Are you looking to take your analytical skills to the next level? Do you have some experience of working in a solid dose pharmaceutical environment? Do you have some experience working in a regulated analytical laboratory setting with a strong background inHPLC and GC?
This is an exciting opportunity to join a global pharmaceutical organisation, working as an Analytical Scientist. You will support the application of chromatography methods to understand impurities in a broad range of excipients and active pharmaceutical ingredients.
The role is an 18-month contract and it’s based in Sandwich, Kent. There is a competitive hourly rate ranging from £17 to £23, working through an umbrella company.
SKILLS NEEDED:
Proven experience with the application of chromatography methods to quantify impurities
Demonstrated application of wider suite of analytical methods to build understanding of material attributes.
Understanding of analytical approaches to evaluate elemental impurities
Ability to work independently, and to present analytical results and conclusions.
Excellent communication and interpersonal skills, both written and verbal are required.
Design, follow and review protocols, scientific methods, and departmental procedures.
Experience with HPLC/UPLC method development & validation
• Strong written and oral communication skills.
• Independent, accountable, attention to detail, ability to effectively balance multiple projects, and strong interpersonal/communication skills are required.
• Must be highly motivated and self-directed
• Demonstrates good interpersonal skills and works well with personnel at all levels.
ROLE RESPONSIBILITIES:
Support the development and application of chromatography methods for the quantitation of small molecule impurities.
Evaluate chemical properties of a broad range of excipients using suite of analytical methods.
Determine the elemental chemical profiles of APIs, excipients and drug products to enable understanding of composition and impurities to support product investigations and process understanding.
Perform experiments in accordance with good laboratory practices (GLP), established business processes and protocols, and applicable SOPs.
Document laboratory work that is detailed, timely and in compliance with GLP requirements
Conduct technical data reviews, and present data interpretation and conclusions to customers for making informed decisions.
Prepares and reviews technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.