Analytical Professional QC Lab SupportManufacturing QualityDo you want to play a key role in ensuring stable and compliant processes in a QC environment that supports our laboratory operations? We are looking for an Analytical Professional to join our reagent group, where you will drive documentation, quality processes and continuous improvements together with skilled laboratory technicians and chemists.Your new roleAs our new Analytical Professional, you will be responsible for maintaining high-quality documentation, driving quality processes and ensuring compliance across reagent manufacturing and sample handling activities. You will:
Develop, implement and maintain SOPs and work instructions for reagent manufacturing, sample receipt and material handling.Lead change control processes, including risk assessments, coordination of implementation activities and documentation.Manage investigations and handle deviations, including documentation, root-cause analyses and CAPA follow-up.Prepare and review protocols and reports related to reagent production and associated QC activities.Support regulatory signals assessments by identifying requirements, coordinating actions and ensuring documentation.Your new departmentYou will join a team consisting of two functional groups. One group manages global LIMS and Empower systems, ensuring their local implementation and maintenance. The reagent group comprises laboratory technicians and chemists responsible for producing reagents for the QC laboratory and managing the receipt of samples and materials. You will work closely with the reagent group while collaborating with the LIMS/Empower group when data transfer, document control or tracking processes are required.Your skills and qualificationsTo succeed in this role, we expect that you have:A degree in chemistry, life sciences, pharmacy or a similar field.Experience from a QC laboratory, preferably with analytical processes or reagent manufacturing.Experience preparing and reviewing SOPs, protocols and reports.Knowledge of change control, deviation handling and CAPA processes.Strong IT skills; familiarity with document management systems and LIMS is an advantage.Your personal strengths include a structured approach to documentation, strong collaboration and communication skills, an analytical mindset and the ability to drive tasks to completion. You thrive in an environment where you support both daily laboratory operations and long-term quality initiatives.Working at [xxxxx]Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.What we offerThere is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.ContactFor further information about the position, please contact Manager, Yasemin, Camur, at [xxxxx] Be advised Yasmin will not support queries about your recruitment status.
Application Deadline21 May 2026, Applications are reviewed on an ongoing basis.Please apply in English and refrain from adding a photo to your CV to ensure fair and efficient processing. We are committed to an inclusive recruitment process and equality of opportunity for all applicants. Also, beware we use automatic screening questions in this job advert.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At [xxxxx], we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 12.5.2026, men kan have været deaktiveret og genaktiveret igen.
