Quality Document Manager

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support...

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support...

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support...

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support...

Due to ambitious growth plans and high volume of project wins my scaling SME client in the Thames Valley requires a Document Controller to join their UK team. They provide high quality automated blinds and shading solutions to some of the world's biggest names and - put simply - need an organised and talented star to help them meet the demand for their...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support...

Job Description As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. We are...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. We are looking for a full...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. We are looking for a full...

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regulatory Intelligence Triage Manager, responsible for driving...

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization.  The position holder responsibility includes the entire CSL product portfolio and development pipeline.Be one of the first applicants, read the complete overview of the role below, then send your application...

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline.Responsibilities include: -Acts as a Regulatory Intelligence Triage Manager, responsible for driving initial...

Job Title: QA Officer – Supply ChainSalary: Highly competitive with 8% annual bonus (dependent on experience)Location: Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well established Quality team, focusing on the supply chain.We are...

Job Title: QA Officer – Supply ChainIf the following job requirements and experience match your skills, please ensure you apply promptly.Salary: Highly competitive with 8% annual bonus (dependent on experience)Location: Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who...

Job Title: QA Officer – Supply ChainSalary: Highly competitive with 8% annual bonus (dependent on experience)Location: Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well established Quality team, focusing on the supply chain.We are...

Job Title : QA Officer – Supply Chain Salary: Highly competitive with 8% annual bonus (dependent on experience) Location : Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well established Quality team, focusing on the supply chain. We...

Job DescriptionJob Title: QA Officer – Supply ChainSalary: Highly competitive with 8% annual bonus (dependent on experience)Location: Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well established Quality team, focusing on the supply...

Job Title: QA Officer – Supply ChainSalary: Highly competitive with 8% annual bonus (dependent on experience)Location: Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well established Quality team, focusing on the supply chain.We are...

Job Title: QA Officer – Supply ChainSalary: Highly competitive with 8% annual bonus (dependent on experience)Location: Maidenhead (Hybrid, minimum 1 day on site but ideally 2-3 days). SRG is exclusively working with a global pharmaceutical company who require a QA Officer to join their well established Quality team, focusing on the supply chain.We are...