研发高级质量经理（所有性别）| 奥地利
R&D Senior Quality Manager (all gender) | Austria
我们是为明天的世界设计的设计师。
作为全球领先的工程服务提供商之一，ALTEN致力于积极塑造合作伙伴的未来、员工的职业发展以及社会和环境所面临的挑战。
30个国家已有超过5万名员工在航空航天、可再生能源、医疗技术、铁路技术和汽车等各个工程和IT领域开发创新解决方案。
你将负责：
· 对复杂研发项目和全球质量计划进行质量监督
· 作为跨职能利益相关者和项目团队的关键质量合作伙伴
· 审核、批准并发布与GMP相关的文件和质量交付物
· 推动包括风险评估、偏差、变更控制、CAPA和培训计划在内的质量活动
· 支持验证、确认和持续改进项目
· 提供关于cGMP合规性和质量标准的专业指导
· 参与审计、检查和尽职调查活动
· 在整个组织中推动运营卓越和强大的质量文化
你将具备：
· 药品质量、QA、开发或运营领域的学士学位+5年以上或硕士学位+3年以上经验
· 熟悉cGMP法规、质量体系和监管要求
· 具有质量风险管理、偏差、变更控制和CAPA流程的经验
· 展现出强大的项目管理、利益相关者管理和决策能力
· 在制药行业具备扎实的科学、技术和合规知识
· 英语流利
加分项：具有验证、分析开发、监管机构检查和全球项目环境的经验。
薪资：起薪为每月4000欧元税前，根据资质和专业经验有明确的加薪意愿。
我们重视多样性，因此欢迎所有申请，无论性别、国籍、种族或社会背景、宗教或信仰、残疾、年龄、性取向或身份。
同等条件下，严重残疾申请人将获得优先考虑。
有任何问题？
欢迎联系我：Maja Kujundzic（手机：+43 699 10979556）。
- 人才管理 – 我们支持你的职业成长，帮助你发展事业。
- 工作与生活平衡 – 灵活的工作时间
查看英文原文
We are the designers of today for the world of tomorrow.
As one of the world’s leading engineering service providers, we at ALTEN are committed to positively shaping the future of our partners, the careers of our employees and the challenges facing our society and environment.
More than 50,000 employees in 30 countries are already working on innovative solutions in various engineering and IT sectors such as aerospace, renewable energy, medical technology, railway technology and automotive.
YOU
· ensure quality oversight for complex R&D projects and global quality initiatives
· act as the key QA partner for cross-functional stakeholders and project teams
· review, approve, and release GMP-relevant documentation and quality deliverables
· drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives
· support validation, qualification, and continuous improvement projects
· provide expert guidance on cGMP compliance and quality standards
· contribute to audits, inspections, and due diligence activities
· promote operational excellence and a strong quality culture across the organization
YOU
· hold a Bachelor's degree with 5+ years or a Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations
· have strong knowledge of cGMP regulations, quality systems, and regulatory requirements
· bring experience in quality risk management, deviations, change controls, and CAPA processes
· demonstrate strong project management, stakeholder management, and decision-making skills
· possess solid scientific, technical, and compliance knowledge within the pharmaceutical industry
· communicate fluently in English
Nice to have: Experience with validation, analytical development, health authority inspections, and global project environments.
Salary: Starting from €4,000 gross per month, with a clear willingness to offer a higher salary depending on qualifications and professional experience.
We value diversity and therefore welcome all applications, regardless of gender, nationality, ethnic or social background, religion or beliefs, disability, age, sexual orientation, or identity.
Applicants with severe disabilities will be given preferential consideration if equally qualified.
Any questions?
Feel free to contact me: Maja Kujundzic (Mobile: +43 699 10979556).
- Talent Management – We support your professional growth and help you develop your career.
- Work-Life Balance – Flexible working hours and the opportunity for mobile working.
- Green Mobility – Benefit from our public transportation subsidy and enjoy discounted commuting.