Warehouse QA Officer
- Location
- Braine-l'Alleud, Walloon Brabant
- Work type
- Consultancy
- Work model
- Fulltime, Hybrid
We are looking for a Warehouse QA Officer who is a team player and customer oriented to join our Pharma & Injectable Quality department.
Responsibilities
You will work closely with management to ensure the implementation and maintenance of an effective Quality Management System.
• Monitor and adjust Braine warehousing and cold stream operations in order to assure they comply with applicable national and/or international regulations and guidelines (GMP/GDP/21CFR), relevant Quality Policies and Level of Quality requirements.
• Continuously assess the Level of Quality of procedures and practices to identify gaps and opportunities for improvement and simplification
• Support QA and Manufacturing Management to ensure requested Level of Quality within the warehousing areas and cold stream operations
• Pro-actively help operations, identify, develop, and implement quality and operation excellence improvements in response to business requirements, technical changes and regulatory requirements in the relevant scope.
What you’ll do :
Under the responsibility of the Head of QA Dry Forms/Warehouses and in close collaboration with the Cold Chain & Logistic Operations department, you will:
• Ensure alignment with regulatory and cGMP/21 CFR expectations regarding following activities
• Ensure the cold chain and controlled temperature process in order to maintain/ improve the GDP practice.
• Review and approve change controls, failure investigations, deviations, follow-up of complaints, CAPAs, and action plans
• Performing continuous GAP analysis between new expectations and Quality Management System documentation and between UCB documentation and actual practice (update Risk Register regularly)
• Support the preparation, execution, and follow-up of internal and external audits and inspections.
• Handle QA aspects with external customers and partners.
• Assist the Manager in achieving team objectives and act as a backup for other QA Officers as needed.
Requirements
• Scientific Master’s Degree.
• Minimum of 2 years in a regulated pharmaceutical environment, including at least one year in Quality Assurance (QMS & audit included). Experience with GMP is required.
• Knowledge of worldwide regulations pertaining to cGMP
• Excellent interpersonal and communication skills.
• Strong decision-making skills, accountability, and a delivering attitude.
• Fluency in French and English (written and spoken)
Offer
- Enjoy a competitive salary package with extra perks that recognize your talent.
- Advance your career with a clear growth path, coaching, and mentoring to support you.
- Thrive in a dynamic and supportive environment where you can truly make an impact.
- Work when and where you perform best, ensuring an optimal work-life balance.
- Choose a flexible transport solution, from a company car to a public transport subscription.
- Expand your network and enjoy unforgettable moments at exclusive events and afterworks.
- Grow your skills with external courses and our in-house Pauwels Academy.
- Work on exciting projects with industry leaders in Life Sciences, Engineering & Digital.
- Seize opportunities at every level, from a strong start to career acceleration and expert collaboration.
Thank you for your interest. Unfortunately, job applications are not available in your region. To ensure a high-quality match for our clients and streamline the application process, we have certain regional limitations in place. We value all potential candidates and encourage you to explore opportunities with us in the future.
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