49 r d intern jobs found in Philadelphia, PA

Apex Systems, Inc. Job#: 2072623 Job Description: Seeking a Lab Tech to join a company in Malvern, PA. Only local candidates will be considered. Responsibilities: The Lab Technician safely performs advanced specialized technical functions involving testing, analyzing, improving, installing, operating, and/or solving problems concerning gypsum boards (fire, lightweight, mold and moisture) and its raw materials. JOB OBJECTIVES : Supports engineers and scientists in the R&D team with their projects. Executes and/or supports commercial and manufacturing support requests. Manages and documents projects by creating concise and technically accurate summary reports effectively with supervision. Conducts hands-on experimental work and ensures all products are tested and approved according to the company SOP. Performs research and a variety of experiments, makes detailed observations, analyzes data, and interprets results. Identifies opportunities...

Repligen Overview Repligen is a bioprocessing-focused life sciences company bringing over 30 years of expertise and innovation to our customers. We are inspiring advances in bioprocessing through the development and commercialization of high-value products and flexible solutions that address critical steps in the production of biologic drugs. We are seeking a US- based Field Application Scientist to technically support the upstream product lines in the bioprocess industry. This individual will use their knowledge of cell culture process development, filtration and manufacturing to support customers and our sales team in pre- and post- sales opportunities. The successful candidate will also work closely with Repligen colleagues including sales account managers, product management, quality assurance, and R&D scientists/engineers to ensure our products continue to serve the evolving needs of our customers in the bioprocessing industry. This is a US east coast...

Guild Mortgage Guild Mortgage Company , closing loans and opening doors since 1960. As a mortgage banking firm we are dedicated to serving the home owner/buyer. Our goal is to provide affordable home financing for our customers, utilizing the best terms available while providing a level of professionalism and service unsurpassed in the lending industry. Position Summary The AI Engineer is responsible for the development and implementation of advanced artificial intelligence systems. This role involves designing, programming, and training complex algorithms that emulate human cognitive processes. Key responsibilities include managing and processing large datasets, developing, and testing machine learning models, and integrating these models into applications using API calls or embedded code. The position requires a strong foundation in software development, data science, and data engineering, as well as a deep understanding of machine learning principles. The AI Engineer...

Site Name: USA - Pennsylvania - Upper Providence, Home Worker - USA Posted Date: Nov 20 2024 Study Strategic Planning Lead (Associate Director) As R&D efforts follow science without constraint, we need to take full advantage of our internal data and expertise, as well as leverage solutions and technology, to inform, optimize and validate our clinical trial protocols and study delivery plans. The Study Strategic Planning Lead will support study teams in creating optimal clinical trials plans that deliver on the asset and study strategy. These plans will be driven by the analysis of internal and external data, and the inclusion of the necessary Digital Health and other recruitment levers to accelerate patient enrolment and meet patient diversity targets. The SSPL is responsible for advising on data-driven actionable intelligence and high quality insights, partnering with internal discipline experts and study team members. This role will project manage a team of experts...

Site Name: USA - Pennsylvania - Philadelphia, USA - Massachusetts - Waltham, USA - North Carolina - Durham Posted Date: Nov 27 2024 As the Director, Regulatory Advertising & Promotion Policy , you will be responsible for leading assigned products providing sound regulatory advice for advertising and promotion of prescription drug products and biologics that minimizes the risk of regulatory action, competitively positions assigned products and is consistent with applicable FDA regulations and GSK policy. This role will act as a credible, influential, respected spokesperson for assigned products during interactions with the Office of Prescription Drug Promotion (OPDP) and/or the Advertising and Promotional Labeling Branch (APLB) reviewers. The Director will provide consultative support to Global Regulatory Affairs therapeutic project teams for issues/strategies relating to continuity between development plans and commercial objectives. Key Responsibilities : This role...

Site Name: USA - Pennsylvania - Philadelphia, USA - Massachusetts - Waltham, USA - North Carolina - Durham Posted Date: Nov 27 2024 Are you passionate about regulatory advertising and promotion review with oncology experience? Within the Oncology space, we are in a period of very dynamic growth, as we continue to expand and develop our pipeline and portfolio. We are looking for a driven and motivated regulatory professional who will be instrumental in supporting the growth of our expanding oncology portfolio. As the Director, Regulatory Advertising & Promotion Policy , you will be responsible for leading assigned products providing sound regulatory advice for advertising and promotion of prescription drug products and biologics that minimizes the risk of regulatory action, competitively positions assigned products and is consistent with applicable FDA regulations and GSK policy. This role will act as a credible, influential, respected spokesperson for assigned products...

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Dec 13 2024 Do you want to work for one of the world's leading pharmaceutical and healthcare companies, applying your statistical skills and innovative statistical methodology to make key contributions to the manufacture of critical medicines? We have an exciting opportunity for a statistician to join our Digital and Data Science group, dedicated to supporting the launch of medicinal products to market and their subsequent product lifecycle within manufacturing. We are looking for an experienced non-clinical statistician to provide statistical support to manufacturing locations across the globe. In this role you will have the opportunity to collaborate with scientific colleagues in multidisciplinary teams in order to embed statistical thinking within projects whilst designing experiments and analysing data. This is an exciting opportunity to use your applied statistical skills to lead statistics capability build...

Site Name: USA - Pennsylvania - King of Prussia, UK - Hertfordshire - Stevenage, UK - Hertfordshire - Ware RD, USA - Pennsylvania - Upper Providence Posted Date: Dec 13 2024 Are you excited about a role in compliance? If so, the Compliance Solutions Lead may be a role for you! The Job Purpose To ensure Quality Management System (QMS), Data Verification (DV), Digital Data Analytics Compliance and Document/Submission Content Mappings are simple, clear and readily embedded with MDS staff To demonstrate the above processes are operating in compliance with quality/ business expectations and to prioritize and pursue continuous improvement or significant transformation activities, where agreed and/or aligned across Medicines R&D and Vaccines R&D To build partnerships based on leadership and trust within and outside RMC to define and implement strategic initiatives that improve business unit core value drivers. For example, Medicines R&D and Vaccines R&D. For...

Site Name: USA - Pennsylvania - King of Prussia, UK - County Durham - Barnard Castle, UK - Hertfordshire - Ware, USA - Maryland - Rockville, USA - Pennsylvania - Upper Providence Posted Date: Nov 26 2024 Job Description The Reference Material and Reagents Director is accountable for ensuring critical reagents and analytical standards are available for the GSK network. They must be of the required regulatory standards and coordination and supply to GSK sites, CMO and LOC to support end to end supply chain of products to the patient. The role will ensure long term availability and lifecycle management of reference materials for existing and new GSK products. You will ensure outsource partners are maintained, ensuring a priority service to GSK is maintained and that bulk materials are effectively supplied to the outsource partner in a timely manner, along with supporting information to maintain a secure supply of reference materials. Also, ensure GSK customer changes, risks...

CSL Are you ready to build the future product pipeline in a high-impact, strategic leadership role? The Senior Director of Medical Affairs, Cardiovascular & Renal (CVR) in Global Medical Affairs at CSL Vifor is responsible for the development and execution of global medical affairs strategies and tactics across the entire CVR Therapeutic Area (TA). These responsibilities are primarily focused on the pipeline and working closely with R&D and Commercial Strategy at the TA Leadership Team (TALT) membership level. This role works closely with regional and country teams to ensure global strategies and tactics are pulled through into the market and that impactful regional and country input from major markets are represented in global strategies. This role is also a key member of the CVR Therapeutic Area Leadership Team (TALT), and CSL Vifor Global Medical Affairs Leadership Team (MALT), contributing to the cross functional development of TA strategy and individual global...

CSL The Opportunity: As the Global Product Lead (GPL), you will be a senior, cross-functional strategic leader in the CSL organization, reporting to the R&D Therapeutic Area Co-Lead. You will be accountable for all product strategy and delivery in your portfolio and, in that capacity, to the respective Therapeutic Area Leadership Team (TALT) and TA Co-Leads. You will be a member of the GPL Leadership Team (grass roots/informal team) and a core member of TALTs. Depending on specific product(s) and its stage of life cycle, you will have high-level accountabilities that are critical to the delivery of CSL business objectives and portfolio value targets. These may include: Create and lead a cross-functional team of global functional senior leaders responsible for the delivery of the product portfolio. Create development plans and options for each of your assets, with the goal of managing the trade-off between time, risk, cost and value. Accountable for the development and...

CSL CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives. With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. Could you be our next Director, Business Development and Licensing? This is a hybrid role located in our King of Prussia PA or Waltham MA...

CSL For our Clinical Trial Supply department, in Marburg, Bern, Zürich or King of Prussia, we are looking for a Global Planner, Clinical Trial Supply (m/f/x) R-251735 Fulltime / permanent / tariff Internal job title: Global Planner CTS Supply Chain Internal closing date: 08.04.2025 The Opportunity Monthly Forecast Planning and updating on study specific Demands in close cooperation with Study Managers and CMC Creation and maintenance of delivery schedules (Supply) for clinical goods in close cooperation with CSL global and regional product planners and CMOs Recording of the requirements planning in the global CSL planning tool (RapidResponse), ensuring and tracking the transfer of quantities to SAP S4 Hana Coordination of a timely and complete delivery of all clinical studies by CSL Behring worldwide with the required test goods Participation and initiation of international task force meetings as CTS representatives to coordinate requirements Creation...

