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We are looking for a multiple Engineering resources to join our Life Sciences team to support major projects for various pharmaceutical clients in the Massachusetts and Southern NH areas (or other locations depending on interest). Ideal candidates should have a strong understanding of GMPs and experience providing engineering support in highly regulated or pharmaceutical/biotech facilities.
Job Responsibility:
Operational support for GMP manufacturing sites
Supporting/troubleshooting equipment
Ownership of small projects and quality systems
Familiarity of Manufacturing Systems Lifecycle approach
Must be familiar with CAPAs, deviations, and change control protocols
Requirements:
2+ years’ of experience working within a GMP or highly regulated engineering environment
Ability to work independently on projects with applicable client stakeholders in Validation, Quality, Manufacturing, Maintenance, and other relevant personnel
Strongly motivated, well-organized, and shows professional initiative
Takes ownership of assignments, can work both independently and as part of the team
Ability to work in a fast-paced and challenging environment
Excellent organization skills with the ability to manage multiple tasks simultaneously
Bachelors Degree in Mechanical or Chemical Engineering or related field experience
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