Regulatory Affairs Associate - Oral Health Chemical Manufacturing Control Review

The role involves processing the regulatory impact of changes made to existing oral health products. This includes evaluation of the regulatory impact, communication with relevant stakeholders and preparation of submission documents. Additionally I am tasked with managing core dossiers, creating and updating them.

Yes, I was allowed to head projects and be heavily involved in ones of critical business importance. I was also encouraged to get involved in heading voluntary initiatives around the office which allowed me to develop my leadership abilities. I have been treated as a trusted member of the team from the start

Time management, professional networking and interaction, presentation skills, initiative and innovation, communication and negotiation, boundary setting and enforcement

I was thrown in the deep end quite early on, but was supported throughout and the team was open and helpful at all times, never failing to explain something that I should have known by that point in time once more.

Friendly, pleasant and generally good at keeping things human. Especially when it came to direct line management, my experience was that of finding a mentor and friend above all else and it seems I wasn't the only one. Focus on deliverables with an understanding of extenuating circumstances. Effort is expected and doing a few hours of overtime a week is practically unavoidable, but not purposefully oppressive

The social opportunities, the chances to participate in voluntary work and support my community definitely contributed greatly to my enjoyment. The respect and responsibility given to me by my team also made it a lot more interesting and pleasant than what could have been. I found myself in a team that was quite overloaded and in the process of making staff changes which made the experience more difficult, but generally pleasant.

Yes