QA Project Manager

Are you looking for an exciting opportunity to shape the quality strategy for device development projects? We are seeking a highly motivated Device development QA Project Manager to play a vital role in ensuring the quality and safety of our products for clinical trials. Don't miss this chance to make a significant impact in a dynamic and innovative industry. Apply now for a life-changing opportunity! The position Due to an increasing project portfolio, we are expanding and looking for a new colleague who is experienced and skilled in Project management from a QA point of view. You will be part of our team and cover the quality perspective in multiple device development projects across DMD (Device Manufacturing Development), working in close collaboration both with the management group consisting of 3 managers and 1 director, the team of 12 project QAs and of course our stakeholders in Line of business (LoB). In this role, you will manage the broader quality perspective across multiple projects with high complexity and help build the best process, system and governance to maintain overview of progress and quality risks. You will get a broad range of exciting challenges with an impact on the results for the CVP area feeding into your personal and professional development.
In this role, you will have the opportunity to:

Drive, coordinate, and facilitate resource estimates overview, quality-related activities between LoB and QA, such as project risks, strategic Quality direction and document reviews.

Identify and contribute to strengthening and simplifying our working processes with projects in DMD QA.

Foster collaboration with our stakeholders.

Have an impact on defining own role and tasks.

Take important decisions and oversee the quality of projects going into clinical trials. We maintain the product responsibility until end of life cycle so you will also have a unique opportunity to keep up with the products impact on our patients.

Contribute with review and approval of documents.

Overall, this is a great opportunity to make a meaningful impact in the pharmaceutical industry and help drive the development of high-quality products. Our working environment is flexible, dynamic, and informal with a strong culture of cross-functional collaboration. Qualifications To succeed in this role, we imagine that you:

Hold a master’s degree in pharmacy, biotechnology or similar.

Have proven solid experience with governance of multiple projects. You also have project management and/or coordination experience.

Have solid experience from pharmaceutical companies, and profound knowledge of the important aspects of QA and GXP relevant regulations, requirements and guidelines for Devices and pharmaceutical development for clinical trials. You might have worked e.g. as a QA specialist or QA project manager within the field of QA and/or Device manufacturing.

Are fully proficient in English.

As a person, you are structured, keen on having the holistic overview, open-minded, quality- and goal-oriented. You thrive in having the opportunity to make decisions and you are eager to find systems and solutions to complex challenges. Managing a large network of people is something that drives you. You have great collaboration and communication skills on all organizational levels and are a self-driven and independent person with a high sense of responsibility and initiative. You efficiently set up processes and structure that creates overview and thrive working in a dynamic environment, where teamwork is on the top of the agenda. About the department At Device Manufacturing Development Quality Assurance (DMD QA), we are a department of 42 highly qualified professionals based at our site in Hillerød, with diverse backgrounds and interests. In team Product development QA we are 12 highly skilled professionals waiting for you to join us. We are responsible for ensuring the quality and compliance of all processes in Device Manufacturing Development (DMD), including product development and life cycle management, design control, testing an producing for clinical trials phase 3. We take pride in our work and are constantly seeking to improve our competencies and processes through a focus on simplicity and collaboration. By joining our team, you will have the chance to make a real difference in the lives of patients through the development and life cycle management of crucial medical devices. Working at [xxxxx] At [xxxxx], we are a life-science company dedicated to improving the lives of patients around the world. We offer a dynamic and international work environment, with opportunities for professional and personal development. Contact For further information, please contact QA manager Jane Frederiksen +[xxxxx]. Deadline
20th of June 2024
You may submit your application in English or in Danish.
We will review applications received on an ongoing basis, so do not hesitate to apply today. 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 in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At [xxxxx] 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.