Post Market Quality Lab Supervisor - Ludwigshafen am Rhein, Deutschland - AbbVie

AbbVie

Geprüftes Unternehmen

Ludwigshafen am Rhein, Deutschland

vor 3 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Company Description

Job Description A career where all your skills can come into play? We Offer That.**
A task that meets your passionate approach? We Offer That.

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

In our Post Market Quality Organization at the Ludwigshafen site, you will join a team of talented people and experienced experts in the manufacturing and global distribution of our approved and pipeline products - working with some of the most advanced technologies in the world.

Join our team as
Post Market Quality Lab Supervisor (all genders).

As Post Market Quality Assurance Laboratory Supervisor you are responsible for leading the complaint laboratory analyst team.

Make an impact - being:

- responsible for maintaining Data Integrity standards and assure GMP documentation standards.

Qualifications This is how you can make a difference**:
Bachelor's Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/scientific area least 5 years experience in quality assurance, quality oversight or relevant least 3 years Supervisory experience, quality assurance experience preferred (solid understanding of GxP requirements)

Technical knowledge in as many of the following areas as possible:
Quality, Regulatory, Process Sciences, Manufacturing Operations.
Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological or device related products.
Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, combination and pharmaceutical products.

Ability to utilize scientific education and leadership experience to support laboratory testing within a GMP environment to oversee personnel and product complaint return sample testing activities.

Experience with working in both team setting, cross functionally and independently.

Project management experience and strong leadership ability, ability to communicate quality requirements effectively and timely and manage small to medium sized quality related projects.

Strong oral and written communication skills needed.

What we offer:

a diverse area of work where you can make a real differencean open company cultureattractive remunerationintensive onboarding by a mentorflexible work models for a healthy work-life balancecorporate health management with comprehensive health and exercise programscorporate social benefitsdiverse career options in an international organizationhigh-level, attractive career development opportunitiesa 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

**Additional Information