Welcome to Next Phase Recruitment! Please see below our current jobs that match your search criteria. For a broader job search please visit the home page or call us on 01403 216216 to discuss career options in other areas of Life Science and Technology.
Quality Assurance (QA) is a vital function within all Pharmaceutical and Medical Device companies. Job titles within the QA area can vary a great deal across different companies, with titles including QA Associate, QA Officer, QA Specialist and QA Scientist, then progressing to QA Manager, QA Lead etc. The QA terms, especially at junior-to-intermediate level, are often quite interchangeable.
The QA team is typically responsible for ensuring that the quality standards and systems followed in the manufacture of drugs is in compliance with Good Manufacturing Practice (GMP) and meets the specific quality standards laid out in the company’s Quality Management System (QMS). A QMS will include quality standards for internal audits, deviations, change controls, corrective actions, quality review reports, clean room monitoring, batch record review, and external documentation reviews.
A pharmaceutical QA professional’s responsibilities will include analysing the production process of pharmaceuticals, identifying areas where errors prevail, root cause analysis, observing every activity, monitoring the drugs being manufactured or packed for visible defects, testing the drugs (or at least interpreting the data from lab-based QC analysis), noting down observations gathered from the quality control process, and accepting or rejecting batches of drugs on the basis of samples (Batch Release). Quality Assurance teams will often be divided into different QA groups, with some more focused on batch record review while others are more involved in non conformance investigations and SOP (Standard Operating Procedure) updates.
Skills and Experience required for a career in Quality Assurance
- Science degree (this is not always essential)
- Experience gained in a GMP / ISO environment
- QA processes and systems
- Batch record processing
- Ability to multi-task
QA salaries can vary enormously depending on what specific duties the person will be undertaking. If the role is a relatively entry-level or administrative one, focused on batch review or entry and processing of QA documents / data, salaries could be in the £18k - £24k range. Salaries can then increase steadily once you start to specialise in a particular area, especially if this means getting involved in hosting / conducting internal or external audits, continuous improvement initiatives, team leadership, or training. QA offers a varied and interesting career path and you could earn up to £40k in a non-management role and significantly more than this once you are in a management-level position.
Arundel is an historic town located in the South Downs National Park in West Sussex in the South East region of England. Arundel is approximately 49 miles from London, 18 from Brighton, 40 from Portsmouth and 10 from Chichester, the county town of West Sussex. Other towns within easy reach include the seaside resorts of Worthing, Littlehampton and Bognor Regis. Arundel lies on the River Arun and has many beautiful listed buildings including a castle, home to the Duke of Norfolk and a cathedral which dominate the skyline. Arundel’s location in the South Downs National Park makes it an ideal base for walkers, cyclists and wildlife watchers. There are also numerous individual shops, galleries, restaurants and pubs in the town and surrounding villages national park.
Although many Arundel residents commute to Brighton, London and elsewhere, a number of large companies do provide more local employment opportunities including the worldwide HQ of Body Shop in Littlehampton, Butlin’s holiday camp in Bognor Regis and Goodwood Race course which stages regular horse racing and motor racing events such as the Festival of Speed and Revival. Goodwood is also the home of a large Rolls Royce factory.