Validation Engineer

Morgan McKinley; Carlow; On-site; EUR 41,000 - 69,000; Full time

Job summary

Morgan McKinley is seeking a Validation Engineer for a 12-month hourly rate contract with a leading Pharmaceutical company in Carlow, Ireland.

The role involves project validation support, qualifications, and documentation. The ideal candidate has a degree in Engineering or science and at least 3 years in validation within pharma or medical devices, with experience in equipment and sterilization validation.

Qualifications

• 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.

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

Engineering degree

Validation experience

Equipment validation

Sterilization validation

Technical writing

Communication skills

Education

Engineering or scientific degree

Job description

We are looking for a Validation Engineer to join our client, a leading Pharmaceutical 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.