HOF Pharma Hiring QC Analyst – Quality Control

QC Analyst – B.Pharm/M.Pharm | 2–5 Yrs | Sanand Ahmedabad

HOF Pharma hiring QC Analyst for OSD formulation unit at Sanand, Ahmedabad. Apply now with B.Pharm/M.Pharm/M.Sc & 2–5 yrs QC experience.

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HOF Pharma Pvt. Ltd., a trusted name in pharmaceutical formulation manufacturing, is inviting applications for the position of Quality Control (QC) Analyst at its Sanand, Ahmedabad facility. This is an exciting opportunity for analytical professionals with experience in pharma formulations (OSD) who want to work in a quality-driven, growth-oriented environment.

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Company Overview

HOF Pharma Pvt. Ltd. is a reputed pharmaceutical formulation company based in Gujarat, specializing in Oral Solid Dosage (OSD) and other regulated market products. With a commitment to excellence, compliance, and continuous improvement, HOF Pharma ensures every product meets global regulatory standards like USFDA, WHO-GMP, and MHRA.

The organization focuses on innovation, precision, and scientific integrity while maintaining a collaborative environment that encourages learning and growth. HOF Pharma is known for its high-quality infrastructure, modern analytical laboratories, and a dedicated workforce that contributes to global healthcare improvement.

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Job Role & Responsibilities

Position: QC Analyst – Pharma Formulation
Department: Quality Control
Location: Sanand, Ahmedabad
Industry: Pharmaceutical Formulation (OSD)

Key Responsibilities:

• Perform routine and stability analysis of raw materials, intermediates, and finished products in accordance with specifications.
• Conduct stability studies, trend analysis, and analytical data reviews.
• Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, IR, Dissolution Tester, and KF Titrator.
• Ensure strict adherence to Good Laboratory Practices (GLP) and data integrity in analytical documentation.
• Review and verify analytical data, COAs, and ensure compliance with pharmacopeial standards (IP, BP, USP, EP).
• Support method validation and method transfer activities as per regulatory guidelines.
• Participate in OOS (Out of Specification) and OOT (Out of Trend) investigations, implementing effective CAPAs.
• Coordinate with QA, ADL, and Production teams for timely batch release and analytical support.
• Follow cGMP, GDP, and safety protocols within the Quality Control laboratory.

Technical Expertise:

• Hands-on experience with analytical instruments and regulatory documentation.
• Familiarity with stability protocols and analytical trend report preparation.
• Strong understanding of ICH, FDA, and WHO regulatory requirements.

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Eligibility / Qualifications

Educational Qualifications:
B.Pharm, M.Pharm, B.Sc, or M.Sc in Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, Industrial Chemistry, or related fields.

Experience:
2–5 years in Quality Control within pharma formulation (OSD / Injectable / API) industries.
Preferred Background: Experience in regulated or semi-regulated market plants.

Core Competencies:

• Proficiency in HPLC, GC, UV, IR, and other analytical systems.
• Strong knowledge of cGMP, GLP, and GDP documentation.
• Excellent analytical, communication, and teamwork skills.
• Ability to troubleshoot analytical issues and support audits effectively.

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Location & Salary

Work Location: Sanand, Ahmedabad (Gujarat)
Department: Quality Control (QC)
Salary: Competitive; commensurate with industry standards and candidate experience.
Work Type: Full-time, on-site

Facilities:

• Advanced analytical laboratory setup
• Professional and learning-friendly environment
• Exposure to global regulatory systems

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Application Process

Interested candidates may apply by sending their updated resume to:
Email: Recruitment@hofpharma.com
Contact: 6353534507

Please mention “QC Analyst – Sanand” in the email subject line.
Shortlisted candidates will be contacted for further interview rounds.

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Why Join HOF Pharma?

• Work with a globally recognized pharmaceutical formulation manufacturer.
• Opportunity to learn from experienced professionals in analytical and regulatory compliance.
• Exposure to state-of-the-art equipment and global pharmacopeial standards.
• Competitive salary and growth-oriented environment.
• Contribution to global healthcare advancement through quality formulations.

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Frequently Asked Questions (FAQs)

Q1. Who can apply for the QC Analyst position at HOF Pharma?
Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc degrees and 2–5 years of experience in QC formulation analysis.

Q2. What analytical techniques are essential for this role?
HPLC, GC, UV, IR, Dissolution testing, and KF titration techniques.

Q3. What is the work location for this position?
The position is based at Sanand, Ahmedabad, Gujarat.

Q4. What experience level is required?
Applicants should have 2–5 years of hands-on QC experience in the pharma formulation industry.

Q5. What type of products does HOF Pharma manufacture?
The company focuses on pharmaceutical formulations (OSD and related dosage forms) catering to domestic and global markets.

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Category	Details
Company	HOF Pharma Pvt. Ltd.
Vacancies	QC Analyst – Quality Control Department
Required Education	B.Pharm, M.Pharm, B.Sc, M.Sc (Chemistry or related)
Experience	2–5 years
Location	Sanand, Ahmedabad, Gujarat