Job Description: Shift: Day Shift: 7:00 Am to 7:00 Pm Summary: The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute proc...
Description: Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols. Participates in protocol review discussions concerning scientific and procedural aspects of study design. Prep...
Description: Official Job Title: Research Associate - Process Development Location: Onsite (5 days a week) Philadelphia, PA Key Responsibilities: Works independently under the guidance of Scientists to execute laboratory experiment ...
Supervisory Organization : Supply Chain Title: Operational Buyer Direct Level II Schedule: 5 days/week onsite Duration: 6 Months with opportunites for extension Job Description: Summary: Proactively manage the performance of raw...
Job Description: Shift Day Shift: 7:00 Am to 7:00 Pm Summary: The Manufacturing Services Associate I is responsible for supporting all cGMPmanufacturing production suites. They support the production groups by ensuring the suites are...
This is a Day shift role. *Ideal candidates will have Pharma experience, SAP experience, knowledge of warehouse...
Title - QA Specialist QA compliance Job Description: The QA Specialist QA Compliance is responsible for supporting and maintaining the site's Quality Management System (QMS) by ensuring alignment between local quality procedures and Cli...
Job Description: Summary: Responsible for overseeing and executing MES validation activities related to the gLIMS implementation. This role ensures that all validation deliverables are completed on time and in full compliance with globa...