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Biocompatibility Coordinator
Blue Ash, OH, US
Scientific
Bachelors Degree
Full Time, Temporary
37.00
Experienced (Non-Manager)
On-site
Medical Devices and Supplies
First Shift (Day)
Blue Ash, OH, US
37.00
Experienced (Non-Manager)
Full Time, Temporary
Medical Devices and Supplies
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
At Kelly® Science, Engineering, Technology & Telecom (SETT), we’re passionate about helping you find a job that works for you. We’re hiring a Biocompatibility Coordinator for a long-term opportunity in Blue Ash, Ohio. With us, it’s all about finding the job that’s just right.
Biocompatibility Coordinator
Blue Ash, Ohio
Mon – Fri 8am-5pm (Hybrid) 3 days on site/2 days remote
Hourly Rate: $37/hr W2
Long-term engagement at one of our Global medical device clients. The role is eligible for medical benefits, paid time off including vacation (PTO), and holidays, 401K, and annual performance reviews.
Responsibilities
- Manage incoming R&D Biocompatibility requests for SME support for Regulatory, external standards and guidance, audits, and material selection and evaluations via the R&D Biocompatibility mailbox.
- Capture and report on R&D Biocompatibility metrics and resource mapping.
- Coordinate interactions with external partners to support R&D Biocompatibility initiatives and processes.
- Act a key source and point of contact of R&D Biocompatibility SME input for design changes, including potential future changes, and SPCRs.
- Project management of design changes, associated milestones, and identification and mitigation of timing challenges to meet the schedules of critical business projects.
- Assist toxicologists by preparing risk assessments and quarterly implant testing documentation.
- Develop R&D Biocompatibility procedures to streamline and increase the efficiency of processes.
- Become an expert in R&D Biocompatibility practices by supporting other group members as needed.
Qualifications
- The ideal candidate should have a background in engineering, materials or biomedical related area.
- Bachelor’s degree in Material Engineering or Material Science is preferred.
- Experience with medical device/pharmaceutical industry is preferred.
- Familiarity with ISO 10993, FDA 21 CFR Part820, and ISO 13485 is preferred.
- Knowledge of manufacturing processes (injection molding, cleaning, machining, etc.) and experience with engineering drawings is preferred.
- Must possess solid communication skills as they will be interacting with internal and external customers.
- Must possess solid collaboration skills and be able to work in a team environment.
- Work independently with little to no supervision and have initiative to drive projects forward.
- Able to work on a variety of projects and shift priorities as needed.
- Able to prioritize, organize, and plan with adherence to deadlines, and communicate any deadline obstacles in a timely manner.
- Attention to detail and organization of data with high degree of confidentiality.
- Able to follow procedures with accuracy and precision, including a sequence of tasks.
- Able to ask questions, present different options in group consultation, and accept reinstruction on tasks.
- Computer skills required –Windows, MS Office (with an emphasis on Excel and Word).
What happens next
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
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