Staff Data Scientist MozillaStaff Data ScientistPhiladelphia, PADevelop and maintain a deep understanding of user growth dynamics: how acquisition, activation, and retention interact to drive growth, and use that understanding to diagnose metric movements, explain trends to leadership, and anticipate emerging risks or opportunities. This Staff Data Scientist will own the analytical strategy for a major product area: identifying the right questions, defining how success is measured, and driving decisions that shape Firefox’s growth trajectory.
Senior Product Manager, Fortary - Remote Ava LabsSenior Product Manager, Fortary - RemotePhiladelphia, PARemoteThe ideal candidate brings a strong track record of building and launching products in fintech or crypto, thrives in fast-paced environments, and operates with a high degree of ownership and execution rigor. The company was founded by Cornell computer scientists, who partnered with Wall Street veterans and early Web3 leaders to execute a promising vision for redefining the way people build permissionless networks.
Sr. Scientist Stat Programming, Late-Stage Development (Hybrid) Merck & Co IncSr. Scientist Stat Programming, Late-Stage Development (Hybrid)PA$117,000–$184,200 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Education Minimum Requirement: BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years SAS programming experience in a clinical trial environment.
Principal Scientist, Drug Product Steriles Primary Packaging GSK plcPrincipal Scientist, Drug Product Steriles Primary PackagingCollegeville, PAApply project management skills to deliver priority tasks aligned to project and portfolio milestones Assessment of external partners and collaborations Leads the characterisation of the selected container closure system and its compatibility with the intended drug product e.g., glass delamination, silicone distribution, USP/EP/JP/ChP Compliance, and Container Closure Integrity Support the development of regulatory, quality, and legislative strategies for packaging to ensure cost effective development and provide guidance across teams, projects, and functional areas. Site Name: USA - Pennsylvania - Upper Providence Posted Date: May 11 2026 Principal Scientist, Drug Product Steriles Primary Packaging Onsite role located at Upper Providence, PA At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade.
Principal Data Product Scientist, DDSAI Immunology Johnson & JohnsonPrincipal Data Product Scientist, DDSAI ImmunologyNJRemote$117,000–$201,250 / yearAll Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Johnson & Johnson Innovative Medicine is recruiting for a Principal Data Product Scientist, DDSAI Immunology to join our Immunology R&D Data, Data Science & Artificial Intelligence (DDSAI) team and to enable and scale high‑value data assets across Immunology Research & Development.
Sr. Scientist, Biologics Analytical Development 6084-Janssen Research & Development Legal EntitySr. Scientist, Biologics Analytical DevelopmentMalvern, PennsylvaniaAnalytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Coaching, Consulting, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Pharmacogenetics, Pharmacovigilance, Process Improvements, Quality Assurance (QA), Relationship Building, Research Documents, Scientific Research, Technologically Savvy The experienced and motivated Senior Scientist will be responsible for development, validation, and transfer of separation assays for protein biotherapeutics including but not limited to monoclonal antibodies, bi- and tri-specific antibodies and antibody drug conjugates to be used in support of clinical and commercial development.
Sr. Scientist, Biologics Analytical Development Johnson & JohnsonSr. Scientist, Biologics Analytical DevelopmentMalvern, PARequired Skills: Preferred Skills: Analytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Coaching, Consulting, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Pharmacogenetics, Pharmacovigilance, Process Improvements, Quality Assurance (QA), Relationship Building, Research Documents, Scientific Research, Technologically Savvy. The experienced and motivated Senior Scientist will be responsible for development, validation, and transfer of separation assays for protein biotherapeutics including but not limited to monoclonal antibodies, bi- and tri-specific antibodies and antibody drug conjugates to be used in support of clinical and commercial development.
Principal Scientist, Drug Product Sterile Solutions GSK plcPrincipal Scientist, Drug Product Sterile SolutionsCollegeville, PAWe are seeking professionals with the following required skills and qualifications to help us achieve our goals: PhD in Pharmaceutics, Chemical Engineering, Biomedical Engineering, Chemistry, or related scientific discipline; or MS with 5+ years' relevant experience; or BS with 10+ years' relevant experience. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.
