Packaging Line Lead — GMP Champion with Team Impact

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 48,000 - 68,000; Full time

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism starting day 1

PTO 13 days per year

Wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing is seeking a Packaging Lead to oversee the execution of packaging tasks, lead operators, and ensure cGMP compliance. You will guide labeling and packaging lines, direct post-run activities, and support terminal wash and PFA operations.

You will collaborate with QA and manufacturing to maintain schedules, review batch records, and keep thorough documentation. This role requires at least 1 year in regulated pharma packaging and readiness for overtime as needed.

Qualifications

• 1+ years of relevant pharma/biopharma manufacturing experience.
• Experience with packaging of regulated products and CFR guidelines.
• Knowledgeable of GDPs and quality systems.
• Willing to work overtime/weekends when required.
• Proficient in MS Word, Excel and Outlook.

Responsibilities

• Provide direction and support to the packaging team to ensure cleanliness and maintenance.
• Support training processes, procedures, and records for labeling and packaging.
• Coordinate with manufacturing and QA to prioritize finishing schedules.
• Review Master Batch Records and related documentation for GDP compliance.
• Perform material transactions in GRAM's QAD system.
• Participate in quality investigations related to labeling and packaging.
• Assist troubleshooting and resolution of quality events.
• Communicate clearly with cross-functional teams and shift leads.

Skills

QA knowledge

cGMP familiarity

FDA guidelines understanding

GMP standards

Overtime availability

Microsoft Word / Excel / Outlook

Tools

Microsoft Word

Excel

Outlook

Job description

Grand River Aseptic Manufacturing is seeking a Packaging Lead to oversee the execution of packaging tasks, lead operators, and ensure cGMP compliance. You will guide labeling and packaging lines, direct post-run activities, and support terminal wash and PFA operations.

You will collaborate with QA and manufacturing to maintain schedules, review batch records, and keep thorough documentation. This role requires at least 1 year in regulated pharma packaging and readiness for overtime as needed.