November 2025

Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance tasks on equipment as required.

Review of stability data. Review of analytical method validation data. Review of analytical method transfer.

Ph.D. or Master in Life Sciences, Biotechnology, Pharmacology, or related field. Strong understanding of the drug discovery pipeline and integrated biology workflows.

Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk.

Looking for talented QC professionals with strong analytical skills and hands-on experience in pharmaceutical Quality Control operations. The ideal candidate should have a strong understanding of GLP, GMP, documentation, and regulatory compliance.

Hands-on experience in Blister, Strip, and Bulk Packaging (Primary & Secondary), Experience in QMS activities (handling of SOPs preparing, Training, Change Control/Deviations), Familiarity with Track & Trace and Serialization Systems.

Experience and having knowledge of raw material analysis, finished product analysis, qualification & calibration of laboratory instruments. SOP preparation, change control, deviation management and knowledge of LIMS. DMS and QMS, etc.

Masters degree/ diploma, life sciences, pharmacy, public health, healthcare for clinical trial monitoring or clinical trial / study coordinator, or clinical trial/study associate. THSTI

Graduate in B.PHARM / D.PHARM and Pharmacy council Board registration is required. Candidate Should possess the basis computer course certificate and Computer knowledge will be tested during Interview.