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Coordinator for Manufacturing Deviations and CAPA Management

3 mesi fa


Rieti, Lazio, Italia Takeda A tempo pieno

Position Overview

Job Title: Manufacturing Deviation and CAPA Management Coordinator

Location: Rieti

In the role of Manufacturing Deviation and CAPA Management Coordinator, you will play a critical role in ensuring the effectiveness of production support activities. Your responsibilities will include overseeing manufacturing deviations, developing and managing corrective action plans (CAPA), and pinpointing areas for enhancement to boost compliance with Good Manufacturing Practices (GMP) in production.

Key Responsibilities:

  • Management of deviations and identification of root causes.
  • Implementation of corrective actions within specified timelines.
  • On-site problem-solving capabilities.
  • Identification of opportunities for improvement to enhance GMP compliance in production.
  • Assistance in the preparation and execution of both internal and external audits.
  • Application of investigation quality standards.
  • Enhancement of investigation skills through coaching and mentoring.
  • Ability to influence team dynamics to drive decisions, alignment, and resolution of complex cross-functional issues.
  • Promotion of Takeda's culture, safety, and quality within the organization.
  • Commitment to understanding diverse perspectives and fostering effective collaboration.
  • Facilitation of teamwork and engagement in challenging discussions.
  • Focus on priorities to deliver exceptional results.
  • Minimum of 2 years of manufacturing experience.
  • Strong background in Deviation/Root Cause Analysis and CAPA Management.
  • Knowledge of current Good Manufacturing Practices (cGMP) relevant to production processes.
  • Proven ability to inspire and align diverse groups.
  • Excellent communication and collaboration skills.
  • Strong problem-solving orientation and results-driven mindset.
  • Proficient in English and familiar with key IT applications.

About Takeda:

At Takeda, we are dedicated to transforming patient care through the development of innovative specialty pharmaceuticals and exemplary patient support programs. We are a patient-focused organization that encourages personal growth through impactful work.

Recognized as a Global Top Employer, Takeda promotes stimulating career paths, fosters innovation, and strives for excellence in all endeavors. We cultivate an inclusive and collaborative work environment, where our teams are united by a steadfast commitment to delivering Better Health and a Brighter Future to individuals worldwide.

Commitment to Diversity:

Takeda is committed to building a diverse workforce and providing equal employment opportunities to all employees and applicants 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.

Work Environment

Employee Type: Regular

Time Type: Full time