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DATE ADDED: Thu 11/10/2018

Process Engineer / Medical Device Manufacturing Validation

La Jolla, USA
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COMPANY: CELERE, INC.

Job Description

We are seeking a Process Engineer, Medical Device Manufacturing, Validation to join our team! 

** Chemical, Electrical, Mechanical engineering degree required (Bachelors of Science) .
** 7-10 years experience working as Process Control Engineer or Manufacturing Process Engineer in Pharmaceutical, Medical Device, Biotechnology facilities (west cost preferred).

Responsibilities:

  • Perform process engineering studies, develop work instructions, requirements.
  • Develop Validation Plan, Risk Assessment, Protocol, and reports
  • Supervise Validation Execution (coordinate with manufacturing personnel)
  • Serve as point of contact between production, quality, and validation teams

Qualifications:

  • 7-10 years Process Control Validation, or Process Validation experience in Pharmaceutical environment
  • Previous experience in QC and manufacturing in a pharmaceutical and/or device manufacturing company
  • Strong project management skills
  • Ability to prioritize and multitask
  • Excellent written and verbal communication skills
  • Ability to work well in teams

Company Description
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Role: Process Engineer / Medical Device Manufacturing Validation
Job Type:
Location: La Jolla,

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