A leading organisation in the pharmaceutical industry is seeking a Regulatory Affairs associate to join their dynamic team based in Kent. This role offers a hybrid working pattern and you will play a crucial role in ensuring the accuracy and timely delivery of publishing activities, contributing to the successful delivery of the portfolio.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Regulatory Affairs associate will be varied however the key duties and responsibilities are as follows:
1. As the Regulatory Affairs associate, you will support publishing activities, ensuring accuracy and timely delivery against challenging deadlines.
2. As the Regulatory Affairs associate, you will collaborate effectively with team members to ensure successful delivery of the portfolio.
3. As the Regulatory Affairs associate, you will support the implementation of future digital solutions to streamline publishing processes.
4. As the Regulatory Affairs associate, you will contribute to business testing and validation activities to ensure system functionality and regulatory compliance.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Technical Publisher we are looking to identify the following on your profile and past history:
1. Relevant degree in a related field.
2. Proven industry experience in a technical or publishing role.
3. A working knowledge and practical experience with document management systems and regulatory submissions.
This entry-level position provides full training, making it an excellent starting point for those eager to enter the pharmaceutical industry. The role focuses on delivering high-quality regulatory submissions to national and international markets, securing health authority approval, and ultimately delivering essential medicines to patients worldwide.
Key Words:
Technical Publisher / Regulatory Affairs Associate / Regulatory Submissions / eCTD / CTD / Document Management Systems / Publishing Software / Pharmaceutical Industry / Life Sciences / Publishing Activities / Submission Management / Health Authority Submissions / Digital Transformation / Regulatory Compliance / System Validation / Business Testing / Data Integrity / Quality Assurance / SOPs / Regulatory Documentation / Global Submissions / Electronic Publishing / Validation Activities / Workflow Optimisation / Process Improvement / Stakeholder Collaboration / Cross-Functional Teams / Attention to Detail / Compliance Standards / Training and Development / Change Management / Submission Timelines / Project Coordination / Regulatory Lifecycle Management / Clinical Documentation / User Acceptance Testing (UAT) / System Implementation / Data Management / Innovation in Publishing / Continuous Improvement / Operational Efficiency / Industry Regulations / EMA / FDA / MHRA / Document Control / Audit Readiness / Submission Publishing Tools
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.