Regulatory Affairs Associate - Hybrid/Pharma/Contract

Orion Group Life Sciences are currently recruiting a Regulatory Affairs Associate on behalf of our Multinational Biopharmaceutical Client based in Buona Vista, Singapore on an initial 12-Month contract with potential to extend. Hybrid role.

Key responsibilities

• Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.

• Acts as Submission Management support to project teams providing guidance and communication of established submission processes and standards. Provides input to project publishing timelines and deliverables.

• Participates in submission team meetings. Expedites, manages, and coordinates multiple concurrent interrelated activities for submission projects in the delivery of low to moderately complex published submissions within the required timelines. Anticipates obstacles and proposes solutions within the team.

• Coordinates submission publishing with offsite publishers/provides notification to ensure resources are available to meet submission timelines. Prepares content planner for publishing and works with vendor to resolve publishing issues

• Facilitates the creation or procurement of submission content deliverables such as cover letters and forms

• Performs detailed quality reviews of published output to ensure compliance with Regulatory Standards and Health Authority guidance’s including verification of content, bookmarks, hypertext links and tables of content in low to moderately complex submissions. Facilitates team reviews.

• Contributes to the development of optimal business processes and standards within the department to ensure high levels of customer support and to achieve high quality submissions. Contributes to the implementation of internal process and standards documents relating to publishing and publishing deliverables.

• Suggests and contributes to process improvements, including changes to software and business processes. May participate on internal project teams to update business software.

• Demonstrates ability to influence without direct authority. Builds and maintains positive relationships internally and externally.

Qualifications

• Bachelor’s degree
• PMP and RAC certificates desirable.

Competencies

• Pharmaceutical or industry related experience

• Experience working in a complex and matrix environment

• Strong communication skills both oral and written

• Experience in Regulatory Affairs preferred but may consider QA, R&D/support, Scientific affairs, operations or related area

• Experience in Regulatory Operations, including regulatory submission project management and/or submission publishing is preferred.