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25048_Analytical Study Manager (f/m/d) 100%

Solvias AG

Infos sur l'emploi

Date de publication :29 mai 2025
Taux d'activité :100%
Type de contrat :Durée indéterminée
Lieu de travail :Kaiseraugst

Résumé de l'emploi

Solvias, leader en solutions analytiques, recherche un manager.

Tâches

Coordonner les équipes de laboratoire avec les chefs de projets.
Superviser l'exécution des projets en respectant les délais et coûts.
Gérer la documentation analytique et assurer la qualité.

Compétences

BSc ou MSc en sciences de la vie avec 3 ans d'expérience.
Compétences organisationnelles et communicationnelles solides.
Compréhension des processus de développement pharmaceutique.

Est-ce utile ?

Company information
Solvias is an internationally recognized provider of integrated solutions in contract analytical research, development and manufacturing. The company offers a broad spectrum of services and solutions in the Pharmaceutical, Biotech, Medical Device, Cell&Gene Therapy and Cosmetic industries. With headquarters near Basel, Switzerland, over 800 highly qualified employees take pride in putting science at the heart of serving customers to bring safer and better products to market faster.

We're looking for an analytical study manager to act as the key link between our lab teams and project leaders. With a sharp analytical mindset and strong communication skills, you’ll ensure seamless coordination and high-quality project delivery for our clients.

25048_Analytical Study Manager (f/m/d) 100%

Step up as the key link between lab teams and customer-focused project leaders!

Your Role

Understand and cover the analytical aspects during the project development cycle for biologics (NBEs, biosimilars, ATMPs)

Act as interface between the operational teams and the dedicated project lead

Implement project plans with respect to customer expectations and requirements into operations and supervise project execution considering scope, quality, time and cost

Supervise cross-functional teams in a matrix setting

Preparation and management of project deliverables (protocols, reports, CoAs, etc)

Overlook compilation and review of analytical documentation

Perform risk analysis and support with quality event generation

Support and trigger troubleshooting activities

Your Profile

BSc or MSc in Life Sciences (e.g. Analytical Chemistry, Biochemistry, Biology, or Pharmacy), with at least 3 years of relevant industry experience in an analytical or development setting

Strong technical, organizational, and communication skills to collaborate effectively across cross-functional teams

Solid understanding of the pharmaceutical development process, both theoretical and practical

Experience with quality control standards

Proficient in English, both written and spoken; German is a plus

Familiarity with GMP guidelines and project management experience is a strong advantage

Our Offer

Comprehensive onboarding to ensure a smooth start

Flexible working models with a 40-hour work week and at least 28.5 vacation days annually

Diverse opportunities for professional development and career growth

Attractive pension plans and commuter subsidies for public transport users

Generous family benefits, including above-average child allowances and voluntary family support

Access to discounts via a voucher platform and subsidized Reka-Checks

An excellent on-site cafeteria

We are looking forward to meeting you.

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