- Merck & Co. (Rahway, NJ)
- …device development activities including engineering design, engineering analysis and testing, medical device design controls, risk management , test ... and leading cross-disciplinary project teams.Has broad knowledge of medical device development, design controls and risk management , alongside deep knowledge… more
- Merck & Co. (Rahway, NJ)
- …and managing external vendors/research partners.Preferred Experience and Skills:Experience with medical device development with understanding of Design Controls ... Job DescriptionOur Company's Device Product and Process Development (DPPD) Team is...(21 CFR 820.30)Familiarity with the following standards: Quality Management - ISO 13485, Risk Management -… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …clinical data management medical coding experience in a medical device , pharmaceutical company, or similar environment (eg, CRO) requiredOncology, ... and relevant regulatory requirements. This position has experience working within the medical device and/or pharmaceutical industry across complex disease areas,… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... (PSCS) deliverable which is the development of robust compositions, processes and device / packaging that enable patient centric products for patients. The successful… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …systems (Ethernet) 10 plus years of experience at a medium to large scale medical device , Pharmaceutical or biotechnology process firm in an automation role is ... the system administrator and quality system interface for Siemens Building Management System (BMS) and Environmental Monitoring System (EMS). Relationships Reports… more
- Aequor (Cincinnati, OH)
- …/ facility / equipment for the cGMP manufacture, particularly in pharmaceutical and medical device industries. Individual will work closely with and/or lead ... engineering, management , and finance.Qualifications 3-5 years of experience in engineering field, prefer in pharmaceutical or medical device industries more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the global TA strategy by working closely with global marketing and medical leaders. Embody NN leadership behaviors, embracing innovation, leadership over process, ... teams, including Feld Sales, Marketing, Strategic Partnership and Engagement, Medical Affairs, Market Access and Public Affairs (MAPA), Portfolio Strategy,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Twist BioScience (South San Francisco, CA)
- …Sciences or Engineering.5+ years of experience managing projects in biotech, medical device or pharmaceutical industry, with prior technical ... Bioscience is at an exciting phase of growth in business. The Program Management Office (PMO) is seeking an experienced, highly-motivated program manager to enable… more
- Aequor (Devers, TX)
- …the relevant industry. o Prior cGMP experience in biopharmaceuticals, pharmaceuticals, and/or medical device industry is highly preferred. o Experience in SAP ... along with a strong attention to detail and time management skills. Key Responsibilities: Business Process Lead for Procurement...Lead consistent site and global ways of working. Change Management : Serve as the designated Change Champion for the… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …possess strong knowledge manufacturing within a regulated industry such as medical device , automotive, or defense.Must be detail-oriented with exceptional ... of repeat CAPAs, CAPA On Time, and Validation on Time.Job ResponsibilitiesChange Management - evaluate the impact to product, processes, and equipment changes on… more
- Aequor (Fort Worth, TX)
- …Under guidance, update technical documentation files to align with EU MDR medical device requirements Submit Regulatory Impact Assessments to countries using ... submission package and manage country timelines to support approval of lifecycle management changes for medical devices Under guidance, collect data from… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Aequor (Newbury Park, CA)
- …experience in a regulated industries in a similar role (eg Biotechnology, Medical Device , Aerospace) Demonstrated strong Knowledge of industry and business ... be required to present on topics or issues to management May support audit & Inspections requests as needed...independently and to effectively interact with various levels of management Ability to lead and influence staff outside QA… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relevant includes clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...(ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and… more
- Lundbeck (Fargo, ND)
- …from an accredited college or university 2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must ... based on customer needs and organizational goals, incorporating "total office" account management . Local Market & Therapeutic Area Expertise - Gather and validate… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …equipment, and quality and regulatory requirements important to pharmaceutical and medical device manufacturing labs.Able to write detailed investigation summary ... instrumentation, and computerized systems.Knowledge of quality systems including exception management , change control, document control.Knowledge of operating and troubleshooting… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …corporate environment required Experience in pharmaceutical, healthcare, Information Technology, or medical device industry is required Privacy or compliance ... Spend and Risk Evaluation and Mitigation Strategy (REMS) including the management and oversight of systems supporting these processes. It involves coordinating… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …more than 3 year of experience.Engineering experience in the Pharmaceutical, Biotech or Medical Device industries.Experience in WFI and HVAC systems, clean and ... design and operations.Experience with maintenance, reliability, and computerized maintenance management systems (CMMS)Engineering experience in a Facilities, Utilities, Maintenance,… more
- Aequor (West Greenwich, RI)
- …related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation and documentation ... mathematical skills including the ability to trend data. Basic project management skills. Independently understand, follow and implement instructions. Strong word… more
Related Job Searches:
Device,
Management,
Medical,
Medical Device,
Medical Device Marketing Management,
Medical Device Project Management,
Medical Management,
Risk Management Medical Device