Hi
Hope you are doing great. This is Neha from Deegit Inc. Please go through the below job description and please let me know if you are interested. Job Description - 1 *Below is the job details:* *Job Role: R and D Engineer III* *Location: Plymouth, MN* *Duration: 6+ Months* *Senior Process Development Engineer* *Job Description:* · Plans and coordinates the execution of process characterization and validation · Successfully complete all the Process Development Engineering elements of the PDP by the milestone dates · Work with drafting and documentation departments to create all required documents (manufacturing processes, drawings, protocols, reports, etc.) · Ensures process capability and yield targets are met · Provide mentoring and direction to more junior technical staff · Hands-on development of manufacturing processes · Present status of plans and projects to larger team. · Develop requirements and procure equipment for manufacturing processes · Lead small team(s) for process development or problem solving Minimum Qualifications · BS degree (Mechanical, or related technical field) with 5 years’ experience · Good verbal and written communication skills · Good presentation skills · Leadership and self-starter qualities · Experience developing and validating medical device manufacturing processes (IQ, OQ, PQ, and PPQ) · Working knowledge of PFMECAs, sampling plans, normality assessment, and capability assessment · Process validation protocol and report writing · Demonstrated problem solving skills · History of successfully transfering projects to manufacturing · Excel and Word skills Preferred Qualifications · MS degree (Mechanical, or related technical field) with 10 years’ experience · Six Sigma training; Minitab and Design Expert skills (DOE and other statistical analysis) · Stent or balloon catheter manufacturing experience · Experience with polymer extrusion, thermal bonding, and adhesive bonding Job Description -2 *Below is the job details:* *Job Role: Systems Engineer* *Location: Fridley, MN* *Duration: 6+ Months* *Job Description:* *POSITION RESPONSIBILITIES:* • Plans and schedules integration and test efforts for all assigned projects and monitors progress to schedule. • Influence product/component integration and test plans in order to assist in incremental system maturity. Works with engineers in various departments to achieve results. • Create maturity strategy and plan. Lead/execute system integration, verification, and validation activities. • Lead/execute system characterization efforts. Align characterization efforts with need to understand design capability. • Assures activities comply per relevant SOP. • Understand use conditions and help establish or review system requirements to assure adequacy and testability of requirements relative to those use conditions. More broadly, participate as a reviewer of requirements and design to understand/determine test method. • Plan and execute test method validation. • Perform regression, HALT/HAST testing as required. • Identify opportunities for test automation. • Prepare data summary reports and other relevant inputs for submission by Regulatory Affairs to regulatory agencies in support of market release review and approval. *BASIC QUALIFICATIONS:* • 2+ years of job-related experience with a Bachelor’s degree; or a Master’s *DESIRED/PREFERRED QUALIFICATIONS:* • Bachelor's or Master's Degree in Biomedical Engineering, Systems Engineering, Electrical Engineering, Computer Science, Reliability Engineering, or Mathematics. • Experience in engineering and testing mission critical systems and/or medical device systems. • Experience working to and with detailed requirements and traceability. • Demonstrated experience developing test plan/protocols (e.g. N-square interface matrices or equivalent) for interface testing, use-case testing, stress testing, characterization, design verification, design validation. • Experience working in cross-functional team effort. • Demonstrated strong verbal/written communication and influence management skills. • Proven ability to accomplish critical project level objectives in a team environment. • Experience working with DRM, DMAIC, DMODV or DFSS principles. • Experience working in a regulated and/or FDA medical device environment. Experience working with ISO and Quality System Regulation requirements. *PHYSICAL JOB REQUIREMENTS:* • The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Ability to work for extended periods of time at a computer. • Ability to sit/stand/bend for up to 8 hours a day. Best Regards, Neha Srigadi | Technical Recruiter [image: Description: Description: cid:[email protected]] *DeegitTM Inc* | Technology Consulting 1900 E Golf Rd., Suite 925 | Schaumburg, IL 60173 *Phone* (847) 440 2436 Ext. 368 *Email* [email protected] [image: Description: Description: cid:[email protected]] www.deegit.com [image: Description: Description: cid:[email protected]] The information transmitted is intended only for the person or entity to which it is addressed and may contain confidential and/or privileged material. Any review, retransmission, dissemination or other use of, or taking of any action in reliance upon this information by persons or entities other than the intended recipient is prohibited. If you received this in error, please contact the sender and delete the material from any computer. -- You received this message because you are subscribed to the Google Groups "Exact Match" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/exact-match. For more options, visit https://groups.google.com/d/optout.
