Job Description SummaryJoin Novartis as our QA Operations Head and play a pivotal role in ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an opportunity to lead a
At Duke Health, were driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we
Job Overview Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines,
Protecting our tomorrow Job Title: Senior QA Specialist, External Manufacturing, US Location: Remote, East Coast Preferred Department: Quality Assurance Reports To: Head of External QA & Global EHS Salary Range: $120k - $155k About Bavarian Nordic At Bavarian
The QA Compliance Lead Auditor (Host) is a senior‑level role that is US remote based with preference for candidates near Durham, NC location. This position is within Fortrea’s Global Quality Assurance organization, responsible for providing regulatory expertise,
Job Description: Note: Fidelity will not provide immigration sponsorship for this position. The Role We are seeking a Senior QA Automation Engineer passionate about latest technologies, modern frameworks, and design patterns to join our Human Resource Technology
JOB SUMMARY The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists are expected to provide sound guidance to Manufacturing
Job Description SummaryLocation: Morrisville, NC Join Novartis as our QA Compliance and Systems Head and help shape the quality foundation that enables the delivery of medicines to patients worldwide. This is a unique opportunity to join our
About the Department For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our
Job descriptions may display in multiple languages based on your language selection. What we offer: At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest
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Job Description:The CV Invasive Specialist II (CVIS II) performs duties necessary for catheterization procedures at a technical and professional level requiring minimal supervision of technical detail. The CVIS II performs a variety of technical procedures that
Validation Project Lead / Documentation Audit LeadMajor Pharmaceutical Facility Construction Project Location: Durham, NC - FST Life Science office FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a
JOB DESCRIPTION: This position is on a 2-2-3 shift, Day Shift (7am-7pm) The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and
With a company culture rooted in collaboration, expertise and innovation, we aim to promote progress and inspire our clients, employees, investors and communities to achieve their greatest potential. Our work is the catalyst that helps others
JOB SUMMARY *Nightshift: 7PM-7AM, 2-2-3 rotating schedule The Senior Manufacturing Associate I/II (Nights) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must
JOB SUMMARY This position is on a 2-2-3 rotating schedule, dayshift (7am-7pm) The Manufacturing Associate I/II is responsible for performing upstream processing for biopharmaceutical products. The Manufacturing Associate must follow written, approved procedures and forms to
JOB SUMMARY *Nightshift: 7PM-7AM, 2-2-3 rotating schedule The Senior Manufacturing Associate I/II (Nights) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must
Why UKG: At UKG, the work you do matters. The code you ship, the decisions you make, and the care you show a customer all add up to real impact. Today, tens of millions of workers
Why UKG: At UKG, the work you do matters. The code you ship, the decisions you make, and the care you show a customer all add up to real impact. Today, tens of millions of workers