Quality Associate and Quality Control

Meet Life Sciences Ltd.; North Carolina; On-site; USD 70,000 - 90,000; Full time

Job summary

Meet Life Sciences Ltd. is seeking experienced Quality Assurance professionals for multiple opportunities in the Raleigh-Durham area.

Positions span QA Specialist, QA Associate, QA Compliance, batch record review, deviations, CAPA, change control, and document control in GMP-regulated pharmaceutical/biotech environments. Candidates with CDMO experience and strong quality systems knowledge are encouraged to apply, with roles potentially available across various experience levels and quality

Qualifications

• Previous experience working in a GMP-regulated environment is required.
• CDMO experience is highly preferred.
• Experience supporting pharmaceutical or biotechnology manufacturing, quality systems, or laboratory operations.
• Knowledge of applicable quality standards, documentation practices, and regulatory requirements.
• Strong attention to detail, organizational skills, and a commitment to product quality and compliance.

Responsibilities

• Quality roles include QA Specialist, QA Associate, QA Compliance.
• Perform batch record reviews and deviations investigations.
• Support CAPA, change control, and document control processes.
• Ensure compliance with GMP and regulatory requirements in manufacturing environments.

Skills

GMP environment

CDMO experience

Quality systems

Deviations handling

CAPA

Change Control

Document Control

Attention to detail

Job description

We are seeking experienced Quality Assurance professionals for multiple opportunities with established Contract Development and Manufacturing Organization (CDMO) clients in the Raleigh-Durham area.

If you have experience working in a GMP-regulated pharmaceutical, biotechnology, or life sciences environment, we encourage you to apply!

Quality Assurance (QA)

Quality Specialist, QA Associate, QA Compliance, Batch Record Review, Deviations, CAPA, Change Control, and Document Control.

Qualifications

• Previous experience working in a GMP-regulated environment is required.
• Previous CDMO experience is highly preferred.
• Experience supporting pharmaceutical or biotechnology manufacturing, quality systems, or laboratory operations.
• Knowledge of applicable quality standards, documentation practices, and regulatory requirements.
• Strong attention to detail, organizational skills, and a commitment to product quality and compliance.

Why Apply?

Explore multiple opportunities with CDMO clients throughout the Raleigh-Durham area, with positions potentially available across different experience levels and quality functions.