Manufacturing Change Control Specialist

2 settimane fa


Roma, Lazio, Italia Takeda Pharmaceutical A tempo pieno

About the Role: We are seeking a highly skilled Manufacturing Change Control Specialist to join our team. In this role, you will be responsible for overseeing GMP documentation management and revision, ensuring thorough and accurate processing.

Key Responsibilities:

  • Executing training programs to maintain high levels of competency
  • Managing change requests and conducting risk assessments to mitigate potential issues
  • Supporting various projects and playing a key role in preparing for both internal and external audits

Requirements:

  • BS in life sciences or related field
  • Manufacturing experience of at least 1 year
  • Good science knowledge and main principles of pharmaceutical manufacturing equipment

What You Bring:

  • Knowledge of cGMP with respect to the production process
  • Quality risk management experience
  • GMP documentation experience
  • Experience supporting MES implementation

About Takeda:

  • We are a patient-focused company that will inspire and empower you to grow through life-changing work
  • We are committed to creating a diverse workforce and providing equal employment opportunities to all employees and applicants

Location: Rieti, ITA

Worker Type: Employee

Worker Sub-Type: Fixed Term

Time Type: Full time



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