We are seeking a Quality Systems Specialist to join our client, a global pharmaceutical company.
This permanent opportunity offers a hybrid work arrangement.
Main Responsibilities and Reporting Structure:
* Support the ongoing management of electronic Quality Management Systems (eQMS), including documentation management, change controls, deviation management, CAPAs, customer complaints, and laboratory investigations.
* Lead and execute the development and/or modification of the company's eQMS.
* Develop and approve written procedures and documents, such as SOPs, WISOPs, technical agreements, quality policy, and other compliance-related documents, required for eQMS.
* Develop and maintain dashboard reports, ensuring accurate, complete, and consistent data is available for meaningful trending and analysis of data across all quality systems.
* Participate in training preparation and delivery on-site.
* Collaborate with the corporate Quality Systems Specialist to contribute to the development and maintenance of quality systems.
* Work collaboratively with site departments to ensure high levels of GMP.
* Participate in the preparation and follow-up of regulatory and external inspections.
Position Requirements:
* At least 3 years' experience in the pharmaceutical industry and a 3rd-level qualification in a scientific discipline.
* Strong communication skills and interpersonal skills.
* Strong IT skills.
* Strong writing skills.
* Strong attention to detail.