• Merck & Co. (Durham, NC)
    Specialist will primarily support vaccine drug manufacturing via Validation program execution and partnering with cross-functional teams (ie Maintenance, ... Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation . Position Description: GENERAL INFORMATION A Senior Engineer will… more
    HireLifeScience (06/14/24)
    - Related Jobs
  • BioAgilytix (Durham, NC)
    …therapeutics to the patients who need them.The Senior Laboratory Automation Specialist will be primarily responsible for leading the programming and implementation ... project plans to implement automated solutions to support (GxP) validation and implementation, including protocol/throughput analysis; instrumentation specification; drafting… more
    HireLifeScience (05/21/24)
    - Related Jobs
  • Novo Nordisk Inc. (West Lebanon, IN)
    …system to implement changes associated with technical operations, engineering, and/or validation (generate, execute, and evaluate change requests) Revise and create ... records, reports) associated with technical operations, production, engineering, and validation Incorporate technical pre-planned process improvements and cost reduction… more
    HireLifeScience (05/22/24)
    - Related Jobs
  • Merck & Co. (Rahway, NJ)
    …job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the Director, Engineering, ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:Site Operations (GWES)… more
    HireLifeScience (06/01/24)
    - Related Jobs
  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking a CQV Specialist (Contract Position) as part of the Technical Operations team based in Raritan, ... This position will be responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing… more
    HireLifeScience (05/30/24)
    - Related Jobs
  • Merck & Co. (Durham, NC)
    …and reviewDirect support of regulatory inspections and auditsDirect support of validation activities and all other associated quality functionsOther duties as ... requested by managementPROBLEM SOLVING:Identifies and solves a range of problems in straightforward situations; analyzes possible solutions and assesses each using standard proceduresINTERNAL CLIENT/EXTERNAL CUSTOMER FOCUS:Responds to standard requests from… more
    HireLifeScience (06/05/24)
    - Related Jobs
  • Novo Nordisk Inc. (Plainsboro, NJ)
    …membership work instructions and procedures Verify contract membership data testing and validation with IT is properly performed Work with Chargeback personnel to ... research and adjudicate membership discrepancies Physical Requirements 0-10% overnight travel required. Qualifications A Bachelors degree or equivalent experience required Familiar with enterprise-wide integrated application systems such as SAP, Model N, or… more
    HireLifeScience (06/04/24)
    - Related Jobs
  • 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 ... reporting/trending Reviews manufacturing and support records to certify compliance with specifications and procedures Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, walk through audits of the… more
    HireLifeScience (05/25/24)
    - Related Jobs
  • 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 ... Participates in Regulatory Inspections Other duties as assigned Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes Incorporates the Novo Nordisk… more
    HireLifeScience (05/09/24)
    - Related Jobs
  • Aequor (Thousand Oaks, CA)
    …following functions: a) Review and approve product MPsb) Approve process validation protocols and reports for Mfg. processes. c) Approve Environmental ... in site audits) Approve change-over completion) May perform work of QA Specialist EDUCATION/LICENSES Doctorate degree or Master's degree and 3 years of directly… more
    HireLifeScience (06/12/24)
    - Related Jobs