Job Description
ELISA experience desired for this role.
The focus of this role is development, validation of Immunoassay assays, and analysis of samples using these assays. This work will be performed within a regulatory (GLP/GCP) framework to deliver high quality results to our customers.
Responsibilities:
* Development and validation of Immunoassay methods for quantitation of drugs and biomarkers.
* Application of these methods to routine analysis of samples from pre-clinical toxicology, and clinical safety studies
* Record keeping in compliance with GLP
* Be familiar with, and work in accordance with, SOPs and Study Documents
* Be able to accurately communicate the outcomes of your experiments
* Make suggestions for how processes can be improved
* Take an interest in your own personal development, seek out training, and look for opportunities to grow
* Embrace the Laboratory Charter, keeping your work areas clean and tidy and being respectful to your colleagues
* Be flexible and productive; realise that timelines, priorities and requirements will change regularly and respond to these challenges positively.
* Be familiar with, and work to the Resolian Health and Safety Policy relevant to your role, paying particular attention to COSHH in the lab.
* Complete any mandatory training appropriate for your role.
Experience, Skills & Qualifications
* Degree in biological science, or equivalent relevant experience (essential)
* Experience in a GXP accredited laboratory (desirable)
* Familiarity with ELISA techniques (essential)
* Ability to communicate effectively to peers and customers (essential)
* Excellent attention to detail (essential)