Training Supervisor- API Manufacturing

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: Pharmaceutical / API Manufacturing.

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