Senior Construction Materials Field Technician Engineering Consulting Services LtdSenior Construction Materials Field TechnicianAllentown, PAField Activities: Perform observation, testing, sampling, and inspection of materials, including soils, aggregates, concrete, grout, masonry, asphalt, and structural steel placement on construction sites; Execute tasks based on project requirements under the guidance of other senior technicians, staff professionals, and project managers. Communication: Maintain daily communication with site contractors, other technicians, and project managers; Keep supervisor and project teams informed of changing site conditions and additional testing requested; Attend project meetings with senior staff as requested.
Senior Structural Engineer 1 - Nuclear Sargent & LundySenior Structural Engineer 1 - NuclearReading, Pennsylvania$84,762–$129,498 / yearFull timeSince 1954, we’ve been a trusted leader in nuclear engineering, design, and licensing, with expertise spanning small modular reactors (SMRs), advanced reactor technology (ART), and first-of-a-kind commercial reactor restart projects. Depending on the role, employees may use data, automation, artificial intelligence, and other digital tools to support research, analysis, engineering and design activities, workflow improvement, or other aspects of their work.
Senior Structural Engineer 1 Nuclear Sargent & Lundy LLCSenior Structural Engineer 1 NuclearReading, PA$84,762–$129,498 / yearIn this role, we expect people to be willing or able to lead others who use modern tools: You are expected to lead others in taking engineering problems from issue to solution by setting expectations for using data and modern tools such as automation and AI to improve workflows, reduce rework, and deliver cost-effective designs. Leaders in these roles often direct automation and process-improvement work, for example, how teams automate calculations, summarize technical documents, or generate design documentation and guiding when and how AI or agentic AI tools are used while ensuring results are checked.
Senior Director, Commercial Learning and Development and Onboarding Celldex Therapeutics IncSenior Director, Commercial Learning and Development and OnboardingNJ$203,157–$263,841 / yearCelldex is now entering an exciting new chapter - building a commercial team to launch barzolvolimab - the most advanced anti-KIT therapy in pivotal development that has the potential to redefine treatment for multiple allergy and dermatological diseases with Phase 3 studies in CSU, ColdU, SD and phase 2 studies in AD and PN. 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.
Senior Director Regulatory Affairs Liaison- General Medicine Merck & Co IncSenior Director Regulatory Affairs Liaison- General MedicineUpper Gwynedd, PA$190,800–$300,300 / yearRequired Skills: Corporate Commercial, Cross-Cultural Awareness, Drug Development, Exercises Judgment, Global Health, Global Market, Healthcare Innovation, Interpersonal Relationships, In Vitro Diagnostics (IVD), Multiple Therapeutic Areas, Oral Communications, Orphan Drugs, Pharmaceutical Regulatory Affairs, Process Improvements, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Communications, Regulatory Compliance, Regulatory Issues, Regulatory Management, 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 Vice President of Marketing (Remote) M3 USA CorpSenior Vice President of Marketing (Remote)Fort Washington, PARemoteThe Vice President of Marketing will lead and evolve M3 MR Group's global marketing strategy to accelerate revenue growth, strengthen the Group's position as a trusted healthcare market research and insights partner, and support continued expansion across regions, panels, solutions, and operating brands. M3 services incorporate all of the most advanced statistical and attitudinal methodologies allowing clients to provide world-class offerings and support services to their end-client customers throughout multiple industry sectors.
SERM Senior Medical Director, Oncology GSK plcSERM Senior Medical Director, OncologyCollegeville, PA$284,625–$474,375 / yearGSK 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. Clinical Development, Drug Regulatory Affairs, Evidence Based Decision Making, Good Clinical Practice (GCP), Influencing Without Authority, Learning Agility, People Management, Project Management, Scientific Presentations, Strategic Thinking.
Sr. Director, Medical Evidence Generation, Immunology Hampton, NJ Celldex Therapeutics IncSr. Director, Medical Evidence Generation, Immunology Hampton, NJHampton, NJ$203,157–$263,841 / yearThis role will lead evidence generation strategies, provide strategic oversight, and co-lead initiatives including post-marketing Ph3b/Ph4 studies in collaboration with Clinical Sciences & Clinical Development, Investigator Initiated ResearchStudies (IIRs), collaborative research efforts, real-world evidence (RWE) initiatives, outcomes research, and integrated evidence planning activities. HEOR), Clinical Development, Clinical Science, Biostatistics, Regulatory, Market Access, Commercial, and external scientific experts to identify evidence gaps and drive the generation of clinically meaningful, scientifically rigorous, and impactful evidence supporting Celldex programs across the product lifecycle.
Sr. Director, Project Management Hampton, NJ Celldex Therapeutics IncSr. Director, Project Management Hampton, NJHampton, NJ$203,157–$263,841 / yearWe have built a culture where innovative and talented people thrive-focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. 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.
Senior Project Manager Linde plcSenior Project ManagerAllentown, PAYou will direct all project phases - engineering (basic and detailed), procurement, fabrication, construction and commissioning/start-up, as well to maintain a strategic focus for the project with frequent interaction with the business area and the client to ensure a balance between the immediate project needs and the long term goals of the company. Areas of expertise include hydrogen solutions, air separation, carbon capture, adsorption, gas processing, deep cryogenics, liquefied natural gas (LNG) and fired process equipment.
