln@harmanfinochem.com
chetank@harmanfinochem.com
Why Apply for This Pharma Job?
This opportunity is ideal for professionals who want to build a strong career in pharmaceutical quality assurance. Working at Harman Finochem Limited provides hands-on exposure to regulatory audits, documentation systems, and compliance practices that are essential in the pharma industry.
The company’s focus on global standards ensures that employees gain valuable experience in handling quality systems and regulatory requirements. Candidates will also have the opportunity to work on advanced QA processes, making it a suitable role for long-term career growth.
For experienced professionals aiming to enhance their expertise in QA and regulatory affairs, this position offers both stability and advancement opportunities.
Important Note / Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.
Final Call-to-Action
Eligible candidates with relevant experience are encouraged to apply as soon as possible by sending their resumes via email. Early applications may increase the chances of selection for these quality assurance roles.
