Technical Staff - Production

Piramal Pharma Ltd; Madhya Pradesh; On-site; INR 250,000 - 360,000; Full time

Job summary

Piramal Pharma Ltd is seeking a Technical Staff - Production to support sterile product manufacturing. The role involves executing manufacturing tasks in the Sterile Department, managing manpower across shifts, and ensuring strict adherence to cGMP and documentation standards.

Responsibilities include line supervision, participation in validation activities, calibration checks, and preparation of SOPs as required. A B.Sc or B.

Qualifications

• No explicit language requirements stated beyond basic education.

Responsibilities

• Allocates workmen for different workstations on shift-to-shift basis.
• Ensure no stoppage of operation due to manpower or machine issues.
• Supervises line operations and participates in validation activities.
• Maintains cGMP practices and documentation.

Education

B.Sc

B. Pharma

Tools

SAP

Job description

Job Description

Technical Staff - ProductionJob Description Well-versed in sterile product manufacturing techniques, including drug manufacturing, autoclaving, FFS (Form–Fill–Seal) filling, aseptic filtration, and other processing operations. Responsible for executing manufacturing activities in the Sterile Department on a shift-to-shift basis and completing all documentation in accordance with cGMP requirements.

Key Responsibilities Key Roles/Responsibilities:

• 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 participate in Validation activities as per the protocol.
• Maintains c-GMP practices along with documentations in various records.
• Involvement in the processing and documentation of trial batches.
• Fills and checks BMR before submission to the superiors.
• Handles minor parametric setting issues in various machines and products.
• Monitors speed of machine and output according to the run time.
• Imparts on job/ Classroom training to the concern workmen and supervisor for SOP and cGMP systems.
• Imparts induction activity to all new joining.
• Monitors and reports the unauthorized movement of workmen from line.
• Takes up the responsibilities of the immediate supervisor for the section in his absence.
• Helps section in charge in preparation of SOP.
• Reports on day-to-day basis activities in SAP system. (If SAP user id is available)
• Verifies the balances on daily and monthly basis.
• Participate in machine qualification activities.
• Checks all the calibration tags of equipment, instruments and fire extinguisher for their due date time to time.
• Knowledge and involvement in Daily Management System.
• Knowledge and involvement in ISO 14000 & 13485.
• Any other activity from time to time which his supervisor / company feels appropriate.
• Checking of line clearance during batch change over.
• In process testing as defined in Batch Manufacturing Record.
• Preparation of Material Return Note (MRN), Material Requisition Note (MRQN), Line rejection Note (LRN) of Processing area.
• Review the Batch Manufacturing and other quality documents.

Essential Qualification

B.Sc / B. PharmaFull time