Senior Analyst
Description✓Leading Analytical Development company seeks an experienced Senior Analyst.
✓About the role:
✓To carry out and monitor the progress of Analytical work to GMP requirements to ensure that project schedules are met and that the work is carried out efficiently and accurately
✓Duties may include:
✓Develop or verify methods for the testing of incoming materials as well as developing methods for intermediates and products manufactured using these materials.
✓Carry out analysis to GMP standards and monitor the levels of compliance within the Laboratory.
✓Maintain records of all analytical work carried out on incoming materials, intermediates and products.
✓Monitor the systems in place within the Laboratory to ensure that procedures are being followed
✓Review analytical documentation that has been generated.
✓Report and investigate incidents of out of specifications results within the Laboratory.
✓Advise and assist staff in troubleshooting methods.
✓Review new methods with respect to their application within the Laboratory.
✓Delegate and monitor the progress of work on a daily basis with regard to the overall schedule of work within the department.
✓Liaise with senior department staff and other departments to update them on the progress of work.
✓Compile SOP's specifications and protocols for various development projects
✓Skills and experience:
✓BSc
✓[or equivalent] in Chemistry or a Life Science subject with a significant chemistry component.
✓Experience in supervising or line managing a team of analysts.
✓Significant experience working in a GMP drug product development laboratory.
✓GMP raw material testing for API, excipients and packaging components.
✓Cleaning validations and verifications.
✓Stability Testing for drug products including assay/related substances, dissolution analysis
✓For more information apply now Show more →
✓About the role:
✓To carry out and monitor the progress of Analytical work to GMP requirements to ensure that project schedules are met and that the work is carried out efficiently and accurately
✓Duties may include:
✓Develop or verify methods for the testing of incoming materials as well as developing methods for intermediates and products manufactured using these materials.
✓Carry out analysis to GMP standards and monitor the levels of compliance within the Laboratory.
✓Maintain records of all analytical work carried out on incoming materials, intermediates and products.
✓Monitor the systems in place within the Laboratory to ensure that procedures are being followed
✓Review analytical documentation that has been generated.
✓Report and investigate incidents of out of specifications results within the Laboratory.
✓Advise and assist staff in troubleshooting methods.
✓Review new methods with respect to their application within the Laboratory.
✓Delegate and monitor the progress of work on a daily basis with regard to the overall schedule of work within the department.
✓Liaise with senior department staff and other departments to update them on the progress of work.
✓Compile SOP's specifications and protocols for various development projects
✓Skills and experience:
✓BSc
✓[or equivalent] in Chemistry or a Life Science subject with a significant chemistry component.
✓Experience in supervising or line managing a team of analysts.
✓Significant experience working in a GMP drug product development laboratory.
✓GMP raw material testing for API, excipients and packaging components.
✓Cleaning validations and verifications.
✓Stability Testing for drug products including assay/related substances, dissolution analysis
✓For more information apply now Show more →