Teil II Primäres Ziel der Stelle / Part II Primary Job Objective |
The Quality System Lead is a key role within the German QA. This person will play a pivotal role in ensuring the highest standards of professional excellence regulatory adherence and quality within the business with overall responsibility and accountability of the site Quality Management System. |
Teil III Mindestanforderungen an die Stelle / Part III Minimum Requirements |
Bildungshintergrund und Erfahrung / Education Background and Experience |
- At least 10 years experience working in a GMP environment as part of a quality assurance quality control technical services or manufacturing operations function or other combination of experience and educational background that may otherwise satisfy the requirements of the role
- At least 3 years managerial experience as people manager and/ or project manager
- Must be familiar with general GMP requirements of EMA FDA and other relevant standards e.g. ICH and WHO guidelines
- Proven track record of accomplishments in the Quality and GMP
- Experience in development manufacturing and testing of biological products
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Besondere Kenntnisse / Special Knowledge |
- Very good leadership skills
- Good organizational skills
- Good interpersonal communication skills
- Excellent oral & written communication skills (English; German is preferable)
- Task-oriented team player with partnering and stakeholder management skills
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Teil IV Berufliche Verantwortung / Part IV Job Responsibilities |
- Provide technical and managerial leadership to the QMS and Compliance team lead and team
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- Provide technical and managerial leadership to the QA training team lead and team
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- Provide technical and managerial leadership to the QA auditing team lead and team
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- Provide technical and managerial leadership to the QA document team lead and team
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- Ensure cross functional collaboration and leadership execution for the site Quality Management System inclusive of GMP standards compliance programs and owner of QA GMP system such as Master Control Trackwise.
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- Participate in global QMS projects and ensure global implementation and delivery aligned with regulatory and client expectations.
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- Oversee and manage the document lifecycle of SOPs and all related GMP documents at the German Manufacturing sites and QC locations.
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- Oversee and manage the Quality System for the German Manufacturing sites and Quality Control locations
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- Oversee and manage the Training System for the German Manufacturing sites and Quality Control locations
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- Manage review and/ or approve deviations CAPA and changes within the area of responsibility
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- The role will require extensive liaison with stakeholders at the Manufacturing sites incl. QA counterparts as well as clients during initial contacts due diligence and visits with a focus on quality topics
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- Responsible for the planning and oversight of the annual self-inspection programs
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- Support audits and inspections response to findings from client audit and regulatory inspection and follow up CAPAs
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- Point of contact for authority communication
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- Develop quality risk management strategy and have oversight of annual risk planning and execution of risk assessments
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- Support and guide the planning preparation and follow-up for authority inspections client audits and corporate audits performed at the German Manufacturing sites and Quality Control locations
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- Lead the periodic management review and annual product process review/CPV.
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- Ensure the engagement of the teams with learning and development initiatives and the performance management system
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- Act as a role model for your team member and within German Quality in adherence to the WuXi corporate core values and local requirements.
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20. Perform other quality-related duties and responsibilities as assigned by the supervisor. |