R&D Engineer II — Medical Device (Onsite — Maple Grove) Contract at Pharmavise Corporation

Maple Grove, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

15 May, 26

Salary

0.0

Posted On

14 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Polymer Science, Research, Development, Material Characterization, Test Method Development, Prototyping, Analytical Chemistry Testing, Data Interpretation, Product Development, Biomaterials, Cardiovascular Implants, Regulatory Compliance, Quality, Manufacturing Science, Technical Expertise, Decision Making

Industry

Business Consulting and Services

Description

Overview: From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp Our F500 Medical Device client has an exciting opportunity for a R&D Engineer III Job Summary: To apply polymer science expertise to research, develop, and optimize polymer-based materials and technologies that enable innovative, high-performance, and manufacturable products to be used for the development of novel cardiovascular implants. Responsibilities: • Design, development and integration of next generation technology to meet customer and market demands in rapidly growing and evolving medical device marketplace. • Material characterization testing and analysis. • Test method development for novel product testing. • Apply scientific and engineering principles to manage and support decision making around key technical issues for the overall system and technical workstreams. • Prototyping and development of concept ideas, processes and tests. • Leverage internal/external partners as necessary to achieve project objectives. • Work cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects. • Document development and analysis by writing documents, reports, memos, change requests. • Solve engineering problems by analyzing the situation and recommend solutions or alternative actions. • Ability to work both independently and in a team setting. Required Qualifications: • BS degree or more from an accredited school in Biomedical Engineering, Chemical Engineering, Materials Science or related field. • 3+ years of engineering experience with a Bachelor’s degree OR 1+ years with Master’s Degree. • New product development experience in implants or cardiovascular products. • Experience in medical device polymers and/or biomaterials. • Experience in analytical chemistry testing and data interpretation. • Experience being a self-starter with a hands-on approach. • Ability to provide technical insights as it relates to product design and leadership. Preferred Qualifications: • Experience in exploratory or early phase product development. • Experience in adhesives, material coatings, and coating techniques. • Experience in managing and supporting technical trade-off decisions to optimize design, performance, usability, manufacturability, cost-efficiency and reliability. • Strong written and verbal communication, judgment, decision-making, and critical thinking skills. • Experience in medical device Product Development Planning (PDP) lifecycle process environment. • Ability to exercise a solution focused and flexible mindset.

Responsibilities

The role involves applying polymer science expertise to research, develop, and optimize polymer-based materials for novel cardiovascular implants. Responsibilities include designing next-generation technology, conducting material characterization testing, developing test methods, and prototyping concepts.