Zoological Park Attendant, Central Park Zoo Wildlife Conservation SocietyZoological Park Attendant, Central Park ZooNew York, NYAbility to represent WCS in a professional manner and to establish and maintain positive, effective working relationships with employees, colleagues, and the general public. We are committed to cultivating an inclusive work environment and looking for future team members who share that same value.
Zoological Park Maintainer, Central Park Zoo Wildlife Conservation SocietyZoological Park Maintainer, Central Park ZooNew York, NYAt least five years hands on experience in some or all fields such as plumbing, electrical, carpentry, HVAC, painting, and use of power tools. We are committed to cultivating an inclusive work environment and looking for future team members who share that same value.
Principal Scientist, Early Pipeline Development Novartis AGPrincipal Scientist, Early Pipeline DevelopmentEast Hanover, NJ$119,700–$222,300 / yearInternal Job Title: Principal Scientist I/IIPosition Location: Onsite, San Diego, CAKey Responsibilities:Lead and manage a 3-5 person downstream process team and provide technical support, training, and SME knowledge to assist with the professional development of direct reports. Desired Requirements:Experiences in AAV gene therapyExperience with viral gene therapyThe salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II.
Principal Scientist - Analytics Team Lead Novartis AGPrincipal Scientist - Analytics Team LeadEast Hanover, NJ$119,700–$222,300 / yearantibodies, fusion proteins, ADCs, bi- and trispecifics, AAVs, Lentiviruses) transitioning into clinical developmentAct as senior analytics expert in project teams ensuring optimal project support and high quality for all deliverables of your groupFoster streamlined processes and optimal use of capacities as well as continued innovation, incorporating latest technologies and knowledgeEffectively manage resources, project activities, timelines, maintain a strong customer focus and set respective objectives for your teamProvide leadership and clear guidance to the team, optimally leveraging the expertise and experience of individualsDrive a culture of collaboration, integrity, and team development, and ensure a safe, empowering, and inspiring working environmentEssential Requirements:PhD degree or equivalent in biochemistry, biotechnology, chemistry or a related field with 3+ years of related experience in the pharmaceutical industry, with 2+ years of experience as a people manager Strong scientific background in analysis of recombinant proteins (mAb, bi/tri-specific mAbs, therapeutic proteins) by techniques such as mass spectrometry, chromatography, capillary electrophoresis, and light scattering technologiesImplementation and supervision of cutting-edge characterization of PCA techniques for analyzing novel biologics modalities, e.g. Experience interpreting CDMS results for AAV analysis is beneficial, direct instrument experience not requiredExperience with data analysis workflows and report generationProven ability to lead, coach and develop peopleDistinguished team spirit and scientific driveHigh flexibility combined with excellent organizational and communication skillsCompensation & Benefits:The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II.
Senior Principal Scientist/Associate Director Clinical PBPK (Dual Level Posting) Novartis AGSenior Principal Scientist/Associate Director Clinical PBPK (Dual Level Posting)East Hanover, NJ$122,500–$227,500 / yearKey responsibilities:Expert PBPK modeler to provide translational modeling support for global drug discovery and development projectsPerform translational PBPK analyses to predict clinical drug exposure in specific populations, assess potential for DDI, understand clinical impact of disease on drug exposure, as well as apply biopharmaceutic PBPK modeling to support formulation changes and achieve clinical biowaiversIntegrate PK/ PD data, ADME and DDI findings Ability to interpret and communicate modeling results and potential impact to project teamsPrepare summary documents for use in regulatory submissions and ability to respond independently to health authority questionsEssential requirements PhD in pharmaceutical sciences or related discipline with experience in ADME/DMPK sciences, biopharmaceutics, and modeling and simulation. #LI-Hybrid Internal Title: Senior Principal Scientist or Associate DirectorLocation: Basel, SwitzerlandThe Modeling & Simulation group within PK Sciences is looking for a Principal Scientist to Associate Director level modeler, to develop and apply translational physiologically based pharmacokinetic (PBPK) modeling along with data analysis techniques to facilitate drug discovery, development, and translational research across disease areas.
Principal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AGPrincipal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/ToxicologyEast Hanover, NJ$119,700–$222,300 / yearEssential Requirements: Degree in biological related sciences8+ years of relevant experience working in a pharmaceutical settingExperience working in GLP setting, and general regulatory compliance and animal welfare knowledge related to conduct of toxicology studiesGood communication skills, and excellent logistical/planning skillsFluent in English (spoken and written)Desirable Requirements: Previous experience with SEND packages is desirablePrevious experience with software for online information and program management is a plusThis is a dual level posting. Support SEND package creation and quality review for FDA submissionsSupport the Study Quality and Compliance team's effort for tracking and managing study-related information through input of information types from the areas of responsibility above and generally support the effort in various workstreams or initiatives.
