NewManufacturing Operations Graduate Program, Upper Merion, US, 2027 GSK plcManufacturing Operations Graduate Program, Upper Merion, US, 2027King of Prussia, PAEducation required: Bachelor of Science/BSc; Master of Science/MSc - Engineering, Biomedical Engineering, Pharmaceutical Engineering, Biologics & Process Technology, Chemical & Pharmaceutical Technology, Chemical Engineering, Pharmaceutical Science, Microbiology, Biochemistry, Biotechnology, Computer Science with a focus on AI, Data management, digital technologies. You will gain an insight into the manufacturing side of our business, developing your expertise in production, engineering, quality and technical services or supply chain management, while broadening your global business perspective: Pharmaceutical Manufacturing: Gain hands-on exposure to production processes, manufacturing systems, and equipment performance.
Associate Director, Device Lead GSK plcAssociate Director, Device LeadCollegeville, PA$142,725–$237,875 / yearThese responsibilities include some of the following: Be the SPOC technical SME interface between Device/Component suppliers and GSK MSAT site teams - providing device-related technical management to MSAT where required for business improvement projects and risk management activities, represent MSAT at supplier technical and project meetings. Drive innovation through the introduction of new and novel device technologies and/or ways of working and champion business cases for sustainable manufacturing technology implementation or other strategic projects including those related to quality by design, design for manufacturing, product and process understanding, design control, and digital data management, and analytical competency.
Scientist, Downstream Vaccines and Advanced Biotechnologies (VAX) Process R&D Merck & Co IncScientist, Downstream 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. Preferred Experience and Skills: Prior hands on experience with any of the following purification bioprocesses: Tee-mixing, Extrusion, Tangential Flow Filtration, Dead-End Filtration, Microfiltration or Homogenization.
Associate Director, Device Lead GSK, Plc.Associate Director, Device LeadUpper Providence, PA$142,725–$237,875 / yearThese responsibilities include some of the following: Be the SPOC technical SME interface between Device/Component suppliers and GSK MSAT site teams - providing device-related technical management to MSAT where required for business improvement projects and risk management activities, represent MSAT at supplier technical and project meetings. Drive innovation through the introduction of new and novel device technologies and/or ways of working and champion business cases for sustainable manufacturing technology implementation or other strategic projects including those related to quality by design, design for manufacturing, product and process understanding, design control, and digital data management, and analytical competency.
Facility Project Manager Genscript Biotech CorpFacility Project ManagerPennington, NJ$100,000–$130,000 / 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.
Senior Clinical Algorithm Specialist Globus MedicalSenior Clinical Algorithm SpecialistAudubon, PennsylvaniaNevro also recently added a minimally invasive treatment option for patients suffering from chronic sacroiliac joint ("SI joint") pain and now provides the most comprehensive portfolio of products in the SI joint fusion space, designed to meet the preferences of physicians and varying patient needs in order to improve outcomes and quality of life for patients. HFX iQ, Nevro’s latest innovation, is the first and only SCS System that uses Artificial Intelligence to optimize and maintain pain relief using each patient's response1.Nevro’s unique support services provide every patient with an HFX Coach throughout their pain relief journey and every physician with HFX Cloud insights for enhanced patient and practice management.
Product Manager, Imaging Globus MedicalProduct Manager, ImagingAudubon, PennsylvaniaGather Voice of Customer (VOC) feedback from surgeons, healthcare professionals, and key opinion leaders (KOLs) to define product requirements and guide development activities. · 3-6 years of experience in Product Management, Product Development, Product Marketing, or related commercial roles within the medical device industry.
PRODUCT MANAGER, IMAGING Globus Medical IncPRODUCT MANAGER, IMAGINGPAGather Voice of Customer (VOC) feedback from surgeons, healthcare professionals, and key opinion leaders (KOLs) to define product requirements and guide development activities. 3-6 years of experience in Product Management, Product Development, Product Marketing, or related commercial roles within the medical device industry.
Director, Clinical Pharmacology Madrigal Pharmaceuticals IncDirector, Clinical PharmacologyConshohocken, PA$228,074–$264,393 / yearThis individual will be responsible for developing integrated clinical pharmacology strategies that support dose selection, characterization of pharmacokinetics, pharmacodynamics, exposure-response characterization, intrinsic and extrinsic factors, drug-drug interactions, cardiac safety, special populations, and regulatory submissions. The successful candidate will collaborate closely with Clinical Development, Translational Medicine, Biostatistics, Regulatory Affairs, Medical Writing, and external partners to deliver high-quality Clinical Pharmacology strategies that enable informed development and regulatory decision making.
Associate Director - Life Sciences Advisory - Market Access (Global) Guidehouse IncAssociate Director - Life Sciences Advisory - Market Access (Global)Philadelphia, PA$135,000–$225,000 / yearSpecific responsibilities for the Global Market Access position include: Track record of success developing, leading, and delivering global (e.g., EU, APAC, LATAM) pricing and access / reimbursement projects, with subject matter expertise on HTA assessment frameworks, pricing & reimbursement archetypes, and national / regional pricing & reimbursement mechanisms. Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle today's challenges, while anticipating tomorrows.
