Compliance Expert for Pharmaceutical Solutions
4 weeks ago
Do you want to play a key role in delivering software systems that meet the regulatory demands of the pharmaceutical industry? As a QA Engineer at CIM A/S, you will work together with project managers, software developers, and customers' validation teams to ensure our solutions are compliant and meet their expectations.
In this role, your primary responsibilities include participating in project execution, designing phase, development phase, and supporting the rest of the organization in day-to-day tasks. You will have the opportunity to update validation documentation for our software products, ensuring they remain compliant as new features and versions are developed.
To be successful in this position, you should hold a degree in a technical field, have experience with the validation process, and be familiar with technical deliveries such as URS, SDS, FS, RTM, and Test Plans. Additionally, you must possess excellent communication skills, work in a structured way, and have a high degree of credibility.
We offer a competitive salary, estimated around 65000-85000 DKK per year, depending on location and experience. This includes working in a flexible environment where you can adapt your schedule to fit your lifestyle. We encourage anyone qualified to apply, regardless of age, gender, religion, or ethnicity.
This is an exciting opportunity to reimagine the pharmaceutical industry and contribute to the development of innovative software solutions. If you're interested in this role, please send your CV and a short application by email to Anders Rohde, Site Director, or call him directly for any questions.
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