Niagen Bioscience Inc jobs

Pricing Associate Director, Waters Biosciences Division 2 Locations posted: Posted 4 Days Ago

Senior Quality Assurance Manager - BioScience Cincinnati, OH posted: Posted 21 Days Ago

Principal Scientist Metabolism Bioscience Research, CVRM US - Gaithersburg - MD posted: Posted 3 Days Ago

Field Application Scientist, Biosciences, Southeast Asia Singapore, Singapore Embrace the opportunity to become a Field Application Scientist, Biosciences, and support cutting-edge Cell Biology solutions for leading clients. Deliver hands-on training, technical expertise, and customer success in a dynamic, global environment. Grow your career with Thermo Fisher Scientific and make a real impact in advancing scientific discovery across Southeast Asia.

Quality Systems and Standards Manager-- BioScience Cincinnati, OH posted: Posted 21 Days Ago

Senior Quality Control Manager - BioScience Cincinnati, OH posted: Posted 21 Days Ago

Biosciences Account Manager, Sales Rep - Chicago Chicago, Illinois, United States of America Embrace the opportunity to become a Biosciences Account Manager, Sales Representative and drive scientific innovation by managing key accounts and building strong customer relationships. Leverage your expertise in life sciences sales and laboratory solutions to make a global impact. Grow your career with Thermo Fisher Scientific and help advance the world's health and safety.

Principal Scientist, Discovery BioSciences – Integrative New Targets, Oncology Cambridge Crossing - MA - US posted: Posted 30+ Days Ago

Sr. Manager/Associate Director QC Scientist (Analytical–Late Stage Development & Process Excellence) Brighton, Massachusetts Sr. Manager/Associate Director QC Scientist (Analytical-Late Stage Development & Process Excellence)

Senior Quantum Field Engineer - Bioscience Remote, US; Toronto, Ontario, Canada About IonQ: IonQ, Inc . [NYSE: IONQ] is the world's leading quantum platform and merchant supplier - delivering integrated quantum solutions across computing, networking, sensing, and security. IonQ's newest generation of quantum computers, the IonQ Tempo, is the latest in a line of cutting-edge systems that have been helping customers and partners including Amazon Web Services, and AstraZeneca achieve 20x performance results and accelerate innovation in drug discovery, materials science, financial modeling, logistics, cybersecurity, and defense. In 2025, the company achieved 99.99% two-qubit gate fidelity, setting a world record in quantum computing performance . Headquartered in College Park, Maryland, IonQ has operations in California, Colorado, Massachusetts, Tennessee, Washington, Italy, South Korea, Sweden, Switzerland, Canada, and the United Kingdom. Our quantum computing services are available through all major cloud providers, while we also meet the needs of networking and sensing customers across land, sea, air, and space. IonQ is making quantum platforms more accessible and impactful than ever before. We are looking for a Senior Quantum Field Engineer. As a Senior Quantum Field Engineer, you'll be part of a team whose mission is to lead IonQ on its journey to build the world's best quantum solutions for the Bioscience vertical and solve the world's most complex problems. Field Engineering sits at the intersection of customers, markets, products and product teams, algorithms, applications, innovation and strategy - this is the team where ideas become applied and have impact. Join a nimble

Director, Global Service Operations – Flow Cytometry - Hybrid California Milpitas, CA, US Overview Waters Biosciences is seeking a Global Director, Service Operations Excellence to lead critical operational capabilities across our global service organization, with a strong focus on Flow Cytometry platforms and designing serviceability into current and next generation products. This role is central to driving service value capture, operational excellence, and service quality as Waters continues the integration of the Biosciences and Diagnostics portfolios. The successful candidate will serve as a key bridge between Service, Engineering, R&D, and Quality, ensuring our Flow Cytometry solutions are scalable, serviceable, and deliver exceptional customer outcomes throughout the product lifecycle. This position requires being onsite at the Milpitas California location. Hybrid 4 days per week, remote Friday. Relocation assistance may be considered. Responsibilities The Director, Global Service Operations Excellence will be responsible for: Driving service value capture initiatives across cost productivity, and install‑base optimization. Establishing and advancing standardized global operating mechanisms for Biosciences service operations to promote consistency, scalability, and adherence to regulatory requirements as well as company quality policies and procedures. Defining and owning the global service strategy to consistently deliver exceptional and measurable service performance at all Biosciences service touchpoints. This also involves collecting best practices from

