- 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
- 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
- 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
- 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
- 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
