Select Oh | Regulatory Affairs Manager

An excellent opportunity has arisen for a Regulatory Affairs Executive to join my client based in Berkshire and focusing on cGMP, solid dosage generic pharmaceuticals.Responsibilities: Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure.These include new licence applications, variations (including...

Are you a skilled professional looking for a challenging opportunity in regulatory affairs?About the RoleWe are seeking a highly motivated and experienced Regulatory Affairs Executive to join our team at Select OH, based in Berkshire. This exciting role will focus on cGMP, solid dosage generic pharmaceuticals.As a key member of our team, you will be...

Job DescriptionAn exciting opportunity has arisen for an experienced Regulatory Affairs Manager to join our team at Select OH. As a key member of our post-approval team, you will be responsible for managing licenses and maintaining regulatory relationships.The ideal candidate will have a strong understanding of the generic pharmaceutical industry and be able...

Are you ready for a new challenge in regulatory affairs? We are currently seeking an experienced Regulatory Affairs Executive to join our team at Select OH, based in Berkshire.About the JobThis is an exciting opportunity to join a dynamic team focused on cGMP, solid dosage generic pharmaceuticals. As a key member of our team, you will be responsible for...

Join us at Select OH, a leading generic pharmaceutical company, where we are seeking an experienced Regulatory Affairs Manager to join our team. As part of our continued growth, this is an exciting opportunity to take on a new challenge in a dynamic environment.About the RoleThis key position will be responsible for ensuring that all post-approval activities...

An excellent opportunity has arisen for a Regulatory Affairs Executive to join my client based in Berkshire and focusing on cGMP, solid dosage generic pharmaceuticals.Scroll down to find the complete details of the job offer, including experience required and associated duties and tasks.Responsibilities: Prepare and submit applications of reliable quality in...

An exciting opportunity has become available with my client, a growing pharmaceutical company, for an experienced and enthusiastic Regulatory Affairs professional wishing to expand their experience and knowledge in a growing Reg team.With a focus on post-approval activities, the successful candidate will gain exposure to many aspects of Regulatory compliance...

An excellent opportunity has arisen for a Regulatory Affairs Executive to join my client based in Berkshire and focusing on cGMP, solid dosage generic pharmaceuticals.Responsibilities: Prepare and submit applications of reliable quality in a timely manner to MHRA (UK) via National Procedure.These include new licence applications, variations (including...

Job SummarySelect OH is seeking a Deputy Regulatory Manager to play a critical role in the preparation and submission of Marketing Authorization applications. The successful candidate will be responsible for collecting, organizing, and tracking documentation in eCTD format.Responsibilities:Verifying documents for accuracy and completeness.Compiling CTD...

We are looking for a skilled Pharmaceutical Regulatory Affairs Specialist to join our team at Select Pharma Limited. As a key member of our regulatory affairs department, you will play a crucial role in ensuring compliance with regulatory requirements.About the Role:In this position, you will be responsible for converting existing applications to eCTD...

**Job Summary**Select Pharma is looking for an enthusiastic and experienced Regulatory Affairs professional to join its growing Reg team. The ideal candidate will have a strong background in Regulatory compliance and a proven track record of successfully managing post-approval activities.The estimated salary for this role is around $90,000 - $120,000 per...

An exciting new opportunity has arisen for a Regulatory Affairs Associate to join my client, a growing pharmaceutical company based in Berkshire.This role will suit a regulatory professional at the beginning of their career please note that 6 months to 1 year of regulatory experience is required.Interested in learning more about this job Scroll down and find...

An exciting opportunity has become available with my client, a growing pharmaceutical company, for an experienced and enthusiastic Regulatory Affairs professional wishing to expand their experience and knowledge in a growing Reg team.If your skills, experience, and qualifications match those in this job overview, do not delay your application.With a focus on...

An exciting opportunity has become available with my client, a growing pharmaceutical company, for an experienced and enthusiastic Regulatory Affairs professional wishing to expand their experience and knowledge in a growing Reg team.With a focus on post-approval activities, the successful candidate will gain exposure to many aspects of Regulatory compliance...

An exciting new opportunity has arisen for a Regulatory Affairs Associate to join my client, a growing pharmaceutical company based in Berkshire. This role will suit a regulatory professional at the beginning of their career please note that 6 months to 1 year of regulatory experience is required.++ Please note that this role is fully office based (5 days...

Responsible for collecting, organising, and tracking of documentation required for Marketing Authorisation application and response to questions in eCTD format.Check documents for accuracy, consistency, deficiencies, and compliance with regulatory submission requirements Compile module 1-5 CTD registration package for new Marketing Authorisation...

Are you an enthusiastic Regulatory Affairs professional looking to expand your experience and knowledge in a growing pharmaceutical company? We have an exciting opportunity for a skilled Chemical Regulatory Specialist to join our team!About the Role:We are seeking an experienced professional to lead post-approval activities, ensuring compliance with...

**Job Description**Select Pharma is a rapidly expanding pharmaceutical company that requires an experienced Regulatory Affairs professional to join its team. The successful candidate will have a strong background in Regulatory compliance and be able to effectively manage post-approval activities.The estimated salary for this role is around $100,000 -...

Key ResponsibilitiesDocument Accuracy and Compliance: Check documents for accuracy, consistency, deficiencies, and compliance with regulatory submission requirements.Compilation and Submission: Compile module 1-5 CTD registration package for new Marketing Authorisation submissions and submit necessary applications through electronic channels.Collaboration...

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan...