Regulatory Affairs - Pharma jobs

• United States of America
• Negotiable
• Posted 4 days ago

MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a US based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the USA. In this role you will: Serve as the CMC Product Lead for assigned products and be accountable for the delivery ...

• United States of America
• Negotiable
• Posted 4 days ago

We are currently hiring a Global Labelling Associate (GLA) for one of our global Pharmaceutical clinets to support their end-to-end non-US/Central EU (Most of World) labeling development and implementation. This position provides innovation and technical expertise for the creation, maintenance an...

• Belgium
• Negotiable
• Posted 4 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...

• High Wycombe
• £35 - £38 per hour
• Posted 4 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 ...

• California
• US$150000 - US$180000 per annum + Bonus and Benefits
• Posted 4 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 4 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 4 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...

• Belgium
• Negotiable
• Posted 4 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...

• England
• Negotiable
• Posted 4 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• Cambridge
• Negotiable
• Posted 10 days ago

MSI Pharma have partnered with a global pharmaceutical organisation in the US who are seeking a Global Regulatory Director to spearhead transversal projects for the success of the business and company goals. Responsibilities You will ensure the development of robust regulatory strategies for mult...

• New Jersey
• US$15 - US$25 per hour
• Posted 14 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...

• United States of America
• Negotiable
• Posted 14 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• Belgium
• Negotiable
• Posted 14 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 18 days ago

Specialist consultancy are looking to hire a dedicated consultant to support a Veeva implementation for a Switzerland based Pharmaceutical company, but the role can be done remotely from anywhere in Europe. As you are aware, the EMA are publishing a lot of detail around EU IDMP Implementation Gui...

• New Jersey
• US$15 - US$25 per hour
• Posted 18 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 18 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...