Lab QC & LIMS Coordinator — GMP & Inventory

PPL Healthcare LLC; Sellersville (Bucks County); On-site; USD 42,000 - 64,000; Full time

Job summary

Piramal Pharma Solutions in the United States is seeking a Laboratory Coordinator to support daily QC operations, log samples into LIMS, and assist with inventory and safety procedures.

The role requires a High School Diploma or equivalent with 1–2 years in a GMP-regulated lab; Associate degree in a scientific field is preferred. Strong documentation and equipment handling skills are essential.

Qualifications

• High School Diploma or equivalent required.
• Associate degree in a scientific field preferred.
• Minimum 1–2 years in GMP-regulated lab.
• LIMS experience preferred.
• Knowledge of cGMP and USP requirements.
• Proficiency with laboratory safety practices.

Responsibilities

• Receive, verify, review, and log samples into LIMS.
• Maintain accurate laboratory records and documentation per cGMP.
• Wash, inspect, and store laboratory glassware.
• Operate and maintain laboratory equipment including balances and pH meters.
• Coordinate shipment of QC samples to external testing laboratories.
• Clean and maintain laboratory equipment and work areas.
• Monitor inventory levels and order chemicals, standards, consumables, and supplies.
• Support Quality Control personnel with routine laboratory activities.
• Ensure compliance with safety, quality, and regulatory requirements.
• Perform other duties as assigned.

Skills

cGMP knowledge

USP knowledge

Microsoft Office

LIMS experience

Lab equipment operation

Communication skills

Attention to detail

Time management

Multitasking

Education

High School Diploma or equivalent

Associate degree in a scientific field (preferred)

Tools

LIMS software

Microsoft Office suite

Job description

Piramal Pharma Solutions in the United States is seeking a Laboratory Coordinator to support daily QC operations, log samples into LIMS, and assist with inventory and safety procedures.

The role requires a High School Diploma or equivalent with 1–2 years in a GMP-regulated lab; Associate degree in a scientific field is preferred. Strong documentation and equipment handling skills are essential.