IT Quality
2 semanas atrás
Kuehne+Nagel's goal is to accelerate digital technologies for our global customers, focusing on developing new mission-critical products, e-solutions, and new digital services following Kuehne+Nagel's strategy. Join our fascinating and international working environment and be part of the team responsible for developing our digital logistics processes.
** Your Responsibilities**:
- You keep up to date with regulations and closely collaborate with our globally distributed units (Information Security, Data Protection, QSHE, and Pharma & Healthcare) so that you can streamline how teams can best meet the requirements of customers and regulated industries.
- You explore issues and challenges pertaining to quality and compliance in the IT Product Portfolios and provide support, advice, and coaching to help our Business Units/Operations and product development teams raise their quality and compliance levels.
- You position yourself as a competent contact for all questions concerning our quality standards and practices and assist in customer meetings and audits.
- You launch and lead internal awareness and training programs for our quality standards.
- Provide support and mentoring for development team members working in quality management or compliance.
- You are a competent advisor in all matters relating to process documentation.
**Your Skills and Experiences**:
- Working with Management Systems, ideally for Quality and Information Security, including handling audits, documentation requirements, and compliance reporting (e.g. ISO 9001, ISO 90003:2018, or ISO 27001).
- Good understanding of complex enterprise software solutions, both self-developed and commercial off-the-shelf, with a strong focus on quality, information security, and data protection.
- Experience in auditing IT processes.
- Ability to communicate complex contexts on different levels of management.
- Ability to teach and train people.
- Willingness to learn from each other and to share knowledge and experience, to effectively improve the quality level of the organization.
- Knowledge of existing regulation in the Pharmaceutical industry (FDA 21 CFR part 11 and 820, EU GMP Annex 11), as well as experience in Computerized System Validation (CSV) methodologies and processes (preferably based on the GAMP5 framework), is beneficial.
**Good Reasons to Join**: You will have a direct influence on the future of logistics and IT. Your colleagues are experts who shape the IT industry in Portugal and worldwide. We want you to feel comfortable in your working surroundings. Therefore, we are offering you flexible working hours and mobile working arrangements. We value teamwork, continuous learning, and diversity. Kuehne+Nagel offers you a custom-made career - through individual planning and supervisors who support and advise you in every way. You get supported by many work-life balance offerings and supplementary health insurance.
**About Kuehne+Nagel***
With over 80.000 employees at some 1,300 locations in over 100 countries, the Kuehne+Nagel Group is one of the world’s leading logistics companies.
CONTACT
Carlos Correia
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