Scientist II/III, LCMS Method Development (Bioanalysis) Pharmaron Beijing Co LtdScientist II/III, LCMS Method Development (Bioanalysis)Exton, PA$65,000–$85,000 / yearFounded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. In this role, you will contribute to the development and validation of innovative bioanalytical methods supporting drug discovery and development programs across a diverse range of therapeutic modalities, including small molecules, peptides, oligonucleotides, PROTACs, biologics, and emerging therapies.
Principal Scientist, Analytical Comparability & Product Characterization – Advanced Therapies Johnson and JohnsonPrincipal Scientist, Analytical Comparability & Product Characterization – Advanced TherapiesMalvern, PAFull timePromote positive relationships and collaboration with Process Development functional leaders, data sciences, Janssen Supply Chain leaders, Quality Assurance, and Discovery. •Contribute to technical forums both internal and external to the company to share knowledge and approaches related to deep product characterization strategies as they relate to cell and gene therapy products. •Optimally communicate comparability study plans, statistical justifications, and results and scientific data to cross-functional teams, project teams, and health authority as needed.
NewAssociate Principal Scientist, Sterile Drug Product Commercialization Merck & Co IncAssociate Principal Scientist, Sterile Drug Product CommercializationWest Point, PA$142,400–$224,100 / yearLead and/or serve on cross-functional biologics drug product (DP) working group and manage DP activities through filing and Process Performance Qualification (PPQ), including registration stability study execution, process characterization plan and execution, tech transfer control strategy, process development, PPQ readiness, PAI (Pre‐Approval Inspection) readiness, approval, launch, and post‐launch support. As part of our Manufacturing Division, the Sterile Drug Product Commercialization (SDPC) group provides technical process leadership and laboratory expertise for late‑stage and commercial sterile drug products, including vaccines, biologics, and pharmaceutical and combination products.
NewFormulation Development Scientist Eurofins Scientific SEFormulation Development ScientistPhiladelphia, PAEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
High Throughput Process Development Scientist Eurofins Scientific SEHigh Throughput Process Development ScientistWest Point, PAIt is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Purification Development Scientist (Philadelphia) GenentechPurification Development Scientist (Philadelphia)Philadelphia, PennsylvaniaThe Downstream Process Development (DSPD) team is seeking a highly motivated Scientist with a specialized focus on filtration processing and relevant biopharmaceutical industry experience. The successful candidate will drive laboratory execution, contribute to process optimization, and collaborate cross-functionally to support the advancement of breakthrough therapeutics.
FSP Senior Research Scientist-Dissolution Method Development Thermo Fisher ScientificFSP Senior Research Scientist-Dissolution Method DevelopmentCollegeville, PennsylvaniaWithin our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Scientist: Steriles Packaging Development Thermo Fisher ScientificScientist: Steriles Packaging DevelopmentCollegeville, PennsylvaniaWith clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. • Maintain packaging lab component and lab inventory, including ordering, receiving, and organization of lab space to enable dynamic, flexible laboratory workspace.
Scientist, Analytical Development Genscript Biotech CorpScientist, Analytical DevelopmentPennington, NJ$90,000–$120,000 / yearGenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy. QC Manager is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials and participating in the technology transfer.
Scientist, Analytical Development GenScript/ProBioScientist, Analytical DevelopmentPennington, NJ$80,000–$110,000 / yearProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
Executive Director, Product Development Team Leader, Clinical Research, Hematology Merck & Co IncExecutive Director, Product Development Team Leader, Clinical Research, HematologyNorth Wales, PA$310,900–$489,400 / yearWorking closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility. Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.
Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma Merck & Co IncExecutive Director, Product Development Team Leader, Clinical Research, Hematology - LymphomaPA$310,900–$489,400 / yearWorking closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility. Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.
Associate Director, Early Stage Drug Product Development Acadia Pharmaceuticals IncAssociate Director, Early Stage Drug Product DevelopmentPrinceton, NJ$154,000–$192,700 / yearThe incumbent will be responsible for management of activities relating to the above at the Contract Service Providers (CSPs) and will contribute both internally and externally in resolution of complex technological issues The role will be critical in ensuring that we select developable drug candidates, reduce risk and accelerate the introduction of new chemical entities into the Acadia pipeline. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.
