Quality Assurance Manager

von: Solvias AG | Ort: Kaiseraugst
N: SolviasAG
 
Quality Assurance Manager
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.
Do you have a passion for all Quality-related topics? Are you interested to join a mid-sized company with local roots in Switzerland and global appeal? You are convinced that "teamwork" is more than just a phrase and you live up to it? If yes, then we might have the perfect role for you. Our quality team is looking for a Quality Assurance Manager on senior level. Your impact will matter and we are looking forward getting to know you – don't wait and apply!
Job Description
  • You review and approve SOP's, protocols, reports, Certificate of Analysis and other quality-related documents
  • You have a high sense of detail orientation and support investigations of deviations and out of specifications (OOS) 
  • You maintain, record and process corrective and preventive measures (CAPA's) 
  • You act as a Quality Assurance point of contact for our customers 
  • You have a high level of customer orientation and you organize and manage customer audits and inspections
  • You apply and interpret audit and compliance requirements
  • You perform internal audits and provide support for GMP training
Requirements
  • You have a scientific education (Master degree) in analytical chemistry, biochemistry or life sciences 
  • You are fluent in English and are willed to learn German 
  • You worked for at least 7 years in the analytical-pharmaceutical environment having preferably proven experience in Quality Assurance
  • You have profound expertise in the regulatory framework in the GMP environment such as ICH, FDA, USAP, Ph. Eur.
  • You have a background in data integrity and computerized systems, risk assessment and project support
  • You convince us with your problem-solving skills and outstanding communication skills to collaborate with your future team-members and various stakeholders 
  • If you have gained experience as an auditor, then this is an asset 
  • A well-structured onboarding program
  • An intensive training in the beginning to bring you up to speed
  • The possibility for further development
  • Flexible working time models
  • 40 hours week
  • At least 28.5 vacation days per year (depending on your age)
  • Commuter contribution for using public transport
  • Contribution to German and English language courses
  • An excellent staff restaurant
Our employees are very close to our hearts. Each individual can make a difference and develop both professionally and personally. Does this appeal to you? We are looking forward to receiving your online application.

N: SolviasAG

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