| Hiring- C2C contract-Bio and Materials development Engineer-Blue Ash - OH. 100% Onsite at Remote, Remote, USA |
| Email: [email protected] |
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Hi Hope you are doing well! My name is Javid, and I am a Senior Technical Recruiter with MindPro Solutions Inc. Please review the job description below and share your updated resume and employer details if you find the position suitable. Role: Bio and Materials development Engineer Type: Contract Location: Blue Ash - OH. 100% Onsite Duration: Long term contract Job description: Quality review of Spec Engineering documentation (processes, specifications, etc.) for accuracy of content, formatting, and spelling/grammar. Maintain metrics on document rework and reason Draft and review documentation related to procedures, special instruction, reports, and standards/gap assessments or Polymer SME review for WE001156 updates Convert the supplier names from existing supplier and split specification when multiple material are identified on a single specification Update / standardize reference standards and transfer them to WE001156 and Rename specification per WE0138 guidelines Find out the linked drawings or documents with existing material specification and link with updated material specification Facilitate document management and material specific engineering changes Update iMOE database with material and biocompatibility data (e.g., medical grade, sustainable grade, sterilization documentation, chemicals, risk assessments, etc.) Product development support including support to regulatory team to provide documentation for approval process. Strong Knowledge about Biocom process. Gather supporting document for specification updates (e.g., COA/COC, SDS, etc.) for WE0138 process execution or regulatory requests (e.g., submissions, tenders) Process the changes through the system per CP0150 (e.g., CRs, CNs, Mod Code listings) Preparation and quality review of biocompatibility documentation for EES R&D Biocompatibility Digitization/archival of biocompatibility files iMOE database updates to archive and integrate evaluation and chemical data. Mechanical Design (Medical Device) and development services Mechanical Engineering Material using medical grade plastics services Design and development of Buyers product and process development that meets product requirements Develop verification and validation strategies for end-to-end product validation Top Skills: Materials engineering experience, Biomaterials and its process for using it in the Medical device design & development. **Additional Details provided by HM** Evaluating medical device products for safety per internal procedures, US and international regulations, and the ISO 10993 Standard series. Assisting in the design and implementation of biocompatibility testing systems and procedures for Ethicon and across the Johnson & Johnson Medical Device sector. Ensuring appropriate documentation is established and maintained to support that the biocompatibility and toxicity testing meets all US and international test requirements per ISO, FDA (US Food and Drug Administration), and GLPs (good laboratory practices). Coordinating, designing, implementing, and analyzing testing systems, procedures and test results for biocompatibility / toxicology evaluations and in vivo / in vitro studies. Reviewing, interpreting, and summarizing toxicological and material chemistry raw data from reports. Applying technical expertise to solve complex biocompatibility problems, utilizing ingenuity and business experience. Serving as the sponsor for applicable GLP / non-GLP biocompatibility studies per current, global regulatory and compliance requirements. Thanks & Regards Javid Ahmad Sr Technical Recruiter MindPro Solutions Inc E: [email protected] L: linkedin.com/in/javid-ahmad-598111158 W: www.mindprosolutions.com Keywords: access management rlang information technology Ohio Hiring- C2C contract-Bio and Materials development Engineer-Blue Ash - OH. 100% Onsite [email protected] |
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| 03:03 AM 05-Mar-25 |