Exciting pharma jobs at HOF Pharma! A WHO-GMP certified formulation manufacturing facility in Sanand, Gujarat, specializing in Tablets, Capsules, and Oral Liquids, is hiring for roles in Quality Control, Analytical Development Lab, Production, Documentation, and Regulatory Affairs.
Great opportunity for freshers and experienced professionals in pharmaceutical careers in India, focusing on quality, method development, and international regulatory compliance.
Contents
About the Company
HOF Pharmaceuticals Limited is a dynamic, WHO-GMP certified pharmaceutical company based in Sanand, Gujarat, India. Established around 2019-2021, the company specializes in streamlined formulation development and manufacturing of high-quality Tablets, Capsules, and Oral Liquids.
With a state-of-the-art facility spanning significant land area and adhering to cGMP and international standards, HOF Pharma aims for global accreditations including EU-GMP and PIC/S.
The company exports pharmaceutical products worldwide, emphasizing innovation, quality assurance, and patient-centric solutions. Led by experienced leadership with decades in the industry, HOF Pharma fosters a collaborative environment for professional growth and excellence in formulation manufacturing.
Job Details
- Company Name: HOF Pharmaceuticals Limited (HOF Pharma)
- Experience: Freshers to 7 years (varies by role)
- Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc (in relevant fields)
- Location: Sanand, Gujarat (Facility: Survey No. 211-4/5/6, Opp. Rathi Agro Industries, Sanand-Bavla Road, Village Pipan, Sanand, Ahmedabad – 382110)
- Work Type: On-site
Job Description
HOF Pharma, a WHO-GMP certified formulation unit producing Tablets, Capsules, and Oral Liquids, is expanding its team with openings across Quality Control (QC), QC Documentation, Analytical Development Lab (ADL), Production, Documentation Quality Assurance (DQA), and Regulatory Affairs (RA) departments.
QC – Micro Section
- Department: Quality Control (QC)
- Designation: Officer / Sr. Officer
- Experience: 1-2 years
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
QC-Doc Cell
- Department: QC Documentation Cell
- Designation: Officer / Sr. Officer
- Experience: 3-5 years
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
QC – HPLC Analyst
- Department: Quality Control (QC)
- Designation: Officer / Sr. Officer
- Experience: 2-5 years
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
ADL (Analytical Development Lab)
- Department: Analytical Development Lab (ADL)
- Designation: Executive / Sr. Executive
- Experience: 5-7 years
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
Production
- Department: Production
- Designation: Trainee Officer
- Experience: Freshers
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
DQA (Documentation Quality Assurance)
- Department: DQA
- Designation: Sr. Officer / Executive
- Experience: Relevant (knowledge-based)
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
RA (Regulatory Affairs)
- Department: Regulatory Affairs (RA)
- Designation: Sr. Officer / Executive
- Experience: 3-5 years
- Education/Qualification: B.Pharm / M.Pharm / M.Sc / B.Sc
Skills/Qualifications
- Experience in microbiology testing for QC micro section
- Proficiency in QC documentation, specification, and STP preparation
- Hands-on HPLC analysis and instrumentation skills
- Expertise in analytical method development, validation, and related documentation
- Knowledge of QMS, ADL, and F&D documents for DQA
- International regulatory affairs experience for global markets
- Strong GMP compliance, documentation, and analytical abilities
- Freshers with pharma qualifications welcome for production trainee roles
Key Responsibilities
- Conduct microbiological testing and analysis in QC micro section
- Prepare and manage QC documents, specifications, and STPs
- Perform HPLC analysis for quality testing
- Develop and validate analytical methods with proper documentation
- Support production operations as trainee officer
- Oversee QMS, ADL, and formulation development documents
- Handle international regulatory submissions and compliance
Benefits/Perks
- Professional growth in a WHO-GMP certified facility
- Opportunities in formulation manufacturing and exports
- Collaborative work environment focused on innovation
- Exposure to international quality standards and global markets
- Platform for skill development in QC, ADL, and regulatory functions
How to Apply
Send your updated resume to recruitment@hofpharma.com. Mention the department and designation in the subject line for quick processing. Shortlisted candidates will be contacted for further rounds. Apply now to join this growing WHO-GMP facility!
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the HOF LinkedIn page.
For more pharma jobs and opportunities in Gujarat and across India, visit Pharma Recruiter.
Why You Should Join
HOF Pharma offers a promising career in a modern, WHO-GMP certified manufacturing setup dedicated to high-quality formulations and global exports.
Benefit from a supportive culture, opportunities to work on Tablets, Capsules, and Oral Liquids, continuous learning in analytical and regulatory areas, and long-term stability in a company committed to innovation and healthcare excellence. Ideal for aspiring professionals building pharmaceutical careers in India in a quality-driven environment.
FAQs
What qualifications are needed for HOF Pharma jobs in Sanand?
B.Pharm, M.Pharm, M.Sc, or B.Sc; experience varies from freshers (Production Trainee) to 5-7 years (ADL Executive).
How do I apply for these positions?
Email your resume to recruitment@hofpharma.com with the relevant department/designation in the subject.
Where is the HOF Pharma facility located?
Sanand, Gujarat – Survey No. 211-4/5/6, Opp. Rathi Agro Industries, Sanand-Bavla Road, Village Pipan, Ahmedabad – 382110.
What growth opportunities exist at HOF Pharma?
Strong focus on professional development, exposure to international regulatory markets, and advancement in QC, ADL, production, and RA roles.
