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Quality Assurance Associate Jobs in Springfield, PA

Quality Assurance (QA) Specialist / Manager - DMPK Location: Exton, PA Department: DMPK (Drug Metabolism & Pharmacokinetics) Reports To : Senior VP, DMPK Employment Type: Full-Time Company Frontage ...

Position Summary The Quality Assurance Manager is responsible for ensuring that all consumer-packaged goods (CPG) appliances and electronic products meet or exceed quality, safety, regulatory, and ...

New

QA Engineer

King Of Prussia, PA · On-site

$120K - $140K/yr

We are seeking a QA Engineer to lead quality assurance across our software products and help ensure we deliver reliable, high-quality experiences for customers. This person will own test strategy ...

We are currently accepting resumes for the position of Quality Assurance Supervisor, conveniently ... Customer Service Associates will be required to work in person on-site prior to the end of training.

Showing results 41-60

Quality Assurance Associate information

See Springfield, PA salary details

$12

$27

$58

How much do quality assurance associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality assurance associate in Springfield, PA is $27.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.69 and $32.40 per hour, depending on experience, location, and employer.

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.

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 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 the most commonly searched types of Quality Assurance jobs in Springfield, PA?

The most popular types of Quality Assurance jobs in Springfield, PA are:

What cities near Springfield, PA are hiring for Quality Assurance Associate jobs?

Cities near Springfield, PA with the most Quality Assurance Associate job openings:

Infographic showing various Quality Assurance Associate job openings in Springfield, PA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $57,473 per year, or $27.6 per hour.

Quality Assurance Manager

Focus Laboratories

Cherry Hill, NJ • On-site

$110K - $120K/yr

Full-time

Posted 9 days ago


Job description

Who We Are
TPM Laboratories, Inc. is an independent contract testing laboratory providing personalized analytical services to the pharmaceutical and chemical industries. TPM Labs specializes in Analytical Research and Development Testing Services, Quality Control Testing and Stability Storage & Testing Services.
Our goal is to provide high quality, cost effective and timely service, personalized to meet your needs.
Scope of the Role
The QA Manager leads TPM Laboratories' quality system and ensures laboratory work meets cGMP, FDA, ICH, USP, and internal requirements. This role exists to protect data integrity, keep the site inspection-ready, and provide clear QA governance across documentation, investigations, and releases.
Key responsibilities include leading QA staff; maintaining QA policies, SOPs, and controlled documents; approving methods, specifications, and validation protocols; reviewing analytical data for accuracy and compliance; overseeing OOS/OOT, deviations, CAPA, and change control; trending quality events; managing internal audits; supporting client and regulatory audits; and driving GMP training and continuous improvement.
Required qualifications/skills:
- Bachelor's in Chemistry (or related discipline)
- 6-8 years in a regulated pharmaceutical/laboratory environment
- Strong QA systems, audit, and compliance oversight experience
- Proven review/approval of scientific and regulatory documentation
- People leadership experience; strong knowledge of ALCOA+ and 21 CFR 210/211
Apply if you can set direction, make sound quality decisions, and lead a compliant, audit-ready lab.
Your Typical Day
You start by checking the status of open quality events and the lab's inspection-readiness items, then confirm priorities with senior leadership. Mid-morning is focused time for document review-data packages, controlled records, and technical reports-so releases and client timelines stay on track.
As the day moves on, you shift between short, agenda-led team touchpoints and deeper problem-solving sessions where you align QA expectations with operational realities. You may host or prepare for a client audit, review responses and commitments, or brief teams on a regulatory update.
Before the day ends, you look ahead: confirm resources and schedules, ensure projects are logged correctly in Pryme, and identify one practical improvement to strengthen compliance without slowing delivery.