- Merck & Co. (Rahway, NJ)
- …Reporting to the Director responsible for this area, you will partake in medical device assembly and process development using semi-automated and automated ... as needed. Key Responsibilities: Experience with, and a fundamental understanding of medical device assembly equipment to enable development of product specific… more
- Merck & Co. (Rahway, NJ)
- …and effective implementation and oversight model to maintain best in industry regulatory compliance .The Vice President Regulatory Affairs, General Medicine ... cross-functional impact, including drug device /combination products and software as medical device platforms.- Reviews and resolves issues that span diverse… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Experience10+ years of experience in GxP-regulated IT system implementation, validation, and compliance in pharma/biotech/ medical device industry - Required ... while ensuring alignment with the Global Digital Transformation (DX) strategy, regulatory compliance framework, and overall quality assurance standards. This… more
- Merck & Co. (Rahway, NJ)
- …in alignment with the company's business goals, and quality and regulatory compliance .-Essential Duties and Responsibilities:Strategic Leadership and Project ... performance of team members, fostering a collaborative and innovative team environment. Regulatory Compliance and Quality Assurance:Ensure that all activities are… more
- Merck & Co. (Rahway, NJ)
- …Capital Process having participated on a large capital project teamExperience in regulatory compliance expectations across all phases of product development to ... robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward… more
- Merck & Co. (Durham, NC)
- …Experience and Skills: Manufacturing - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination ... compliance requirements governing development and manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU Medical Device … more
- Cardiovascular Institute of Central Florida (Lady Lake, FL)
- …in electronic medical records (EMR). Ensure compliance with regulatory guidelines and best practices for device management. Proficiency of reading ... Institute of Central Florida is looking for a qualified Device Technician - CVI Tavares & CVI The Villages...of Central Florida is seeking a skilled and detail-oriented Device Technician to join our team at our Tavares… more
- Eisai, Inc (Salt Lake City, UT)
- …with 3+ years experience in two or more of: infusion, diagnostic, biologic, medical device , buy and bill, rare disease, specialty pharmacy, and/or neurology; ... systems (including buy & bill, specialty pharmacy, distribution models, medical device and/or biologics experience) strongly preferred.Additional commercial… more
- Lundbeck (Edmond, OK)
- …from an accredited college or university 2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must ... issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources. Pharmaceutical Environment/ Compliance - Ability to apply knowledge of pharmaceutical and … more
- Eisai, Inc (Phoenix, AZ)
- …approved promotional clinical trials, patient access to medication, and regulatory / compliance guidelines preferred.Experience with account planning and ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...customer stakeholders in a compliant way.Monitor operating costs and compliance with territory budget.Seek out mentorship to learn and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and establishes the oversight model for timely and quality delivery and regulatory compliance of outsourced activities.Ensures inspection readiness of all data ... of relevant experience preferredData management and/or related work experience in a medical device or pharmaceutical company, or similar environment (eg, CRO)… more
- Merck & Co. (Rahway, NJ)
- …stability manufacturing by designing, developing, and scaling-up the formulation, device , and manufacturing process.- Driving drug product design from the ... individual will drive a culture of perpetual adherence to safety and compliance standards. A successful candidate should have extensive drug product development… more
- Eisai, Inc (Boston, MA)
- …Area Business Leader- ADBachelor's degree with 10+ years of pharmaceutical, biotech, or medical device sales with 5+ years successfully hiring, developing, and ... local markets and healthcare systems).Experience working with pharmaceutical manufacturer compliance & regulatory requirements.Experience networking, establishing, and… more
- Lundbeck (Raleigh, NC)
- …an accredited college or university 2-5 years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience. Must ... issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources. Pharmaceutical Environment/ Compliance - Apply knowledge of pharmaceutical and regulatory … more
- BioSpace (Washington, DC)
- …of quality professionals overseeing external mechanical device suppliers Ensure compliance with scientific, regulatory , and quality standards across global ... with these qualifications. Basic Qualifications: Doctorate degree and 2 years of Medical Device , Pharmaceuticals or Biotechnology experience Or Masters degree… more
- Kaiser Permanente (Bellevue, WA)
- Description: DEVICE RN - EXPERIENCE IN EP, ED, CCU, PCCU Job Summary: Provide nursing care to a defined group of patients, adhering to Kaiser Foundation Health Plan ... all members of the health care team with dignity and respect. Medical Specialties include areas such as Allergy, Cardiology, Neurology, Pulmonology, Dermatology,… more
- Michael Page (Hudson, NH)
- …in improving lives & advancing tech About Our Client My client is a medical device manufacturer specializing, supporting a variety of surgical fields (eg, ... 2-5 years of experience in a lean manufacturing environment, preferably within the medical device sector. Ability to identify issues, analyze root causes, and… more
- Geosyntec Consultants, Inc. (Seattle, WA)
- Overview Gradient, a Geosyntec Company, is seeking a Senior Medical Device Toxicologist to assist colleagues and clients in toxicological risk assessments and ... variety of backgrounds in chemistry, engineering, toxicology, epidemiology, ecotoxicology, medical device and pharmaceuticals, exposure sciences, industrial… more
- BioSpace (Indianapolis, IN)
- …Expert (SME) Oversight : Demonstrate a strong ownership and stewardship for medical device design, manufacturing, labelling, and/or packaging processes you ... technical change agendas. Understand key regulations and their impact to the medical device design transfer and post-launch surveillance process. Engage… more
- Lexington Medical (Bedford, MA)
- …new products and global expansion. This is a terrific opportunity for an experienced medical device regulatory professional to grow with our company. ... Affairs, or other technically related field. 5-8+ years of experience in medical device regulatory affairs, including prior 510(k) submission and… more
