Regulatory Document Specialist

Job DescriptionEli Lilly And Company is a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.We are committed to...

Company OverviewEli Lilly And Company is a global healthcare leader headquartered in Indianapolis, Indiana. We unite caring with discovery to make life better for people around the world.We are dedicated to improving human health and well-being through the discovery and development of innovative medicines and services.Job DescriptionThe GSC Regulatory...

The PM Group is seeking a skilled Documentation Specialist to join its dynamic OTS team.This role involves creating, maintaining, and improving technical documentation related to manufacturing processes, regulatory compliance, and operational procedures.Develop high-quality technical documents, including SOPs, work instructions, batch records, equipment...

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...

ref.01233Documentation Specialist Exciting opportunity for a Documentation Specialist with our client, a leading multinational Pharmaceutical company based in Brinny, Co. Cork.This is an 11-Month contract opportunity with hybrid working options.Responsibilities • Creating, editing, and formatting of SOPs, Work Instructions, and other documents on the EDMS...

Role OverviewWe are seeking a highly skilled Regulatory Documentation Writer to join our team at eir evo talent. As a key member of our team, you will be responsible for creating high-quality clinical trial documents that meet regulatory and company-specific guidelines.Your primary responsibilities will include:Developing and finalizing clinical trial...

Key ResponsibilitiesThis contract role requires a Medical Writer to possess a strong understanding of clinical pharmacology, therapeutic areas, and medical science. The ideal candidate will have experience in writing regulatory or clinical trial documents and have demonstrated mastery of written English. Additionally, they will be able to lead the scientific...

Company OverviewLeveraging our extensive network and expertise in life sciences recruitment, we provide tailored solutions for clients and candidates alike. Our commitment to excellence drives us to deliver results-oriented recruitment services that meet the evolving needs of our clients.Role Description:This Medical Writer role presents an exciting...

We are seeking a highly skilled Quality Documentation Specialist to join our team in Cork. The successful candidate will be responsible for reviewing and maintaining the accuracy of Production Batch Records, GMP Documentation and Electronic Systems associated with the Site Production Teams.Main duties and responsibilities:Upload documents in line with site...

About the RoleWe are looking for a highly skilled Documentation Specialist to join our team in Cork. As a key member of our project team, you will play a critical role in ensuring that all documents related to our products are accurate, complete, and compliant with regulatory requirements.Your responsibilities will include creating, editing, and formatting...

Company OverviewWe are a leading consultancy services provider, dedicated to delivering high-quality solutions in the pharmaceutical industry. Our team is passionate about excellence and committed to driving growth and expansion.Job DescriptionThe role of Documentation Specialist is crucial in ensuring the smooth operation of our facility. As a key member of...

About the RoleThis is an excellent opportunity to work as a Clinical Trials Document Specialist with Eir Evo Talent. We are seeking an experienced medical writer to develop comprehensive and scientifically rigorous protocols, as well as high-quality clinical study reports and initial investigator's brochures. The successful candidate will have a strong track...

Job Overvieweir evo talent is seeking a highly skilled Clinical Research Document Specialist to join our team. As a key member of our medical writing department, you will be responsible for creating high-quality clinical trial documents that meet regulatory requirements.

Senior Regulatory Affairs Specialist (Contract) Position SummaryWe are seeking a dynamic and experienced Self-Employed/Freelance Senior Regulatory Affairs Specialist. This role is pivotal in ensuring our products and services adhere to all relevant regulations and standards. The successful candidate will collaborate with cross-functional teams to facilitate...

At Hibernia Services Limited, we are seeking a highly skilled Clinical Research Document Specialist to join our team. As a key member of our team, you will be responsible for developing and managing high-quality clinical trial documents that meet regulatory standards.Key Responsibilities:Develop comprehensive and scientifically rigorous study protocols that...

Job Summary:This is a hybrid role, located in Cork, Ireland. As a Senior Regulatory Affairs Specialist with our client, you will provide strategic, tactical, and operational direction to expedite CMC development of the portfolio and technical agenda by supporting global clinical trial, market registration submissions, and post-approval submissions.Oversee...

About UsEli Lilly And Company is a leading developer of innovative medicines and services that improve human health and well-being.We are committed to advancing science and addressing the most pressing medical needs of our time.Job SummaryThe GSC Regulatory Specialist will be responsible for supporting the delivery of GSC regulatory documents, ensuring...

ResponsibilitiesThe Specialist, GSC Regulatory Delivery plays a crucial role in supporting the delivery of GSC regulatory documents with all aspects of regulatory document planning, tracking, and compliance. Key responsibilities include:Managing and maintaining regulatory document planning and tracking tools.Generating status, productivity, and other metrics...

Job OverviewWe are seeking a skilled Regulatory Compliance Specialist to join our team at Recruitment by Aphex Group.About the RoleThe primary function of this position is to ensure compliance with Good Manufacturing Practice (GMP) regulations and Company SOPs. This role will be responsible for reviewing and approving production and analytical documentation,...

OverviewThe Outsourced Technical Services (OTS) Department at PM Group partners with Global leaders across a range of industries to find the best people for their current and ongoing business needs. Partnering with PM Group and our clients means that you will gain unrivalled experience working with global brands.We are looking for a Technical...