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.