Hobson Prior are seeking a Quality Specialist to join a Swiss global healthcare organisation who are focused on offering medical solutions in order to transform patients' lives. You will join them on a contract basis in Basel, Switzerland.

Job Responsibilities:

• Supports establishment of GxP Global Procedural Documents throughout all of the organisation's development related organizational enterprises (gRED, pRED, PD, GPS and Affiliates).
• Builds and maintains strong relationships with key business stakeholders and ensures that PDQ is providing an efficient, effective and compliant process landscape to the functions.
• In partnership with supported functional areas and key business stakeholders, identifies needs for process standardization, regulatory compliance direction and areas for improvement.
• Ensures that business partner expectations for Procedural Document strategy, materials and deployment are met.
• Supports internal process improvement projects.
• Ensures, 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.
• Co-operates with a network of subject matter experts across the functional areas, supporting the Global Procedural Documents development.
• Contributes 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.
• Is knowledgeable of all services and activities provided by PDQS, Standards, Systems and Processes Governance in order to provide business stakeholders with a comprehensive overview and effectively communicates this to stakeholders.

Key Skills:

• Capability to analyse and simplify complex systems or processes into pragmatic solutions.
• Ability to assimilate new and emerging compliance information or trends.
• Excellent verbal and written communication skills (including presentations) and ability to influence and lead without authority.
• Ability to work effectively in an international multicultural matrix organization.

Requirements:

• Bachelor's degree or equivalent in scientific or quality-related field or equivalent combination of education, training, and experience.
• A minimum of 3-5 years 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.
• Demonstrated knowledge of GCP and/or GVP regulatory requirements, as well as analytical, organizational and planning skills.
• Organizational awareness (e.g., interrelationship of departments, business priorities), including experience successfully working cross-functionally and in global teams.
• Broad understanding of global expectations of Regulatory Authorities in the area of pharmaceutical development.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.