Pharma Sampling Coordinator - GMP & Compliance

Paylocity; Grand Rapids (MI); On-site; USD 38,000 - 56,000; Full time

Benefits offered by this job

Benefits from day 1

Volunteer time off

PTO

Wellness time off

Paid holidays

Competitive pay discussed at interview

Job summary

Grand River Aseptic Manufacturing (GRAM) in Grand Rapids, Michigan, is seeking a Finishing Technician I to coordinate internal sample pulls and inspections. You will partner with Sample Coordinators, Supply Chain, Quality, Operations, CI, Validation, MSAT, and Project Management to support site objectives.

This role requires a High School Diploma, proficiency in Word/Excel/Outlook, and experience with pharmaceutical packaging and cGMP standards.

Qualifications

• High School Diploma or GED required.
• Proficiency in Word, Excel and Outlook.

Responsibilities

• Perform sample pulls with pertinent documentation (SOPs, protocols, reports).
• Pull, inspect and complete GMP/non-GMP docs for Sample Management including in-process, PPQ/ENG, media fill, incoming, finished goods, logs, forms, and Master Batch Records.
• Collaborate cross-functionally with Operations, Engineering, Maintenance, Project Management, Quality, MSAT and others to gather data for timely sample submissions.
• Follow procedures on communication of sample pull, shipments, operations, quality, compliance, custody, storage, and GDPs.
• Assist with roadblocks affecting sample pull and inspections; raise issues to Sampling Management and Sample Coordinators.
• Adhere to KPIs and project timelines; take corrective action through creative problem-solving.

Skills

Microsoft Word

Microsoft Excel

Outlook

Education

High School Diploma/GED

Associate degree or equivalent

Job description

Grand River Aseptic Manufacturing (GRAM) in Grand Rapids, Michigan, is seeking a Finishing Technician I to coordinate internal sample pulls and inspections. You will partner with Sample Coordinators, Supply Chain, Quality, Operations, CI, Validation, MSAT, and Project Management to support site objectives.

This role requires a High School Diploma, proficiency in Word/Excel/Outlook, and experience with pharmaceutical packaging and cGMP standards.