Validation Engineer I - Pharma (cGMP, FDA)

Perrigo; Allegan Township (MI); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Total Rewards program

Career development opportunities

Job summary

Perrigo in Allegan, Michigan is seeking a Validation Engineer I to support validation activities (process, packaging, cleaning and equipment) across manufacturing operations.

The role focuses on preparing and reviewing plans, protocols and studies, coordinating validation events, assessing deviations, and revising master plans and SOPs to meet regulatory requirements and product specifications.

Qualifications

• Bachelor's degree in Engineering, Chemistry, Pharmacy or closely allied field with 1 year pharma industry experience.
• Strong analytical, problem-solving and interpersonal skills.
• Experience with FDA requirements and cGMP.
• Ability to write technical documents of medium complexity.
• Excellent organizational and communication skills.

Responsibilities

• Prepare and review validation plans, protocols, reports, and studies for validation activities (Process, Packaging, Cleaning, Equipment).
• Coordinate timing of validation events; assess deviations and recommend corrective actions.
• Review and revise master plans and SOPs to align with regulatory requirements and product specifications.

Skills

Analytical skills

Problem-solving

Interpersonal skills

Oral communication

Written communication

Organizational skills

Education

Bachelor's degree in Engineering, Chemistry, Pharmacy or closely allied field

Job description

Perrigo in Allegan, Michigan is seeking a Validation Engineer I to support validation activities (process, packaging, cleaning and equipment) across manufacturing operations.

The role focuses on preparing and reviewing plans, protocols and studies, coordinating validation events, assessing deviations, and revising master plans and SOPs to meet regulatory requirements and product specifications.