• Novo Nordisk Inc. (Durham, NC)
    …help us make what matters. The Position Plan, manage & perform laboratory validation activities. Routine review of laboratory validation procedures & completed ... all deliverables. Relationships Manager. Essential Functions Ensure accuracy & compliance of validation & equipment records Responsible for validation of QC… more
    HireLifeScience (04/25/24)
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  • Merck & Co. (Rahway, NJ)
    …build Quality Management System elements into the end-to-end computer system validation process , thereby promoting permanent inspection readiness.Develop and ... community, provide for and lead Quality Assurance oversight for computer system validation matters within the Global Development Quality organization and for the… more
    HireLifeScience (05/08/24)
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  • Merck & Co. (Durham, NC)
    Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... for supporting qualification of Fermentation Process Automation at our Company's Durham, NC facility. Responsibilities include:- supporting commissioning and… more
    HireLifeScience (05/15/24)
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  • Novo Nordisk Inc. (Durham, NC)
    …approval - components/raw material, batch records, change control requests, deviations & validation documents Performs QA presence & process confirmation on shop ... Deviations & other documentation (in conjunction with LoB) & QA presence & process confirmation on shop floor. Handles release of raw materials & provides quality… more
    HireLifeScience (04/24/24)
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  • Merck & Co. (Durham, NC)
    …areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation . - ... vaccines, including our HPV vaccines. - The Senior Engineering Specialist will troubleshoot and maintain process and process support equipment utilized in a… more
    HireLifeScience (05/11/24)
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  • Eisai, Inc (NJ)
    …of the PSSS, including MedDRA coding. This may include participating in the validation process for the PSSS. 70%Ensure accurate and timely submissions to ... (Product Safety Surveillance System) consistent with the ARISg coding manual, SOPs/WIDs, process flows and established time frames within the ARISg workflow. Full… more
    HireLifeScience (05/02/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …of multiple myeloma. Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role Overview The ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...per inspection plan and record results to complete receipt process . Reviews inspection documentation (C of A or other… more
    HireLifeScience (03/13/24)
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  • Blanchard Valley Hospital (Findlay, OH)
    …OF THIS POSITION The primary purpose of the Professional Coding Integrity Specialist (PCIS) is to review, enter and/or modify charges as appropriate, including ... claim-scrubber edits (Quadax) resulting from charges entered by the Revenue Integrity Validation team; collaborate with clinical areas, coding, PFS, etc. to support… more
    JobGet (05/14/24)
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  • Software Galaxy Systems, LLC (Parma Heights, OH)
    Title: Data Entry Specialist (Business Process Outsourcing Tech, BSS. Offsite MS) Duration: 4 Months (Temp to Perm) Location: Parma, OH 44130 Shift: Sun to Thu ... entry and verification from incoming digital images. Provides document classification validation of automatically classified documents. Provides data validation more
    JobGet (05/16/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …SOPs, + state, federal + local laws. Test raw materials, In- process , extended release Intermediates, Finished Product + Stability samples, incl dissolution, ... by Laser Diffraction/Sieve Analysis, Bulk + Tapped density, cleaning verification/ validation according to analytical methods, United States Pharmacopeia (USP)… more
    HireLifeScience (05/06/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …Possess signature authority for deviation closure Reviews and approves Validation Documentation Reviews and assesses Corrective and Preventive Action Reports ... data requires evaluation of identifiable factors We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo… more
    HireLifeScience (05/09/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …tracking, follow-up, and reporting / trending Reviews and approves Validation Documentation Reviews and assesses Corrective and Preventive Action Reports. ... Junior team members in QA Best Practices We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we… more
    HireLifeScience (05/09/24)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …Review and assess Corrective and Preventive Actions Reviews and approves validation documentation Reviews and assesses deviations; includes tracking, follow-up and ... with flexibility for changes in work priorities We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk… more
    HireLifeScience (05/09/24)
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  • Novo Nordisk Inc. (Durham, NC)
    …problems solving Understand & execute GMP & compliance protocols for instrument validation Executes work according to schedule & department plan Evaluates instrument ... performance & responds to potential issues Contributes to process confirmations Maintains training qualifications on time. Supports training others as required… more
    HireLifeScience (03/29/24)
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  • Rose International (St. Louis, MO)
    …Hiring Organization: Rose International Position Number: 464039 Job Title: Salesforce Specialist Job Location: Saint Louis, MO, USA, 63167 Work Model: Hybrid ... Rate ($): 39.00 Must Have Skills/Attributes: Audit, CRM, MS Office, Salesforce, Validation Job Description **Only those lawfully authorized to work in the designated… more
    JobGet (05/14/24)
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  • Nesco Resource (Rensselaer, NY)
    Work for a well-regarded biotechnology company in Rensselaer, NY as a MSAT Specialist ! This position is a one-year contract; with potential for extension or ... cGMP environment or equivalent preferredA typical day as a MSAT Specialist might include: Supporting the Drug Product Manufacturing Sciences and Technology… more
    JobGet (05/19/24)
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  • Hired by Matrix (Orlando, FL)
    …so, our client is hiring a Digital Analytics Integrations Specialist !What You'll Do:Essential Job Responsibilities: Analytics Tools Integration Management: Oversee ... from digital channels. Conduct rigorous testing utilizing debugging tools and validation methods to ensure precision in reporting metrics. Data Collection Accuracy:… more
    JobGet (05/16/24)
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  • Schaeffler Group (Fort Mill, SC)
    …requirements and secures the implementation by defining respective application rules, TCO validation and packaging process requirements for the steering of ... Lifecycle Management, including planning of packaging introduction and packaging cost validation . Validate and prove that packaging systems meet the requirements in… more
    JobGet (05/03/24)
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  • Arthrex (Naples, FL)
    …for regular, full time employees.Arthrex Inc. is actively seeking a Payroll Tax Specialist for our corporate office in Naples, FL. This position will maintain all ... ensure annual tax filings are correct. Per pay period validation with IRS deposits posted by 3rd party vender....Office skills required. SAP & ADP experience a plus. Ability to process payroll transactions via a computerized HRIS… more
    JobGet (04/30/24)
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  • Sunrise Systems Inc (Seattle, WA)
    …cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client ... Above-site organization, including the document approvals, document change control process , periodic review and system reporting. Experience Basic Qualifications:… more
    JobGet (05/12/24)
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