QC Manager Jobs in Microgen Healthcare, Kala Amb - Sirmaur, Himachal Pradesh

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QC Manager Jobs in Microgen Healthcare, Kala Amb - Sirmaur, Himachal Pradesh

work outline icon10 - 15 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Microgen Healthcare, Kala Amb, Sirmaur

time outline iconSirmaur, Himachal Pradesh, India

Posted on 31-01-2026

1 Vacancy

Description

  1. Job Title: QC Manager
  2. Qualification: BPharm/MPharm
  3. Location: Microgen Healthcare, Kala Amb - Sirmaur, Himachal Pradesh
  4. Work Experience: 10 to 15 Years

Job Description

  1. Lead and manage the Quality Control department.
  2. Ensure compliance with GMP / GLP / regulatory guidelines.
  3. Review and approve raw material, in-process, and finished product test results.
  4. Supervise QC team and manage training, performance, and scheduling.
  5. Investigate deviations, OOS/OOT results, and implement corrective actions (CAPA).
  6. Conduct internal audits and support regulatory inspections.
  7. Maintain QC documentation, SOPs, and data integrity.
  8. Coordinate with Production, QA, and R&D teams for quality improvement.
  9. Monitor analytical instruments and ensure proper maintenance.
  10. Prepare reports and present QC metrics to senior management.

Take this opportunity to join Microgen Healthcare, Kala Amb - Sirmaur, Himachal Pradesh as a QC Manager in Sirmaur, Himachal 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 Control (QC)

Preferred Education

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

Key Skills

Communication SkillsManagementLeadership SkillsDecision-Making Skills

About Organization

Microgen Healthcare, Kala Amb – Sirmaur, Himachal Pradesh, is a well-established pharmaceutical manufacturing company known for its strong quality systems and regulatory compliance. The company invites applications for QC Manager positions to lead and manage quality control operations. The role involves overseeing laboratory activities, ensuring compliance with GMP/GLP standards, review and approval of analytical data, and coordination with QA and production teams. Responsibilities also include handling OOS/OOT investigations, method validation, stability studies, and audit preparedness. This opportunity offers leadership exposure and long-term career growth in a structured, quality-driven pharmaceutical environment.

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