As a QC Analyst, you will perform analytical testing on pharmaceutical products and ensure accurate reporting of results within a GMP-regulated laboratory environment.

Responsibilities

- Perform and evaluate analytical tests including HPLC, GC, TLC, pH, spectroscopy, dissolution, microscopy, density, and viscosity testing.
- Accurately document test results in the LIMS system.
- Review analytical results generated by fellow analysts.
- Report out-of-specification results to the Senior Analyst or Supervisor.
- Follow cGMP guidelines and laboratory SOPs.
- Support laboratory housekeeping, stock management, and inventory control.
- Assist with training activities and onboarding of new team members.

Profile

- Bachelor's degree in a scientific discipline (Chemistry, Biochemistry, Biotechnology,



Pharmaceutical Sciences, or similar).
- Minimum 2 years of experience in a GMP laboratory is an asset.
- Hands-on experience with HPLC is required.
- Knowledge of Waters HPLC systems is a plus.
- Familiarity with analytical laboratory techniques.
- Good knowledge of MS Office applications.
- Good command of English.
- Able to work in a shift-based environment.

Skills

- Strong attention to detail and accuracy.
- Ability to work independently.
- Sense of ownership and responsibility.
- Problem-solving mindset.
- Positive and proactive attitude.
- Strong communication skills.

📌 Qc analyst (España)
🏢 Arcadis
📍 España