Working within a small team, the Validation Engineer role will primarily involve preparing and executing validation/ qualification protocols.
Inizio Engage have the pleasure of working with one of the fastest growing privately owned businesses in the UK involved in the development, manufacture and testing of pharmaceutical and biotechnology products and medical devices.
The ideal candidate will have a good understanding of manufacturing practice and background knowledge of clean rooms but our Client will also consider new to industry candidates with a science degree for this role.
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.
Spurgeon's College is looking to appoint a dynamic Head of Validation to provide management and active delivery of our validation processes as they pertain to programme design, development, academic validation and managing the College's approach to collaborative partnerships (validation and franchise).
The Head of Validation, working with the Vice-Chancellor and Deputy Vice-Chancellor, will be responsible for the active oversight of the quality and standards of higher education (HE) and non-HE programmes offered by collaborative academic partners.
Working closely with the College's Senior Management Team (SMT), the Head of Validation will play a key role in ensuring that the College's new academic programmes are project managed to successful completion and the 'in prospect' and potential academic collaborative partnerships are project managed to successful implementation.
This opportunity is for a QC Analytical Validation Specialist to join the QC Technical Services Team on a contract basis.
The duration of the contract will be 23 months.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
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.
The Customer Verification Risk Analysis department is responsible for identifying and mitigating the risk of syndicated activity, while ensuring genuine customers are able to utilise the full product range on offer.
As a Specialist in the Customer Verification Risk Analysis department, you will be responsible for reviewing the legitimacy of customer verification documents and identifying fraudulent account profiles.
You will be part of the team playing a key role at the verification stage of the customer journey, protecting the business from threats, related to abusive and syndicated activity.