If you have a strong analytical background and experience in pharmaceutical environments, this could be your next opportunity. We are seeking a motivated and detail-oriented Quality Control Scientist to join our team.
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This role requires strong technical expertise, leadership skills, and a solid understanding of regulatory compliance within a GMP environment.
Key Responsibilities
* Design, supervise, and execute studies forDrug substance and drug product control, Stability studies
and Quality control testing
* Utilize analytical techniques including HPLC, GC, Potentiometry, Karl Fischer titration, UV spectroscopy, Dissolution testing
* Lead and manage assigned projects, ensuring adherence to deadlines and maintaining direct communication with clients.
* Draft, review, and manage technical documentation, including:Protocols, study reports, Standard Operating Procedures (SOPs), Certificates of Analysis
* Supervise and mentor laboratory analysts and technical staff, promoting scientific excellence and strict GMP compliance.
* Ensure all work is conducted in accordance with GMP regulations.
Education and Skills:
* Bachelor's degree in Chemical Sciences (Analytical Orientation). A Master degree is highly valued.
* Knowledge in HPLC, GC techniques, and have a basic understanding of an analytical development department.
* Some experience in the development and validation of new analytical methods for quality control of pharmaceuticals is valued.
* Previous experience in chemical analysis of active ingredients and pharmaceutical formulations in a Quality Control or Analytical Development department of a pharmaceutical or related company is preferred.
* Experience working with GLP and GMP is required.
* Minimum English language proficiency level: First Certificate.
* Availability for afternoon shift (14:00-22:00).
If you join us, you will enjoy:
* 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. xsgfvud
Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic