Ofertes d'ocupació a SIEGFRIED

• Nivell d'experiència---
• Tipus de contracteA temps complert
• PublicadaNova

. QA

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.

Your Role:

The Site Quality Head is responsible of managing the QA and QC departments, ensuring the compliance with the overall strategy of Quality. He/She is responsible of managing the department in terms of operations, projects, resources and policies.

Main responsibilities of the Site Quality Head are:

• Ensure compliance with GMP requirements, ISO 13485 standards, ICH guidelines, the Siegfried Quality Manual, and all applicable SOPs across site operations.
• Lead and manage the Quality Assurance (QA) and Quality Control (QC) functions.
• Ensure that all site products, projects, processes, strategies, and decisions comply with applicable GMP, ISO 13485, and Siegfried Quality requirements.
• Serve as the primary point of contact for Global Quality matters and ensure the effective implementation and ongoing adherence to Siegfried Quality policies and standards.
• Define, execute, and monitor the annual departmental budget. Ensure the effective allocation and utilization of human and financial resources to achieve departmental objectives efficiently.
• Foster a quality-first culture and continuous improvement mindset across the site.
• Provide overall leadership and accountability for product quality, patient safety, regulatory compliance, and quality performance.
• Lead the site's Quality Strategy and Quality Plan, ensuring continuous improvement and alignment with corporate objectives
• Act as the Medical Devices Management Representative, assuming the responsibilities and authority defined in ISO 13485.
• Ensure compliance with all applicable Safety, Health, and Environment (SHE) requirements and standards.
• Ensure sustained MRP II Class A performance through robust planning, governance, and cross-functional collaboration.
  
  

• Pharmacy degree
• MBA will be valued
• Knowledge in FDA, MHRA, EMA, WHO, GxP and ICH regulations
  
  

• Annual Bonus
• Company car
• Free parking
• Subsidized canteen on-site or restaurant ticket: to use when eating out or working from home
• Medical, life, and accident insurance
• Access to "Club Siegfried": an exclusive platform with discounts and offers on over 400 services.