Pharma Packaging Shift Lead - Quality & Compliance

Grand River Aseptic Manufacturing, Inc.; Grand Rapids (MI); On-site; USD 60,000 - 85,000; Full time

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism starting day 1

PTO 13 days/year

Wellness time off

Paid holidays

Pay depends on experience

Job summary

Grand River Aseptic Manufacturing, Inc. is seeking a Packaging Lead to oversee packaging operations for parenteral products, ensuring GMP compliance and timely production in a fast-paced environment.

You will coordinate with QA, Finishing, and other departments, train staff, manage supplies, and document batch records while supporting continuous quality and safety improvements. This is an on-site, full-time role with competitive pay and day-one benefits.

Qualifications

• Lead packaging tasks for parenteral products in a GMP environment.
• Coordinate with QA, Finishing and other departments to ensure schedule adherence.
• Ensure adequate supplies and maintain equipment readiness for production.
• Train staff on safety, cGMP, and standard operating procedures.
• Write and revise batch records and packaging department procedures.

Responsibilities

• Lead all packaging activities for parenteral products and ensure GMP compliance.
• Coordinate cross-functionally with QA, finishing, and production teams.
• Maintain adequate levels of operating supplies for the packaging line.
• Train staff on safety practices and enforce safety regulations.
• Document data, review batch records, and support calibration of equipment.
• Assist with scheduling and performance of routine maintenance and audits.

Skills

Packaging leadership

Cross-functional communication

Attention to safety

Documentation

Training staff

Education

Associate’s degree in life sciences or equivalent

Tools

QAD systems

MS Office Suite (Word/Excel/Outlook)

Job description

Grand River Aseptic Manufacturing, Inc. is seeking a Packaging Lead to oversee packaging operations for parenteral products, ensuring GMP compliance and timely production in a fast-paced environment.

You will coordinate with QA, Finishing, and other departments, train staff, manage supplies, and document batch records while supporting continuous quality and safety improvements. This is an on-site, full-time role with competitive pay and day-one benefits.