Aseptic GMP Process Engineer

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Benefits starting day 1 (medical, Rx,-

Paid volunteerism - 16 hours/year

PTO + WTO + Holidays

Job summary

Grand River Aseptic Manufacturing (GRAM) seeks a Manufacturing Process Engineer to execute technical tasks within GMP operations in a multi-product Formulation/Fill CMO facility. You will contribute to solving technical problems in aseptic filling and formulation prep, ensuring safety, quality, and performance.

The role supports cGMP initiatives, change control, and process optimization across manufacturing and QA teams, with on-site responsibilities and some off-shift work as needed.

Qualifications

• Bachelor’s degree or equivalent in engineering or life sciences.
• Proficient MS Word, Excel and Outlook.
• Flexible for off-shift and/or on-call work as needed.

Responsibilities

• Execute Change Control and CA/PA projects for manufacturing/finishing departments.
• Assess and correct cGMP discrepancies.
• Assist with batch process data, analyze datasets, and generate reports.
• Maintain and operate equipment in the assigned area; support aseptic fill/finish techs.
• Perform minor preventive maintenance and assist with more complex PMs.
• Engage in process optimization and troubleshooting of equipment and software.
• Collaborate with leadership to minimize error, failure, and contamination.

Skills

MS Office

Off-shift availability

Analytical thinking

Education

Bachelor’s degree in mechanical or electrical engineering, automation, or life sciences OR equivalent experience

Master’s degree with 1 year of relevant experience or Bachelor’s degree with 2 years of relevant experience or 7 years of training/experience

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) seeks a Manufacturing Process Engineer to execute technical tasks within GMP operations in a multi-product Formulation/Fill CMO facility. You will contribute to solving technical problems in aseptic filling and formulation prep, ensuring safety, quality, and performance.

The role supports cGMP initiatives, change control, and process optimization across manufacturing and QA teams, with on-site responsibilities and some off-shift work as needed.