ADME Scientist, Antibody-Oligonucleotide Conjugates (Principal Scientist I/II) Novartis AGADME Scientist, Antibody-Oligonucleotide Conjugates (Principal Scientist I/II)East Hanover, NJ$108,500–$201,500 / yearEssential requirementsPhD, MSc, or BSc in pharmaceutical sciences, biochemistry, analytical chemistry, pharmacology, molecular biology, bioengineering, or a related discipline, with relevant industry experience in ADME, DMPK, biotransformation, or biologics/new modality research. #LI-Onsite,Location: San Diego, CaliforniaNovartis is seeking a highly motivated ADME scientist for a laboratory-based role supporting the discovery and early development of antibody-oligonucleotide conjugates, including antibody-siRNA and antibody-PMO modalities.
Principal Scientist, Digital Enablement Kenvue IncPrincipal Scientist, Digital EnablementSummit, NJ$127,075–$179,400 / yearThis individual will lead the identification, development, and deployment of digital tools and frameworks that improve scientific workflows, enhance knowledge management, and drive greater efficiency, productivity, and decision-making across R&D. The Principal Scientist, Digital Enablement will play a key role in accelerating innovation across Kenvue by embedding digital technologies, AI capabilities, and data-driven solutions into product development teams.
Principal Scientist, Biologics Development Merck & Co IncPrincipal Scientist, Biologics DevelopmentRahway, NJ$173,200–$272,600 / yearWithin Our Company's Manufacturing Division, Biologics Drug Substance Commercialization (BDSC) provides upstream process leadership and laboratory capabilities that advance late-stage pipeline and commercial drug substance manufacturing for biologics. The Principal Scientist/ Director position in BDSC-Upstream team is a senior scientific and leadership role supporting late stage and commercial biologics programs, with a primary focus on biologics upstream processing.
Associate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent) Merck & Co IncAssociate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent)Rahway, NJ$142,400–$224,100 / yearRequired Skills: Collaborative Development, Combination Products, Commercialization, Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Method Validation, Product Risk Management, Project Leadership, Quality Management Systems (QMS), Release Testing, Self Motivation, Testing Methodology, Test Method Validation, Test Procedure Development, Troubleshooting. This role has a primary focus on design verification while encompassing the full spectrum of testing activities, including test method development and validation, analytical transfers, incoming testing, in-process, release testing, and testing readiness to enable successful clinical introduction and commercialization.
Associate Principal Scientist, Analytical R&D Merck & Co IncAssociate Principal Scientist, Analytical R&DRahway, NJ$142,400–$224,100 / yearJoin us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. Your main responsibilities will include: Driving Pipeline: Leading or participating on analytical teams driving the development of drugs in the company's pipeline, with a deep understanding of product development from early stage through commercialization.
Sr. Principal Scientist (Sr. Director) - Regulatory Liaison Merck & Co IncSr. Principal Scientist (Sr. Director) - Regulatory LiaisonRahway, NJ$190,800–$300,300 / yearRequired Skills: Biological Sciences, Clinical Reporting, Drug Development, Global Health, In Vitro Diagnostics (IVD), Multiple Therapeutic Areas, Pharmaceutical Regulatory Affairs, Process Improvements, Product Approvals, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Communications, Regulatory Compliance, Regulatory Issues, Regulatory Strategies, Regulatory Strategy Development, Written Communication. As the Global Regulatory Lead (GRL), the Senior Principal Scientist functions as the regulatory single, accountable, global point of contact on the project team and interacts with the global regulatory agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more company investigational and marketed drugs/biologics in early- and/or late-stage development.
Senior Principal Scientist / Associate Director- Soluble Biomarkers, Molecular & Cellular Sciences (MCS) Novartis AGSenior Principal Scientist / Associate Director- Soluble Biomarkers, Molecular & Cellular Sciences (MCS)East Hanover, NJ$122,500–$227,500 / yearExpected Annual Base Salary Range for role: 122,500.00 - 227,500.00 CHF AnnualThe base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offeredBenefits & Rewards At Novartis, we're committed to reimagining medicine together - and rewarding the people who make it happen.
