- Cepheid (Miami, FL)
- …science field.Related work experience in Quality with a focus on assay development in a medical device or IVD l industry with applicable knowledge of FDA QSR, EU ... the Danaher Business System which makes everything possible.The Sr. Quality Specialist is responsible for supporting quality systems activities related to assay… more
- LinTech Global Inc. (Chantilly, VA)
- …work cooperatively as part of a cross-functional team. Nice to Have 1-3 years of Medical Device industry experience. Familiarity with FDA 21 CFR Part 820, EU ... coordinating, and conducting technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE) constructs. This… more
- ATR International (Minneapolis, MN)
- …Working level understanding of implantable procedures. Proficient knowledge of medical device industry standards, regulations compliance requirements Experience ... costs May be responsible for the transfer from R&D to manufacturing SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a… more
- Ascend Performance Materials (Alvin, TX)
- …Asia, we develop essential solutions that drive safer vehicles, cleaner energy, advanced medical devices , and durable consumer goods. Guided by a strong focus ... primary purpose of the Manufacturing Engineer is to provide engineering support to operate the unit safely, reliably, and...and manage job scope for outages and turnarounds - specialist Participate in PHA's Obtain Six Sigma Green Belt… more
- West Pharmaceutical Services (Exton, PA)
- Senior Specialist , Regulatory Affairs - Medical Device Requisition ID: 69746 Date: Jul 10, 2025 Location: Exton, Pennsylvania, US Department: Regulatory ... of the time. **Additional Requirements** + Ability to comprehend principles of math, science, engineering , and medical device use. + Ability to handle… more
- Mallinckrodt Pharmaceuticals (Madison, WI)
- …Locations Job Description Summary Job Description The Medical Device Specialist assembles medical devices and components within a controlled ... Job Title Medical Device Specialist Requisition...with 2-3 years in a regulated manufacturing environment, preferably medical devices . + Familiarity with manufacturing documentation… more
- Amazon (Seattle, WA)
- …across Amazon devices . Key job responsibilities As a senior sustainability specialist , you will be working with Amazon devices cross-functional teams (across ... In this role, you be part of the Amazon Devices Sustainability Science and Engineering team. Your...Devices & Services organization is hiring a Sustainability Specialist to provide expert knowledge, analyses, tools, and data… more
- Stryker (Portage, MI)
- **We are hiring for 2 roles.** As a Medical Device Technical Support Specialist (Hybrid), you'll be at the forefront of delivering exceptional customer ... experiences by supporting innovative medical technologies. In this dynamic, customer-facing role, you'll troubleshoot product issues, analyze implementations, and… more
- Meta (Burlingame, CA)
- … products with distribution into many worldwide markets. **Required Skills:** Medical Devices Regulatory Affairs Strategy Specialist Responsibilities: ... form factors can do. We are seeking an experienced medical devices regulatory affairs professional to help...9. Knowledge and experience in the application of the Medical Device Directive & European Union … more
- Meta (New York, NY)
- **Summary:** We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a ... Medical Device (SaMD) applications for the US...wearables, and other innovative devices . **Required Skills:** Medical Devices , Regulatory Specialist Responsibilities:… more
- Abbott (Lake Forest, IL)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... in software development, cybersecurity, validation, and/or quality systems in a medical device regulated environment. + Experience in product cybersecurity… more
- Lilly (Indianapolis, IN)
- …(SME) Oversight** : + Demonstrate a strong ownership and stewardship for medical device design, manufacturing, labelling, and/or packaging processes you support ... technical change agendas. Understand key regulations and their impact to the medical device design transfer and post-launch surveillance process. + Engage… more
- Gilead Sciences, Inc. (Foster City, CA)
- …factors, design controls, and risk management regulations, standards, and guidance for medical devices and combination products. + Excellentverbal, written, and ... communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ability… more
- Abbott (St. Paul, MN)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... in documentation control or technical writing in a regulated industry ( medical device , pharmaceutical, or biotech preferred). Apply Now… more
- Catalent Pharma Solutions (Harmans, MD)
- … or Biotech field with 6 years' experience within the biologic, pharmaceutical or medical device industry performing direct hands-on work in a Quality function ... **Lead Specialist , QA Validation & Engineering ** Catalent...8 plus years' experience within the biologic, pharmaceutical or medical device industry performing direct hands-on work… more
- Snap Inc. (Palo Alto, CA)
- …and own the accuracy and comprehensiveness of BOMs at the SKU-level, including device , accessories, packaging, and artwork + Enforce process compliance of all change ... SMT and FATP build matrices for Proto, EVT, and DVT builds + Device Allocations & Distribution + Interface with Technical Program Managers, Optical Engineering… more
- Terumo Neuro (Aliso Viejo, CA)
- …and designs from engineers, support the development of products/processes for medical devices , including writing or verifying specifications and/or manufacturing ... **12850BR** **Title:** Specialist II, Engineering **Job Description:** Perform...knowledge of Good Laboratory Practices. 8. Experience in the medical device industry. 9. Working knowledge of… more
- L3Harris (Cincinnati, OH)
- …sea and cyber domains in the interest of national security. Job Title: Specialist , Electrical Engineering Job Code: 24214 Job Location: Cincinnati, OH Schedule: ... qualification, and manufacture of numerous Electronic and Electro-Mechanical fuzing devices for numerous large defense contractors and direct government customers.… more
- Medtronic (Boston, MA)
- …multiple teams to execute concurrent, interdependent projects. + Knowledge of medical device R&D, product development, and clinical/regulatory procedures; ... up to 10%, primarily in US. As a Principal Engineering Project Management Specialist , you will lead...as a Subject Matter Expert + Comprehensive knowledge of medical device standards and regulations (eg, IEC… more
- L3Harris (Anaheim, CA)
- …sea and cyber domains in the interest of national security. Job Title: Sr Specialist , Project Engineering Job Code : 24853 Job Location: Anaheim, CA Schedule: ... DE specializes in the design and manufacture of fuses, ignition safety devices , proximity sensors, GPS navigation systems, aerospace status indicators, and range and… more
