Atrandi Biosciences is a biotechnology startup founded and built in Vilnius, Lithuania, working at the frontier of single-cell analysis. Our technologies are used by researchers around the world to advance discoveries in CRISPR, cancer, immunology and other fields shaping the future of biology. Our goal is simple: help scientists make discoveries faster, easier, and at a larger scale.
We're a team of curious, ambitious people who collaborate across disciplines to solve hard problems, take ownership, and turn bold ideas into real products. And we're comfortable not having everything figured out, because that's where the most interesting questions are waiting.
We are looking for an experienced Quality Control Specialist to join our growing Quality Control team. This role is ideal for someone who thrives on precision, enjoys working with both laboratory testing and technical documentation, and takes pride in identifying issues others might overlook. The successful candidate will play a key role in ensuring the quality of reagents, devices, and incoming materials while contributing to continuous improvement of QC processes in a fast-paced biotechnology environment.
- Degree in Life Sciences, Biotechnology, Biochemistry, Chemistry, Engineering, or related fields.
- At least 2 years of experience in Quality Control, Quality Assurance, laboratory testing, manufacturing, or a similar technical environment.
- Experience working with SOPs, technical documentation, and controlled records.
- Ability to interpret technical drawings and specifications; experience with measuring equipment is an advantage.
- Strong analytical thinking, problem-solving skills, and attention to detail.
- Ability to work independently, prioritize tasks, and communicate effectively.
- Ability to communicate in English and Lithuanian (written and spoken).
- Perform quality control testing of reagents, consumables, and device-related products according to approved procedures.
- Conduct functional testing and incoming quality inspections of products, raw materials, and components.
- Review, complete, andmaintain QC documentation in compliance with internal quality requirements.
- Investigate non-conformities, analyze QC data, identify trends, and support corrective actions.
- Verify components against specifications, technical drawings, and dimensional requirements.
- Contribute continuous improvement initiatives and collaborate with Manufacturing, R&D, Supply Chain, and Quality teams.
- The chance to be a part of the team that is making a significant impact in the global industry of biotechnology.
- Engage in a vibrant, collaborative, and rapidly growing workspace that encourages creativity and teamwork. You’ll work alongside passionate professionals dedicated to pushing the boundaries of innovation.
- Flexibility in working hours.
- Following a successful probation period, you will have access to private health insurance or a dedicated budget on Perks.lt platform.
- Have fun together in quarterly team-buildings, summer and winter festivals, and other important occasions.
- Additional vacation days for tenure - extra paid vacation days recognizing loyalty and long-term commitment.
- Internal and external training opportunities.
- Parking spot near the office or public transport pass – whatever works best for you.
- Referral bonus.