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

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

work outline icon3 - 5 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

  • Job Title:  QC Executive
  • Qualification: BPharm/MPharm
  • Location: Microgen Healthcare, Kala Amb - Sirmaur, Himachal Pradesh
  • Work Experience: 3 to 5 Years

Job Description

  • Perform QC testing of raw materials, in-process samples, and finished products.
  • Ensure all testing follows SOPs and GMP guidelines.
  • Maintain laboratory records and batch test reports accurately.
  • Report deviations or discrepancies to QC/QA Manager.
  • Assist in environmental monitoring and calibration of instruments.
  • Participate in internal audits and support external audits if needed.
  • Follow safety guidelines in the laboratory and production areas.
  • Coordinate with Production and QA for smooth workflow.
  • Support QC Manager in daily laboratory operations.

Take this opportunity to join Microgen Healthcare, Kala Amb - Sirmaur, Himachal Pradesh as a QC Executive 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

TeamworkAttention to DetailCoordinationBasic Computer Knowledge

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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