Rosemont & You
Life at Rosemont
At Rosemont it’s our mission to be a rapid developer, reliable manufacturer and global supplier of novel delivery, patient focused medicines.
Our people are important to us and with them we can make a real difference to our patients.
We pride ourselves on being a great place to work where you can grow and be at your best. Our diverse talent allows us to embrace different ideas that reflects the diversity of our patients, as well as creating a truly inclusive environment.
I joined Rosemont in 2016 in operations working on the bottling line and then moved into manufacturing. I got involved with cleaning validation and became interested in what the quality department do which led to a move into Quality Control. I’m now doing a Level 3 Lab Technician apprenticeship, learning how to test materials & products.
Ross Parker, QC Technician
I love that no two days are the same, from a regulatory affairs perspective I get to deal with all stages of a product; we write the dossier, publish it, maintain it and deal with the MHRA. There are lots of challenges & it keeps my role interesting.
Charlotte Brendon, Regulatory Affairs Manager
Rosemont is a great place to work, the culture and environment created is one that encourages progression and emphasises the importance of supplying quality medicines to the market.
Liam Szyczak. Quality Assurance Officer
My job requires a lot of multitasking. It never gets boring, this allowed me to strengthen, develop, and learn new skills. I enjoy working closely with my team members and we all always make sure to listen to everyone’s perspective.
Maria Verdesca, Principle QPPV Officer and UK dQPPV
Latest Vacancies
- Apply by 24/10/2025
Regulatory Affairs Associate Director (US-based role)
This role will ensure that pharmaceutical products are developed, manufactured, and distributed in compliance with all U.S. applicable regulatory requirements and standards. The Regulatory Affairs Associate Director serves as a strategic partner across cross-functional teams, providing regulatory strategy and guidance throughout the product lifecycle — from development to marketing approval and post-approval surveillance. This role is critical in securing timely application approvals from the FDA, maintaining product compliance, and supporting the company’s commitment to patient safety and product quality. Use the ‘general responsibilities and skills and qualifications’ for the rest of the advert.
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- Apply by 24/10/2025
Quality Manager (US-based role)
The Quality Manager is responsible for leading the quality assurance functions for Sabal Therapeutics and its client companies. This role will commence with an evaluation of company GMP Quality Systems and gap analysis. Creation and implementation of necessary processes and procedures will be an integral part of the first six months. Oversight of third party CMO activities, outsourced packaging facilities and API providers as well as on-going product release, change control, CAPA, employee training and vendor auditing are key functions of this position.
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