Vital Sign Jobs in Durham County, NC
Vital Sign Jobs in Durham County, NC
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This application is for a 12week internship role from June August 2025. Resume review begins in January 2025. The Annual Product Review (APR) is a GMP (Good Manufacturing Process) requirement for all countries where Biogens products are marketed. This project corresponds w More...
Manufacturing Technician Iii Maintenance - Nights
Shift and Schedule: 11 PM to 7 AM rotating weeks: 1 week Mon Thu 1 week TueFriAbout this roleA Manufacturing Technician III performs preventative standard and repair maintenance on process equipment and utility equipment such as bioreactors water and CIP systems pumps agitators gearbo More...
Job Title: Clinical Data Associate Duration: 06 months contract with possible extension Shift Details: Day shift/ Fully Remote Pay Range: $30$37 /hr w2 Essential Duties and Responsibilities: Works collaboratively with Process Engineers and Statisticians in Global Manufact More...
Sr Associate Iii Quality Assurance Quality Engineering
The schedule for this position is MF Business hours (full time onsite)About This RoleThe Sr. Associate III of Quality Engineering is responsible for understanding quality systems and maintaining oversight of GMP activities while supporting Automation Engineering Facilities Manufacturi More...
Manufacturing Associate Iv - Clinical Label And Pack
About This RoleAs a Manufacturing Associate at our Research Triangle Park (RTP) facility you will be essential to our Labeling and Packaging operations for bottles vials blisters and syringes playing a key role in delivering lifechanging therapies to patients. This position offers a u More...
This application is for a 12week internship role from June August 2025. Resume review begins in January 2025. The global technology transfer team is responsible for the facilitation management and leadership of all drug substance and drug product technology transfers both intern More...
This is a full time on site position with MF business hours About This Role The Sr Manager Planning leads the material planning function for the RTP Bio DS Manufacturing Site for both clinical and commercial programs. This individual is responsible for planning /managing a l More...
This application is for a 6month student role from July December 2025. Resume review begins in January 2025.The Quality Control Raw Materials (QCRM) team is responsible for ensuring that all materials needed within manufacturing are inspected sampled tested and released in order to m More...
This application is for a 12week internship role from June August 2025. Resume review begins in January 2025.As an intern you will work closely with the Site Training Team to identify learning needs an align learning priorities with expected outcomes. This position offers exposure to More...
Program Manager Patient Services Voice Of Customer Analytics
This position reports MF business hours at our Research Triangle Park NC facilityAbout This RoleThe Program Manager Patient Services will be a pivotal role within the Quality Monitoring and Experience Optimization team driving the advancement of our Customer Experience (CX) monitoring More...
This application is for a 12week internship role from June August 2025. Resume review begins in January 2025. The Facilities Engineering team supports the utility and facility equipment associated with bioprocessing capital projects and ensures continuous improvement and enginee More...
This application is for a 6month student role from July December 2025. Resume review begins in January 2025. Biogen Engineering at the RTP Pharma site supports two sterile filling lines and an Automated Visual Inspection Machine at the Parenteral Facility and a smallscale fillin More...
100% TELECOMMUTEResponsibilities:Individual will be assisting with the flow of work to ensure that the team is working at full capacity and no projects fall behind We are looking for someone who takes initiative and drives important production design projects to the finish line. Assis More...
100% TELECOMMUTEResponsibilities:Individual will be assisting with the flow of work to ensure that the team is working at full capacity and no projects fall behind We are looking for someone who takes initiative and drives important production design projects to the finish line. Assis More...
Manufacturing Associate Ii - Parenteral Filling
This position will work 12hour Night SHIFTS (approx. 6:00PM 6:00AM) on a 223 rotationAbout This RoleManufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations More...
About This RoleThe Sr. Specialist I Instrumentation& Controls (I&C) position supports the daily activities of the I&C technicians and management at the 5000 Davis Drive Drug Substance site. The site includes laboratory facilities central utilities warehouse drug substance More...
Sr Manager Manufacturing - Parenteral Filling
About This RoleBiogen is seeking an experienced manufacturing leader who is responsible for establishing and maintaining accountability and ownership of Parenteral Filling operations. Fostering a collaborative working environment throughout the manufacturing area the Sr. Manager will More...
Manufacturing Process Maintenance Specialist Ii
A Manufacturing Process Maintenance Specialist III will provide customeroriented service and support in a fastpaced manufacturing environment. Performs corrective and preventative maintenance on manufacturing Filling equipment Isolators Vial Washers Autoclaves Parts Washers More...
Manufacturing Process Maintenance Specialist Ii
A Manufacturing Process Maintenance Specialist III will provide customeroriented service and support in a fastpaced manufacturing environment. Performs corrective and preventative maintenance on manufacturing Filling equipment Isolators Vial Washers Autoclaves Parts Washers More...
Description: Works collaboratively with Process Engineers and Statisticians in Global Manufacturing Sciences and Technology (GMSAT) Statistical Sciences & Analytics (SS&A) team to meet project deliverables and timelines to author and approve Continued Process Verification (CPV) relat More...
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