Reviewer – Elemental Analysis (m/f/d)
Reviewer – Elemental Analysis (m/f/d)
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.