BIOPHARMA EXCEPTION REPORT INVESTIGATION AUTHOR
2 weeks ago
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
Are you looking for a challenging and rewarding opportunity in the field of Biopharma Investigation? Look no further We are seeking a highly motivated candidate to join our team as the Biopharma Investigation Author.
The Sr Specialist Quality Systems is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.
If you thrive in a fast-paced environment, enjoy problem-solving, and have a passion for writing and project management, this is the perfect opportunity for you. Join our team and contribute to the world of Biopharma Investigation.
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Biopharma Exception Report Investigation Author
2 weeks ago
Worcester, United States AbbVie, Inc Full timeCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services...
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Biopharma Exception Report Investigation Author
4 weeks ago
Worcester, United States AbbVie Full time**Company Description** The Sr Specialist Quality Systems is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA....
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Biopharma Exception Report Investigation Author
2 weeks ago
Worcester, United States AbbVie, Inc Full timeCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services...
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RESEARCH NURSE COORD II
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UM NURSE
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PATIENT AUTHORIZATION COORDINATOR
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Tulsa, OK 74120, USA, United States Viemed Healthcare Inc. Full timeDuties:* Responsible for obtaining re-authorization requirements for on-going coverage of durable medical equipment.* Review and obtain necessary compliance documents, medical records and prescriptions in order to submit for re-authorization.* Responsible for assisting patients in the re-authorization process* Responsible for working with sales and clinical...
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Scientist, Quality Control
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Worcester, Massachusetts, United States AbbVie Full timeJob Description Purpose: Independently performs routine and non-routine testing. Performs laboratory testing within a GMP environment in support of one or more of the following areas: raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data, evaluates results, and forms conclusions with minimal outside input....
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PATIENT AUTHORIZATION COORDINATOR
2 weeks ago
Fairfield, NJ 07004, USA, United States Res-Care, Inc. Full timeOur CompanyAmeritaOverviewThe Patient Authorization Coordinator - Lead has primary responsibility for the timely clearance of new referrals. In addition, this position provides support and training for Patient Authorization Coordinator team members as well as other specialty intake staff as necessary.Responsibilities* Obtains core initial authorizations and...
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AUTHORIZATION COORDINATOR
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Tuscaloosa, AL 35487, USA, United States DCH Full timeOverviewCoordinates the clinical review and obtaining authorizations for the procedures performed in the SpineCare Center. Requires attention to detail and the ability to work in multiple computer systems to verify insurance eligibility and determine requirements for precertification of insurance.ResponsibilitiesReviews order report to initiate and obtain...
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PATIENT AUTHORIZATION REPRESENTATIVE
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Los Angeles AFB, CA 90009, USA, United States UCLA Health Full timeGeneral InformationPress space or enter keys to toggle section visibilityWork Location: Los Angeles, USAOnsite or RemoteFlexible HybridWork ScheduleMonday - Friday, 9:00am-5:30pm PSTPosted Date09/15/2023Salary Range: $28.34 - 44.5 HourlyEmployment Type2 - Staff: CareerDurationIndefiniteJob #12604Primary Duties and ResponsibilitiesPress space or enter keys to...
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Plant Controller
4 weeks ago
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Financial Assistant IV-Hybrid
2 weeks ago
Worcester, United States University of Massachusetts Medical School Full timeOverview: GENERAL SUMMARY OF POSITION: Under the general supervision of the Department Administrator or designee, the Financial Assistant IV is responsible for the preparation of fiscal reports related to grant and contract proposal budgets and the processing and review of all grant, contract and school fund expenditures. The position provides personnel...