Viatris Specialty LLC At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via Access Providing high quality trusted medicines regardless of geography or circumst

Site Name USA Pennsylvania Upper Providence, Belgium Wavre, Durham Blackwell Street, USA Massachusetts Waltham Posted Date Apr 15 2024 Associate Director Epidemiology Vaccines Would you like to be part of GSK's Epidemiology team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportuni

Site Name USA Pennsylvania Upper Providence Posted Date Mar 11 2024 Are you a scientist in sterile product formulation and injectables eager to lead the development of life changing drug products? Are you eager to unite science, talent, and technology to get ahead of disease together? This may be the right opportunity for you! As a Scientific Leader/Associate Director, yo

The Regulatory Affairs Specialist (RA Specialist) is responsible for supporting registration of West's Administration and Safety System devices, with primary responsibility for obtaining device regulatory approvals/clearances in the APAC regions. This includes the authoring, preparation, and review of technical dossiers. The RA Specialist ensures timely execution in prepa

To be responsible for Epidemiological studies within a large program or group of related programs (led by a senior epidemiologist) within the context of the GSK Vaccines process in order to ensure the high quality and on time delivery of all epi data that will allow and support world wide registration in compliance with the clinical and epi development plan, applicable go

We are looking to fill a position for a Validation Engineer Laboratory working as a full time employee of Parexel FSP on long term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. Responsibilities Executes analytical methods, including total organic carbon (TOC) and co

We are looking to fill a Facility Engineer Suite Coordinator position working as a full time employee of Parexel FSP on long term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. Description The Facility Engineer Suite Coordinator supports facility readiness and compli

Assist Philadelphia office in leveraging existing client base while performing market research and outreach on new potential clients and opportunities. Participate in Philadelphia regional industry events and organizations. Work with Senior Leadership to define local business development strategies and goals. Collaborate with firm wide business development team on cross o

Develops and maintains enterprise software applications Collaborates with the product team on requirements elicitation to deliver software Authors and reviews unit/integration test Participates in code and software review processes Collaborates with members of the product, test, and software engineering organizations Develops expertise for all aspects of a software produc

Develops and maintains enterprise software applications Collaborates with the product team on requirements elicitation to deliver software Authors and reviews unit/integration test Participates in code and software review processes Collaborates with members of the product, test, and software engineering organizations Develops expertise for all aspects of a software produc

As a Contract Negotiation Analyst, you will prepare, analyze, and negotiate customer contracts, with a primary focus on standard template agreements. Manage contract negotiation process from sale date to execution, as well as contract renewals and retention. Work within the framework of sales contracting and legal strategies, law, administrative regulations, and company p

Collaborate with stakeholders to define and document reporting requirements, data models, and queries. Design and create supporting data models. Integrate, test, and validate new data sources into production data models. Design and develop visually compelling reports and dashboards. Author efficient SQL queries with a strong understanding of relational data modeling Adapt

Authors and reviews test scripts Conducts manual testing (included construction of test data) and collects test evidence Collaborates with the product team on requirements elicitation to make sure requirements are complete and testable Collaborates with quality assurance team to ensure teams compliance responsibilities are met (our products are GxP and ISO compliant) Tria

Conduct bioanalytical work to a high degree of quality and rigor, ensuring compliance with regulatory guidelines Develop regulated bioanalytical methods for the quantitation of biotherapeutic drug candidates using ligand binding assay based platforms such as Meso Scale Discovery, Gyrolab, Ella, and other emerging technologies Contribute to immunogenicity assay development

The Robotics Institute at Carnegie Mellon University was established in 1979 to conduct basic and applied research in robotics technologies relevant to industrial and societal tasks. Seeking to combine the practical and the theoretical, we have diversified efforts and approaches to robotics science while retaining the original goal of realizing the potential of the roboti