In-Demand Regulatory affairs specialist Jobs in Ryde, Nsw

Senior Regulatory Affairs Specialist
Fresenius Medical Care —North Sydney NSW
- Full-time
- Management
- Engineering
- ERP systems
Specialist, Clinical Research (12 months contract)
Edwards Lifesciences —North Ryde NSW
- Full-time
- Management
- Patient monitoring
- Microsoft Office
Labelling Systems Specialist (12-Month Contract)
ResMed —Bella Vista NSW
- Full-time
- AI
- Communication skills
Senior Manager, Regulatory Affairs
Cencora —North Sydney NSW
- Full-time
- Hybrid work
- Master's degree
- Education
- Bachelor's degree
Quality Assurance Specialist
Device Technologies Australia —Sydney NSW
- Full-time
- Communication skills
Senior Remuneration Regulations Consultant (Senior Manager level)
ING Bank —Sydney NSW
- Financial services
- Communication skills
5d
PR & Media Relations Specialist
Woolworths Group —Bella Vista NSW
- Full-time
- Hybrid work
- Communication skills
Post Market Quality Assurance Reporting Specialist
AbbVie —Sydney NSW
- Full-time
- Hybrid work
- Clinic
- Bachelor's degree
- Communication skills
4d
MCO Medical Lead - Adult Vaccines
Sanofi —Sydney NSW
- Medicine
- Doctoral degree
- Marketing
12d
Senior Specialist, Medical Science Liaison
Organon —Sydney NSW
- Full-time
- Medicine
- Doctoral degree
- Writing skills
Quick Apply
MCO Medical Lead - Paediatric Vaccines
Sanofi —Sydney NSW
- Medicine
- Doctoral degree
- Marketing
12d
Senior Marketing Specialist
Solventum —North Ryde NSW
- Full-time
- Sales
- Marketing
- Organisational skills
Medical Advisor - Specialty Care
Sobi —Sydney NSW
- Full-time
- Medicine
- Doctoral degree
- Writing skills
Quick Apply
13d

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Senior Regulatory Affairs Specialist

Fresenius Medical Care -
North Sydney NSW

Apply Now

Job Details

Full-time

Qualifications

Management
Engineering
ERP systems
English
Microsoft Office
Finance
Databases
Education
Risk management
SharePoint
Communication skills
FDA regulations

Full Job Description

Scope of Role:

The role is based in Sydney and may require some local and interstate travel. The role encompasses a range of pre and post market product activities and requires:

interaction and negotiation with regulatory agencies in Australia and New Zealand;
collaboration across local, regional and cross functional regulatory, quality, clinical and pharmacovigilance teams to support the ANZ business and maintain regulatory compliance;
working closely with key internal stakeholders namely, S&M, Finance, Legal, Clinical, Supply chain and Technical teams to ensure no interruption to product supply within ANZ and to drive commercial initiatives and new products to market to grow the ANZ business.

The role supports 3 key business areas within ANZ– FMC Devices/Medicines (including Smithfield manufacturing), Packs, Seating.

Responsibilities

Maintain regulatory compliance across all ANZ device and medicine related pre- and post- marketing activities for the 3 key business areas
Review and maintain all medical device and medicine registration requirements to support the ANZ businesses within required timelines
Prepare and submit medical device applications to TGA and notifications to WAND, including managing post-market variations and change notifications to ensure continuous compliance throughout the product lifecycle
Lead the preparation and submission of registration application for medicines with the TGA & Medsafe, including submissions of variations/changes for updates in Safety related, Product and Consumer Medicine Information
Monitor and interpret changes in TGA/Medsafe/WAND regulations to provide strategic advice on submission timelines and impact on existing product portfolios
Review S&M related materials, promotions and for compliance to ANZ advertising regulations and MTAA/MTANZ codes
Review device change controls and complete risk assessments based on regulatory impact to ANZ as requested
Maintain a database of all ANZ product certification and manufacturer’s evidence submitted to regulatory authorities to ensure it is contemporaneous and accessible for all FMC teams
Act as the Primary LSO for ANZ: Responsible for the assessment and determination of safety events. Manage direct communications with the TGA and serve as the main regulatory contact point for all device-related incident reporting and Post-Market Surveillance (PMS) activities
Serve as Deputy CCA and Deputy PVRP: Provide essential support for complaint management and medicine safety. This includes the timely and accurate data entry of complaints into the global quality system and assisting the Primary PVRP to ensure all regulatory timelines are met
Maintain compliance with post market activity such as recall, FSNs/FSCAs and liaising with regulatory authorities, distributors and customers to complete all required regulatory actions
Support the maintenance and update of Local Quality Management System (QMS) documentation and SOPs to ensure alignment with FMC global policies and local ANZ standards

Other responsibilities

Support the S&M team with documentation required for tender submissions
Support SE Asian market with documentation requests
Support HQ/AP regional project teams impacting ANZ
Ad hoc regulatory and quality related tasks as required to support the ANZ business

Competencies

Knowledge of regulatory requirements for management of medical devices and medicine in Australia and New Zealand
Experience in preparing, submitting and handling medical device and medicine applications, change applications, variations and updates to the TGA & WAND
Understanding of MAH responsibility including Sponsor requirements, device and medicine lifecycle management
Understanding of GMP, QSR & ISO 13485 Quality Management Systems
Knowledge of device incident reporting, adverse event reporting; pharmacovigilance experience desirable but not essential
Understanding of 3PL supply chain management
Strong organisational and interpersonal skills and able to work autonomously as well as in cross functional teams
Strong problem solving and decision making skills
Knowledge of risk management techniques
Computer literacy with Microsoft Office/Office 365, sharepoint, and knowledge of ERP systems, databases such as Trackwise, QDoc and Doc control platforms

Experience

At least 5 years previous regulatory affairs experience in the medical device or life sciences industry; pharmaceutical experience is desirable but not essential
Experience working in a GMP and/or ISO13485 environment
Direct experience with medical device Conformity Assessment processes; CE marking and MDR experience desirable
Proven history of successful submissions of device applications (Class I-III) to TGA and WAND
Proven engagement, both verbal and written, with regulatory authorities and notified bodies such as TGA, Medsafe, US FDA, TUV SUD, BSI
Proven QMS experience relating to medical devices including complaint handling, reporting to regulatory authorities (incidents, events), recalls, FSNs/FSCAs

Education

Degree qualified in a science, engineering or healthcare discipline

Communication Effectiveness

Fluency in English
Strong verbal and written communication skills
Ability to comprehend and effectively translate complex regulatory information to internal stakeholders and external contacts
Ability to collaborate regularly and respectfully with local, regional and cross functional teams to achieve positive business outcomes

Apply Now

Refine Your Search

regulatory affairs specialist jobs in ryde, nsw

Senior Regulatory Affairs Specialist

Specialist, Clinical Research (12 months contract)

Labelling Systems Specialist (12-Month Contract)

Senior Manager, Regulatory Affairs

Quality Assurance Specialist

Senior Remuneration Regulations Consultant (Senior Manager level)

PR & Media Relations Specialist

Post Market Quality Assurance Reporting Specialist

MCO Medical Lead - Adult Vaccines

Senior Specialist, Medical Science Liaison

MCO Medical Lead - Paediatric Vaccines

Senior Marketing Specialist

Medical Advisor - Specialty Care

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