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Iovance is seeking a Specialist, Quality Assurance (QA) Compliance with experience in the Pharmaceutical / Biotechnology industry. This individual will be responsible for Quality System and Compliance activities to ensure GXP compliance in accordance with local and country regulations and guidelines, as well company policies and procedures. The selected team member should be innovative, energetic, collaborative, express a strong desire to learn and take ownership and accountability for Quality. The Specialist will support and oversee Quality Compliance activities including, but not limited to: ensuring that Iovance facilities and staff are inspection/audit ready at all times, ensuring and supporting Internal audits (L1, L2, & L3) have been scheduled and completed, and driving Quality System records such as CAPAs/ Change Controls, Deviations to closure, and related Quality Systems and Compliance task. The successful candidate will be a key member of an established team who is passionate about working with others in complex, changing, and fast-paced environments.