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Quality Control Pharma Jobs in Raleigh, NC (NOW HIRING)

... quality service to clients in order to meet timelines and budget deliverables. He/she acts as the ... control process and as agreed to by the client and other stakeholders Liaise with client, taking ...

Associate Director, Operations

Durham, NC ยท On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... quality control laboratories. The Associate Director is accountable for building and leading the ... A Master's Degree AND at least six (6) years of working in the Manufacturing, Pharma, Biotech, and ...

Associate Director, Operations

Durham, NC

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... quality control laboratories. The Associate Director is accountable for building and leading the ... A Master's Degree AND at least six (6) years of working in the Manufacturing, Pharma, Biotech, and ...

New

Senior Quality Engineer - Continuous Improvement

Pittsboro, NC ยท On-site

$61K - $83K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... change control and complaints. Perform effectiveness checks. * Facilitate investigations to ... Master's or advanced degree in relevant field. * 5+ years in pharma or medical device manufacturing ...

Senior Quality Engineer - Continuous Improvement

Durham, NC ยท On-site

$83K - $113K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... change control and complaints. Perform effectiveness checks. * Facilitate investigations to ... Master's or advanced degree in relevant field. * 5+ years in pharma or medical device manufacturing ...

Senior Quality Engineer - Continuous Improvement

Pittsboro, NC ยท On-site

$61K - $83K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... change control and complaints. Perform effectiveness checks. * Facilitate investigations to ... Master's or advanced degree in relevant field. * 5+ years in pharma or medical device manufacturing ...

Senior Quality Engineer - Continuous Improvement

Durham, NC ยท On-site

$83K - $113K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... change control and complaints. Perform effectiveness checks. * Facilitate investigations to ... Master's or advanced degree in relevant field. * 5+ years in pharma or medical device manufacturing ...

Principal CQV Consultant

Cary, NC ยท Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Act as the primary CQV SME during pre-sales discussions with pharma/biotech clients. * Identify new qualification/validation opportunities across labs, manufacturing, QC, and QC IT landscapes.

Showing results 41-60

Quality Control Pharma information

See Raleigh, NC salary details

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How much do quality control pharma jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for quality control pharma in Raleigh, NC is $20.38, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $22.45 per hour, depending on experience, location, and employer.

Is quality control pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It offers stable employment, opportunities for advancement, and requires attention to detail, knowledge of laboratory techniques, and often certifications such as GMP training.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What is the role of quality control in pharma?

The role of quality control in pharma involves testing and inspecting raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. QC professionals use analytical techniques and follow Good Manufacturing Practices (GMP) to identify and prevent defects, supporting regulatory compliance and product consistency.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What are popular job titles related to Quality Control Pharma jobs in Raleigh, NC?

For Quality Control Pharma jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Raleigh, NC look for?

The top searched job categories for Quality Control Pharma jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Quality Control Pharma jobs?

Cities near Raleigh, NC with the most Quality Control Pharma job openings:

Infographic showing various Quality Control Pharma job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $42,394 per year, or $20.4 per hour.

(Contract) Quality Technical Writer

Kymanox

Morrisville, NC โ€ข Remote

Contractor

Posted 23 days ago


Job description

Job Description:

Is Kymanox the right fit for you?

You want to make a difference and have an impact...

You enjoy having an influence in your day-to-day work...

You are motivated by working alongside a team filled with

subject matter experts who will help you learn and grow...

You wake up every day and do what you do

... because patients deserve better.

If this sounds like you, you've come to the right place.

The Technical Writer - General QMS (Contract)will perform technical writing and client support on a site readiness project authoring a range of engineering, compliance, and commercialization Standard Operating Procedures (SOPs).

Responsibilities:

  • Technical writing may include any of the following focus areas:
    1. Manufacturing equipment and processes
    2. Quality Control Laboratory instruments and methods
    3. Utility systems
    4. Facilities and maintenance equipment
    5. Logistics and warehousing processes
    6. Quality Assurance processes
    7. Environment, Health, and Safety processes
    8. Warehouse and Supply Chain
    9. Information Technology
    10. Training content.

Educational Background:

  • The ideal candidate will have a bachelor's degree in any Engineering discipline (prefer Biomedical, Mechanical, or Chemical engineering) or other STEM discipline (Biology, Chemistry, other) from an accredited institution or equivalent.

Experience:

  • A minimum of 3 to 5 years of experience in development and/or manufacturing in the pharmaceutical, biotechnology, combination product, and/or medical device sectors is required.
  • Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired.

Desired Aptitude and Skill Set:

  • Resourceful
  • Extremely detail oriented
  • Ability to work effectively with remote team members
  • Highly organized
  • Self-directing, self-pacing
  • Excellent written and oral English communication skills
  • Understanding of own limitations
  • Ability to solicit and utilize subject matter expert input
  • Fast learner
  • Pleasant and positive communication style
  • Strong customer-service aptitude
  • Ability to motivate self, team members, and direct reports
  • High energy level
  • Excellent problem-solving skills
  • Seasoned soft skills (i.e., high EQ)
  • Team player

Compensation:

Hourly rate is commensurate with experience, qualifications, and other intangibles evident during the interview process - as well as market conditions.

Travel:

Travel may be necessary to support client work.

About Kymanox:
Join Kymanox - a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today's biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement. Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox's service offerings and the life science industry as a whole.

Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market. Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC.

To learn more about our company, please visit our website:Life Science Solutions | Kymanox

Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.

Employment Type: Contractor