- 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 ... research areas centered around rare diseases and immune disorders.Summary: The Associate Director, Regional Marketing Conventions & Field Programs will be… 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 ... research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC… 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 ... CCDS; Ensures implementation of CCDS/labeling agreements with licensing partners.Conduct Label Review Committee Meetings: Prepares documents for review by… 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 ... of CDx and data collectionSupports Regulatory affairs in providing content and providing review of documents supporting CDx submissions to the FDA and other health… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …experience and 4+ years direct or related CMC regulatory experienceSuccessful track record in preparation, management of review and approval of NDA/MAA/BLA ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Insmed Incorporated (San Diego, CA)
- …has responsibility for the QA oversight of Insmed Gene Therapy (GTx) analytical laboratories, review and approval of GMP analytical records . Will also provide QA ... applicable for internal or external manufacturing/analytical testing)Evaluate completed test records and other relevant information to ensure procedures were… more
- Novo Nordisk Inc. (WA)
- …in good standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records .; May be required to work company holidays ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and… more
- Insmed Incorporated (San Diego, CA)
- …lead planning activities for process characterization and PPQ planning activities. Review batch records , SOPs, raw material specifications, development reports ... and Best Medium Workplaces™ lists.OverviewJoin the Technical Operations team as an Associate Director of MSAT where you will support pipeline programs that change… more
- Merck & Co. (Upper Gwynedd, PA)
- … medical affairs or clinical development experience with proven track record of contribution to medical or clinical development strategiesCustomer expertise, ... Job DescriptionThe Executive Director, Global Medical and Scientific Affairs (EDMA) GYN Malignancies is...team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …within sub-function. Solid NN value chain understanding and execution. Proven track record of creating business results with impact on VP/CVP level. Motivated, ... US East Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics,… more
- Novo Nordisk Inc. (Durham, NC)
- …& equipment outside of own expertise (with the appropriate experience & skill level) Record / review production data in BPR & associated forms Follow all safety & ... 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases,...returns, etc. Participate actively in & support event response Review & author SOPs & other documents as required… more
- Novo Nordisk Inc. (Boulder, CO)
- …all applicable environmental, health and safety regulations. Relationships Reports to Associate Director, EHS at US headquarters in MA. Internal relationships ... incidents. Ensure follow-up is done to minimize future exposure and proper records /documents are maintained Create, conduct, coordinate and track various training to… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our success is backed by ethical integrity, forward momentum, and ... have 8-10 direct reports composed of experienced, senior and associate biopharmaceutic scientists.- The successful candidate will effectively partner with… more
- Eisai, Inc (Fort Worth, TX)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... oral markets with approved indications, helping targeted customers, such as Medical Oncologists, Hematologists, Endocrinologists, and nurses, etc. learn about the… more
- Eisai, Inc (San Diego, CA)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... oral markets with approved indications, helping targeted customers, such as Medical Oncologists, Hematologists, Endocrinologists, and nurses, etc. learn about the… more
- Sun Pharmaceutical Industries, Inc. (Lexington, MA)
- …regulatory compliant Quality System for QC laboratory system Plan, direct and coordinate QC batch record review , logbook review , QC test review , and lot ... Job Summary Performs QA review of testing records of raw...in cGMP compliance and conduct inspections and internal audits Record and review GMP data, monitor and… more
- Sun Pharmaceutical Industries, Inc. (Hopewell, NJ)
- Responsible for batch certification review of site QA activities related to manufacturing batch records , packaging records , QC lab records , certificates ... of analysis/compliance and all related supporting documentation (ie documentation review , SOP compliance, laboratory application data reviews, batch release,… more
- CHS Inc (Thompson, ND)
- …soil sampling and use GIS to create field maps based on GPS data to record and assess the impact of farm management decisions. Use data sensors to monitor soil ... what information means and how it can be used Ability to monitor and review information from events and/or the environment, to detect or assess problems Ability to… more
- Healthcare Recruitment Counselors (Jamestown, ND)
- …review health and medical histories, exam patients, review pertinent records /imaging Evaluate patients neuromusculoskeletal systems and the ... are flexible in our need and can accommodate an associate looking for either full time or part time...nutrition, and home exercises Documentation/progress notes- accurate and timely records Re-exams for progress checks, adjustments, and ensure the… more
- Adecco US, Inc. (Beaverton, OR)
- …seeking a dedicated and detail-oriented Customer Service Specialist to join our team as a ** Medical Record Review Associate ** . The ideal candidate will ... information. **JOB SUMMARY** The candidate will work as a Medical Record Review Associate...+ Record Types: Understanding different types of medical records such as patient histories, diagnostic… more
