<p>Job Description (Posting).</p> <p>Job: Biocompatibility and toxicology engineer</p> <p>Location:Waukesha, WI</p> <p>JD:</p> <ul> <li>Support and consult on projects related to biocompatibility issues and challenges to resolve. </li><li>Author biocompatibility strategy and toxicological risk assessment per ISO 10993 - 1, ISO 10993 - 18, ISO 10993 - 17, ISO 18562 - 1, 2, 3, and 4. </li><li>Perform biocompatibility gap analysis and write summary report. </li><li>Review biocompatibility test reports, raw data, and protocols for accuracy, quality, and correctness. </li><li>Familiar with medical devices used in breathing gas pathways (e.g., Incubator, Warmer, Anesthesia systems, etc.) </li></ul> <p>Qualification:</p> <ul> <li>Bachelor's in chemistry, Biology, Pharmacology, Material Science, or related field (or higher) </li><li>At least 3 - 5 years of experience in medical device or pharmaceutical industry or contract research laboratory </li><li>Knowledge of ISO 10993 series of requirements, ISO 18562 series requirements, and FDA guidance for biocompatibility </li><li>Strong time management skills to prioritize, organize, track details, and meet deadline for multiple projects. </li></ul> <p>Job Description (Posting).</p> <p>Job: Biocompatibility and toxicology engineer</p> <p>Location:Waukesha, WI</p> <p>JD:</p> <ul> <li>Support and consult on projects related to biocompatibility issues and challenges to resolve. </li><li>Author biocompatibility strategy and toxicological risk assessment per ISO 10993 - 1, ISO 10993 - 18, ISO 10993 - 17, ISO 18562 - 1, 2, 3, and 4. </li><li>Perform biocompatibility gap analysis and write summary report. </li><li>Review biocompatibility test reports, raw data, and protocols for accuracy, quality, and correctness. </li><li>Familiar with medical devices used in breathing gas pathways (e.g., Incubator, Warmer, Anesthesia systems, etc.) </li></ul> <p>Qualification:</p> <ul> <li>Bachelor's in chemistry, Biology, Pharmacology, Material Science, or related field (or higher) </li><li>At least 3 - 5 years of experience in medical device or pharmaceutical industry or contract research laboratory </li><li>Knowledge of ISO 10993 series of requirements, ISO 18562 series requirements, and FDA guidance for biocompatibility </li><li>Strong time management skills to prioritize, organize, track details, and meet deadline for multiple projects. </li></ul> <p>Job Description (Posting).</p> <p>Job: Biocompatibility and toxicology engineer</p> <p>Location:Waukesha, WI</p> <p>JD:</p> <ul> <li>Support and consult on projects related to biocompatibility issues and challenges to resolve. </li><li>Author biocompatibility strategy and toxicological risk assessment per ISO 10993 - 1, ISO 10993 - 18, ISO 10993 - 17, ISO 18562 - 1, 2, 3, and 4. </li><li>Perform biocompatibility gap analysis and write summary report. </li><li>Review biocompatibility test reports, raw data, and protocols for accuracy, quality, and correctness. </li><li>Familiar with medical devices used in breathing gas pathways (e.g., Incubator, Warmer, Anesthesia systems, etc.) </li></ul> <p>Qualification:</p> <ul> <li>Bachelor's in chemistry, Biology, Pharmacology, Material Science, or related field (or higher) </li><li>At least 3 - 5 years of experience in medical device or pharmaceutical industry or contract research laboratory </li><li>Knowledge of ISO 10993 series of requirements, ISO 18562 series requirements, and FDA guidance for biocompatibility </li><li>Strong time management skills to prioritize, organize, track details, and meet deadline for multiple projects. </li></ul> <p>Job Description (Posting).</p> <p>Job: Biocompatibility and toxicology engineer</p> <p>Location:Waukesha, WI</p> <p>JD:</p> <ul> <li>Support and consult on projects related to biocompatibility issues and challenges to resolve. </li><li>Author biocompatibility strategy and toxicological risk assessment per ISO 10993 - 1, ISO 10993 - 18, ISO 10993 - 17, ISO 18562 - 1, 2, 3, and 4. </li><li>Perform biocompatibility gap analysis and write summary report. </li><li>Review biocompatibility test reports, raw data, and protocols for accuracy, quality, and correctness. </li><li>Familiar with medical devices used in breathing gas pathways (e.g., Incubator, Warmer, Anesthesia systems, etc.) </li></ul> <p>Qualification:</p> <ul> <li>Bachelor's in chemistry, Biology, Pharmacology, Material Science, or related field (or higher) </li><li>At least 3 - 5 years of experience in medical device or pharmaceutical industry or contract research laboratory </li><li>Knowledge of ISO 10993 series of requirements, ISO 18562 series requirements, and FDA guidance for biocompatibility </li><li>Strong time management skills to prioritize, organize, track details, and meet deadline for multiple projects. </li></ul>