- Exela Pharma Sciences, LLC (Lenoir, NC)
- …deviations, CAPAs, and/or managing change controls in the Veeva Digital system. The Quality Systems specialist will support GMP activities to ensure compliance ... Position Summary: The Specialist , QA - Systems will be responsible for...building and approving CAPAs in Veeva.Write/update SOPs and other documentation pertaining to Quality SystemsPotential participation in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Specialist , Sterile Engineer This Sterile Pharm Operations Engineer position will provide engineering support to sterile ... various partner groups such as operations, equipment vendors, site maintenance, quality .Provide quality engineering support that includes authoring and executing… more
- Merck & Co. (Rahway, NJ)
- …of immediate and future state business objectives.The SAP Cloud Infra Planning, Sr. Specialist will play a critical role in driving releases within our global ... work independently on high-profile tasks.The SAP Cloud Infra Planning, Sr. Specialist is responsible for the following:Plan, schedule, and coordinate global… 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
- Merck & Co. (Durham, NC)
- …make our products. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement. We work in the local plant ... connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. POSITION OVERVIEW The successful… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Associate Specialist - Engineering Auto Eng position will report to the Director, ... process control systems to improve production efficiency and product quality .Collaborate with cross-functional teams, including operations, maintenance, 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma. Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... Overview We are actively seeking a proficient Master Data Governance Sr. Specialist with a specific focus on Materials orchestration throughout the End-to-End… 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
- Merck & Co. (Rahway, NJ)
- …Database Services (CDS) staff to communicate issues and ideas to improve quality and efficiency.Participate in extra activities including, but not limited to, study ... language, development theory and techniques, testing methodologies, and software documentation .Qualifications, Skills & ExperienceA minimum of 2 years of database… more
- 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, ... outside contractors/vendors to complete tasks Supports and/or owns technical and quality investigations, CAPAs and corrections Develops and performs any required… 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
- Novo Nordisk Inc. (West Lebanon, IN)
- …write up Deviations events utilizing Root Cause Analysis Utilize the quality system to implement changes associated with technical operations, engineering, and/or ... (generate, execute, and evaluate change requests) Revise and create documentation (SOP, batch records, reports) associated with technical operations, production,… more
- Shimadzu Scientific Instruments (Los Angeles, CA)
- …technical training to customers, service, and technical support personnel. (daily) Accurate documentation and reporting of all repairs and product failures and when ... with necessary telephone technical support, repair parts shipments and documentation required to effect instrument repairs, maintenance, and installations. (daily)… 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
- Merck & Co. (North Wales, PA)
- …lake and data warehouse.Work with data governance team and implement data quality checks and maintain data catalogs.Use Orchestration, logging, and monitoring tools ... proof of concepts using Jupyter Notebooks and create technical documentation as needed.Requirements:Bachelor's degree or equivalent in Mathematics, Computer Science,… more
- Merck & Co. (Rahway, NJ)
- …( Global Clinical Trial Operations) organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance in ... document disclosure, and data sharing with external researchers. - The Specialist (Disclosure Medical Writer) will be primarily responsible for preparing clinical… more
- Merck & Co. (Rahway, NJ)
- …and proceduresExperience with agile developmentExperience with software testing, Micro Focus ALM/ Quality Centre, and Good Documentation PracticesWhat we offer: ... for tomorrow. The position of ServiceNow CMDB & Discovery Specialist has responsibility for s upporting the standardization, design,...(GOM) function, and collaborate with colleagues from IT Data Quality , IT Analytics & Reporting , IT Service… more
- Merck & Co. (Rahway, NJ)
- …procedures, workflow, job aids, training, knowledge articles, and other supporting documentation .Marketing and increasing awareness of Data Quality leading ... The position of CMDB & Discovery Analyst / Sr. Specialist has responsibility for s upporting the standardization, design,...(GOM) function, and collaborate with colleagues from IT Data Quality , IT Analytics & Reporting , IT Service Management… more
- Aequor (Thousand Oaks, CA)
- …about 1 week a month - multiple short trips. In support of 's Quality Assurance program manages and oversees the operations of a specific area(s) of responsibility ... 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
