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Medical Device Jobs in Oak Park (IL)

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Search Results - Medical Device Jobs in Oak Park (IL)
Icon Clinical PLC-Oak Park (IL)
related field  •  3-5 years of CRA monitoring experience in CRO/pharma  •  Experience managing complex protocols  •  Medical device experience is a plus but not required  •  Orthopedic experience is a plus but not essential  •  Experience as an CRA with strong...
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Tempus-Oak Park (IL)
Overview In this role you will lead verification, validation, and quality activities for Tempus Medical Device software and AI systems. You’ll drive risk assessments, CSF/HSV/CSV strategies, and regulatory compliance aligned with FDA and ISO...
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Medline-Oak Park (IL)
or relevant experience  •  4+ years of experience in design/operation of medical device or drug combination product platforms and compliance with QSR/GMP/ISO (21CFR 820, ISO 13485, ISO 14971, MDSAP, MDR)  •  Broad knowledge of relevant standards and regulations...
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Lumenis-Oak Park (IL)
Collaborate cross-functionally to ensure customer success  •  Travel approximately 50% within territory and for meetings/events Key requirements  •  Bachelor's degree or equivalent experience  •  4+ years of outside B2B sales or capital medical device sales...
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Legacy MedSearch-Oak Park (IL)
Overview As Senior Quality Manager, you own the Quality function during a critical manufacturing transfer for a Class II medical device. You will lead the QMS, supplier quality, and post-market processes while hands-on in daily operations. You’ll...
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Deloitte-Oak Park (IL)
and medical device clients at scale. You’ll join a mission-driven firm that values continuous learning and cross-functional collaboration. Responsibilities  •  Oversee day-to-day sales operations and process improvements for Life Sciences Cloud projects...
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Slalom-Oak Park (IL)
shaping how pharma and medical device companies use technology to enable value for people and processes. You’ll work across client teams to translate requirements into scalable architectures and drive successful outcomes. This is a chance to influence go...
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Philips-Oak Park (IL)
and analytics  •  Support continuous improvement through change management and problem-solving across CAPA processes Key requirements  •  Minimum 5 years of relevant experience in the medical device industry with at least 3 years as a CAPA Facilitator/Manager...
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Abbott-Oak Park (IL)
to deliver scalable, compliant medical device software. You’ll partner with development teams to translate requirements into robust designs and drive process improvements to boost quality and efficiency. This role offers impact on product architecture...
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BD, Becton and Dickinson-Oak Park (IL)
support Key requirements  •  Bachelor's degree in Business, Marketing, Engineering, or related scientific field  •  Minimum of 5 years of successful sales experience in medical device industry with emphasis on OEM, kitting, or contract manufacturing  •  Proven...
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Deloitte-Oak Park (IL)
biotechnology, medical device, diagnostics, or healthcare commercial operations  •  Bachelor’s degree in business, IS, CS, Engineering, Life Sciences, or related field or equivalent  •  Effective written and verbal communication  •  Relationship-building...
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Veeva Systems-Oak Park (IL)
practices as part of post‑implementation programs for ongoing success Key requirements  •  8+ years of GMP systems ownership or software consulting  •  5+ years of Complaints Management for Medical Device  •  Strong understanding of FDA, EU MDR/IVDR requirements...
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Guidehouse-Oak Park (IL)
Overview In Guidehouse Life Sciences, you will partner with pharmaceutical, biotech, medical device, and diagnostic clients to support product planning, pricing, reimbursement, product commercialization, and regulatory/compliance efforts. You work...
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Deloitte-Oak Park (IL)
or technology implementation  •  2+ years experience with Salesforce, Veeva CRM, Microsoft Dynamics, Oracle CPQ, Salesforce Revenue Cloud, SAP CPQ, or similar platforms  •  1+ years experience in pharmaceutical, biotechnology, medical device, diagnostics...
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Tempus-Oak Park (IL)
internal systems, CRO operations, and medical device studies  •  Mentor cross-functional teams on clinical validation architectures and compliance  •  Shape QA organization design, scale operations, and optimize collaboration of quality roles  •  Lead regulatory...
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