Junior Validation Engineer - Pharma, cGMP Ready

Biopharma Careers; Michigan; On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Total Rewards

Forbes recognition as America's Best

Job summary

Perrigo is seeking a Validation Engineer to work at our Allegan, Michigan facility. You will prepare and review validation plans, protocols, reports and studies for processes, packaging, cleaning, and equipment, ensuring adherence to approved procedures and regulatory requirements.

The role involves coordinating validation events, assessing deviations, and updating master plans and SOPs to maintain compliance with quality standards. Strong writing and communication skills are essential.

Qualifications

• Bachelor's degree in Engineering, Chemistry, Pharmacy or a closely allied field and 1 year pharma experience.
• Ability to interpret FDA requirements and cGMP regulations.
• Ability to write technical documents for applications and systems of medium complexity.
• Strong organizational skills to manage multiple tasks and changing priorities.

Responsibilities

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

Skills

Analytical skills

Problem solving

Written communication

Interpersonal skills

Organizational skills

Statistical understanding

Computer literacy

Education

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

Job description

Perrigo is seeking a Validation Engineer to work at our Allegan, Michigan facility. You will prepare and review validation plans, protocols, reports and studies for processes, packaging, cleaning, and equipment, ensuring adherence to approved procedures and regulatory requirements.

The role involves coordinating validation events, assessing deviations, and updating master plans and SOPs to maintain compliance with quality standards. Strong writing and communication skills are essential.