In-Demand Program associate Jobs in Adelaide, Sa

Regulatory Affairs Associate
Mayne Pharma —North Haven SA
- Laboratory experience
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- Full-time
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Travel + Leisure Co. —Adelaide SA
- $76,000 - $80,000 a year
- Weekend availability
- Hotel experience
- Resort
- Kitchen
- Professional development assistance
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Regulatory Affairs Associate

Mayne Pharma -
North Haven SA

Apply Now

Job Details

2 days ago

Qualifications

Laboratory experience
Pharmacy

Full Job Description

Are you experienced in Regulatory Affairs and thrive on achieving excellence in a dynamic environment? Do you deliver standout results first time, every time?

If so, you’ll fit right in at Mayne Pharma. What’s in it for you? You’ll help us achieve our mission of delivering better, safer and more accessible medicines.
At Mayne Pharma, the results speak for themselves

About Mayne Pharma

Mayne Pharma is a global pharmaceutical company offering end-to-end pharmaceutical development and manufacturing to customers around the world. Our heritage makes us one of the most well-known and respected pharmaceutical companies in Australia.

Mayne Pharma Australia are passionate about bringing globally valued pharmaceuticals to Australian patients and consumers. Our values of Passion, Integrity, Accountability, Creativity, Empowerment and Agility are the foundation for everything we do.

Why Join Us?

Attractive remuneration packages
Professional Development
Mayne Perks: Enjoy exclusive discounts and savings
Community Service
Recognition and Team Events
Exclusive Health Insurance Benefits
Well-being Programs

Here’s where you come in

Are you a Regulatory Affairs Associate who wants a new challenge in the pharma industry and wants to build your experience? If so, you’ll join a fast-paced environment that pushes you to achieve your best as you partner with the business to deliver its products and improve its processes. But you won’t do it alone. You’ll be supported every step of the way as part of a large, high-achieving Regulatory Team.

Your responsibilities, at a glance, will include:

Compile documentation necessary for local and overseas regulatory submissions (new product registrations, variations to existing licenses etc.) in line with international regulatory guidance for prescription and non-prescription pharmaceutical products.
Review change control documents and ascertain Regulatory impact.
Assist in maintaining regulatory records.
Write regulatory submission content for CTD Modules 1 and 3.
Any other duties considered appropriate for the position, as required

Additionally, collaborate with cross-functional teams within Mayne Pharma’s production facility in Salisbury, South Australia, and its commercial partners.

You need to tick these boxes

We pick applicants based on capability and aptitude. But we also emphasise cultural fit.

Therefore, you’ll need to have a positive mindset and be prepared to take ownership of your performance.

You’ll also need to hold a science degree or higher in chemistry, pharmacy, pharmacology, or another related discipline. You will have a minimum of 2+ years’ experience working in a laboratory.

Ready to become part of the Mayne Pharma story?.

How To Apply - Click the APPLY NOW button

Apply Now

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program associate jobs in adelaide, sa

Regulatory Affairs Associate

Associate Primary Engineer

Associate Cable Engineer

Lawyer to Associate, Insurance

Chef De Partie

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