This is a full time, 12 month fixed term contact position, working a 37 hour flexible week Monday - Friday.
The purpose of this job is to support analysis of pharmaceutical Drug Product for early stage projects.
Responsibilities:
Perform routine and non-routine analysis using traditional and modern analytical techniques like HPLC, dissolution, KF, and spectroscopic analysis, as required by the Lead Scientist or customer representative. Support development and validation of analytical procedures used for Drug Products in line with experience. Work with a high level of flexibility due to the nature of the service area where project demands regularly change. Support work activities across multiple projects. Think logically with the ability to plan own work. Effectively collaborate and communicate scientific ideas to both internal and external partners. Prepare and approve results for tests in which they have received the appropriate training and are deemed competent. Support the authoring of documentation. Minimum Requirements:
Educated to degree level in a relevant scientific discipline. Relevant practical lab skills, as well as experience of key analytical techniques (HPLC, Dissolution, KF, Particle Size Analysis, and pH). Analytical method development and validation skills would be beneficial. Understanding in conducting forced degradation studies. Experience operating in a GMP environment. Proven ability to work with a high level of flexibility, ownership, and understanding where to apply capacity proactively. Experience handling Drug Products – Tablets and Parenterals. Ability to use literature databases. Good collaboration skills. Excellent analytical thinking and problem-solving skills, with a focus on detail.
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Perform routine and non-routine analysis using traditional and modern analytical techniques like HPLC, dissolution, KF, and spectroscopic analysis, as required by the Lead Scientist or customer representative. Support development and validation of analytical procedures used for Drug Products in line with experience. Work with a high level of flexibility due to the nature of the service area where project demands regularly change. Support work activities across multiple projects. Think logically with the ability to plan own work. Effectively collaborate and communicate scientific ideas to both internal and external partners. Prepare and approve results for tests in which they have received the appropriate training and are deemed competent. Support the authoring of documentation. Minimum Requirements:
Educated to degree level in a relevant scientific discipline. Relevant practical lab skills, as well as experience of key analytical techniques (HPLC, Dissolution, KF, Particle Size Analysis, and pH). Analytical method development and validation skills would be beneficial. Understanding in conducting forced degradation studies. Experience operating in a GMP environment. Proven ability to work with a high level of flexibility, ownership, and understanding where to apply capacity proactively. Experience handling Drug Products – Tablets and Parenterals. Ability to use literature databases. Good collaboration skills. Excellent analytical thinking and problem-solving skills, with a focus on detail.
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