At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
Eaton’s IS VEH VGNA division is currently seeking a Lead Quality Engineer. This is a full time, on-site position based at our Roxboro,NC manufacturing facility. Relocation assistance is available to those within the US/PR. The expected
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
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
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,
*Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts ( Nights 6p to 6a) on a 2-2-3 calendar rotation About This Role Our Manufacturing Associates perform processing steps and manufacturing support activities in our
Position Overview The QC Associate I role in Quality Control Microbiology is crucial for performing operational functions of the QC Microbiology laboratory. This position holds the responsibility for conducting environmental and clean utility monitoring and standard
Retail Service Specialist The Retail Service Specialist will support the Store Manager and Assistant Managers in areas of sales, customer service, store appearance, and store operations. This position will also assume shift management responsibilities in the