Dynamic job in an international environment

For Agilent in Glostrup, we are currently looking for a skilled Design Control Process specialist to become part of The Development Office team.

Agilent Technologies is a world-leading laboratory instrument manufacturer, selling and supporting instruments like gas chromatography, liquid chromatography, mass specs, elemental and molecular products and a wide range of genomic & cell analysis products.

If you are looking for challenges and want to work with a dynamic team centered in a global company with state-of-the-art technology - this is the job for you! We offer a dynamic job within an international organization that prioritizes a healthy work environment.

About the job

As a Design Control Process specialist, you are responsible for generation of new and revised versions of Product development and Design Control related documents as well as best practice/guideline documents supporting efficient development, covering early feasibility to end-of-life phases. Stakeholder-design and Change Management will be a vital part of your role ensuring clear communication, collaboration and networking.

The job contains no direct opportunities for product innovation, but process innovation in close collaboration with the New Product Development project groups should be considered in all activities as applicable.

You will have the following responsibilities:

• Driver of optimization and further development of existing product development processes and supporting documents.

• Ensure clear roles and responsibilities, consistent language and consistency among processes and procedures.

• Interact with partners to ensure relevant input on new needs.

• Involve collaborators in development of new processes and documents.

• Drive implementation of new processes, tools and language, including training and post approval follow up as applicable.

• Support project development activities as relevant.

• Collaboration with relevant parties in the Agilent organization to align and seek synergies among design control and support tools in the broader organization.

You will need to ensure that activities are performed in accordance with Agilent and Dako business as well as QMS processes. You will get the necessary training when you begin in the position.

The key to success

We are looking for a talented and motivated individual with a Master degree or equivalent in biological sciences, technical sciences or related fields. Ideally you have experience with QA (Quality Assurance).

Furthermore, we are seeking a profile with;

• Knowledge with Design Control Support to product development projects.
• Proven experience in product development of Medical Devices and CE/IVD Class I-III devices.
• Demonstrated ability with process improvement activities.
• Strong knowledge of quality systems and regulatory requirements like ISO13485, 21 CFR part 820, GxP and IVDR.
• Required proficient in the English language, both written and verbal; Danish is highly desired.

On a personal level, you are a strong communicator and have collaboration skills. You are great at networking and building alliances around internally.

Practical information

We offer an attractive salary package.

The position is located in the Glostrup Office.

Work hours: From 08 a.m. – 4 p.m.

We offer a 10-12 months contract at Agilent.

Please do not hesitate to apply for the position. We would like the position to be filled as soon as possible.