07.06.25 | Vollzeit | Couvet | JobLeads GmbH | CHF 100’000 - CHF 125’000 And Pharmacopeia requirements - Thorough knowledge of quality systems as well as deviations and investigations handling. - Takes a structured and analytical approach to problem solving. Is familiar with problem-solving and investigation tools and methodologies - Able to present topics as Subject Matter Expert
Später ansehen07.06.25 | Vollzeit | Couvet | JobLeads GmbH | CHF 100’000 - CHF 125’000 And Pharmacopeia requirements - Thorough knowledge of quality systems as well as deviations and investigations handling. - Takes a structured and analytical approach to problem solving. Is familiar with problem-solving and investigation tools and methodologies - Able to present topics as Subject Matter Expert
Später ansehen05.06.25 | Vollzeit | Couvet | JobLeads GmbH | CHF 100’000 - CHF 125’000 And transfer per ICH guidelines. - Proven proficiency in a wide range of analytical techniques. - Solid understanding of GMP, data integrity, and regulatory requirements. - Excellent communication, technical writing, and organizational skills. - Familiarity with LIMS, Empower, and quality software tools
Später ansehen05.06.25 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Writes or reviews all types of GMP documents (e.g. test method, SOP, WPR, validation protocols and reports, investigation reports etc.) - Handles deviations and OOS in the applicable software tool - Handles change control in the applicable software tool - Supports internal and external audits - Takes
Später ansehen04.06.25 | Vollzeit | Couvet | JobLeads GmbH | CHF 100’000 - CHF 125’000 And transfer per ICH guidelines. - Proven proficiency in a wide range of analytical techniques. - Solid understanding of GMP, data integrity, and regulatory requirements. - Excellent communication, technical writing, and organizational skills. - Familiarity with LIMS, Empower, and quality software tools
Später ansehen04.06.25 | Vollzeit | Couvet | JobLeads GmbH | CHF 100’000 - CHF 125’000 Understanding of GMP, data integrity, and regulatory requirements. - Excellent communication, technical writing, and organizational skills. - Familiarity with LIMS, Empower, and quality software tools. - Excellent team spirit. - Open-minded, adaptable, and solution-oriented, with a collaborative mindset. - Very
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