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.

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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. xugodme
- 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)

📌 QC & Analytical Scientist (Sallent)
🏢 Randstad España
📍 Sallent