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Rieti, Italia Takeda A tempo pienoDescription Job Title: Manufacturing Deviation and CAPA Management Coordinator Location: Rieti As the Manufacturing Deviation and CAPA Management Coordinator, you will guarantee production support activities by managing manufacturing deviations, defining and managing action plans (CAPA), and identifying improvement opportunities to increase...
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Manufacturing deviation and CAPA management Coordinator
4 mesi fa
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.
Job DescriptionSarà considerato requisito preferenziale l'appartenenza alle categorie protette (legge n. 68/99)
Job Title: Manufacturing Deviation and CAPA Management Coordinator
Location: Rieti
OBJECTIVES/PURPOSE:
As the Manufacturing Deviation and CAPA Management Coordinator, you will guarantee production support activities by managing manufacturing deviations, defining and managing action plans (CAPA), and identifying improvement opportunities to increase compliance with GMP in production.
ACCOUNTABILITIES:
Deviations management and root cause identification
Corrective actions implementation respecting the due date
Problem solving on the floor
Identification of improvement opportunities to increase compliance with GMP in production.
Support on preparation and execution of internal and external audit
Investigation Quality Standard application
Augment investigation skills capabilities through coaching/mentoring activities
Ability to influence within teams to drive decisions, alignment, and conflict resolution for complex cross-functional issues
Displays and drives Takeda culture, safety, and quality into the organization
Makes the extra effort to meet with people, understand diverse perspectives and effectively work together
Enables the team to work collaboratively and have challenging discussions
Focus on the priorities and delivers superior result.
WHAT YOU BRING TO TAKEDA:
Manufacturing experience at least 2 years
Strong exposure with Deviation/Root cause and CAPA Management
Knowledge of cGMP with respect to the production process
Proven ability to align and inspire diverse populations
Strong communication and collaboration skills
Problem solving and result driven mindset
Good knowledge of English and the main IT applications
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 status, or any other characteristic protected by law.
Locations ITA - Rieti Worker Type Employee Worker Sub-Type Regular Time Type Full time