Leading role in quality control and laboratory analysis

About Us

Magle Group is a dynamic organisation within the life science sector, developing life-changing products for patients in need. We are currently looking for an experienced QC Teamlead for our Danish unit, Magle Biopolymers, which operates at two locations: Hårlev and Køge. Our QC team is based in Hårlev and supports production at both sites. The QC organization is led by a QC Director based in Malmö, Sweden.

About the role

As QC Teamlead, you will hold a leading position within our QC team in Hårlev. You are responsible for managing and developing a team of five experienced laboratory technicians, as well as ensuring that quality work meets the expected standard. You have personnel responsibility and work closely with other departments, both on analytical tasks and documentation.

Role Responsibilities

· Lead and coach the QC team to ensure efficient and high-quality work.

· Conduct development discussions and follow up on performance.

· Plan and allocate tasks within laboratory analyses of raw materials, intermediates, finished products, and stability studies, as well as document-related tasks.

· Be responsible for accurate documentation and reporting of results in both digital and paper-based systems to ensure full traceability.

· Review and approve quality documents, such as SOPs, protocols, reports, and analytical methods, as well as handle change requests and deviations.

· Stay updated on current regulatory requirements and contribute to ensuring that operations adhere to applicable analytical standards (ISO, GMP).

· Drive improvement initiatives and develop laboratory processes for more efficient and precise analysis.

· Be responsible for the onboarding and development of team members.

Qualifications

· A university degree in analytical chemistry, biomedicine, or a related field.

· At least three years’ experience in a leadership role within quality control, preferably in the pharmaceutical or biotechnology sector.

· Experience with GMP and ISO13485.

· Proven experience with personnel responsibility and team leadership.

· Strong expertise in laboratory work, analytical methods, and quality documentation.

· Excellent proficiency in Danish and English, both spoken and written.

· Good computer skills and a willingness to learn new systems.

We offer

At Magle Biopolymers, you will join a highly skilled and dedicated team that values cooperation, creativity, quality, and accountability. We provide a stimulating work environment with substantial individual responsibility and opportunities for development in pharmaceutical analysis and quality control. Our organization is driven by values, and we seek individuals who share our ambition to make a difference for patients - by being innovative, motivated, positive, responsible, customer-focused, and a true team player. If you recognize yourself in this description and the role matches your experience, we look forward to hearing from you!

Application

We conduct interviews on an ongoing basis, so please submit your application as soon as possible, but no later than April 1st, 2026.

We look forward to hearing from you!

If you have any questions regarding the role and QC, please reach out to our QC Director; sofia.bergfors@maglegroup.com