Validation Engineer

Morgan McKinley; Munster; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

Morgan McKinley is seeking a Validation Engineer to join a leading Pharmaceutical company in Tipperary for a 12-month hourly rate contract. You will support project validation, author master plans, SOPs, protocols and final reports, and perform data analysis.

The role requires equipment and sterilization validation experience, strong technical writing, and excellent communication skills. Collaborative, cross-functional work is expected.

Formación

• Degree in Engineering or a scientific discipline.
• Minimum 3 years in a Validation role within Pharmaceuticals or Medical Devices.
• Equipment Validation and Sterilization Validation experience.
• Strong technical writing and oral communication skills.

Responsabilidades

• Support project validation including equipment performance qualifications (cleaning and sterilization).
• Author validation master plans, SOPs and documentation updates.
• Author validation protocols and final reports; execute validation studies and analyze data.
• Resolve issues encountered during study execution.
• Work in a cross-functional team and independently to achieve validation objectives.

Conocimientos

Technical writing

Oral communication

Educación

Engineering or scientific discipline

Descripción del empleo

We are looking for a Validation Engineer to join our client, a leading Pharmaceutical company in Tipperary 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.
• Strong technical writing and oral communication skills.