HOF Pharmaceuticals Hiring IPQA Officer/Executive

IPQA Officer / Executive – B.Pharm, M.Pharm | HOF Pharmaceuticals Ahmedabad

HOF Pharmaceuticals hiring IPQA Officer / Executive in Ahmedabad. B.Pharm/M.Pharm with 2–5 yrs experience. Apply now and join a WHO-GMP certified company.

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HOF Pharmaceuticals Limited, a WHO–GMP Certified pharmaceutical company, is expanding its Quality Assurance (IPQA) team at its Sanand, Ahmedabad facility. If you’re a motivated QA professional seeking to work in a reputed formulation manufacturing setup, this is an excellent opportunity to grow your career in compliance and quality assurance.

This position is ideal for professionals passionate about Good Manufacturing Practices (GMP), regulatory compliance, and maintaining the highest standards of pharmaceutical quality.

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Company Overview

HOF Pharmaceuticals Limited is one of India’s fastest-growing pharmaceutical manufacturing companies, known for its high-quality Oral Solid Dosage (OSD) products. With a robust global presence and a commitment to innovation, HOF Pharma provides healthcare solutions that adhere to international regulatory and quality benchmarks.

The company’s manufacturing units are WHO–GMP and ISO certified, equipped with state-of-the-art technology to ensure product efficacy, consistency, and patient safety.

At HOF Pharmaceuticals, employees are valued as integral contributors to the company’s mission of improving global healthcare access. The organization fosters a culture of learning, teamwork, and continuous improvement—ideal for professionals in the pharmaceutical quality and manufacturing domain.

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Job Role & Responsibilities

The IPQA Officer / Executive will play a vital role in ensuring quality assurance during manufacturing and packaging operations. This role requires deep understanding of in-process checks, GMP documentation, and cross-functional coordination to maintain product quality and compliance.

Key Responsibilities:

• Perform in-process checks during manufacturing and packing operations to ensure product quality.

• Monitor adherence to SOPs, GMP, and cGMP guidelines on the production floor.

• Provide line clearance for production and packaging activities.

• Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure accuracy and completeness.

• Identify and report deviations promptly and assist in deviation investigation and CAPA (Corrective and Preventive Actions).

• Support the QA team in internal and external audits and regulatory inspections.

• Coordinate with the Production and QC departments for real-time quality compliance.

• Ensure proper documentation control and maintain records in accordance with company SOPs and regulatory expectations.

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Eligibility / Qualifications

Education Required:

• Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm) from a recognized university.

Experience:

• 2 to 5 years of experience in pharmaceutical manufacturing (formulations), preferably in Oral Solid Dosage (OSD) or IPQA roles.

Key Skills:

• Excellent knowledge of GMP / cGMP and documentation systems.

• Hands-on experience with shop floor IPQA activities.

• Strong understanding of quality systems, deviation management, and change control.

• Good communication and teamwork skills.

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Location & Work Environment

Location: Sanand, Ahmedabad, Gujarat
Work Type: Full-time, Onsite

HOF Pharmaceuticals provides a safe, modern, and compliance-driven work environment, supported by experienced professionals and robust QA systems. Employees enjoy opportunities for career advancement, professional learning, and exposure to international quality standards.

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Salary & Benefits

Salary: Competitive, based on experience and qualification.
Benefits:

• Provident Fund (PF)

• Employee State Insurance (ESIC)

• Subsidized canteen and transport facilities

• Training and skill development programs

• Performance-linked growth opportunities

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Application Process

Interested candidates can apply directly by sending their updated resume to:

hr@hofpharma.com

Documents to Prepare:

• Updated CV

• Educational Certificates

• Experience Letters

• ID Proofs (Aadhar, PAN)

Apply before 10th November 2025 to secure your opportunity at one of India’s leading WHO–GMP certified pharma companies.

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Why Join HOF Pharmaceuticals?

• WHO–GMP certified company with a strong reputation in the OSD segment.

• Exposure to cutting-edge manufacturing technologies.

• Opportunity to work with a highly experienced QA team.

• Career growth within a quality-focused, compliance-driven organization.

• Commitment to innovation, excellence, and employee well-being.

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Frequently Asked Questions (FAQs)

1. What qualifications are required for this role?
You must hold a B.Pharm or M.Pharm degree from a recognized institution.

2. How much experience is required?
Candidates should have 2–5 years of experience in QA or IPQA, preferably in OSD formulation manufacturing.

3. Where is this role based?
The position is based in Sanand, Ahmedabad (Gujarat).

4. What are the key skills needed?
Strong understanding of GMP, documentation, and line clearance procedures is essential.

5. How do I apply for this position?
Send your updated CV to hr@hofpharma.com before the application deadline.

6. Is this a WHO–GMP certified company?
Yes. HOF Pharmaceuticals is WHO–GMP certified, ensuring compliance with international manufacturing standards.

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