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Quality Assurance Associate I Jobs (NOW HIRING)

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

SECOND SHIFT Position Title : QA Associate I - Operations Location: Madison, Wisconsin Department: Quality Assurance Reporting To: Quality Assurance Operations Supervisor Responsible For (Staff): No ...

Conduent, Inc.

Quality Assurance Associate I

Erlanger, KY · On-site

$26K - $33K/mo

Quality Assurance Associate I ONSITE - Erlanger, KY Pay: $16.00 This pay rate may be below your state's minimum wage. Please take this into consideration when applying. Monday - Friday | 3:00PM - 11 ...

Conduent, Inc.

Quality Assurance Associate I

Erlanger, KY · On-site

$26K - $33K/mo

Quality Assurance Associate I ONSITE - Erlanger, KY Pay: $16.00 This pay rate may be below your state's minimum wage. Please take this into consideration when applying. Monday - Friday | 3:00PM - 11 ...

PCI Pharma Services

Qa Associate I - Ops

Madison, WI · On-site

SECOND SHIFT Position Title : QA Associate I - Operations Location: Madison, Wisconsin Department: Quality Assurance Reporting To: Quality Assurance Operations Supervisor Responsible For (Staff): No ...

Senior plc

Quality Assurance Associate I

Oceanside, CA · On-site

$25 - $27/hr

... Quality Assurance Associate I, you will: Conduct internal audits, documentation, data analysis, control of non-conforming material, authorization of customer returns, and support overall product ...

Senior plc

Quality Assurance Associate I

Oceanside, CA · On-site

$25 - $27/hr

... Quality Assurance Associate I, you will: Conduct internal audits, documentation, data analysis, control of non-conforming material, authorization of customer returns, and support overall product ...

CEDENT

Quality Assurance Associate I

Cumberland, RI · On-site

The QA Associate II/III independently conducts quality assurance audits of production records ... i.e., batch documentation, investigations, timelines and data related issues). 12. Authors or ...

Powermatic Associates Inc

Quality Assurance

Georgetown, TX · On-site

$57K - $72K/yr

Georgetown, TX 78628 Position Type: Full Time Salary Range: $57,000.00 - $72,000.00 Salary/year Job Purpose The Quality Assurance Associate I (QA I) will perform the quality assurance functions under ...

New

AVANTech, LLC

Quality Assurance Associate I

Columbia, SC · On-site

$18 - $23/hr

We are seeking an experience Quality Control Associate I to join our team in the Quality Assurance Department. A Day in the Life: * File physical and electronic documents exactly as received * Scan ...

Powermatic

Quality Assurance

Georgetown, TX · On-site

The Quality Assurance Associate I (QA I) will perform the quality assurance functions under the direction of the QA Supervisor and in accordance with Powermatic's Quality Management System (QMS)

Thompson Pipe Group

QA Associate I

Conroe, TX · On-site

... assurance requirements. Essential Functions: * Record product conformance to engineering and ... ACPA Quality or NPCA PQS I or PCI Level I : Required * Precast Concrete Experience or related field ...

Owens & Minor

Quality Assurance Associate I

Louisville, KY · On-site

$20 - $22/hr

Assists with documentation and review of inspection records and basic quality assurance activities ... High school diploma or equivalent required (Associate's degree a plus) * 0-2 years of experience in ...

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How much do quality assurance associate i jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for quality assurance associate i in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is a quality assurance associate I?

A Quality Assurance Associate I is an entry-level professional responsible for assisting with the maintenance and enforcement of quality standards within an organization, typically in industries like pharmaceuticals, manufacturing, or food production. Their duties often include inspecting products or processes, documenting findings, supporting audits, and ensuring compliance with regulatory requirements. They work under the direction of more senior quality assurance staff to help identify and resolve quality issues, contributing to the overall reliability and safety of the company's products or services.

What are the key skills and qualifications needed to thrive as a quality assurance associate I, and why are they important?

To thrive as a Quality Assurance Associate I, you need a solid understanding of quality control principles, attention to detail, and a bachelor's degree in a scientific or technical field. Familiarity with quality management systems (QMS), documentation software, and regulatory guidelines such as GMP or ISO standards is typically required. Strong analytical thinking, effective communication, and teamwork skills help you identify issues and collaborate with cross-functional teams. These abilities are crucial for maintaining product standards, ensuring compliance, and supporting continuous improvement within the organization.

