Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
About This Role As a Scientist II within Pharma Validation, Transfer and Registration (VTR), you will serve as a subject matter expert supporting analytical method validation, transfer, investigation, and regulatory filings for small molecule and antisense oligonucleotide (ASO)
This job is with Biogen, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. About This Role As a Scientist
Associate Director Or Director In Program Design Join a high-impact team shaping end-to-end biologics programs for clients across the globe. As an Associate Director or Director in Program Design, youll lead technical engagements, design robust development-to-cGMP manufacturing strategies, and
Program Manager, Electromechanical Systems Group: Eng Materials Group N. America Division: Noise Vibration & Harshness (NVH) Location: USA Bldg E Cary NC LORD Job Family: Engineering Job Type: Regular NVH is a best-in-class innovator in the industrial
Job Title This individual will provide thought-leadership, expertise, and management of managed validation services to the IT Validation & Compliance infrastructure in a Contract Development and Manufacturing Organization (CDMO) setting. Job Responsibilities: Provide oversight of enterprise software validation from
Program Manager, Director - Cancer Research Exp Durham, North Carolina DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering and integration, and digital transformation. Our experts in public
Duration: 24 months Contract, strong chances of extension Job Description: Reporting to the Director of Sterility Assurance and Contamination Control, the Associate Director of Quality for Capital Programs is responsible for quality assurance oversight from early design
California, US residents click here. The job details are as follows: Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose
Team Description: Kitware is seeking a Software Engineer to join the Computer Vision team. This position offers an opportunity to help Kitware’s customers build meaningful software that will stand the test of time. Through this position,
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific
About This Role We are seeking an experienced technical contributor to join our Automation Systems Engineering team at the Biogen RTP Bio site. The Senior Automation Engineer I will support Syncade (MES) system administration within a
About This Role The Automation Engineer II/III provides 24/7 process controls/automation technical site support to the Biogen 900 Davis drive, NC manufacturing site. In addition, this role manages multiple small OPEX/CAPEX projects and continuous improvement initiatives
Shift Details: Schedule: Alternating schedule, Monday–Thursday one week; Tuesday–Friday the following week Hours: 10-hour shifts About this role As a Senior Manufacturing Technician, you will play a critical role in supporting manufacturing and laboratory operations by
About This Role A Sr. Engineer I/II in Automation & MES is a key member of the RTP Bio Automation & MES team, supporting both day-to-day manufacturing operations and large-scale capital and improvement projects. This role
About This Role: The Biologics VTR (Validation, Transfer, and Registration) and AIV (Analytical Instrument Validation) leader oversees the VTR team across Biologics and Combination Drugs as well as the AIV teams within Biogen Global Product and Quality Control
About This Role As a Senior Associate II, Technical Quality, you will play a critical role in ensuring quality and compliance across manufacturing, laboratory, engineering, and quality operations. You will lead and support investigations, change controls,
Position schedule: 2nd shift The schedule for this position can be either Tues-Fri 2PM to midnight OR Mon-Fri 2PM to 10PM (dependent on applicant preference). There is a rotational on-call schedule for weekends for this position.
About this role As an Engineer III, you will serve as a key technical resource supporting manufacturing equipment within our production areas, with a focus on solid dose (OSD/ASO) operations. This role plays a critical part