Quality Assurance Jobs in Microgen Healthcare - Ujjain, Madhya Pradesh

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Quality Assurance 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: Quality Assurance
  2. Qualification: B.Pharm / M.Pharm
  3. Location: Microgen Healthcare - Ujjain, Madhya Pradesh
  4. Work Experience: 0 to 5 Years

Job Description

  1. Implement and maintain Quality Management Systems.
  2. Ensure compliance with GMP / regulatory guidelines.
  3. Prepare, review, and control SOPs, formats & records.
  4. Review batch manufacturing & packing records.
  5. Investigate deviations, OOS, complaints & implement CAPA.
  6. Coordinate internal, customer & regulatory audits.
  7. Ensure data integrity and documentation accuracy.
  8. Support validation, qualification & change management.
  9. Conduct GMP training for employees.
  10. Work closely with QC, Production & Regulatory teams.
  11. Ensure product quality and regulatory compliance.

Take this opportunity to join Microgen Healthcare - Ujjain, Madhya Pradesh as a Quality Assurance 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

Pharma Quality Assurance (QA)

Preferred Education

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

Key Skills

Coordination SkillsAttention to DetailRisk Management SkillsGood Communication

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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