12 medical lab technician jobs found in fairless hills, pennsylvania

job summary: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate quality

job summary: This role will perform QC Microbiology laboratory testing including bioburden, endotoxin, sterility, and microbial ID testing to ensure timely generation and reporting of test results (for In-Process, Drug Substance, Drug Product, and Stability samples) in support of manufacturing operations. This will include performing utilities sampling of Water for Injection, Purified Water, Clean Steam and Process gases. This role will also perform envir

job summary: This person will be responsible for operational support of the MS&T and QC labs, including scheduling and overseeing maintenance of laboratory and process equipment. You will also be responsible for scheduling and tracking maintenance/repair activities within the CMMS. This is a 6-month contract requiring 100% on-site work from 8:30 AM to 4:00 PM. location: Philadelphia, Pennsylvania job type: Contract salary: $40 - 50 per hour wo

job summary: Real-World Evidence & Biostatistics ~ Exclusive Summer Internship Opportunity We're looking for a highly motivated PhD student to join our Real-World Evidence (RWE) and Biostatistics research team for a Summer Internship. This role will focus on the application of Double Machine Learning in Causal Inference, providing exposure to real-world healthcare data and advanced statistical modeling techniques. The intern will work with cross-function

job summary: The Global Regulatory Operations Publishing Intern prepares and delivers high quality, timely, and compliant regulatory submissions to global health authorities. The Publishing Intern represents Global Regulatory Publishing in cross-functional project teams, provides regulatory submission support for products and contributes to regulatory initiatives location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9

job summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinical

job summary: The Cell Culture Manufacturing Senior Technician position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. location: Pennington, New Jersey job type: Contract salary: $45.13 - 53.10 per hour work hours: 9 to 5 education: High School responsibilities: Hands-On cGMP Operations: Focused on execution of c

job summary: Job Description As we expand our business, we seek a motivated and skilled API Programming Intern to join our team and help develop advanced APIs that power our products and services location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors responsibilities: Job Responsibilities Support EDC User Management and Site Administration activities.Understand how to build RESTful AP

job summary: Biostatistics Intern ~ Summer 2024 Are you a PhD student in Statistics, Biostatistics, Data Science, or Mathematics looking to gain hands-on experience in the pharmaceutical industry? Our 10-week Data Science Internship Program offers an exciting opportunity to apply your statistical expertise to real-world drug development challenges. As a Biostatistics Intern, you will: Gain a deeper understanding of the drug development process and stati

job summary: SUMMARY Assist in leading a team that supports Financial Advisors enterprise wide within the mainframe environment. Responsibilities: Work closely with the Manager and on-shore mainframe developers to ensure design, build and delivery is reliable.Will be responsible for running SQL, looking at data, giving estimates, reviewing requirements and conducting impact analysis.Provide direction and oversight to ensure deadline

job summary: A Project Controls Professional Senior is needed for an engineering consulting company in the Philadelphia, PA area. This role involves managing project cost controls, scheduling, and financial reporting for EPCMV Bio/Pharma projects, utilizing Primavera P6, earned value management, and risk analysis while collaborating with engineering, construction teams, subcontractors, and clients. location: Philadelphia, Pennsylvania job type: Contra

job summary: Job Description Intern, Global Patient and Site Engagement, will be a member of the GPSE team under GCDO. The Intern will work cross functionally across the portfolio supporting the vision to bring the patient and site voice into the clinical design and clinical trial working group teams, as well as study feasibility and global monitoring with activities related to site relationship management, strategic planning for new and ongoing studies,