Position: Associate

Job type: Full-time

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Microbiologist - Pharmaceutical development
Lucerne, Switzerland

Are you looking to become a valued member of an award-winning clinical research organisation, with a collective goal of positively improving the health and wellbeing of people? Clintec is looking to expand our team to join our clients pharmaceutical development and manufacturing site located in Lucerne area.

You will have the opportunity to work dedicated to a world-renowned company, on some of the most prestigious and ground-breaking drug development projects impacting lives all over the world. Every employee strives to find innovative ways to overcome obstacles together, and this team centric ethos is crucial to the continued success of Clintec.

Our management team recognise that every employee is different, so we offer individual training and development plans to suit your goals and expectations. You’ll enjoy a fast-paced and dynamic environment, where we value inclusion and promote teamwork.

What We Can Offer You
  • A competitive salary and benefits package; performance related bonus, private healthcare allowance, pension contribution and flexible working options
  • 25 days annual leave per year plus 15 days bank holiday entitlement
  • Career development/training opportunities and a life-long career with an innovative, forward-thinking clinical research company
  • Team focussed social events throughout the year, subsidised food canteen and a high-quality working environment


Qualifications
  • Completed apprenticeship (lab technician EFZ subject Biology) or Bachelor in Biology
  • Practical experience in microbiological techniques
  • Ideally experienced in GMP guidelines
  • Fluent German, English language skills desirable
  • Knowledge of MS Office
  • Team player
  • Willingness to work occasionally on weekends


Responsibilities
  • Conducting microbiological sampling for environmental monitoring in the production areas (water, air and surface monitoring)
  • Execution and evaluation of microbiological analyses (analysis of water, microorganism identification, endotoxin and bioburden determinations)
  • Quality control and storage organization of media, reagents and test kits
  • Maintenance of equipment
  • Documentation and management of analytical results according to applicable GMP requirements
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Deadline: 10-05-2024

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