Current jobs related to Snr Development Analyst - Northumberland Northumberland - Catalyst Life Sciences
-
System Support Analyst
2 weeks ago
Prestwick, Northumberland, United Kingdom Bellway Homes Full timeSystem Support AnalystWhen registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed.At Bellway we recognise that people are the key to our success and our goal is to provide a rewarding and fulfilling career in line with our values of...
-
QA Test Analyst
2 days ago
Northumberland, United Kingdom Reed Technology Full timeThe Role Hybrid working You will be developing and implementing test plans and test cases Conducting functional and non-functional tests ensuring the software is fit for purpose Working closely with internal and external teams to contribute to the overall success of running projects Stay up to date with the latest technologies with the support from the...
-
QA Test Analyst
3 days ago
Northumberland, United Kingdom Reed Technology Full timeThe Role Hybrid workingYou will be developing and implementing test plans and test casesConducting functional and non-functional tests ensuring the software is fit for purposeWorking closely with internal and external teams to contribute to the overall success of running projectsStay up to date with the latest technologies with the support from the...
Snr Development Analyst
4 months ago
Senior Pharmaceutical Laboratory Analyst
Company Background
A dynamic and innovative pharmaceutical company. They specialise in supporting research, development, manufacture, and licensing of unique and vital pharmaceutical products.
The Role
A fantastic opportunity has arisen for an experienced Senior Analyst to join their growing laboratory team working in the pharmaceutical industry.
The successful candidate will be responsible for the following:
Analysis of pharmaceutical, medical device and nutritional samples
Analytical method development, verification, validation activities to current ICH standards
Second person review of associated data
Preparation, review, and approval of analytical documents to a high standard (e.g., Laboratory notebook, analytical methods, protocols, and reports)
Adherence to GMP standards, inhouse standards and other regulatory guidelines.
Supporting & Contributing to the maintenance of all laboratory equipment (performance qualifications, troubleshooting, and routine maintenance)
Supporting Contributing to the completion of quality tasks within the analytical team (including the completion and review of change controls, deviations, CAPAs, OOS investigations and SOPs)
Supporting the technical development of junior members of the analytical team
Adhering to all current health & safety requirements and contributing to housekeeping activities
Leading and driving laboratory continuous improvement projects.
Qualifications and Experience
The candidate should have a formal academic qualification of at least a BSC degree in chemistry or relevant scientific degree.
At least 5 years’ experience, GMP, pharmaceutical analytical laboratory. Experience of QC, Stability, Method development and validation would be advantageous.
The candidate should have a strong understanding of analytical techniques commonly used within the pharmaceutical industry (e.g., HPLC, GC, dissolution, KF, auto-titration). They should also have significant hands-on experience with at least one chromatographic technique.
