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

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.

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.

Apply now