Scientist II, R&D

Werfen

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.

Position Summary

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.

The annual base salary range for this role is currently $80,000 to $100,000. This is a bonus-eligible position. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.

This role is eligible for medical, dental, and vision insurance, 401k plan retirement benefits with an employer match, as well as paid vacation and sick leave.

Key Accountabilities

Essential Functions:

• 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.

Networking/Key Relationships:

• To be determined based on department needs

Minimum Knowledge & Experience Required for the Position

• Bachelor's degree, or equivalent.
• Minimum of three (3) years of previous experience required; medical device industry and/or whole blood hemostasis experience preferred.

Skills & Capabilities

• 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). 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.
• 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.

Travel requirementsNo travel required.

If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.

Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.

We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.

www.werfen.com