Executive Medical Science Liaison _ Northwest Celldex TherapeuticsExecutive Medical Science Liaison _ NorthwestHampton, New Jersey$153,616–$245,387 / yearThe role maintains and develops relationships across a range of stakeholders, including key opinion leaders, investigators, and as appropriate, large group practices and private equity-backed dermatology organizations , contributing to a broader understanding of evolving clinical and practice dynamics. The Associate Director is expected to deliver complex, data-driven scientific discussions , synthesize meaningful insights from the field, and navigate real-world clinical dynamics while maintaining a strong focus on regional ownership and high-impact engagement .
Sr. Distinguished Scientist - Psts Neuroscience Disease Area Lead Johnson & JohnsonSr. Distinguished Scientist - Psts Neuroscience Disease Area LeadSpring House, PA$173,000–$299,000 / yearRequired Skills: Preferred Skills: Design Mindset, Drug Discovery Development, EHS Compliance, Emergency Planning, Interpersonal Influence, Performance Measurement, Process Hazard Analysis (PHA), Process Optimization, Program Management, Risk Management, Safety Audits, Safety Investigations, Safety-Oriented, Scientific Research, Stakeholder Engagement, Strategic Thinking, Technical Writing. The DAL will serve as a coach and mentor for PSTS team leaders working in their portfolio including providing expert advice and review of PSTS plans and regulatory submissions at assigned stages and PSTS functional reviews with the purpose of assuring scientific and regulatory questions are proactively addressed.
Senior Scientist, Discovery Process Research Johnson & JohnsonSenior Scientist, Discovery Process ResearchSpring House, PennsylvaniaOur goal is to facilitate medicinal chemistry research by finding solutions to synthetic bottlenecks, enabling access to novel chemical space and translating chemistry innovations to the development of efficient routes for the synthesis of small molecules, oligonucleotides, peptides and other emerging modalities advancing into development. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Scientific Publication Manager - III (Senior) Talent Software Services, Inc.Scientific Publication Manager - III (Senior)North Wales, PA$55–$61.54 / hourSpecialist Publication Manager coordinates publication planning and implementation, tracks and reports the progress of publication development, aids in the selection of appropriate journals and congresses for scientific data dissemination, and allocates resources for writing, editing, formatting and submitting articles to peer-reviewed scientific journals and scientific conferences. Ability to plan, prioritize, and execute multiple projects; ability to multitask and work both independently and within multi-disciplinary teams, and keep both team members, departmental colleagues (as appropriate) and management fully apprised of project / initiative status and issues.
Sr Lab System Support Engineer TechDigital CorporationSr Lab System Support EngineerWest Point, PAThe Sr Lab System Support Engineer plays a key role in supporting laboratory operations by ensuring the smooth functioning of lab systems, analytical instruments, and data workflows. Lab System Lifecycle Management: Manage end-to-end lab system lifecycle, including implementation, validation, maintenance, and decommissioning.
Senior Scientist, Engineering Merck & Co IncSenior Scientist, EngineeringWest Point, PA$117,000–$184,200 / yearRequired Skills: cGMP Regulations, Chemical Engineering, Chemistry, Chromatographic Techniques, Clinical Judgment, Commercialization, Design of Experiments (DOE), Good Manufacturing Practices (GMP), Pharmaceutical Industry, Pharmaceutical Research, Process Development (PD), Process Optimization, Process Scale Up, Process Transfers, Scientific Presentations, Scientific Writing, Small Molecule Synthesis, Strategic Planning, Technical Evaluation, Technical Reviews, Technology Transfer, Writing Technical Documents. Education Minimum Requirement: Bachelor's degree and 6 years related experience, master's degree and 4 years related experience, or PhD (no additional experience required) in Chemical/Biochemical Engineering, Materials Science/Engineering, Pharmaceutical Sciences, or related discipline.
NewSenior Director of Operations - Easton II-VI Optical Systems, Inc.Senior Director of Operations - EastonEaston, PAThe Senior Director of Operations - Easton, PA provides senior leadership for the Easton Garnet manufacturing operation, with primary accountability for the successful execution of the Easton expansion, operational readiness, and production ramp. The position reports to the Senior Director, Garnet Operations and works closely with Engineering, R&D, Quality, Supply Chain, Finance, Human Resources, Facilities, EHS, and other functions to align expansion, staffing, equipment, process qualification, and manufacturing execution.
Sr. Research Scientist, Dissolution Method Development Thermo Fisher Scientific IncSr. Research Scientist, Dissolution Method DevelopmentCollegeville, PAWithin 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.