PerkinElmer Responsibilities Location Collegeville, PennsylvaniaUS Job ID REQ-053845 Job Responsibilities: Work as a principal engineer/scientist in a multi-disciplinary development team, liaising efficiently with Formulators, Modelers, automation experts, data scientists and device engineers, to deliver the work packages required to understand drug product unit operations and scale these-up effectively. Actively participate in technical reviews on projects, lead the scale-up of processes, and ensure timely execution. Contribute to CMC and MPD team planning, agreeing priorities and coordinating PE&A activities that support delivery of objectives. Ensure proper Process Engineering and PAT related decisions are taken at appropriate milestones within the project plan to accelerate early phase formulation and process design and minimize number of DOE's for scalability assessments and API consumption throughout the development life-cycle. Make innovative...

PerkinElmer Responsibilities Location Collegeville, PennsylvaniaUS Job ID REQ-055020 Job Responsibilities Provide high quality laboratory support to the ETCT team. Support multiple ongoing large-scale cell-based projects that are critical to the success and future of the department. Lab work will include flow cytometry, mammalian cell culturing, cell proliferation, protein isolation, and viral transduction. Generate and analyze data with the highest Data Integrity standards. Operate and maintain laboratory instrumentation and robotics, including liquid sample handling platforms. Continue technological improvements to increase productivity and cost-efficiency. Data reporting, management, and interactions as appropriate with the teams. Develop organization skills, presentation skills and attention to detail. Interact with senior staff members as necessary. Ensure compliance with all R&D data integrity practices, ethics codes, standards and training, and...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Canada - Ontario - Mississauga, USA - Massachusetts - Cambridge, USA - Massachusetts - Waltham Posted Date: Sep 16 2024 Would you like to be part of GSK’s Global Epidemiology, Vaccines team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportunity to explore. Job Purpose The Associate Director in Epidemiology will support epidemiological strategy for programs led by the Epidemiology Cluster Head- Bacterial vaccines. The goal is to ensure high quality and on-time delivery of epidemiology data that will allow and support world-wide registration in compliance with the epidemiology plan, applicable good practices, and non-interventional studies standard operating procedures (SOP). As an Associate Director in Epidemiology, you will provide scientific leadership in the application of epidemiological expertise and methods to...

Site Name: Upper Providence, Belgium-Wavre, Mississauga, USA - Massachusetts - Waltham Posted Date: Aug 20 2024 Would you like to be part of GSK’s Global Epidemiology, Vaccines team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportunity to explore. Job Purpose The Director in Epidemiology will support epidemiological strategy for programs led by the Epidemiology Cluster Head- Bacterial vaccines. The goal is to ensure high quality and on-time delivery of epidemiology data that will allow and support world-wide registration in compliance with the epidemiology plan, applicable good practices, and non-interventional studies standard operating procedures (SOP). As a Director in Epidemiology, you will provide scientific leadership in the application of epidemiological expertise and methods to answer key challenges identified across all phases of vaccine development for an asset or...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Oct 31 2024 We are seeking a highly motivated, flexible, and experienced scientist with demonstrated expertise in reagent generation and characterization. This individual will support for generation and characterization of critical reagents in a timely manner for development, validation, and execution of bioanalytical, immunogenicity and biomarker assays to support clinical development. The successful candidate will work closely with bioanalytical, immunogenicity and biomarker assay groups and cross-functional teams in GSK to identify, generate, select, and qualify critical reagents, as well as their monitoring, tracking, and storage. The role is based in our R&D hub at Upper Providence US. In this role you will Participate in laboratory activities and provide scientific expertise to prepare and analyze critical protein reagents in support of the bioanalytical laboratory. Conduct day-to-day experimental...

Site Name: Collegeville TSA, Durham Blackwell Street Posted Date: Nov 8 2024 Purpose of this role is to provide independent Pharmacovigilance (PV) Quality Assurance within GSK R&D by delivering comprehensive risk-based audit programs. This role will define audit scope and methodology to conduct audits and ensure the delivery of audit reports with and end-to-end process driven approach. This role involves identifying compliance issues, trends, within the scope of R&D to ensure compliance with relevant international regulatory agency regulations/guidelines, GSK policies/procedures and accepted principles and improving overall processes. Additionally, the role includes supporting QA activities during regulatory inspections, building solid working relationships with stakeholders, and maintaining knowledge of local regulatory frameworks and global regulatory reporting requirements. This role will provide YOU the opportunity to lead key activities to progress YOUR career,...

Site Name: USA - Pennsylvania - Upper Providence, Home Worker - USA Posted Date: Nov 20 2024 Study Strategic Planning Lead (Associate Director) As R&D efforts follow science without constraint, we need to take full advantage of our internal data and expertise, as well as leverage solutions and technology, to inform, optimize and validate our clinical trial protocols and study delivery plans. The Study Strategic Planning Lead will support study teams in creating optimal clinical trials plans that deliver on the asset and study strategy. These plans will be driven by the analysis of internal and external data, and the inclusion of the necessary Digital Health and other recruitment levers to accelerate patient enrolment and meet patient diversity targets. The SSPL is responsible for advising on data-driven actionable intelligence and high quality insights, partnering with internal discipline experts and study team members. This role will project manage a team of experts...