Document Management Specialist

Job Title: Document Management SpecialistWe are seeking an experienced Document Management Specialist to join our Compliance, Technology & Innovation team based in Trumpington, Cambridgeshire.This role will play a pivotal part in setting up, managing and maintaining our document control systems across the firm.The successful candidate will lead the design...

At Ridgeway and Co, we are seeking a skilled Document Management Specialist to coordinate all activities related to our document control procedure. The successful candidate will be responsible for managing technical documents, drawings, and commercial correspondence. This role requires strong knowledge of electronic document management systems, as well as...

About the RoleWe are seeking a highly organized and detail-oriented Document Management Specialist to join our dynamic team at Phoenix ME. This is an exciting opportunity for an individual with excellent communication skills and a passion for construction projects.The successful candidate will be responsible for managing and maintaining project...

About the RoleAt uWorkin, we are seeking a skilled Document Management Specialist to support our document management process and contribute to continuous improvement efforts.This is an excellent opportunity to join a clean renewable company with a legacy of 100+ years.You will have the chance to make a lasting impression by supporting contemporary ways of...

We are seeking a skilled Document Control Specialist to join our team at the Henry Martin Group. This role is pivotal in ensuring the efficient management and control of all project documentation.Key Responsibilities:Manage and maintain accurate records of project documents and drawings using Viewpoint/4Projects.Ensure all project documentation is...

We are looking for a highly skilled Scientific Document Specialist to join our team at Costello Medical.About the RoleThis role involves working on projects that require the creation of high-quality scientific documents, including posters, slide sets, value dossiers, reports, and peer-reviewed publications. You will work in project teams alongside...

We are seeking an experienced professional to join our Compliance, Technology & Innovation team based in Trumpington, Cambridgeshire.This role will play a pivotal part in setting up, managing and maintaining our document control systems across the firm.You will be responsible for leading on the design and implementation of new corporate Knowledge Management...

About the roleKey ResponsibilitiesIssuing project documentation, including technical submittals and drawings.Managing electronic filing systems for easy document retrieval.Coordinating with clients and subcontractors to ensure timely submission and review of documents.RequirementsA high level of organization and attention to detail.Excellent communication...

Costello Medical is a leading global healthcare agency specializing in medical communications, market access, and health economic and outcomes research. We are currently seeking a skilled Scientific Document Specialist to join our team.In this role, you will be responsible for developing high-quality scientific documents, including literature reviews,...

Job OverviewWe are seeking a highly skilled Regulatory Document Specialist to join our team at VCLS. As a key member of the team, you will be responsible for creating high-quality medical documents for various client projects.The ideal candidate will have a strong background in regulatory affairs and excellent writing skills. You will work closely with...

Welcome to Vivify Talent LimitedWe're a small consultancy with big ambitions, seeking an experienced Regulatory Document Specialist to spearhead key documents and projects. As a fully remote role, you'll enjoy autonomy and flexibility while collaborating with our passionate team.Your Key ResponsibilitiesDevelop top-tier regulatory documents, ensuring...

Senior/Principal Medical WriterWe are currently looking for a Senior/Principal Medical Writer to join our team in the UK. As a key member of our clinical development team, you will be responsible for producing high-quality regulatory documents for the international pharmaceutical industry.About the Role:You will prepare a variety of clinical regulatory...

Gilead Sciences is a global biopharmaceutical company that is committed to making a difference in the lives of people with life-threatening diseases. We are seeking a highly skilled Senior Medical Writer to join our dynamic team. As a Senior Medical Writer, you will be responsible for authoring complex regulatory documents, including clinical study reports,...

About the Role">As a Scientific Document Specialist, you will play a vital role in the detailed analysis and presentation of data from clinical trials, driving the successful uptake of novel therapies. You will work on projects involving the assimilation and creative presentation of analysis in different formats, including posters, slide sets, value...

We're looking for a skilled and reliable Document Control Specialist - Hydro Tasmania to join our team. As a key member of our asset management team, you will ensure all asset information and project documentation is managed and available as needed.The salary for this position is approximately $98,000 per annum, plus super. With opportunities to work across...

As a Project Documentation Manager at the Henry Martin Group, you will be responsible for ensuring the smooth flow of project documentation. This includes managing and maintaining accurate records of project documents and drawings using Viewpoint/4Projects.Responsibilities:Manage document control systems to ensure compliance with company and project-specific...

Imagine working with a clean renewable energy company that has been fuelling the future of energy for over 100 years. As a Hydro Document Manager, you will play a vital role in ensuring all asset information and project documentation is managed and available as needed.The salary range for this position is $89,558 – $110,146 plus super. With opportunities...

Unlock the Power of Industrial Software">We are seeking a talented Senior Technical Writer to join our global technical writing group at AVEVA, a leading provider of industrial software solutions.In this role, you will collaborate with skilled software engineers to create high-quality technical documentation and associated content for our products and...

Our client is seeking a highly skilled and experienced Document Controller to join their team in Cambridge. This role is pivotal in ensuring the efficient management and control of all project documentation. The ideal candidate will have a strong background in document control, with specific expertise in using Viewpoint/4Projects. Key Responsibilities: *...

Our client is seeking a highly skilled and experienced Document Controller to join their team in Cambridge. This role is pivotal in ensuring the efficient management and control of all project documentation. The ideal candidate will have a strong background in document control, with specific expertise in using Viewpoint/4Projects. Key Responsibilities: *...