Reviewer – Titration Techniques (Karl Fischer) (m/f/d)
Reviewer – Titration Techniques (Karl Fischer) (m/f/d)
Reviewer – Titration Techniques (Karl Fischer) (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 on-time delivery of analytical results for customer orders related to titration analyses
- Ensure compliance with applicable scientific and quality standards (GMP, ISO) throughout the analytical and documentation process
- Perform data review of titration techniques, with a strong focus on Karl Fischer titration (volumetric and coulometric)
- Act as an interface between laboratory teams, Quality Assurance (QA), and Project Managers to ensure clear communication and efficient issue resolution
- Support the preparation, review, and approval of technical documentation such as analytical reports, investigations, and validation or verification documents related to titration methods
- Provide subject-matter support for titration-related deviations, OOS/OOT assessments, and method-related questions
Our requirements
- Degree in chemistry, analytical sciences, or a related field; alternatively, experienced laboratory technicians with solid theoretical and practical understanding of titration techniques
- Proven experience with titration methods, especially Karl Fischer titration
- Experience with Metrohm TiAmo software (or comparable titration software) is required
- Familiarity with pharmacopeial requirements (e.g., Ph. Eur., USP) related to titration methods is an advantage
- Experience working with LIMS systems (preferably LIMS 7) for data review and result approval in a regulated environment is a plus
- Experience working in a GMP- and/or ISO-regulated environment is required
- Very good communication skills in English (written and spoken); German is an advantage
- Interest in a non-laboratory role with close interaction with laboratory staff and cross-functional teams
- Strong organizational skills, attention to detail, and a high level of personal responsibility
- Collaborative and proactive team player with a strong quality and compliance mindset
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.