Drive business performance through financial planning and forecasting, management reporting, evaluation of initiatives and business partnering with commercial functions to achieve business and financial objectives, including growth drivers, costs and return on investment. Provide decision support insight, analysis and recommendations on initiatives and investments, to help the business allocate resources optimally. Support on the commercial areas of the long-range strategic planning, budgeting, and financial forecasting processes.

Physical movement of raw materials, packing materials, other materials and finished good – Using Forklift Trucks where necessary (authorised personnel only). Receipts into the warehouse for storage – from the warehouse to production, as defined by the collation procedures – and from the warehouse to dispatch. The picking and preparation of customer orders to be dispatched following checks to ensure that customers’ orders are correct, and are as specified by sales documentation. Prepare correct documentation to accompany goods being shipped using the dispatch system.

Ensures Supplier Qualification and Material management activities are planned and executed in line with Rosemont SOPs and GMP Requirements and Regulations

Accountable for growing volume and net sales across a designated geography to maximise Rosemont profit. Accountable for optimal distribution of Rosemont portfolio through hospitals and CCGs.

Perform a variety of accounting activities in accordance with accounting principles and standards to control the organisation’s financial resources and ensure that it complies with all relevant regulations, laws, and reporting requirements.

The Data and Digital Solutions Architect will play a crucial role in supporting our IT strategy, enhancing capabilities of our data and solutions architecture, data governance, BI & reporting, automation, and systems integration, working closely with key business leaders to support them in accelerating their business through data & insights. A key aspect of this role involves supporting the execution of our digital roadmap and AI initiatives, you’ll be pivotal in assessing our current tools and capabilities to build and execute the digital roadmap.

Fills and reconciles bulk liquids into bottles and performs cleaning of equipment post fill in adherence to standard operating procedures and current good manufacturing practices.

Rosemont Pharmaceuticals is a company, dedicated to improving the health and wellbeing of people through the development, manufacture and supply of liquid medicines for patients who have difficulty swallowing solid medications or those who need a precise measured dose not available in a solid tablet. As such QC employees must be able to demonstrate full compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Health and Safety requirements.

The Senior HRBP will partner with the Operations Director and Quality Director and their senior leadership teams to drive organisational efficiency, effectiveness, and development to ensure the business areas are equipped with the mindset, capability, and capacity to deliver today and in the future. They will support and enable Functional teams in building and maintaining functional excellence and on their specific journey to high performance.

Effective, efficient and rigorous delivery of all aspects of accounts payable and employee expenses and optimisation of creditors. Responsible for ensuring supplier spend follows the company policies and procedures. Ensuring accurate recording of all transactions in the ledgers, including credit notes and staff expenses.

Provide analytical development support to the business for problem solving and continuous improvement projects. This will include drug substance and excipient changes, product investigations,
updating and where necessary developing new analytical methods as below.
To develop and validate, under supervision, suitably rugged physical and chemical analytical methods that will determine all necessary product parameters including physical characteristics, determination of
active, degradation products, preservatives, and, if necessary, volatiles using the most suitable analytical instruments available to the company in compliance with standard operating procedures and international scientific, quality and regulatory standards.

Drive compliance to MHRA Regulatory and Company requirements/standards by working and collaborating with multifunctional teams and providing quality leadership. To act as site QP, ensuring that site is maintained in a state of compliance and each batch is released according to cGMP and product registration.