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SENIOR LAB SCIENTIST

Interfuse Staffing

SENIOR LAB SCIENTIST

Irvine, CA
Full Time
Paid
  • Responsibilities

    The Sr. Lab Scientist - Product Development Specialist, will work in the lab on development of

    diagnostic assays as well as support commercialization activities for our client’s proprietary

    diagnostic assays and assays developed for external clients. This role will work closely and

    collaboratively with the Vice President of Development on the development of single and

    multiplexed point of care assays. Depending on experience, this roll may include lead a team of

    1-3 individuals for specialized projects.

    Our client a public company and offer salary, stock and great

    benefits.

    REQUIREMENTS

    • Master’s or PhD degree in chemistry, biochemistry, bioengineering, or a related field

    • 5+ years of experience in immunoassay development

    • Demonstrated track record of solving challenging issues with assay design and development

    • Excellent organizational and project management capabilities to facilitate internal and external

    scientific interactions

    • Experience managing direct reports

    • Excellent verbal and written communication skills for generating high-quality proposals,

    presentations, and reports for internal and external stakeholders.

    • Effective at communicating issues and proposes and implementing solutions

    • Ability to manage multiple projects and rapidly learn new techniques and approaches.

    • Ability to work effectively in a cross-disciplinary environment.

    • Strong Microsoft office skills (Excel, Word, PowerPoint)

    DESIRED SKILLS

    • Demonstrated track record of bringing point-of-care diagnostics from feasibility through

    transfer to manufacturing

    • Direct, hands-on experience generating analytical assay development, optimization, and

    validation data packages in accordance with regulatory requirements

    • Previous experience with ELISAs, antibody conjugation, protein purification, and fluorescent

    labeling

    • Experience with cGMP / ISO 13485 compliant quality systems and the 510k approval process

    • Drafting and release of standard operating procedures and batch production records

    • Highly motivated and innovative problem solver able to independently design, execute,

    troubleshoot, and interpret experiments within a co-operative matrixed team environment.

    Employment Type: -

    Full-time