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Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders.  

PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management.  

PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs. 

For more details, please visit https://www.piramalcriticalcare.com/global/ 

Job Title

Job Description

• . Experience from industry like specialty chemicals having experience in handling of hazardous chemicals like HF, Chlorine, Bromine, HCl etc. DCS exp is essential
• Achieving the targeted production in each shift.
• Contribute to the planning of work programmes to maximise overall efficiency; and to assist other members of the team as required to carry out the planned work programmes.
• Meeting all the delivery schedules for the products as committed in the Plan.
• Co-ordination with maintenance, Quality Assurance, Quality Control and stores/Warehouse functions to ensure compliance to the committed Plan.
• Review of GMP documents like BMR, deviation reports, SOP etc without taking much time.Coordination for product dispatch.Issuance of BMR, BPR and ECR
• Completing analysis of in process samples within the standard time of analysis and communicating to plant once analysis is completed.
• Coordinate with production team during the pre-validation batches and validation batches of new product and technology transfer from lab scale to plant.
• Training the plant personnel on critical steps of new process.
• To continuously interact with service departments to carry out the process in the plant without breakdowns.
• Updating the knowledge of GMP by reading and understanding the SOPs.
• To ensure the safety of co-workers in the plant and adherence to the EHS and safety regulations.
• Manufacture of GMP products with right quality.
• Operation of all sections of the plant, monitoring & control systems, pipelines and metering systems, and mentoring and training of Junior staff in their relevant operations.
• Reporting the Accidents/ incidents and near misses and unsafe conditions to superiors.

Customer satisfaction.Meeting GMP and safety audit requirements