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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Visit our Career Opportunities Page



Posted On: Monday, October 8, 2018
Compensation: DOE



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