Aktuelle Jobs im Zusammenhang mit QA Manager Clinical GCP audits and compliance - Zürich, Zürich - gloor & lang ag life science careers
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Zürich, Zürich, Schweiz Takeda VollzeitAbout the Role:We are seeking an experienced Associate Director, Clinical Quality Compliance to join our team at Takeda. As a key member of our Clinical Quality Compliance function, you will be responsible for providing quality oversight to our clinical trial delivery quality systems, promoting operational and compliance excellence, quality risk management,...
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Associate Director, Clinical Quality Compliance Specialist
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Clinical Project Manager
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Compliance Operations Lead, Associate Director
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Compliance Operations Lead, Associate Director
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Pharmacovigilance Audit Manager
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Pharmacovigilance Audit Manager
vor 2 Wochen
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vor 2 Wochen
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Compliance Operations Lead, Associate Director
Vor 2 Tagen
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Audit Manager
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Technical Software License Compliance Specialist
vor 2 Wochen
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Clinical Excellence Manager
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Compliance Manager
Vor 4 Tagen
Zürich, Zürich, Schweiz Alpinum Solutions AG VollzeitJob OpportunityWe are seeking a highly skilled Compliance Manager to join our team at Alpinum Solutions AG.About the RoleThe successful candidate will be responsible for developing and implementing a robust Compliance Management System (CMS) tailored to our industrial operations. This will involve ensuring the CMS aligns with international standards and...
QA Manager Clinical GCP audits and compliance
vor 3 Monaten
For further support with the growing QA activities we seek to recruit an experienced QA person, familiar with GCP audit activities.
The position is defined on a temporary base and has high chance to develop into a perm role still this year.
We are looking for an independent, experienced hands-on professional, able to manageand keep QA oversights related to GXP incl coordination of internal trainings, manage related projects andsupport cross-fct teams. On site presence up to 4 days/week required.
Your tasks:
Oversight for QMS Quality Management System
Provides Quality Oversight prior to/ during/ close-out of clinical trials
Leads GCP/GMP/GLP Vendor Qualifications
Organize and lead audits at GCP/GMP vendors
Coordinates the conduct of internal audits and regulatory inspections
Your profile:
B.Sc, M.Sc. Life Sciences
3-5 years of experience in Clinical QA Operations
Experience in CRO and Clinical Vendor Management
Excellent knowledge in GCP and GMP regulations
Your autonomy, your integrity, and your initiative are of particular value. Your service-oriented approach will be of help to liaise with all internal and external stakeholders involved. Join our customer as the next reliable team member in this familial work environment. Working place is close to public transportation within Zurich area.
