Manufacturing Change Control Specialist
2 mesi fa
About the Role:
We are seeking a highly skilled Manufacturing Change Control Specialist to join our team at Takeda. As a key member of our quality assurance team, you will be responsible for overseeing GMP documentation management and revision, ensuring thorough and accurate processing.
Key Responsibilities:
- Issue and review of GMP documentation
- Support the maintenance of the GMP documentation archive related to own department
- Project management and change request opening and management
- Support MES project implementation
- Carrying out activities relating to GMP compliance in the field and operational problem solving
- Identification of improvement opportunities to align GMP compliance in production
- Writing/Executing/reviewing RA
- Performance of staff training regarding specific operating procedures
- Support in preparing and carrying out 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
- Knowledge of cGMP with respect to the production process
- Quality risk management
- GMP documentation experience
- Experience supporting MES implementation
- Organizational and personnel management skills
- Relationship and communication skills
- Good knowledge of the English language
About Takeda:
Takeda is a patient-focused company that is transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. We are committed 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.
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