Senior Scientist I - Ludwigshafen am Rhein, Deutschland - ABBVIE

ABBVIE

Geprüftes Unternehmen

Ludwigshafen am Rhein, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

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 work closely with us to address the health challenges of tomorrow.

Do you have a passion for improving health care around the world and for using your expertise to improve patients' quality of life? In a challenging work environment that allows you to broaden and develop your own skills? You've found the right place

As part of our
Research and Development team, you will be contributing to finding solutions and helping pave the way for innovative therapies that address complex diseases using innovative research approaches and state-of-the-art technology.

Further develop your expertise and join our team as

Senior Scientist I (all genders) Quality Risk Management - Overarching Projects

With a lot of experience and even more passion, you will be joining our team as QRM expert and QRM project lead in Biologics DPD.

This means:

Developing globally aligned, standardized, qualitybydesignbased development approaches for Biologic Drug Products from early development to late stage and transfer to Operations.

Developing state of the art and globally aligned Quality Risk Management approaches.

Leading and participation in international initiatives to improve Drug Product Development processes and alignment between different development sites
Actively accompanies Quality Risk Management and Quality by Design based project specific documentation. Assures state of the art and aligned approaches for individual projects.
Leading of Change Management Processes
Ensures compliance with regulatory and environmental requirements.
Interface with e.g. Biologics Technical Leads, Analytical Technical Leads, Product Development Directors, NBE functional heads, ABC, NBE-LC, ABR, CMC-RegA, outside industry partners

This is how you can make a difference:

Bachelor's degree or equivalent and typically 10 years of professional experience, Master's degree or equivalent and typically 8 years of professional experience, Doctorate with initial professional experience
Relevant knowledge/experience in the area of formulation, manufacturing process, primary packaging and device development for New Biological Entities and Quality Risk Management
Demonstrated expert knowledge and experience in more than one discipline in development or operations or related field
Demonstrated communication skills in English
Experience in a crossfunctional, global environment
Understanding of both scientific and regulatory requirements in the area of responsibility

What we offer you:

- a diverse area of work where you can make a real difference
- an open company culture
- diverse career options in an international organization
- high-level, attractive career development opportunities
- a strong international network

At AbbVie, your individual contributions count - help us achieve more together. Be a part of it and grow with us - go above and beyond