Responsibilities
Work to laboratory SOPs and adhere to cGMP record keeping and procedures.
Provide right first-time analytical data to agreed schedules using techniques such as LC-MS, GC-MS and other separation techniques.
Provide verbal and written reports, both internally and externally.
Perform data review.
Lead development, validation and sample analysis on regulated and non-regulated projects, ensuring delivery to time, budget and providing excellent customer service.
Supervise and share knowledge with more junior scientists on scientific and regulatory issues.
Suggest and lead process improvements.
Contribute to the Quality Assurance programme of laboratory audits, investigations, and CAPA.
Personal Attributes
Excellent written and verbal communication skills.
Ability to successfully manage large amounts of information.
Good organisational skills to perform tasks in a meticulous manner with close attention to detail.
Flexible attitude to changing priorities and timelines, responding to these challenges positively.
Good time management skills and ability to work and deliver to tight deadlines.
Highly motivated and willing to get involved with new initiatives.
Enthusiastic, with a positive attitude.
Education, Skills & Qualifications
Degree or higher in analytical chemistry, chemistry or related subject.
At least 5 years’ experience of working in an analytical laboratory.
Confident in separation science and/or Mass Spectrometry.
Experience of working within GxP regulations.
Experience in managing complex analytical projects.
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