Regulatory Compliance Professional – QA Expertise
6 days ago
CIM A/S is seeking a Regulatory Compliance Professional to join our team. As a QA expert, you'll play a key role in ensuring our software solutions meet the pharmaceutical industry's regulatory demands.
We provide globally leading pharmaceutical companies with end-to-end production software solutions. As our QA Engineer, you'll work together with project managers, software developers, and our customers' validation teams to ensure our solutions are compliant and meet their expectations.
Your primary responsibilities will include participating in project execution, helping shape a solution that meets regulatory demands, and participating in the design phase to write Software & Hardware Design Specifications and a Requirement Traceability Matrix.
In addition to this, you'll support the rest of the organization in their day-to-day tasks, including updating validation documentation for our own software products as new features and versions are developed, and updating our QMS as we continuously find more efficient ways of working.
You'll have the opportunity to focus on doing what you do best with minimal meetings and time-consuming processes. You'll also choose whether you want to be based in our office or work remotely.
We imagine that you hold a degree in a technical field, have some experience with the validation process, and know your way around technical deliveries for a project like URS, SDS, FS, RTM, Test Plans etc.
You'll be a high-degree credibility professional who takes pride in delivering high-quality projects, works in a structured way with overview and attention to detail, possesses excellent communication skills, and understands how to communicate with different profiles and navigate unexpected situations.
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Århus, Århus Kommune, Denmark CIM AS Full timeCIM A/S is looking for a highly skilled QA Engineer to join our team and ensure compliance with pharmaceutical regulations. In this role, you will work closely with project managers, software developers, and customers' validation teams to deliver software solutions that meet regulatory demands.Your primary responsibilities will include participating in...
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Århus, Århus Kommune, Denmark CIM AS Full timeCIM A/S is seeking a highly skilled QA Engineer to join our team and ensure compliance with pharmaceutical regulations. As a key player in delivering software systems, you will work closely with project managers, software developers, and customers' validation teams to guarantee that our solutions meet regulatory demands.We provide leading pharmaceutical...
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Århus, Århus Kommune, Denmark CIM AS Full timeAt CIM A/S, we're seeking a talented Quality Assurance Specialist to join our team. As a regulatory compliance expert, you'll play a key role in delivering software systems that meet the pharmaceutical industry's stringent demands.We provide globally leading pharmaceutical companies with end-to-end production software solutions. As our QA Engineer, you'll...
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Århus, Århus Kommune, Denmark CIM AS Full timeDo you want to play a key role in delivering software systems that are in compliance with the regulatory demands of the pharmaceutical industry? Do you want to be part of a talented team in a company at the forefront of production software solutions? And do you dream of a flexible work week with room for a life in balance?If that's three times yes, you might...
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Århus, Århus Kommune, Denmark CIM AS Full timeDo you want to play a key role in delivering software systems that are in compliance with the regulatory demands of the pharmaceutical industry? Do you want to be part of a talented team in a company at the forefront of production software solutions? And do you dream of a flexible work week with room for a life in balance? If that's three times yes, you...
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