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Trainee – Production

Piramal Pharma
0-2 years
INR 2.5 LPA – 4 LPA
Pithampur, India
2 June 10, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding

Trainee – Production

Location: Pithampur, Madhya Pradesh
Company: Piramal Pharma Solutions
Department: Production / Manufacturing
Employment Type: Full-Time
Experience: Freshers to 2 Years
Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma in Pharmacy or relevant discipline


About the Company

Piramal Pharma Solutions is a leading Contract Development and Manufacturing Organization (CDMO) providing integrated drug development and manufacturing solutions across the pharmaceutical lifecycle. The company serves global innovator and generic pharmaceutical companies through its network of facilities across North America, Europe, and Asia.


Job Summary

We are looking for a motivated and detail-oriented Trainee – Production to support pharmaceutical manufacturing operations involving tablet and capsule dosage forms. The candidate will assist in production activities, maintain cGMP compliance, support documentation practices, and contribute to process efficiency, quality, and safety standards.


Key Responsibilities

Production Operations

  • Support tablet and capsule manufacturing activities including Granulation, Compression, Coating, and Encapsulation.

  • Allocate and coordinate manpower across production workstations during shifts.

  • Ensure uninterrupted manufacturing operations by minimizing machine downtime and manpower shortages.

  • Monitor machine performance, production output, and process parameters.

  • Handle basic machine settings and troubleshoot minor operational issues.

Batch Manufacturing & Documentation

  • Perform manufacturing and documentation of pilot, trial, exhibit, and commercial batches.

  • Record process parameters and maintain Batch Manufacturing Records (BMR).

  • Review and verify manufacturing documentation before submission.

  • Prepare process summaries after completion of manufacturing stages such as compression and coating.

  • Review quality and production-related documents for compliance.

Quality & Compliance

  • Maintain compliance with cGMP, SOPs, and regulatory requirements.

  • Conduct line clearance during batch changeovers.

  • Perform in-process checks as specified in Batch Manufacturing Records.

  • Verify calibration status of instruments, equipment, balances, and fire extinguishers.

  • Participate in machine qualification and validation activities.

  • Support implementation of 5S, SFTI, ISO 14000, and ISO 13485 initiatives.

Training & Team Support

  • Provide on-the-job and classroom training on SOPs and cGMP practices.

  • Conduct induction training for new employees.

  • Monitor workforce discipline and report deviations when necessary.

  • Assume additional responsibilities during supervisor absence.

Continuous Improvement

  • Participate in process improvement initiatives and operational excellence programs.

  • Support safety, quality, productivity, and compliance objectives.

  • Perform additional responsibilities assigned by management.


Required Skills

Technical Skills

  • Knowledge of tablet and capsule manufacturing processes.

  • Understanding of Granulation, Compression, Coating, and Encapsulation operations.

  • Familiarity with cGMP documentation practices.

  • Basic understanding of pharmaceutical manufacturing equipment.

Behavioral Skills

  • Good communication and teamwork abilities.

  • Strong attention to detail.

  • Problem-solving and troubleshooting mindset.

  • Planning and scheduling skills.

  • Willingness to learn and adapt in a manufacturing environment.


Preferred Qualifications

  • Exposure to pharmaceutical manufacturing environments.

  • Understanding of validation and qualification activities.

  • Knowledge of ISO standards and quality systems.

  • Basic computer proficiency (MS Office).


Why Join Piramal Pharma Solutions?

  • Opportunity to build a career in pharmaceutical manufacturing.

  • Hands-on exposure to global manufacturing standards.

  • Learning and development opportunities with industry experts.

  • Exposure to cGMP-compliant manufacturing facilities.

  • Career growth within a leading global pharmaceutical CDMO.