GMP QC Analyst, Life Sciences Lab

ALTEN; Lisboa; On-site; EUR 30,000 - 38,000; Full time

Benefits offered by this job

Possibility to work with cutting-edge技

Job summary

ALTEN Portugal is seeking a Quality Control Analyst to join the Pharmaceutical Quality Control Laboratory. You will perform routine chemical testing, support investigations, and help maintain product quality and patient safety.

The role involves operating analytical techniques like HPLC, GC, UV/Vis, FTIR, and Karl Fischer, while ensuring compliance with GMP and regulatory requirements. Collaboration with QA, Manufacturing, and Regulatory Affairs is essential.

Qualifications

• Bachelor's degree in a chemical or life sciences field.
• Experience in GMP-regulated pharmaceutical or biotech labs.
• Experience with analytical techniques (HPLC, GC, UV/Vis, FTIR, Karl Fischer).
• Strong documentation and technical writing skills.
• Knowledge of GMP regulations and data integrity.

Responsibilities

• Perform testing of raw materials, packaging components, in-process samples, finished products, and stability samples.
• Operate, calibrate, and maintain laboratory instruments.
• Support investigations of deviations, OOS/OOT and incidents.
• Assist in method verification, validation and transfer activities.
• Participate in audits and regulatory inspections.

Skills

Attention to detail

Analytical thinking

Documentation skills

Regulatory compliance

Education

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering

Tools

HPLC

GC

UV-Vis Spectroscopy

FTIR

Karl Fischer Titration

pH and conductivity measurements

Job description

ALTEN Portugal is seeking a Quality Control Analyst to join the Pharmaceutical Quality Control Laboratory. You will perform routine chemical testing, support investigations, and help maintain product quality and patient safety.

The role involves operating analytical techniques like HPLC, GC, UV/Vis, FTIR, and Karl Fischer, while ensuring compliance with GMP and regulatory requirements. Collaboration with QA, Manufacturing, and Regulatory Affairs is essential.