Associate Director Quality Management Oss • Joinuz

Vacature in het kort

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Wij bieden
What do we offer you? A dynamic, innovative and international working environment. You are part of the development process of new drugs that can make a difference in the lives of cancer patients and their loved ones. The opportunity to further develop yourself, for example, into a position offering even more responsibility. International growth (within AstraZeneca) is also one of the possibilities. Good primary & secondary benefits including 8% holiday allowance, 25 holidays on a full-time basis plus office closure between X-mas and New Year + Good Friday. Collective pension with a fixed percentage personal contribution, bonus scheme. Personal budget which can be used for vitality, home office equipment, sustainability or personal development. Access to internal training and learning and development offerings. You can partly work from home (2 days per week on a full time base).

Wij vragen
what do you bring: degree in life sciences or equivalent discipline. demonstrable experience in clinical compliance or quality-related position. in-depth knowledge of drug development process and gxp activities. understanding of skills required for successful clinical study delivery. experience with oncology and/or haematology studies is an advantage. excellent knowledge of international regulations and guidelines. strong analytical, problem-solving, negotiation, and conflict resolution skills. outstanding interpersonal and communication skills with influence capabilities. ability to multitask and work efficiently and independently under pressure. fluency in english.

Wat ga je doen
join us in oss as an associate director of quality management and be our key player in maintaining and elevating our global standards in clinical studies. in this role, you will provide invaluable compliance and process advice to our clinical operations teams, driving quality improvements on a worldwide scale. what will you be doing? as our associate director quality management, you will collaborate with a passionate group of professionals to uphold our commitment to excellence. you will be responsible for maintaining, enhancing, as well as communicating high-quality standards throughout the clinical study delivery process. key responsibilities include: collaborate effectively with colleagues and stakeholders to champion quality across r&d. drive strategic focus on quality for the haematology portfolio. ensure adherence to gcp and clinical operations quality objectives. provide first-line quality advice to study management operations and program management. drive a culture of quality in clinical operations, striving for an 'always inspection ready' mindset. support study/program level activities during regulatory inspection support team (rist) events. provide insights from quality metrics analysis for continuous performance improvement. facilitate quality review meetings with clinical operations leadership team. collaborate with other quality functions in the clinical operations quality network for sustainable issue resolutions. continually seek opportunities for improvement and feedback, fostering a culture of knowledge sharing and learning.

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Over Joinuz

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