The Model Risk Management (MoRM) team provides independent oversight and governance of model analytics and their implementation into the risk architecture that drive valuation, risk and stress results.
The algorithmic trading model validation team is responsible for the independent review and validation of models used within bank's algorithmic trading business across all asset classes.
The Model Risk Management (MoRM) team provides independent oversight and governance of model analytics and their implementation into the risk architecture that drive valuation, risk and stress results.
After around six months, the Verification & Validation duties will reduce, allowing you to focus your work into Mechanical Engineering duties.
A growing Biotech company, based in Cambridge, are currently looking for a Mechanical Engineer who help with the company's successful Verification & Validation activities, from a mechanical engineering viewpoint.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst to join the QC Technical Services Team on a contract basis.
Key Responsibilities as the QA Validation Specialist
Performing validation activities at the site including Facility, equipment, and process validation.
General
As the QA Validation Specialist, you will be responsible for performing a range of validation activities at the site.
Walker Cole International is searching for a QA Validation Specialist to join an exciting Global Pharmaceutical company based in the South-West of the UK.
Design or plan validation protocols and other documentation for equipment, processes or products meeting internal and external safety and quality requirements.
The purpose of this role of Quality Validation Specialist is to ensure product and system quality.
Your will be evaluating engineering systems based on safety and performance standards and analyse results and update activity logs
Fantastic Validation Technician position within a sought-after employer based in North Kent!
Monday to Friday Hybrid; Excellent company benefits
This role has the opportunity to work in a small, state of the art laboratory environment, completing all allocated formulation sample requests, working to deadlines.
You will be the site Lead for equipment, facility and utility validation to ensure regulatory compliance to established internal and external criteria.
Dechra Pharmaceuticals are looking for an experienced Validation Specialist to join our global manufacturing site.
Your duties will also make you responsible for developing the overall validation program within Dechra and providing guidance in establishing and maintaining cGMP compliant processes and site validation master plan.
Play a pivotal role in crafting, enhancing, and managing intricate data ingestion pipelines, ensuring their efficiency, scalability, and dependability.
Defining and executing equipment validation activities, ensuring all equipment meets the required standards.
General
We are seeking a highly motivated Equipment Validation Specialist to play a vital role in maintaining the integrity and efficiency of pharma manufacturing processes.
Do you have a keen eye for detail and a passion for ensuring top-notch equipment performance?