Lavori attuali relativi a Quality On The Shop Floor - Pisa - Takeda Pharmaceutical
-
Quality On The Shop Floor
4 mesi fa
Pisa, Italia Takeda Pharmaceutical A tempo pieno**Sarà considerato requisito preferenziale l'appartenenza alle categorie protette** (legge n. 68/99) **Job Title: Quality on the shop floor** **Location: Pisa - Italy** Key Responsibilities of Quality on the shop floor are the following: - Ensure compliance with regulatory requirements; develop and maintain standard operating procedures (SOPs) for...
-
Quality Assurance On The Floor
3 mesi fa
Pisa, Italia Inclusyon A tempo pienoInclusyon è la società di ricerca e selezione specializzata nel recruiting di personale qualificato appartenente alle categorie protette. Conoscenza dettagliata della normativa (Legge 68/99) e consolidata esperienza in ambito HR si fondono in un approccio consulenziale in grado di soddisfare le esigenze di recruitment della tua azienda, in qualunque...
-
Pisa, Italia Takeda Pharmaceutical A tempo pieno**Sarà considerato requisito preferenziale l'appartenenza alle categorie protette** (legge n. 68/99) **Job Title**:Manufacturing Deviation & GMP Documentation Supervisor **Location**:Pisa **_ OBJECTIVES/PURPOSE: _** - Supervision and management of all activities related to all GMP production documentation; that includes: - critical revision, approval,...
-
Pisa, Italia Takeda Pharmaceutical A tempo pieno**Job Title**:Manufacturing Deviation and GMP Documentation Lead **Location**:Pisa **_ OBJECTIVES/PURPOSE:_** - Assure management of all activities related to all GMP production documentation; that includes: - critical revision, approval, issuance, maintenance of documentation according to GDDP rules, cGMP compliance. - execution of training on production...
-
Pisa, Italia Takeda Pharmaceutical A tempo pienoJob Title: Manufacturing Deviation and GMP Documentation LeadLocation: PisaOBJECTIVES/PURPOSE: Oversee all activities related to GMP production documentation, ensuring compliance with established guidelines.Conduct critical reviews, approvals, and maintenance of documentation in accordance with GDDP regulations and cGMP standards.Facilitate training on...
-
Calibration Coordinator
3 mesi fa
Pisa, Italia Takeda Pharmaceutical A tempo pieno**Sarà considerato requisito preferenziale l'appartenenza alle categorie protette** (legge n. 68/99) **Job Title: Calibration Coordinator** **Location: Pisa** **_ OBJECTIVES/PURPOSE _** - Ensure the management and execution on the shop floor of calibration activities, according to the annual planning and in compliance with GMP - Collaborate for the...
-
Pisa, Italia Takeda Pharmaceutical A tempo pienoBy clicking the "Apply" button, I acknowledge that my employment application process with Takeda will commence and that the information I provide in my application will be processed in accordance with Takeda's Privacy Notice and Terms of Use.I further affirm that all information I submit in my employment application is accurate to the best of my...
-
Pisa, Italia Takeda Pharmaceutical A tempo pienoBy 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...
-
Pisa, Italia Takeda Pharmaceutical A tempo pienoBy clicking the "Apply" button, I acknowledge that my employment application process with Takeda will commence and that the information I provide in my application will be processed in accordance with Takeda's Privacy Notice and Terms of Use.I further affirm that all information I submit in my employment application is accurate to the best of my...
-
Quality System Analyst
4 mesi fa
Pisa, Italia Takeda Pharmaceutical A tempo pieno**Sarà considerato requisito preferenziale l'appartenenza alle categorie protette** (legge n. 68/99) **Job Title**:Quality System Analyst **Location**:Pisa The _Quality System Analyst_ will report to the Quality System Supervisor and will be responsible for ensuring maintaining the Change Control process, ensuring compliance with relevant regulations and...
-
Quality Assurance Specialist
3 settimane fa
Pisa, Toscana, Italia Adecco Italia A tempo pienoJob Description:Adecco Italia is seeking a Quality Assurance Trainee to join our team in the pharmaceutical industry. As a Quality Assurance Trainee, you will be responsible for supporting the management and supervision of the Quality System for Deviations and CAPA.Key Responsibilities:Ensure that all deviations and CAPA comply with regulatory requirements,...
-
Quality Assurance Specialist
3 settimane fa
Pisa, Toscana, Italia Adecco Italia A tempo pienoJob Description:Adecco Italia is seeking a Quality Assurance Trainee to join our team in the pharmaceutical industry. As a Quality Assurance Trainee, you will be responsible for supporting the management and supervision of the Quality System for Deviations and CAPA.Key Responsibilities:Ensure that all deviations and CAPA comply with regulatory requirements,...
-
Quality Assurance Specialist
2 settimane fa
Pisa, Toscana, Italia ADECCO ITALIA A tempo pienoJob DescriptionCompany: ADECCO ITALIAJob Title: Quality Assurance SpecialistLocation: PisaJob Type: Full TimeJob SummaryWe are seeking a Quality Assurance Specialist to join our team in Pisa. The successful candidate will be responsible for supporting the management and supervision of the Quality System for Deviations and CAPA.Key ResponsibilitiesEnsure that...
