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)

📌 QC & Analytical Scientist (El Vallés Occidental)
🏢 Randstad España
📍 El Vallés Occidental