Principal Scientist, Bioassay and Impurity Assay Development Bristol Myers SquibbPrincipal Scientist, Bioassay and Impurity Assay DevelopmentNew Brunswick, NJ$134,900–$163,461 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. PhD in Immunology, Cell Biology, Molecular Biology, or a related scientific discipline with 4–6 years of relevant industry experience; or a Master’s degree with 6–9 years of experience; or a Bachelor’s degree with 9–12 years of experience.
NewPrincipal Scientist (Director), Translational Medicine - Infectious Diseases Merck & Co IncPrincipal Scientist (Director), Translational Medicine - Infectious DiseasesRahway, NJ$260,300–$409,700 / yearPrimary responsibilities for the Principal Scientist include the following: Working with basic science teams on specific diseases and therapeutic areas, providing clinical expertise for identification and validation of novel targets, including the design of preclinical and clinical experiments to validate targets and/or pathways, and leveraging this work for development of novel therapeutics. Translational Medicine is specifically responsible for: Contributing to the identification of novel targets by partnering with Discovery Sciences to bring a clinical perspective into the earliest stages of target identification and validation, and to execute clinical studies to evaluate the relevance of potential targets to human disease in order to justify full development.
Associate Principal Scientist, Small Molecule Chemical Engineering Merck & Co IncAssociate Principal Scientist, Small Molecule Chemical EngineeringRahway, NJ$142,400–$224,100 / yearThe candidate must demonstrate a strong commitment to safety, quality, and compliance, including adherence to current Good Manufacturing Practices (cGMPs), Good Documentation Practices (GDPs), data integrity principles, and participation in risk assessments, deviation investigations, change control activities and continuous improvement initiatives. Required Skills: API Manufacturing, Bioprocessing, Chemical Engineering, Chemical Processes, Commercialization, Manufacturing, Manufacturing Processes, Manufacturing Scale-Up, Manufacturing Technologies, Pharmaceutical Process Development, Process Design, Process Development (PD), Small Molecule Drugs, Technology Transfer.
Principal Scientist I, Soluble Biomarkers- Molecular & Cellular Sciences (MCS) Novartis AGPrincipal Scientist I, Soluble Biomarkers- Molecular & Cellular Sciences (MCS)East Hanover, NJ$108,500–$201,500 / yearLI-OnsiteInternal job title: Principal Scientist ILocation: Cambridge, United StatesWe are seeking a motivated soluble biomarker expert to lead the development, validation, and implementation of fit-for-purpose soluble biomarker assays, with a focus on immunoassay and LC-MS based methods supporting neuromuscular and muscle disease clinical programs within the Biomarker Development (BMD) Molecular & Cellular Sciences group. This role requires strong hands-on assay development and validation expertise, scientific leadership, and the ability to translate disease biology and program needs into robust biomarker assay strategies that inform clinical decision-making.
Principal Scientist, Regulatory CMC ImmunityBio IncPrincipal Scientist, Regulatory CMCSummit, NJBachelor's Degree in life sciences or technical discipline with 10+ years relevant progressive experience required; or • Master's Degree in life sciences or technical discipline with 8+ years relevant progressive experience required; or • Doctorate degree in life sciences or technical discipline with 6+ years relevant progressive experience required • Experience in the preparation of the submission of CMC modules in eCTD format required • Familiarity with organizing responses to Health Authority requests required • Familiarity with regulatory submissions outside of the US desired. ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells.
Principal Scientist, Large Molecule Analytical Merck & Co IncPrincipal Scientist, Large Molecule AnalyticalRahway, NJ$156,900–$247,000 / yearThe Principal Scientist is a highly visible and impactful senior scientific role tasked with working closely with the group Director to define analytical strategy and to lead a team of scientists in solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of biologics active pharmaceutical ingredients (APIs). Required Skills: Analytical Method Development, Assay Development, Bioanalytical Analysis, Chromatographic Techniques, Clinical Judgment, Cross-Functional Teamwork, Dosage Forms, Ethical Compliance, Liquid Chromatography (LC), Matrix Management, Mentoring Staff, Method Validation, Personal Initiative, Stability Testing, Technical Writing.
NewPrincipal Scientist, Clinical Biomarker, Immunology & Immuno-Oncology (Hematology) Legend Biotech USPrincipal Scientist, Clinical Biomarker, Immunology & Immuno-Oncology (Hematology)Somerset, New JerseyLeverage advanced single-cell technologies (e.g., scRNA-seq) to deeply profile immune cell compartments, particularly T-cell states and exhaustion markers, to inform patient stratification and biomarker hypotheses. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases.