Process Validation Engineer – Pharma/Biotech, 24/7 Ops

TEST369; Grand Rapids (MI); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical benefits

Prescription coverage

Dental insurance

Vision insurance

Life insurance

Disability benefits

401(k) immediate vesting

Paid volunteer time

Job summary

TEST369 is seeking a Process Validation professional to support validation of cGMP equipment, facilities, and processes in a fast-paced, high-standards environment. The role includes validating manufacturing processes and production equipment, and coordinating with Technical Services, Quality Control, and Manufacturing teams.

Ideal candidates will have pharma/biotech manufacturing experience, strong project management skills, and comfort with 24/7 operations.

Qualifications

• A minimum level of project management and leadership experience is required.
• Proficiency with Microsoft Word, Excel, and Outlook is required.

Responsibilities

• Assist with maintaining and revising validation procedures.
• Establish and maintain good practices to support aseptic environments.
• Develop and execute validation programs for manufacturing processes, equipment, and cleaning.
• Provide validation support to internal customers and attend client meetings.
• Write, review, and execute protocols and studies for process improvement and scale up.

Skills

Project management

Leadership

Education

Bachelor's degree in engineering or life sciences

Tools

Microsoft Word

Microsoft Excel

Outlook

Job description

TEST369 is seeking a Process Validation professional to support validation of cGMP equipment, facilities, and processes in a fast-paced, high-standards environment. The role includes validating manufacturing processes and production equipment, and coordinating with Technical Services, Quality Control, and Manufacturing teams.

Ideal candidates will have pharma/biotech manufacturing experience, strong project management skills, and comfort with 24/7 operations.