Für ein international erfolgreiches Pharmaunternehmen im Großraum Mainz suchen wir zum nächstmöglichen Eintritt, zunächst im Rahmen der ANÜ
Senior Specialist QA GMP | M/W/D – Referenz 601
Ihre Aufgaben:
In your new role as Senior Specialist Quality Assurance GMP you process, assess, and decide on quality incidents during manufacturing, release, packaging / labelling, and distribution of investigational medicinal products (IMPs).
You manage and drive different kinds of quality incidents together with globally organized functional departments and with external partners.
Additionally, you further develop and improve the internal quality processes and the supporting IT systems.
You are responsible to present quality incidents in management meetings, audits, and inspections.
In addition, you contribute to international and interdisciplinary quality working groups and ensure that deliverables are achieved.
Ihr Profil:
Bachelor degree or professional training with additional qualification (e. g. „Industriemeister“)
Several years of practical and proven experience in drug manufacturing or analytics, quality assurance and/or development in the pharmaceutical industry
Advanced knowledge of development processes for investigational medicinal products as well as in-depth knowledge of cGMP regulations for IMPs
Expert knowledge of health authorities’ requirements (cGMP regulations e.g., EU-GMP Guide, CFR etc.)
Conceptual thinking, high customer focus and result orientation
Strong oral and written communication skills in English and German
Interessiert?
Dann senden Sie uns Ihre aussagekräftige Bewerbung mit Angabe Ihres möglichen Eintrittstermins und Ihren Gehaltsvorstellungen über das unten folgende Bewerbungsformular oder per Email an bewerbung@consult16.de oder rufen Sie uns an! Diskretion ist selbstverständlich.
Bitte geben Sie bei Email-Bewerbungen immer die Referenznummer an !