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Morepen Laboratories is Hiring for QC, QA & ADL Roles

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Morepen Laboratories

B.Sc, M.Sc, B.Pharm and M.Pharm

Baddi

2-10 Years

Verified Job

Walk In Interview
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Morepen Laboratories Limited has announced a walk-in interview drive for its Manufacturing Unit located in Baddi, Himachal Pradesh. The company is inviting experienced professionals from Quality Control, Quality Assurance, and ADL departments for multiple positions including Chemist, Executive, and Senior Executive roles.

Candidates with qualifications such as B.Sc, M.Sc, B.Pharm, and M.Pharm and relevant pharmaceutical industry experience can attend the interview directly at the venue on 24 May 2026.

About Morepen Laboratories

Morepen Laboratories Limited is a well-known pharmaceutical company with strong expertise in research, development, and manufacturing of APIs and formulations. The company is recognized for its advanced manufacturing facilities and focus on quality-driven pharmaceutical production.

Walk-In Interview Details

  • Interview Date: 24 May 2026 (Sunday)
  • Time: 10:30 AM onwards
  • Venue: Morepen Laboratories Limited, Baddi, Himachal Pradesh
  • Mode: Walk-In Interview

Open Positions Available

Quality Control Department

Qualification

  • B.Sc
  • B.Pharm
  • M.Sc (Chemistry)

Experience

  • 2 to 8 Years

Required Skills

  • Instrumentation
  • HPLC
  • UV
  • GC
  • Dissolution
  • Reviewers
  • QMS
  • GLP

Designation

  • Chemist
  • Executive

Quality Assurance Department

Qualification

  • B.Pharm
  • M.Pharm

Experience

  • 2 to 10 Years

Required Skills

  • Stability
  • IPQA
  • Qualification Validation
  • CSV

Designation

  • Sr. Chemist
  • Sr. Executive

ADL Department

Qualification

  • M.Sc
  • M.Pharm

Experience

  • 3 to 7 Years

Designation

  • Sr. Chemist
  • Executive

Roles and Responsibilities

Quality Control

  • Perform analytical testing using HPLC, GC, UV, and Dissolution instruments
  • Maintain laboratory documentation and GLP compliance
  • Handle QMS activities and analytical reviews
  • Ensure quality standards during testing procedures

Quality Assurance

  • Manage IPQA activities and validation processes
  • Maintain stability documentation and compliance records
  • Support qualification and CSV-related activities
  • Ensure adherence to GMP and regulatory standards

ADL

  • Conduct analytical method development activities
  • Prepare and review analytical reports
  • Support formulation and validation studies
  • Coordinate with cross-functional departments

Salary and Benefits

Selected candidates can expect an attractive salary package based on experience and current industry standards. The estimated salary range for these positions may vary between ₹3.5 LPA to ₹9 LPA depending on role and experience.

Additional benefits may include:

  • Growth opportunities in pharmaceutical manufacturing
  • Learning and development programs
  • Professional work environment
  • Employee benefits as per company policy

How to Apply

Interested candidates can directly attend the walk-in interview with:

  • Updated Resume
  • Recent Passport Size Photograph
  • Current CTC Details
  • Relevant Educational & Experience Documents

Candidates who are unable to attend the interview may send their resumes to:

For additional information, candidates can visit the official website of Morepen Laboratories

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