Business Development Manager- Product & Services BiocytogenBusiness Development Manager- Product & ServicesPhiladelphia, PennsylvaniaYou will have the best opportunity to learn and utilize the science and business in the fields of immuno-oncology, animal model gene engineering, preclinical pharmacology, etc. The biggest advantage of working in Biocytogen is that your career will have the best combination of biopharmaceutical science and applications, and you will grow with Biocytogen with confidence and strength.
Senior Principal Scientist, Outcomes Research Merck & Co IncSenior Principal Scientist, Outcomes ResearchWest Point, PA$210,400–$331,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. The Senior Principal Scientist leads a team of health economists to develop and implement health economics and modeling strategies that enable the Company to understand and communicate the full economic value of the Company's oncology products to payers, health technology agencies, policy makers, and other decision-makers in order to optimize market access and patient outcomes.
Senior Scientist, DSCS Digital Technologies - Laboratory Automation (Hybrid) Merck & Co IncSenior Scientist, DSCS Digital Technologies - Laboratory Automation (Hybrid)West Point, PA$117,000–$184,200 / yearThis includes, but is not limited to, developing digital and data integration platforms for PAT, delivering solutions for digitally integrating analytical instrumentation and sensors, leveraging state-of-the-art data engineering tools to enable frictionless flow of PAT data streams, and inventing data science approaches to enable optimal extracting of information from vast PAT data sets. Required Skills: Analytical Instrumentation, Biology, Biopharmaceuticals, Bioprocessing, Chemistry, Data Analysis, Data Science, Digital Technology, Flow Cytometry, Innovative Thinking, Laboratory Automation, Laboratory Techniques, Pharmaceutical Development, Pharmaceutical Sciences, Process Analytical Technology (PAT), Process Optimization, Scientific Research.
Principal Scientist (Director) - Regulatory Affairs-CMC Merck & Co IncPrincipal Scientist (Director) - Regulatory Affairs-CMCNorth Wales, PA$190,800–$300,300 / yearThe Principal Scientist / Director responsibilities include but are not limited to: • Serve as a Regulatory CMC Project Lead and provide CMC Regulatory leadership within Regulatory and on cross-functional teams for the assigned biological products in development or commercial products. Under general supervision of an Executive Director/Senior Director, the Principal Scientist /Director is responsible for developing and implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for our organizations biologics product franchises in accordance with domestic and international regulations and guidance.
Research Scientist (Polymers) Trinseo PlcResearch Scientist (Polymers)Exton, PAManage multiple concurrent projects with clear governance (scope, schedule, budget, risk, and deliverables) and disciplined application of stage gate methodologies, including gate readiness and decision reviews. As a global materials solutions provider focused on delivering innovative and sustainable solutions to our customers, we need people to feel respected and included so they can be more creative, innovative, and successful.
Scientist, Vaccines and Advanced Biotechnologies (VAX) Process R&D Merck & Co IncScientist, Vaccines and Advanced Biotechnologies (VAX) Process R&DWest Point, PA$87,300–$137,400 / yearVaccines and Advanced Biotechnologies (VAX) Process R&D is responsible for the development and clinical manufacturing of Drug Substance (DS) and Drug Product Intermediates (DPI) for the vaccine and advanced therapy pipeline, spanning from preclinical to commercialization stages. Education Minimum Requirement: BS, MS or PhD in engineering or bio/chemical sciences: Chemical Engineering, Bioengineering, Biomedical Engineering, Chemistry, Biochemistry, Molecular Biology, Biotechnology.
Sr. Scientist, Preclinical Dev. Merck & Co IncSr. Scientist, Preclinical Dev.West Point, PA$117,000–$184,200 / yearRole Summary: Vaccines and Advanced Biotechnologies Process R&D (VaxPRD) is responsible for the development and clinical manufacturing of Drug Substance (DS) and Drug Product Intermediates (DPI) for the vaccine and advanced therapy pipeline, spanning from preclinical to commercialization stages. The successful candidate is expected to work with other upstream scientists and engineers, typically focusing on one to two vaccine programs at a time, while also supporting the overall program management and governance activities across larger multi-functional and cross-divisional teams.
