We are seeking a highly motivated Scientist to join our Biologics and Advanced Therapies Quality Control team. This role, reporting to the Department Manager, focuses on the analysis of biological products in a GMP-regulated environment. Key...
We are seeking a highly motivated Scientist to join our Biologics and Advanced Therapies Quality Control team. This role, reporting to the Department Manager, focuses on the analysis of biological products in a GMP-regulated environment.
Key responsibilities:
Requirements:
Key responsibilities:
- Design, execution, and oversee of analytical method development and validation studies for biologic products, including monoclonal antibodies, recombinant proteins, and advanced therapies.
- Hands-on experience with techniques such as HPLC, capillary electrophoresis, ELISA, protein quantification (e.g., BCA, UV), and other relevant biochemical methods.
- Lead and manage assigned development and validation projects, ensuring timely execution, compliance with regulatory requirements, and effective communication with internal and external stakeholders.
- Draft, review, and manage technical documentation including method validation protocols and reports, SOPs, risk assessments, and technical justifications.
- Collaborate with cross-functional teams including Quality Assurance and Marketing to support method development and validation.
- Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.
Requirements:
- Bachelor's or higher degree in Biochemistry, Biotechnology, Pharmacy, or a related life science field.
- Solid hands-on experience in analytical method development and validation for biologics, particularly using HPLC, capillary electrophoresis, and immunoassay-based techniques.
- In-depth understanding of GMP requirements and ICH guidelines relevant to analytical method validation.
- Experience with HPLC and Capillary electrophoresis development will be considered a strong asset.
- Excellent organizational and documentation skills, with the ability to manage multiple projects simultaneously.
- English level equivalent to Cambridge First Certificate (B2) or higher.
- Willingness and availability to work the afternoon shift (2:00 PM – 10:00 PM).
- Working in a dynamic company with a highly qualified growing team
- Professional development and collaborative environment and a culture of empowerment.
- Flexible Working Hours and intensive schedule on Friday.
- Hybrid work, but mainly in the office.
- Access to the employee benefits flexibility platform.
- 23 vacation days per year plus 24th and 31th of December.
- Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
- Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.
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