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Kyowa Kirin, Inc.

Full-time|$155K/yr - $170K/yr|On-site|Princeton, New Jersey

Join Kyowa Kirin, a rapidly expanding global specialty pharmaceutical company dedicated to harnessing cutting-edge biotechnologies to innovate and provide groundbreaking therapies across four critical disease areas: bone and mineral disorders; intractable hematologic conditions; hematology oncology; and rare diseases. With our headquarters located in Princet…

Feb 18, 2026

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Associate Director of GLP/GCP Quality Audits and Compliance

Acadia Pharmaceuticals

Full-time|$145.2K/yr - $181.5K/yr|Hybrid|Princeton, New Jersey, United States; San Diego, California, United States; San Francisco, California

About Acadia Pharmaceuticals At Acadia Pharmaceuticals, we are dedicated to transforming scientific breakthroughs into impactful solutions for underserved populations affected by neurological and rare diseases globally. Our portfolio features the first and only FDA-approved therapies for Parkinson’s disease psychosis and Rett syndrome. We are advancing innovative treatments through a diverse pipeline, including programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis. At Acadia, we strive to be the difference for those in need.Please be aware that this role can be located in San Diego, CA; Princeton, NJ; or San Francisco, CA. Acadia operates under a hybrid work model, requiring in-office attendance three days per week on average. Position OverviewThe Associate Director of GLP/GCP Quality Audits and Compliance is pivotal in safeguarding data integrity and ensuring regulatory compliance across the company's nonclinical and clinical operations. This role encompasses the planning, execution, and reporting of both internal and external GLP/GCP audits, ensuring adherence to U.S. and international regulations while promoting ongoing enhancements in quality systems.As a valued quality partner, this role will provide expert advice on GLP/GCP compliance, assist in regulatory inspections, and collaborate closely with internal teams and Contract Service Providers (CSPs) to sustain inspection-ready operations. The ideal candidate will possess strong audit leadership skills, sound regulatory judgment, and the ability to positively influence quality practices throughout the organization.Key ResponsibilitiesPlan, schedule, coordinate, and conduct internal and external GLP/GCP audits of company functions and Contract Service Providers (CSPs) according to company standards and global regulatory requirements.Manage the complete audit lifecycle, including preparation, execution, documentation, reporting, follow-up, and validation of corrective and preventive actions.Prepare, review, and approve clear, compliant audit reports, ensuring that observations, risks, and responsibilities are effectively communicated to relevant stakeholders.

Feb 11, 2026

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Senior Manager of R&D Learning & Development

Acadia Pharmaceuticals

Full-time|$139.6K/yr - $174.5K/yr|On-site|Princeton, New Jersey, United States; San Diego, California, United States

About Acadia Pharmaceuticals Acadia Pharmaceuticals is dedicated to transforming scientific potential into innovative solutions that significantly benefit underrepresented communities facing neurological and rare diseases globally. Our commercial offerings include the first and only FDA-approved treatments for Parkinson’s disease psychosis and Rett syndrome. We are at the forefront of developing a new wave of therapeutic innovations with a robust pipeline that encompasses mid- to late-stage programs targeting Alzheimer’s disease psychosis and Lewy body dementia psychosis, as well as earlier-stage programs addressing various unmet patient needs. At Acadia, our mission is to make a tangible difference in patients' lives.We are seeking talent near: Princeton, NJ; San Diego, CAPosition SummaryThe Senior Manager of R&D Learning & Development plays a pivotal role in designing, implementing, and continuously refining onboarding and training strategies, systems training, and learning processes aimed at enhancing scientific, operational, and future-ready capabilities within the Research and Development organization and its pipeline.Primary ResponsibilitiesContribute to the design, implementation, and ongoing enhancement of a comprehensive onboarding and capability-building curriculum that aligns with the dynamic needs of the R&D pipeline, covering discovery, early development, and late-stage programs.Employ experiential learning methodologies to effectively engage adult learners and facilitate successful knowledge transfer.Assist in managing GxP, congress, and data training in collaboration with internal stakeholders.Work collaboratively with R&D subject matter experts to develop focused training on disease areas, modalities, platforms, and pipeline initiatives, including education on investigational assets and emerging scientific advancements.Lead and support training initiatives in partnership with internal stakeholders.Facilitate the management and development of learning modules in collaboration with external vendors.Oversee the creation of advanced, recurrent, and future-focused training materials.

