Join Cytiva as a Senior QA Specialist to enhance quality management systems and ensure compliance in life sciences projects. Collaborate with cross-functional teams to support vital projects and drive improvements that impact human health.
Key Responsibilities
Represent QA in cross-functional projects
Support the organization within QMS processes; Change Control, CAPA, NC, and batch release
Review and approve Change Control, CAPA, NC
Perform batch release
Approve qualification activities to meet project timelines
Conduct risk assessments and review qualification documentation
Drive improvement activities within QMS
Required Qualifications
Relevant Bachelor's degree in chemistry, pharmacy, or equivalent
Experience in a similar QA role within Life Science companies (e.g., ISO 9001, ISO 13485, GMP)
Experience in QA for projects
Experience in qualification activities for automation, equipment, and analytical methods
Prior experience in risk assessments/FMEA, batch release, and deviations/NC