Quality Control Scientist

Repligen Sweden; Lunds kommun; On-site; SEK 40,000 - 60,000; Full time

Job summary

Repligen Sweden is seeking a Scientist in analytical development and validation to join the QC department in Lund. This dynamic role involves developing and validating analytical methods, contributing to customer projects, and ensuring product quality.

The ideal candidate will have a relevant post-secondary education and experience in a laboratory environment. Proficiency in both Swedish and English is required. This position offers the chance to work in a collaborative setting focused on continuous improvement.

Qualifications

• A post-secondary education, for example in microbiology, biochemistry, biotechnology, biomedicine, or equivalent.
• Experience working in a laboratory environment.
• Experience with GMP/ISO 9001.
• Fluent Swedish and good English skills.

Responsibilities

• Develop and validate analytical methods.
• Perform analyses primarily within projects and stability studies.
• Write protocols/reports and handle deviations.
• Drive changes and improvements within QC.
• Collaborate with colleagues on analytical challenges.
• Contribute to developing work processes with a LEAN mindset.

Skills

Analytical methods development

Quality Control (QC)

GMP/ISO 9001

Fluent Swedish

Good English

Education

Post-secondary education in microbiology, biochemistry, biotechnology, biomedicine or equivalent

Job description

About the Position

Repligen Sweden is looking for a Scientist in analytical development and validation for the QC department. Are you a driven and ambitious scientist who wants to take the next step in your career? Would you like to be part of an innovative company that develops and produces ligands for the pharmaceutical industry? Then this opportunity could be for you! We are now looking for a Scientist in analytical development and validation for our QC department in Lund. You will work in a dynamic environment where you will have the opportunity to work on exciting customer projects. You will play a key role in the development and validation of analytical methods to ensure the right quality in our products. This role is expected to model our Leadership Behaviors – Integrity & Compliance, Customer Focus, Collaboration, Courage, Team Empowerment, and Accountability & Results in all aspects of work.

Responsibilities

• Develop and validate analytical methods.
• Perform analyses primarily within projects and stability studies, while also being able to support and perform other analyses in QC.
• Write protocols/reports, SOPs, handle deviations, changes and CAPA.
• Be responsible for implementing and driving changes and improvements within QC.
• Be an active part of our QC team and collaborate with colleagues to find solutions to analytical and technical challenges.
• Contribute to the development of our work processes and routines with a LEAN mindset.

Qualifications

• A post‑secondary education, for example in microbiology, biochemistry, biotechnology, biomedicine, or equivalent.
• Experience working in a laboratory environment.
• Experience with GMP/ISO 9001.
• Fluent Swedish and good English skills.