Lavori attuali relativi a Technical Documentation Specialist - Pisa, Toscana - Canonical
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Production Documentation Specialist
1 settimana fa
Pisa, Toscana, Italia Takeda A tempo pienoPurpose and ScopeThe Production Documentation Specialist will oversee the management of all activities related to production documentation ownership, ensuring cGMP compliance and the execution of related training. This role will be responsible for executing documentation revision, issuance, and maintenance according to GDDP rules.Key ResponsibilitiesExecute...
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GMP Documentation Specialist
6 giorni fa
Pisa, Toscana, Italia Takeda A tempo pienoDescriptionJob Title: GMP Documentation SpecialistLocation: PisaEnsure GMP compliance through effective management of production documentation, including critical revision, approval, issuance, and maintenance.Develop and execute training programs on production documentation, focusing on strong training efficacy.Manage logistics for manufacturing and visual...
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Production Documentation Specialist
4 settimane fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:Takeda is seeking a highly skilled professional to join our team as a Production Documentation Specialist. In this role, you will be responsible for managing production documentation, including the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications. You will also oversee production changes...
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Production Documentation Specialist
4 settimane fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:Takeda is seeking a highly skilled professional to join our team as a Production Documentation Specialist. In this role, you will be responsible for managing production documentation, including the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications. You will also oversee production changes...
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Production Documentation Specialist
1 mese fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:Takeda is seeking a highly skilled professional to join our team as a Production Documentation Specialist. In this role, you will be responsible for managing production documentation, including the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications. You will also oversee production changes...
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Manufacturing Deviation and GMP Documentation Specialist
2 settimane fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:As the Manufacturing Deviation and GMP Documentation Specialist, you will oversee the management of all activities related to GMP production documentation. This includes the critical review, approval, issuance, and maintenance of documentation in accordance with GDDP rules and cGMP compliance standards. Additionally, you will be responsible...
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GMP Compliance Documentation Specialist
6 giorni fa
Pisa, Toscana, Italia Takeda Pharmaceutical A tempo pienoAbout the Role:As the Manufacturing Deviation and GMP Documentation Lead, you will oversee the management of all activities related to GMP production documentation. This includes the critical review, approval, issuance, and maintenance of documentation in accordance with GDDP rules and cGMP compliance standards.Key Responsibilities:Guarantee production...
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Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:Takeda is seeking a highly skilled Manufacturing Deviation and GMP Documentation Lead to join our team in Pisa, Italy.Job Summary:The Manufacturing Deviation and GMP Documentation Lead will be responsible for managing all activities related to GMP production documentation, including critical revision, approval, issuance, and maintenance...
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Production Documentation Specialist
2 settimane fa
Pisa, Toscana, Italia Takeda Pharmaceutical A tempo pienoAbout the Role:In the realm of production, effective management of documentation is crucial for ensuring compliance and excellence in production standards. As a subject-matter expert, overseeing production changes and conducting related risk assessments is a key responsibility. Moreover, leading projects that enhance production processes and continuous...
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Manufacturing Deviation and GMP Documentation Specialist
1 settimana fa
Pisa, Toscana, Italia Takeda A tempo pienoJob Description:Purpose: We are seeking a highly skilled Manufacturing Deviation and GMP Documentation Specialist to join our team at Takeda. The successful candidate will be responsible for ensuring the management of all activities related to GMP production documentation, including critical revision, approval, issuance, and maintenance according to GDDP...
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Production Documentation Specialist
2 settimane fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:In the realm of production, management of documentation is crucial. This encompasses the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications, all in strict adherence to GDDP and cGMP standards.As a subject-matter expert, overseeing production changes and conducting related risk assessments is...
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Production Documentation Specialist
2 settimane fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:In the realm of production, management of documentation is crucial. This encompasses the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications, all in strict adherence to GDDP and cGMP standards.As a subject-matter expert, overseeing production changes and conducting related risk assessments is...
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Production Documentation Management Specialist
1 settimana fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:In the realm of pharmaceutical production, proper documentation management is crucial for maintaining quality and compliance. As a subject-matter expert, you will oversee production changes, conduct risk assessments, and lead projects to enhance production processes and continuous improvement initiatives.Your Key Responsibilities:Complete and...