Senior Medical Director, Pulmonary Hypertension, Global Medical Affairs Merck & Co IncSenior Medical Director, Pulmonary Hypertension, Global Medical AffairsNorth Wales, PA$282,200–$444,200 / yearCommunicates pertinent information to stakeholders [e.g., Executive Director Medical Affairs (EDMA), Regional Strategy Leads (RSL), Regional Director Medical Affairs (RDMA), U.S. Director Medical Affairs (US DMA), Payor and Access Strategy Leads (PASLs)] to inform and influence country and regional planning. Engages with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about our company's emerging science, building an important network and partnership internally and externally.
Senior Therapist Eagleville HospitalSenior TherapistPAEagleville Hospital, located in Montgomery County, Pennsylvania, is a private non-profit organization dedicated to the treatment, education, and prevention of substance abuse, co occurring disorders, and acute psychiatric disorders. Assists clients in maintaining contact with external systems when necessary including: Probation or Parole Officer, DPA, DHS, Employers, Funding Sources, and other case management as required.
Sr HVAC Technician CBRE Group IncSr HVAC TechnicianFort Washington, PAAbout the Role: As a CBRE HVAC Technician, you will be responsible for maintaining mechanical and electrical equipment for commercial HVAC systems at facilities by conducting proactive performance testing and ongoing scheduled maintenance. Meet the physical requirements of this role including stooping, standing, walking, climbing stairs/ladders, and the ability to lift/carry heavy loads of 50 lbs.
Senior Director, Team Lead - U.S. Medical Affairs, Payers & Health Systems Merck & Co IncSenior Director, Team Lead - U.S. Medical Affairs, Payers & Health SystemsNorth Wales, PA$210,400–$331,100 / yearEffectively communicates and coordinates with Commercial, Country MA, V&I Global Medical and Value Capabilities (V&I GMVC), and V&I Outcomes Research (V&I OR) leadership to oversee strategic account plans and associated medical account plans; ensures execution of medical activities in alignment with agreed plans. Supports the PHS Executive Director Medical Affairs (PHS EDMA) and PHS Payor & Access Strategy Lead (PHS PASL) in developing and executing the PHS MAP across the full company portfolio and across key account segments (e.g., payer, IDN, government).
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.
Senior Scientist, Regulatory Affairs- CMC - Synthetic Moieties of ADC''''s and Bioconjugates Merck & Co IncSenior Scientist, Regulatory Affairs- CMC - Synthetic Moieties of ADC''''s and BioconjugatesNorth Wales, PA$117,000–$184,200 / yearManage preparation and execution of Chemistry, Manufacturing and Control documentation including Investigational New Drug Applications, Investigational Medicinal Product Dossiers, original Biologics License Applications, Marketing Authorization Applications, post-approval submissions/variations, agency meeting background packages, and responses to health authority questions. Required Experience and Skills: At least 5 years of Regulatory CMC or directly relevant pharmaceutical development experience in small molecules or other chemically synthesized modalities, including experience in process chemistry, analytical development, manufacturing, testing, quality, technical operations, or CMC product development.
Senior Scientist, Biology-Discovery Merck & Co IncSenior Scientist, Biology-DiscoveryWest Point, PA$117,000–$184,200 / yearRequired Skills: Animal Models, Antiviral Drugs, Assay Development, Biochemical Assays, Biomarkers, Cell Culture Techniques, Drug Target Identification, Enzyme Linked Immunosorbent Assay (ELISA), Flow Cytometry, Immunoassays, Immunology, Infectious Disease Research, In Vitro Research, In Vivo Models, Molecular Biology, Pathogenesis, Tissue Collection, Transcriptomics, Virology. EDUCATION REQUIREMENT: BS/BA degree in Biology or Biomedical Sciences with a minimum 7 years of experience in industry and/or academia, or a MS degree in Biology or Biomedical Sciences with 4 years of experience in industry and or academia, or PhD with >1-year postdoctoral experience.
Sr. Materials Planner Veeco Instruments IncSr. Materials Plannerhorsham, PAFrom the smartphones in our pockets that access the world's collective knowledge, to the cloud-based services where all that information lives, to high-speed wireless communication and computing power needed to drive artificial intelligence, augmented and virtual reality, gaming and so much more, our technology is all around us. Change Management & Continuous Improvement: Evaluate and implement Engineering Change Notices (ECNs) with minimal disruption to production and aftermarket operations, and drive planning adjustments related to obsolescence, redesigns, and part substitutions.
Senior Turbomachinery Design Engineer Air Products and Chemicals IncSenior Turbomachinery Design EngineerBethlehem, PAKey Job Responsibilities: Perform aerodynamic design activities for awarded customer projects, including flowpath optimization of impellers, vanes, centrifugal compressors, turboexpanders, and related rotating equipment to improve efficiency, performance, and operating range. In this hands-on engineering design role, you will deliver advanced aerodynamic designs, performance predictions, and engineering tool improvements for turboexpanders, centrifugal compressors, and related turbomachinery systems.
Senior Quality Technician - In-Process Inspection (PSP) Veeco Instruments IncSenior Quality Technician - In-Process Inspection (PSP)Horsham, PAFrom the smartphones in our pockets that access the world's collective knowledge, to the cloud-based services where all that information lives, to high-speed wireless communication and computing power needed to drive artificial intelligence, augmented and virtual reality, gaming and so much more, our technology is all around us. We design, develop, manufacture, and service highly complex, cutting-edge machines used by our customers to create the essential devices that drive the digital age, connect the world, and improve the human experience.