-
Pisa, Italia Takeda Pharmaceutical A tempo pienoBy 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...
-
Pisa, Italia Takeda Pharmaceutical A tempo pienoBy 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...
-
Quality & Certification Specialist
4 mesi fa
Pisa, Italia Mediate A tempo pienoAs a **Quality and Certification Specialist**, you will play a crucial role in ensuring the highest standards of quality and compliance for our products. Working within a dynamic and innovative team, you will be responsible for overseeing all aspects of product quality control, certification, and compliance with relevant regulations and standards. Your...
-
Quality Assurance Specialist
1 settimana fa
Pisa, Toscana, Italia Adecco Italia A tempo pienoJob DescriptionCompany: Adecco ItaliaJob Title: Quality Assurance TraineeLocation: Pisa, ItalyJob Type: Full-timeIndustry: PharmaceuticalJob Description:We are seeking a Quality Assurance Trainee to join our team at Adecco Italia. As a Quality Assurance Trainee, you will be responsible for supporting the management and supervision of the Quality System for...
-
Pisa, Italia Takeda A tempo pienoDescription Job Title: Manufacturing Deviation and GMP Documentation LeadLocation: PisaAssure management of all activities related to all GMP production documentation; that includes:critical revision, approval, issuance, maintenance of documentation according to GDDP rules, cGMP compliance.execution of training on production documentation (SOPs, MBRs, JA,...
-
Quality & Certification Specialist
4 giorni fa
Pisa, Italia Mediate A tempo pienoAs a Quality and Certification Specialist, you will play a crucial role in ensuring the highest standards of quality and compliance for our products. Working within a dynamic and innovative team, you will be responsible for overseeing all aspects of product quality control, certification, and compliance with relevant regulations and standards. Your duties...
-
Pisa, Italia Takeda A tempo pienoDescription Job Title: Manufacturing Deviation and GMP Documentation Lead Location : Pisa Assure management of all activities related to all GMP production documentation; that includes: critical revision, approval, issuance, maintenance of documentation according to GDDP rules, cGMP compliance. execution of training on production...
Quality On The Shop Floor
3 mesi fa
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: Quality on the shop floor Location: Pisa – Italy The Quality on the shop floor will ensure that the production processes for the manufacturing of sterile products are executed following cGMP/Annex 1 regulations and in adherence to the internal and global procedures. The candidate must have a strong microbiological background and have gained experience in relevant investigations and data analysis, with robust aptitude for problem solving.
Key Responsibilities of Quality on the shop floor are the following: Promote the application of good manufacturing practices in terms of aseptic behavior and ensure training and oversight of activities related to aseptic process.Ensure compliance with regulatory requirements; develop and maintain standard operating procedures (SOPs) for sterile processes.Ensuring that aseptic processing aligns with international standards by providing technical oversight.Support the definition and implementation of the appropriate contamination control strategies (CCS) and promote the continuous improvement in aseptic technique culture/behavior.Conduct risk assessments and develop mitigation strategies to minimize the risk of contamination, identifying potential sources of contamination and developing strategies to mitigate the risk.Collaborate with cross-functional teams to ensure that all products are manufactured in compliance with sterility requirements.Provide training to employees on sterilization processes, GMP/Annex 1 requirements and procedures. ensuring that all employees are trained in the appropriate processes and procedures.Participate in audits and inspections to ensure compliance with regulatory requirements.Provide technical support and Subject Matter Expert inputs for manufacturing-related process improvements, change control, deviation investigation, and CAPA implementation.Coordinate the process to guarantee the site inspection readiness; participate to site self-assessments.Identify and implement, in close collaboration and partnership with the production/warehouse/engineering departments, actions to improve and simplify activities, always in full compliance with GMP requirements, regulatory and corporate requirements.Critically evaluate environmental monitoring data, perform a trend data analysis.Collaborate at global level to harmonize the practices/procedures/processes between the various sites across the network. Qualifications: Bachelor's degree in a relevant field such as microbiology, biology, or biochemistryMinimum of 3+ years of experience in the same role or quality assurance Dept. in a pharmaceutical manufacturing environment.Knowledge of current regulatory requirements for Aseptic manufacturing that use RABs and isolator technologies and cGMP /Annex 1Experience in investigations and data analysis, with aptitude for problem solvingKnowledge of Aseptic manufacturing process and related microbiological aspectKnowledge of MODA, Labware, Trackwise, JDE (ERP system) systemsCommunication and interpersonal skills to collaborate with cross-functional teams and provide training to employees.Be able to work in a dynamic environment to ensure that all products are manufactured in compliance with sterility requirements.Ability to work under pressure and to organize and prioritize multiple tasks. 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 - Pisa Worker Type
Employee Worker Sub-Type
Regular Time Type
Full time
