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The role of the Qualified Person is integral to the success of the Quality Department in delivering expert advice and ensuring release of clinical supplies, in line with customer expectations and regulatory demands. The Qualified Person will ensure that finished products are not released until their quality has been judged to be satisfactory as measured against specifications and regulatory requirements.
The CTM ensures that all clinical deliverables meet the customer's time/quality/cost expectations, by managing the clinical team to work efficiently and within project scope. Dependent on the needs of the project, the CTM may also take responsibility for budget management and oversight of other functional groups on the project e.g. regulatory, safety.
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Senior Account & Account Director - Healthcare / Pharmaceuticals - North West Our client is a leading player in the Healthcare / Pharms marketplace and are well renowned for delivering fully integrated marketing communications for their array of well known clients.
Development Analyst - Pharmaceutical - Middlesex, South EastAn excellent opportunity has arisen for a Pharmaceutical Development analyst in a growing organisation in the Middlesex area. The role will involve carrying out analytical method development and validation of analytical techniques for numerous pharmaceutical products.
Site and Project Managers - Pharmaceutical - Sites throughout UK, UKMy client is a specialist contractor, currently seeking experienced site and project managers, who have experience of construction projects within pharmaceutical environments, which will need to include internal finishing.
COMPLIANCE ENGINEER - PHARMACEUTICAL - Oxford, OxfordshireCOMPLIANCE ENGINEER - PHARMACEUTICALC35,000 + pension, healthcare, life assurance, share ownershipOxford 1502/60/saJOB ROLE: COMPLIANCE ENGINEER - PHARMACEUTICAL: * Co-ordinating and directing compliance issues within the Operations Engineering department to ensure a consistent approach is taken to resolving quality issues including ERs, CAPAs, Calibration Alerts and Post investigations.
Quality Control Technician (Pharmaceutical) - Great Yarmouth, East AngliaQuality Control Technician (Pharmaceutical)Great YarmouthFull Time (One year FTC) possibly permanent20 - 22kAn opportunity has arisen for a QC technician / analyst.
GMP Packaging Technician: Pharmaceutical - Brighton, East Sussex* Job Title: Packaging Technician (permanent)* GMP experience ESSENTIAL* Packaging experience PREFERRED* FOUR new vacancies, all due to expansion* Location: Brighton, East Sussex* Double Day Shifts (see below)* Salary: Around 6.
Quality Assurance Manager.   c£ Negotiable plus benefits.   You will be required to manage all quality assurance functions necessary to ensure compliance with good distribution practice guidelines and conditions of the wholesale dealer&rsquo s licence   To act as the management representative to ensure compliance with ISO9001:2008   To act as the nominated Responsible Person for the company.
We are currently looking for a Formulation Development Manager to join a leading Pharmaceutical company based in United Kingdom.
Overview Our client is a leading global system integrator who are expanding their presence in the pharmaceutical markets. With a turnover in excess of $6b and a year on year growth percentage over 30% they are keen to bring on board new, experience talent within the Life Sciences Markets).
The role of the Qualified Person is integral to the success of the Quality Department in delivering expert advice and ensuring release of clinical supplies, in line with customer expectations and regulatory demands.
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