QA Compliance Specialist Responsible for review and approval of Deviations and CAPAs in support of GMP manufacturing operations. Support timely review of events for classification, initiation in EtQ and closure. Support external client review and resolution of
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
About this role The Sr. Associate III, Compliance - Data Integrity is a key leadership role supporting the RTP Drug Substance Manufacturing site, with a strong focus on ensuring data integrity, compliance, and inspection readiness. This
About this role The Sr. Associate III, Compliance – Risk Management provides operational leadership for Biogen’s RTP drug substance manufacturing site, with a focus on quality risk management (QRM), inspection readiness, data integrity, and compliance systems.
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
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 Overview The Senior QA Technical Specialist acts independently and provides QA subject matter knowledge in the GMP domain to systems and projects with focus on key quality activities and deliverables in accordance with company policies/SOPs
About this role We are seeking an experienced and motivated QC Manager, Lab Support to lead the lab support function within our biologics drug substance manufacturing facility. This role is critical to ensuring seamless QC laboratory
Job Title: GMP Quality Assurance Duration: 06/29/2026- 04/04/2027 with possible extension Office: Research Triangle Park, NC 27709 Pay rate: $40/hr. on W2 Job Description: The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality
About this role Our factories run 24/7 operations. Our maintenance team currently works 10-hour shifts (either Days or Nights) Shift Details: Alternating schedule, Monday–Thursday one week; Tuesday–Friday the following week Hours: 10-hour Shifts on Days Note:
About this role Our factories run 24/7 operations. Our maintenance team currently works 10-hour shifts (either Days or Nights) Shift Details: Alternating schedule, Monday–Thursday one week; Tuesday–Friday the following week Hours: 10-hour Shifts on Nights (15%
Position Job Title: Senior Principal Risk Based Quality Management Data Monitor Location: Research Triangle Park, NC (preferred, not mandatory) About This Role As a Senior Principal Risk Based Quality Management Data Monitor, you will be a
About This Role The Facilities Engineer is responsible for support of both GMP and non-GMP utility systems at a dynamic and diverse biologics manufacturing site with great opportunities for personal and career growth. This position is
Job Description This position follows a traditional 2-2-3 format from 6a-6P ( RED Day Shift) About This Role: The Manufacturing Lead performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment,
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 Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts (either Days or Nights) on a 2-2-3 calendar rotation. Shift Details: This role follows a 2-2-3 calendar rotation on days (6:00 AM
Clinical Research Coordinator Opportunity Unique opportunity to make an impact in the healthcare industry. Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival
Oncology Sr. CRA 2 Our FSP team is currently seeking an Oncology Sr. CRA 2 with 5+ years of monitoring residing in the Midwest (IL, IN, IA, KS, MI, MN, MO, ND, SD, WI, OH) area.
Lead Technician, Drug Product Operations Responsibilities may include but are not limited to: Ability to effectively coach new trainees to build their skills so that they may become effective operations technicians and SMEs. Support production activities