Scientist , Chemistry

Position Summary

Primary focus of this position is to support the development, optimization, implementation, and validation of components and elements of a medical device. The candidate will perform hands‑on testing, conduct process development activities to understand process inputs and outputs, assist/write technical documents, validation protocols and reports, prepare work instructions and standard operating procedures, and support equipment development. The role will also involve data analysis and simulations, and collaboration across R&D, Quality, Operations, and Regulatory Affairs.

• Design components of a medical device, translating design inputs into engineering specifications and drawings, selecting materials, processes, and vendors, and validating designs against standards and clinical scenarios.
• Assist in the development and optimization of processes, using statistical methods such as DOE, and support new process equipment and tooling development.
• Prepare work instructions, SOPs, technical documents, and reports; assist in the preparation of verification and validation protocols and reports.
• Develop new engineering and clinically relevant test methods, and assist in their validation.
• Perform lab bench and analytical testing, conduct engineering and competitor evaluations, unit testing, and verify and validate activities.
• Train technicians and operators on new designs, processes, and test methods; conduct training with operations and quality assurance.

• Support Manufacturing, Quality, Regulatory, and R&D to ensure system compliance with internal and external guidelines.
• Assist in design and process root cause analysis and support non‑conforming product and complaint investigations.

• B.S. or M.S. in chemistry, biomedical engineering, chemical engineering, or a related scientific discipline.
• 1–3 years of industrial experience in R&D or process development, preferably in a medical device or regulated FDA/QSR and ISO environment.
• Hands‑on technical aptitude and excellent oral and written communication skills.
• Ability to work in cross‑functional teams and think creatively through interpretation of patents, technical papers, and clinical literature.
• Skilled in polymer science, physical chemistry, or colloidal chemistry.
• Know‑how in surfactants and formulation technologies (granulation, emulsion, encapsulation).
• Knowledge of characterization test methods for nanoemulsion (DLS particle sizing and zeta potential).
• Mechanical aptitude and knowledge of engineering principles.
• Experience transferring products from lab to manufacturing scale.
• Demonstrated record of achievement in formulation research and development from discovery to commercialization.

• Proficiency in statistical software for data analysis and report writing.
• Knowledge of cGMP and GLP practices.

The employee regularly stands, walks, sits, uses sight and hands to manipulate tools and equipment, and communicates verbally with associates. Occasional reaching, stooping, kneeling, or crouching may be required.

Employees may work in an open cubicle office and must be able to thrive in a team‑oriented, fast‑paced setting. Occasional work may be required in preclinical labs, cadaver labs, or clinical case observations.

BD is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.