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