Plandent seeks a Compliance & Quality Manager for a newly created key function in Vallensbæk

Do you want to help ensure compliance, quality and regulatory compliance in one of Denmark's leading companies in the dental industry?

At Plandent in Vallensbæk, we are seeking an ambitious and structured Compliance & Quality Manager who will take daily responsibility for driving and developing our overall compliance and quality function across Plandent.

You will become the central specialist and executional driving force across software, IT, information security, MDR, product compliance, warehousing, laboratory and other regulatory areas. You must ensure that Plandent continues to comply with applicable laws, group requirements and internal quality standards, while supporting the company's growth and development. The role reports directly to the COO, who has the overall management responsibility for the area.

We work purposefully with digitalisation, sustainability, customer satisfaction and responsible business operations – and we are now looking for a key person who can raise the compliance and quality area to the next level.

Your responsibilities

You will be responsible for developing and driving Plandent's overall compliance and quality work across IT, software, MDR, product compliance, warehousing and laboratory.

You will, among others,

• Ensure compliance with laws, regulatory requirements and group standards.
• Drive work on GDPR, information security, MDR and other compliance areas.
• Maintain procedures, documentation and quality management processes.
• Plan and conduct audits, risk assessments and improvement actions.
• Support compliance in Nexta, DentalSuite as well as other products and services.
• Ensure quality and compliance in warehousing and laboratory functions.
• Drive training and embedding of a strong compliance and quality culture.

We imagine that you have

• A relevant education in law, quality, compliance, IT, medtech or similar.
• Minimum 3-5 years' experience with compliance, quality or regulatory areas.
• Experience with GDPR and information security.
• Experience with audits, governance and risk management.
• Gerne experience with MDR, GDP, GMP, medical devices or medical software.
• Experience with document control and quality management systems.
• Ability to translate complex requirements into practical and operational solutions.
• Danish and English in writing and speech.

It would be advantageous if you have experience with

• ISO 13485, ISO 9001, ISO 3000 or similar quality standards
• Medico-, software- or healthcare sector
• SaaS or cloud solutions
• NIS2
• Vendor management
• Internal and external audits

As a person, you are

• Structured, analytical and detail-oriented
• Independent and proactive
• Curious and solution-oriented
• Good at building relationships and collaborating across the organisation
• Robust and persistent in following up on complex tasks
• Business-oriented and pragmatic in your approach to compliance
• Motivated by creating order, quality and transparency

We offer

• A newly established key function with significant influence on Plandent's future development.
• Close collaboration with the COO and the company's leadership.
• Opportunity to set the direction for compliance, quality and regulatory processes across the entire organisation.
• Responsibility for a high-growth area with strategic importance.
• Opportunity to work with modern software solutions, medico-related products and the future digital dental clinic.
• An informal and ambitious working environment with competent colleagues and short decision-making paths.
• Good opportunities for professional and personal development.
• A company with high ambitions and strong values
• Pension, health insurance and dental insurance
• An informal, professional and ambitious working environment

Do you want to help ensure that Plandent continues to be the industry's most professional, responsible and innovative collaboration partner?

We are calling for interviews on an ongoing basis, and we will hire when we have found the right candidate. If you have questions about the position, you are welcome to contact COO Julie Quass: [email protected] / 22 25 86 90

Application deadline: September 11, 2026