Distinguished Scientist, Vaccines & Advanced Biotechnologies Process R&D Merck & Co IncDistinguished Scientist, Vaccines & Advanced Biotechnologies Process R&DWest Point, PA$210,400–$331,100 / yearRequired Skills: Bioprocessing, Bioproducts, Cross-Functional Teamwork, Detail-Oriented, Evaluating New Technologies, Exercises Judgment, Good Laboratory Practices (GLPs), Innovation, Mentoring Staff, Process Scale Up, Professional Networking, Protein Characterization, Protein Purifications, Scientific Analysis, Scientific Leadership, Strategizing. We are seeking an esteemed scientific leader in the process development and manufacturing of vaccine drug substances for the role of Distinguished Scientist (equivalent to the Executive Director level), in the Vaccines & Advanced Biotechnologies Process R&D (VAX PR&D) department, located in West Point, PA.
NewSenior Scientist, Biostatistics Merck & Co IncSenior Scientist, BiostatisticsNorth Wales, PA$117,000–$184,200 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Required Skills: Biostatistics, Business Decisions, Clinical Trials, Clinical Trials Analysis, Data Management, Data Science, Global Health, Manufacturing, Numerical Analysis, Regulatory Compliance, Regulatory Requirements, Scientific Modeling, Statistical Analysis, Statistical Programming, Strategic Management, Strategic Planning.
Associate Principal Scientist, Biostatistics Merck & Co IncAssociate Principal Scientist, BiostatisticsNorth Wales, PA$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and other Research & Development Division Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.
NewDistinguished Scientist, Biologics Discovery Process Research Integrator Johnson & JohnsonDistinguished Scientist, Biologics Discovery Process Research IntegratorSpring House, PARequired Skills: Preferred Skills: Analytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Collaboration, Consulting, Design Mindset, Drug Discovery Development, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Product Licensing, Program Management, Representing, Scientific Research. Building trusted cross‑functional partnerships and influencing decision‑making across Therapeutics Discovery (TD), Preclinical Sciences & Translational Safety (PSTS), Therapeutic Areas (TAs), and TDS in matrixed governance and technical forums.
Assoc Principal Scientist Statistical Programming, Late-Stage (Hybrid) Merck & Co IncAssoc Principal Scientist Statistical Programming, Late-Stage (Hybrid)Upper Gwynedd, PA$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Strong project management skills; A program leader; Determines appropriate programming methodology, assures programming consistency across protocols and projects, completes programming tasks, and directs the program development effort of other programmers; an experienced programming mentor; ability to engage key stakeholders.
Associate Principal Scientist, Molecular Modeling Merck & Co IncAssociate Principal Scientist, Molecular ModelingWest Point, PA$142,400–$224,100 / yearThe tools that we develop are as diverse as the teams developing them, and in this Associate Principal Scientist role, the successful candidate will leverage their expertise in atomistic modeling of drug substance and drug formulations with an ability to apply predictive sciences to support our Company's pipeline of antibodies, small molecules, peptides, biologics, conjugates, and vaccines. We aspire to embed digital technologies into the fabric of DSCS culture to drive transformational impact, by innovating solutions through strong partnership in the domains of Data Science, Data Analysis, Informatics, Multi-Omics, Predictive Science, and Data Engineering.
Research Scientist – Applied Artificial Intelligence in Chemistry Universal Display CorporationResearch Scientist – Applied Artificial Intelligence in ChemistryEwing Township, New Jersey$115,000–$140,000The ideal candidate has hands-on experience applying AI/ML to chemistry problems, can work across data curation, model development, and workflow deployment, and is motivated by close collaboration with computational scientists, synthetic chemists, and device engineers to advance new materials from concept toward experimental validation. Build and maintain applied AI workflows, including agentic AI systems, tool-harnessed LLM workflows, and scientific application components that support chemistry-focused decision making.