Senior Manager, R&D Data, Data Science, And AI - Digital Health For Neuropsychiatry Johnson & JohnsonSenior Manager, R&D Data, Data Science, And AI - Digital Health For NeuropsychiatryTitusville, NJRemote$137,000–$235,750 / yearDigital Endpoints & Tools: Execute the neuropsychiatry-focused digital health strategy by applying AI/ML, modeling, and longitudinal analytics to support patient stratification, endpoint development, and clinical trial optimization, in partnership with disease experts, statisticians, and platforms and clinical teams on study design and validation of digital measures, balancing their informativeness with low clinical burden for patients and study teams. All 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.
Regulatory Affairs Manager West Pharmaceutical ServicesRegulatory Affairs ManagerExton, PASupport Regulatory Affairs digital transformation by serving as a functional subject matter expert for AI and digital enablement, including identifying and evaluating AI-enabled solutions, defining compliance-critical use cases, supporting implementation planning, and ensuring regulatory workflows, submissions, document automation, and data traceability are aligned with regulatory, quality, and business needs. In addition, this role will play a key role in advancing Regulatory Affairs digital transformation by identifying, shaping, and supporting the adoption of compliant AI-enabled tools, automation solutions, and RA-focused digital capabilities that improve productivity, scalability, data traceability, submission quality, and operational efficiency across Regulatory Affairs.
Senior Manager, R&D Data, Data Science, and AI - Digital Health for Neuropsychiatry Johnson & JohnsonSenior Manager, R&D Data, Data Science, and AI - Digital Health for NeuropsychiatrySpring House, PARemote$137,000–$235,750 / yearDigital Endpoints & Tools: Execute the neuropsychiatry-focused digital health strategy by applying AI/ML, modeling, and longitudinal analytics to support patient stratification, endpoint development, and clinical trial optimization, in partnership with disease experts, statisticians, and platforms and clinical teams on study design and validation of digital measures, balancing their informativeness with low clinical burden for patients and study teams. All 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.
IONM Technologist Neuro PathwayIONM TechnologistPhiladelphia, PennsylvaniaReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: While performing the essential duties of this job, the associate is required to: stand, walk, sit; use hands to grasp, handle or feel objects, tools or controls; reach with hands and arms; stoop, kneel, crouch; talk or hear. Set up neurophysiological equipment following any indicated biomedical electrical safety checks, with equipment properly located in operating room and assembled with respect to reduction of recording artifact.
Simulation Technician Gwynedd Mercy UniversitySimulation TechnicianPAThis state-of-the-art facility features immersive simulation and skills labs where students practice clinical skills and manage complex patient scenarios in a safe, realistic environment. Maintain and oversee simulation equipment, coordinating purchases, repairs, and vendor relationships for service and upgrades, while also managing a complete inventory of all equipment, supplies, materials, and other technologies used in the laboratory.
Senior Director, Quality Assurance & Regulatory Affairs ConcertAISenior Director, Quality Assurance & Regulatory AffairsPlymouth Meeting, PAConcertAI brings together a portfolio of purpose-built solutions, including TeraRecon, an industry leader in advanced imaging and AI-driven visualization, and CancerLinQ, the ASCO-originated oncology platform advancing care quality and large-scale discovery. Leaders are expected to embrace an AI-first mindset by leveraging AI to improve efficiency, enhance quality, automate routine work, accelerate decision-making, and foster continuous innovation while ensuring responsible, ethical, and compliant use of AI technologies.
NewManaging Consultant - Life Sciences Advisory - Market Access (Us) GuidehouseManaging Consultant - Life Sciences Advisory - Market Access (Us)Philadelphia, PA$122,000–$204,000 / yearGuidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle today's challenges, while anticipating tomorrows. As Managing Consultants hone their project management skills, ability to manage multiple work streams, professional expertise, and client and business development skills, they progress to the position of Associate Director.
Cast Tech- Orthopedics- EHN PHL Thomas Jefferson UniversityCast Tech- Orthopedics- EHN PHLPhiladelphia, PAJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Jefferson Health, nationally ranked as one of the top 15 not-for-profit health care systems in the country and the largest provider in the Philadelphia and Lehigh Valley areas, serves patients through millions of encounters each year at 32 hospitals campuses and more than 700 outpatient and urgent care locations throughout the region.
Director, Medical & Scientific Affairs - Metabolic Disease Imaging ICON PlcDirector, Medical & Scientific Affairs - Metabolic Disease ImagingBlue Bell, PARemoteYou will serve as a key scientific advisor to internal stakeholders and external clients, helping to shape imaging strategies, support study design, and ensure the successful implementation of imaging endpoints across clinical trials. Working in close partnership with Commercial Development, Operations, Product Development, and Marketing teams, you will help drive business growth, advance imaging innovation, and strengthen ICON's leadership position in metabolic disease imaging research.
Senior Scientist, R&D, Primary Drug Packaging West Pharmaceutical ServicesSenior Scientist, R&D, Primary Drug PackagingRadnor, PAThe Senior Scientist, Primary Drug Packaging, will be responsible for leading technical activities related to the development, evaluation, selection, and lifecycle management of primary packaging systems for pharmaceutical and drug products including biologics, vaccines, cell and gene therapies, mRNA/LNP-based products, high-value injectables, and other complex drug products. The person will work cross-functionally with R&D, Analytical Services, Quality, Regulatory, Technical Customer Support, Product Development, and Commercial teams to generate scientifically sound data that supports product development, customer programs, technical investigations, and lifecycle management.