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<h1>Analytical Study Manager (m/f/d)</h1>
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. 
Description of your role 
We are searching for an analytical study manager to act as a key link between our lab teams and project leaders. With a sharp analytical mindset and solid communication skills, you'll ensure seamless coordination and high-quality project delivery for our clients. 
Your tasks 
<ul>
<li>Understand and cover the analytical aspects during the project development cycle for biologics (NBEs, biosimilars, ATMPs)</li>
<li>Act as interface between the operational teams and the dedicated project lead</li>
<li>Implement project plans in line with customer expectations and requirements into operations and supervise project execution with regard to scope, quality, time and cost</li>
<li>Supervise cross-functional teams in a matrix setting</li>
<li>Preparation and management of project deliverables (protocols, reports, CoAs, etc)</li>
<li>Oversee the compilation and review of analytical documentation</li>
<li>Perform risk analyses and support quality event management</li>
<li>Support and initiate troubleshooting activities</li>
</ul>
Our requirements 
<ul>
<li>BSc or MSc in Life Sciences (e.g. Analytical Chemistry, Biochemistry, Biology, or Pharmacy), with at least 3 years of relevant industry experience in analytical or development environments</li>
<li>Solid understanding of the pharmaceutical development process, both theoretical and practical</li>
<li>Experience with quality control standards</li>
<li>Familiarity with GMP guidelines; project management experience is a strong advantage</li>
<li>Proficient in English, both written and spoken; German is a plus</li>
<li>Strong technical, organizational, and communication skills to collaborate effectively across cross-functional teams</li>
</ul>
What we offer 
<ul>
<li>Fair and market‑competitive compensation</li>
<li>Opportunity for a permanent position, depending on mutual fit and business development</li>
<li>State‑of‑the‑art infrastructure at a modern work location</li>
<li>Excellent staff restaurant offering high quality meals at fair prices</li>
<li>Flat hierarchies and a collaborative and international working environment</li>
</ul>
*Please note that, as part of this recruitment process, we cooperate with an external recruitment partner.

Analytical Study Manager (m/f/d)

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Treuhänder:in / Buchhalter:in (m/w/d)

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Treuhänder:in / Buchhalter:in (m/w/d)

Chemielaborant:in Analytik (befristet auf 5–6 Monate)

Operator Abfüllung / Filling (m/w/d)

QA Systems Manager (m/f/d)

QA Systems Manager (m/f/d)