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Quality Control Associate Jobs in Springfield, PA

The Laboratory Specialist within the Quality Operations department, with guidance from the Associate Director of Quality Operations, provides support to Laboratory Operations. The Laboratory ...

At WSFS Bank, we empower our Associates to grow their careers, guide our customers to secure their ... The Quality Control Specialist will act as gatekeeper to ensure that the highest quality standards ...

At WSFS Bank, we empower our Associates to grow their careers, guide our customers to secure their ... The Quality Control Specialist will act as gatekeeper to ensure that the highest quality standards ...

At WSFS Bank, we empower our Associates to grow their careers, guide our customers to secure their ... The Quality Control Specialist will act as gatekeeper to ensure that the highest quality standards ...

Requirements Essential Duties of the QC Lac Tech: PRIORITY - Product sample testing as required ... Associate degree preferred. * Computer proficiency - Microsoft Windows/Outlook, Microsoft Office ...

QC Lab Technician

Moorestown, NJ · On-site

$20 - $21/hr

Requirements Essential Duties of the QC Lac Tech: PRIORITY - Product sample testing as required ... Associate degree preferred. * Computer proficiency - Microsoft Windows/Outlook, Microsoft Office ...

OR Associate degree in a scientific discipline with 5+ years of hands-on microbiology laboratory ... GMP QC Microbiology Laboratory * Advanced experience with testing microbiological compendial ...

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Quality Control Associate information

See Springfield, PA salary details

$10

$24

$36

How much do quality control associate jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for quality control associate in Springfield, PA is $24.02, according to ZipRecruiter salary data. Most workers in this role earn between $17.45 and $29.23 per hour, depending on experience, location, and employer.

What is a QC Associate job description?

A Quality Control (QC) Associate is responsible for inspecting and testing products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like measurement instruments and quality management systems. The role typically requires attention to detail, knowledge of quality procedures, and adherence to safety protocols.

What does a Quality Control Associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a Quality Control Associate, and why are they important?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges Quality Control Associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

Which pays more, QA or QC?

Quality Assurance (QA) and Quality Control (QC) roles often have similar pay scales, but QA positions typically offer higher salaries due to their focus on process improvement and prevention. Factors such as industry, experience, certifications, and location can influence compensation for both roles.

What do quality control associates do?

Quality control associates inspect products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or production environments to identify defects and ensure product consistency.

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

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

Is QC a high paying job?

The salary for a Quality Control Associate varies depending on industry, experience, and location, but it is generally considered an entry-level to mid-level position with moderate pay. Higher salaries are often associated with advanced certifications, specialized skills, or supervisory roles within quality control departments.
What are the most commonly searched types of Quality Control jobs in Springfield, PA? The most popular types of Quality Control jobs in Springfield, PA are:
What are popular job titles related to Quality Control Associate jobs in Springfield, PA? For Quality Control Associate jobs in Springfield, PA, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Springfield, PA look for? The top searched job categories for Quality Control Associate jobs in Springfield, PA are:
What cities near Springfield, PA are hiring for Quality Control Associate jobs? Cities near Springfield, PA with the most Quality Control Associate job openings:
Infographic showing various Quality Control Associate job openings in Springfield, PA as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $49,962 per year, or $24 per hour.
Specialist, Quality Control

Specialist, Quality Control

MSD

West Point, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


Job description

Job Description

The Laboratory Specialist within the Quality Operations department, with guidance from the Associate Director of Quality Operations, provides support to Laboratory Operations. The Laboratory Specialist will support sample tracking and scheduling, perform performance trends, manage inventory, facilitate collaboration meetings, engage in project work, and support other business needs at the direction of the Associate Director.

The Laboratory Specialist will work closely with the assigned laboratory in a team environment to ensure timely turnaround of laboratory testing and to ensure that documentation is completed right the first time. The Laboratory Specialist will work with Laboratory Operations staff and management coordinate day-to-day schedule and perform historical performance trends. They may also assist Laboratory Operations in conducting investigations associated with sample scheduling or other related topics. Additionally, the Laboratory Specialist will also support project work as needed and lead collaboration meetings within the department and participate in those outside the department.

The Laboratory Specialist will also be trained to support Quality Assurance system functions and to support End to End Quality Operations as needed.

Primary Activities:

  • Responsible for the scheduling of lab testing and performing sample tracking from receipt to approval.

  • Maintain metrics and tracking associated with this testing and approval.

  • Complete remediation activities for all samples, to ensure roadblocks are appropriately corrected in a timely manner.

  • Actively participate in the Tier process and use this forum to make concerns visible and to partner with Laboratory Quality on resolution.

  • Facilitate collaboration meetings with the Quality team to drive on-time testing and participate in meetings with external customers to provide testing updates.

  • Collaborate with team members in the identification and implementation of continuous improvement initiatives and action plans.

  • Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence, and lean practices.

  • Work with members from Quality and Technical Services to properly handle unplanned events impacting laboratory samples.

  • Maintain media inventory.

  • Participate in design and implementation of training and development programs.

  • Foster a customer service attitude across the network.

  • Assist with training of incoming personnel.

  • Provide support to Regulatory Agency inspections as needed.

  • Develop, Update and Modify SOP's as needed.

Education:

Bachelor's Degree in life science, scientific discipline or engineering preferred OR M.S. degree in life science, scientific discipline or engineering.

Required Experience and Skills:

Minimum 1-2 years' experience in GMP Manufacturing environment, Pharmaceutical / Biological Quality, Operational, Technical or Regulatory function supporting manufacturing or testing operations, or related industry experience in a laboratory, manufacturing, science related or regulated setting.

Preferred Experience and Skills:

Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work in a team environment.

Demonstrated analytical aptitude, critical thinking skills and problem solving skills.

Demonstrated ability to upskill / coach others.

Strong written and verbal communication skills.

Strong organizational skills.

Experience in pharmaceutical laboratory operations or related environment

Required Skills:

Adaptability, Analytical Instrumentation, Biological Sciences, Driving Continuous Improvement, GMP Compliance, Laboratory Documentation, Laboratory Safety, Problem Solving, Teamwork, Technical Issues, Troubleshooting, Use of Laboratory Equipment, Written Communication

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$87,300.00 - $137,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

07/20/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.