Walk-in || Executive/Sr Executive - QC, QA, Engineering & Packing Development

About the Company

Responsibilities

• ● Experience in OSD (Tablets & Capsules) for FP, RM, Stability & Packaging Materials analysis.
• ● Conduct Preventive and Breakdown Maintenance of production and packing equipment like Fluid bed driers (FBD), Rapid mixture grinders (RMG), Compression machines, Coating machines, Blenders, Capsule filling machines, Blister packaging, Bulk counting lines, Sachet filling lines, Serialization equipment & inspection systems.
• ● Performing all in-process checks & Ensure Line clearance at every stage of manufacturing.
• ● Sampling activity during different stages of Production.
• ● Review audit trail of the QC chromatography and non-chromatography instrument (IR, UV, SOR, HPLC, GC) in line with 21CFR part 11.
• ● Analytical Method validation and verification study, Assay review, Related substance, Residual solvents & Dissolution.
• ● Establish and implement an integrated packaging development strategy for regulatory markets, partnering closely with Formulation Development and Manufacturing.
• ● Oversee end-to-end product lifecycle initiatives, including new launches, commercialization, site variations, cost optimization, and automation.
• ● Drive technology transfer and operational readiness by establishing Master Packaging Records, artwork, material specifications, and equipment change parts.
• ● Resolve quality issues and streamline manufacturing processes through continuous improvement, standardization, and variety reduction.

Requirements

• ● 2-5 years in pharma industry
• ● B.Pharm/M.Pharm/M.Sc.
• ● Diploma/B.Tech (Mechanical/Electrical/Instrumentation)
• ● B.Pharm/M.Pharm
• ● Graduation/Diploma in Packaging Technology
• ● 2-8 years in pharma industry