Training Supervisor- API Manufacturing

Emcure; Pune District; On-site; INR 1,600,000 - 2,100,000; Full time

Job summary

Emcure in Kurkumbh is seeking an experienced QA professional to lead Site Training and Document Control functions, ensuring GMP compliance and regulatory readiness across the site. You will oversee training programs, TNI, e-LMS, and DMS lifecycle management while supporting regulatory inspections and QMS activities.

The role requires an M.Sc. in Science with 8-10 years of QA, technical training, and document control experience in the pharma/API space, including site-wide training leadership and

Qualifications

• M.Sc. in Science.
• 8-10 years of QA, Technical Training, Quality Systems, or Document Control experience in Pharma/API.
• Site-wide training experience as Training Lead with GMP and regulatory exposure.

Responsibilities

• Act as Site Training Lead and manage GMP, SOP, OJT, and compliance training programs.
• Oversee Training Need Identification (TNI), training compliance, e-LMS administration, and training effectiveness.
• Manage document control activities including SOP issuance, review, archival, and lifecycle management through DMS/Fine Doc.
• Support regulatory inspections, customer audits, and QMS activities (TrackWise).
• Review and approve quality documents, protocols, reports, and change requests.
• Drive continuous improvement in training and documentation systems.

Skills

GMP knowledge

Regulatory compliance

LMS

DMS

TrackWise

Audit management

Site-wide training

Education

M.Sc. (Science)

Tools

DMS/Fine Doc

TrackWise

Job description

Job Title: Supervisor - Technical Training & Document Control (QA) Location: Kurkumbh
Qualification: M.Sc. (Science)

Experience: 8-10 Years

Role Overview

We are seeking an experienced QA professional to lead Site Training and Document Control functions, ensuring GMP compliance, regulatory readiness, and effective quality systems management across the site.

Key Responsibilities

• Act as Site Training Lead and manage GMP, SOP, OJT, and compliance training programs.
• Oversee Training Need Identification (TNI), training compliance, e-LMS administration, and training effectiveness.
• Manage document control activities including SOP issuance, review, archival, and lifecycle management through DMS/Fine Doc.
• Support regulatory inspections, customer audits, and QMS activities (TrackWise).
• Review and approve quality documents, protocols, reports, and change requests.
• Drive continuous improvement in training and documentation systems.

Candidate Profile

• M.Sc.
• 8-10 years of experience in QA, Technical Training, Quality Systems, or Document Control within the Pharmaceutical/API industry.
• Proven experience in handling site-wide training activities as a Training Lead.
• Strong knowledge of GMP, Regulatory Compliance, LMS, DMS, TrackWise, and Audit Management.

Preferred Industry:

• Strong exposure to regulatory inspections, quality systems, and documentation management in a cGMP environment.