Junior CSV Engineer Opportunity
Deliver stable manufacturing systems optimized for operational efficiency and compliance in the Pharmaceutical and Biotechnology Manufacturing stack.
Key Responsibilities
* Implement automation solutions using Delta V and MES platforms
* Ensure data integrity and GAMP compliance in a GMP environment
* Collaborate with cross-functional teams to deliver end-to-end solutions
Requirements
* 4+ years of experience with Automation, preferably Delta V
* 1-3 years of experience with Computer Systems Validation
* 5+ years of experience working in a GMP environment
* BS in Computer Science or Engineering field or equivalent experience
Preferred Qualifications
* Experience with Data Integrity, 483 compliance consent decree, and 21 CFR Part 11
* Biotech and pharma industry experience preferred over medical device
* Knowledge of MES Delta V PI, Rockwell, GE, Emerson, ABB, Werum, Siemens, Honeywell, and their associated platforms
What We Offer
Excellent opportunity to work with a leading Life Sciences company. Collaborative team environment with opportunities for growth and development.
The ideal candidate will have strong technical skills, excellent communication skills, and the ability to work effectively in a fast-paced environment.