MANUFACTURING CHANGE CONTROL & GMP DOCUMENTATION

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 Since , Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases.
These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors.
As a partner of the National Health System, we transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program.
We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia.
Across Italy and the world, Takeda is recognized as a Top Employer by the Top Employers Institute based on our commitment to career development, inclusion, learning, sustainability, wellness, and, most importantly, our values.
Join us to make a difference.
About the Role.
As a Manufacturing Change Control & GMP Documentation, you will issue and review GMP documentation.
You will support the maintenance of the GMP documentation archive related to own department, including the responsibility to collect and destroy documents.
How you will contribute.
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 Can speak and write in English Manufacturing experience, at least 1 year Good computer system knowledge and main software and applications used in the pharmaceutical industries Good science knowledge and main principles of pharmaceutical manufacturing equipment Quality risk management Organizational and personnel management skills Relationship and communication skills Data analysis Knowledge of cGMP with respect to the production process Good knowledge of English and the main IT applications What Takeda can offer.
We want our employees to succeed in everything they do - at work, at home, and in the community.
This is why we offer world-class benefits and access to resources that can support people.
Health and Finance Health Care Assistance Insurance Employee Stock Purchase Plan Employee discount programs on commercial establishments, shops, medical services Training and Development Technical skill training and professional development Job Rotation programs for working in other departments Spontaneous employee groups for awareness on Diversity, Equity, and Inclusion issues and community engagement activities Value-based culture Individual Support Wellness programs On-site cafeteria and bar Resources for mental, physical, financial, and spiritual health Parental Leave NOTE.
Belonging to protected categories (Law No.
) will be considered a preferential qualification.
Important Considerations.
At Takeda, our patients rely on us to create quality products, and we aim to create a safe environment for our team members.
As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product or putting anyone at the site in harm's way.
In this role, you may.
Work in a controlled environment requiring special gowning and wearing protective clothing.
Need to remove all make-up, jewelry, contact lenses, nail polish, and/or artificial fingernails while in the manufacturing environment.
More About Us.
At Takeda, we are transforming patient care through the development of innovative specialty medicines and first-class patient support programs.
Takeda is a patient-oriented 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 aims for excellence in everything we do.
We promote an inclusive and collaborative work environment where our teams are united by an unwavering commitment to delivering Better Health and a Brighter Future to people worldwide.
Empowering our people to shine.
Takeda is proud of its commitment to creating a diverse workforce and offering equal employment opportunities to all employees and applicants without distinction of race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, marital status, or any other characteristic protected by law.
#GMSGQ #LI-LA1 Locations ITA - Rieti Worker Type Employee Worker Sub-Type Regular Time Type Full time