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Research Development Scientist/Engineer II Regenity Oakland, NJ Job Details Full-time $85,000 - $95,000 a year 1 day ago Benefits Wellness program AD&D insurance Paid holidays Health insurance Dental insurance 401(k) Tuition reimbursement Paid time off Employee assistance program Vision insurance 401(k) matching Qualifications Developing medical devices Engineering research Research data analysis Materials science Technical writing experience within technology Research & development Cross-functional communication Full Job Description Position Summary/ Objectives The Research and Development Scientist/Engineer II is responsible for the design, development, and improvement of implantable regenerative medical devices from concept through commercialization. This role applies engineering and scientific principles to support product innovation while ensuring compliance with design control and quality system requirements. The ideal candidate combines strong technical expertise with hands-on laboratory and product development experience and is capable of working independently to support both strategic and operational objectives.

Essential Job Functions:

Independently contribute to the development of implantable regenerative medical devices in compliance with design control requirements. Execute and document design control activities, including design inputs/outputs, risk management, verification, validation, and design transfer. Design and conduct experiments, including feasibility studies, prototype fabrication, and characterization. Analyze and interpret experimental and engineering data to support product development decisions. Troubleshoot technical challenges across prototyping, process development, validation, and manufacturing scaleup. Develop and maintain product specifications, test methods, and acceptance criteria. Create and execute experimental protocols, technical reports, and documentation to support verification, validation, and regulatory submissions. Collaborate with Quality, Regulatory, Manufacturing, and external partners to ensure compliance and timely project execution. Support R D equipment calibration and maintenance programs in accordance with quality system requirements. Develop and revise SOPs, work instructions, and technical documentation. Maintain accurate and compliant design history file (DHF) documentation, including lab notebooks, protocols, and reports. Ensure laboratory operations meet safety, organization, and inspectionreadiness standards. Train and support R D personnel on procedures, equipment, and test methods. Contribute to continuous improvement initiatives through established quality and change control processes. Participate in crossfunctional and special projects as needed.

Competencies:

1. Innovation and Scientific Curiosity 2. Ownership and Accountability 3. Execution and Efficiency 4. Collaboration and Teamwork 5. Integrity and Ethical Practice 6. Resilience and adaptability

Education, Experience and Certification:

Bachelor's or Master's degree in Biomedical Engineering, Biological Sciences, Material Science or related field required. Minimum of 3 years of experience with a Bachelor's degree, or minimum of 2 years with a Master's degree, in medical device R D, preferably in regenerative or implantable technologies. Experience with experimental design, material characterization, data analysis, and laboratory techniques. Ability to work independently with minimal supervision while managing multiple priorities. Strong analytical and problemsolving skills with a datadriven approach. Effective collaborator with crossfunctional teams. Strong written and verbal communication skills, including technical documentation Experience with CAD software, prototyping tools or model software is a plus. Ability to work independently with minimal supervision while managing multiple priorities. Strong analytical and problemsolving skills with a datadriven approach. Effective collaborator with crossfunctional teams. Strong written and verbal communication skills, including technical documentation. Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Total Rewards & Benefits:

Regenity offers a comprehensive rewards package, including: Company performance bonus eligibility 401(k) plan with company contribution Paid time off and paid holidays Medical, prescription, dental, and vision insurance Companypaid life and AD&D insurance Wellness Program and Employee Assistance Program (EAP)

Tuition Reimbursement Salary Range:

$85,000-$95,000 per year Regenity Biosciences, Inc. is an Equal Opportunity Employer. We consider applicants for all positions without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, sexual orientation or any other legally protected status. Regenity Biosciences celebrates the diversity of our team. We believe that talent, drive, and experience are the only relevant criteria for considering new team members. About Regenity Collagen Matrix is now Regenity Biosciences. Regenity Biosciences advances new frontiers in regenerative science, turning bioabsorbable materials into life-changing solutions. Sought after for our novel resorbable technologies and distinct approach to contract manufacturing and contract development, our team brings the urgency and vision to deliver breakthrough medtech solutions for medical technology and medical device manufacturers of all sizes. For more than 25 years, Regenity Biosciences has been transforming bioabsorbable materials into regenerative solutions to repair and regenerate tissue and bone we have since introduced numerous bioresorbable technologies with more than 71 product lines commercially available worldwide. Most recently, Regenity expanded its product portfolio to include versatile bioresorbable polymer technologies via the acquisition of Polyganics, which was the impetus behind the new name and brand direction.