Quality Control Scientist

Randstad España; Cataluña; Presencial; EUR 42.000 - 56.000; Jornada completa

Descripción de la vacante

Randstad España is seeking an experienced QC Scientist for an analytical laboratory environment focused on biologic analysis. You will oversee testing workflows, manage client project timelines, and ensure strict GMP compliance.

Responsibilities include designing and performing HPLC-based QC assays, generating GMP documents, and mentoring junior technicians to ensure accurate and safe workflows. English proficiency is required, with shifts 6h–14h or 14h–22h.

Formación

• Education: Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Chemistry, or closely related life sciences.
• Hands-on experience developing and running HPLC methodologies.
• Background in a Pharmaceutical Quality Control laboratory operating under GMP regulations.
• Exposure to protein characterization techniques (e.g., Western Blot, ELISA, electrophoresis) is advantageous.
• Professional proficiency in English (written and spoken).
• Scheduling flexibility for morning or afternoon shift.

Responsabilidades

• Design, oversee, and conduct quality control assays for biological products, focusing on HPLC.
• Serve as technical contact for external clients to meet milestones and maintain clear communication.
• Generate, review, and manage GMP documentation including SOPs, CoA, deviations, OOS investigations, and CAPAs.
• Mentor and supervise junior laboratory technicians to ensure accurate and safe experimental workflows.

Conocimientos

Project management

Team leadership

Regulatory documentation

Quality control

English communication

Educación

Bachelor’s or Master’s 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)