About the job

We are looking for a Validation Engineer to join our client, a leading Biopharmaceutical company in Carlow for a 12 month hourly rate contract.

Key Responsibilities

• Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilization validation)
• Authoring project validation master plans; SOP and documentation updates; Authoring validation protocols and final reports, executing validation studies, analysis of validation data; Resolving technical issues encountered during study execution.
• This individual will be required to work in a cross-functional team and independently to accomplish validation project objectives.
• Works with moderate work direction and is skilled and knowledgeable to the position.

Skills, Attributes & Experience

• Degree in Engineering or a Scientific related discipline.
• Minimum of 3 years + experience working in a Validation role within Pharmaceuticals or Medical Device.
• Equipment Validation and Sterilization Validation experience.
• The successful candidate must have strong technical writing and oral communication skills.