- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and relevant regulatory requirements. This position has experience working within the medical device and/or pharmaceutical industry across complex disease areas, ... around rare diseases and immune disorders. Job Summary: The Manager , Medical Coding is accountable for delivery...data management medical coding experience in a medical device , pharmaceutical company, or similar environment… 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 ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... areas centered around rare diseases and immune disorders. Job Summary: The Manager , Clinical Data Repository Administration is a member of the Biostatistics and… more
- Merck & Co. (Rahway, NJ)
- …BS Required Experience and Skills: Experience in the pharmaceutical, biotechnology, chemical, medical device , or closely related industry.- Experience in one or ... Job Description Job Description: The Rahway based Senior Specialist, Global Development Quality Operations - API, is responsible for independent review and approval… more
- Novo Nordisk Inc. (Durham, NC)
- …of QA and/or cGMP related experience required, preferably in the pharmaceutical or medical device industry General knowledge of Batch Review Processes (BRP), ... 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases,...life-changing careers, and the opportunity to help improve the quality of life for millions of people around the… 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… 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 ... The Program Management Office (PMO) is seeking an experienced, highly-motivated program manager to enable the tremendous growth of Twist's Next Generation DNA… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …corporate environment required Experience in pharmaceutical, healthcare, Information Technology, or medical device industry is required Privacy or compliance ... Implements and oversees automation processes to improve data reviews and data quality for ensuring government obligations Tracks all policy and contract template… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …The Quality Engineer will participate in Internal Audits as directed by the Quality Manager . In addition, the Quality Engineer will lead continuous ... Position SummaryThe Quality Engineer is responsible for overseeing the health...strong knowledge manufacturing within a regulated industry such as medical device , automotive, or defense.Must be detail-oriented… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …FDA and EMEA Regulatory requirements Experience at a medium to large scale medical device , pharmaceutical or biotechnology process firm in an automation role ... to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a...will be commisserate with experience. Relationships Reports to: Automation Manager Essential Functions Responsible for assisting with the design,… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …and quality and regulatory requirements important to pharmaceutical and medical device manufacturing labs.Able to write detailed investigation summary memos ... performance and other areas. You will report to the Manager , Microbiology.Job ResponsibilitiesProvide general oversight, plan, organize, direct, and evaluate… 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 ... to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a...(BMS) and Environmental Monitoring System (EMS). Relationships Reports to: Manager of Automation Engineering Essential Functions Lead, plan, organize… 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
- Actalent (Neptune, NJ)
- Job Title: Quality Manager Job Description We are seeking a dedicated Quality Manager to oversee Quality Management functions. In this role, you will ... 9001 standards. Essential Skills + Experience working in the Medical Device or Pharmaceutical Industry. + 3+...Device or Pharmaceutical Industry. + 3+ years of Quality Management experience. + 3+ years of experience managing… more
- Pfizer (Rocky Mount, NC)
- …applicable FDA CAPA requirements. + SME during internal and external inspection related to Medical Device Quality Systems. + Work with all functional areas ... governance processes. + Experience at a medical device manufacturer in a design quality role....medical device manufacturer in a design quality role. **Physical/Mental Requirements.** The position may require lifting,… more
- US Tech Solutions (San Bruno, CA)
- …align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process Verification, ... Device Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management Systems (QMS). + 3+ years of technical program… more
- Takeda Pharmaceuticals (Lexington, MA)
- …PSDQ's Quality Risk Management program, activities and documentation, both for medical device products and pharmaceutical development. Serves as a key point ... knowledge of current Good Manufacturing Practice requirements for the biopharmaceutical and medical device industries + Experience in compliance and systems… more
- Amazon (Sunnyvale, CA)
- …key features for device makers. Basic Qualifications - 6+ years of quality assurance engineering experience - 4+ years of delivering test automation, test tools, ... Work hard. Have fun. Make history. As a Senior Manager , you will be responsible to innovate and drive...you will be responsible to innovate and drive new Quality initiatives, establish new test methodologies, frameworks and processes… more
- Vanderbilt University Medical Center (Nashville, TN)
- …Team **Job Summary:** Manages vision, roadmap, deliverables to support the growing medical device and software support needs of the enterprise. Translates ... in the future. . **KEY RESPONSIBILITIES** * Leads vision, roadmap, deliverables for medical device software and hardware. * Translates customer needs into… more
- Insight Global (Cincinnati, OH)
- Job Description An employer is seeking a Medical Device Project Manager for their New Product Development team in Blue Ash, OH. This will be a long-term ... and a unique chance to convert full time with a leader in the Medical Device space. The day-to-day responsibilities for this role will include developing… more
