Clinical Method Development & Validation Team Lead
Newry, Co. Down
CPL are continuing to work closely with one of the top veterinary pharmaceutical companies globally as they continue their exciting growth plans across Europe and specifically within Northern Ireland.
I am currently recruiting for a Clinical Method Development & Validation Team Leader on a full time, permanent basis.
You will be joining a very experienced R&D team to be based in Newry, Co. Down.
So what’s in it for you?
The business strategy is supported by their Values – Customer Value, One Team, Results Driven, Excellence, Innovation, and Quality – and they support their employees to live the behaviours that creates the culture. the on-going success is based on the expertise, knowledge and innovation of our employees.
· An excellent salary accompanied by an endless benefits package
· 34 Days annual leave
· Enhanced pension contribution
· Annual Bonus
Roles & Responsibilities;
We are currently recruiting for the role of Clinical Method Development & Validation Lead. You will lead the team in the development and validation of accurate, precise, robust bioanalytical methods of analysis within the GLP Clinical Research Section of R&D.
You will provide expertise in method development planning and execution and ensure all validation activity conducted within the laboratory is in compliance with GLP, VICH guidance and in-house SOPs/SOMS. All work under their direction will be conducted in compliance with H&S requirements and other quality standards detailed within the Research Division GLP Policy Document. You will manage the team and their work schedules within the GLP Laboratory to ensure delivery.
What we are looking for;
At least four years lab experience in a GxP laboratory, 2 years consisting of management.
A minimum of 4 years’ experience working in a laboratory environment with HPLC, UPLC and frequent use of a chromatography data management system.
Proven ability to successfully develop, optimise and validate analytical methods.
Proven ability to problem solve and troubleshoot complex problems with methods and equipment
Highly motivated with excellent analytical technique
Good knowledge of Regulatory Guidelines.
Demonstrated ability to work in a high pressured environment.
Experience of preparing and reviewing validation protocols, SOMs & SOPs
Next Steps
If this sounds like an opportunity that could potentially be of interest to you, simply get in touch with Seamus Moore by applying to this advertisement or giving me a call.