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.
Senior Machine Learning Engineer, Biologics Discovery Johnson and JohnsonSenior Machine Learning Engineer, Biologics DiscoverySpring House, PAFull timeArtificial Intelligence (AI), Coaching, Cognitive Computing, Critical Thinking, Cross-Functional Collaboration, Curious Mindset, Data Structures, Distributed Computing, Emerging Technologies, Human-Computer Relationships, Machine Learning (ML), Persistence and Tenacity, Program Management, Research and Development, SAP Product Lifecycle Management, Scripting Languages, Technologically Savvy . This role builds and operates the integration, deployment, lifecycle management, and governance capabilities that enable machine learning (ML) models and AI solutions developed by partner organizations to run reliably in Biologics Discovery environments.
Sr. Data Architect Judge GroupSr. Data ArchitectWorcester, PA$130,000–$150,000 / yearThis role serves as the senior-most subject matter expert (SME) for Microsoft Fabric, OneLake, advanced analytics, and Copilot-enabled architectures, ensuring the enterprise is positioned to fully leverage data as a strategic asset. · Microsoft Fabric & OneLake Authority: Serve as the definitive technical authority for Microsoft Fabric architecture, including OneLake, lakehouse design, real-time analytics, semantic models, and AI-enabled workloads at enterprise scale.
Sr. Manager Quality Systems & Compliance Piramal PharmaSr. Manager Quality Systems & ComplianceSellersville, PennsylvaniaThis enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. The incumbent will be primarily responsible to ensure the Quality Assurance team delivers the following through effective leadership, mentoring and management: Audits: Support internal and external audits and regulatory inspections.
Senior Medical Writer Health InteractionsSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Sr. CSV/CSA/Validation Engineer Katalyst HealthCares & Life Sciences IncSr. CSV/CSA/Validation EngineerRaritan Township, NJCSV/CSA/Validation Engineer leads and independently executes computerized system validation, computer software assurance, infrastructure qualification, and business system validation activities within GxP-regulated pharmaceutical, biotechnology, or medical device environments. Ability to manage end-end from Inventory, assessments, remediations to final dispositions; Infrastructure Qualifications & Business Systems Validations 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources.
Senior Manager, Clinical Project Management Job Details | Olympus Corporation Of The Americas OlympusSenior Manager, Clinical Project Management Job Details | Olympus Corporation Of The AmericasCenter Valley, PAThis role manages study timelines, budgets, vendors, and operational deliverables while coordinating cross-functional study teams in a hub-and-spoke model to ensure efficient study execution. Serve as the central hub for the study core team, coordinating activities across Clinical Strategy, Data Management, Biometrics, Monitoring, Site Management, Data Systems, and Clinical Trial Associates.
Senior Manager, Clinical Project Management Olympus CorpSenior Manager, Clinical Project ManagementPAThis role manages study timelines, budgets, vendors, and operational deliverables while coordinating cross-functional study teams in a hub-and-spoke model to ensure efficient study execution. Serve as the central hub for the study core team, coordinating activities across Clinical Strategy, Data Management, Biometrics, Monitoring, Site Management, Data Systems, and Clinical Trial Associates.
Senior Controls Engineer Barry-Wehmiller Companies IncSenior Controls EngineerEaston, PADesign Group is widely known as an industry leader, recognized as a top system integrator, ranking #7 in the 2023 System Integrator Giants; as a Rockwell Platinum Integrator, the highest designation given to Rockwell partners; and as an Ignition Enterprise Premier Integrator. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world.
Sr. Manager Quality Systems & Compliance Piramal Enterprises LtdSr. Manager Quality Systems & ComplianceSellersville, PAThis enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. The incumbent will be primarily responsible to ensure the Quality Assurance team delivers the following through effective leadership, mentoring and management: Audits: Support internal and external audits and regulatory inspections.
Senior Veeva Technical Architect Tata Consultancy Services LtdSenior Veeva Technical ArchitectTitusville, NJ$140,000–$180,000 / yearStrong architecture expertise across Veeva QualityDocs, Veeva eTMF, Veeva PromoMats, and Veeva MedComms, with the ability to provide cross-platform architectural leadership across ECM and Commercial content domains. Demonstrated ability to lead distributed cross-functional teams, including architects, product owners, business analysts, configuration teams, integration teams, QA/validation teams, vendors, and implementation partners.
Senior Medical Writer Nucleus Global LtdSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.