Associate Engineer, Device Development

South San Francisco, CA 94080

Posted: 06/02/2020 Employment Type: Contract Industry: Clinical & Scientific Job Number: 17534

Job Description

Bayside Solutions is seeking a Associate Engineer, Device Development to be part of our client’ s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at

Associate Engineer, Device Development

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Product Testing and Design Verification
  • Execute GMP Testing Protocols (Design Verification, Test Method Validation, and Complaints Investigations) using knowledge of Design Requirements, Validated Test Methods, and analytical instruments.
  • Record GMP Data in Laboratory Notebook and Document Control systems Review GMP data for technical accuracy, completeness, and cGDP compliance.
  • Execute R&D / characterization testing or special Test Requests as needed to support the development and selection of device designs, components, test methods or operating procedures.
  • Collection of mechanical testing data to aid in the characterization, selection, Design Verification, and commercialization of drug delivery devices.

Summary of Qualifications:
  • BS/BA in an engineering or life sciences field (mechanical, biological, biomedical, chemical)
  • 0-2 yrs of experience in the Pharmaceutical, Biotech, or Medical Device industry or an equivalently-regulated research/development environment (e.g. ISO compliant) is required.
  • Experience in R&D and GMP environments is desired, and an understanding of the differences between these environments is critical.
  • Direct experience in executing physical/functional Test Methods and following SOPs / Protocols is highly desired.
  • Familiarity with tensile/torque testing systems is highly desired (Instron, Zwick, Mecmesin).
  • Familiarity with dimensional analysis/metrology equipment is highly desired (Microscopes, Gages, Calipers, Vertex).
  • Familiarity with Operational Excellence Initiatives, Lean Six Sigma, 5S, Kaizen, and/or Value Stream Mapping is a plus.

Meet Your Recruiter

Allison Glogovac

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