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Piramal 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

Job Description

• To maintain department cleanliness.
• To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.
• To implement QEHS policy & objectives.
• To ensure participation and consultation of worker.
• Ensure use of PPE.
• To identify & communicate incidents, QEHS nonconformities, investigate and take corrective actions on the same. 
• To ensure work permit system during maintenance activities.
• To implement QEHS continual improvement projects at site and monitor.
• To ensure disposal of waste. 
• To prepare and review departmental SOPs & load final SOPs in ENSUR.
• To prepare and review departmental documents.
• To Coordination, Monitoring and controlling of departmental activities as per cGMP norms.
• To get optimum productivity within specified quality by effective utilization of available resources so as to deliver the product as per market requirement.
• Responsible for providing quality product and maintaining quality system of company.
• Ensuring avoidance of breach of data integrity at all the levels.
• Ensuring implementation of effective sanitation activities at all the levels.
• To allocate manpower.
• Verification of raw materials and packing materials.
• To check and monitor the dispensing, granulation and compression and Coating activities in the department as per plan.
• To update departmental documents and records.
• To do online completed batches entries and close process orders in SAP system.
• To impart training to the operators and workers and maintain records.
• To maintain inventory of machine accessories and change parts and miscellaneous items required in granulation and compression department.
• To train workmen and subordinates.
• To give requisition of BMRs and BPRs to the QA department.
• To check the raw material and packing material availability in SAP.
• Intimate material shortages to planning department.
• To Update KPIs.
• To investigate and find out root cause analysis of any identified problem.
• To report near miss incident to Human resources and safety department.
• To make a plan of manpower requirement to meet the expected output and delivery schedules under the guidance of HOD.
• To utilize man, machine and material including natural resources like Electricity, Water, Steam and Compressed air to get higher productivity.
• To ensure proper segregation of material, quality of products, cleanliness of machines, walls, flooring, ceiling, windows and scrap area.
• To improve product quality and productivity.
• To co-ordinate with QA, QC, Stores, HR, IT, EHS and Engg. Department.
• To ensure compliance to the safety measures.
• To ensure that preventive maintenance of the machines done by maintenance department.
• To complete monthly production plan.
• To do monthly verification of weighing balances.
• To coordinate to external party to do quarterly and yearly calibration of instruments.
• To impart training to the workmen and operators for GMP, Personal Hygiene and SOP’s, Processes and Company Policies.
• Preparation of Documents for ISO 9001:2015, 14001:2015 & 18001:2007 & its Compliance. Authorised to prevent improper workplace conditions.
• Authorised for reporting of Hazards, Incident, accidents and near Miss Reporting.
•  Authorised to prepare OH&S performance document.
•  Authorised to conduct training of workmen related to OHSMS.
• To handle QMS documentation.

To review stage wise Batch Manufacturing Record