Pharma CSV & Automation Engineer - Part-Time On-Site PR

Legalpmpartners

Barceloneta (PR)

On-site

USD 55,000 - 83,000

Part time

6 days ago

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Job summary

Legalpmpartners in Puerto Rico seeks a part-time Automation Engineer to support CSV and automation activities for pharmaceutical projects in Manatí. You will contribute to validation strategies, requirements, and documentation throughout lifecycle activities for manufacturing systems and equipment.

The ideal candidate has hands-on CSV experience, data integrity focus, and strong writing skills in English. On-site work in Manatí with cross-functional collaboration, adhering to cGMP and FDA

Qualifications

Experience with CSV and validation lifecycle activities.
Hands-on validation, data integrity, and documentation.
Knowledge of cGMP and FDA requirements.

Responsibilities

Support CSV and automation activities for pharmaceutical systems.
Develop/review system requirements, specs, and validation docs.
Prepare validation packages and risk assessments.
Collaborate with Quality, Validation, Engineering, IT and vendors.
Support commissioning/qualification of autoclaves and equipment.

Skills

CSV

Automation

Validation

Documentation

Data integrity

Technical writing

Problem solving

Independent work

Cross-functional collaboration

Education

Bachelor’s Degree in Engineering, Computer Science, IT, Automation, Electrical Engineering, or related field

Tools

ALM or similar validation lifecycle system

Microsoft Office 365

Job description

The ideal candidate has hands-on CSV experience, data integrity focus, and strong writing skills in English. On-site work in Manatí with cross-functional collaboration, adhering to cGMP and FDA

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