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Expert in connecting top Regulatory Affairs & C-suite talent with Biotech, CRO, and Pharmaceutical clients across Europe and the US. Are you passionate about cutting-edge science and ready to make an impact in the world of gene therapy and biologics? We’re looking for an Analytical Scientist to join a dynamic and growing biotech company in the Barcelona area. This is a fantastic opportunity to be part of a cross-functional team focused on developing innovative therapies from early to late phases.
Key Responsibilities:
1. Execute analytical methods (SDS-PAGE, WB, ELISA, qPCR, potency assays) according to SOPs and regulatory guidelines (FDA, EMA, ICH).
2. Report, analyze, and review analytical data with accuracy and attention to detail.
3. Perform molecular biology work across bacterial, mammalian, and fungal expression systems.
4. Design and conduct potency assays aligned with regulatory expectations.
5. Support gene therapy programs through analytical and molecular biology techniques.
6. Collaborate closely with cross-functional teams including upstream and downstream processing (USP & DSP).
7. Participate in laboratory management activities, including equipment calibration and maintenance.
8. Ensure smooth communication between departments and contribute to overall project success.
Requirements:
1. Bachelor’s or Master’s degree in Biomedical Sciences or related field.
2. Minimum of 2 years’ experience in a CRO, CMO, CDO, or the biopharmaceutical industry.
3. Hands-on experience with biochemical methods (SDS-PAGE, WB, ELISA, qPCR).
4. Solid understanding of potency assays; physico-chemical methods (HPLC, CE) are a plus.
5. Familiarity with molecular biology techniques for mammalian and bacterial systems.
6. Strong motivation to work in a biotech environment with a collaborative mindset.
7. Excellent communication skills and ability to work cross-functionally.
What We Offer:
1. A chance to grow in both molecular biology and biochemical methods.
2. Exposure to end-to-end biologic product development.
3. Involvement in in-process control analytics alongside USP and DSP teams.
4. Opportunity to work with advanced technologies and regulatory frameworks (EMEA, FDA, ICH).
5. A flexible and supportive work environment within a forward-thinking company.
Seniority level: Associate
Employment type: Full-time
Job function: Research and Science
Industries: Pharmaceutical Manufacturing, Research Services, and Biotechnology Research
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