Automation Project Manager

Tek Support; Pune District; Remote; INR 1,200,000 - 1,500,000; Part time

Job summary

A leading pharmaceutical automation company seeks a Senior Automation Engineer to drive automation initiatives in manufacturing systems while ensuring compliance with GMP standards. The candidate should have over 10 years of experience, specifically in automation system management, control logic development, and cross-functional collaboration. This part-time role offers the opportunity to enhance equipment reliability and process efficiency in a remote work setting.

Qualifications

• 10+ years of experience in pharmaceutical automation.
• Understanding of GMP compliance in manufacturing.
• Ability to guide junior engineers and technicians.

Responsibilities

• Oversee automation initiatives across manufacturing systems.
• Manage automation for production and cleanroom environments.
• Ensure compliance with validation standards and data integrity.

Skills

Automation systems management

Control logic development

Troubleshooting and root cause analysis

Technical documentation preparation

Collaboration with cross-functional teams

Tools

PLC

SCADA

HMI

Job description

Job Title: Senior Automation Engineer – Pharmaceutical Manufacturing

Location: Remote

Experience: 10+ years

Industry: Pharmaceutical / Biotech Manufacturing

Job Summary:

The Senior Automation Engineer is responsible for driving automation initiatives across pharmaceutical manufacturing systems, ensuring compliance with GMP, and enhancing equipment reliability and process efficiency. This role involves overseeing automation design, programming, validation, and maintenance of PLC, SCADA, and related control systems used in production and utility areas.

Key Responsibilities:

• Managed automation systems supporting production, utilities, and cleanroom environments in compliance with GMP and regulatory requirements.
• Developed, modified, and optimized control logic for PLC, HMI, and SCADA systems (Siemens, Allen-Bradley, DeltaV, or equivalent).
• Supported the design, configuration, and integration of new automated equipment and systems into existing production lines.
• Performed troubleshooting and root cause analysis of automation and instrumentation failures to minimize downtime.
• Executed system upgrades, patches, and changes following change control procedures and validation standards (GAMP 5).
• Prepared and reviewed technical documentation including URS, FDS, FAT, SAT, IQ/OQ/PQ, and SOPs.
• Ensured data integrity and compliance with 21 CFR Part 11 for electronic records and automation systems.
• Collaborated with cross-functional teams (Engineering, QA, Validation, and Manufacturing) for project execution and continuous improvement.
• Guided junior engineers and technicians in automation programming, troubleshooting, and documentation practices.

Seniority Level

Mid-Senior level

Employment Type

Part-time

Job Function

Training

Industries

Pharmaceutical Manufacturing and Automation Machinery Manufacturing