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Senior Officer, Mechanical Engineering Documentation at Amneal India
Ahmedabad, gujarat, India -
Full Time

Start Date

Immediate

Expiry Date

12 Aug, 26

Salary

0.0

Posted On

14 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Mechanical Engineering Documentation, Records Management, P&ID Governance, Change Management, Validation Records, Regulatory Compliance, Technical Writing, Audit Readiness, Version Control, Quality Systems, Pharmaceutical Manufacturing, Cross-functional Coordination

Industry

Pharmaceutical Manufacturing

Description
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 environment. 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:
Responsibilities
Responsible for the preparation, review, and governance of mechanical engineering documentation and records within a pharmaceutical manufacturing environment. The role ensures compliance with regulatory standards and supports audit readiness through accurate technical documentation and version control.