Description
Job Summary:
Grupo Azevedos is strengthening its Quality Control team with a Laboratory Analyst (m/f) for the Chemistry area, responsible for inspections, testing, and documentation handling.
Key Highlights:
1. Join a solid pharmaceutical group with over two centuries of history
2. Perform quality control work in the field of Chemistry
3. Opportunity to work with technologies such as HPLC and GC
Grupo Azevedos, a brand with over two centuries of service to medicine, has always been at the forefront of pharmaceutical development.
We are one of the most solid national pharmaceutical groups, responsible for developing the first medication in Portugal and, since then, have continued producing high-quality, trustworthy pharmaceutical products. We have earned our partners’ trust through competence and rigor—principles that have consistently guided our market presence—as well as through shared values we have always upheld.
Beyond trust—which distinguishes us and has placed us at the forefront throughout these two centuries of history—our expertise in quality control across the entire pharmaceutical supply chain, from development and manufacturing to marketing and distribution, makes us a solid and competitive Group.
We are strengthening our Quality Control team in Cacém with a Laboratory Analyst (m/f) for the Chemistry area.
Key responsibilities include:
\- Performing inspections and tests using HPLC and/or GC;
\- Handling documentation \- Development protocols/reports;
\- Conducting analytical validation;
\- Performing dissolution testing;
\- Preparing reagents required for testing.
Profile:
\- Degree in Chemistry / Biochemistry / Laboratory Analysis or related fields;
\- Two years’ experience in a quality control laboratory setting;
\- Experience with HPLC / GC;
\- Knowledge of GMP standards applied to quality control (preferred);
\- Availability to work rotating shifts.
If interested, apply at:
https://www.grupoazevedos.com/pt/carreiras/tecnicoa\-de\-laboratorio\-quimica\-mf
Work location: On-site