Regulatory Affairs Project Manager (m/w/d) in Teilzeit

Auf einen Blick: Penzberg | Teilzeit | Pharmaindustrie

Sie suchen spannende Aufgaben, Raum für Ihre Ideen und ein mitarbeiterfreundliches Arbeitsumfeld?

Dann sind Sie bei uns genau richtig!

Im Rahmen der Arbeitnehmerüberlassung suchen wir für unseren Kunden Roche Diagnostics GmbH in Penzberg ab dem nächstmöglichen Zeitpunkt für 6 Monate mit Option auf Verlängerung einen Regulatory Affairs Project Manager (m/w/d) in Teilzeit (20h/Woche).

Das bieten wir Ihnen:

• Unbefristetes Arbeitsverhältnis bei HEADWAY
• Abwechslungsreiche Tätigkeiten in einem dynamischen Umfeld
• Übertarifliche Bezahlung nach Qualifikation und Erfahrung
• Urlaubs- und Weihnachtsgeld
• Zuschüsse zur Altersvorsorge
• Persönliche Betreuung durch HEADWAY

Ihre Aufgaben:

• Projekthintergrund: Peak Periode bezüglich der Zulassung von IVDs in China

• Regulatory document and submission compilation: Good understanding of complexities and challenges in a global regulatory environment. Advanced understanding of internal processes and procedures. Oversees the development of submission/product registration dossiers of more complex products. Uses their broader expertise and experience for more difficult assignments.

• Regulatory knowledge & strategy: Deep understanding of healthcare regulatory frameworks and how to maintain compliance while accelerating innovation for customers and patients. Using appropriate knowledge to manage complex issues. Ability to interpret and apply understanding of the regulators' thinking to projects and apply strategies to the different needs of different regions without significant guidance.

• Manage Stakeholders: Effectively communicate and partner with stakeholders to understand and provide best solutions. Take initiative to address problems or opportunities and involves stakeholders for best solutions. Develops relationships that significantly influence the current and future direction for Roche and our products. Understands the structure, key roles and responsibilities of external customers/stakeholders.

• VACC Leadership and Influencing: Starting to live the spirit of we all lead - identifies opportunities to develop VACC competency. Acts with integrity, courage, passion and honors commitments. Contributes an inclusive environment which supports all dimensions of diversity. Explores the opportunity of leadership and future contribution. Fosters an exchange of ideas and support amongst colleagues.

• Decision Making and Innovation: Ability to work day to day with minimal guidance to no supervision to correctly complete daily scheduled and unscheduled activities. Develop solutions and present both issues and solutions. Drive innovation within their own area of influence. Learn how to apply good decision making principles. Consistently generates new ideas. Leverages the unique talents and viewpoints of others. Seeks new opportunities and tries new approaches.

• Problem Solving: Able to troubleshoot issues as they arise, independently develop and implement cost effective and non-complex actions solutions to ensure that daily work is completed without jeopardizing compliance. Ability to find solution options for highly complex problems and to make decisions to implement.

• Agile Mindset and communication: Change ambassador for their environment. Actively develops their agile mindsets and behaviors and encourages others to do so as well. Identifies and acts on opportunities for improvement within across Q&R. Embraces new technologies and other means to simplify and increase productivity. Owns their regulatory data and promotes data stewardship within their RA teams and uses and promotes the usage of all regulatory tools.

• Teamwork and Collaboration: Is able to pull people together around a common goal. Seeks to understand and build on different perspectives to enhance outcomes. Addresses and resolves conflict by creating an atmosphere of openness and trust. Brings out the best in people and teams.

Das bringen Sie mit:

• Bachelor's / Master degree in Life Science, Data Science or related subject or equivalent experience; completed training as a technician or laboratory technician; or equivalent qualification for the tasks
• At least 5 years experience, 5-7 Years preferred, in Regulatory, R&D, Quality, Operations and/or Clinical Some experience in Healthcare regulatory affairs. Advanced degree is considered an advantage
• Can manage more complexity work and/or global projects, or equivalent experience
• English fluent in spoken and written
• Working mostly independently, confident to approach interfaces (e.g. R&D, QC, and the Chinese Regulatory Affairs colleagues)
• Nice to Have: Experience from Regulatory Affairs in China would be very desirable

Bewerben Sie sich in wenigen Minuten - wir freuen uns auf Ihren Lebenslauf!

Wir melden uns innerhalb eines Werktages bei Ihnen zurück.

Über HEADWAY

HEADWAY ist ein erfahrener Personaldienstleister und begleitet Sie persönlich auf Ihrem Weg zu einer neuen beruflichen Perspektive. Unser Ziel ist es, gemeinsam den passenden Job für Sie zu finden. Wir legen Wert auf Vielfalt und Chancengleichheit. Bewerbungen begrüßen wir unabhängig von Alter, Geschlecht, Behinderung, ethnischer Herkunft, sexueller Orientierung oder sozialem bzw. religiösem Hintergrund.