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Job Title: Research Chemist (Medical Device)

Job Description:

+ The R&D Chemist plays a key role in advancing innovative medical devices based on regenerative technologies.

+ This position combines hands-on laboratory research with product development responsibilities, including experimental design, material characterization, prototype development, and compliance with design control requirements.

+ The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing.

+ This role bridges early discovery and applied development, requiring both strong scientific skills and practical problem-solving.

Responsibilities:

+ Plan, execute, and analyze laboratory experiments involving biomaterials, regenerative matrices, and medical device components.

+ Contribute innovative ideas for new products, testing methods, or process improvements to enhance R&D capabilities.

+ Develop, build, and refine prototypes to meet defined specifications and clinical needs.

+ Generate accurate technical documentation, reports, and protocols in compliance with FDA and Control requirements.

+ Characterize materials and prototypes using analytical, biochemical, and mechanical testing methods.

+ Perform risk assessments, troubleshoot technical issues, and propose solutions to improve product performance or process robustness.

+ Support technology transfer from R&D to manufacturing, including process documentation, validation support, and training of personnel.

+ Collaborate with cross-functional teams (Manufacturing, Quality, Regulatory, Marketing, and Clinical) to align product development with business and clinical requirements.

+ Engage with external consultants and customers to gather feedback and translate needs into product features.

+ Mentor and provide technical guidance to junior staff on laboratory practices, data analysis, and project tasks.

+ Present findings and project updates to management, peers, and cross-functional stakeholders.

+ Maintain laboratory operations, including equipment calibration, safety compliance, and method updates.

Essential Skills:

+ Strong proficiency in laboratory research and development.

+ Expertise in biomaterials, regenerative technologies, or medical device research and development.

+ Knowledge of laboratory techniques for material characterization, tissue-derived biomaterials, or device testing.

+ Familiarity with Design Controls, GLP/GMP, and industry standards.

+ Proficiency in experimental design, data/statistical analysis, and technical problem-solving.

+ Strong organizational skills with the ability to manage multiple studies and projects simultaneously.

+ Excellent communication and presentation skills for cross-functional collaboration.

+ Demonstrated ability to work independently, manage multiple priorities, and deliver high-quality results.

Additional Skills & Qualifications:

+ MS with 1–2 years or BS with 3–5 years in Biomedical Science, Materials Science, Chemistry, or related field.

+ Experience with CAD or modeling software is a plus.

Work Environment

The role involves working within a team of one other Scientist and three Engineers in a GMP environment. The position requires collaboration with a cross-functional team and adherence to safety and operational standards.

Job Type & Location

This is a Permanent position based out of Paramus, New Jersey.

Pay and Benefits

The pay range for this position is $85000.00 - $95000.00/yr.

Great benefits / medical benefits start 1st day, 401k requiring no employee contribution, frequent employee activities

Workplace Type

This is a fully onsite position in Paramus,NJ.

Application Deadline

This position is anticipated to close on Oct 16, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.