We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Director, Assay Development

Werfen
United States, California, San Diego
Aug 27, 2025
Job Information
Number
ICIMS-2025-9293
Job function
R&D
Job type
Full-time
Location
San Diego - AID - 9900 Old Grove Road San Diego, California 92131-1638 United States
Country
United States
Shift
1st

About the Position
Introduction

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.

Overview

Job Summary

The Director of Assay Development, within Autoimmunity's (AID) Research & Development function, oversees the entire reagent lifecycle of assay development, from concept through commercialization and on-market support. Position is responsible for designing, validating, and optimizing autoimmunity-based assays, ensuring they meet the highest standards of performance and regulatory compliance. This role requires deep knowledge of autoimmunity, biotechnology, quality & regulatory requirements, strategic leadership, and excellence in developing management staff and high performing teams. As a senior member of the R&D leadership team, this position is responsible for overall management and leadership of Autoimmunity's assay development business planning and operations management. Ensure all work is carried out in accordance with the Autoimmunity's Quality Management System.

Responsibilities

Key Accountabilities

Leadership and Team Management:

  • Develops and provides strategic direction to AID's assay development team, fostering a culture of collaboration, innovation, and continuous improvement.
  • Ensures effective management and collaboration of internal staff, external collaborators, and third-party vendors to lead the successful design, development and optimization of assays.
  • Mentors and develops people managers and individual contributors, instilling excellence in bench skills, scientific thought, technical writing, and project management.
  • Role models Werfen Values in the quality of work and working relationships. Strategic Planning:
  • Serves as the subject matter expert for assay design and development for Autoimmunity, advising senior leadership on strategic initiatives to enhance assay products and services.
  • Collaborates with Marketing, Quality Systems, Product Management and other stakeholders to define assay development goals and roadmaps that align with overall business objectives.

Assay Design, Development and On-Market Support:

  • Leads the design and optimization of autoimmunity-based assays, to ensure high quality products, scientific procedures, quality standards and efficient business practices.
  • Ensures assay development is conducted with rigorous adherence to Design Control practices, following Autoimmunity's Quality Management System (QMS).
  • Ensures thorough documentation of development processes, experimental results, and data analyses to support internal decision-making and regulatory submissions.
  • Ensures robostness of assays and facilitates design transfer to other departments including, but not limited to Manufacturing, Qualty Systems, Regulatory Affairs and Marketing.
  • Leads on-market efforts for escalated complaints and analyzes need to design changes through the product change request (PCR) process.
  • Serves as the R&D representative on core teams. Where appropriate, acts as the core team leader on product development projects.

Technical Excellence and Innovation:

  • Stays abreast of emerging technologies and industry trends in autoimmunity diagnostics to drive innovation and continuous improvement in assay development.
  • Partners with the Quality team to establish and maintain robust quality systems and standard operating procedures ensuring the highest standards of assay performance and reliability.
  • Fosters partnerships with external collaborators, academic institutions, and industry experts to enhance Werfen's assay development capabilities.

Resource Management:

  • Plans, presents and manages department budgets, resource allocation, and project timelines to optimize leadership of AID's assay development business.
  • Recruits, onboards, and retains top-tier talent, building a strong and dynamic team committed to advancing Werfen's purpose of Powering Patient Care.
  • Responsible for workforce planning to ensure positions and teams are structured to optimize resources and achieve company goals.
  • Ensures staff comply with applicable Standard Operating Procedures (SOPs), Work Instructions (WIs), Standard Work (SW), Quality Management System (QMS) regulations, as well as Environmental Health & Safety (EHS), Human Resources and other regulatory and company policies.

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.Networking/Key Relationships

  • AID R&D teams
  • AID Quality, Regulatory & Compliance teams
  • AID Marketing & Service teams
  • AID Manufacturing teams
  • AID Finance team
Qualifications

Minimum Education & Experience

Education:

  • Master's degree in biological or related science required, Ph.D. degree highly preferred.

Experience:

  • 10+ years' experience leading assay development businesses in an IVD or autoimmunity regulated medical device environment required.
  • 5+ years in a senior leadership position, including strategic planning, product development and developing high performing management teams required.
  • Experience in autoimmunity-related diagnostic platforms such as ELISA, indirect immunofluorescence, chemiluminescence immunoasssys and multi-analyte technologies strongly preferred.
  • Proven track record of taking medical device products from concept through development and successful commercialization.

Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement.

Skills & Capabilities

  • Understanding of design controls, quality system regulation and relevant regulatory requirements for the design, development and commercialization of diagnostic technologies and products.
  • Experience developing budget proposals and managing to multiple budgets.
  • Ability to analyze and interpret scientific data, technical journals, financial reports, government regulations and legal documents required.
  • Financial acumen and aptitude (P&L, ROI, NPV, etc.) required.
  • Demonstrated experience and a track record of success in leading high performing management teams required.
  • Innovative mindset, unafraid to champion new ideas and technologies.
  • Exceptional attention to detail and ability to perform under changing circumstances and environments.
  • Superior communication, analytical and problem-solving skills.
  • Ability to anticipate challenges and opportunities and gain alignment throughout the organization to drive organizational strategy.
  • Ability to provide strong technical product and project leadership.
  • Ability to develop and execute an effective, action-oriented plan.

Travel Requirements10-20% travel, including international travel.

Work Environment:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to communicate. Must be able to detect, identify and inspect scientific data. The employee will be required to stand and/or walk up to 8 hours per day and/or sit for up to 8 hours per day. Must be able to use hands to feel objects, including keyboard, telephone and pipettes or other lab equipment. May need to reach with hands and arms, climb stairs, balance, stoop, kneel or crouch. Will be required to talk and hear and have specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. May occasionally have to lift and/or move up to 25 pounds. The noise level in the work environment will vary but is usually moderate.

Other Duties and Acknowledgement:

The above statements are intended to describe the general nature and level of work being performed by the incumbent. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of this position. Note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. This job description does not constitute or contain a contract or employment promise of any kind. Nothing contained herein modifies the at-will nature of employment with Werfen.

The salary range for this position is currently $175,000 - $225,000. Individual compensation is based on the candidate's qualifications for the position, including experience, skills, knowledge, education, certifications, internal equity, budget and/or other business and organizational needs.

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

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

Apply Now
Applied = 0

(web-5cf844c5d-tthkl)