Description:
The role is responsible for engineering operations across the organization with specialized ownership of mechanical engineering documentation and records management supporting pharmaceutical manufacturing. The role ensures quality, safety, reliability, cost, timeliness, and performance standards are met through accurate preparation, review, control, and governance of engineering documentation. It supports interpretation of engineering plans, drawings, specifications, and validation records, ensures compliance with internal procedures and external regulatory standards, and monitors documentation quality and audit readiness outcomes. The position contributes to technical, functional, cost, and schedule targets, supports validation and inspection activities, and drives continuous improvement in documentation practices within a regulated manufacturing setting.

Essential Functions:
- Lead preparation, review, and control of mechanical engineering documentation
- Govern drawings, layouts, P&IDs;, manuals,



and technical records
- Ensure documentation complies with quality systems and regulatory requirements
- Review and approve maintenance, qualification, and validation documents
- Coordinate documentation support for audits, inspections, and assessments
- Ensure effective document version control and change management
- Support engineering teams with accurate technical documentation
- Monitor documentation accuracy, completeness, and traceability
- Drive continuous improvement initiatives in documentation processes
- Coordinate with cross-functional teams and external vendors

Mentor junior staff on documentation standards and best practices

Additional Responsibilities:
Education:
- B.E.
- M.Tech
- B.Pharm/ M.Pharm

Experience:
- in 1 - 4 Years

Specialized Knowledge: Licenses:

📌 Senior Officer, Mechanical Engineering Documentation (Ahmedabad)
🏢 Amneal Pharmaceuticals
📍 Ahmedabad