Quality Specialist (m/f/d)

REFERENCE NUMBER:

459804/1

MY DUTIES:

- Support establishment of GxP Global Procedural Documents throughout all of the development related organizational enterprises to ensure a consistent GxP process landscape for standards and processes and procedures related to clinical development and safety/pharmacovigilance which meet internal and external standards of regulatory compliance, as well as industry best practices and interpretations
- Build and maintain strong relationships with key business stakeholders and ensure that PDQ is providing an efficient, effective and compliant process landscape to the functions
-In close collaboration with supported functional areas and key business stakeholders, identify needs for process standardization, regulatory compliance direction and areas for improvement
- Ensure, in collaboration with business partners, that Global Procedural Documents in the GxP process landscape are up-to-date and regulatory compliant versus current Clinical and safety/pharmacovigilance international regulations
- Collaborate with a network of subject matter experts (SMEs) across the functional areas, supporting the Global Procedural Documents development
- Contribute to the PDQS Standards, Systems & Processes Governance Team to set strategies and achieve the long-term goals and objectives of PDQS and PDQ as a whole

MY QUALIFICATIONS:

- Bachelor’s degree or equivalent in scientific or quality-related field or equivalent combination of education, training, and experience
- Experience in the pharmaceutical industry, preferably in pharmaceutical development and working in a GxP regulated area
- Experience in preparation, development and administration of GxP standards and processes
- Organizational awareness (e.g., interrelationship of departments, business priorities), including experience successfully working cross-functionally and in global teams
- Demonstrated knowledge of GCP and/or GVP regulatory requirements, as well as analytical, organizational and planning skills

MY BENEFITS:

- You will work in an international environment
- Extension possible

ABOUT HAYS:

With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

MY CONTACT AT HAYS:

My contact person
Zlatan Mujagic

Reference number
459804/1

Contact
E-Mail: [email protected]
Phone: +41-(0)61-2250587