QC Analyst – Diamyd Medical

Do you enjoy working hands-on in the lab and solving problems with data? Are you ready to grow in a collaborative QC environment?
On behalf of Diamyd Medical, Haeger & Carlsson Executive Search and Interim is looking for a motivated Quality Control (QC) Analyst to join their QC team at their state-of-the-art Biologics Manufacturing facility in Umeå.
As a QC Analyst, you will work with analytical techniques such as SDS-PAGE, and ELISA to characterize protein-based pharmaceuticals and different microbiological techniques to monitor cleanroom environment. You will collect, document, and analyse data to ensure accuracy and reliability, and contribute to quality control processes that meet regulatory and internal standards. The role includes maintaining clear documentation and may involve tech transfer of analytical methods. You will be part of a team focused on continuous improvement and scientific excellence.
We are looking for someone with experience in analytical methods, chemometrics, and ideally previous work in a QC setting. You enjoy working with statistics, multivariate data analysis, and are comfortable with techniques like SDS-PAGE, ELISA, possibly cell culture and microbiological analysis. You are a social, collaborative and flexible team player who thrives in an environment where not everything is predefined. You value structure but are not afraid to adapt when needed. Familiarity with GLP is important, and while GMP is not required, it is a plus.
Diamyd Medical develops precision medicine therapies for Type 1 Diabetes. The drug candidate, Diamyd, is an antigen-specific immunotherapy for the preservation of endogenous insulin production. DIAGNODE-3, a confirmatory Phase III trial is actively recruiting patients with recent-onset Type 1 Diabetes in eight European countries and in the US. A biomanufacturing facility is being set up in Umeå for the manufacture of recombinant human GAD65, the active ingredient in the antigen-specific immunotherapy Diamyd. The long-term goal for the facility is to produce enough rhGAD65 to meet the market demand for Diamyd, as well as to be a key player in the production of biological substances for other drug projects.
Diamyd Medical lives by its core values: Innovation, Teamwork, Resilience, and Compassion — principles that shape how the company collaborates, finds solutions, and drives progress in its field.
Read more:
https://www.diamyd.com/docs/Manufacturing.aspx
Key responsibilities:
- Prepare and handle protein drug samples for analysis.
- Perform analytical techniques such as SDS-PAGE, ELISA, absorbance measurements and microbiological analysis.
- Collect, document, and analyse experimental data to ensure accuracy and reliability.
- Participate in quality control processes to meet regulatory and internal standards.
- Maintain detailed records and contribute to reports and publications.
- Collaborate with scientists and technicians to optimize methods and solve technical challenges.
- Ensure compliance with GLP standards and maintain a safe laboratory environment.
- Support process development including cell culture, protein purification, and formulation.
- Conduct experimental research to evaluate and document new process parameters.
Key Requirements:
- Bachelor’s degree in Biochemistry, Molecular Biology, or a related field.
- Experience with laboratory techniques and analytical methods.
- Familiarity with SDS-PAGE, ELISA, and cell culture.
- Knowledge about microbiological analytical techniques.
- Interest in statistics and chemometrics is highly valued.
- Knowledge of GLP is required; GMP experience is a plus but not mandatory.
- Strong attention to detail and ability to work effectively in a team.
- Proficiency in data analysis and laboratory data management systems.
- Strong problem-solving skills.
- Excellent communication skills, both written and verbal.
- Ability to manage multiple tasks and prioritize in a dynamic environment.
- Fluent in spoken and written Swedish and English.
This is an exciting opportunity to contribute to the development of life-changing therapies and grow within a forward-thinking, research-driven organization. You will be part of a passionate team working at the forefront of biopharmaceutical innovation. Whether you are early in your career or looking for your next step, this role offers a great opportunity to grow in a supportive and innovative team. We look forward to your application!
We are reviewing applications continuously, and the desired start date is January 2026.

Please apply through haegercarlsson.com
Questions are answered by:
Anna Freese +46 (0)76-174 75 81, anna.f@haegercarlsson.com
- Avdelning
- Quality
- Platser
- Umeå

Om Haeger & Carlsson | Executive Search & Interim AB
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