Validation Engineer I — Pharma Quality & Compliance

Perrigouk; Michigan; Hybrid; USD 75,000 - 110,000; Full time

Benefits offered by this job

Competitive compensation

Career development opportunities

Benefits tailored to you and family

Job summary

Perrigo in Allegan, Michigan is seeking a Validation Engineer to prepare and review validation plans, protocols, reports and studies for processes, packaging, cleaning and equipment. The role ensures events occur in line with procedures and regulatory expectations.

The candidate should hold a Bachelor's degree in Engineering, Chemistry or Pharmacy with pharma experience, strong analytical and writing skills, and familiarity with FDA/cGMP requirements.

Qualifications

• Bachelor's degree in Engineering, Chemistry, Pharmacy or closely allied field, plus one year of pharmaceutical industry experience.
• Analytical skills with problem-solving ability and good interpersonal skills.
• Experience with FDA requirements and cGMP.
• Ability to write technical documents for applications and systems of medium complexity.
• Ability to organize multiple tasks and changing priorities to meet deadlines.
• Excellent oral and written communication and interpersonal skills.
• Basic understanding of statistics; computer literacy.

Responsibilities

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

Skills

Analytical skills

Problem-solving ability

Interpersonal skills

Oral and written communication

Statistical understanding

Time management

Technical writing

Education

Bachelor's degree in Engineering, Chemistry, Pharmacy

Job description

Perrigo in Allegan, Michigan is seeking a Validation Engineer to prepare and review validation plans, protocols, reports and studies for processes, packaging, cleaning and equipment. The role ensures events occur in line with procedures and regulatory expectations.

The candidate should hold a Bachelor's degree in Engineering, Chemistry or Pharmacy with pharma experience, strong analytical and writing skills, and familiarity with FDA/cGMP requirements.