QC Lab Coordinator - LIMS & cGMP Support

Piramal Pharma Ltd; Sellersville (AL); On-site; USD 42,000 - 62,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Lab Coordinator to support daily Quality Control laboratory operations by receiving, reviewing, and logging samples, chemicals, reagents, standards, solvents, and other materials into the Laboratory Information Management System (LIMS).

The role ensures compliance with cGMP and company requirements, maintains accurate records, and assists with inventory and sample shipments across QC activities.

Qualifications

• High School Diploma or equivalent required.
• Associate degree in a scientific field preferred.
• 1–2 years of GMP-regulated laboratory experience.
• Experience with LIMS and lab inventory management preferred.

Responsibilities

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

LIMS proficiency

MS Office

Equipment operation

Communication skills

Detail-oriented

Multitasking

Education

High School Diploma or equivalent

Associate degree preferred

Tools

LIMS software

Microsoft Office suite

Job description

Piramal Pharma Solutions is seeking a Lab Coordinator to support daily Quality Control laboratory operations by receiving, reviewing, and logging samples, chemicals, reagents, standards, solvents, and other materials into the Laboratory Information Management System (LIMS).

The role ensures compliance with cGMP and company requirements, maintains accurate records, and assists with inventory and sample shipments across QC activities.