Senior Manager CQA (all genders) – fulltime, permanent

In our Quality Assurance team in Ludwigshafen you will join a group of experienced professionals dedicated to ensuring quality compliance and operational excellence across a complex commercial pharmaceutical environment. Working at the interface of local quality oversight MAH responsibilities for centrally filed products in Europe and cross-functional collaboration you will help shape robust quality systems and drive continuous improvement. If you are passionate about leading teams navigating regulatory complexity and partnering with stakeholders across the business to enable compliant and efficient operations we invite you to join us as Senior Manager CQA (all genders)!

Your Responsibilities:

• Providing leadership and oversight of quality compliance matters at an operational and regulatory complex commercial entity
• Oversight of quality at the affiliate level as well as MAH responsibilities for centrally filed products in Europe
• Integration and support of German regulations at the affiliate level for drugs biologics device and/or combination products
• Driving the design of effective quality systems procedures and/or processes within cross functional teams to ensure compliance as well as efficiency
• Managing the Wholesale Distribution Authorization (WDA) and hosting internal external and MoH inspections & audits in support of this licence
• Responsible for the management and oversight of a team including hiring setting performance expectations providing performance feedback development of staff and handling of personnel issues

Qualifications :

• . or . preferably in a technical field
• 5 years of experience in Quality Assurance Operations or a regulatory environment
• Proven experience leading and managing teams including setting priorities coaching team members and driving results through collaboration and accountability
• Business-fluent proficiency in both German and English is required
• Experience working in a GxP-regulated pharmaceutical environment is imperative
• Strong understanding of how Quality Assurance supports broader business objectives with the ability to foster a culture of continuous improvement and leadership development
• Knowledge of regulatory requirements for complex finished products including storage distribution product complaints supplier management risk management and inspections
• Excellent stakeholder management skills including collaboration with Regulatory Commercial and Site Manufacturing teams

Heres how we can grow together:
 

with a diverse work environment where you can have a real impact

with an open corporate culture

with an attractive salary

with an intensive onboarding process with a mentor at your side

with flexible work models for a healthy work-life balance

with a corporate health management that offers comprehensive health and exercise programs

with company social benefits

with a wide range of career opportunities in an international organization

with top-tier attractive development opportunities

with a strong international network
 

Multiple times we have been globally recognized as a Great Place to Work and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality equity diversity and inclusion (EED&I) a commitment that is fundamental to us. This includes appreciating different perspectives creating an inclusive culture and treating all employees with dignity and respect.
 

Any questions Feel free to email us at we look forward to hearing from you!

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

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Work :

No

Employment Type :

Full-time