WHO ARE WE?

At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Now, we are powered by 53,000 employees globally who nurture a diverse, collaborative, and inclusive culture. We believe that if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve.
ROPU MIDI is a Regional Operating Unit consisting of 8 mid-sized countries: Belgium, Denmark, Norway, Finland, Greece, Portugal, Sweden, and The Netherlands. MIDI is a multicultural and diverse work environment. More than 1.800 employees are striving to work together to improve lives for patients and animals in our region.

THE OPPORTUNITY – DO WORK THAT MATTERS

We are seeking a highly motivated Quality Assurance Manager at Boehringer Ingelheim Veterinary Medicine Belgium (BIVMB). At BIVMB we focus on the equine mesenchymal stem cells platform, addressing the unmet needs of multiple veterinary patients.
In this exciting role, you will be responsible for daily management and operation of the quality management system. You will be working with state-of-the-art technologies.
At Boehringer Ingelheim, your development is a priority. If you aspire – in the role you will get the opportunity to develop yourself into the role of Qualified Person.
This position is based in Evergem, Belgium, and reports directly to the Head of Quality.

YOUR KEY RESPONSIBILITIES

• Promote quality achievement and performance improvement throughout the organization and train the personnel.
• Detect and analyze the needs concerning quality within the business unit and initiate projects to improve the quality in an efficient and effective way.
• Write and maintain procedures, work instructions and instructions for maintenance and calibration.
• Ensure correct handling of OOS/OOT, deviations, complaints, CAPA's and changes in the relevant scope, with their associated actions Ensure compliance with national and international standards and legislation.
• Organize and perform internal audits throughout the entire production process and report its results to guarantee the quality of the product.
• Perform external audits for qualification of suppliers and subcontractors.
• Organize and check the maintenance and qualification of premises and equipment.
• Quality Review of quality documentation, process records, batch records and labels.
• Aid in continuous improvement of the Quality System.
• Ensure that quality documentation from and for suppliers comply with BIVMB requirements.

WHAT YOU SHOULD BRING TO THE TEAM

• At least 3 years of experience in Quality for aseptic pharma or biotech products.
• At least 10 years of experience in a pharmaceutical manufacturing environment.
• Master’s degree in Life Sciences, Veterinary Medicine or similar.
• If you meet the formal requirements to grow into a Qualified Person role this is considered a plus.
• In depth knowledge about Good Manufacturing Practices (GMP) regulations and quality pre-requisites in a controlled environment.
• Experience in implementing and managing quality systems.
• Excellent command of the English language. Dutch is a plus!
• Excellent communication skills.
• Flair for electronic data handling and reporting.
• Strong skills in documentation, detail-oriented, analytic, administrative Quality-conscious, well-organized, and attentive to detail.

Please note: this requisition will be posted until 17th October.

WHAT WILL YOU GET IN RETURN?

• Work in a wellbeing-oriented organization (Premium access to Headspace and ongoing support and initiatives related to ways of working to help our employees to stay healthy and constantly improve the physical, emotional, mental, and spiritual well-being).
• Customized Development plan based on your role and aspirations, with several learning platforms such as Linked In Learning Premium, and access to international development opportunities and languages + training programs.
• Good balance between work and free time (Mix of working from home within the respective country / office as well as flexible working hours).
• Working in a passionate team within a fun, diverse, and multicultural working environment.
• Full time basis with 20 legal holidays and 12 time reduction days.
• Competitive salary package and extralegal benefits.

What’s next?

DIVERSITY & INCLUSION

At Boehringer Ingelheim we share the opinion that diversity and inclusion is essential for the growth of our business and that our strengths and competitive advantage are also the result of the diversity of our company – diversity across the three dimensions of inclusion: Gender, Geography and Generation. Our people are part of a deep-rooted, family company philosophy that welcomes everyone! We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
Screening:
In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.