Scientific Documentation Expert

About the PositionWe are seeking a detail-oriented Scientific Documentation Coordinator to join our team at Life Science Recruitment. As a key member of our team, you will be responsible for coordinating and reviewing scientific documents, preparing reports, and implementing change control procedures.ResponsibilitiesDocument coordination and reviewReport...

About the JobWe are seeking a skilled Scientific Documentation Professional to join our team at evo talent. In this role, you will be responsible for the development and management of high-quality clinical trial documents, including study protocols, initial investigator's brochures, and clinical study reports.The ideal candidate will have a strong background...

Life Science Recruitment Ltd is currently recruiting for a Medical Writer to join their team. In this role, you will work closely with cross-functional teams to facilitate external scientific publications and regulatory documents.About the Role:You will plan, write, edit, review, and coordinate the publication of scientific data through peer-reviewed...

Job SummaryHibernia Services Limited is seeking a Regulatory Documentation Expert to join our team. As a Regulatory Documentation Expert, you will be responsible for developing and finalizing high-quality clinical trial documents, including study protocols, protocol amendments, investigator brochures, and clinical study reports.You will work closely with...

**Senior Analytical Scientist Position:**We are seeking an experienced Senior Analytical Scientist to join our team at ThermoFisher Scientific in Cork, Ireland. In this role, you will be responsible for developing, validating, and transferring quality methods to support the manufacture of high-quality products.Develop, validate, and transfer quality methods...

Company OverviewAt Thermo Fisher Scientific, we enable our customers to make the world healthier, cleaner and safer. Our team of 100,000+ colleagues shares a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support...

About the OpportunityWe have an exciting opportunity for a Laboratory Development Expert to join our team at Scientific Update Ltd.Develop and maintain detailed knowledge of process chemistry, including mechanisms and impurity control.Provide technical support for Capital engineering projects relating to new customer products and major process...

Job Summary:\TN Ireland is seeking a skilled Medical Writer to create high-quality clinical trial documents that meet regulatory requirements and support the advancement of innovative therapies. As a Medical Writer, you will develop scientifically accurate and regulatory-compliant documents, conduct literature reviews, and collaborate with cross-functional...

Job OverviewClinical trials documentation requires a high level of expertise in medical writing, regulatory compliance, and project management. As a Medical Document Specialist at Hibernia Services Limited, you will be responsible for authoring, reviewing, and finalizing clinical trial documents, including study protocols, investigator brochures, and...

Job DescriptionWe are looking for a motivated and detail-oriented Regulatory Affairs Specialist II to join our team at Boston Scientific. As a key member of our regulatory affairs team, you will be responsible for providing regulatory support to our product sustaining process, including submissions, maintenance of regulatory files, and regulatory...

**Join Our Team**We're seeking an experienced Analytical Development Manager to join our team at Scientific Update Ltd. In this role, you'll lead analytical discussions with customers, communicate with subject matter experts, and ensure safety standards are met.Lead analytical technology transfer activities and transfer analytical methods to QC and IPC...

Job Title: Laboratory Process ExpertJob Summary:We are seeking an experienced Laboratory Process Expert to join our team at Scientific Update Ltd. The successful candidate will be responsible for providing expert guidance on process chemistry, supporting laboratory operations, and collaborating with cross-functional teams to drive process improvement...

Our Company CultureWe value innovation, collaboration, and continuous learning at EPM Scientific. Our team members are encouraged to share their ideas and contribute to the company's growth and success. As a Technical Development Specialist, you will have the opportunity to work with experienced professionals in the field and develop your skills through...

Boston Scientific Gruppe is a leader in medical science, dedicated to advancing science for life by transforming lives through innovative medical solutions.We are seeking an experienced High-Yield Manufacturing Expert to join our team on a permanent basis. As a key member of our R&D Engineering and Manufacturing teams, you will be responsible for developing...

Job Description:\In this role, you will play a critical part in the development of high-quality clinical trial documents. Your primary focus will be on developing scientifically accurate and regulatory-compliant documents that support the advancement of innovative therapies.\This position requires extensive experience in medical writing within the clinical...

Social network you want to login/join with:Publications Scientific Communications Associate, CorkClient:Location:Cork, IrelandJob Category:OtherEU work permit required:YesJob Reference:1df29500b86cJob Views:143Posted:21.01.2025Expiry Date:07.03.2025Job Description:Publications Scientific Communications AssociateOur client, a global pharmaceutical...

**Quality Control and Assurance Specialist:**We are looking for a highly skilled Quality Control and Assurance Specialist to join our team at ThermoFisher Scientific in Cork, Ireland. In this role, you will be responsible for ensuring the quality and integrity of our products by developing, validating, and transferring quality methods.Develop, validate, and...

Key ResponsibilitiesPlan and manage timelines for document development, ensuring timely delivery of high-quality deliverables.Conduct quality checks to ensure accuracy, consistency, and completeness of data and content.Provide expert guidance to team members on medical writing best practices, regulatory requirements, and document standardization.

Quanta Consultancy Services Ltd is seeking a skilled Documentation Expert to join our team. As a key member of our organization, you will play a crucial role in ensuring the accuracy and compliance of our technical documentation.About the RoleWe are looking for an experienced Technical Documentation Specialist who can create, edit, and maintain high-quality...

Job DescriptionDocument Development: Author, review, and finalize high-quality clinical trial documents, including study protocols, investigator brochures, and clinical study reports.Regulatory Compliance: Ensure all documents comply with ICH GCP, regulatory requirements, and internal SOPs.Scientific and Literature Support: Conduct thorough literature...