Jobs › Companies › Abbott › Regulatory Affairs Manager

About this Regulatory Affairs Manager role at Abbott

Abbott · Onsite · Australia - New South Wales - Eastwood

     

JOB DESCRIPTION:

About Abbott

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.  Our Rapid Diagnostics division is about providing innovative ways to screen, diagnose and monitor a vast range of health conditions with greater speed, accuracy and efficiency.  Abbott's rapid diagnostic tests allow healthcare professionals and their patients to get same-day results. For healthcare workers, this means they can diagnose and advise their patients in a single office visit. For patients, quicker results means earlier treatment, less anxiety, less time and money spent on repeat doctor visits and a faster return to good health.

 

The Role

We are seeking an experienced and motivated Regulatory Affairs Manager to lead regulatory compliance activities across our Australia, New Zealand, and Pacific Islands business. This is an exciting opportunity to play a critical role in bringing innovative healthcare solutions to market while ensuring compliance with applicable regulatory requirements.

Based in Macquarie Park, NSW and reporting to the Director Regulatory Affairs APAC, you will act as the key regulatory expert and primary liaison with regulatory authorities, supporting a diverse portfolio across Infectious Disease, Cardiometabolic, Informatics, and Toxicology products.

 

Key responsibilities

  • Manage product registrations and regulatory submissions with relevant authorities, ensuring compliance and timely approvals.
  • Maintain existing product registrations and manage regulatory changes throughout the product lifecycle.
  • Lead post-market surveillance activities, including adverse event reporting, recalls, and field safety actions.
  • Review and approve promotional and external communication materials to ensure regulatory compliance.
  • Manage biological and controlled substance import permits where required.
  • Monitor and interpret regulatory developments impacting medical devices and related healthcare products.
  • Serve as the primary point of contact for regulatory agencies and external stakeholders.
  • Support clinical trials by reviewing protocols, assisting with ethics submissions, and coordinating sponsorship requirements.
  • Maintain regulatory databases and tracking systems to support compliance and reporting activities.
  • Contribute to industry consultations and represent the organisation within relevant industry associations and working groups.
  • Provide regulatory guidance, support, and training to internal stakeholders across the business.

 

What we’re looking for:

To be successful in this role, you will have:


Essential Qualifications & Experience

  • Bachelor of Science (BSc) or equivalent qualification.
  • Minimum 3 years' experience in a Regulatory Affairs role within the medical device, diagnostics, healthcare, or related industry.
  • Demonstrated experience working with the Australian Therapeutic Goods Administration (TGA) Medical Device Regulatory Framework.
  • Strong understanding of regulatory requirements across Australia and New Zealand.

Key Skills & Attributes

  • Strong leadership and influencing capabilities.
  • Excellent analytical and problem-solving skills.
  • Ability to interpret and apply complex regulatory requirements.
  • High level of attention to detail and commitment to quality.
  • Strong project management and organisational skills.
  • Excellent communication and stakeholder management abilities.
  • Ability to work independently while managing multiple priorities.
  • Knowledge of Quality Management Systems and regulatory compliance frameworks.
  • High levels of integrity, professionalism, and confidentiality.

 

Why Abbott?

At Abbott, you'll be part of a purpose-driven organisation focused on helping people live healthier lives. You'll work with passionate and talented colleagues in a collaborative environment where innovation, continuous improvement, and professional growth are encouraged.

We also provide some fantastic benefits for our employees such as:

  • Discounted Healthcare
  • Access to Fitness Passport
  • Discounted Shares program
  • Learning and development opportunities
  • Onsite parking and a barista
  • And Lots more…

     

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Regulatory

     

DIVISION:

ID Infectious Disease

        

LOCATION:

Australia > Macquarie Park : 299 Lane Cove Road

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Not specified

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

     

     

     

Ready to apply to Abbott?
Apply to Abbott

About Abbott

​ Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, ent

See all jobs at Abbott →

Similar jobs

Hims & Hers
Sr Manager, Global Regulatory Affairs (AI/ML)
Hims & Hers
⚡ Apply early US Remote · location restricted $170,000–$200,000
● New 👁 Seen ✓ Applied 4h ago
Ōura
Senior Regulatory Affairs Specialist
Ōura
⚡ Apply early Remote - United States · location restricted
● New 👁 Seen ✓ Applied 7h ago
Gilead Sciences
Manager, Regulatory Affairs CMC
Gilead Sciences
⚡ Apply early United States - California - E... Hybrid $133,195–$172,370
● New 👁 Seen ✓ Applied 11h ago
ME
Associate Regulatory Affairs Systems Specialist
Medtronic
⚡ Apply early Taguig City, National Capital... Onsite
● New 👁 Seen ✓ Applied 20h ago
Gilead Sciences
Manager, Kite Regulatory Affairs CMC
Gilead Sciences
⚡ Apply early Japan - Tokyo Onsite
● New 👁 Seen ✓ Applied 20h ago
ME
Associate Regulatory Affairs Specialist - Temporary
Medtronic
⚡ Apply early Madrid, Madrid, Spain Onsite
● New 👁 Seen ✓ Applied 20h ago
AB
Senior CMC Regulatory Affairs Manager
AbCellera
⚡ Apply early Vancouver Onsite CA$150,000–CA$180,000
● New 👁 Seen ✓ Applied 23h ago
Pulmovant
Senior Manager, Regulatory Affairs, Pulmovant
Pulmovant
⚡ Apply early Remote, US · location restricted
● New 👁 Seen ✓ Applied 1d ago
Olema Oncology
Associate Director, Global Regulatory Affairs, Compliance and Project Management 
Olema Oncology
⚡ Apply early Boston, Massachusetts Onsite $185,000–$205,000
● New 👁 Seen ✓ Applied 1d ago

Sign up for suggestions tailored to the jobs you open and the searches you save.

More jobs at Abbott

See all jobs at Abbott →

Apply now
🤖

Whoa — hold up

JobsRadar was built for real people having a rough time in their job search — not for automated requests. You're clicking way too fast and you're now temporarily blocked.

Come back later. If you're genuinely job hunting, we've got your back — just act like a human.

Catch your next role the second it’s posted.

Create a free account and we’ll watch the boards for you — the instant a job matches your search, it lands in your inbox or Telegram. No digging, no refreshing.

Create free account

Free forever · takes 30 seconds · already have one?

Get an edge on your job hunt.

Join our Telegram channel for the stuff that helps you land the role — salary benchmarks, the weekly market pulse, and new-feature drops. No spam, just signal.

Join the channel — it's free