- job summary: The Global Regulatory Affairs and Drug Safety (GRADS) Alliance Management Summer Internship opportunity is designed to expose a selected individual to the roles and responsibilities of alliance and vendor management within the pharmaceutical industry setting. The selected individual will gain exposure to alliance and vendor management processes such as business partner agreements and commitment reporting, pharmacovigilance exhibits, and vendojob summary: The Global Regulatory Affairs and Drug Safety (GRADS) Alliance Management Summer Internship opportunity is designed to expose a selected individual to the roles and responsibilities of alliance and vendor management within the pharmaceutical industry setting. The selected individual will gain exposure to alliance and vendor management processes such as business partner agreements and commitment reporting, pharmacovigilance exhibits, and vendo
- job summary: This person will support the manufacturing of gene-modified autologous T-cell products in a cGMP-regulated facility. The role includes cell processing, media formulation, product sampling, and ensuring quality compliance in an aseptic cleanroom environment. Prior experience in cell culture, aseptic techniques, and cGMP practices is required. This is 100% on-site in Philadelphia, PA. 6-month contract, some potential to extend/convert locatijob summary: This person will support the manufacturing of gene-modified autologous T-cell products in a cGMP-regulated facility. The role includes cell processing, media formulation, product sampling, and ensuring quality compliance in an aseptic cleanroom environment. Prior experience in cell culture, aseptic techniques, and cGMP practices is required. This is 100% on-site in Philadelphia, PA. 6-month contract, some potential to extend/convert locati
- job summary: 40 hour per week, remote Nonclinical Writer with demonstrated experience writing clinical pharmacology and bioanalytical reports that go into Modules 2.7.1 and 2.7.2 (will not be writing the modules, just the reports that will go into the modules). location: Wayne, Pennsylvania job type: Contract salary: $80 - 90 per hour work hours: 9 to 5 education: Doctorate responsibilities: Regulatory Writers prepare high quality djob summary: 40 hour per week, remote Nonclinical Writer with demonstrated experience writing clinical pharmacology and bioanalytical reports that go into Modules 2.7.1 and 2.7.2 (will not be writing the modules, just the reports that will go into the modules). location: Wayne, Pennsylvania job type: Contract salary: $80 - 90 per hour work hours: 9 to 5 education: Doctorate responsibilities: Regulatory Writers prepare high quality d
- job summary: We are seeking a Senior Engineer - Equipment and Utilities to support GMP manufacturing operations by ensuring the proper maintenance and functionality of building systems, utilities, and manufacturing equipment. This role involves 70% desk-based responsibilities and 30% vendor management, requiring a strong technical background and the ability to oversee third-party maintenance activities effectively. This is a 6-month contract 100% on-sitejob summary: We are seeking a Senior Engineer - Equipment and Utilities to support GMP manufacturing operations by ensuring the proper maintenance and functionality of building systems, utilities, and manufacturing equipment. This role involves 70% desk-based responsibilities and 30% vendor management, requiring a strong technical background and the ability to oversee third-party maintenance activities effectively. This is a 6-month contract 100% on-site
- job summary: The Facility Technician must have hands on experience performing preventative/corrective maintenance and calibrations in a complex GMP commercial environment. Proper calibration and maintenance of utilities, process equipment and instruments is critical to data accuracy required in GMP pharmaceutical operations. Previous experience working with a CMMS system preferred. location: Philadelphia, Pennsylvania job type: Contract salary: &#xjob summary: The Facility Technician must have hands on experience performing preventative/corrective maintenance and calibrations in a complex GMP commercial environment. Proper calibration and maintenance of utilities, process equipment and instruments is critical to data accuracy required in GMP pharmaceutical operations. Previous experience working with a CMMS system preferred. location: Philadelphia, Pennsylvania job type: Contract salary: &#x
- 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: Contrajob 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: Manager, Global Medical Affairs (IST Operations) 1 Year Contract (potential tor extend) Remote | EST Hours Join a leading biopharma team supporting the execution and oversight of Investigator Sponsored Trials (ISTs) within Global Medical Affairs. T his operations-focused role is ideal for a detail-oriented professional with 3+ years of industry experience and a strong background in Project Coordination, Resource Planning, and Cross-functionaljob summary: Manager, Global Medical Affairs (IST Operations) 1 Year Contract (potential tor extend) Remote | EST Hours Join a leading biopharma team supporting the execution and oversight of Investigator Sponsored Trials (ISTs) within Global Medical Affairs. T his operations-focused role is ideal for a detail-oriented professional with 3+ years of industry experience and a strong background in Project Coordination, Resource Planning, and Cross-functional
