5+

Ability to manage shift plans for formulation activities. Operate and maintain equipment such as autoclaves and blending vessels CIP and SIP skids. Ability to manage shift plans for filling activities. Operate and maintain equipment such as a Vial Washer, Tunnel Sterilizer, filling and Capping Machine.

Perform real-time monitoring of production processes to ensure adherence to quality standards. Conduct routine inspections and in-process checks to verify compliance with specifications and protocols.

Review qualification protocols, reports, and documentation for accuracy, completeness, and compliance. Collaborate with cross-functional teams, including Quality Assurance, and Engineering, to ensure alignment and consistency in qualification practices.

Set and agree written goals and objectives, perform annual appraisal interviews and end of probation appraisals; submit promotion requests to management as appropriate. Ensure resource and recruitment are well aligned and timely managed in collaboration with relevant parties, participate in interviews for potential new hires.

B.Pharm, B.Sc, M.Sc. OSD - Coating, Compression, Granulation, Ointment-External Preparation General Manufacturing and Sterile Manufacturing. IPQA - OSD and Injectable, AQA, APQR, Documentation, Validation, QMS, CQA, Artwork. Injectable, Aseptic, SIP, CIP, Batch Manufacturing, Bulk Manufacturing, Dry Powder, Oral Liquid. HPLC Operating, Dissolution, Assay

Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule.

Method transfer of Pharmaceuticals Products and Materials. Analysis of In-process, Finished products, Stability study samples and raw material. Sampling and testing of Raw Materials, Packaging Materials and Water samples. Calibration and Handling of Laboratory Instruments like - GC, HPLC and Autotitrator etc

Responsible for upkeep of Encapsulation area in Production and Supervising area in production. Preparation and review of SOPs and other documentation in manufacturing areas.

ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.