Officer/Sr. Officer-QC (RM) Jobs in Oxalis Labs, Baddi - Solan, Himachal Pradesh

Officer/Sr. Officer-QC (RM) Jobs in Oxalis Labs, Baddi - Solan, Himachal Pradesh

work outline icon1 - 7 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Oxalis Labs, Baddi, Solan

time outline iconSolan, Himachal Pradesh, India

Posted on 26-03-2026

1 Vacancy

Description

  • Job Title: Officer/Sr. Officer-QC (RM)
  • Qualification: BPharm/MPharm
  • Location: Oxalis Labs, Baddi - Solan, Himachal Pradesh
  • Work Experience: 1 to 7 Years

Job Description

  • Conduct microbiological testing of raw materials, in-process samples, and finished products.
  • Perform sterility testing, microbial limit tests, bioburden testing, and environmental monitoring.
  • Ensure compliance with cGMP, GLP, and other regulatory guidelines.
  • Prepare and maintain accurate QC microbiology documentation and reports.
  • Investigate and document microbiological deviations / OOS (Out of Specification) results.
  • Monitor cleanroom environments and hygiene standards.
  • Ensure proper calibration and maintenance of microbiology lab instruments.
  • Support validation and qualification activities of lab equipment.

Take this opportunity to join Oxalis Labs, Baddi - Solan, Himachal Pradesh as a Officer/Sr. Officer-QC (RM) in Solan, 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

Preferred Education

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

Key Skills

TeamworkAttention to DetailDocumentationCoordination Skills

About Organization

Oxalis Labs is a pharmaceutical company engaged in the manufacturing of high-quality formulations while maintaining strict regulatory and quality standards. The role involves handling quality control activities for finished goods and ensuring product compliance. Responsibilities include testing samples, reviewing specifications, and maintaining documentation as per GMP guidelines. It requires coordination with production teams and supporting audits and quality checks. The position focuses on product quality, regulatory compliance, and maintaining high pharmaceutical standards.

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