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Technical Leader
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Manufacturing Deviation and GMP Documentation Specialist
1 settimana fa
Pisa, Toscana, Italia Takeda Pharmaceutical A tempo pienoJob Title: Manufacturing Deviation and GMP Documentation LeadWe are seeking a highly skilled Manufacturing Deviation and GMP Documentation Lead to join our team at Takeda Pharmaceutical. As a key member of our quality assurance team, you will be responsible for ensuring the management of all activities related to GMP production documentation, including...
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Advertisers Technical Support Specialist
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Pisa, Toscana, Italia Atlean World A tempo pienoAbout the RoleWe are seeking a highly skilled and motivated Advertisers Technical Support Specialist to join our team at Atlean World. As a key member of our international recruitment company, you will play a vital role in providing exceptional customer service and technical support to our clients.Key ResponsibilitiesProvide technical support and...
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Advertisers Technical Support Professional
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Pisa, Toscana, Italia Atlean World A tempo pienoRole OverviewWe are seeking a highly motivated and experienced Technical Support Specialist to join our team at Atlean World. As a Technical Support Specialist, you will be responsible for providing exceptional customer service and technical support for our clients in the Italian-speaking market.Key ResponsibilitiesProvide technical support and...
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IT System Administrator
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Pisa, Toscana, Italia List Group A tempo pienoAbout LIST GroupWe're a diverse group of visionary innovators who provide trading and workflow automation software, high-value analytics, and strategic consulting to corporations, central banks, financial institutions, and governments. Our company has achieved tremendous growth by bringing together some of the best and most successful financial technology...
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AI/ML Software Engineer R&D Specialist
1 settimana fa
Pisa, Toscana, Italia Michael Page A tempo pienoAI/ML Software Engineer R&D Specialist RoleWe are seeking a talented Ai/Ml Software Engineer to join our R&D team in a highly innovative and dynamic environment.The successful candidate will contribute to cutting-edge R&D activities in AI and ML areas, collaborating with our expert team to design, develop, and integrate AI/ML solutions.Main...
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Production Specialist
6 giorni fa
Pisa, Toscana, Italia Takeda A tempo pienoAbout the Role:Takeda is seeking a highly skilled Production Specialist to oversee production documentation, manage change control, and ensure compliance with GMP regulations. The ideal candidate will have experience in aseptic production and a strong understanding of sterile manufacturing processes.Key Responsibilities:Develop, revise, and approve...
Technical Documentation Specialist
2 mesi fa
As a Technical Author at Canonical, you will play a crucial role in shaping the company's documentation strategy and ensuring that our products and services are well-documented and user-friendly.
Key Responsibilities- Create, maintain, and improve software documentation to ensure accuracy and consistency.
- Collaborate with engineering team members to develop effective documentation contributions.
- Influence product development as an expert user, providing valuable insights on product function and design.
- Engage with user communities to ensure that our documentation meets their needs and expectations.
- Encourage and support community engagement in and contribution to documentation.
- Help standardize the structure, presentation, style, and language of content across products.
- Collaborate with documentation peers to advance the state of the art in documentation at Canonical.
- Challenge and advance documentation understanding and best-practice as part of a disciplinary team.
- Cares deeply about functional written communication.
- Is a technical writer with a programmer's mindset, or a programmer with a record of producing excellent documentation.
- Has a record of community engagement in open-source software, documentation, research, or other disciplines.
- Is sympathetic to the needs and challenges of open-source software and its communities.
- Demonstrates technical curiosity and is fascinated by software technology and its challenges.
- Has demonstrable documentation skills, insight, and enthusiasm.
- Has experience of software development contexts, including Linux, working on the command line, application deployment, system operations, and infrastructure management, Git, documentation markup languages.
- Has excellent written and verbal communication skills.
- Holds a BSc/BA degree or equivalent.
- Is able to travel twice a year for up to two weeks for events.
- We consider geographical location, experience, and performance in shaping compensation worldwide.
- We revisit compensation annually (and more often for graduates and associates) to ensure we recognize outstanding performance.
- We provide all team members with additional benefits that reflect our values and ideals.
- We balance our programs to meet local needs and ensure fairness globally.
- Distributed work environment with twice-yearly team sprints in person.
- Personal learning and development budget of USD 2,000 per year.
- Annual compensation review.
- Recognition rewards.
- Annual holiday leave.
- Maternity and paternity leave.
- Employee Assistance Programme.
- Opportunity to travel to new locations to meet colleagues.
- Priority Pass, and travel upgrades for long haul company events.
