- Option Care Health (Dublin, OH)
- …a diverse workforce. Job Description Summary:Hiring Range From $18+The Specialist , Patient Registration is responsible for facilitating new patient's transition ... partners feel Option Care Health makes it easy to transition care. The Specialist , Patient Registration works in conjunction with Sales to prepare patients for OCH… more
- Aequor (Thousand Oaks, CA)
- …Cause Analysis (RCA) investigative and deviations experience. Experience 3-4 YOE Quality GMP/GLP experience and working in a regulatory environment. Processing all ... process by determining follow-up required for complaint return samples and documentation of communication attempts, partnering with call centers providing tactical… more
- Merck & Co. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded Quality Control Laboratory Associate Specialist that can help drive our Strategic Operating ... bulk active ingredient, finished product and support laboratory testing for vaccines.The Quality Control Laboratory Associate Specialist participates on a team… more
- Novo Nordisk Inc. (Boulder, CO)
- …to support analytical and process development, the CMC team works alongside Quality , Regulatory, Technical Operations and RNAi Early Development professionals at our ... are driving change. Are you ready to make a difference? The Position The Specialist , API Manufacturing works in Novo Nordisk's Boulder, Colorado Pilot Plant and is… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything ... is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything ... is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... Performs walk-through audits of NNUSBPI Manufacturing facilities Releases product based on Quality Assurance record review and approval by Manager, Quality … more
- Merck & Co. (Rahway, NJ)
- …Description Position Description: As a member of our company's Research Laboratories Quality Assurance community, provide for and lead Quality Assurance ... oversight for computer system validation matters within the Global Development Quality organization and for the company's R&D division.For company's Clinical Supply,… more
- Merck & Co. (Durham, NC)
- …are seeking a highly motivated individual to partner with the Operations, Quality Operations, and Technical Operations to meet the targeted supply and compliance ... vaccines in the Global Vaccine and Sterile Manufacturing organization.The successful Specialist candidate will be energetic and technically sound, with strong… more
- Merck & Co. (Durham, NC)
- …in equipment validation, process validation, and GMP laboratory readiness.- The Quality Operations Laboratory Associate Specialist performs laboratory testing on ... and energize individuals at all levels in the organizationFUNCTIONAL EXPERTISE: The Specialist , Quality Control will be responsible for activities that support… more
- Aequor (Bothell, WA)
- …skills include- strong cross-functional experience, strong interpersonal skills *Job Description: The Quality Assurance Specialist position plays a key role in ... regulated cGMP environment. The primary focus of the QA Specialist role will be to support routine clinical and...industry expectations. Assist the QA department in maintaining the Quality focused culture at Jump by ensuring documentation… more
- Novo Nordisk Inc. (Durham, NC)
- …with Regulations, ISO standards, corporate & local SOPs Reviews & approves documentation for Quality approval - components/raw material, batch records, change ... life-changing careers, and the opportunity to help improve the quality of life for millions of people around the...Production Records (BPRs), Change Requests (CR's), Deviations & other documentation (in conjunction with LoB) & QA presence &… more
- 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:The automation engineer… more
- American Honda Motor Co Inc (Marysville, OH)
- …HR initiatives to support our associates so we can continue to build high quality products that contribute to the power of the Honda Brand! Key AccountabilitiesAct ... Manage and support associate internal movement process, including evaluation of documentation and ensuring alignment with company policies, budgets, etc. Support… more
- Novo Nordisk Inc. (Durham, NC)
- …our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate ... with IT, metrology & other key stakeholders to ensure the right quality , cost & timely completion of all deliverables. Relationships Manager. Essential Functions… more
- Merck & Co. (Durham, NC)
- …work with shop floor production personnel and interface with Technical Support and Quality Operations. Furthermore, the candidate must be able to work efficiently in ... which may require change controls or have regulatory impact.Author and update GMP documentation including but not limited to SOPs and batch records.Serve as a… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …to support manufacturing operations. Focus areas may include Training, Documentation , Deviations, Change Control and Projects. Drives the coordination and ... execution of process and equipment improvement programs, reviews completed quality records, generates quality deviation responses, drive investigations and has… more
- Catalent (Manassas, VA)
- … Specialist - 2nd Shift is responsible for creating and maintaining the Quality System documentation . Communicate any deviations to management. Assist the ... based positionThe Role:Support the creation and maintenance of all documentation related to the Quality System utilizing...maintenance of all documentation related to the Quality System utilizing technical writing skills to ensure proper… more
- Novo Nordisk Inc. (Durham, NC)
- …our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate ... party instrument services Accurately & legibly records all activities in appropriate documentation . Writes work orders Reviews documentation for accuracy &… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …promise 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...on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support… more
