About the role This is your chance to join a company that unites people across the world through its unique and innovative product line of medical devices! Be part of a small but truly global company, with manufacturing plants in Switzerland and the US and a presence in 3 of the world's major continents.
My client is one of the worlds most respected & successful pharmaceutical companies. They are currently looking for a Regulatory Affairs Manager to join their team in Maidenhead. This is a rare opportunity to join one of the industries most innovative companies! An opportunity not to be missed for any experienced Regulatory Affairs Professional!
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Regulatory Affairs Manager - Global Office based with home working Cambridge Permanent
Company/Role Overview: This fast paced worldwide CRO organization is seeking talented individuals to join their team. The role will be mostly office-based but would offer 2 days home working. Working in the global team the Regulatory Manager is a high visibility role which would include direct line management of junior staff.
Our client is searching for an experienced Regulatory Affairs CMC Manager / Lead who can provide expert advice with the pharmaceutical industry.
Within the role you will be responsible and will be part of the Project management team overseeing successful initiation, execution and completion of Regulatory, CMC and Publishing programs for their global clients.
This unique opportunity is for a Consultancy based in London, which offers the flexibility of home working. ...
Opportunity for an experienced Emerging Market Regulatory Affairs Manager to join this global Pharma Company on a permanent basis. Remit includes line managing 2 Senior Regulatory Associates, ensuring effective strategic input to Global Regulatory Plans, and that teams / functional groups are provided with clear, constructive regulatory input to assist planning and issue resolution across lifecycle activity. Excellent promotional / development opportunities.
Regulatory Affairs Manager - Germany
Baden-Wurttemberg, Office-based. An exciting opportunity has arisen for an experienced Regulatory Affairs Manager looking for a new, diverse challenge in Regulatory Affairs. My client, a global pharmaceutical company is looking for a Manger to provide leadership to a team of associates and consultants, provide a variety of consulting services, and to work within project guidelines to achieve project objectives and address client issues.
Regulatory Affairs Manager - Switzerland
Basel or Geneva, office-based. An exciting opportunity has arisen for an experienced Regulatory Affairs Manager looking for a new, diverse challenge in Regulatory Affairs. My client, a global pharmaceutical company is looking for a Manger to provide leadership to a team of associates and consultants, provide a variety of consulting services, and to work within project guidelines to achieve project objectives and address client issues.
Regulatory Affairs Manager - Belgium
An exciting opportunity has arisen for an experienced Regulatory Affairs Manager looking for a new, diverse challenge in Regulatory Affairs. My client, a global pharmaceutical company is looking for a Manger to provide leadership to a team of associates and consultants, provide a variety of consulting services, and to work within project guidelines to achieve project objectives and address client issues.
The role of Regulatory Affairs Manager is responsible for planning regulatory submissions, mentoring and supervising a team for provision and maintenance of core dossiers and co-ordination of labelling activities. Through leading cross functional project teams, you’ll ensure preparation of high quality documentation for all regulatory submissions, both medicinal products and devices, whilst building relations with Reg bodies in order to expedite approval.
My innovative and expanding medium sized Pharmaceutical client is seeking a regulatory affairs snr manager with broad experience for a regulatory affairs role covering both pre and post marketing phases for a range of therapeutic categories and dosage forms. Contact Theo Moore for full details or to apply on 0207 801 3384 or via email at Cv@advregulatory.com
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