Denmark Job Openings
Ferring Pharmaceuticals, Inc.
QA Manager GCP and GVP Compliance
Kastrup
FULL TIME
November 15, 2024
If you are looking for a job where you can unfold the full palette of your knowledge within Good Clinical Practice & Good Pharmacovigilance Practice this is the right job for you. In Ferring you will join a successful, global market leader and work with a broad and exciting product portfolio – and you will do it together with highly skilled colleagues in a well-functioning team.
Your day at Ferring
Your primary focus is optimization of our clinical and pharmacovigilance processes in collaboration with stakeholders such as compliance functions within the Clinical Development, Regulatory Affairs and Pharmacovigilance business areas. By focusing on continuous improvement, advisory and compliance support you will have ample opportunities to influence our way forward. Your primary tasks will be to:
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Participate and support quality improvement projects including reviewing procedures related to areas such as clinical operations, PV system, regulatory affairs and discovery including non-clinical development.
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Support and facilitate implementation of quality aspects in Ferring processes
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Support the assessments of quality risks covered by the supported stakeholder areas including implementation of mitigating actions
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Lead and support quality harmonization both locally and globally across Ferring Clinical Development sites along with compliance related to the use of computerised systems
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Contribute to the follow up on clinical and pharmacovigilance audit observations and deviations together with trending of observations and CAPAs
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Prepare relevant quality training programs and act as trainer
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Participate in preparation for and coordination during and after Regulatory Inspections
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Develop and maintain departmental quality metrics
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Write and update relevant SOPs owned by the department
We are looking for a profile with knowledge, experience and drive to take on a role as outgoing support and enabler for the business. You must bring:
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At least 4+ years’ experience with clinical and/or pharmacovigilance activities/processes.
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An insight and understanding of important quality processes such as deviation, audit and inspection management as well as management review.
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Extensive stakeholder management skills
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Previous experience from working in a compliance or QA role is a preference but not a prerequisite for applying.
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Experience in working cross-organizationally and ability to create sustainable relationships – across cultural, professional and geographical borders.
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Very good communication skills
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Fluent English, written and spoken
People come first at Ferring
You will join a global team with 11 competent and dedicated colleagues which are responsible for the overall quality assurance of Ferring’s Global R&D, Marketing and Sales and Pharmacovigilance activities. The working atmosphere is characterized by respect, helpfulness and a shared passion for improving life for our patients.
Contact and application
For additional information, please contact Head of Global Clinical Quality Caroline Sandström on +452878 7211. Your CV in English should be sent as soon as possible as we review applications on an on-going basis.
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