Regulatory Affairs Manager
- Sydney
- Salary:$140000 - $145000 per annum, Benefits: + Super + Bonus
Job details
- Location
- Sydney
- Salary
- $140000 - $145000 per annum, Benefits: + Super + Bonus
- Job Type
- Full Time
- Ref
- BH-39898
- Contact
- Gemma Staddon
- Contact email
- Email Gemma
- Contact phone
- +612 8877 8776
- Posted
- 7 days ago
Job details
- Location
- Sydney
- Salary
- $140000 - $145000 per annum, Benefits: + Super + Bonus
- Job Type
- Full Time
- Ref
- BH-39898
- Contact
- Gemma Staddon
- Contact email
- Email Gemma
- Contact phone
- +612 8877 8776
- Posted
- 7 days ago
Benefits
• Competitive income with opportunities for growth and advancement.
• Career development prospects in a multinational company.
• Work-life balance with a flexible work environment.
• Competitive salary package
About the Company
Our client is a globally recognised multinational company specialising in consumer products. They have a strong presence in the industry and are renowned for their commitment to quality and compliance.
About the Opportunity
In this role, you will manage compliance policies and programs for medical devices, listed medicine, registered medicine, and electrical products. Reporting to the Regional Regulatory Lead, you will collaborate with cross-functional teams and stakeholders to ensure regulatory compliance and support new product launches. Your contribution will be crucial to the company's success and market impact. This role is hybrid and offers the flexibility to work from home as well as the office.
Duties
• Contribute to compliance policy development and implementation.
• Oversee new product launches and ensure regulatory compliance.
• Collaborate with cross-functional teams and stakeholders.
• Support regulatory inspections and certification audits.
• Maintain accurate documentation and reports.
Skills and Experience
• Experience working with related products
• Experience in a Senior Regulatory role within Healthcare
• In-depth knowledge of TGA requirements and quality standards for medical devices.
• Strong communication skills, both verbal and written.
• Demonstrated experience in regulatory affairs.
• Experience leading a team
• Ability to prioritise and to handle multiple projects simultaneously.
• Ability to work with all levels of management and to build relationships across disciplines.
• Excellent influence, persuasion, communication, and presentation skills
• Well organised and high initiative
Culture
Our client fosters a culture of innovation, collaboration, and professional growth. They value diversity and provide a supportive and flexible work environment.
How to Apply
Click "Apply" or contact Gemma Staddon, Specialist Manager, at 02 8877 8776 for a confidential discussion.
• Competitive income with opportunities for growth and advancement.
• Career development prospects in a multinational company.
• Work-life balance with a flexible work environment.
• Competitive salary package
About the Company
Our client is a globally recognised multinational company specialising in consumer products. They have a strong presence in the industry and are renowned for their commitment to quality and compliance.
About the Opportunity
In this role, you will manage compliance policies and programs for medical devices, listed medicine, registered medicine, and electrical products. Reporting to the Regional Regulatory Lead, you will collaborate with cross-functional teams and stakeholders to ensure regulatory compliance and support new product launches. Your contribution will be crucial to the company's success and market impact. This role is hybrid and offers the flexibility to work from home as well as the office.
Duties
• Contribute to compliance policy development and implementation.
• Oversee new product launches and ensure regulatory compliance.
• Collaborate with cross-functional teams and stakeholders.
• Support regulatory inspections and certification audits.
• Maintain accurate documentation and reports.
Skills and Experience
• Experience working with related products
• Experience in a Senior Regulatory role within Healthcare
• In-depth knowledge of TGA requirements and quality standards for medical devices.
• Strong communication skills, both verbal and written.
• Demonstrated experience in regulatory affairs.
• Experience leading a team
• Ability to prioritise and to handle multiple projects simultaneously.
• Ability to work with all levels of management and to build relationships across disciplines.
• Excellent influence, persuasion, communication, and presentation skills
• Well organised and high initiative
Culture
Our client fosters a culture of innovation, collaboration, and professional growth. They value diversity and provide a supportive and flexible work environment.
How to Apply
Click "Apply" or contact Gemma Staddon, Specialist Manager, at 02 8877 8776 for a confidential discussion.
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