Research Scientist - Applied Artificial Intelligence in Chemistry Universal Display CorpResearch Scientist - Applied Artificial Intelligence in ChemistryNJ$115,000–$140,000 / yearThe ideal candidate has hands-on experience applying AI/ML to chemistry problems, can work across data curation, model development, and workflow deployment, and is motivated by close collaboration with computational scientists, synthetic chemists, and device engineers to advance new materials from concept toward experimental validation. Build and maintain applied AI workflows, including agentic AI systems, tool-harnessed LLM workflows, and scientific application components that support chemistry-focused decision making.
NewSenior Scientist Merck & Co IncSenior ScientistWest Point, PA$117,000–$184,200 / yearThe Senior Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of vaccine adjuvants supporting process development, formulation development, vaccine investigations and method lifecycle management. The Vaccine Analytical Research & Development department of our Research & Development Division is seeking applicants for a Senior Scientist position available at its West Point, Pennsylvania research facility.
Principal Scientist, Stat. Programming - A&R Standards, Innovation (Hybrid) Merck & Co IncPrincipal Scientist, Stat. Programming - A&R Standards, Innovation (Hybrid)North Wales, PA$173,200–$272,600 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Superior knowledge and significant experience in setting strategy and developing analysis and reporting statistical programming deliverables (datasets, statistical analyses, report tables, and graphics) according to quality, compliance and timeliness requirements.
NewDistinguished Scientist, Biologics Discovery Process Research Integrator 6084-Janssen Research & Development Legal EntityDistinguished Scientist, Biologics Discovery Process Research IntegratorSpring House, PennsylvaniaAnalytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Collaboration, Consulting, Design Mindset, Drug Discovery Development, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Product Licensing, Program Management, Representing, Scientific Research Building trusted cross‑functional partnerships and influencing decision‑making across Therapeutics Discovery (TD), Preclinical Sciences & Translational Safety (PSTS), Therapeutic Areas (TAs), and TDS in matrixed governance and technical forums.
Principal Data Scientist - Immunology - (2 positions) Johnson & JohnsonPrincipal Data Scientist - Immunology - (2 positions)PARemote$117,000–$201,250 / yearAll Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Work with Data Science & Digital Health colleagues, IT and DevOps teams to deploy and manage the graph database infrastructure, focusing on high availability, scalability, and recovery operations specifically geared toward Immunology R&D needs and applications.
Senior Analytical Scientist AltasciencesSenior Analytical ScientistHarleysville, PennsylvaniaExtensive hands-on experience with Quantitative tests such as Assay, Content Uniformity, Dissolution, Particle Size Distribution, Preservative Assay, Related Substances, Residual Solvents, Resuspend ability, Viscosity, and other techniques for testing Drug Product Oral Solid dosage forms and data review in a pharmaceutical development and quality control laboratory setting. A Senior Analytical Scientist in the Pharmaceutical and Analytical development function is a senior-level technical role focused on developing, validating, and applying analytical methods to support drug discovery, development, and quality assurance.
Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology GSK plcDirector, Global Real-World Evidence & Health Outcomes Scientist, OncologyCollegeville, PA$204,000–$340,000 / yearThe role of Director, Global Real-World Evidence & Health Outcomes Research Scientist is critical to achieving this ambition by supporting asset teams to ensure that each medicine GSK brings to market is supported by scientifically credible, high quality, evidence that drives competitiveness and strong evidence-based product positioning, value propositions and value-based pricing. We need to better understand how our customers define value and to effectively collaborate with them to ensure we are generating value evidence data that includes real world evidence and cost effectiveness analyses that are impactful for payers, health systems, providers, and patients.
Director, Patient Safety Scientist Bristol-Myers Squibb CoDirector, Patient Safety ScientistPrinceton, NJ$217,520–$263,577 / yearCreates strategy for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development, support Structured Benefit Risk, and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance, including collaboration with Epidemiology on risk minimization effectiveness, non-interventional research (NIR) activities for post-authorization safety studies (PASS). The Director, Patient Safety Scientist, is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks.
