Regulatory Affairs - Pharma jobs

• London
• Negotiable
• Posted 13 days ago

Global professional services company need a Senior strategic OTC Regulatory Affairs manager to manage Health Authority approvals for their clients pharmaceutical portfolio. This role involves guiding regulatory strategy, overseeing submissions, and maintaining critical dossier information. Specif...

• London
• Negotiable
• Posted 13 days ago

Professional services company need a Global Strategic Regulatory affairs manager to Support the RA Partner business leading implementing global regulatory strategies for marketed brands. The assignment will be 12 months, with the likelihood of an extension. Duties: Develops and implements global ...

• England
• £40 - £60 per hour
• Posted 13 days ago

The Role: Prepare and maintain national labelling (SmPC, PIL and labels) Prepare dossiers to meet national submission requirements for new licences, licence renewals, variations, PSURs and DSURs Maintain national aspects of global regulatory systems 1. To prepare and maintain national labelling (...

• California
• US$150000 - US$180000 per annum + Bonus and Benefits
• Posted 13 days ago

MSI Pharma is currently hiring a Regulatory Affairs Associate Director for one of our Pharma clients in the US. The Associate Director Regulatory Affairs will be responsible for the regulatory review and approval of all labeling, based on development and management of a target product profile (TP...

• San Francisco
• Negotiable
• Posted 19 days ago

Sr Compliance Manager, USA, Hybrid, Competitive Pay Rate! Key responsibilities include: - Compliance SME - Generating compliance metrics and data - Leading cross functional initiatives - Strategic partner for study teams - Developing SOPs, job aids etc

• High Wycombe
• £35 - £38 per hour
• Posted 25 days ago

MSI Pharma is partnering with one of the largest and diversified healthcare organizations in the world on a Regulatory Data (XEVMPD) role on an initial 12-month contract - with the possibility of extension. This is a global role supporting data needs in the EU, US and the Rest of the World; with ...

• England
• Negotiable
• Posted 25 days ago

MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a UK based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the UK Responsibilites: Manage the timely preparation (may include authoring) and delivery of CMC contributions to the r...

• High Wycombe
• £35 - £38 per hour
• Posted 27 days ago

MSI Pharma is partnering with one of the largest and diversified healthcare organizations in the world on a Regulatory Data (XEVMPD) role on an initial 12-month contract - with the possibility of extension. This is a global role supporting data needs in the EU, US and the Rest of the World; with ...

• New Jersey
• US$15 - US$25 per hour
• Posted 27 days ago

Interacts with complainants and obtains essential information required to document technical complaints Provides customer service and support to meet the needs of the complainants Evaluates complaints for severity and risk to public safety. Monitors and tracks sample receipt from critical complai...