Manager - R&D External Partners Oversight (all genders) (full-time)

Allergan Aesthetics; Ludwigshafen am Rhein; Vor Ort; EUR 70.000 - 100.000; Vollzeit

Zusammenfassung

Als Manager - R&D External Partners Oversight bei einem führenden Unternehmen haben Sie die Möglichkeit, die Qualität externer Partner sicherzustellen und an strategischen Projekten mitzuwirken. Sie werden Teil eines dynamischen Teams, das Lösungen für unerfüllte medizinische Bedürfnisse arbeitet und eine echte Auswirkung auf die globalen Gesundheitsversorgung hat.

Leistungen

Vielfältige Arbeitsumgebung

Attraktives Gehalt

Flexible Arbeitsmodelle

Umfassende Gesundheitsprogramme

Karrieremöglichkeiten in einer internationalen Organisation

Qualifikationen

• Mindestens 8 Jahre Erfahrung in der pharmazeutischen, medizinischen Geräte- oder Kombinationsproduktindustrie.
• Fundiertes Verständnis der internationalen GxP-Regulierungsstandards.
• Vorzüge eines professionellen Akkreditierungsnachweises sind wünschenswert.

Aufgaben

• Leiten und Durchführen von Qualitätsvereinbarungen.
• Zusammenarbeiten mit externen Partnern zur Behebung von Qualitätsproblemen.
• Überwachung der GxP-Anforderungen und Unterstützung bei der rechtlichen Einhaltung.

Kenntnisse

Einsatzbereitschaft

Kommunikation

Organisationsfähigkeit

Urteilsvermögen

Zusammenarbeit

Ausbildung

Bachelor-Abschluss in einem technischen oder wissenschaftlichen Fach

Jobbeschreibung

Unternehmensbeschreibung

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and TikTok.

Stellenbeschreibung

People. Passion. Possibilities. Three words that make a world of difference.

More than a job. It's a chance to make a real difference.

Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity to address some of tomorrow's unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities to develop and enhance your skills? You've come to the right place!

Together, we break through – as Manager - R&D External Partners Oversight (all genders) (full-time)

In this role, you primarily provide direction and execution in compliance and quality of R&D External Partners. You ensure that activities are performed and documented in accordance with applicable worldwide quality and regulatory requirements to guarantee the quality, effectiveness, and safety of our clinical materials and drug development activities.

Additionally, you deliver relevant and constructive evaluations of external partners that provide materials and services to AbbVie R&D. This may include API suppliers, third-party manufacturers, contract labs, contract research organizations, and other GXP service providers supporting ongoing development projects.

Make your mark:

• Act as an expert in GXP requirements, focusing on early detection and prevention, followed by correction of issues.
• Collaborate with GXP functional areas and assist in resolving external partner quality issues.
• Lead or participate in technically complex and strategic cross-functional projects to improve compliance with regulatory requirements and standards.
• Manage the lifecycle of Quality Agreements and lead their creation.
• Conduct periodic reviews of Quality Agreements to ensure they remain current or to withdraw them as applicable.
• Create a learning environment, embrace ideas from others, and manage innovation to implementation.

Qualifikationen:

This is how you make a difference:

• Bachelor’s Degree in a technical or scientific field (Chemistry, Pharmacy, Biology, Microbiology, or Engineering) or equivalent industry experience (minimum 8 years) with sufficient exposure to pharmaceutical, medical device, or combination product industries.
• Thorough understanding of international GxP regulatory standards (e.g., GMP, GLP, GCP, GDP, GCLP) and the audit process, along with extensive knowledge of worldwide quality system requirements.
• Understanding of various quality and operational systems supporting study/product design, drug development, facility, production, and distribution, and principles of quality management.
• Excellent communication, organizational, and interpersonal skills, along with openness, decisiveness, self-reliance, and sound judgment.
• Effective, collaborative working style across GXP functions, technical areas, and outside the company.
• Professional accreditation is desirable, e.g., ASQ Certified Quality Manager (CQM), RQAP, or CQA.
• Proficiency in English, both oral and written.

What we offer you:

• A diverse work environment where you can have a real impact
• An open corporate culture
• An attractive salary
• An intensive onboarding process with a mentor
• Flexible work models for a healthy work-life balance
• Comprehensive health and exercise programs
• Company social benefits
• Wide range of career opportunities in an international organization
• Top-tier development opportunities
• A strong international network

We have been recognized multiple times as a "Great Place to Work" and are committed to equality, diversity, and inclusion. We focus on giving back to our communities and take our environmental and social responsibilities seriously. Your individual contributions are valued—help us move mountains together. Join us, grow with us, and accomplish more than you imagined. If this sounds like the perfect career opportunity, we look forward to your application! Please send us your complete CV, and we will discuss everything else in person.

Any questions? Feel free to email us at [e-mail]. We look forward to hearing from you!