Sr. Manager/Associate Director QC Scientist (Cell Based Assays-ELISA–Late Stage Development & Process Excellence) Brighton, Massachusetts Sr. Manager/Associate Director QC Scientist (Cell Based Assays-ELISA-Late Stage Development & Process Excellence)

Account Manager (Instrument Sales, Biosciences Division) Gangnam-gu, Seoul, Korea, Republic of Embrace the opportunity to become an Account Manager in the Instrument Sales division, driving key account success and delivering outstanding customer experiences in the life sciences sector. Leverage your expertise in instrument sales and account management to exceed targets, manage territories, and collaborate with industry leaders. Grow your career with Thermo Fisher Scientific in a dynamic, global environment.

Custom Project Manager, Biosciences Santa Ana, CA, US Position Overview We are hiring a Custom Project Manager-Bioprocessing. The Custom Project Manager will oversee the end-to-end lifecycle of custom media orders (CMOs) from initial Marketing Review through to Shipping, ensuring on-time, in-full delivery to customers. This role will serve as the central point-of-contact for custom/make-to-order (MTO) projects, accurately capturing and translating requirements, coordinating cross-functional activities, and driving effective communication between requirements to ensure seamless coordination across internal teams and external partners. Company Overview At FUJIFILM Biosciences, we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Biosciences. Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic b

Principal Scientist, Biologics Process Development US Principal Scientist, Biologics Process Development

Associate Director, Process Development and Manufacturing US Associate Director, Process Development and Manufacturing

Executive Director, Clinical Quality Assurance Boston; San Francisco; Seattle About Jade Biosciences Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn . Role Overview The Executive Director, Clinical Quality Assurance (CQA) will be responsible for all aspects of Quality Assurance focused on Good Clinical Practice (GCP), Good Pharmacovigilance Practices (GPvP) and Good Laboratory Practices (GLP) activities to ensure quality assurance and compliance of Jade sponsored clinical trials with applicable regulations, ICH guidelines, OECD Principles of GLP, Jade procedures and policies, and current industry standards and practices. The Executive Director, Clinical Quality Assurance will perform day-to-day clinical quality operations and compliance activities to support the success of our clinical programs in addition to being a strategic partner to Clinical Development and Operations. This role will maintain and ensure effectiveness of quality programs and documentation to assure compliance and inspection readiness with all applicable quality requirements and regulatory standards. The ideal candidate brings hands-on expertise in GCP, GPvP and GLP QA operations, a proactive

Senior/Executive Director, Quality Management System Boston; Chicago; San Francisco; Seattle About Jade Biosciences Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn . Role Overview The Senior/Executive Director, Quality Management System (QMS) will be responsible for driving and delivering the activities necessary to develop, implement, and continuously improve a phase appropriate GxP QMS. This role will be directly involved with both strategy development and day-to-day tactical execution related to QMS processes such as Document Management, Training Management, Change Control, Management Review (MR), Annual Product Quality Review (APQR), Deviation, CAPA, Risk Management, and GxP Computer System Assurance. The Sr./Exec. Director will be responsible for the maintenance of both paper-based and electronic processes and lead quality initiatives to support the pace and growth of the organization. This role will maintain and ensure effectiveness of quality programs and documentation to assure compliance and inspection readiness with all applicable quality requirements and regulatory standards. The ideal candidate brings hands-on expertise in creating and maintaining a GxP

