Quality Control Scientist

Planet Pharma; Ceuta; Presencial; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Ceuta, Spain, seeks a detail-oriented Quality Control Technician to oversee quality control studies for biological products. Candidates should have a Bachelor’s or Master’s degree in a relevant field and at least 3 years of experience with HPLC and chromatography techniques. The role involves project management, technical documentation, and interaction with clients. Proficiency in English is essential. Join us to contribute to high-quality pharmaceutical products.

Formación

• Minimum of 3 years of hands-on experience with HPLC and chromatography techniques.
• Proven experience in Quality Control within a pharmaceutical company.
• Familiarity with electrophoretic techniques, Western Blot, ELISA, and protein quality control is a plus.

Responsabilidades

• Design and execute quality control studies for biological products.
• Manage assigned projects, ensuring timely delivery and communication with clients.
• Oversee technical documentation preparation and maintenance.

Conocimientos

HPLC proficiency

Chromatography techniques

Strong organizational skills

Communication skills

Educación

Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Chemistry

Descripción del empleo

Quality Control (QC) Technician – Biologics

Morning Shift 6am-2pm. We are seeking a highly motivated and detail‑oriented Quality Control Technician to join our team, specializing in the analysis of biological products.

Key Responsibilities

• Design, supervise, and execute quality control studies for biological products, with a strong focus on chromatography and HPLC techniques.
• Manage assigned projects, ensuring timely delivery and maintaining direct communication with clients.
• Oversee the preparation and maintenance of technical documentation, including SOPs, certificates of analysis, deviations, OOS reports, and CAPAs.
• Provide direction and supervision to technical staff, ensuring high‑quality experimental execution and compliance with regulatory standards.

Requirements

• Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Chemistry, or a related field.
• Minimum of 3 years of hands‑on experience with HPLC and chromatography techniques.
• Proven experience in Quality Control within a pharmaceutical company, with a solid understanding of GMP regulations.
• Familiarity with electrophoretic techniques, Western Blot, ELISA, and protein quality control is a strong plus.
• Strong organizational and communication skills.
• Proficiency in English (written and spoken) is required.

Equal Opportunity Statement

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.