Regulatory Affairs - Pharma jobs

• California
• US$150000 - US$180000 per annum + Bonus and Benefits
• Posted 15 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...

• Belgium
• Negotiable
• Posted 16 days ago

We currently have an exciting role, looking for a GRA Documentation and Learning Officer to join the headquarters office of a global Pharma company in Belgium. Key Job Functions: LEARNING Entirely review GRA training matrices (inc. IT GRA systems matrices) Set-up a training matrix in line with GR...

• High Wycombe
• £35 - £38 per hour
• Posted 17 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 ...

• Belgium
• Negotiable
• Posted 17 days ago

Please find below a brief description of the role: Start date: ASAP Duration: 6-month initial contract (with potential to extend) Location: Anderlecht, Belgium Language: English Key Job Functions: LEARNING Entirely review GRA training matrices (inc. IT GRA systems matrices) Set-up a training matr...

• Belgium
• Negotiable
• Posted 17 days ago

We are looking for a GRA Documentation and Learning Officer to join the headquarter office of a global Pharma company in Belgium. Key Job Functions: LEARNING Entirely review GRA training matrices (inc. IT GRA systems matrices) Set-up a training matrix in line with GRA, LRA (Local Regulatory Affai...

• New Jersey
• US$15 - US$25 per hour
• Posted 17 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...

• Belgium
• Negotiable
• Posted 17 days ago

We currently have an exciting role, looking for a GRA Documentation and Learning Officer to join the headquarters office of a global Pharma company in Belgium. Key Job Functions: LEARNING Entirely review GRA training matrices (inc. IT GRA systems matrices) Set-up a training matrix in line with GR...

• United States of America
• Negotiable
• Posted 17 days ago

We are hiring a experienced CMC Compliance Expert to work on a fully remote basis within the US! Key Functions include: * Experienced in authoring of assessment reports * Reviewing of quality documents (e.g. reformulation studies, process validations, particle size method implementation and speci...

• England
• Negotiable
• Posted 17 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...

• England
• Negotiable
• Posted 17 days ago

Global professional services Consultancy require several Data Scientists and Data Engineers for a project to start in November / December. The team of consultants will help with the continual advancement of their AI core extraction and classification engine by leveraging Natural Language Processi...

• United States of America
• Negotiable
• Posted 17 days ago

Global professional services Consultancy require several Data Scientists and Data Engineers for a project to start in November / December. The team of consultants will help with the continual advancement of their AI core extraction and classification engine by leveraging Natural Language Processi...