Work Location:Mount Laurel, New Jersey, United States of America Hours:40 Pay Details:$98,160 - $159,270 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. Growth opportunities and skill development are defining features
Be an integral part of an agile team thats constantly pushing the envelope to enhance, build, and deliver top-notch technology products. As a Senior Lead Software Engineer- Python Distributed Development and AI Modernization at JPMorganChase within
If you are a software engineering leader ready to take the reins and drive impact, we’ve got an opportunity just for you. As a Director of Software Engineering – Payment Data Platform Infrastructure at JPMorgan Chase
Description Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have
Calling all innovators - find your future at Fiserv. Were Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations,
Description Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have 150 US
ADP is hiring an Oracle Developer Locations: Parsippany NJ (preferred), Alpharetta GA, Pasadena CA Are you empathetic to client needs and inspired by transformation and impacting the lives of millions of people every day Are you
Calling all innovators - find your future at Fiserv. Were Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations,
Quality Planner Opportunity Avantor is looking for a Quality Planner to join our Quality group! The Quality Planner is central to communicate batch and sample investigations, ensuring smooth progress and timely updates. Youll act as a key
NOI Investigations Specialist The NOI Investigations Specialist plays a critical role in ensuring product quality, compliance, and patient safety by conducting comprehensive investigations into quality events that may impact the manufacturing, release, distribution, or shelf life of
Manufacturing Supervisor For Cell Therapy Operations We are seeking an innovative and highly motivated Manufacturing Supervisor for Cell Therapy Operations to join our team who will be responsible for ramp-up and oversight of the cGMP operations
Quality Assurance Technician It is an essential and basic job responsibility, as a Quality Assurance Technician to comply with all Standard Operating Procedures, Work Instructions, and current Good manufacturing practices. A quality assurance technician will work
QA Director GMP ESO Biotechnologies This position is with Recordati Rare Diseases, Inc. (RRD), North America, an affiliate of Recordati. At Recordati, we are united by a clear purpose: unlocking the full potential of life. With
Director of Quality & Compliance The Director of Quality & Compliance is responsible for leading the companys Quality Management System (QMS) and ensuring the consistent delivery of safe, compliant, and high-quality products across all manufacturing, packaging,
IT Technical Project Manager Key Skills: 12+ years of IT experience with at least 6+ years in technical project/program management delivering data and analytics solutions. Strong AI/ML background understanding of ML lifecycle, Vertex AI / MLOps,
QA Support Contractor The contractor will provide temporary QA support to maintain quality and compliance oversight of sterile pharmaceutical products manufactured by third-party partners. The focus will be on batch release, issue resolution, and regulatory compliance for the
Associate Director-Quality Assurance (QA-CMC) Company is seeking a highly experienced, motivated, and innovative quality leader with strong experience in early and late-stage development to join our Quality team as Associate Director, Quality Assurance to support drug
QA Product Manager (Sterile Products) Location: Florham Park, New Jersey Type: Contract Compensation: $45-$59 per hour dependent on years of experience and education. Contractor Work Model: Hybrid onsite and remote Hours: 40.0 hours per week Responsibilities
Inprocess Quality Assurance Associate I Location: US-NJ-East Windsor High School Diploma or Equivalency. Up to 2 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment. Responsibilities: Collaborates with other
Sr. Director of Quality Operations Ledgewood, NJ Harrow (Nasdaq: HROW) is a leading provider of ophthalmic disease management solutions in North America. Harrow is an incredible entrepreneurial company where we celebrate the ability of every member