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Gigg från: Randstad AB

Quality Supplier Manager, Södertälje

  • Övrigt

Södertälje

Job description Randstad is now looking for a consultant placed at Astra Zeneca as a Quality supplier manager. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. Responsibilities At Astra Zeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person. The Global Supplier Quality (GSQ) organisation leads Supplier Quality oversight for externally sourced materials to ensure that they align with the Astra Zeneca Quality Standard, are safe and effective and meet the required regulatory standards. We do this through execution of the key Pharmaceutical Quality System (PQS) and supplier management business processes, by experienced and qualified Quality Professionals. This is a diverse and exciting role working with Suppliers, Contractors and a broad range of Astra Zeneca sites and functions. You will collaborate with colleagues and customers across many countries and interact cross-functionally with supply chain, supplier relationship, technical and project roles. Qualifications Key accountabilities In this role, you will be responsible for assuring the quality of materials received by Astra Zeneca from the designated supplier portfolio and will proactively ensure GMP and regulatory compliance during supplier related projects. The role includes the responsibility for the Quality System oversight of Supplier related product quality complaints, change controls, deviation investigations, issue management, and Quality Agreements between Astra Zeneca and External Suppliers; and the preparation and submission of Supplier Quality Risk Assessments, and support to Regulatory Agency inspections of supplier sites and site transfers. You will drive quality improvements at the supplier as part of a cross functional team. Your role will also include the quality review and approval of Chemistry and Manufacturing Control (CMC) documents associated with changes or product establishment at suppliers. Key to this role will be maintaining an understanding of relevant production processes and quality systems. Essential skills: - University Degree in a science / technical field such as Pharmacy, Biology, Chemistry, Engineering or equivalent experience - Broad experience with a minimum of 5 years relevant work experience in either the pharmaceutical operations environment or a pharmaceutical Quality Assurance and/or Qualified Person role - Excellent oral and written communication skills - Strong proven knowledge of c GMPs, Quality Systems and the pharmaceutical supply chain environment. Also, strong understanding of industry standards such as Pharmacopoeia, ISO standards, etc. - Shown experience working cross-functionally and leading significant improvement initiatives (e.g. project management skills) - Strong problem-solving skills - Strong negotiating/influencing skills - Strong and proven collaboration skills - High ability to work independently under your own initiative - Ability to travel nationally and internationally as required, up to approximately 10% of their time Desirable skills: - Experience working in a PCO/PET organization or Lean/Six Sigma training - Multi-site / multi-functional experience - particularly within a manufacturing site environment - Shown strong experience in Quality Assurance or combination of Quality and Technical - Previous experience working with quality assurance of sterile manufacturing is qualifying Application Selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible. Last day for application 2021-02-25 About the company Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus.

Randstad AB

Villkor

  • Antal platser: 1
  • Timmar per vecka: 32 - 40 timmar
Sista ansökningsdag: 2021-02-25
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