Pharmaceutical Engineering Opportunity with a Growth-Oriented Company - Process | Validation
Vista Technology
- Lexington, MA, United States
NEW POSITION | NEW OPPORTUNITY
MANUFACTURING / VALIDATION PROCESS ENGINEER
Primary Responsibilities:
- Develop quality characteristics for qualification and validation activities on critical manufacturing systems.
- Develop and execute engineering trials as well as validation (IQ, OQ, PQ) of equipment.
- Provide support to the plant during maintenance activities
- Research and purchase new manufacturing equipment, technology and processes to reduce cost, improve sustainability, and develop best practices.
Background Profile:
- Working knowledge of cGMP practices, 21 CFR Part 210, 211, USP, ISPE trends and guidelines.
- Experience in commissioning, qualification and validation.
- BS in Engineering with 3+ years or equivalent experience.
Would you like more information on this opportunity?
Feel free to reach out for more details:
Call: 978.686.2200 OR
Email: rich@vista-technology.com OR
Schedule a Time To Talk With The Recruiter:
https://calendly.com/richconnors
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Posted On: Monday, October 8, 2018
Compensation: DOE