QC Analyst I

Evotec

Working within the pilot plant production shift team supporting all the cGMP pilot plant manufacturing through analysis of Raw materials, intermediates, final products and reaction profiling.
Analysis is required over a wide range of techniques, including HPLC – (area%; assays; MS); GC – (area%; solvents); standard pharmacopoeia methodology (FTIR, NMR, XRPD and Karl Fischer etc.).
As part of the wider integrated team the role is integral to ensuring that Aptuit produce work of the highest quality. Experience in carrying out the following analytical techniques is essential to this role: HPLC – (area%; assays); GC – (area%); standard pharmacopoeia methodology at an intermediate level (NMR and Karl Fischer etc.).
Experience in a method development environment would be an advantage.

Degree in Chemistry/Analytical Chemistry or other related discipline.
Excellent time management and prioritisation capabilities. Ability to successfully manage multiple tasks simultaneously.
Excellent written and verbal communication skills.
Knowledge of GMP and other regulatory requirements relevant to an analytical environment required.
Prior experience of method development is a distinct advantage.
An understanding of Empower (CDS System) and the ability to use it to capture and process data would be benifical.
Proficiency with email and Microsoft Office applications.
Highly detail orientated with an organised approach to work.
Superior analytical and problem solving skills.
Demonstrated successful planning and organizational skills.
Able to interact effectively and positively with all internal departments.
Able to work on your own and as part of a team.
Flexible and adaptable problem solving skills.
Strong sense of accountability for the outcome.