Clinical trials specialist

Clinical Supplies Qualified Person

Key Responsibilities:

* Ensure compliance with EU GMP and regulatory standards.
* Oversee batch certification for products manufactured globally.
* Participate in Health Authority inspections to maintain site licenses.
* Manage ongoing compliance activities related to clinical trials.
* Coordinate with cross-functional teams to ensure quality and regulatory standards are met.

* Eligibility to be named as a Qualified Person (QP).
* Practical experience with product disposition.
* Recognized pharmacy degree or equivalent.
* Extensive experience in a cGMP environment.
* Strong organizational and communication skills.
* Deliver high-quality services that meet clients' expectations.
* Collaborative team environment.
* Opportunities for professional growth and development.