Computer System Validation Pharmaceutical Jobs

Blackpool, United Kingdom

As a Technical Assistant, your role entails various responsibilities. You'll be responsible for entering and updating raw material information and new product specifications onto the technical MRP program... £25000/annum

from: CV-library.co.uk - 27 days ago

Regeneron - Uxbridge, Middlesex, United Kingdom

We need you to regularly meet with the Statistical Programming management team for close collaboration with the clinical development statistical programming team to evaluate and develop solutions for project... Competitive

from: pharmiweb.jobs - Yesterday

Pharma Partners Recruitment Ltd - London, United Kingdom

Ensure Non-Conformances/Incident Reports are reviewed, assessed and approved using the eQMS ensuring it is contributing to continual quality improvement. Ready to apply Before you do, make sure to read...

from: uk.lifeworq.com - 2 days ago

Pharma Partners Recruitment Ltd - London EC1A, City of London, London

While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required. Conduct QA risk assessments for studies, systems...

from: joblookup.com - 3 days ago

Drebbelogic Ltd - Waterford, County Waterford, Republic of Ireland

* Ensure Automation compliance with Global Policies, Procedures and Guidelines, regulatory requirements, GxP, and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities... £47 - £51/hour

from: CV-library.co.uk - 14 days ago

Hobson Prior - England, London

Ensure that own work, and that of the team, complies with GMP, Good Documentation Practice (GDP) and GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's... Negotiable

from: pharmiweb.jobs (+3 sources) - 8 days ago

United Kingdom

Minimum 4 years of consulting experience in the Life Science industry (pharmaceutical or biotech/biomedical sectors) as either: Google Documents (drafting of documents and letters, minutes, formatting...

from: jobleads.co.uk - 13 days ago

Adepto Technical Recruitment Ltd - Clwyd, United Kingdom

* Lead investigations and reporting for equipment-related deviations, maintaining compliance integrity. * Strong computer skills, including proficiency in QC pharmaceutical automated systems and Microsoft... £48000 - £58000/annum 12 Month FTC Plus Benefits

from: CV-library.co.uk - 28 days ago

Cramlington, England, United Kingdom

In this role you will be ensuring that the EtQ application and its operation are in compliance and fit for intended use in accordance with the associated GMP/GDP process Standard Operating Procedures ...

from: jobleads.co.uk - 10 days ago

Headcount Solutions Limited - Dublin, Dublin City, Republic of Ireland

Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure compliance with regulatory guidelines and internal policies. Support regulatory inspections and audits...

from: CV-library.co.uk - More than 30 days ago