Experienced Stability Professional to Future QC

Would you like to work in a complex stakeholder landscape across business areas? Are you ready to design and build our new QC Facility to ensure a facility that can accommodate our high ambitions for automation and the future way to do QC testing? If yes, then apply today and come join us! The position As an experienced Professional, you will play a key role in putting your experience into use and help us build new critical processes across our stability department, for instance, all flows of samples and materials. You will be part of designing the layout of the future laboratory together with end-users and specialists. You will join the Future QC Processes department that is responsible for securing that our new facility will live up to all requirements and accommodating the future automation within stability testing. Some of your main responsibilities will include:

Preparing requirement and qualification documents and supervising facility design e.g., stability and climate room

Qualification of equipment and validation (FAT, SAT, IQ, and OQ)

Optimizing the processes in Future QC, preparing necessary SOPs, and planning/facilitating workshops

Coordinating, supporting and ensuring execution of all activities needed to build the joined facilities and relocating the existing processes into our new laboratory facility

Participating in a highly important project of introducing new fully automated processes and equipment where needed

Creating a set-up and governance that ensures maintaining the established processes/equipment after implementation

Moreover, you will be expected to identify challenges and secure the necessary agreements or clarifications with stakeholders who can be consulting engineers, end users, QA, regulatory and IT. This also entails being curious about how other teams and departments work, both within and outside [xxxxx]. Qualifications The ideal candidate for this position should possess the following qualifications:

A MSc in pharmaceutical or natural Sciences, engineering, chemistry or similar discipline and experience working in the stability function in the pharmaceutical industry

Experience with qualifying equipment and/or facility areas or processes

Preferably familiarity with the Lean methodology toolbox combined with a natural drive to optimize processes

Ideally, possessing a project management toolbox to facilitate a structured approach

Strong communication skills in both written and spoken English, with a natural ability to establish new relationships across teams and departments

On a personal level you possess strong collaboration skills, and the ability to set direction and motivate junior colleagues. You have the right quality mindset, dare to challenge our way of working and are known for your ability to identify improvements, as well as take the lead for driving the implementation of these improvements. About the project The project will build a multi-functional QC laboratory at [xxxxx] located on Zealnad and be the future workplace for many QC colleagues. Both shared facilities, stability, chemistry and microbial QC laboratories will be established, as well as development laboratories within these areas. When functional the laboratory will deliver analytical support to production units across [xxxxx] covering products for treatment of diabetes, obesity, rare blood and endocrine disorders. The laboratories will be ready for our ambitious goals for QC Automation & Digitalisation. Working at [xxxxx] At [xxxxx], 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 If you want to hear more about the position, contact Maria Berg, Project Director on [xxxxx] or get to know us better by visiting   [xxxxx] Global Manufacturing Careers.  Deadline 16 June 2024. We may conduct interviews before the deadline. Therefore, we may take the liberty to close for new applicants before the deadline. 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.