- Lovelace Biomedical Research Institute (Albuquerque, NM)
- OverviewUnder specific direction, the Payroll Specialist will review and process bi-weekly payroll for approximately 400 employees.Will transmit direct deposit ... to financial institutions and prepare manual checks as needed, maintain and review timesheets submitted through the electronic time collection system, compile and… more
- Merck & Co. (Rahway, NJ)
- Job Description Job Description The Rahway based Senior Specialist , Global Development Quality Operations - API, is responsible for independent review and ... of our company's clinical supply programs. This person will also independently review and approve documentation accompanying the disposition of API materials to… more
- Novo Nordisk Inc. (Hackensack, NJ)
- …by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm ... this job family are as follows: Endocrinology Diabetes Care Specialist I - $102K to $126K Endocrinology Diabetes Care... I - $102K to $126K Endocrinology Diabetes Care Specialist II - $119K to $146K Senior Endocrinology Diabetes… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionTitle: Specialist , Metrology and Validation, Analytical Research & DevelopmentJob Description-The Analytical Research & Development (AR&D) External ... Research Laboratories Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research facility. The… more
- Novo Nordisk Inc. (Boston, MA)
- …as a frontrunner in the cardiometabolic care market. The Ecosystem Portfolio Specialist is responsible for achieving sales targets by effectively promoting Novo ... adherence to approved guidelines. Relationships Externally, the Ecosystem Portfolio Specialist maintains relationships with physicians, pharmacists, nurses, and other… more
- Eisai, Inc (Raleigh, NC)
- …difference. If this is your profile, we want to hear from you. The QA Specialist plays a critical role in ensuring the quality and compliance of commercial and ... effective collaboration across teams.ResponsibilitiesExecute core processes within Quality area: Review manufacturing batch records for completeness, accuracy, and compliance… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Validation Specialist III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Validation Specialist role is an exempt level position with responsibilities...technical, qualification, and validation activities including data or document review and approval as needed. This role will be… more
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. The Sr. Medical Information Specialist is responsible for meeting the medical information needs of internal and external ... medical accuracy of Eisai's materials; this may include assisting with review of Eisai's advertising and promotional and/or medical/scientific materials. May partner… more
- Twist BioScience (South San Francisco, CA)
- The Regulatory Operations Specialist is responsible for ensuring the efficient and compliant management of regulatory documentation, with a primary focus on Safety ... composition data and hazardinformation for accurate SDS generation. Manage the review , approval, and distribution of SDS to internal and external stakeholders.… more
- Merck & Co. (Millsboro, DE)
- …summaries (ISS), outlines of production and special outlines). Alternatively, may review and prepare registration documents for export markets.May serve as point ... lead in creation of GRA standard international dossiers for US Biologicals.May review market advertising and promotions (A&P) for US Biologicals in compliance with… more
- Novo Nordisk Inc. (Tyler, TX)
- …by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm ... D required Minimum one (1) year of experience working in one or more of the following areas preferred: Pharmaceutical/Healthcare, Sales, Consulting, Customer Service or Military Intermediate computer skills required (Windows, Word, Excel); Prior computer… more
- Novo Nordisk Inc. (Walnut Creek, CA)
- …by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm ... D required Minimum of two (2) years of pharmaceutical, medical or healthcare experience required Demonstrated leadership and decision-making ability Ability to navigate PA's in rapidly developing market Health Systems and/or Institutional Account experience is… more
- Novo Nordisk Inc. (Dayton, OH)
- …by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm ... D required Minimum of two (2) years of pharmaceutical, medical or healthcare experience required Intermediate computer skills required (Windows, Word, Excel); prior computer experience using sales data/call reporting software ideal Must be a self-starter and… more
- Merck & Co. (South San Francisco, CA)
- …clarity, accuracy, and conciseness of regulatory documents to facilitate the review process. -Implement strategies to leverage GenAI for improving document quality ... positive change. -Experience with regulatory submissions and understanding of the review process. -Familiarity with cloud-based data platforms and technologies (eg,… more
- Leica Biosystems (Miami, FL)
- …impact.Learn about the Danaher Business System which makes everything possible.The Specialist , Regulatory Compliance for Leica Biosystems is responsible for working ... an on-site role. In this role, you will have the opportunity to:Prepare, review and approve regulatory documentation for submission, including but not limited to… more
- Merck & Co. (Durham, NC)
- …DescriptionJoin our dynamic Engineering, Maintenance, & Utility Department as a Senior Specialist , where you will play a crucial role in enhancing asset reliability ... the highest quality of raw materials, intermediates, and finished products.The Sr. Specialist , Calibration Engineer is a member of the Engineering, Maintenance and… more
- Merck & Co. (Durham, NC)
- Job DescriptionJoin Our Team as a Calibration & Maintenance Specialist !Are you a self-motivated problem solver with a knack for technical guidance and hands-on ... GMP, and calibration/maintenance procedures.Uses the SAP work order system to review work requests, identify required stock and non-stock materials, ensure… more
- Merck & Co. (Durham, NC)
- …manufacturer? If so, then this is the opportunity for you!The Associate Specialist , Calibration is a member of the Engineering, Maintenance and Site Services ... to support investigations and develop appropriate CAPAs which lead to program improvements. Review and approve out of tolerance (OOT) records and ensure quality… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Associate Specialist , is a member of the Site Automation team responsible for the assigned process control systems in support of manufacturing ... all Good Manufacturing Practices (GMPs), safety, and environmental regulations.- Review and approve automation documents, preventive maintenance, and SOPs to… more
- Genmab (NJ)
- …would love to have you join us!Responsibilities:Lead programmer for a trial(s) Review CRFs for adequacy and consistencySupport establishment and maintenance of Genmab ... standards, and templatesRepresent programming in cross-functional team meetingsAct as a specialist to others within teamRequirements" Bachelor's degree in Sc. or… more
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