- Allstate (Chesapeake, VA)
- …Job Description Join Allstate's Litigation Services team as a Paralegal Specialist , where you'll contribute to delivering strong legal outcomes and exceptional ... case documentation, organization, and deadline tracking. Coordinate medical records, expert review , and disclosures as needed. Assist with arbitration and trial… more
- Cipla (Fall River, MA)
- Job Title : Quality Assurance Operation Specialist FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General: 8:30AM - 5:00PM ... Salary Range: $72,800 - $93,600 Purpose: The QA operation specialist (MDI) position is an individual contributor role and...include but are not limited to the following : Review of batch manufacturing/packaging record. Review of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Lab Services, II/III as part of the Quality team based in Raritan, ... NJ. Role OverviewThe QC Specialist , Lab Services is responsible for sample management. The...(LIMS)Prepare documents and coordinate Sample shipment (internal and external shipments) Review logbooks and/ or LIMs to align physical quantities… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Batch Disposition Specialist II/III as part of the Quality team based in Raritan, NJ. Role ... within company policies, procedures, and all applicable regulations.Key Responsibilities Review documentation for all manufacturing activities executed in accordance… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. ... integrityExecutes, owns, assesses and participates in the creation, revision and review of change controls, SOPs, and other documentationParticipates in authoring… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist II/III as part of the Quality Operations team based in Raritan, New Jersey. ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...guidance and determine immediate path forward for manufacturing quality issues. Review of all documentation, in accordance with Good Documentation… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist I/II/III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Document Control Specialist role is an exempt level position with responsibilities...with workflow handling and electronic system usageManage the periodic review process for proceduresIssuance of batch related documentation in… more
- Cipla (Fall River, MA)
- …/ comparison reports and any other study reports. Prepare and review laboratory investigation (OOS/OOT/Deviation) reports and ensure compliance of same. Verifying ... edition, supplement, amendment, or other changes of any Pharmacopoeia are in effect. Review of laboratory audit trials during data review against standard… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …vendor call scripts, including stewarding material through the Promotional Review Board process (if applicable) Optimizes multi-media communication (letters, emails, ... programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance… more
- Merck & Co. (Rahway, NJ)
- …and stakeholder engagement within Decideware. Negotiate supplier contracts from initial review to execution. Develop and execute RFIs/RFPs aligned with strategic ... sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a… more
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