Senior Manager/Associate Director, Marketing Operations Waltham, Massachusetts, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing. The Role: This critical role will manage the tactical execution of marketing operations supporting the launch of bezuclastinib, Cogent Biosciences' key pipeline asset. This role ensures compliant, efficient, and impactful delivery of promotional content, omnichannel campaigns, key marketing KPI's. This role is critical to implementing. evolving and advancing our organization's omnichannel capabilities. The Senior Manager partners closely with brand leads to unify personal and non-personal promotional activities into a seamless customer experience that drives brand performance goals and commercial growth. Responsibilities: - Omnichannel Campaign Orchestration - Work with marketing to ensure the execution of complex customer engagement plans into high-performing omnichannel campaigns across HCP, patient, and caregiver audiences. - Collaborate with analytics teams to integrate insights

Senior Director, Clinical Operations Boston; Chicago; San Francisco; Seattle About Jade Biosciences Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade's lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated in a Phase 1 clinical trial for the treatment of immunoglobulin A nephropathy. Jade's pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn . Role Overview The Senior Director, Clinical Operations is responsible for directing the strategy, management, and oversight of clinical program(s) and functional activities as assigned. Key Responsibilities - Acts as Clinical Operations program lead for assigned program(s) - R epresent Clinical Operations at the Clinical Development Team and /or Global Program Team - Develops and executes program operational strategy - Partners closely and effectively with other functions and functional heads to drive program forward - Provides strategic and technical recommendations to senior leadership - Directs the selection of CROs and other vendors ( IxRS , Central Lab, ancillary/tech vendors) - Acts as an escalation point for CRO/vendor issues - Directs development of vendor Scopes of Work (SOW), scope changes, budgets, and vendor payments - Partners with CRO and other vendors to deliver on study execution - Creates and tracks clinical program

Associate Director, Drug Product Development & Manufacturing US Associate Director, Drug Product Development & Manufacturing

Regional Business Director - Northeast Pennsylvania, United States Overview About Pacira Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Why work with us? Rarely do you have an opportunity to do work that really matters. What drives us is our mission. What makes us successful are our people. At Pacira, you are part of an inclusive culture that fosters collaboration, growth, and innovative thinking - a place where you can make an impact and help change the standard of care in non-opioid pain management. Be part of our movement, let's pursue excellence together. Summary: The Regional Business Director will lead the sales specialty team for their Region, managing Account Managers in promoting and selling healthcare products to healthcare providers. The Regional Business Director will be responsible for working with the Marketing and Commercial organizations in development and execution of the sales strategy and serve as a key information holder regarding the marketplace and thus, be able to react appropriately to that market as needed. They will also be responsible for delivering on all contractual obligations as agreed to by the client and Pacira. Responsibilities Essential Duties & Responsibilities : The following statements are intended to describe the general nature and level of

Regional Business Director- New England Boston, Massachusetts Overview At Pacira, innovation meets purpose. Pacira BioSciences, Inc. is a pioneer in non-opioid pain management and regenerative health solutions. Today, we're building on that legacy with next-generation innovations for chronic, postsurgical, and musculoskeletal pain. Our culture is built on collaboration, innovation, and a shared commitment to helping patients recover faster. We are redefining what's possible in pain management-and we can't do it without talented people like you. Why Join Us? At Pacira, every career is more than a job. Our mission drives us, and every day, we challenge ourselves to achieve the extraordinary. Integrity is at the core of who we are. We value diverse perspectives and the collective strength of a unified team. Join the team in making better possible for patients everywhere. Summary: The Regional Business Director will lead the sales specialty team for their Region, managing Account Managers in promoting and selling healthcare products to healthcare providers. The Regional Business Director will be responsible for working with the Marketing and Commercial organizations in development and execution of the sales strategy and serve as a key information holder regarding the marketplace and thus, be able to react appropriately to that market as needed. They will also be responsible for delivering on all contractual obligations as agreed to by the client and Pacira. Responsibilities Essential Duties & Responsibilities : The following statements are intended to describe the general nature and level of work being performed by an individual assigned to this

Scientist II, Analytical Development (Oligonucleotide) San Diego, CA, US Scientist II, Analytical Development (Oligonucleotide)