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Provides global regulatory leadership of assigned program(s); Develops global regulatory strategies, including risk assessment and mitigation strategies; Participates in strategic...
You will take charge of leading regulatory CMC strategy and execution for one or more transformative medicine programs. This pivotal role involves developing and implementing...
Implementing and maintaining pharmacovigilance activities and associated quality management system at the national level including oversight of such activities in other Hub...
You are responsible for clinical trial sample management in a GCP environment; You are responsible for streamlining processes across all different sample types; You manage/own...
This role will be pivotal in integrating quantitative methods to advance the development of innovative therapeutics, including small molecules, antibodies, and antibody-drug...
Are you an experienced Regulatory Affairs leader with a passion for medical devices? Are you looking for a motivated and diverse department to empower, guide and mentor Applied...
You are responsible for providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical...
Providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace...
The position leads the Global Development Team for the Asset and works in partnership with other global asset functions in accordance with Target Product Profiles (TPP) as jointly...
Accountable for external PV vendor development and oversight, including quality, performance and compliance of cases, support budget review and strategies of tasks outsourced to...
You'll play a crucial role in managing compliance with evolving regulations like REACH, offering a challenging yet rewarding professional environment. In detail, you will...
Provides operational expertise, strategic insights, and cross-functional leadership that enables the delivery of assigned trials within quality standards, agreed upon timelines and...
The right candidate plays a key role in the execution of country medical affairs plans and tactics and delivers regional/national clinical, scientific and technical educational...
As our new Associate Director/Director, Global PV Operations you will become responsible for PV Operations activities and provide strategic and operational PV/quality/safety...
Establish the EMEA regulatory strategy for marketed and pipeline products and ensure it is in line with the global regulatory strategy, taking into account the diverse needs of the...
Develop and implement regulatory strategies for successful product approvals; Provide strategic guidance to cross-functional teams on regulatory requirements and risks Ensure...
The Medical Affairs Manager provides support to the Clinical Evaluation Group for ongoingly assess the safety and performance clinical data of the Bausch+Lomb Surgical Medical...
Provision of regulatory input and support to Post-Approval Regulatory procedures in EU and ROW (document quality and accuracy, coordination of input from other line functions,...
In this role, you will be responsible for leading an operational team that provides a range of services related to laboratory analysis within clinical trials for our clients. This...
Ensure that all products in scope are designed, manufactured and distributed in such a way that they are safe and effective for their intended use and meet applicable regulatory...
Provide strategic medical safety leadership and practical contributions for assigned product(s) in a cross-functional setting; Perform safety signal management and benefit risk...
Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a...