Reviewer – Elemental Analysis (ICP MS / ICP OES / AAS) (m/f/d)

Über den Job

Reviewer – Elemental Analysis (ICP MS / ICP OES / AAS) (m/f/d)

Location: Kaiseraugst | Workload: 100% | Contract time: temporary long-term employment with the possibility of a permanent role

Who we are

Solvias is an internationally recognized provider of integrated solutions for contract research. With its headquarters in Kaiseraugst near Basel, more than 500 highly qualified employees are proud to place science at the heart of customer service, helping to bring safe and high‑quality products to market faster.

At Solvias, we serve the world’s leading pharmaceutical innovators. That offers you the opportunity to make a meaningful impact on the health of patients worldwide, working with brilliant scientists in a fast-moving environment filled with stimulating challenges.

Your tasks

Review and release of raw data, final approval, and timely delivery of analytical results for customer orders related to elemental analysis

Ensure full compliance with applicable scientific, regulatory, and quality standards (GMP, ISO)

Perform independent and critical data review for ICP-MS, ICP-OES, ET AAS, and HG AAS analyses

Assess calibration, QC samples, system suitability, and compliance with internal procedures and pharmacopeial requirements

Act as a key interface between laboratory teams, Quality Assurance (QA), and Project Managers

Support the preparation, review, and approval of analytical reports, method validations/verifications, investigations, and change controls

Contribute expert input to deviations, OOS/OOT assessments, and CAPAs related to elemental analysis

Our requirements

Degree in chemistry, analytical sciences, or a related discipline; alternatively, experienced laboratory technicians with strong elemental analysis expertise

Proven experience with elemental analysis techniques, particularly ICP‑MS and/or ICP‑OES; ET‑AAS and HG‑AAS are strong advantages

Good knowledge of sample preparation and contamination control for trace and ultra-trace analysis

Familiarity with ICH Q3D and pharmacopeial requirements (Ph. Eur., USP) is an advantage

Experience working with LIMS systems (preferably LIMS 7) for analytical data review and result approval is a plus

Experience in a GMP- and/or ISO-regulated environment is required

Very good communication skills in English; German is an advantage

Interest in a non-laboratory reviewer role with close interaction with laboratory and cross-functional teams

Collaborative and proactive team player with strong analytical and quality awareness

Strong organizational skills, attention to detail, and high personal responsibility

What we offer

Fair and market‑competitive compensation

Opportunity for a permanent position, depending on mutual fit and business development

State‑of‑the‑art infrastructure at a modern work location

Excellent staff restaurant offering high quality meals at fair prices

Flat hierarchies and a collaborative and international working environment

*Please note that, as part of this recruitment process, we cooperate with an external recruitment partner.