Scientist II, R&D

WerfenSan Diego, CA
$80,000 - $100,000Onsite

About The Position

The Scientist II within R&D will work on an array of complex and novel assignments in new product development, life cycle management, and sustaining initiatives to support our Patient Blood Management (PBM) product line within Point-of-Care Hemostasis. The Scientist II will contribute to R&D activities to advance our diagnostic product portfolio, from feasibility to validation, by applying technical expertise in assay design, execution, and problem-solving, using the highest standards of quality and performance.

Requirements

  • Bachelor’s degree, or equivalent.
  • Minimum of three (3) years of previous experience required.
  • Must possess extensive diversified knowledge of engineering/scientific principles.
  • Must be able to work with advanced techniques, to modify and/or extend theory and practices.
  • Excellent technical writing and documentation, communication, interpersonal, analytical, and presentation skills are essential.
  • Computer literacy required; knowledge of basic software tools (Excel, Word, PowerPoint, Teams).
  • Scientific knowledge and application.
  • Understanding of program/department objectives, critical issues, and new concepts and able to meet the objectives according to timelines.
  • Ability to complete assignments and document results, using good documentation practices for internal records and regulatory submissions.
  • Structure and logic of project plans.

Nice To Haves

  • medical device industry and/or whole blood hemostasis experience preferred.
  • Knowledge of SAP and statistical software packages preferred.
  • Familiarity with Design of Experiments (DOE) and Design for Six Sigma (DFSS) tools in the product development process preferred.
  • Flexibility and creative thinking to problem solve and develop products are essential.

Responsibilities

  • Coordinate and complete research and development assignments; make sound technical judgments and suggestions.
  • Schedule and prepare work in relation to general program schedule.
  • Complete assignments on time and within budgetary limitations.
  • Test and evaluate work; confer with senior staff and manager, as needed.
  • Prepare technical reports and documentation.
  • Provide recommendations for new product development and see them through to completion.
  • Maintain accurate in-depth knowledge of the scientific principles; keep current on new industry developments.
  • Contribute to scientific discussions pertinent to the Company’s products and development goals.
  • Prepare scientific reports for publications in peer reviewed journals.
  • Provide technical support to Manufacturing, primarily through analytical testing in support of Validation and Verification activities.
  • Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures, and processes.
  • Other duties and/or projects as assigned.

Benefits

  • medical, dental, and vision insurance
  • 401k plan retirement benefits with an employer match
  • paid vacation and sick leave
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