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Pqa Jobs (NOW HIRING)

Kelly Services

PQA Analyst

Barceloneta, PR

How about this one? We're seeking an PQA Analyst to work with one of our top global biopharmaceutical clients in the Barceloneta PR area. With us, it's all about finding the job that's just right The ...

Amgen

Sr Associate QA I - PQA

Holly Springs, NC

The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. This is a unique opportunity to maintain and further build a strong ...

LG

Quality Lab Engineer

Clarksville, TN

$62K - $80K/yr

Quality Management for Production Lines (PQA): Monitor and manage the quality performance of production lines, including root cause analysis and corrective actions. Collaborate with cross-functional ...

LG

Quality Lab Engineer

Clarksville, TN · On-site

$62K - $80K/yr

The Quality Lab engineer will handle PQA (Process Quality Assurance for the mass production line) and AQA (Analytical Quality Assurance) tasks. The primary responsibilities for the Quality Lab ...

Prestage

Truck Washer

Texhoma, OK · On-site

$12.50 - $14.50/hr

PQA Plus Certified. Benefits In addition to very competitive pay employees of Prestage Farms receive: * Vacation Pay * Holiday Pay * 401(k) Plan * Medical Insurance * Voluntary Insurance options such ...

Prestage

Farm Maintenance Technician

Texhoma, OK · On-site

Maintain PQA+ Certification * Ability to work well with others. * Must have a minimum of one-year experience in a maintenance or construction related field. Benefits In addition to very competitive ...

Prestage

Truck Washer

Texhoma, OK · On-site

$12.50 - $14.50/hr

PQA Plus Certified. Benefits In addition to very competitive pay employees of Prestage Farms receive: * Vacation Pay * Holiday Pay * 401(k) Plan * Medical Insurance * Voluntary Insurance options such ...

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Pqa information

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How much do pqa jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for pqa in the United States is $50.32, according to ZipRecruiter salary data. Most workers in this role earn between $37.98 and $60.82 per hour, depending on experience, location, and employer.

What is a PQA?

PQAs, or Performance Qualification Analysts, are professionals who ensure that products and systems meet specified quality and performance standards before they are released or go live. They typically design and execute test plans, analyze test results, and document performance issues. PQAs work closely with development and engineering teams to identify and resolve problems, ensuring that products are reliable and meet regulatory or industry requirements. Their role is crucial in industries such as pharmaceuticals, manufacturing, and software development to maintain high standards of quality and safety.

What are some common challenges faced by a Product Quality Analyst when working with cross-functional teams?

Product Quality Analysts often collaborate closely with developers, product managers, and QA engineers, which can present challenges such as aligning on quality standards, managing tight deadlines, and ensuring clear communication across departments. Balancing priorities between rapid product releases and thorough testing is a frequent hurdle. Successful PQAs proactively facilitate discussions, document requirements, and advocate for quality best practices to help bridge gaps and maintain product integrity.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Quality Assurance professional, and why are they important?

To thrive as a Pharmaceutical Quality Assurance (PQA) professional, you need a solid background in pharmaceutical sciences, regulatory compliance, and quality control, often supported by a relevant degree and familiarity with GMP standards. Experience with quality management systems (QMS), documentation software, and industry certifications such as Six Sigma or ISO 9001 is typically required. Attention to detail, analytical thinking, and effective communication are critical soft skills for this role. These skills ensure products meet regulatory standards, maintain patient safety, and uphold the reputation and integrity of the pharmaceutical company.

What is the difference between Pqa vs Quality Assurance Tester?

AspectPqaQuality Assurance Tester
CertificationsISO, Six Sigma, QA-specific certificationsISTQB, CSTE, QA certifications
Work EnvironmentManufacturing, production, or software developmentSoftware development, IT, or product testing
Industry UsageManufacturing, pharmaceuticals, softwareSoftware, IT, technology
Job FocusProcess control, compliance, quality improvementTesting, defect tracking, software quality

While both Pqa and Quality Assurance Tester focus on quality, Pqa emphasizes process control and compliance across industries like manufacturing and software, whereas Quality Assurance Testers primarily focus on testing software products for defects. The roles overlap in ensuring quality standards but differ in scope and industry application.

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Pqa jobs near you
Infographic showing various Pqa job openings in the United States as of August 2026, with employment types broken down into 71% Full Time, 24% Part Time, 3% Contract, and 2% Nights. Highlights an 100% Physical job distribution, with an average salary of $104,667 per year, or $50.3 per hour.

PQA Analyst

Kelly Services

Barceloneta, PR

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago

Job description

At Kelly® Science, Engineering, Technology & Telecom (SETT), we’re passionate about helping you find a job that works for you. How about this one?
We’re seeking an PQA Analyst to work with one of our top global biopharmaceutical clients in the Barceloneta PR area. With us, it’s all about finding the job that’s just right
The Product Quality Assurance (PQA) Analyst has various objective/functions related to Third Party Manufacturing (TPM) plants and PQA functions. During routine operations, the Senior PQA Analyst is responsible for supporting the day-to-day Quality Assurance activities related to the TPM plants including but not limited to approval of manufacturing direction to the production floor, review and approval of manufacturing, laboratory, and raw material investigations, assess product impact analysis and corrective and preventive action for events, review and approval of changes as applicable. The Senior PQA Analyst also is responsible for evaluating supplier change notification, monitor process track and trending, and perform annual Product Quality Reviews. This person also acts as a liaison between company regulatory areas and TPM plants for regulatory submission.
•Maintains an effective liaison and cooperative relationship with other Customer Areas including but not limited Quality, Regulatory, Technical, Supply Chain, along with the TPM sites.
•Ensures that bulk drug substance and/or drug product production at TPM sites is performed as per current good manufacturing practices, according to local procedures and as per specifications and manufacturing directions provided by Customer QA Operations.
•Ensures TPM procedures including but not limited to raw material specification, product specification, test methods, supplier change notification, shipping, are in compliance with cGMP, policies, regulatory approvals, and Quality Technical Agreement with TPM site. •Review and approve manufacturing directions to the production floor.
•Provide support to PQA in global projects and events to ensure intended results are achieved; including planning, risk analysis, and implementation.
Ensure investigations of TPM plant events related but not limited to process, laboratory, raw materials are completed thoroughly and documented accurately, including adequate product impact analyses and corrective and preventive action for plant events are documented.
•Perform annual Product Quality Review according to Customer global procedure to comply with regulatory requirements. •Participates in Trend Review Board to monitor process track and trending.
•Participates in the Global Change Review Board (GCRB) meeting as TPM representative to evaluate global changes related but not limited to supplier change notifications, process, laboratory, and regulatory submissions that impacts all sites.
•Generates detailed change management plans related to TPM plants changes to ensure intended results are achieved; including planning, risk analysis, and implementation. .
Qualifications:
•Bachelor’s degree preferably in Engineering or Science
•Six years of experience within pharmaceutical operations, preferably Biologic manufacturing process
•Knowledge of GMP regulations and standards affecting pharmaceutical products •Comprehensive knowledge and application of business and quality concepts
•Strong analytical skills and attention to detail
•Change plan, Exception Reports, SAP and LRMS experience is highly preferred •Proven ability to adapt communication style for a variety of modes as well as for multicultural audiences
•Strong interpersonal relations / communications skills. Ability to effectively communicate across all levels of the organization. Assures the quality of manufactured products and processes per standard operating processes (SOP'S) and GMP (Good Manufacturing Practices).
Daily Work Schedule Expectations Monday to Friday 8-5PM
 
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.