• Resize Text
    • Small Text
    • Medium Text
    • Large Text
    • Connect

Working at Rosemont you’ll get a sense of purpose 

Rosemont has a long heritage in the UK Pharmaceutical industry, originally established in 1967 by two Pharmacists in response to the lack of liquid medicines available for their patients.

Our ambition is to maintain this momentum and continue to expand and develop our product range to enable us to support even more patients and healthcare professionals. We have a reputation as a market leader and innovator within the UK for oral liquid medicines.

Here at Rosemont, our values underpin how we deliver for our patients.

Working at Rosemont

By working at Rosemont, you will be part of a great team and together we can help improve the lives of our patients.

Learn more
Rosemont Pharmaceuticals - Woman working in a laboratory

Benefits & Perks

We provide employees with benefits that are more than just payWe offer benefits that are centred around what our employees value.

Learn more
Rosemont Pharmaceuticals - Woman working in a laboratory

Latest News

See what we are up to at Rosemont

Learn more
Rosemont Pharmaceuticals - Man and woman smiling in an office looking at a tablet device

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.

 

Read more
  • 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.

 

Read more
Rosemont Pharmaceuticals - Lady using a test tube in a laboratory