Associate Principal Scientist, Analytical R&D Merck & Co IncAssociate Principal Scientist, Analytical R&DWest Point, PA$142,400–$224,100 / yearThis broad role includes 1) working with Analytical Product Leaders (APLs) to develop and implement analytical strategies, with special focus on transition from clinical to commercial stages; 2) driving method alignment and supporting consistent executional excellence across multiple testing laboratories; 3) developing and maintaining a robust assay monitoring effort and supporting method procedure life cycle management, including automation and/or modernization as applicable. In partnership with the BCR hub, develop short and mid-term strategy for sustainability in BCR inventory and antisera generation needed to support all testing laboratories in the network and connect BCR performance with assay performance as noted above.
Principal Data Scientist - Immunology - (2 positions) 6084-Janssen Research & Development Legal EntityPrincipal Data Scientist - Immunology - (2 positions)Titusville, New JerseyRemoteCambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of AmericaJob Description: Work with Data Science & Digital Health colleagues, IT and DevOps teams to deploy and manage the graph database infrastructure, focusing on high availability, scalability, and recovery operations specifically geared toward Immunology R&D needs and applications.
NewPrincipal Scientist, Biopharmaceutics Johnson & JohnsonPrincipal Scientist, BiopharmaceuticsMalvern, PARequired Skills: Preferred Skills: Analytical Reasoning, Biochemistry, Biotechnology, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Coaching, Critical Thinking, Drug Discovery Development, Emerging Technologies, Molecular Diagnostics, Organizing, Pharmacovigilance, Presentation Design, Process Improvements, Productivity Planning, Scientific Research. We are seeking a highly motivated Principal Scientist to join the Biopharmaceutics team in the Drug Product Development and Delivery (DPD&D) organization, focusing on biologics biopharmaceutics (monoclonal antibodies, multispecifics, antibody drug conjugates (ADCs), fusion proteins, and other therapeutic protein modalities).
Lead Polymer R&D Scientist DuPont de Nemours IncLead Polymer R&D ScientistWilmington, DECustomer & cross-functional collaboration: Serve as a customer-facing technical expert, partnering with medical device customers and collaborating internally with marketing, product management, regulatory, quality, manufacturing, and supply chain teams. You will lead end‑to‑end polymer development programs, applying deep polymer science expertise to design, synthesize, functionalize, and scale novel materials-including sustainable alternatives-tailored for healthcare applications.
Sr. Scientist - Analysis and Reporting Standards, Innovation (Hybrid) Merck & Co IncSr. Scientist - Analysis and Reporting Standards, Innovation (Hybrid)North Wales, PA$117,000–$184,200 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Required Skills: Applied Engineering, Clinical Database Programming, Clinical Trials, Collaborative Communications, Computer Science, Data Management, Data Modeling, Innovation, Mechatronics, Numerical Analysis, Programming Languages, Research Databases, Stakeholder Relationship Management, Statistical Methods, Technical Consulting, Waterfall Model.
Scientific - Quality Control Scientist - Microbiology Ampcus IncorporatedScientific - Quality Control Scientist - MicrobiologyPrinceton, NJ$43–$45 / hourAdditionally, the QC Scientist will mentor junior staff, support audits, and ensure proper maintenance and calibration of laboratory equipment, playing a key role in upholding the laboratory’s operational excellence. The QC Scientist – Microbiology, Bio-Analytical and Raw Material is responsible for performing microbiological, bio-analytical, and raw material testing to ensure the quality and safety of products.
Associate Director, Medical Scientist, Global Medical Oncology, IO Lung Cancer Bristol-Myers Squibb CoAssociate Director, Medical Scientist, Global Medical Oncology, IO Lung CancerPrinceton, NJ$166,350–$201,571 / yearImplement data generation strategies and collaborate with Medical Evidence Generation (MEG) to oversee the execution of the Investigator-Sponsored Research (ISR) programs from concept through full execution, including reporting the evidence at scientific congresses, in peer-reviewed publications, and proactive/reactive BMS communication tools. Collaborate with the Medical Product Lead with the development and implementation of the GMO medical plan that drives product differentiation, lifecycle management as well as advancing disease specific strategies in alignment with Commercialization and R&D, translating strategies into meaningful impact for patients.