Apr 9, 2026

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Senior Director of R&D Outsourcing and Business Optimization

Acadia Pharmaceuticals Inc.

Full-time|On-site|Princeton, New Jersey, United States

Join Acadia Pharmaceuticals Inc. as the Senior Director of R&D Outsourcing and Business Optimization, where you will play a pivotal role in enhancing our research and development capabilities. You will lead strategic initiatives to optimize business processes and manage outsourcing operations, ensuring our projects align with our mission to advance innovative therapies for patients.

Mar 19, 2026

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Associate Director of Clinical Quality Management

Kyowa Kirin, Inc.

Full-time|$190K/yr - $190K/yr|On-site|Princeton, New Jersey

Join Kyowa Kirin, a rapidly expanding global specialty pharmaceutical company, committed to innovating life-changing medicines through cutting-edge biotechnologies. We focus on four key disease areas: bone and mineral disorders, intractable hematologic conditions, hematology oncology, and rare diseases. Our mission is to convert scientific advancements into therapeutic solutions, ensuring that patients receive the care they need when existing treatments fall short. Our North America headquarters is based in Princeton, NJ, with additional offices in California, North Carolina, and Mississauga, Ontario.Position Overview:The Associate Director of Clinical Quality Management acts as the primary Risk-Based Quality Management (RBQM) Lead within Clinical Operations. This pivotal role oversees proactive risk management strategies across clinical trials, implementing a comprehensive RBQM framework that encompasses risk identification, assessment, mitigation, centralized monitoring, lessons learned, and the upkeep of a clinical risk library. This ensures uniform risk management practices across studies, programs, vendors, and regions. Collaborating with various departments, this role integrates risk-based decision-making into all aspects of study design, execution, oversight, and continuous enhancement, in accordance with ICH E6 (R3), GCP, and global regulatory standards.

Feb 3, 2026

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Information Assurance Manager (U.S. Citizenship Required)

SciTec, a Firefly Aerospace Company

Full-time|$160K/yr - $160K/yr|On-site|Princeton, New Jersey, United States

SciTec, a proud subsidiary of Firefly Aerospace, stands as an innovative leader among defense contractors, providing cutting-edge technologies that bolster U.S. National Security and Defense initiatives. With over 45 years of experience, we have been at the forefront of supporting Department of Defense clients by creating groundbreaking remote sensing algorithms, tools, and techniques that enhance data exploitation capabilities across various missions, including missile defense, intelligence, surveillance, reconnaissance, space domain awareness, and aircraft survivability.Important Notice: All positions at SciTec are exclusively for U.S. citizens due to the nature of our government contracts. We do not offer sponsorship for work visas. U.S. citizenship is essential for obtaining and maintaining security clearance. Candidates who do not meet these criteria will not be considered.We are currently seeking an experienced Information Assurance Manager to spearhead, develop, and mentor a dedicated team charged with ensuring that our information systems and associated data adhere to stringent security, compliance, and risk management standards as mandated by federal laws and specific agency requirements.

Apr 7, 2026

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Managing Consultant, Air Quality

Ramboll

Full-time|On-site|Princeton

Join our dynamic team at Ramboll as a Managing Consultant in Air Quality, where you will leverage your expertise to drive impactful environmental solutions. In this pivotal role, you will lead projects that enhance air quality standards, working closely with a diverse range of clients including governmental agencies and private sector organizations.Your responsibilities will include developing innovative strategies, collaborating with multidisciplinary teams, and ensuring compliance with regulatory frameworks. This position offers a unique opportunity to make a significant difference in environmental management and public health.

Feb 3, 2026

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Senior Managing Consultant - Air Quality

Ramboll

Full-time|On-site|Princeton

Join Ramboll as a Senior Managing Consultant for Air Quality, where you will play a pivotal role in driving sustainable solutions in air quality management. You will collaborate with a diverse team of experts and contribute to innovative projects that address critical environmental challenges. Your expertise will help shape strategies to improve air quality and promote sustainable practices.

Mar 18, 2026

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Principal Air Quality Specialist

Ramboll

Full-time|On-site|Princeton

Join our dynamic team at Ramboll as a Principal Air Quality Specialist. In this pivotal role, you will leverage your extensive expertise in air quality management to lead innovative projects that enhance environmental performance and compliance. Collaborate with a diverse team of professionals to develop sustainable solutions that address complex air quality challenges.Your contributions will be vital in shaping our approach to air quality assessments, regulatory compliance, and stakeholder engagement. As a leader in the field, you will have the opportunity to mentor junior staff and contribute to the development of best practices within the industry.

Mar 18, 2026

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Senior Consultant - Air Quality Expertise

Ramboll Group

Full-time|On-site|Princeton, New Jersey

Join Ramboll as a Senior Consultant specializing in Air Quality, where your expertise will directly contribute to environmental sustainability. In this pivotal role, you will leverage your analytical skills to assess air quality data and formulate strategies aimed at improving air quality standards. Collaborate with a dynamic team of professionals dedicated to advancing environmental solutions.

Apr 10, 2026

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Enterprise Solutions Quality Tester

Integrated Resources Inc.

Full-time|On-site|Princeton

Join our dynamic team as an Enterprise Solutions Quality Tester in Princeton, NJ. As a key player, you will be responsible for ensuring the quality and reliability of our enterprise software solutions. Your contributions will directly impact our ability to deliver exceptional products to our clients.

Mar 16, 2015

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Managing Consultant in Air Quality Compliance & Permitting - Chemical/Pharmaceutical Sector

Ramboll

Full-time|On-site|Princeton

Join Ramboll as a Managing Consultant focusing on Air Quality Compliance and Permitting within the Chemical and Pharmaceutical sectors. In this role, you will leverage your expertise to guide clients in navigating complex environmental regulations, ensuring compliance, and implementing effective air quality management strategies. Your analytical skills and industry knowledge will contribute to impactful projects that promote sustainable practices and environmental stewardship.

Mar 10, 2026

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Senior Manager, IT Business Analyst - Development & Quality

Kardigan

Full-time|$171K/yr - $223K/yr|On-site|Princeton, New Jersey, United States

Kardigan is dedicated to improving heart health by pursuing both prevention and cures for cardiovascular disease. The company aims to develop several targeted treatments at once, ensuring people with cardiovascular conditions have more options for care. Founded by Tassos Gianakakos, Jay Edelberg, M.D., Ph.D., and Bob McDowell, Ph.D., Kardigan's leadership previously led MyoKardia to discover and develop mavacamten, the first cardiac myosin inhibitor, which was acquired by Bristol Myers Squibb in 2020. Today, the team continues to advance cardiovascular medicine through a strong research platform and a late-stage pipeline focused on patient outcomes. Our Values Patient-centric: Every decision starts with the needs of patients and their families. Authenticity: Honesty and acceptance shape the work environment. Curiosity: Learning and adapting are part of daily work. Collaborative success: Team members support each other, no matter their role. Unlocking innovation: The team embraces risk to advance care, knowing patients depend on progress. These values guide daily work and reflect the impact the team aims to achieve.

Apr 20, 2026

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QUMAS Consultant

Sonsoft Inc.

Contract|On-site|Princeton

Join our dynamic team at Sonsoft Inc. as a QUMAS Consultant, where you will play a crucial role in enhancing our clients' regulatory compliance and quality management systems. As an integral part of our consulting team, you will leverage your expertise to implement effective QUMAS solutions, ensuring that our clients meet industry standards and regulations. This position offers an exciting opportunity to work with cutting-edge technology and contribute to the success of various projects.

Jan 18, 2017

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Drug Supply Manager

Artech Information Systems LLC

Full-time|On-site|Princeton

Join our dynamic team as a Drug Supply Manager where you will play a crucial role in managing the supply chain of pharmaceutical products. In this position, you will be responsible for ensuring the timely delivery and distribution of medications, maintaining inventory levels, and collaborating with various departments to optimize supply chain operations. If you are passionate about improving patient care and have a strong background in supply chain management, we want to hear from you!

Jul 18, 2017

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Clinical Operations Manager

Noom Inc.

Full-time|$121K/yr - $158K/yr|On-site|New York, New York, United States; Princeton, New Jersey, United States