What are some common challenges faced by a quality assurance associate I and how can they be managed effectively?

As a Quality Assurance Associate I, you may encounter challenges such as balancing multiple testing projects with tight deadlines, understanding evolving regulatory requirements, and ensuring effective communication with cross-functional teams. To manage these effectively, it's important to prioritize tasks, stay organized with detailed documentation, and proactively seek clarification when requirements are unclear. Building strong relationships with colleagues in production, research, and regulatory departments also helps ensure smooth workflow and quick resolution of issues.

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

AspectQuality Assurance Associate IQuality Control Technician
CredentialsTypically requires a bachelor's degree in life sciences or related fieldOften requires a diploma or associate degree in a technical field
Work EnvironmentInvolves documentation, process audits, and compliance activities within labs or manufacturingFocuses on testing, sampling, and inspecting products or materials
Industry UsageCommonly used in pharmaceutical, biotech, and manufacturing industries

The main difference is that a Quality Assurance Associate I focuses on ensuring processes meet quality standards through documentation and audits, while a Quality Control Technician primarily tests and inspects products to identify defects. Both roles are essential in maintaining product quality but differ in their specific responsibilities and focus areas.

What cities are hiring for Quality Assurance Associate I jobs?

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What states have the most Quality Assurance Associate I jobs?

States with the most job openings for Quality Assurance Associate I jobs include:

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For Quality Assurance Associate I jobs, the most frequently searched job titles are:

Quality Assurance Associate I jobs near you

Qa Associate I - Ops

Madison, WI • On-site

PCI Pharma Services
See more jobs at PCI Pharma Servicesexternal

Full-time

Re-posted 3 days ago

Key responsibilities

  • Perform QA on-the-floor activities supporting manufacturing, including room release, auditing critical processes, reviewing documentation, and resolving issues during production

  • Review executed batch records and supporting documentation for completeness, accuracy, and compliance, and support lot disposition of intermediates and finished products

  • Act as first responder for on-the-floor quality issues, document events and investigations, and implement immediate corrective actions

PCI Pharma Services rating

6.3

Company rating: 6.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
SECOND SHIFT
Position Title: QA Associate I - Operations
Location: Madison, Wisconsin
Department: Quality Assurance
Reporting To: Quality Assurance Operations Supervisor
Responsible For (Staff): No
The Quality Associate I - Operations is the first of two levels within the QA Associate job family The associate I provides real-time QA support on the floor for GMP Manufacturing of drug product. The work scope includes floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products
ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Perform QA On-the-Floor activities supporting client projects, including room release, auditing critical processes, reviewing documentation in real time, and resolving issues that occur during manufacturing
  • Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and Good Documentation Practices
  • Review executed Manufacturing Batch Records and supporting documentation for completeness, accuracy and compliance
  • Support the evaluation and lot disposition of intermediates, finish bulk drug substance and drug product
  • Act as first responder for on the floor quality issues in a timely manner, documentation of all events/investigations and required immediate corrective actions
  • May participate in root cause analysis using methodologies, such as: fishbone, 5 whys, etc.
  • Act as QA reviewer for deviations and CAPA issuance; with limited approval authority as designated by QA Management
  • Perform Acceptable Quality Limit (AQL) visual inspection of drug product
  • Participate in SOP revision as it pertains to process improvements
  • Participate in site quality and process improvement initiatives. Represent QA on project teams and represent QA perspective as necessary
  • Guide personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements and industry best practices

QUALIFICATIONS:
Required:
  • Bachelor's Degree in a relevant scientific discipline preferred with a minimum of 0-2 years of pharmaceutical or biotech industry experience with 1+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production preferred
  • Exposure to RCA, technical writing, and working with quality related investigations
  • Exposure to lean operation excellence highly desirable
  • Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH
  • Knowledge and ability to apply basic scientific principles to solve operational, as well as routine quality tasks
  • Knowledge and exposure to using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9 preferred
  • ASQ certification preferred

#LI-RS1
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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