Assistant Manager - Engineering Documentation

Amneal Pharmaceuticals LLC; Visakhapatnam; On-site; INR 1,500,000 - 2,500,000; Full time

Job summary

Amneal Pharmaceuticals LLC in Visakhapatnam seeks an experienced Documentation Specialist to manage and maintain engineering records for facilities, HVAC, utilities, and equipment in compliance with GMP. You will coordinate with QA, Production, Validation, and external vendors, ensuring traceability and proper archival of documents.

The role requires 10–12 years in pharma engineering documentation, strong GMP knowledge, and proficiency with document-management systems and MS Office.

Qualifications

• 10–12 years of experience in engineering documentation, preferably in pharmaceutical manufacturing.
• Strong knowledge of GMP documentation, qualification, validation, and audit requirements.
• Good understanding of HVAC, utilities, equipment, and facility-related documentation.

Responsibilities

• Prepare, review, update, and maintain engineering documents, records, and reports.
• Manage documentation related to HVAC, utilities, equipment, facilities, and projects.
• Prepare and maintain engineering SOPs, specifications, protocols, reports, drawings, checklists, logbooks, and qualification documents.
• Coordinate with Engineering, QA, Production, Projects, Validation, and external vendors for timely completion of documentation.
• Review engineering documents for accuracy, completeness, traceability, and compliance with approved procedures.
• Support preparation and execution documentation for DQ, IQ, OQ, PQ, commissioning, qualification, and validation activities.
• Maintain documentation for change controls, deviations, CAPA, risk assessments, and engineering modifications.
• Ensure proper document numbering, revision control, approval, issuance, archival, and retrieval.
• Review vendor documents, drawings, manuals, test certificates, and technical dossiers.
• Ensure engineering records are maintained in accordance with GMP and data-integrity requirements.
• Support audits by providing engineering documentation and evidence.
• Track documentation status and follow up for closure of pending documents.

Skills

Document control

GMP knowledge

MS Office

Coordination

Attention to detail

Communication skills

Education

Bachelor's degree (B.Tech/B.E.)

Master's degree (M.Tech)

Tools

Document-management systems

Job description

Job Description:

Description:

Responsible for managing, reviewing, maintaining, and controlling engineering documentation related to facilities, utilities, equipment, HVAC, and engineering projects in compliance with applicable GMP, quality, and documentation requirements.

Key Responsibilities

• Prepare, review, update, and maintain engineering documents, records, and reports.
• Manage documentation related to HVAC, utilities, equipment, facilities, and engineering projects.
• Prepare and maintain engineering SOPs, specifications, protocols, reports, drawings, checklists, logbooks, and qualification documents.
• Coordinate with Engineering, QA, Production, Projects, Validation, and external vendors for timely completion of documentation.
• Review engineering documents for accuracy, completeness, traceability, and compliance with approved procedures.
• Support preparation and execution documentation for DQ, IQ, OQ, PQ, commissioning, qualification, and validation activities.
• Maintain documentation for change controls, deviations, CAPA, risk assessments, and engineering modifications.
• Ensure proper document numbering, revision control, approval, issuance, archival, and retrieval.
• Review vendor documents, drawings, manuals, test certificates, and technical dossiers.
• Ensure engineering records are maintained in accordance with GMP and data-integrity requirements.
• Support internal, customer, and regulatory audits by providing engineering documentation and evidence.
• Track documentation status and follow up with concerned departments for closure of pending documents.
• Maintain an organized engineering document repository and ensure timely archival of obsolete documents.
• Participate in engineering projects and provide documentation support from project initiation through commissioning and qualification.

Qualification

• B.Tech / B.E. in Mechanical, Electrical, or relevant Engineering discipline.
• Candidates with relevant pharmaceutical engineering documentation experience will be preferred.

Required Experience & Skills

• 10–12 years of overall experience in engineering documentation, preferably in the pharmaceutical/API manufacturing industries
• Strong knowledge of engineering documentation and document-control practices.
• Experience with GMP documentation, qualification, validation, and audit requirements.
• Good understanding of HVAC, utility systems, equipment, and facility-related documentation.
• Good coordination and communication skills.
• Strong attention to detail and ability to maintain document accuracy and traceability.
• Working knowledge of MS Office and document-management systems.

Qualifications

Education:

• Bachelors Degree (BA/BS) B.Tech - Required

• Master Degree (MS/MA) M.Tech - Preferred

Experience:

• 5 years or more in 5 - 8 Years

Specialized Knowledge:

Licenses:

Requirements: