Vacant job

Are you looking for a central and influential role in a competent and engaged QC organization, where your analytical skills, structure, and drive for improvement can truly impact pharmaceutical products?

About the position

Unimedic, based in Matfors, Sundsvall, is an established manufacturer of sterile and non-sterile pharmaceuticals, specializing in liquid formulations for the European market. With over 60 years of experience, approximately 90 employees, and as a wholly-owned subsidiary of MedCap within Life Science, we combine stability with development. Our vision is to enable a better life through high quality and flexible solutions.

The QC department is responsible for quality control and analysis of, among other things, environment, water, raw materials, products, and input materials. The department consists of receiving, raw material, product, and microbiological laboratories, with a total of 15 dedicated employees.

Your mission

As a quality engineer, you play a key role in ensuring and further developing the quality system within QC. You serve as expert support to both the QC manager and the laboratory operations and actively contribute to improvement and development work.

In this role, you will among other things:

• Review, update, and develop instructions and governing documents within QC

• Drive and document deviation investigations, CAPA and change requests, as well as risk analyses

• Follow up and verify the effects of implemented changes

• Participate in internal and external inspections

• Engage in improvement projects, development work, and internal training as needed

• Work with method and instrument development as well as qualification and validation documentation

• Represent QC in internal company projects

• Contribute to annual reports and trend analyses

We are looking for someone who

Has an academic background in chemistry, biomedicine, natural sciences, or equivalent experience.

Has experience working in a lab and has knowledge in chemistry, analytical chemistry, and/or microbiology.

Is accustomed to working in a regulated environment and understands the importance of adhering to quality requirements and documentation.

Speaks and writes fluent Swedish and English as required for the operations.

Experience in the pharmaceutical industry and GMP, particularly in quality control, as well as knowledge of HPLC and practical method development work is meritorious.

As a person, you are structured, quality-conscious, and solution-oriented. You are flexible, take responsibility, and thrive in collaboration with others in an environment characterized by change and development.

We offer With us, you will receive a secure employment in an organization with short decision-making paths and a strong focus on employee well-being. We offer flexible working hours, wellness benefits, and access to a small gym.

The position is a permanent employment with placement in Matfors. Start date according to agreement, preferably as soon as possible. The last application date is February 27, 2026, but selection is ongoing.

Under special circumstances, a temporary employment may become relevant.

Welcome with your application via Teamtailor.