Hiring for Quality Control and Quality Assurance at Zenotech Laboratories

Zenotech Laboratories Limited is an India-based pharmaceutical company operating out of Hyderabad, India. The Company is engaged in a business of manufacture and marketing of pharmaceuticals products. The Company is a pharmaceutical specialty generic injectables company engaged in the area of manufacturing Oncology, bio-technology and General Injectables products.

Zenotech Laboratories HIRING

Quality Control
Qualification : B.Pharma/M.Pharma/MSc Sub-Analysis-OSD
Designation : Senior Officer
Experience : 2–4 Years
Responsibility : Operation, calibration, and maintenance of GC, HPLC, and analytical instruments. Analysis of raw materials, finished products, cleaning samples, and stability samples.

Quality Control
Qualification : B.Pharma/M.Pharma/MSc Sub-Analysis – General Injectable
Designation : Senior Officer
Experience : 2–4 Years
Responsibility : Operation, calibration, and maintenance of GC, HPLC, and analytical instruments. Analysis of raw materials, finished products, cleaning samples, and stability samples.

Quality Assurance
Qualification : B.Pharma/M.Pharma/MSc Sub-QMS – General Injectable
Designation : Senior Officer
Experience : 2–4 Years
Responsibility : Manage and monitor QMS activities, including Change Controls, Deviations, CAPA, OOS, and Product Quality Complaints. Review, track, and ensure timely closure and effectiveness of CAPA and quality systems. Control and maintain SOPs, protocols, training records, and EDMS documentation. Support regulatory compliance, product recalls, audits, and continuous quality improvement.

Quality Assurance
Qualification : B.Pharma/M.Pharma/MSc Sub-QMS – General Injectable
Designation : Executive
Experience : 5–8 Years
Responsibility : Manage and monitor QMS activities, including Change Controls, Deviations, CAPA, OOS, and Product Quality Complaints. Review, track, and ensure timely closure and effectiveness of CAPA and quality systems. Control and maintain SOPs, protocols, training records, and EDMS documentation. Support regulatory compliance, product recalls, audits, and continuous quality improvement.

Quality Assurance
Qualification : B.Pharma/M.Pharma/MSc Sub-AQA – General Injectable
Designation : Executive
Experience : 5–8 Years Responsibility :
• Handle QMS activities such as Change Controls, Deviations, CAPA, OOS, and PQC.
• Manage SOPs, training, EDMS, and quality documentation.
• Ensure CAPA effectiveness, compliance, and regulatory readiness.
• Support product recalls, audits, and continuous quality improvement.