QC Lab Coordinator — LIMS & cGMP Compliance

Piramal Pharma Limited; Sellersville (Bucks County); On-site; USD 52,000 - 65,000; Full time

Job summary

Piramal Pharma Solutions, a global CDMO, is seeking a Laboratory Coordinator to support daily QC laboratory operations. You will log samples into LIMS, manage inventory, and assist with routine testing shipments while ensuring adherence to cGMP and company requirements.

This role emphasizes meticulous record-keeping and cross-functional support. The position requires 1–2 years of GMP-regulated lab experience, High School Diploma or equivalent, and preferred Associate degree in a scientific

Qualifications

• Must have knowledge of cGMP and USP requirements.
• Proficient in operating laboratory equipment.
• Strong written and verbal communication skills.
• Attention to detail and accuracy.
• Problem-solving and time-management abilities.
• Ability to multitask and prioritize activities.
• LIMS experience preferred.

Responsibilities

• Receive, verify, review, and log samples, chemicals, reagents, standards, solvents, and other materials into LIMS.
• Maintain accurate laboratory records in accordance with cGMP requirements.
• 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.
• Monitor inventory levels and order laboratory chemicals, standards, 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

MS Office proficiency

LIMS proficiency

Equipment operation

Communication skills

Attention to detail

Time management

Multitasking

Education

High School Diploma or equivalent

Associate degree in a scientific field

Tools

LIMS

Microsoft Office

Job description

Piramal Pharma Solutions, a global CDMO, is seeking a Laboratory Coordinator to support daily QC laboratory operations. You will log samples into LIMS, manage inventory, and assist with routine testing shipments while ensuring adherence to cGMP and company requirements.

This role emphasizes meticulous record-keeping and cross-functional support. The position requires 1–2 years of GMP-regulated lab experience, High School Diploma or equivalent, and preferred Associate degree in a scientific