- Outlier AI (Wichita, KS)
- …Have you got what it takes to succeed The following information should be read carefully by all candidates. Outlier is committed to improving the intelligence & ... safety of AI models. Owned and operated by Scale AI , weve recently been featured in Forbes for partnering experts with top AI labs to provide the high quality data for LLMs. We believe AI can only perform as well as the data its trained on. Thats why we work… more
- Cipla (Fall River, MA)
- Job Title : Mfg. Validation Engineer FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM (may vary ... is searching for experienced candidates for the position of Manufacturing Validation Engineer . The Manufacturing Validation Engineer is responsible… more
- Merck & Co. (Rahway, NJ)
- …DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process Development ... of product design and development; manufacturing process development, qualification, and validation ; and design control and risk management techniques to positively… more
- Cipla (Fall River, MA)
- Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall River, MA Work Hours: General Shift: 08:30 AM - 5:00 PM ... Lead Salary Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is responsible for managing controlled documents to… more
- Eisai, Inc (Chicago, IL)
- …If this is your profile, we want to hear from you. The Associate Director of Global Submission Management (GSM) is responsible for leading, managing, strategizing, ... technical oversight to support the objectives of Global Regulatory Operations. The Associate Director will collaborate with the Heads of Submissions Management for… more
- Aptyx (Charlotte, NC)
- …and reliability testing plans for catheter systems, including the development and validation of accurate in-vitro and in-vivo models and methods Develop pilot and ... for devices Assess feasibility of processes and support manufacturing with validation plans and time studies Support product manufacturing until the project… more
- Aequor (Thousand Oaks, CA)
- …improvement projects from problem definition through vendor/technology evaluation, piloting/ validation , SOP generation, and handoff into operations while also ... critical reagents. End-to-end ownership: Lead projects through definition, pilot, validation , SOP documentation and handoff; deliver measurable outcomes. Practical… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Associate Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) ... Under the broad guidance of the DSCS Digital Program Mgmt Lead, the Associate Director, DSCS Digital Project Manager, will be responsible for implementing improved… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting into the Director, Logistics and Distribution Technology the Associate Director, Logistics and Distribution Technology will be responsible and ... to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible providing… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director, Engineering as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Associate Director of Engineering is a strategic and operational leader responsible for the management, development, and performance of… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:We're looking for an Associate , Regulatory Operations on the Regulatory team to help us expand what's possible ... document authoring, review, approval, and publishing workflows.Conduct technical checks ( validation , bookmarking, hyperlinking) to ensure submissions pass regulatory agency… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …requirements. They are responsible for the development of cleaning processes, the validation of those processes, and for monitoring those processes during routine ... acrylics, perfume/cologne, and personal cell phones. Relationships Reports to: Associate Manager Essential Functions Assist with SOPs, JIs, Deviations,cand other… more
- Insmed Incorporated (NJ)
- …the future of science, we're in. Are you?About the Role:The Associate Director, Programming provides technical leadership and ensures adequate programming support ... to statistical programming practices Contributes to the creation, maintenance, and validation of internal standards for programming tools, outputs, and macros… more
- ACROBiosystems Inc. (San Jose, CA)
- …support drug development and clinical applications from target discovery and validation , candidate drug screening and optimization, CMC development, preclinical and ... encouraging cross-functional collaboration and continuous learning. Job Summary The Associate Regional Manager will lead commercial activities across Northern… more
- Merck & Co. (Rahway, NJ)
- …lifecycle. Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs ... and good programming practices.Maintain and manage a project plan including resource forecasting.-Coordinate the activities of a global programming team that includes outsource provider staff.Membership on departmental strategic initiative teams Education and… more
- Insmed Incorporated (NJ)
- …and Electronic SignaturesExperience with GAMP 5 guidelines and validation lifecycle processesIT System Project managementExperience managing vendor relationships ... for multiple software platformsWhere You'll WorkThis is a hybrid role based out of our Bridgewater NJ HQ office. You'll have the option to work remotely most of the time, with in-person collaboration when it matters most.This role requires occasional Up to 10%… more
- Christus Health (San Antonio, TX)
- …validated through successful completion of the designated organizational entry competency validation and an Emergency Department- specific competency validation . ... certification will apply, dependent on your experience level. Any Candidate/ Associate with at least one year of acute care...within the past three years is considered an Experienced Associate . Any Candidate/ Associate who does not have… more
- Christus Health (San Antonio, TX)
- …through successful completion of the designated organizational entry competency validation and a Critical Care Department-specific competency validation . ... certification will apply, dependent on your experience level. Any Candidate/ Associate with at least one year of acute care...within the past three years is considered an Experienced Associate . Any Candidate/ Associate who does not have… more
- Christus Health (San Antonio, TX)
- …are validated through successful completion of the designated organizational entry competency validation and a MedSurg specific competency validation . All newly ... certification will apply, dependent on your experience level. Any Candidate/ Associate with at least one year of acute care...within the past three years is considered an Experienced Associate . Any Candidate/ Associate who does not have… more
- Christus Health (San Antonio, TX)
- …validated through successful completion of the designated organizational entry competency validation and an Emergency Department- specific competency validation . ... certification will apply, dependent on your experience level. Any Candidate/ Associate with at least one year of acute care...within the past three years is considered an Experienced Associate . Any Candidate/ Associate who does not have… more
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