Method Development & Validation Supervis
Method Development & Validation Supervisor- Mayo. Key Purpose: Our Client is looking to recruit an experiencedAnalytical Supervisor with extensive knowledge in method development and validationfor their Biologics Department. This role shall have approximately 8 Direct Reports and will bereporting to theAnalytical Services Manager. Key Responsibilities: Responsible for the daily running of the department overseeing the day to day activity with specific responsibility for the organising of work in the area and training. Conduct of water, drug substance and finished product analysis using multiple techniques. Accurate recording of all data. Reporting of results to Manager and Clients. Maintenance of equipment qualification status. SOP writing. Follow up on Quality issues. Compliance with requirements of GMP. Qualifications & Experience: Degree in chemistry, biochemistry or biological subject with analytical component. 5+ years’ experience of working in an Analytical and GMP environment. Good attention to detail and high level of accuracy. Experience of writing study plans and reports preferable but not essential. Ability to work on own initiative as well as part of a team. Excellent interpersonal & communication skills both written and verbal. Enthusiasm for laboratory work. Ability to work under strict hygiene conditions. Excellent IT skills. Proven track record in Supervisory experience. Flexibility to work overtime, weekends and public holidays as required. Experience of working in a GMP environment essential. This job originally appeared on RecruitIreland.com.
384 days ago