QA / Quality Operations Consultant

Wilson

Contract

Negotiable

Quality

CR/607876_1787905558

Overview

We are seeking experienced quality professionals to support a major pharmaceutical manufacturing client in Greenville, North Carolina. This engagement focuses on strengthening quality oversight, manufacturing compliance, remediation activities, and inspection readiness efforts within a regulated GMP environment.

Consultants will join an established project team and provide onsite support for approximately 6 to 7 months. The role follows a two-week rotational onsite schedule with limited remote responsibilities during off-site periods.

Responsibilities

Provide quality assurance oversight across manufacturing operations.
Support shop floor quality activities within GMP-regulated environments.
Partner with manufacturing teams to ensure compliance with quality standards and procedures.
Assist with deviation investigations and corrective and preventive action (CAPA) activities.
Contribute to inspection readiness programmes and regulatory compliance initiatives.
Support remediation and quality improvement efforts.
Review manufacturing documentation and quality records.
Identify compliance risks and escalate quality concerns as appropriate.
Collaborate with cross-functional teams including Quality, Manufacturing, and Compliance functions.
Assist in maintaining regulatory expectations across sterile and aseptic operations when applicable.

Requirements

Experience within pharmaceutical, biotechnology, biologics, or related GMP manufacturing environments.
Strong background in Quality Assurance or Quality Operations.
Experience supporting manufacturing compliance programmes.
Understanding of deviation management and CAPA processes.
Knowledge of FDA and GMP regulatory requirements.
Prior exposure to inspection readiness or remediation projects preferred.
Experience in sterile manufacturing, aseptic processing, or fill-finish operations is highly desirable.
Ability to work onsite in Greenville, NC on a rotational schedule.
Strong communication, documentation, and stakeholder engagement skills.

Ideal Candidate Profile

The ideal candidate is a hands-on Quality Assurance or Quality Operations professional with experience supporting GMP manufacturing environments. They have worked closely with production teams on the shop floor, possess strong compliance knowledge, and are comfortable managing deviations, CAPAs, inspection readiness activities, and remediation programmes. Experience within sterile, aseptic, biologics, or fill-finish manufacturing environments is especially valuable.

FAQs

I have applied for a role, what happens next?

Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your CV and details on file so when we see similar roles or see skillsets that drive growth in organisations, we will always reach out to discuss opportunities.

This role doesn’t 100% suit my next professional move, can you help?

Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.

We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business.

That's why we recommend registering your CV so you can be considered for roles that have yet to be created.

Can you help with resume preparation, interviews, and offer negotiation?

Yes, we help with CV and interview preparation. From customised support on how to optimise your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.