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.
Worthing is a large seaside town located in West Sussex in South East England. The cities of Brighton and Chichester are close by and London is only 50 miles away. Worthing is a great place to live and work with good schools and transport links as well as a pier, sports facilities, a theatre, cinemas and a wide variety of shops, restaurants and bars. Worthing also benefits from being located at the foot of the South Downs, the UK’s most recent National Park, which offers fabulous scenery, marked trails for walking, horse riding and mountain biking. Worthing was first inhabited in the Bronze Age, became a farmstead in the Roman era and remained a small agricultural fishing village for centuries after that. Thanks to Princess Amelia, who decided to visit Worthing in 1798 to help her recuperate from TB, Worthing became a fashionable destination for wealthy members of London’s Society to try out the beneficial effects of bathing in the sea. Tourism is still a major employer in Worthing together with pharmaceuticals, medical devices production and financial services.