Officer/Sr. Officer-QC Jobs in Gufic Biosciences Ltd - Navsari, Gujarat

Officer/Sr. Officer-QC Jobs in Gufic Biosciences Ltd - Navsari, Gujarat

work outline icon3 - 10 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Gufic Biosciences Ltd.

time outline iconNavsari, Gujarat, India

Posted on 12-03-2026

1 Vacancy

Description

  • Job Title: Officer/Sr.Officer-QC
  • Qualification: MPharm/BPharm
  • Location: Gufic Biosciences Ltd - Navsari, Gujarat
  • Work Experience: 3 to 10 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 Gufic Biosciences Ltd - Navsari, Gujarat as a Officer/Sr. Officer-QC in Navsari, Gujarat 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 DetailDocumentationCoordination Skills

About Organization

Gufic Biosciences Ltd is a pharmaceutical company known for manufacturing high-quality medicines and injectable products while maintaining strict regulatory and quality standards. The company operates advanced production and laboratory facilities to ensure safe and effective pharmaceutical products. The role involves performing quality control testing of raw materials, in-process samples, and finished products in the laboratory. Responsibilities include maintaining laboratory records, following GLP and GMP guidelines, and ensuring compliance with quality standards. The position focuses on accurate testing, documentation, and maintaining high pharmaceutical quality and regulatory compliance.

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