Product Test Engineer - Req Instron Mechanical Testing & Medical Device Industry Exp

Product Test Engineer - Req Instron Mechanical Testing & Medical Device Industry Exp

Join to apply for the Product Test Engineer – Req Instron Mechanical Testing & Medical Device Industry Exp role at Millennium Soft Inc
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Location: Franklin Lakes, NJ
Duration: 12 Months
Total Hours/week: 40.00
Shift: 1st Shift
Client: Medical Devices Company
Job Category: Engineering/Technical
Level of

Experience:

Entry Level
Employment Type: Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

• The primary role of the Combination Product Test Engineer is the timely and accurate execution of testing as scoped within individual projects and per client requirements.
• This includes but is not limited to sample receipt, prep, storage, and shipping, as well as protocol and report generation, data review and summary.
• This role utilizes standard and custom laboratory equipment.

• Conducts timely sample intake, including receipt, proper identification, storage and return shipments as needed.
• Conducts testing as assigned utilizing appropriate test methods, protocols, specifications and equipment (includes product and/or equipment testing), including adhering to test schedules (e.g. stability pulls, aging pulls).
• Conducts data analysis as per protocol or specifications utilizing a variety of data analysis tools (e.g. Excel, JMP, Mini Tab).
• Communicates challenges, scheduling or testing conflicts and other issues to management in a timely manner.
• Maintains inventory of lab supplies, including but not limited to general supplies (e.g. PPE, wipes, cleaners…) and chemicals used for routine testing and/or cleaning.
• Conducts routine sample disposition (e.g. return to client, disposal), including coordination of hazardous waste disposal.
• Responsible for maintaining the lab and storage areas in a clean and organized manner, including routine lab cleaning and housekeeping.
• Adheres to Zebra Sci Quality Systems, including but not limited to timely identification and notification of potential quality events (e.g. OOS, deviations, CAPA) and the subsequent forward processing and investigation of such events.
• Follows established standard operating procedures, makes recommendations for edits, enhancements, and/or new procedures.
• Reviews and may draft equipment or other lab documents (e.g. SLP, LWIs) under supervision from lab management.
• Reviews test results, including data analysis and draft reports.
• Interacts with clients to provide updates and technical overviews as needed under supervision from lab management.
• Reviews and may author test methods/protocols/reports under supervision from lab management.
• Works and communicates openly, collaboratively, and respectfully with colleagues and staff.
• Communicates with clients under supervision from lab management.

• Associates degree with 0-2 years of experience.
• A combination of education and experience in laboratory services, medical device, IVD and/or pharmaceutical industry, preferably in a contract testing and/or laboratory environment will be considered.
• Knowledge of GLP, cGMP, ISO, and ASTM methodologies beneficial. Technical written/oral communication skills with working knowledge of Excel and other data analysis tools required.
• Attention to detail with the ability to multi-task in a fast‑paced environment and manage changing priorities while effectively communicating across the organization.