glp

10,000 glp job listings in United States. Find daily updated positions from leading job boards.


  • Alpharetta, Georgia, United States Arxada Full-time $65,000 - $70,000 Contract

    Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of...


  • Exton, Pennsylvania, United States Frontage Laboratories Full-time

                                               Quality Assurance Specialist Bio-Analytical GLPLocation: Exton PAReports to: Director BIO GLP Quality assuranceFull-timePosition/Job Summary:Are you ready for a role that will combine your thirst for scientific knowledge and eye for quality.   Then you are the perfect fit for our team of...


  • Savannah, Georgia, United States Lummus Group Full-time

    Lummus Group is a family of companies which includes three lines of business: Agriculture, Manufacturing and Intralogistics.  The Lummus Group vision is to be a leading entrepreneurial player in our lines of business in terms of size, global reach, game-changing offerings and assumption-busting innovations.   Lummus Corporation Ginning Leadership...


  • San Diego, California, United States RPM ReSearch Full-time $125,000 Contract

    Associate Director, GCP/GLP Quality Assurance Boutique GLP Contract Research Organization (CRO) | San Diego, CaliforniaYou know GLP. Now you may be ready to own more of it.There comes a point in a Quality career when being good at auditing studies is no longer enough.You want your judgment to matter.You want to work directly with the Study Directors,...


  • Indianapolis, Indiana, United States Corteva Agriscience Full-time

    Corteva Agriscience is seeking a GLP Software Administrator to support R&D laboratory systems and applications in a regulated environment. This role will serve as a key partner to researchers, lab staff, IT, and business teams by maintaining system reliability, troubleshooting issues, supporting upgrades and implementations, and ensuring GLP compliance and...


  • Redwood City, California, United States Revolution Medicines Full-time $211,000 - $264,000 Contract

    Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target...


  • San Francisco, CA, United States EPM Scientific Full-time

    A leading CRO is seeking a Senior Scientist / Principal Investigator with extensive experience in bioanalysis to lead scientific projects. You will design and validate bioanalytical methods while overseeing regulatory compliance and mentor junior staff. Ideal candidates will possess a relevant advanced degree and a strong background in GLP/GCLP practices....


  • Swiftwater, Pennsylvania, United States Sanofi Full-time $113,250 - $163,583 Contract

    Job Title: GLP and GCLP Compliance ExpertLocation: Swiftwater, PAAbout Job:The R&D GLP & GCLP Compliance Expert position is globally responsible for support to internal and external nonclinical GLP and GCLP activities within Sanofi R&D Vaccines to ensure compliance with applicable regulatory standards, industry guidance and Sanofi requirements. The incumbent...


  • Solana Beach, California, United States, California RPM ReSearch Full-time

    Director, GLP Quality Assurance & ComplianceBuilding a Culture of Quality & Compliance in a Leading In Vivo Research FacilityCompany OverviewWe are a pioneering research organization dedicated to translational medicine, bridging the gap between research and real-world applications to improve human health. As we expand our in vivo research capabilities,...

  • Sr. Manager, GLP

    4 days ago


    , NJ, United States, NJ Legend Biotech, Inc. Full-time

    Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric...


  • milford, massachusetts, United States Waters Full-time

    Business Development Professional Waters is seeking a strategic and commercially minded Business Development professional to establish and accelerate our presence in the rapidly growing GLP-1 market. This is a unique opportunity to manage the development of our GLP-1 market strategy, identifying customer needs, informing cross-divisional product strategies...

  • Sr. Manager, GLP

    4 days ago


    NJ, United States Legend Biotech, Inc. Full-time

    Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric...


  • Fall River, Massachusetts, United States Celldex Therapeutics Full-time $76,374 - $99,189 Contract

    About Celldex Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a...

  • Senior Director

    1 day ago


    Boston, Massachusetts, United States Vertex Pharmaceuticals Full-time $215,000 - $322,400 Contract

    Job DescriptionPosition Summary: This role has overall accountability for strategic leadership and oversight of the end-to-end quality assurance strategy for proactive, risk-informed, and sustainable quality oversight and compliance with regulatory expectations across Vertex processes for clinical evidence generation and product...


  • Lincolnshire, IL, United States SmartRecruiters Full-time

    SGS is seeking a Senior Manager, Microbiology to lead the Microbiology team within the pharmaceutical division. You will guide method development, design analytical plans, and ensure flawless project execution in collaboration with technical, operational, and project managers. The role is client- and internal-facing with emphasis on multitasking and timely...


  • Florida, United States, Florida RPM ReSearch Full-time

    Job Description: QA/QC Manager for In Vivo Research Facility (GLP Compliance Journey)Bi-Lingual English/Spanish requirement Company OverviewWe represent a visionary research organization dedicated to advancing scientific discovery and innovation. Our mission is to bridge the gap between research and real-world applications, focusing on transformative...


  • United States Berry Street Remote Full-time

    DescriptionBerry Street is on a mission to transform how Americans eat and manage their weight through evidence-based care. Berry Street's platform connects individuals with an expansive network of Registered Dietitians and, now, licensed clinicians to deliver integrated weight management programs. From GLP-1 prescribing and metabolic health to diabetes,...


  • Carlsbad, California, United States | RPM ReSearch Full-time

    🌟 Join Our Cutting-Edge Team in Carlsbad, CA: Senior Scientist & Study Director for Cell and Gene Therapy🌟The Opportunity:  How would you like to pioneer a significant role in an exciting new division of a leading life sciences R&D provider? Picture yourself at the forefront of groundbreaking studies in cell and gene therapy, leading an enthusiastic...


  • Kendall Park, NJ, United States Eurofins USA BioPharma Services Full-time

    Eurofins USA BioPharma Services seeks a qualified supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will assist in protocol development, design, and reporting while supervising scientific staff. Position is full-time, Monday–Friday, with overtime as needed. Minimum 5 years of experience in biocompatibility studies and...


  • Chicago, IL, United States Sword Bio Full-time

    Company Description At Sword Bio, we are a leading Contract Research Organization (CRO) dedicated to providing high-quality nonclinical research services that accelerate the development of innovative therapeutics. Our commitment to scientific excellence, regulatory compliance, and client satisfaction has established us as a trusted partner across the...