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

Key information

  • Publication date:29 May 2025
  • Workload:100%
  • Contract type:Permanent position
  • Place of work:Kaiseraugst

Job summary

Join Solvias, a leader in integrated solutions for biotech! Enjoy a collaborative work environment with excellent benefits.

Tasks

  • Oversee analytical aspects in biologics project development.
  • Act as a key interface between operational teams and project leads.
  • Manage project deliverables and ensure quality execution.

Skills

  • BSc/MSc in Life Sciences with 3+ years in analytical settings.
  • Strong communication and organizational skills required.
  • Familiarity with GMP guidelines and quality control standards.

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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.

Categories:

Human Resources / Staff Management, Management / Project Management

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