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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