Walk In Drive for Experienced Professionals in Production, QA, QC at Cronus Pharma

Cronus Pharma is a fast-growing, privately held veterinary pharmaceutical company located in New Jersey, dedicated to providing innovative and cost effective products to the animal health market. Our team of seasoned industry professionals have been intimately involved in the establishment, and growth of several pharmaceutical manufacturing, and distribution firms in both the human and animal health pharmaceutical industries.

WALK-IN DRIVE for Experienced Professionals

Production (OSD)
Qualification : ITI, Diploma, B.Sc
Experience : 2–4 years
Area : Granulation, Blending, Compression Machine Operation
Key Responsibilities :
• Operate and monitor granulation, blending and compression machines.
• Ensure optimal machine performance and adherence to batch manufacturing records.
• Perform line clearance, equipment cleaning and changeover activities.
• Follow cGMP guidelines, SOPs and ensure documentation compliance.
• Troubleshoot machine issues and support process improvement initiatives.

Quality Control (QC)
Qualification : B.Pharm, M.Pharm, M.Sc in Chemistry
Experience : 2–6 years
Key Responsibilities :
• Hands-on experience with HPLC, Dissolution, IR and other analytical instruments with LIMS.
• Analyze raw materials, in-process samples and finished products as per pharmacopoeial guidelines.
• Ensure accuracy of results, maintain instruments and perform method validation.
• Ensure laboratory compliance with cGMP and data integrity.

Injectables - QA Validation
Qualification : B.Pharm, M.Pharm, M.Sc in Chemistry
Experience : 2–6 years
Key Responsibilities :
• Qualification & validation of injectable manufacturing line, including vial washing, tunnel, filling, sealing, autoclave, vessels and area qualification.
• Execute DQ, IQ, OQ, PQ and PV as per validation protocols.
• Prepare and review validation documents and reports.
• Ensure compliance with regulatory and cGMP requirements.

IPQA - Injectables
Qualification : B.Pharm, M.Pharm, M.Sc in Chemistry
Experience : 2–6 years
Key Responsibilities :
• Perform in-process quality checks at various stages of injectable manufacturing.
• Ensure adherence to SOPs, BMR/BPR and cGMP guidelines.
• Monitor and review critical process parameters and area documentation.
• Coordinate with Production & QA teams for timely issue resolution.