QA Microbiologist (Reviewer) Jobs in Acme Generics LLP - Nalagarh, Himachal Pradesh

QA Microbiologist (Reviewer) Jobs in Acme Generics LLP - Nalagarh, Himachal Pradesh

work outline icon6 - 8 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Acme Generics LLP

time outline iconNalagarh, Himachal Pradesh, India

Posted on 24-03-2026

1 Vacancy

Description

  • Job Title: QA Microbiologist (Reviewer)
  • Qualification: MSc
  • Location: Acme Generics LLP - Nalagarh, Himachal Pradesh
  • Work Experience: 6 to 8 Years

Job Description

  • Conduct laboratory testing and analysis of biological samples to detect microorganisms, pathogens, and contaminants.
  • Perform microbiological cultures, staining, and biochemical tests to identify bacteria, viruses, fungi, and parasites.
  • Maintain and operate laboratory equipment, ensuring calibration and proper functioning.
  • Record, analyze, and interpret laboratory data accurately for research or clinical reporting.
  • Ensure compliance with biosafety protocols, infection control, and laboratory safety standards.
  • Prepare reports, maintain detailed lab documentation, and present findings to supervisors or stakeholders.

Take this opportunity to join Acme Generics LLP - Nalagarh, Himachal Pradesh as a QA Microbiologist (Reviewer) in Nalagarh, 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

Paramedical / Technician

Preferred Education

MSc Microbiology

Key Skills

Analytical SkillsCommunications SkillsInfection Control KnowledgeAttention to Detail

About Organization

Acme Generics LLP is a pharmaceutical company engaged in the manufacturing of high-quality medicines and formulations while maintaining strict regulatory and quality standards. The company operates advanced production facilities and focuses on compliance with global pharmaceutical guidelines. The role involves managing quality management system activities and ensuring adherence to GMP and regulatory requirements. Responsibilities include handling documentation, audits, deviations, and CAPA processes. It requires coordination with production and quality teams to maintain compliance. The position focuses on quality assurance, regulatory adherence, and continuous improvement of quality systems.

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