Manufacturing Change Control & GMP Documentation

Job title:

Manufacturing Change Control & GMP Documentation

Company:

Takeda

Job description

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 and . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionSarà considerato requisito preferenziale l’appartenenza alle categorie protette (legge n. 68/99)Job Title: Manufacturing Change Control & GMP DocumentationLocation: RietiAbout 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 DocumentationSupport the maintenance of the GMP documentation archive related to own department, including the responsibility to collect and destroy documentsProject management and change request opening and managementSupport MES project implementationCarrying out activities relating to GMP compliance in the field and operational problem solvingIdentification of improvement opportunities to align GMP compliance in productionWriting/Executing/reviewing RAPerformance of staff training regarding specific operating procedures, in compliance with the principles of Lean ManufacturingSupport in preparing and carrying out internal and external auditsWhat you bring to Takeda:BS in life sciences or related fieldManufacturing experience of at least 1 year

Good science knowledge and main principles of pharmaceutical manufacturing equipmentKnowledge of cGMP with respect to the production processQuality risk managementGMP documentation experienceExperience supporting MES implementationOrganizational and personnel management skillsRelationship and communication skillsGood knowledge of the English languageMore 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.LocationsITA – RietiWorker TypeEmployeeWorker Sub-TypeFixed Term (Fixed Term)Time TypeFull time

Expected salary

Location

Santa Rufina, Rieti

Job date

Tue, 01 Oct 2024 07:17:47 GMT

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