Executive - Production

Piramal Pharma; Mahad; On-site; INR 350,000 - 550,000; Full time

Job summary

Piramal Pharma Solutions in Maharashtra, India, seeks an Executive - Production to support daily manufacturing in the G-Block area. The role involves manpower allocation, monitoring dispensing, granulation, compression and packaging as per plan, and updating production records.

You will ensure GMP adherence, train operators, and interact with QA/QC, Stores, HR, IT, EHS and Engg. departments to maintain quality and productivity.

Qualifications

• B. Pharma qualification is required.
• Experience in a pharmaceutical production area preferred.
• Strong documentation and record-keeping skills expected.

Responsibilities

• Allocate manpower and ensure cleanliness of area and machines.
• Monitor dispensing, granulation, compression & packaging activities as per plan.
• Update departmental documents and records and close SAP process orders.
• Impart training to operators and workers and maintain records.
• Coordinate with QA, QC, Stores, HR, IT, EHS and Engg. departments.
• Follow GMP practices and maintain QEHS standards in production.

Skills

GMP knowledge

Documentation

Training operators

Education

B. Pharma.

Tools

SAP

Job description

Be the First to ApplyDivisionPiramal 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.comJob TitleExecutive - ProductionJob DescriptionJD - Executive ProductionJOB RESPONSIBILITY, ACCOUNTABILITY & AUTHORITYName of the Employee: Mayur A. Randive Employee ID No.: 70091612Date of Joining: 12.12.2024 Designation: Production ExecutiveQualification: B. Pharma. Department: G-Block ProductionUpward Reporting: Mr. Ravindra R. Mujumale - Manager ProductionTo allocate manpower.Checking cleanliness of area and machines.Balance verificationVerification of Raw materials in granulation.To check and monitor the dispensing, granulation, compression & packaging 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 give requisition of BMRs 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 report 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 follow Good Manufacturing Practices in the department.To maintain quality products and maintain quality norms.To maintain sanitation in production area.Ensuring upkeep of area and equipment.Imparting training to colleagues / subordinates.To raise change control, deviation and CAPA.To ensure avoidance of breach of data integrity at all levels.To ensure compliance to the safety measures.To ensure the cleaning of riser filters as per SOP.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 maintain record of cycle time of products.To maintain change over data of products.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.Ensure use of PPE.To ensure compliance to Safety Measures. Implementation and Documentation of ISO 9001:2015, ISO14001:2015 and ISO 45001:2018.To identify & communicate incidents, QEHS non conformities, 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 participation and consultation of worker.To ensure disposal of waste.Authorized to prevent improper workplace conditions.Authorized for reporting of Hazards, Incident, accidents and near miss Reporting.Authorized to prepare OH&S performance document.Authorized to conduct training of workmen related to OHSMS.In case of absence, Executive Production shall take care of his/her job responsibilities.Apart from above Resources, Roles, Responsibility, Accountability and Authority the Head of Department can assign additional job responsibility on need basis.Prepared By (Sign) :Date:Accepted By (Sign) :Date:Mr. Manoj KotkarMr. Mayur A. Randive(Name of Department Head)(Name of Employee)To allocate manpower.Checking cleanliness of area and machines.Balance verificationVerification of Raw materials in granulation.To check and monitor the dispensing, granulation, compression & packaging 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 give requisition of BMRs 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 report 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 follow Good Manufacturing Practices in the department.To maintain quality products and maintain quality norms.To maintain sanitation in production area.Ensuring upkeep of area and equipment.Imparting training to colleagues / subordinates.To raise change control, deviation and CAPA.To ensure avoidance of breach of data integrity at all levels.To ensure compliance to the safety measures.To ensure the cleaning of riser filters as per SOP.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 maintain record of cycle time of products.To maintain change over data of products.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.Ensure use of PPE.To ensure compliance to Safety Measures. Implementation and Documentation of ISO 9001:2015, ISO14001:2015 and ISO 45001:2018.To identify & communicate incidents, QEHS non conformities, 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 participation and consultation of worker.To ensure disposal of waste.Authorized to prevent improper workplace conditions.Authorized for reporting of Hazards, Incident, accidents and near miss Reporting.Authorized to prepare OH&S performance document.Authorized to conduct training of workmen related to OHSMS.