Our client – Northway Biotech – a group of companies in the biopharmaceutical sector, developing innovative and biosimilar biologic products for clinical use and large-scale production. Company aims to be the leader in development & production of biopharmaceuticals for a better life for patients. As CDMO (Contract Development and Manufacturing Organization), company supports the global pharmaceuticals market with the capability to develop biopharmaceuticals from the gene to the manufacturing of the final drug product.
We are looking for a motivated Analyst (junior and mid-career specialist roles) to join modern BIO CITY facilities in Vilnius, a leading gene therapy center in the Baltic States, dedicated to development and manufacturing of gene therapies.
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.
Job 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.
- 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.
