Overview: We are seeking a highly experienced and detail-oriented CQV (Commissioning, Qualification, and Validation) Manager to lead the execution of commissioning qualification, and validation activities at our pharmaceutical manufacturi...
Overview: Company Overview Job Summary The Quality Assurance Manger will lead the implementation and maintenance of the Quality Management Systems (QMS) at our new manufacturing facility. This leadership role involves designing and im...
Responsibilities CQV Program Oversight Lead the development and execution of CQV plans for facilities, utilities, equipment (FUE), and process systems. Coordinate with engineering, quality, manufacturing teams and IT to ensure alignment...
Overview: Company Overview Job Summary The Quality Specialist will work closely with operations and manufacturing personnel to ensure compliance with SOPs. The ideal candidate is a detail-oriented professional with a strong backgrou...
Responsibilities Maintenance Operations & Equipment/Controls Reliability Support the installation, testing, and commissioning of equipment systems to ensure proper functionality and performance Support the maintenance, repair, and servi...
Overview: STA Pharmaceuticals is constructing a new Greenfield CDMO facility to manufacture finished drug products in Middletown, Delaware. To manage deliver the manufacturing system engineering, construction, CQV activities, start-up an...
Responsibilities Responsibilities Overall responsible for drug products manufacturing system engineering management in Middletown project over the whole project lifecycle, includes business strategic planning and site master planning, R...
Overview: We are seeking a skilled and experienced Equipment Maintenance & Reliability Engineer to support the maintenance, repair, and reliability of base building and manufacturing equipment in our pharmaceutical manufacturing facility....
Responsibilities Key Responsibilities Provide on-the-floor operational and manufacturing support. Participate in the implementation of the QMS at the new manufacturing site, including developing and documenting processes for solid oral...
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