Job Description
Job Description
Senior Regulatory Affairs Associate
Looking for an exciting opportunity as a Senior Regulatory Affairs Associate with an Innovator Research-intensive biopharmaceutical Company?
Permanent Full-time position with competitive renumeration and benefits
Location Sydney, Australia
Hybrid, work from home and office environment, joining a dedicated and welcoming team
Upskill and growth in an area you’re passionate about, whilst being fully supported and encouraged
What You Will Do
Responsibilities include, however not limited to
Regulatory Project Management
Review, compile and submit complex registration dossiers and data packages, within timeframes agreed with manager and in accordance with government, industry and corporate requirements to maintain regulatory compliance and facilitate product supply.
Manage and support (including evaluating regulatory probability of success) the technical and scientific requirements of more complex regulatory applications during the pre-submission, submission, and evaluation process, ensuring timely and high-quality justifications or consultations with the Health Authorities or responses to questions from the Health Authorities in line with global guidance.
Ensure cost effective project management and coordination of work with others (including leading teams), compliance to global and local policies, and effective and timely communication of new or amended registered details to stakeholders within the company.
Regulatory and Technical Support
Provide regulatory and technical advice to other parts of the organization on complex issues to ensure that correct and compliant information is used in decision making and strategy development.
Develop and Maintain Key Relationships
Effectively participate in designated Product Life-Cycle Planning Teams, with regular and prompt attendance, completion of designated action items within agreed timeframes and appropriate contribution to discussions. Proactively recognize and communicate important PLP issues to others outside the team. Develop and maintain effective working relationships with all members of Product Lifecycle Planning team.
Actively collect, analyse and disseminate regulatory intelligence and other information and formulate strategies for best practices for a changing regulatory environment.
Effectively participate in Regulatory team discussions, bringing forward issues for consideration and contributing to the development of solutions and strategies.
Foster professional relationships with individuals within TGA and Medsafe who would be responsible for evaluating our company’s submissions.
What You Must Have
Pharmacy degree or life sciences degree, with at least four years’ experience in regulatory affairs for prescription products.
Competencies And Skills Include
Collaboration & Partnering - thinking and acting beyond one's silo - bridging boundaries across teams, functions, liaisons, geographies, external stakeholders and customers
Project Management - the ability to organise work efforts by prioritising tasks, using resources optimally, establishing appropriate deadlines and ensuring on-time delivery of tasks, deliverables and/or project results
Productive Communication - planning and delivering ideas and information to others in an impactful manner. Demonstrating the ability to listen to others, and to speak and write clearly and concisely
Strategic thinking - visualise the way forward, identify opportunities that add value to the work, to the business and to our customers
Problem solving - gathering and analysing data and effectively responding to new, complex or problematic situations; creating solutions that drive value for our company and our customers, incorporating innovative approaches where relevant
Regulatory & Compliance Management
What You Can Expect
Work autonomously whilst being supported, encouraged and being part of a trusted Global Leading organisation
Exposure to upskill and develop in your role
Flexibility and opening doors to other opportunities and skillsets
Joining a collaborative team of like-minded individuals
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status
Regular
Relocation
No relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable
Shift
Valid Driving License
Hazardous Material(s)
Job Posting End Date
0+/13/2026
A job posting is effective until 11 5+ 5+PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Job Posting End Date 0+/13/2026
A job posting is effective until 11 5+ 5+PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID R2+03+6
Senior Regulatory Affairs Associate
Looking for an exciting opportunity as a Senior Regulatory Affairs Associate with an Innovator Research-intensive biopharmaceutical Company?
Permanent Full-time position with competitive renumeration and benefits
Location Sydney, Australia
Hybrid, work from home and office environment, joining a dedicated and welcoming team
Upskill and growth in an area you’re passionate about, whilst being fully supported and encouraged
What You Will Do
Responsibilities include, however not limited to
Regulatory Project Management
Review, compile and submit complex registration dossiers and data packages, within timeframes agreed with manager and in accordance with government, industry and corporate requirements to maintain regulatory compliance and facilitate product supply.
Manage and support (including evaluating regulatory probability of success) the technical and scientific requirements of more complex regulatory applications during the pre-submission, submission, and evaluation process, ensuring timely and high-quality justifications or consultations with the Health Authorities or responses to questions from the Health Authorities in line with global guidance.
Ensure cost effective project management and coordination of work with others (including leading teams), compliance to global and local policies, and effective and timely communication of new or amended registered details to stakeholders within the company.
Regulatory and Technical Support
Provide regulatory and technical advice to other parts of the organization on complex issues to ensure that correct and compliant information is used in decision making and strategy development.
Develop and Maintain Key Relationships
Effectively participate in designated Product Life-Cycle Planning Teams, with regular and prompt attendance, completion of designated action items within agreed timeframes and appropriate contribution to discussions. Proactively recognize and communicate important PLP issues to others outside the team. Develop and maintain effective working relationships with all members of Product Lifecycle Planning team.
Actively collect, analyse and disseminate regulatory intelligence and other information and formulate strategies for best practices for a changing regulatory environment.
Effectively participate in Regulatory team discussions, bringing forward issues for consideration and contributing to the development of solutions and strategies.
Foster professional relationships with individuals within TGA and Medsafe who would be responsible for evaluating our company’s submissions.
What You Must Have
Pharmacy degree or life sciences degree, with at least four years’ experience in regulatory affairs for prescription products.
Competencies And Skills Include
Collaboration & Partnering - thinking and acting beyond one's silo - bridging boundaries across teams, functions, liaisons, geographies, external stakeholders and customers
Project Management - the ability to organise work efforts by prioritising tasks, using resources optimally, establishing appropriate deadlines and ensuring on-time delivery of tasks, deliverables and/or project results
Productive Communication - planning and delivering ideas and information to others in an impactful manner. Demonstrating the ability to listen to others, and to speak and write clearly and concisely
Strategic thinking - visualise the way forward, identify opportunities that add value to the work, to the business and to our customers
Problem solving - gathering and analysing data and effectively responding to new, complex or problematic situations; creating solutions that drive value for our company and our customers, incorporating innovative approaches where relevant
Regulatory & Compliance Management
What You Can Expect
Work autonomously whilst being supported, encouraged and being part of a trusted Global Leading organisation
Exposure to upskill and develop in your role
Flexibility and opening doors to other opportunities and skillsets
Joining a collaborative team of like-minded individuals
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status
Regular
Relocation
No relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable
Shift
Valid Driving License
Hazardous Material(s)
Job Posting End Date
0+/13/2026
A job posting is effective until 11 5+ 5+PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Job Posting End Date 0+/13/2026
A job posting is effective until 11 5+ 5+PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID R2+03+6
💡 Quick Summary
Seeking a career-building opportunity? The Senior Regulatory Affairs Associate position is now open for candidates interested in the Work from home Jobs sector. This role in Macquarie Park offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Work from home Jobs is a plus.
