Seeking Vector Drug Product Bioprocessing Associate II for cGMP manufacture of viral vectors. Perform aseptic filling of advanced therapeutics, ensure compliance, troubleshoot deviations, and support validation activities. Requires teamwork, multitas...
Seeking a meticulous CSV Specialist in King of Prussia, Philly for 6-12 months. Validate computerized systems in pharmaceutical manufacturing, ensuring compliance. Lead validation efforts, maintain audit readiness, and collaborate for regulatory comp...
Exciting opportunity in King of Prussia! Join a global pharmaceutical leader revolutionizing medicine production. Seeking an MES Engineer to optimize manufacturing systems. Must have BS/BA in relevant field and 3+ years of Emerson Syncade experience....
Seeking a Clinical Research Associate to oversee clinical trials phases, ensuring compliance with regulations, protocols, and GCPs. Conduct site visits, monitor data quality, and address issues promptly. Ideal candidate has a Bachelor's Degree, 4-5 y...
Seeking QA Validation Specialist for Breakthrough Medicines. Oversee validation activities in a Cell and Gene Therapy facility. Review protocols, SOPs, reports, and maintenance docs for GMP compliance. Collaborate with cross-functional teams for cont...
Seeking an experienced Process Engineer to oversee gene therapy manufacturing systems. Develop and implement efficient, cost-effective processes ensuring high-quality production. Collaborate with various teams, lead improvement projects, and offer t...
Seeking Controller for $200 million manufacturing company in Chester/Montgomery County. Must have solid cost accounting background in manufacturing/pharma, extensive financial reporting experience, and strong presentation skills. Opportunity to work ...
Join an award-winning tech client in King of Prussia as an Automation Engineer. Requires a Bachelor's in Electrical/Computer Engineering, 2-5 years of test software design experience, Microsoft SQL proficiency, and strong troubleshooting skills. Cont...
Seeking a GxP Test Lead Model N for a Pharma validation role. Requires 12+ years' GxP testing exp in pharma, 3+ years in Model N. Skills in test planning, strategy, stakeholder management, and various test types. Familiar with HP ALM or Code Beamer.
Join Center for Breakthrough Medicines as a Senior QA Manufacturing Operations Specialist. Lead quality operations, oversee manufacturing activities, and ensure regulatory compliance. Manage QA systems, guide technical staff, and drive growth while m...
