QA AND VALIDATION ENGINEER – BALLERUP

We are experiencing significant growth and are seeking additional colleagues to focus on QA and validation tasks, for a wide range of customers within the life science industry. Together with skilled colleagues, you will take part in the exciting journey!

Your Role in Future Projects

As an employee at DIS, you will become part of an ambitious environment with exciting projects. As a QA and Validation Engineer, you will work as a consultant, either on-site with the customer or from a DIS office. Your tasks will involve providing solutions for a diverse customer base in multiple industries. You will be involved in both large and small projects and will independently oversee agreements and project execution. Your focus will be on quality assurance, documentation, as well as handling deviations and changes.

The tasks are diverse, and not limited to the

• Develop and review GMP documents.
• Plan and create validation strategies.
• Work on quality improvements and analyze quality data.
• Contribute to the establishment and maintenance of QA systems.
• Perform testing, mapping, qualification/validation, supervision, and review.

We Cultivate a Strong Community

DIS expects a lot from you, but we also give back. As a new employee, you will be part of our “buddy program,” where one of your colleagues will be your go-to person in the first months of your employment. We want you to feel welcome and a part of the team. Additionally, we have an Academy Universe where you can further develop your skills in various technologies and areas. Through Communities of Practice, we share knowledge with each other and contribute to shaping the future of DIS together.

We look forward to welcoming you as a part of our team!

What We Expect from You

We expect you to have a relevant educational background and a minimum of 2 years of experience in QA and validation tasks. Since you will be working with various customers on-site, it is important that you understand the significance of working as a consultant and act professionally, technically, and personally.

For the right candidate, we highly value the one or more of the :

• Experience or familiarity with GMP, ASTM E2500, and ICH guides.
• Solid experience with QA and QC systems.
• Experience with risk assessments and quality-related tasks.
• Competencies in areas such as Automation, Process, Compliance etc.

Your Profile

You are an initiative-driven, outgoing, and independent individual who is passionate about your field. You stay updated with technical developments and prioritize quality and professionalism, making you a technically strong and competent partner. As part of a consultancy firm, it’s crucial that you thrive in a dynamic and customer-oriented environment. You are adaptable and an effective communicator in interactions with both clients and colleagues.