Job Overview
Job description
- Location:
- Ludwigshafen, Germany
- Work arrangement:
- On-site
Role Summary
Welcome to Abbvie! As part of an international company with over 58,000 employees worldwide and around 3,500 employees in Germany, you have the opportunity to work closely with us to overcome the health challenges of tomorrow. Are you passionate about improving healthcare around the world? Would you like to use your expertise to improve the quality of life of patients? In a challenging work environment that offers you the opportunity to expand and develop your own skills? Then you've come to the right place!
Demonstrate your know-how and become part of our team at the Ludwigshafen location as Scientist I / II - Qualification and Maintenance Manager, ARD LU (all genders)
In this position, you will be responsible, among other things, for coordinating maintenance and qualification activities in the GMP laboratory. You manage projects to implement new processes, laboratory equipment or software and work in interdisciplinary, global teams and use your enthusiasm to contribute to optimizing processes and workflows and making them future-oriented.
Specifically, this means
Planning and management of instrument & equipment lifecycle projects (e.g. acquisition, consulting, installation, qualification, maintenance & calibration, moves, decommissioning) for the Analytical R&D laboratory areas in Ludwigshafen
Collaborate with external service providers and global functions within AbbVie
Creation, review and management of GMP-relevant documents such as qualification documents (qualification plans and reports), result summaries, data integrity-related documents and SOPs (Standard Operating Procedures)
- Carrying out out of tolerance investigations during instrument calibrations in collaboration with QA and laboratory areas
- Further development and optimization of processes and systems
- Creation of technical documentation, test plans and SOPs
- Project management
- Compliance and implementation of regulatory requirements
Requirements
This is how you make the difference
Bachelor's or equivalent degree and typically 5 years of professional experience or Master's or equivalent degree and typically 2 years of professional experience. Vocational training can be replaced by appropriate professional experience and acquired equivalent knowledge
- Several years of experience in the pharmaceutical or biotechnology industry desired
- Practical experience with qualification and validation processes
- Ability to create, review and manage GMP-relevant documents such as SOPs (Standard Operating Procedures)
- Sound GMP/GSP knowledge
- Knowledge of quality assurance and quality control
- Independent, structured and conscientious way of working
- Ability to adapt to changing requirements and priorities and operate successfully in a dynamic environment
Very good knowledge of German and English, both spoken and written.
- Good computer skills
- High resilience, reliability and flexibility
- Very good teamwork and communication skills, even in global teams
- Knowledge and experience in project management
- How we achieve great things together
- with a diverse work environment where you can make a difference
- with an open corporate culture
- with an attractive remuneration
- with intensive onboarding including a mentor
- with flexible working models for a healthy work-life balance
- with company health management with comprehensive health and exercise programs
- with company social benefits
- with diverse career opportunities in an international organization
- with top-class, attractive development opportunities
- with a strong, international network
- We have been voted a “Great Place to Work” several times around the world and are proud to offer our employees the flexibility that ensures a healthy work-life balance. We take our impact on the environment and society seriously and therefore focus on giving back on a regular basis.
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About the Company
About AbbVie
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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
- Role:
- Scientist I / II - Qualification and Maintenance Manager, ARD LU (all genders) (Vollzeit, befristet für 3 Jahre)
- Industry Type:
- Pharmaceuticals
- Job Type:
- Full-Time
Company profile
AbbVie
abbvie.comAbbVie Inc. is an American pharmaceutical company headquartered in North Chicago, Illinois. It produces drugs to treat a wide range of medical issues. The company ranks sixth on the list of largest biomedical companies by revenue, 77th on the Fortune 500 and 108th on the Forbes Global 2000. Its name combines Abbott, the name of its former parent company, with vie, intended as a reference to a Latin root meaning life.
- Company Size
- 50,000 - 100,000 employees
- Headquarters
- North Chicago, Illinois, United States
- Founded
- 2012
- Funding Stage
- Public