Biological Process Engineer

Portsmouth, NH

Posted: 04/11/2019 Job Number: JN -042019-10624
Biological Process Engineer II, III and Sr. Level (multiple roles)

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Title: Biological Process Engineer II, III and Sr.
Location: Portsmouth, NH
Industry: Biopharmaceutical
Hours: 1st Shift Monday-Friday, 8am-5pm
Salary: Process Engineer II, $75,000-$105k
Process Engineer III, $85,000-$125k
Sr. Process Engineer, up to $145k
Plus relocation assistance for right candidate
Employment Type: Direct hire

Environment: This client is one the world s leading supplier to the pharmaceutical, biotech, biopharmaceutical and specialty ingredients markets. This location focuses on mammalian cell culture and large-scale production of biopharmaceuticals. We create products that support a healthier lifestyle and enhance ones quality of life. Isn t this a company you want to work for?

Job Description Summary
Process Engineers primary responsibility is to be a process owner and primary technical Subject Matter Expert (SME) for downstream manufacturing processes. This person should have experience supporting at-scale downstream processing.

  • Performs all MSAT (Manufacturing Sciences and Technology) functions associated with process transfer and process support. E.g. perform gap analysis / FMEA, generate process models, author / review process documentation (e.g. BRs), author / review / implement quality documents (e.g. change control, CAPA), perform process monitoring (manufacturing data summary and analysis, data presentation), author campaign summary, perform activities for lot release (assess deviations and process changes).
  • May provide guidance on process transfer and support activities to junior members of the team.
  • Assess all major deviations for impact product quality. Take ownership of subsequent CAPA.
  • Authors / present training presentations to manufacturing and other departments.
  • Effectively work with other departments and interface with customers.

  • Minimum Bachelor of Science degree in Biological Sciences or Biomedical/Chemical Engineering
  • 6+ years of biotech industry experience (0 to 5 years for Ph.D.) in process development and process scale up / manufacturing. Experience with large-scale manufacturing support (mammalian preferred), current Good Manufacturing Practices, US / EU regulations.
  • Technical understanding of downstream unit operations: chromatography (e.g. Protein A, IEX, HIC); Ultrafiltration/Diafiltration; and VRF.
  • Experience within a CDMO and/or CMO highly preferred
Search words: process engineer, biopharmaceutical, biomedical, biological, down-stream, up-stream, mammalian, protein, extraction, fermentation, MSAT, Scientist, Engineer

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