- Novo Nordisk Inc. (Tacoma, WA)
- …obesity to maximize sales within an assigned territory. The Obesity Care Specialist (OCS) must achieve sales goals by implementing marketing and sales strategies ... trends, and competitors products or services Maintain required activity records /reports, including timely and accurate transmission of call data...the job titles are the following : Obesity Care Specialist I - $65,850 to $115,240 Obesity Care … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team based in ... Raritan, NJ. Role Overview The QC Specialist , Lab Services, is responsible for sample management. The QC Specialist is encouraged to work independently on… more
- BioAgilytix (Boston, MA)
- …the patients who need them.We're seeking a detail-oriented and proactive Corporate Compliance Specialist to join our team. In this role, you'll play a crucial part ... and internal), by facilitating scheduling and staff coordination, accessing records , addressing inspection/audit requests, and performing other tasks, as… more
- Catalent (Manassas, VA)
- …to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for auditing the products and processes ... of all tasks relating to issuance of Batch production records and maintenance of cGMP and SOP records... records and maintenance of cGMP and SOP records . Participates in all necessary training required to successfully… more
- Merck & Co. (Durham, NC)
- …product inspection, and quality control laboratories. The Quality Assurance Specialist will support this expansion. Project activities requiring support include ... in Aseptic processing, aseptic observations, and techniques.Electronic manufacturing batch records (eMBR) experience.NOTICE FOR INTERNAL APPLICANTSIn accordance with Managers'… more
- Aequor (NV)
- …may not pose an undue hardship to , its operations, or its staff." Specialist Import/Export 's Global Trade Office is an organization within the Trade Compliance ... o Transaction management Broker management Import for export Documentation records Country of origin Classifications Update SAP documents supporting GTS… more
- Catalent (Manassas, VA)
- …to help create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and maintaining the Quality ... Production and Packaging Managers, Supervisors, and R&D to maintain and update records and documentation.Comply with SQF, Food Safety Plan (HACCP), and Food Quality… more
- Novo Nordisk Inc. (Boulder, CO)
- …applicable environmental, health and safety regulations. Relationships Reports to Senior Specialist EHS at US headquarters in MA. Internal relationships include ... 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
- Aequor (Seattle, WA)
- …to ensure availability to users via the LMS File and maintain training records for easy retrieval. Partner with the inspection/audit subject matter expert to ... generate LMS reports and/or retrieve training records to support inspections/audits Build and/or run reports to...offerings in the LMS Ensure Good Manufacturing Practices training records are completed per good document principals (GDP). Monitor… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- The QA Specialist II - Engineering/Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other ... schematics and engineering drawings.Perform Quality review/approval of CMMS asset records .Perform Quality review/approval of equipment/instrumentation/process validation protocols and summary… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for ... This position has QA signature authority on the review of individual batch records , supporting test records and other ancillary support records . Will be a QA… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Position This position will reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all ... position has QA signature authority on the review of individual batch records , supporting test records and other ancillary support records . Will assist in… more
- Novo Nordisk Inc. (Durham, NC)
- …matters. The Position Performs quality review & approval of Batch Production Records (BPRs), Change Requests (CR's), Deviations & other documentation (in conjunction ... & approves documentation for Quality approval - components/raw material, batch records , change control requests, deviations & validation documents Performs QA… more
- Novo Nordisk Inc. (Durham, NC)
- …and help us make what matters. The Position Ensures Batch Production Records (BPRs) & relevant quality processes are compliant with regulations. Performs quality ... local SOPs Reviews & approves documentation for Quality approval - batch records & other documentation Supports & reviews investigations & root-cause analysis… more
- Novo Nordisk Inc. (Montclair, CA)
- …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 Relevant Novo Nordisk experience preferred Intermediate computer skills required (Windows, Word, Excel);… more
- Novo Nordisk Inc. (Durham, NC)
- …Manager. Essential Functions Ensure accuracy & compliance of validation & equipment records Responsible for validation of QC equipment & instrumentation Identify & ... handle deviations per proper appropriate procedures Maintain good standing with stakeholders through engagement & positive cooperation Perform & oversee change control activities for QC equipment & systems Support systematic problem solving related to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records . The incumbent can work remotely anywhere in the United States with reasonable ... access to a major airport. Qualifications A minimum of 1 year of on-site monitoring experience required A minimum of 6 years of progressively responsible clinical trial experience within a pharmaceutical, biotechnology, CRO, and/or healthcare setting required… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …of process and equipment improvement programs, reviews completed quality records , generates quality deviation responses, drive investigations and has ability ... manufacturing equipment and processes Revise and create documentation (SOP, batch records , reports) associated with the manufacture of product, requiring minimal… more
- Novo Nordisk Inc. (Durham, NC)
- …as related to third party instrument services Accurately & legibly records all activities in appropriate documentation. Writes work orders Reviews documentation ... for accuracy & completeness Instrument specifications, scheduled maintenance, repair, & calibration Identifies & handles deviations per proper procedures for measuring equipment Supports cross-functional investigations & participates in systematic problems… more
- Aequor (Durham, NC)
- …any problems encountered. Assist in the preparation and updating of detailed records , documenting the build process. Organize and maintain a system for efficient ... filing and updating of these records . Participate in parts rebuilds as necessary. Acquire and...and costs. Work in tandem with the Quality Control Specialist to address and resolve device repairs. Assist the… more
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