The R&D Engineer is responsible for executing scientific and engineering activities related to the development and sustaining of IVF media products. This role focuses on experimental execution, data analysis, technical problem-solving, and change control, contributing to product performance, robustness, and compliance.
The position works cross-functionally to support the translation of scientific concepts into practical, scalable solutions for assisted reproductive technologies (ART), while building technical expertise in media formulation and product development.
Foundational understanding of cell culture, biochemistry, or related life sciences
Knowledge of IVF/ART media development is desirable
Understanding of solution chemistry (pH, buffers, molarity, osmolality)
Familiarity with GMP, ISO, regulatory requirements and regulated environments
Strong analytical and problem-solving skills
Hands-on laboratory and experimental experience
Well organized with attention to detail}
Ability to follow protocols, document work accurately, and manage multiple tasks
Good organizational and time management skills
Effective communication and teamwork skills
As an employee of CooperSurgical, you''ll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck, we offer a great compensation package, medical coverage, 401(k), parental leave, fertility benefits, paid time off for vacation, personal, sick and holidays, and multiple other perks and benefits. Please visit us at www.coopersurgical.com to learn more about CooperSurgical and the benefits of becoming a member of our team.
To all agencies: Please, no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. In the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired, no fee or payment of any kind will be paid.
We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace. If you are interested in applying and require special assistance or accommodations due to a disability, please contact us at talent.acquisition@coopersurgical.com.
Support design, development, validation, and manufacturing of media products
Design and execute experiments using established scientific and statistical principles
Conduct data analysis, interpret results, and document findings effectively
Support scale-up, process development, and technology transfer activities
Perform chemical and engineering analysis of current and new media formulations
Execute prototype preparation, formulation batches, and lab‑scale studies
Collaborate with cross-functional teams (Quality, Regulatory, Manufacturing, Marketing) to support sustaining and lifecycle activities
Support sustaining activities including product improvements, change management, and troubleshooting
Ensure compliance with applicable regulatory and quality standards (GMP, ISO)
Maintain accurate and complete technical documentation in compliance design control requirements
Support the creation, update, and maintenance of Design History Files (DHFs) to ensure alignment with product development and sustaining activities
Contribute to project execution under guidance of senior technical staff
Support design, development, validation, and manufacturing of media products
Design and execute experiments using established scientific and statistical principles
Conduct data analysis, interpret results, and document findings effectively
Support scale-up, process development, and technology transfer activities
Perform chemical and engineering analysis of current and new media formulations
Execute prototype preparation, formulation batches, and lab‑scale studies
Collaborate with cross-functional teams (Quality, Regulatory, Manufacturing, Marketing) to support sustaining and lifecycle activities
Support sustaining activities including product improvements, change management, and troubleshooting
Ensure compliance with applicable regulatory and quality standards (GMP, ISO)
Maintain accurate and complete technical documentation in compliance design control requirements
Support the creation, update, and maintenance of Design History Files (DHFs) to ensure alignment with product development and sustaining activities
Contribute to project execution under guidance of senior technical staff