Noom is dedicated to empowering individuals to lead healthier, longer lives. As a leading digital health company, we connect users to a wealth of resources, including educational content, personal coaching, a supportive community, and professional clinicians, all aimed at fostering sustainable habits for improved well-being. Our organization thrives on a foundation of scientific research, cutting-edge technology, and exceptional talent. When you join Noom, you’ll witness firsthand the meaningful impact of your contributions on people's lives.About Our Clinical Operations TeamOur Clinical Operations Team plays a vital role in Noom's success in delivering effective, evidence-based health programs. We operate at the crossroads of clinical excellence and operational innovation, collaborating closely with our Product, Engineering, and B2B teams to enhance and expand Noom's clinical and behavioral initiatives.About the RoleAs we embark on an exciting growth phase, we are searching for a Clinical Operations Manager to help scale Noom Med’s clinical offerings, including GLP-1Rx and other medication fulfillment projects. This position combines clinical operations oversight, vendor management, and program implementation to ensure efficient care delivery for patients, clinicians, pharmacies, labs, and internal stakeholders.The ideal candidate will possess robust operational and project management skills, with a talent for translating clinical workflows into efficient and scalable processes while fostering cross-departmental collaboration.Your ResponsibilitiesManage daily clinical operations to facilitate seamless coordination among patients, clinicians, Care Coordinators, pharmacies, and labs.Serve as a pivotal communication link among stakeholders, resolving issues and enhancing the patient and clinician experience.Assist Customer Experience and Care Coordination teams as a point of escalation for complex cases.Lead the rollout of clinical programs, workflows, and tools from design to implementation.Collaborate with Product, Engineering, and Data teams to develop, test, and launch clinical solutions.Create and maintain SOPs, workflows, and documentation to ensure scalable operations.Manage vendor relationships, monitoring performance against KPIs and SLAs.Support operational compliance, vendor management, and licensing requirements.Evaluate performance metrics, identify areas for improvement, and drive ongoing process enhancements.Ensure compliance with clinical protocols, quality standards, and regulatory obligations.Adapt responsibilities as needed to align with the evolving needs of Noom Med.

Apr 30, 2026

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General Manager at Domino's | Princeton

Domino's Pizza, Inc.

Full-time|On-site|Princeton

Role Overview Domino's Pizza is hiring a General Manager for its Princeton, NJ location. This position leads store operations, focusing on team management, sales, and customer satisfaction. What You Will Do Oversee daily store operations and maintain high service standards Drive sales and monitor financial performance Manage staffing, scheduling, and training for team members Handle inventory control and ensure efficient processes Support and motivate a team to deliver strong results What We Look For Management experience, ideally in food service or retail Strong leadership and communication skills Ability to balance operational details with customer needs Interest in building a positive team culture If you enjoy leading teams and want to help shape the Domino's experience in Princeton, consider joining us.

Apr 20, 2026

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Assistant Manager at Domino's | Princeton

Domino's Pizza, Inc.

Full-time|On-site|Princeton

Role Overview Domino's Pizza in Princeton is hiring an Assistant Manager. This role works closely with the management team to keep daily operations running smoothly and maintain high service and quality standards. The Assistant Manager helps guide team members and supports a positive work environment. What You Will Do Support the management team with daily restaurant operations Help ensure service and product quality meet Domino's standards Assist in training and guiding team members Contribute to a welcoming and efficient workplace Who This Role Suits This position fits someone interested in growing their career in the restaurant industry and comfortable working where each day brings new challenges.

Apr 26, 2026

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Adobe Experience Manager Specialist

Artech Information Systems LLC

Contract|On-site|Princeton

Join our dynamic team at Artech Information Systems LLC as an Adobe Experience Manager (AEM) Specialist. We are looking for a passionate and skilled individual to contribute to our innovative projects. As part of our team, you will play a critical role in enhancing digital experiences for our clients through the effective use of Adobe Experience Manager.

May 17, 2017

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Senior Validation Project Manager

cagents

Full-time|On-site|Princeton, New Jersey

Position Overview:Join our dynamic team as a Senior Validation Project Manager, where you will play a pivotal role as a technical leader. Our ideal candidate possesses a robust background in Commissioning, Qualification, and Validation (CQV) strategy, development, and field execution. At cagents, we prioritize cultural fit, as our people are our greatest asset, and exceptional individuals foster exceptional teams!In this role, you will manage projects exceeding $1 million while leading teams of 6 to 8 engineers and consultants on defined scopes of work. As a successful project manager, you will demonstrate direct accountability for project scope, schedule, and budget. We value experienced generalists, particularly those with expertise in facilities, clean utilities, upstream and downstream biotech equipment, single-use disposables, or aseptic fill-finish manufacturing. While a PMP certification is a plus, your hands-on experience is what will enable you to thrive with our team.Your day-to-day responsibilities may include leading budget review meetings, conducting daily huddles with your team, reviewing summary reports, writing protocols, and providing field support to your team. The role of a CAI PM is multifaceted and requires an active participant—desktop project managers need not apply. Typically, you will report to either a client manager or an area manager.

Jan 3, 2023

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