Here at Hays Life Sciences, our Lab Services client in Cork is hiring an Analytical Validation Transfer Scientist. They should have a keen aptitude for implementing and maintaining standards and driving efficiency within the business .

Job Description

A leading lab that provides testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide.

The purpose of this role is to carry out scientific test procedures on client samples and produce accurate results within an acceptable time frame using company procedures and also to be responsible for completion of the more technically challenging analysis. This person will also work to develop any ancillary procedures associated with the methods and technical systems used, ensuring customer samples are completed within their required specifications.

This person will support complex analytical testing and high-knowledge projects. This may be achieved by performing additional duties or functions (e.g. data review) that will be commensurate with your training and skillset.

This person will carry out the non-routine tasks in the laboratory or carry out the particular type(s) of analysis assigned to them, back filling for analysts as required.

Responsible for developing and validating new tests and procedures for company and clients.

Responsible for the completion of specific technological projects and writing up the results of these projects accurately, confidentially and on time for the clients.

Scientists are permitted to sign all technical documents once their training in this task is successfully completed. This includes laboratory reports, SOPs, protocols, investigation reports and any other documentation issued.

Responsible for signing out customer work from the analysts.

Deputising for management as required.

Responsible for keeping the laboratory area clean and tidy in both ‘seen’ and ‘unseen’ areas.

This person will be responsible for providing cover for other members of staff as required and for taking part in the company’s weekend rota and/or overtime schedule.

This person will ensure that all documentation is completed on time, accurately and legibly.

They are responsible for their training, keeping their training records up to date and initiating training where possible when free from work.

Responsible for updating any relevant documentation as required.

Responsible for direct communication with clients appropriately.

Liaise closely with the Section Manager to ensure that resources are available to guarantee that testing activities are completed to customer’s timelines.

Responsible for the review of test methods for quotation purposes.

Responsible for continually liaising with management, customers and other members of the organisation on any relevant problem areas or enhancements to the business.

Adhere to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.

Ensure that customers’ requirements are fully met and, in so doing, be flexible when working in any area of the business as is required.

Identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.

Qualifications
Qualifications/Experience

5 - 7 years experience in HPLC, CE, SDS Page, IEF & Method Validation.

Large Molecule testing,