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Quality Assurance Associate Jobs in Roxboro, NC (NOW HIRING)

The Quality Assurance Associate is primarily concerned with the review of packaging and labeling batch records and the release of clinical supplies. The Quality Assurance Associate assures that no ...

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Quality Assurance Engineer

Oxford, NC Β· On-site

$70K - $95K/yr

Quality * Assesses the impact of deviations, CAPAs, and associated change request on the validation status of equipment and/or systems. * Assist in defining, testing, and implementing comprehensive ...

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Quality Assurance Associate information

See Roxboro, NC salary details

$11

$25

$54

How much do quality assurance associate jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for quality assurance associate in Roxboro, NC is $25.77, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $30.24 per hour, depending on experience, location, and employer.

What does a quality assurance associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What skills and qualifications are needed to be a quality assurance associate?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.

What are common challenges faced by quality assurance associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

What is the difference between Quality Assurance Associate vs Quality Control Inspector?

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Is a Quality Assurance Associate an entry-level job?

A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are the most commonly searched types of Quality Assurance jobs in Roxboro, NC?

The most popular types of Quality Assurance jobs in Roxboro, NC are:

What cities near Roxboro, NC are hiring for Quality Assurance Associate jobs?

Cities near Roxboro, NC with the most Quality Assurance Associate job openings:

Infographic showing various Quality Assurance Associate job openings in Roxboro, NC as of September 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $53,596 per year, or $25.8 per hour.

QA Associate

Durham, NC β€’ On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Almac Group is currently seeking a Quality Assurance Associate for our Durham, NC location. The Quality Assurance Associate is primarily concerned with the review of packaging and labeling batch records and the release of clinical supplies. The Quality Assurance Associate assures that no product is released until its quality has been deemed satisfactory having been manufactured, processed, packed, and held in accordance with Almac Clinical Services Standard Operating Procedures, current Good Manufacturing Practices, and customer specifications.
Mon-Fri 7:30am-4pm
Responsibilities include but are not limited to:
Review and approve documentation from any site associated with packaging and labeling of clinical supplies, including but not limited to:
  • Packaging Specifications
  • Packaging and Labeling methods and design layout
  • Executed packaging and labeling records
  • Medication number lists
Release of clinical supplies upon successful review.
  • Distribution instructions shipping clinical supplies
  • Labeling Instructions for Depots
Release of clinical supplies upon successful review and activation of specific countries to allow shipping activities to commence.
Assist quality management with the following tasks as needed:
  • Report/escalate serious/potentially serious breaches of GMP compliance or matters of concern to QA Team Leader in an open and timely manner for appropriate resolution.
  • Provide support to the Lead Investigators during the conduct of an investigation to enable them to perform a thorough root cause investigation
  • Interface with all levels of Almac Clinical Services personnel in resolving issues by providing QA support.
Notify Client Services of any issues which may impact the customer (i.e. quality issues, batch record completion deadlines).
Qualifications:
Required Experience / Education:
  • HS Diploma (or equivalent)
  • 4+ years Pharmaceutical Experience (with HS Diploma)
  • 2+ years Pharmaceutical Experience (with Associates Degree)
  • 1+ years Pharmaceutical Experience (with Bachelors Degree)
  • Knowledge of Current Good Manufacturing Practices (cGMP)
  • Completing GMP document auditing/reviewing
  • Working with Quality Systems
Preferred Experience / Education:
  • Bachelor’s degree
  • Previous experience working under an established Quality System or within a Pharmaceutical /GXP environment
  • Knowledge of Packaging/Labeling/Storing/Shipping Clinical Supplies
  • Familiar with Clinical Trial Process
What can Almac Group offer you?
  • Medical, Vision amp; Dental benefits from the 1st of the month following start date
  • 20 days PTO per year, accrued monthly following start date
  • 12 holidays per year
  • Company paid Long and Short-term disability along with Life Insurance
  • 401k company contribution
  • Professional development programs/ continuous learning opportunities
Want to see our latest job opportunities? Follow us on LinkedIn
Almac is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years now employing 6,600 highly skilled personnel worldwide. Our US Headquarters is located at Souderton, PA with additional operations scattered around the US and Europe. β€˜Partnering to Advance Human Health’ is more than just a tagline – it is our way of life.
Embracing diversity is at the heart of enhancing Almac Group’s unique culture and reflects our fundamental belief that all people deserve equality, inclusivity and the opportunity for advancement. We are committed to cultivating a welcoming, supportive, and inclusive environment for all. Together, we will build on the strength in our diversity and deliver exceptional solutions to advance human health globally.
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role through our portal. Candidate Resumes/CV’s not submitted through our portal or directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Almac Group, Inc. is an Equal Opportunity Employer - Minorities/Women/Protected Veterans/Disabled - Proudly embracing diversity in all of its expressions.
EEO is the Law
EEO is the Law GINA Supplement
Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at ADARequest@almacgroup.com to request assistance.