Analytical Methods Reviewer Lisboa

Analytical Methods Reviewer
Lisboa
Lisboa, Lisboa, Portugal

ALTEN Portugal, a leading force in the IT, Engineering, and Life Sciences industries, is currently seeking a dedicated and
- oriented Analytical Methods Reviewer to support a key pharmaceutical project with one of our top clients.

ALTEN Group

Within 30 years, ALTEN has become a leader in outsourced Engineering and IT Enterprise Services. Composed of more than 54, 000 employees (88% engineers), ALTEN carries out complex and highly technical projects across the full value chain of 6, 500 clients , including some of the most prestigious companies in industry, services, and telecommunications.

We work with key players in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications, and Services sectors.

Do you want to work on exciting projects with renowned clients?

At ALTEN, we believe that understanding and meeting our consultants' expectations is key to our success.

Our consultants make the difference. Do you want to make the difference too?

In this role, you will be responsible for reviewing and comparing internal analytical methods with major international pharmacopoeias. You will ensure compliance with regulatory standards and support continuous improvement in analytical documentation within a GMP-regulated environment.

Key Responsibilities

Review and analyze existing analytical methods within the internal system.

Compare internal methods with those published in pharmacopoeias (EP, USP, JP, Ch
P).

Evaluate equivalence of methods and identify discrepancies.

Recommend adjustments when necessary to ensure compliance.

Collaborate closely with QA, QC, and Regulatory Affairs teams.

Support in the preparation and improvement of technical documentation.

Ensure adherence to GMP and regulatory guidelines throughout the review process.

Qualifications

Degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or related field.

2–6 years of experience in Quality Assurance, particularly in reviewing analytical and technical documentation.

Solid knowledge of international pharmacopoeias (European, US, Japanese, Chinese).

Fluent in English and Portuguese (spoken and written).

Preferred Skills

Strong attention to detail and analytical thinking.

Good communication skills and ability to work in
- functional teams.

Familiarity with GMP and regulatory frameworks in the pharmaceutical industry.

Proactive attitude and ability to manage multiple priorities effectively.

Location Hybrid – Lumiar (Lisbon), Portugal

Why Join Us?

Work on impactful projects in the Life Sciences industry.

Join a dynamic and collaborative work environment.

Be part of a leading international company with strong growth potential.

Access continuous training and career development opportunities.

Engage in diverse and technically challenging assignments.