Job Description
Be the First to Apply
Division
Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Executive - ProductionJob Description
Seeking a skilled chemical manufacturing professional with 4–6 years of experience in bulk drug production, proficient in process operations, GMP compliance, safety standards, and continuous improvement initiatives to support efficient and compliant manufacturing operations.Key Responsibilities:
- Operating all process equipments Viz. Hydrogenator, Reactor, centrifuge, Tray drier, Vacuum Tray drier / Roto cone vacuum drier / Agitated nutsche filter cum drier / Multi mill / Sifter / Distillation column etc., utility equipments viz. vacuum pump, Ejectors, scrubbers etc. in shifts.
- Safe handling of hazardous chemicals, solvents, catalyst
- Knowledge on static electricity and its controls
- Monitoring & controlling the process parameters as per BMR
- Execution of production batches and meeting the production targets
- Effective utilization of men, utility, equipment, raw materials and power
- Maintaining Good Housekeeping in work place all the time and maintaining the assets in good condition.
- Online Documentation viz. batch manufacturing record, equipment cleaning record etc.
- Identifying and reporting of abnormalities
- Reporting of near miss, unsafe condition, unsafe act
- Packing of Solid / liquid products as per requirement
- Maintaining the inventories of raw material, packing material, solvents, intermediates, finished goods
- Trouble shooting of process equipments, utility systems and process
- Initiating work order and safety permits
- Adherence to CGMP and safety norms
- Knowledge in ISO 9001, ISO 14001, ISO 45001
- Generating new ideas and initiatives
- Involving Yield improvement, time cycle reduction, capacity enhancement initiatives
- Making the plant for the audit readiness
- Carrying out the activities in line with patient centric approach
- Ensuring the safety of self, operating personnel and workmen associated
- Co ordination with the supporting departments viz Engineering, QC, R&D for smooth running of production.
- Participation in training programme and effective communication process
Job Requirements:
- Qualification: Diploma in Chemical / B.Sc. in Chemistry / M.Sc. in chemistry
- Work Experience: 4–6 years experience in Bulk Drugs Industry and exposure to GMP