Production Support Supervisor
JOB TITLE: PRODUCTION SUPPORT SUPERVISOR**:
**LOCATION: RIETI**:
**ABOUT THE ROLE**:
- **Management of work performance and activities of direct reports involved in production business related to**:
- ** Management of all the activities requested to issue, to distribute and to continuously review production documentation, maintenance of cGMP compliance and related training**:
- ** Production Change control management, including related risk assessment**:
- ** Support of site project execution in Production area and continuous improvement processes**:
- ** Support of site project execution in Cleaning, Process Validation, Mixing and Technical Operations**:
- ** Support CAPA identification.
Collaboration for audit execution**:
- ** HOW YOU WILL CONTRIBUTE**:** Guarantee and organize the Production documentation creation, review and distribution (Master Batch Records, SOPs, Forms, Logbooks)**:
- ** Organize the training on production procedures**:
- ** Organize Change Control issuing and activities execution with impacts on production.
Support risk assessment issuing and evaluation (quality risk management)**:
- ** Collaborate with regulatory authorities' audits.
Support preparation and execution.
Support the dossiers renewals.
**:
- ** Support and organize production activities to execute process & cleaning validation, technical operation, mixing studies and all the other activities with impact on Production process/equipment**:
- ** Manage and execute continuous improvement projects in Production area**:
- ** Support the maintenance of the GMP documentation archive related to own department, including the responsibility to collect and destroy documents**:
- ** Good science knowledge and main principles of pharmaceutical manufacturing equipment**:
- ** Quality risk management (ICH9)**:
- ** Leadership**:
- ** Organizational and personnel management skills**:
- ** Relationship and communication skills**:
- ** Data analysis**:
- ** Decision-making and Autonomy**:
- ** Problem solving**:
- ** Risk management**:
- ** Decision making**:
- ** Ability to manage and lead teams of people**:
- ** Interaction**:
- ** Communication skills**:
- ** Ability to lead multi-functions teams (Engineering, Quality, Supply Chain, Validation, Training, ect)**:
- ** Innovation** P**:
- ** Propose innovative and decisive solutions**:
**Complexity**:
- ** Project management**:
- ** Business administration**:
- **_ EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:_****:
- **BS in life sciences or related field**:
- ** Good english knowledge**:
- ** Manufacturing experience at least 4 years**:
- ** BS in life sciences or related field (Chemistry & Pharmaceutical Technologies, Biology, Biotechnology, Chemistry, Engineering)**:
- ** 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**:
Regular
**Time Type**:
Full time
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