Senior Validation Engineer
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Hillerød
Are you an experienced validation engineer seeking new horizons? Do you aspire to embrace the opportunity to collaborate in a dynamic setting, dedicated to achieving excellence while engaging stakeholders effectively? If you're ready for a fresh challenge, join our Device Manufacturing Development (DMD) department, where together we drive innovation and embrace continuous improvement. Apply today and be part of our transformative journey! The position As Senior Validation Engineer, you possess a comprehensive understanding of our engineering procedures, project management, and quality management system (QMS). You collaborate with a small team to ensure alignment of our engineering models, project management, and QMS with regulations and industry standards to effectively support our strategic goals. Your role also involves participating in the development and improvement of methods and processes for engineering, risk management, and validation in accordance with our QMS, regulatory requirements, and standards, implementing and communicating solutions to stakeholders. Your key activities encompass: Improving the QMS within our area on a continuous basis to ensure that it is efficient, effective, and aligned with our strategic goals Facilitating process risk assessments for component production and defining control strategies to mitigate risks Participating in the selection of manufacturers and communicate our requirements to frame and risk matters Providing support and training to internal production as well as external manufacturers where production is already established Staying up-to-date with regulatory requirements and industry standards related to our area and ensure that the QMS is updated accordingly Qualifications To be successful in this role, we imagine you: Hold at least a bachelor’s degree in a pertinent field Showcase a minimum of 4 years of experience in validation and risk management within a regulated industry Demonstrate outstanding organizational and prioritization abilities Display proficiency in both spoken and written English It would be considered as a strong advantage if you possess experience in the medical device/pharma industry. On a personal level, you truly enjoy working with people in a development context. You are humble but confident in your approach and take the time to listen to your team members to understand and clarify their message. You cultivate a collaborative culture in which people feel heard and where decisions are made in a transparent manner. You realize that by trusting and empowering people, you will get ownership and results in return. You excel at keeping things simple and set clear direction to ensure progress. The same simplicity is reflected in your communication style, which enables you to effectively get your message across to all levels in the organization. About the department You will be joining 60+ dedicated colleagues in the Components department within DMD in Hillerød. We develop the equipment and processes that transform great designs into actual products for our patients, bridging the gap between development and production lines. The dosage pen systems that are a big part of the success are always under further development. We strive to ensure they meet and exceed the expectations of a growing and demanding market. We design all the equipment necessary to perform all the processes involved in the manufacturing of the dosage system components. You will be working with experts in the field of device manufacturing development and raw materials for plastic, metal, and electronic components, and you will collaborate with a broad range of stakeholders. We enjoy sharing our knowledge, and we are eager to get to know you and learn from you. If you appreciate collaboration in an innovative and ambitious environment, you will feel at home with us. Working at At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further details about the position, you are welcome to call Mette Mørk Bendtsen at +. Deadline 7 April 2024. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Hillerød.
Jobbet er oprettet på vores service den 22.3.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Projektleder
- Hillerød
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