Manufacturing Chemist Jobs in Microgen Healthcare - Ujjain, Madhya Pradesh

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Manufacturing Chemist Jobs in Microgen Healthcare - Ujjain, Madhya Pradesh

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Microgen Healthcare, Ujjain

time outline iconUjjain, Madhya Pradesh, India

Posted on 31-01-2026

1 Vacancy

Description

  1. Job Title: Manufacturing Chemist
  2. Qualification: BPharm/MPharm
  3. Location: Microgen Healthcare - Ujjain, Madhya Pradesh
  4. Work Experience: 0 to 5 Years

Job Description

  1. Assist in manufacturing of chemical/pharmaceutical products as per SOP.
  2. Prepare raw materials and formulations accurately.
  3. Monitor the production process for quality and compliance.
  4. Maintain batch manufacturing records and production logs.
  5. Ensure adherence to GMP, safety, and environmental standards.
  6. Perform in-process checks and report deviations.
  7. Coordinate with QA and QC for release of materials.
  8. Maintain cleanliness and hygiene of production area.
  9. Troubleshoot minor production or process issues.
  10. Participate in continuous improvement initiatives.

Take this opportunity to join Microgen Healthcare - Ujjain, Madhya Pradesh as a Manufacturing Chemist in Ujjain, Madhya Pradesh and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Production / Manufacturing

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Communication SkillsCoordination SkillsProblem Solving SkillsTeam working

About Organization

Microgen Healthcare, Ujjain, Madhya Pradesh, is a growing pharmaceutical organization known for its focus on quality manufacturing and regulatory compliance. The company invites applications for Quality Control professionals to support routine laboratory operations. The role involves analysis of raw materials, in-process samples, and finished products as per approved specifications. Responsibilities include documentation, adherence to GMP/GLP guidelines, and coordination with QA and production teams. This opportunity offers hands-on industry exposure and long-term career growth in a quality-driven pharmaceutical environment.

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