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HOF Pharma is Hiring for QC, ADL, Production & Regulatory Affairs | 0-7 years exp

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HOF Pharma has announced new hiring opportunities for multiple departments at its WHO-GMP certified formulation manufacturing facility located in Sanand, Gujarat. The company manufactures tablets, capsules, and oral liquid formulations and is expanding its team across several technical and quality functions.

This recruitment drive offers opportunities for both freshers and experienced professionals in departments such as Quality Control, Production, ADL, Regulatory Affairs, and Documentation. Candidates with pharmaceutical and science backgrounds are encouraged to apply.

If you are looking to build your career in the pharmaceutical manufacturing sector, this opportunity at HOF Pharma could be a strong step forward.

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Author: Pharmabharat Editorial Team


Available Job Positions

HOF Pharma is currently hiring for the following departments and roles:

Quality Control (QC)

Designation: Officer / Senior Officer
Experience Areas:

  • Microbiology section experience (1โ€“2 years)
  • HPLC Analyst experience (2โ€“5 years)

QC Documentation Cell

Designation: Officer / Senior Officer

Responsibilities may include:

  • Handling QC documentation
  • Preparation of specifications
  • STP (Standard Testing Procedure) preparation
  • Maintaining regulatory compliance records

Analytical Development Laboratory (ADL)

Designation: Executive / Senior Executive

Responsibilities:

  • Method development
  • Analytical method validation
  • Analytical documentation
  • Support product development and regulatory submissions

Production Department

Designation: Trainee Officer

Opportunity for: Freshers

Responsibilities may include:

  • Supporting tablet, capsule, and oral liquid manufacturing
  • Following GMP procedures
  • Production documentation and batch records

Documentation Quality Assurance (DQA)

Designation: Senior Officer / Executive

Responsibilities:

  • Managing QMS documentation
  • Reviewing ADL and R&D documents
  • Ensuring compliance with regulatory guidelines

Regulatory Affairs (RA)

Designation: Senior Officer / Executive

Responsibilities:

  • Handling international regulatory market documentation
  • Preparing dossiers and regulatory submissions
  • Coordination with regulatory authorities

Required Qualifications

Candidates applying for the positions should meet the following educational criteria:

  • B.Pharm
  • M.Pharm
  • M.Sc
  • B.Sc

Applicants should have relevant knowledge or experience related to their respective department roles.


Salary and Benefits

HOF Pharma generally offers competitive salaries based on role and experience level.

Estimated Salary Range

  • โ‚น2.5 LPA โ€“ โ‚น9 LPA depending on role and experience.

Benefits may include:

  • Industry-standard salary packages
  • Growth opportunities in pharmaceutical manufacturing
  • Exposure to WHO-GMP compliant operations
  • Professional development opportunities
  • Stable pharmaceutical industry career path

Job Location

Sanand, Gujarat, India

HOF Pharmaโ€™s manufacturing facility is located in one of Gujaratโ€™s major pharmaceutical and industrial zones, offering strong career growth in pharma manufacturing.


How to Apply

Interested and eligible candidates can apply by sending their updated resume to the official recruitment email below.

Email your resume to:
recruitment@hofpharma.com

Make sure to include the department or role name in the subject line of your email to help the recruitment team process your application faster.


Conclusion

HOF Pharmaโ€™s latest hiring drive offers excellent opportunities for both freshers and experienced pharmaceutical professionals. With roles across QC, Production, ADL, Documentation, and Regulatory Affairs, candidates can find suitable positions aligned with their expertise.

If you meet the qualification criteria and want to work in a WHO-GMP certified pharmaceutical manufacturing environment, consider applying soon.

HOF Pharma is Hiring for QC, ADL, Production & Regulatory Affairs | 0-7 years exp
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