Validation Engineer: Ensure that a large number of highly complex pieces of process equipment & systems remain within their validated state & regulatory compliance; work w/ Mfg., Facility, & Quality Control design, detailed design, specification procurement, construction & commissioning of process equipment for cGMP production facilities; execute system improvements in conjunction w/ Mfg., Facilities, Quality Assurance, Validation & Regulatory; execute commissioning of equipment FAT/SAT; develop/execute engineering tests, FATs, SATs & commissioning test plans.
Master’s degree in Engineering (Chemical, Mechanical or Biomedical) and 1 year of relevant experience in cGMP Engineering environment with knowledge of FDA regulatory compliance.
Submit Resumes Via Email Only to: Elizabeth.firstname.lastname@example.org. Please include salary requirements. Pharmalucence, Inc, 29 Dunham Road, Billerica, MA 01821.
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The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).
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