Revision of risk analysis, validation plan when applicable.
Your profile:
5-10 years of experience in validation CIP, SIP, Equipment qualification (mechanical and automation part)
Knowledge of filling equipment: Filling line, freeze dryer, depyrogenation tunnel, vials washer, stopper washing and sterilization, isolator
ASTM approach
Writing and execute digitalized protocol (Kneat software)
the application process.
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compliance check.
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reference and background check.
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the perfect job for you.
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the interview.
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For our client, an international pharmaceutical company based in Neuchatel, we are looking for a QA Engineering/Validation Expert.BackgroundThe objective of this resource within the Quality Ops organization is to provide support as a Quality Assurance Expert in the frame of routine GMP operations. He/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory
For our client, an international pharmaceutical company based in Neuchatel, we are looking for a QA Engineering/Validation Expert.BackgroundThe objective of this resource within the Quality Ops organization is to provide support as a Quality Assurance Expert in the frame of routine GMP operations. He/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory
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For our client, an international company based in Neuchâtel, we are looking for an Automation Engineer.In the Global Manufacturing and Supply team, you’ll be part of a rapidly transforming industry that’s applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms.General Information: Start date
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