- Merck & Co. (Rahway, NJ)
- … 4 and Part 820, EU MDR:2017/745, and ISO 13485:2016 for review of Quality Management System documents for the Quality Manual.Previous experience in Medical ... quality issues related to pure Medical Devices and the device constituent part of a Combination Product.Manage activities within electronic computer systems, eg,… more
- Formation Bio (New York, NY)
- …drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the ... values, and every team and individual plays a key part in our mission to bring new treatments to...strategies and operational plans.Responsibilities Leads and manages the writing, review , and finalization of clinical development documents such as… more
- AUROBINDO (Dayton, OH)
- Division OverviewAurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical prouct development and ... assigned work.3. Independently plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction.4. Record data and… more
- Genmab (NJ)
- …ready to make a meaningful impact in oncology drug development and be part of a dynamic, collaborative team that values innovation, quality, and scientific ... to patients-and we want you to grow with us.As part of our Global Medical Writing team, you will...trial teams to manage timelines, facilitate meetings, and lead review cycles.Provide expert peer review and editing… more
- AUROBINDO (Durham, NC)
- … Document work clearly and perform tests accurately.Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.Perform maintenance and calibrations ... Division OverviewAurolife Pharma was founded in 2008 as part of a group of companies that has...supervisor to plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction.Record data… more
- AUROBINDO (Durham, NC)
- Division OverviewAurolife was founded in 2008 as part of a group of companies that have a long history of excelling in generic pharmaceutical product development and ... such as LIMS, Quality Assurance Management System (QAMS),Waters Empower, Document Management System, Training ManagementSystem etc.ResponsibilitiesEnsure key software development… more
- Merck & Co. (Rahway, NJ)
- …human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate ... vials, medical device release testing in a timely manner following GMP procedures. Document the execution, procedure, results, and conclusions of experiments in a… more
- US Bank (St. Paul, MN)
- …working hours between **8:00am - 4:30pm CST,** Monday through Friday. The Document Review Associate performs routine and/or repetitive clerical functions ... and discover what you excel at-all from Day One. **Job Description** This is a ** part - time ** role for a total of **19 hours weekly** . Onsite expectation of **3… more
- Eurofins (Indianapolis, IN)
- …in Europe over the past 20 years. Job Description + Complete data integrity review of analytical data reporting records for the client's portfolio of Bioproducts + ... as needed + Upload new and updated documents into document repository and populate document properties +...perform daily monitoring to meet TAT + Prepare and review job plans, conduct semiannual performance reviews, keep training… more
- Lilly (Pleasant Prairie, WI)
- …Standard Operating Procedures as needed. + Provide technical assistance throughout the document initiation, review , and approval process. + Prepare and route ... on new manufacturing investments and new pioneering technologies. The Senior Specialist - Document Control serves as a site document controller to support GxP… more
- North Wind Group (Richland, WA)
- …and document control fundamentals to facilitate effective communication between the Document Control team and customers. + Review and track daily attendance ... Location: Richland, Washington Title: Document Control and Records Specialist Lead Schedule (FT/PT):...Control and Records Specialist Lead Schedule (FT/PT): Regular Full Time Travel Required: No Clearance: Ability to Obtain North… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …Coordinator** could include, but are not limited to, the following: + Performs document review against standard formats and requirements and ensures appropriate ... cross-referencing, links, and other required meta-data for documents + Processes document requests including intake, coordination, editing, review , and release +… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Document Control Specialist - Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization ... supporting product development, launch, and full life-cycle supply. With time -tested experience in development sciences, delivery technologies, and multi-modality… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …other processes + Executes tasks associated with EDMS outages + Manages document requests including intake, distribution, coordination, editing, review , and ... We are hiring a Lead Document Coordinator to assist our Document ...on-the-floor guidance and support to employees + Ensures employees time sheets are completed on time +… more
- Kratos Defense & Security Solutions, Inc. (San Jose, CA)
- …ensure that documents are reviewed, approved, and released on schedule.* Manage the document change control (ECO) process, including review and approval of ... Inc., a Kratos' company, is looking for an experienced Document Control Manager to work onsite at their San...401(k) savings plan, Employee Stock Purchase Plan (ESPP), paid time off, paid holidays, tuition reimbursement, and more. GENERAL… more
- OTTO Engineering (Carpentersville, IL)
- Lead Document Controller OTTO's opportunity: Our Lead Document Controller is responsible for directing and managing OTTO's Document Control system; including ... managing company technical documentation, procedures and instructions. Lead and direct Document Control Clerks to assure company adherence to requirements and proper… more
- AECOM (Sacramento, CA)
- …leadership, technical teams, contractors, and other stakeholders to ensure timely ** document submission, review , approval, distribution** , and **revision ... for future generations. There has never been a better time to be at AECOM. With accelerating infrastructure investment...bring your bold ideas and big dreams and become part of a global team of over 50,000 planners,… more
- Arena Technical Resources, LLC (WA)
- …Litera Compare, DocXTools, Best Authority, and others as needed). ▪ Conduct document review procedures such asquality check(QC), ensuring requests are fulfilled ... Document Support Specialist Location: Washington, US Job ID:...support services background. ▪ Demonstrated experience working in a time sensitive, high-visibility environment. ▪ Demonstrated experience improving the… more
- Carollo Engineers (Oklahoma City, OK)
- …motivated, talented people to help us reach that goal.We are seeking a full- time Office Administrator/ Document Processor in our Oklahoma City office to ... **Overview** Would you like to be a part of a dynamic team of professionals that...in OneNote. + Using Microsoft Teams for virtual meetings, real- time collaboration, internal messaging, and document storage.… more
- SitusAMC (St. Petersburg, FL)
- …priority and regular mail packages, log, and record package information in the document system daily + Operate document scanner and scanning software which ... documents + Input mortgage doc information into the company's document system + Organize/update documents with VMS barcode system...of relevant experience + Attention to detail in the review and data entry of information from documents +… more
