Scientific Affairs Associate (Part-time or Full-time)
Work From Home (WFH) | 0.5–1.0 FTE | Applications close 22 January 2026
We’re growing!
Enimera RegsPlus is growing, and we are looking for a Scientific Affairs Associate to join our expanding team. We support clients across a wide range of therapeutic and product categories, including prescription medicines, biotechnology, medical technology, consumer medicines, medicinal cannabis, and psychedelics. Our reputation is built on high-quality scientific and regulatory deliverables, trusted relationships, and repeat referral business. This role is ideal for someone who is curious, proactive, detail-oriented, and keen to grow their expertise across regulatory, safety, and quality disciplines in a consulting environment. We are looking for someone who is energetic, proactive, and enjoys solving problems. If you are passionate about healthcare, thrive in a fast-paced, collaborative environment and want variety in your day-to-day work, this role could be an excellent fit.
About the Role
In this work from home position (0.5–1.0 FTE), you will work closely with senior team members to support regulatory, scientific, and compliance activities across Regulatory Affairs, Pharmacovigilance and Quality Assurance (QA) disciplines.
Key responsibilities include:
-
- Preparing, reviewing, and maintaining regulatory submissions
- Supporting pharmacovigilance and safety activities
- Contributing to quality assurance documentation and improvement initiatives
- Conducting scientific literature reviews and technical writing
- Liaising with clients to clarify data needs and project requirements
- Assisting with the development of high-quality, scientifically robust deliverables
About You
We are seeking candidates with:
-
- At least 2 years of industry experience in Regulatory Affairs, Pharmacovigilance, or
Quality Assurance - Strong scientific literacy and analytical skills
- Excellent written and verbal communication
- Ability to manage workload independently in a remote environment
- A collaborative approach and willingness to support team priorities
- At least 2 years of industry experience in Regulatory Affairs, Pharmacovigilance, or
Why Join Enimera?
-
- Exposure to a broad range of product types and regulatory pathways
- Flexible, remote, Australia-based working arrangement (0.5–1.0 FTE)
- Opportunities to develop skills across regulatory, safety, and quality disciplines
- Supportive environment with direct access to senior experts
- Work that is meaningful, varied, and scientifically challenging
How to Apply
To request a position description or for further information, please contact enquiries@enimeraregsplus.com.au
To apply, submit your cover letter and CV to enquiries@enimeraregsplus.com.au
Applications close 22 January 2026.
