- Experience
- 3+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 1 week ago
- Work mode
- In office
- Eligibility
- Professionals with several years of GMP-based analytical laboratory experience who can work in Berlin on-site and communicate in very good German and good English.
- Resume
- Required to apply
Where you'll work
Job description
About the role
Axolabs, part of the LGC Group, is looking for a QC Scientist to join its expanding quality control team at a new production site in Berlin. This role sits within a global, collaborative environment focused on RNA therapeutics and nucleic-acid based medicines. You will work in modern laboratories on meaningful projects with real scope to shape processes and grow professionally.
The wider organization brings together expertise across oligonucleotide chemistry, bioinformatics, molecular biology, process engineering, analytics, and regulatory support. With locations in Petaluma, Kulmbach, and Berlin, the company operates as a CRO and CDMO with an international footprint.
Your role and impact
In this position, you will contribute to pharmaceutical quality control in a GMP-regulated setting and help ensure that all quality standards are consistently met. You will also have the opportunity to support the build-out of a new site and play an active part in a growing team.
Key responsibilities
- Work within a regulated GMP environment and help maintain compliance with quality requirements.
- Design, roll out, and validate modern analytical methods, including supporting method transfer activities.
- Prepare and present data in a clear, structured way for both internal reviews and external communication.
- Take ownership of customer-related projects and communicate directly with clients as needed.
- Support inspections and audits from authorities and customers by contributing specialist expertise.
- Continuously improve internal workflows and help strengthen quality systems and standards.
Required profile
- Several years of experience in an analytical laboratory operating under GMP conditions.
- Solid knowledge of pharmaceutical analysis and the associated regulatory framework.
- Confident use of HPLC, LC-MS, and UV/Vis; experience with NMR and GC is considered an advantage.
- Strong analytical thinking and practical experience in troubleshooting laboratory issues.
- Independent, well-organized working style with a strong sense of accountability.
- Very good German skills and good English skills.
What you can expect
- Thorough onboarding and mentoring to support a successful start.
- The chance to help build a new site from the ground up.
- Permanent employment, company pension provision, and attractive employer contributions.
- Broad employee health and wellbeing programs.
- Relocation assistance for candidates coming from outside the region.
- 30 days of annual leave.
- Subsidy for the job ticket, including the Deutschlandticket.
Additional information
About LGC: LGC is a global life sciences company providing mission-critical components and solutions for fast-growing applications in human health and other markets worldwide. Its portfolio includes essential tools for genome analysis and quality assurance applications that are embedded in customer products and workflows and valued for their performance, quality, and breadth.
Our values: passion, curiosity, integrity, brilliance, and respect.
Equal opportunity: The company promotes openness, mutual respect, and equal employment opportunities regardless of ethnic or social background, gender, age, religion, disability, or sexual orientation and identity. It is committed to an inclusive culture and values the diversity of individual perspectives and experiences as a driver of success and quality.
The organization continues to grow and is looking for people who want to make a difference with commitment and enthusiasm.
Note: This position is based in Berlin and is intended for on-site work.