Piramal Pharma

CDMO and hospital generics, consumer health

Senior Executive-Production

Manufacturing & Production OperationsConfirmed live in the last 24 hours

Full-timeDhar, IndiaNo salary listedIn-person

About the Job

Requirements

B.Pharm or M.Pharm is required.
Maintain current knowledge and involvement in SFTI, OE, and 6S activities.
Know and participate in ISO 14000 and 13485 requirements and EHS compliance, including near-miss reporting, learning incidents, and UA and UC.

Responsibilities

Allocate workmen to different workstations on a shift-to-shift basis.
Ensure operations and machines do not stop due to manpower unavailability or machine breakdowns.
Supervise line operations and related activities, and participate in validation, trial, and qualification activities according to protocol.
Check and cross-verify line clearance during batch or product changeovers.
Maintain c-GMP practices and documentation in required records.
Maintain good hygiene, safety practices, and discipline.
Record in-process parameters and reconciliation in packaging documentation.
Review and check BPR and other documents before submission to the next stage.
Participate in investigations of events and market complaints and implement CAPA.
Handle minor machine-setting issues, serialization, and aggregation.
Monitor machine speed and output against run time.
Provide on-the-job and classroom training to workmen, technical staff, and other employees on SOPs and cGMP systems.
Monitor and report unauthorized movement of workmen from the line.
Prepare new SOPs and update existing SOPs.
Report day-to-day activities in the SAP system when an SAP user ID is available.
Verify balances daily and monthly.
Maintain and calibrate instruments and equipment.
Initiate change controls, deviations, and CAPA in the electronic system when authorized.
Check due dates on calibration tags for equipment, instruments, and fire extinguishers.
Prepare and cross-verify the material return note after completion of a batch or product campaign.
Prepare line rejection notes and material requisition notes when required.
Assume the immediate supervisor's responsibilities for the section in their absence.
Perform other activities assigned by the supervisor or company.

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Job Description

Senior Executive-ProductionJob Description - Allocates workmen for different workstations on shift to shift basis. - Ensure no stoppage of operation / machines due to non-availability of manpower and any kind of machine breakdown. - Supervises the line operations and related activities and participates in Validation /Trial / qualification activities as per the protocol. - Checks and cross-verify line clearance during Batch/Product changeover. - Maintains c-GMP practices along with documentation in various records. - To maintain good hygiene, safety practices and disciplines. - Fills in-process parameters/Reconciliation in packaging documentation. - Review/check BPR and other documents before submission to next stage. - Involve in investigation of event/ market complaints and implementation of CAPA. - Handles minor setting issues, Serialization and aggregation in machines. - Monitors the speed of the machine and output according to the run time. - Imparts on job/ Classroom training to the workmen/Technical staff and other employee for SOP and cGMP systems. - Monitors and reports the unauthorized movement of workmen from the line. - Preparation of new SOPs and updating of existing SOPs. - Reports on day-to-day basis activities in SAP system (If SAP user id is available). - Verifies the balances on daily and monthly basis. - Maintenances and calibration of various instruments and equipment. - Initiate Change controls and deviations, CAPA, Change controls in electronic system as per the need (If authorization is available). - Check all the calibration tags of equipment, instruments, and fire extinguishers for their due date time to time. - Knowledge and involvement in SFTI, OE & 6S Activities. - Knowledge and involvement in ISO 14000 & 13485 and EHS compliance (Near Miss reporting/Learning Incident, UA & UC). - Prepare and cross-verify the material return note (MRN) after the completion batch/product campaign. - Prepare the line rejection note (LRN), material requisition note (MRQN) wherever required. - Take-up the responsibilities of the immediate supervisor for the section in his absence Any other activity from time to time which his supervisor/company feels appropriate. Essential Qualification B.Pharm / M.PharmFull time

About the Company

Piramal Pharma

CDMO and hospital generics, consumer health

Piramal Pharma is a diversified pharmaceutical group with three divisions: Piramal Pharma Solutions (PPS), Piramal Critical Care (PCC), and the Consumer Products Division (CPD). PPS operates as a contract development and manufacturing organization, providing development and manufacturing services across the drug lifecycle for clients in North America, Europe, and Asia through a globally connected network. PCC specializes in complex hospital generics, particularly inhaled anesthetics, serving markets in the USA, Europe, and over 100 countries. CPD leads consumer healthcare in India with brands such as Littles, Lacto Calamine, i-pill, Tetmosol, Polycrol, and Tri Activ, and the company serves pharmaceutical companies, hospitals, and consumers by leveraging its manufacturing scale and distribution network.

Company size: 1,001-5,000
Company stage: IPO
Headquarters: Maharashtra, India
Founded: 2020

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