Key responsibilities:
- Design, supervision and execution of the transfer and validations studies of Biological and Small Molecules Products.
- Hands-on experience with techniques such as chromatography and HPLC.
- Lead and manage assigned the assigned projects keeping the deadlines and establishing a direct communication with the client
- Draft, review, and manage technical documentation associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.)
- Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.
Requirements
- Bachelor's or higher degree in Chemistry, Biochemistry, Biotechnology, Pharmacy, or a related life science field.
- Solid hands-on experience in in HPLC methods, Quality Control of Proteins will be a plus.
- In-depth understanding of GMP requirements
- Experience with electrophoretic techniques, Western-Blot and ELISAs 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
- Availability to work in afternoon shifts (1:30 PM- 9:30 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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