Join the Adjutor Team as a Regulatory Consultant

Are you a knowledgable and details oriented professional with a passion for helping clients navigate complex regulatory landscapes with confidence and compliance? Do you thrive in a remote working environment, collaborating with a high-performing team? If you’re ready to bring best practices and innovative ideas to the development, regulatory and commercialisation of therapeutic goods, Adjutor wants to hear from you!

Job Title: Consultant

Location: Australia (Work from home)

Client Base: Local and International

Department: Operations

Reports to: Head of Development, Regulatory and Commercialisation

Job Type: Full Time

We’re seeking a talented individual to join our collaborative, high-performing team as a consultant. This role offers the chance to gain diverse experience working closely with a team of Consultants and Senior Consultants across multiple clients, markets, products and regulatory pathways.

This is not an entry-level position. We’re looking for a regulatory professional with at least 2 to 3 years of hands-on experience in regulatory affairs and/or development.

Applicants will be interviewed from now until 02nd April and applications may close early if a suitable candidate is identified.

Join us at Adjutor—where your expertise drives business success.

Please submit your resume and a brief covering letter detailing your experience and expertise, against the selection criteria via the application link below.

We look forward to welcoming you aboard!

Adjutor Healthcare is a rapidly growing, agile consulting business delivering expert development, regulatory and commercialisation services across the therapeutic goods industry.

Our team supports local and international clients across the development and commercialisation spectrum for medicines, biologicals, medical devices, and combination products.

Visit us at www.adjutor.com.au to learn more about who we are!  

  • Remote Flexibility: Work from anywhere with a friendly, collegial, supportive and communicative team.
  • Work-Life Balance: Flexible working arrangements.
  • Competitive Salary: Industry benchmark-level compensation.
  • Growth Opportunities: Ongoing training, mentoring & career development.
  • Innovative Environment: Share your ideas for improvement and efficiency—we’re all ears!
  • Compliance-Driven Approach: Be part of a team that values ethics, accuracy, regulatory adherence, and best practice.
  • Degree qualified in life sciences or a related field (postgraduate qualifications highly regarded).
  • High attention to detail without losing sight of the big picture.
  • Strong communication skills and a collaborative approach.
  • Consulting experience is advantageous but not essential.
  • Highly organised with the ability to manage multiple priorities
  • Experience in Australian regulatory affairs, particularly TGA submissions (Cat 1s, Cat 3s, accelerated and collaborative pathways, ODDs).
  • Ability to work independently while staying closely connected with the team.
  • Committed to excellence and client-focused outcomes.
As head of Development, Regulatory and Commercialisation for Adjutor, Dr Rama Gitifar leads multidisciplinary teams to deliver end-to-end strategic support for clients across pharmaceuticals, medical devices and advanced therapies.

Still have questions?

Interested in further information? Let’s have a chat!