The posting
We are welcoming a colleague to join Quality Control & Analytics team, to support analytical testing and development activities for biologic drug substances and products. The successful candidate will perform routine and non-routine analyses, contribute to method development and validation, and ensure the generation of reliable, high-quality data to support manufacturing and regulatory requirements.
Position description
- Perform analytical testing of biologic drug substances, intermediates, and final products using techniques such as HPLC, UV-Vis, SDS-PAGE, ELISA, and others.
- Support method development, optimization, and validation for analytical procedures in compliance with regulatory and internal quality standards.
- Ensure accurate, complete, and timely documentation of all analytical activities in laboratory notebooks, worksheets, and electronic systems.
- Participate in stability studies, in-process control testing, and raw material analysis.
- Contribute to troubleshooting of analytical methods and equipment, proposing solutions for technical challenges.
- Collaborate with cross-functional teams (e.g., Process Development, Manufacturing, QA) to support project timelines and deliverables.
- Maintain laboratory instruments, perform routine calibrations, and ensure compliance with equipment qualification requirements.
- Follow Good Laboratory Practice (GLP), GMP guidelines, and internal SOPs to ensure high data integrity and regulatory compliance.
- Assist in the preparation of technical reports, protocols, and other documentation for internal use or regulatory submissions.
- Participate in continuous improvement initiatives within the QC/R&D laboratory environment.
Expectations for the new colleague
- Bachelor’s degree in Biotechnology, Biochemistry, Molecular Biology, or related life sciences field.
- Practical experience with relevant analytical techniques.
- Familiarity with Good Manufacturing Practice (GMP) guidelines is an advantage.
- Strong analytical and technical problem-solving skills.
- High attention to detail and commitment to quality in a GMP-regulated environment.
- Ability to work independently and effectively in a cross-functional team.
- Proficiency in English and Lithuanian.
- Experience with laboratory information management systems or data analysis software is an advantage.
Company offers
- Competitive salary. Salary range for this position: Junior Analyst 1800 EUR to 2200 EUR gross (before taxes). Analyst 2200 EUR to 2750 EUR gross (before taxes). The final offer depends on competence, qualifications and experience.
- Exposure to a cutting-edge biologics manufacturing environment.
- Opportunities for professional growth, career development in a state-of-the-art biotechnology setting.
- Innovative, hard-working and quality-driven, collaborative, supportive company culture.



