About the Company: Operating as a progressive and highly respected pharmaceutical manufacturer our client is well known for its operational excellence, passion for innovation and its quality branded products. An opportunity has now arisen for a Regulatory Affairs Associate to provide regulatory support for the lifecycle for manufactured products within the Asia Pacific Markets. About the Opportunity: Reporting to the Senior Director, key duties include the following: Be responsible for regulatory submissions such as new licence submissions, applications, renewals, submission of documentation. Lead preparation & contribute to briefing packages associated with established products. Support lifecycle management & actively coordinate documents, packages & dispatch & submission of responses. Prepare operational & strategic project work, preparing applications. Effectively maintain key internal & external stakeholder relationships. About You: The successful candidate will have the following skills & experience: Tertiary qualifications in Science or related industry. Sound experience in pharmaceutical/biotechnology industry essential. Minimum of 3 years experience in similar role. Sound experience in Category 1 and Category 3. Well developed interpersonal and communication skills. Sound organisational skills including planning & time management. Ability to liaise effectively with all internal & external stakeholders. Culture & Benefits: This is an Excellent Contract Opportunity for a Regulatory Affairs Associate to join a global pharmaceutical company & provide regulatory support for lifecycle pharmaceutical manufactured products within the Asia Pacific Markets. This is a Melbourne Based Opportunity and is a HYBRID role offering WFH & Office Based Flexibility. How To Apply To apply for the position, please click APPLY below below. For confidential discussion, please contact Maria Julienne on 0491 694 371 or Sue Campbell on 04147 994 917. NB - Only shortlisted candidates will be contacted.
