GMP Lab Coordinator — Quality & Sample Logistics

Piramal Pharma Limited; Northern (KY); Hybrid; USD 42,000 - 56,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Lab Coordinator to support CDMO activities in a GMP-regulated environment. The role involves logging samples, maintaining records, and ensuring compliance with safety and quality standards across QC and manufacturing interfaces.

The incumbent will handle LIMS data entry, inventory management, and coordination of external laboratory testing while maintaining precise documentation and strong communication with internal stakeholders.

Qualifications

• Education: High School Diploma or equivalent required; Associate degree in a scientific field preferred.

Responsibilities

• Receive, verify, review, and log samples, chemicals, reagents, standards, solvents, and other materials into LIMS.
• Maintain accurate laboratory records and documentation in accordance with cGMP requirements.
• Wash, inspect, and store laboratory glassware using approved procedures.
• Operate and maintain laboratory support equipment including balances, pH meters, and glassware washers.
• Coordinate shipment of QC samples to external testing laboratories.
• Clean and maintain laboratory equipment and work areas.
• Monitor inventory levels and order laboratory 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/USP knowledge

LIMS proficiency

Lab equipment operation

Strong communication

Detail-oriented

Time management

Multitasking

LIMS experience preferred

Education

High school diploma or equivalent

Associate degree in science preferred

Tools

Microsoft Office

LIMS

Job description

Piramal Pharma Solutions is seeking a Lab Coordinator to support CDMO activities in a GMP-regulated environment. The role involves logging samples, maintaining records, and ensuring compliance with safety and quality standards across QC and manufacturing interfaces.

The incumbent will handle LIMS data entry, inventory management, and coordination of external laboratory testing while maintaining precise documentation and strong communication with internal stakeholders.