QC & Analytical Scientist

Randstad España; Cataluña; Presencial; EUR 42.000 - 62.000; Jornada completa

Descripción de la vacante

Randstad España seeks an experienced QC Scientist to join a regulated lab focused on biologic analysis. You will oversee testing workflows, manage client project timelines, and ensure GMP compliance.

Responsibilities include designing and executing QC assays with emphasis on HPLC, producing and reviewing CoA and CAPAs, and mentoring junior staff. English proficiency and GMP background are required, with shift flexibility.

Formación

• Bachelor's or Master's degree in Biotechnology, Biochemistry, Chemistry, or related life sciences discipline.
• Hands-on experience developing and running HPLC methodologies.
• Strong GMP experience in a pharmaceutical QC laboratory.
• Exposure to protein characterization techniques (Western Blot, ELISA, or electrophoresis) is advantageous.
• Professional proficiency in English (written and spoken).
• Flexibility to work designated morning or afternoon shift.

Responsabilidades

• Analytical execution and oversight of QC assays for biological products, with emphasis on HPLC.
• Serve as technical point of contact for external clients, ensuring milestones are met and communication is clear.
• Generate, review, and manage GMP documentation including SOPs, CoA, deviations, OOS investigations, and CAPAs.
• Mentor, direct, and supervise junior laboratory technicians to ensure accurate and safe workflows.

Conocimientos

Analytical thinking

Project management

Regulatory compliance

Leadership

Educación

Bachelor's or Master's degree in Biotechnology/Biochemistry/Chemistry

Herramientas

HPLC

Descripción del empleo

We are seeking an experienced and analytical QC Scientist to join a growing, regulated laboratory environment specializing in biologic analysis. Working closely with lab leadership, you will play a pivotal role in overseeing testing workflows, managing client project timelines, and ensuring strict regulatory compliance.

Key Responsibilities:

• Analytical Execution & Oversight: Design, oversee, and conduct complex quality control assays for biological products, with a heavy focus on advanced liquid chromatography (HPLC).
• Project & Client Management: Serve as a technical point of contact for external clients, ensuring project milestones are met on time and communication remains seamless.
• Regulatory & Documentation Compliance: Generate, review, and manage critical GMP documentation, including standard operating procedures (SOPs), Certificates of Analysis (CoA), deviations, Out-of-Specification (OOS) investigations, and CAPAs.
• Team Leadership: Mentor, direct, and supervise junior laboratory technicians, ensuring experimental workflows are executed accurately and safely.

Qualifications & Requirements:

• Education: Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Chemistry, or a closely related life sciences discipline.
• Technical Expertise: Demonstrated, hands‑on experience developing and running HPLC methodologies.
• Industry Experience: A strong background working within a Pharmaceutical Quality Control laboratory operating under strict GMP regulations is mandatory.
• Preferred Skills: Prior exposure to protein characterization techniques (such as Western Blot, ELISA, or electrophoresis) is highly advantageous.
• Languages: Professional proficiency in English (written and spoken).
• Scheduling: Flexibility to commit fully to either the designated morning (6h - 14h) or afternoon shift schedule (14h - 22h)