QA Disposition Supervisor

Jobinhalt

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

About The Role

Job Description

QA Disposition Supervisor manages the disposition team members (associates and coordinators), ensure Batch disposition activities of Plasma final product and raw materials in line with GMP requirements as well as supply priorities.

How You Will Contribute

• Manage assigned Disposition sub-team (associates and coordinators) by defining, in alignment with site QA objectives, individuals and team objectives. Perform regular quality conversations to prepare end year review.
• Monitor in a regular frame time identified objectives progress.
• Empower people and support them in reaching their full capacity.
• Support team individuals balancing work live and private live and maitain an optimal wellbeing perception.
• Be responsible of Batch Disposition processes and ensure
• Compliance to global guidance and GMP guidelines (GDP, trainings, QMS…etc)
• ,Accuracy and efficiency of process flows, related procedures and trainings
• Support implementation, monitoring and maintenance of those processes through gemba and self auditing programs
• Keep quality system related to processes up to date (process, procedures and trainings)
• Liaise with other departments/up stream partners in order to benchmark and improve common processes and highlight and escalate issues related to practices and propose improvement opportunities
• Actively participate to relevant decisional meetings (change board, PPQ meetings, Ad hoc deviation CAPA meetings, etc.) and reflect/communicate outcomes to disposition team through governance platform in place.
• Keep the team up to date with ongoing projects and strategies.
• Ensure efficient communication, with different internal and external departments involved in the release process (supply chain, QC labs, Exception management department, upstream plants…).
• Support and coach sub-team individuals in their daily activities and ensure batch disposition in line with GMP, Regulatory requirement.
• Support and manage priorities to ensure adherence to planned due dates and align
• Team workload balance and wellbeing
• Quality and regulatory requirement (Disposition registers, PQR, CARE, Quarterly lot release submission, etc.)
• Supply strategy.
• Support and coach sub-team individuals in their daily activities and ensure batch disposition in line with GMP, Regulatory requirement.
• Support and manage priorities to ensure adherence to planned due dates and align
• Team workload balance and wellbeing
• Quality and regulatory requirement (Disposition registers, PQR, CARE
• Quarterly lot release submission, etc.)
• Supply strategy.
• Support batch disposition performance through
• Monitoring of identified KPIs, both specific to batch disposition and quality organization
• Escalating risks and issues to management as appropriate
• Manage sub-team priorities
• Manage sub-team workload to include continuous improvement opportunities implementation
  

What You Bring To Takeda

• Master degree in scientific areas or equivalent by experience Minimum 7 years in pharmaceutical industry
• Rigor, autonomy and proactivity, and well organized
• Good presentation and communication skills (both in French and English)
• Ensure accountability and drive results
• Ability to manage priorities / Stress-resistant
• Demonstrated people management experience
• Good influencing and negotiating skills
• Good Knowledge of quality systems, EU and FDA regulations, cGMP, GDP, Eudralex
• IT knowledgeable
• Cultivate innovation and ‘out of the box’ thinking
• Solution oriented
  

More About Us

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering our people to shine

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, or characteristics, marital or other status. At Takeda, we embrace diversity as a whole.

Locations

BEL - Lessines

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time