HOF Pharma, a WHO-GMP certified pharmaceutical formulation manufacturing company, is expanding its workforce at its Sanand, Gujarat facility. This is an excellent opportunity for pharma professionals looking to build a rewarding career in tablets, capsules, and oral liquids manufacturing.
The company is actively hiring across multiple departments including Quality Control (QC), Documentation Cell, QA (DQA), ADL, Production, Packing, Regulatory Affairs (RA), and Business Development (BD).
If you have relevant pharmaceutical industry experience, this is your chance to join a fast-growing organization focused on innovation and global market expansion.
Job Details
- Company: HOF Pharmaceuticals Limited
- Location: Sanand, Gujarat
- Industry: Pharmaceutical Formulation (WHO-GMP Certified)
- Experience: 2–18 Years
- Employment Type: Full-Time
Open Positions & Responsibilities
1. Business Development (BD) – Manager / Sr. Manager
- Lead generation and client acquisition in ROW (Rest of World) markets
- Build and maintain international client relationships
- Drive business growth strategies and partnerships
2. Quality Control (QC) & Documentation Cell
- Preparation of specifications and STP (Standard Testing Procedures)
- Handling QC documentation and compliance records
- Perform analysis using HPLC and other analytical instruments
3. DQA (Quality Assurance) – Sr. Officer / Executive
- Manage QMS systems including deviation, CAPA, and change control
- Ensure cGMP compliance and documentation practices
- Review batch records and audit processes
4. ADL (Analytical Development Lab) – Sr. Officer / Executive
- Method development and validation
- Documentation and analytical reporting
- Stability studies and troubleshooting
5. Production – Operator (Liquid Sachet)
- Operate liquid sachet machines
- Ensure smooth production operations and GMP compliance
- Maintain equipment and process efficiency
6. Packing – Sr. Officer / Executive
- Handle primary and secondary packaging operations
- Ensure compliance with packaging standards
- Supervise packing line efficiency
7. Regulatory Affairs (RA) – Sr. Officer / Executive
- Manage international regulatory submissions
- Handle ROW market documentation and compliance
- Maintain regulatory lifecycle management
Qualifications Required
- BD Roles: B.Pharm / M.Pharm / M.Sc / B.Sc / MBA
- QC / QA / ADL / RA / Packing: B.Pharm / M.Pharm / M.Sc / B.Sc
- Production Operator: ITI
- Strong knowledge of cGMP, QMS, HPLC, CAPA, regulatory guidelines preferred
Experience Required
- BD: 12–18 years (International markets – ROW)
- QC / RA / Packing: 3–5 years
- HPLC Analyst: 2–5 years
- ADL: 4–6 years
- Production Operator: 4–7 years
Key Skills (SEO Keywords Integrated)
- Pharma jobs in Sanand Gujarat
- QC QA pharma jobs India
- HPLC analyst jobs pharma
- Regulatory affairs jobs India pharma
- ADL method development jobs
- Pharmaceutical production operator jobs
- WHO-GMP pharma company jobs
Benefits of Joining HOF Pharma
- Work in a WHO-GMP certified facility
- Exposure to international regulatory markets (ROW)
- Career growth in a rapidly expanding pharma company
- Hands-on experience in advanced formulation manufacturing
- Collaborative and professional work environment
How to Apply
Interested candidates with relevant pharmaceutical experience can apply by sending their updated CV to:
