Research and Development Engineer I/II

Cresilon • Brooklyn, NY

7d • $70,000 - $120,000 • Onsite

About The Position

Cresilon ® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company’s proprietary hydrogel technology. The company’s plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. The company's current and future product lines target veterinary, human trauma, and human surgical applications. Cresilon's mission is to save lives. Learn more about the company at www.cresilon.com. Description: The R&D Engineer I/II is responsible for supporting product design and process development activities while ensuring compliance with all quality and regulatory requirements. The position has a scientific focus that includes implementation of formulation development through process development, prototype fabrication, and characterization, along with additional process evaluation and data generation through designed experiments. Process development in an R&D environment will be followed by qualification and technology transfer into manufacturing. Collaboration is a key aspect of this role, as the engineer will work within a multidisciplinary team of researchers and engineers. The position offers diverse opportunities in a collaborative cross-functional environment, requiring adaptability, flexibility, and a willingness to learn and innovate in the exploration of new technologies, new approaches, and techniques in pursuit of product/process robustness and innovation. The R&D Engineer I/II is expected to possess expertise in areas including, but not restricted to, polymer, chemical, material science, and process development and engineering. Additionally, they will assist in generating documentation essential for regulatory submissions, ongoing publication initiatives, and direct communication with the Head of Research regarding various tasks. This is a full-time, on-site position, located in Brooklyn, New York. This role is an independent contributor role (i.e. no direct reports). Level is dependent on experience.

Requirements

• BS in Chemical Engineering, Polymer Engineering, Material Science & Engineering, or related engineering discipline.
• Minimum 4+ years previous experience in an industrial environment with a BS degree. (2 years minimum experience if advanced degrees).
• Proficiency as an adept experimentalist with hands-on experience in the product and process development of polymeric materials and their characterization in an R&D or manufacturing environment.
• Mathematically inclined with strong analytical and problem-solving skills with the ability to be observant and to think creatively.
• Demonstrated ability to design experiments and analyze data with the use of appropriate quality and statistical methodologies.
• Demonstrated ability to work independently as well as be a strong team contributor.
• Ability to effectively work within a team and cross-functionally to expedite the completion of critical project tasks.
• Requires understanding of product/process design and engineering. Experience should include process development/validation and/or transfer/verification, protocols, and troubleshooting skills.
• Ability to handle multiple project assignments of medium scope and complexity and able to prioritize and complete work with a sense of urgency on time.
• Ability to lead directly and by influence, including strong problem-solving, conflict resolution, and analytical skills.
• Working knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (cGMP) requirements.
• Proficiency in the use of Microsoft Office, Microsoft Excel, Microsoft Word, Microsoft PowerPoint is required.
• Requires excellent written and verbal communication and presentation skills.
• Legal authorization to work in the United States is required.
• Aseptic Gowning Qualification: Able to be successfully qualified for aseptic gowning, including successful respirator training.
• Wear Appropriate Personal Protective Equipment (PPE): Be able to stand and walk for prolonged periods, with the ability to climb, balance, stoop, bend, reach, and handle equipment.
• Ability to speak, listen, and understand verbal and written communication.
• Possesses hand-eye coordination and manual dexterity for delicate manipulations.
• Ability to lift up to 50 pounds occasionally and to carry, push, pull, or otherwise move objects.
• Visual acuity is required for performing close and distant activities.

Nice To Haves

• An advanced technical degree (MS or PhD).
• Lab experience in an industry setting within cGMP-regulated environments.
• Prior experience developing processes and scaling these up into manufacturing or CDMO
• Mechanical/electrical knowledge with the ability to troubleshoot processing equipment
• Six Sigma green belt or black belt certification preferred.
• Experience implementing process and quality improvements in a manufacturing environment
• Work experience with the medical device or pharmaceutical industries
• Working knowledge of ISO 9001, ISO 13485:2003 and ISO 14971:200.
• Working knowledge of FDA requirements as per 21 CFR 820.

Responsibilities

• Oversee the planning, implementation, and analysis of experiments relevant to project objectives.
• Ensure the application of established scientific and engineering principles to solve complex problems and challenges innovatively and efficiently, adhering to rigorous scientific methodologies and protocols.
• Create and execute product/process enhancement, and new product/process development plans.
• Lead material/design/process changes and their implementation with well-documented research/analyses.
• Process and analyze results, Author protocols and reports including engineering studies and design verification/validation activities.
• Aid in the development and execution of testing methods to aid in exploratory research, product/process development, and quality control; conduct chemical and mechanical property evaluation tests to assess the desirability of process or formulation changes.
• Prepare samples as required for manufacturing, testing, or other evaluations and data analysis.
• Participate in voice-of-customer (VOC) labs and other user needs assessments.
• Interface with external vendors, customers, and suppliers.
• Specify equipment and process requirements for developing and implementing new products, product improvement and new equipment/processes.
• Support process and product transfers to manufacturing or CDMOs.
• Maintain a laboratory notebook and other technical documentation according to required GLP/GMP guidelines.
• Understand and prioritize process improvements, design experiments to make those improvements, and execute these plans in the laboratory.
• Maintain active dialogue with Regulatory Affairs as subject matter expert on all product design elements/documentation about research towards FDA/regulated authority submissions.
• Provide support to the marketing and sales team, with the development of presentations, sales tools, and application data.
• Work with company leadership to evaluate existing research practices and contribute to a culture of ethical, high-quality research operations within the organization.
• Provide other project or product support as needed to support Cresilon’s business objectives.

Benefits

• Competitive annual base salary range of $70,000 - $120,000, depending upon job level and qualifications
• Paid Vacation, Sick, & Holidays
• Monthly MetroCard Reimbursement
• 401(k) & Roth Retirement Savings Plan with company match up to 5%
• Work/Life Employee Assistance Program
• Company Paid Life and Short-Term Disability Coverage
• Medical, Dental, and Vision Insurance, FSA: Dependent & Healthcare, Commuter & Parking Benefits, Long Term Disability Coverage

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 101-250 employees