Process Validation Engineer - Pharma (24/7 Ops)

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Paid volunteer hours

Paid time off

Job summary

Grand River Aseptic Manufacturing Inc. seeks a Process Validation Engineer/Specialist to support validation of cGMP equipment and processes. Applicants should have a bachelor’s degree in Engineering or a life sciences field and experience in pharmaceutical manufacturing.

The position offers competitive benefits including medical and dental insurance starting day one, paid volunteerism, and paid time off for vacations and wellness.

Qualifications

• 1-4 years' work experience in a pharma or biotech manufacturing environment.
• Proficient computer skills in Microsoft applications.
• Open to working in a cleanroom environment.

Responsibilities

• Maintain and revise validation procedures.
• Support manufacturing processes and equipment validation.
• Provide validation support to internal and external customers.

Skills

Project management

Leadership skills

Proficient in Microsoft Word, Excel, Outlook

Education

Bachelor's degree in Engineering or Life Sciences

Job description

Grand River Aseptic Manufacturing Inc. seeks a Process Validation Engineer/Specialist to support validation of cGMP equipment and processes. Applicants should have a bachelor’s degree in Engineering or a life sciences field and experience in pharmaceutical manufacturing.

The position offers competitive benefits including medical and dental insurance starting day one, paid volunteerism, and paid time off for vacations and wellness.