1

Quality Control Inspector Jobs in York, PA (NOW HIRING)

Lead day-to-day QC biochemistry operations to meet testing timelines for product release, raw ... Strong record of managing laboratory documentation and supporting audits or inspections. Preferred ...

[RDJ] QC Technician

Mountville, PA · On-site

$19.75 - $25.25/hr

Must be able to work within a multi-disciplinary team and ensure that Company's quality & food ... Filing of BOLs, Sanitation Records, transfer orders, pre-shift inspection record, drivers access ...

[RDJ] QC Technician

Mountville, PA · On-site

$19.75 - $25.25/hr

Job purpose Responsible for managing all incoming and outgoing documentation of the quality ... Filing of BOLs, Sanitation Records, transfer orders, pre-shift inspection record, drivers access ...

[RDJ] QC Technician

Mountville, PA · On-site

$19.75 - $25.25/hr

... during inspection. • Employee will collect and review all quality audit reports that are ... completed by the QA auditor, ensure they are signed off by the appropriate auditor, and filed. • ...

[RDJ] QC Technician

Mountville, PA · On-site

$19.75 - $25.25/hr

Must be able to work within a multi-disciplinary team and ensure that Company's quality & food ... Filing of BOLs, Sanitation Records, transfer orders, pre-shift inspection record, drivers access ...

Inspect finished products for quality, packaging, and compliance with product specifications ... Monitor and record chlorination levels and other quality control measurements. * Grade incoming ...

Showing results 41-60

Quality Control Inspector information

See York, PA salary details

$11

$21

$32

How much do quality control inspector jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for quality control inspector in York, PA is $21.14, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $23.65 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality control inspector, and why are they important?

To thrive as a Quality Control Inspector, you need a solid understanding of quality assurance procedures, attention to detail, and often a high school diploma or relevant technical training. Familiarity with inspection tools such as calipers, micrometers, and quality management systems like ISO 9001 is commonly required. Strong observational skills, problem-solving abilities, and clear communication are important soft skills in this role. These competencies ensure that products meet quality standards, reduce errors, and maintain customer satisfaction.

What are some common challenges quality control inspectors face when working on a fast-paced production line?

Quality Control Inspectors in fast-paced environments often face challenges such as quickly identifying defects without slowing down production, maintaining accuracy under time pressure, and effectively communicating issues to both production and management teams. Balancing speed with thoroughness requires strong attention to detail and the ability to prioritize tasks. Additionally, inspectors must stay updated on changing quality standards and adapt to new technologies or procedures introduced on the line.

What does a quality control inspector do?

A quality control inspector makes sure that production workers make products according to prescribed guidelines and specifications. Quality control inspectors perform tests to ensure that products meet quality standards, report their findings, then make recommendations for improvement. Quality control inspectors achieve this by using relevant tools, and technical knowledge along with strong attention to detail and analytical skills to perform these duties.

Is quality control inspection a good career?

Quality Control Inspector is a stable career that involves inspecting products and materials to ensure they meet quality standards. It often requires attention to detail, knowledge of industry regulations, and sometimes certifications like ASQ. The job can offer steady employment and opportunities for advancement in manufacturing, production, or industrial settings.

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

AspectQuality Control InspectorQuality Assurance Technician
CertificationsOften requires industry-specific certifications (e.g., ASQ certifications)Similar certifications may be preferred, but focus is on process compliance
Work EnvironmentInspecting products or materials on production lines or in labsDeveloping and implementing quality processes in manufacturing or service settings
Employer & Industry UsageCommon in manufacturing, aerospace, automotive industriesUsed in manufacturing, healthcare, and service industries
Search & Comparison IntentPeople compare roles related to product inspection and quality checksPeople look for roles focused on quality systems and process improvement

The main difference is that Quality Control Inspectors focus on inspecting and testing products to ensure quality standards are met, while Quality Assurance Technicians develop and maintain quality systems and processes to prevent defects. Both roles are essential in quality management but serve different functions within the industry.

What are popular job titles related to Quality Control Inspector jobs in York, PA? For Quality Control Inspector jobs in York, PA, the most frequently searched job titles are:
What cities near York, PA are hiring for Quality Control Inspector jobs? Cities near York, PA with the most Quality Control Inspector job openings:
Infographic showing various Quality Control Inspector job openings in York, PA as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 31% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $43,961 per year, or $21.1 per hour.

QC Biochemistry Manager

GlaxoSmithKline

Marietta, PA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


GlaxoSmithKline rating

8.9

Company rating: 8.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

9th of 86 rated pharmaceutical


Job description

Position Summary
You will lead and grow a quality control biochemistry team that ensures safe and compliant laboratory testing. You will work closely with production, quality assurance, and cross-functional partners. We value clear thinkers who coach others, drive continuous improvement, and focus on reliable results. This role offers career growth, the chance to shape lab strategy, and meaningful impact aligned with our mission: uniting science, technology and talent to get ahead of disease together.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Lead day-to-day QC biochemistry operations to meet testing timelines for product release, raw material, in-process and stability samples.

  • Develop and coach a team of analysts and supervisors to build capability and deliver consistent, high-quality results.

  • Oversee method transfers, validations, and troubleshooting for analytical assays used in release and stability testing.

  • Maintain compliance with good manufacturing practices and regulatory expectations through strong documentation and audit readiness.

  • Drive continuous improvement projects to enhance lab efficiency, quality and equipment uptime.

  • Manage resources including budgets, equipment lifecycle, and sample inventory to support reliable laboratory capacity.


Why You?
Work arrangement
This role is on-site in the United States. Hybrid working is not available for this role due to operational needs.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

  • Bachelor's degree in biochemistry, chemistry, molecular biology or related scientific discipline.

  • Minimum 5 years' experience in a GMP-regulated analytical laboratory environment.

  • Minimum 3 years' experience in a supervisory or manager role overseeing laboratory personnel.

  • Hands-on experience with biochemical or analytical techniques such as chromatography, electrophoresis, protein assays, or similar methods.

  • Demonstrated experience with method validation, method transfer, and laboratory investigations.

  • Strong record of managing laboratory documentation and supporting audits or inspections.


Preferred Qualification
If you have the following characteristics, it would be a plus:

  • Master's degree in a relevant scientific field.

  • Experience in biopharmaceutical or biologics testing environments.

  • Experience leading continuous improvement initiatives such as lean or Six Sigma projects.

  • Familiarity with stability study design and sample management practices.

  • Strong stakeholder management and cross-functional collaboration skills.

  • Experience managing laboratory budgets, equipment qualification, and lifecycle activities.


What we value
We welcome people who bring different perspectives and experiences. We seek candidates who are curious, reliable, and open to learning. If you like mentoring others, improving processes, and ensuring quality that makes a difference, we want to hear from you.
How to apply
If this role matches your skills and career goals, please apply today. We look forward to learning how you can help us deliver high-quality science that serves patients.

#LI-GSK

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at -usrecruitment.adjustments@gsk.com

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/


What GlaxoSmithKline employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


GlaxoSmithKline logo

About GlaxoSmithKline

Sourced by ZipRecruiter

GlaxoSmithKline is a globally recognized pharmaceutical and healthcare company based in Philadelphia, PA, USA. Originated from a merger between Glaxo Wellcome and SmithKline Beecham in 2000, the company excels in the pharmaceutical industry and holds a leading position in making medicines, vaccines, and consumer healthcare products. GSK's mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. They adhere to core values of transparency, integrity, respect for people, and patient-focus, reflecting in their endeavors to conduct research and deliver innovative healthcare solutions to patients and consumers worldwide.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Philadelphia, PA, US