Quality Control Jobs in Acme Generics LLP - Nalagarh, Himachal Pradesh

Quality Control Jobs in Acme Generics LLP - Nalagarh, Himachal Pradesh

work outline icon12 - 22 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: Quality Control
  • Qualification: BPharm
  • Location: Acme Generics LLP - Nalagarh, Himachal Pradesh
  • Work Experience: 12 to 22 Years

Job Description

  • Perform routine QC testing of raw materials, in-process & finished products.
  • Collect samples and perform analysis as per approved methods.
  • Record, review, and report test results accurately.
  • Follow GMP, GLP, and SOP requirements strictly.
  • Assist in OOS / OOT investigations and CAPA activities.
  • Maintain QC documentation, logbooks & reports.
  • Support calibration and maintenance of lab instruments.
  • Coordinate with QA, production & R&D teams.
  • Maintain lab cleanliness, safety & compliance.
  • Support internal and external audits

Take this opportunity to join Acme Generics LLP - Nalagarh, Himachal Pradesh as a Quality Control 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

Pharmaceuticals

Functional Area

Pharma Quality Control (QC)

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

DocumentationGood Communication SkillsData RecordingTeamwork

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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