
Officer/Sr. Officer-QC Job in Pontika Aerotech Limited - Paonta Sahib, Himachal Pradesh
Pontika Aerotech Limited
Paonta Sahib, Himachal Pradesh, India
Posted on 12-03-2026
1 Vacancy
Description
- Job Title: Officer/Sr.Officer-QC
- Qualification: DPharm/BPharm
- Location: Pontika Aerotech Limited - Paonta Sahib, Himachal Pradesh
- Work Experience: 2 to 6 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 Pontika Aerotech Limited - Paonta Sahib, Himachal Pradesh as a Officer/Sr. Officer-QC in Paonta Sahib, 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
Key Skills
About Organization
Pontika Aerotech Limited is a pharmaceutical manufacturing company known for producing high-quality medicines and maintaining strict regulatory and quality standards in production. The company operates modern manufacturing 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 documentation, following GLP and GMP guidelines, and ensuring compliance with quality standards. The position focuses on accurate testing, proper documentation, and maintaining high pharmaceutical quality and regulatory compliance.
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