About This Role We are seeking a skilled Sr. Program Lead, Process Optimization to implement regulatory, legal, and commercial compliance controls for identified areas of promotional risk. This position is responsible for working cross-functionally to develop and
Arcadis is the worlds leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 34,000 people, in over 30 countries, dedicated to improving quality of life. Everyone has
Carolina Senior Marketing Internship Position We are a small group of hard-working, get-it-done kind of people, with a constant focus on new ideas, excellence, and integrity. If youre a task-oriented, detail-driven problem solver who enjoys building
Manufacturing Operator The Manufacturing Operator is responsible for executing a wide range of operations in a cGMP-compliant biopharmaceutical manufacturing environment. This role involves operating, maintaining, and troubleshooting production equipment, performing and documenting complex and critical processes,
Documentation Specialist - I Location: 100 Rodolphe Street, Durham, NC Pay Rate: $29.5/HR Qualifications: Education: Bachelor degree in a Science, Engineering, English, Business or relevant discipline OR Highschool Diploma with two years related GMP Biopharma experience Required
Senior Consultant - Healthcare Clinical Documentation Specialist Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organization. Join our
Senior Business Process Analyst, Revenue Operations Draper, UT EGNYTE YOUR CAREER. SPARK YOUR PASSION. Egnyte is a place where we spark opportunities for amazing people. We believe that every role has a great impact, and every Egnyter
Technical Source is seeking multiple Downstream Process Equipment Engineers to support startup activities for a large-scale biologics manufacturing expansion project. These roles will support installation verification, commissioning, startup, and operational readiness activities for downstream process equipment within a
Technical Source is seeking experienced Upstream Process Equipment Engineers to support a large-scale biologics manufacturing expansion project in Holly Springs, NC. This role will support startup, commissioning, qualification, and operational readiness activities for upstream manufacturing systems within
Process Improvement Specialist Finance Transformation We are seeking a high-impact Process Improvement Specialist Finance Transformation to support the modernization of finance processes through end-to-end process discovery, data-driven analysis, and low-code/no-code automation to join our Raleigh, North Carolina (NC) office!
Finance Transformation Team Manager and Process Design & Reengineering Lead Step into a role where youll help shape the future of finance. As part of our Finance Transformation team, youll collaborate with CFOs, finance leaders, and executive
Accounts Payables Process Improvement Specialist Kimley-Horn is looking for an Accounts Payables Process Improvement Specialist to join our Raleigh, North Carolina office! This is not a remote position. This role supports accounts payable and employee expense processes for
Process Expert Step into a role where your technical expertise directly drives the success of life-changing medicines. As a Process Expert, you will be at the heart of manufacturing operations, ensuring processes run smoothly, compliantly, and efficiently. You
Validation Project Lead / Documentation Audit Lead FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical manufacturing facility construction project. This role is responsible for establishing a standardized
Ambulatory Clinical Documentation Improvement Specialist 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
Clinical Documentation Improvement Spec-Outpatient This position will be responsible for utilizing their clinical/nursing knowledge, and understanding of current CMS coding guidelines, conventions and AHA coding clinics to improve the overall quality and completeness of the patient medical
Manufacturing Equipment Operator You will operate and maintain manufacturing equipment to safely deliver high-quality products. You will work closely with operators, technicians and leads to troubleshoot issues and keep production running. We value problem-solvers who take
Manufacturing Process Associate Location: Durham, NC 27703 Duration: 12 Months (Extension Possible) Shift: Day Shift Monday to Friday, 7:00 AM 3:30 PM Summary The Manufacturing Process Associate supports daily production activities in a GMP-regulated manufacturing environment. This position
Sample Management Coordinator Support daily GMP manufacturing operations by performing production sampling, managing batch documentation and GLIMS activities, and coordinating with cross-functional stakeholders to ensure accurate, timely, and compliant execution of manufacturing processes that enable product quality
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