Manufacturing Change Control

4 settimane fa

Santa Rufina Cittaducale Lazio, Italia Takeda Pharmaceutical A tempo pieno

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 Description

Sarà considerato requisito preferenziale l'appartenenza alle categorie protette (legge n. 68/99)

Job Title: Manufacturing Change Control & GMP Documentation

Location: Rieti

About the role:

The role involves overseeing GMP documentation management and revision, ensuring thorough and accurate processing. It includes executing training programs to maintain high levels of competency, managing change requests and conducting risk assessments to mitigate potential issues. Additionally, the position supports various projects and plays a key role in preparing for both internal and external audits.

How you will contribute:

  • Issue and review of GMP Documentation

  • Support the maintenance of the GMP documentation archive related to own department, including the responsibility to collect and destroy documents

  • 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, in compliance with the principles of Lean Manufacturing

  • Support in preparing and carrying out internal and external audits

What you bring to Takeda:

  • 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

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 status, or any other characteristic protected by law.

Locations

ITA - Rieti

Worker Type

Employee

Worker Sub-Type

Fixed Term (Fixed Term)

Time Type

Full time

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