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Quality Assurance In Pharmaceutical Jobs in Renton, WA

Probi AB

Quality Assurance Specialist

Redmond, WA · On-site

$23 - $26/hr

Rooted in science, and working closely with customers and research partners, Probi aims to empower ... POSITION SUMMARY The Quality Assurance Specialist supports the Quality Assurance team and reports ...

Probi

Quality Assurance Specialist

Redmond, WA · On-site

Rooted in science, and working closely with customers and research partners, Probi aims to empower ... POSITION SUMMARY The Quality Assurance Specialist supports the Quality Assurance team and reports ...

The Greenbrier Companies

QA Manager

Tacoma, WA

We believe in supporting our global workforce through our unwavering attention to Safety, Quality ... Summary The Quality Assurance Manager position is responsible for providing support to the GBX ...

CharacterStrong

Quality Assurance Engineer

Lake Tapps, WA · On-site

$95K - $120K/yr

At CharacterStrong, you will have the opportunity to make a positive impact on education, both in ... Quality Assurance Engineer Responsibilities: * Design and implement test cases for work items each ...

Albertsons

Quality Assurance Manager

Bellevue, WA · On-site

The QA Manager partners cross-functionally with Operations, Maintenance, Supply Chain, Product ... ACI) is a leading food and drug retailer in the U.S. We operate over 2,200 stores, 1,732 pharmacies ...

Albertsons

Quality Assurance Manager

Bellevue, WA · On-site

The QA Manager partners cross-functionally with Operations, Maintenance, Supply Chain, Product ... ACI) is a leading food and drug retailer in the U.S. We operate over 2,200 stores, 1,732 pharmacies ...

Pegasus Northwest Inc

Quality Assurance Inspector

Kent, WA · On-site

$21 - $28/hr

Pegasus Northwest located in Kent, WA is currently looking for Quality Assurance Inspector to join our team in a fast paced, rewarding environment. We are a company that believes in work-life balance ...

B.E. Meyers

Quality Assurance Specialist

Redmond, WA · On-site

$28 - $31/hr

Quality Assurance Specialist Department: Quality Reports To: Quality Manager SUMMARY: The Quality ... Proficiency in the English language demonstrating oral and written communication skills. * Ability ...

B.E. Meyers

Quality Assurance Specialist

Redmond, WA · On-site

Quality Assurance Specialist Department: Quality Reports To: Quality Manager SUMMARY: The Quality ... Proficiency in the English language demonstrating oral and written communication skills. * Ability ...

B.E. Meyers

Quality Assurance Technician

Redmond, WA · On-site

Quality Assurance Technician Department: Quality Reports To: Quality Manager SUMMARY: The Quality ... Previous experience in manufacturing, quality, or production support. * Experience with calibration ...

New

ORION INDUSTRIES

Quality Assurance Supervisor

Auburn, WA · On-site

$73K - $95K/yr

Participates in safety and quality investigations and recommends corrective action. * Provides training to Orion staff and recommends qualification on specific processes and equipment as identified ...

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How much do quality assurance in pharmaceutical jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for quality assurance in pharmaceutical in Renton, WA is $26.09, according to ZipRecruiter salary data. Most workers in this role earn between $19.76 and $27.31 per hour, depending on experience, location, and employer.

Is quality assurance a good career in the pharmaceutical industry?

Quality assurance in the pharmaceutical industry is a stable and growing career, focusing on ensuring products meet safety and regulatory standards. It often requires knowledge of Good Manufacturing Practices (GMP), quality control processes, and relevant certifications, making it a vital role for maintaining product integrity and compliance.

What are some common challenges faced by quality assurance professionals in the pharmaceutical industry, and how can they be effectively managed?

Quality Assurance (QA) professionals in the pharmaceutical industry often face challenges such as keeping up with evolving regulatory requirements, ensuring consistent documentation, and coordinating cross-functional teams during audits. Managing these challenges requires continuous training, strong attention to detail, and effective communication skills. Collaboration with other departments, such as production and regulatory affairs, is key to identifying issues early and maintaining compliance with Good Manufacturing Practices (GMP). Establishing clear quality procedures and staying proactive with process improvements also help QA professionals maintain high standards and reduce risks.

What are the key skills and qualifications needed to thrive as a quality assurance professional in the pharmaceutical industry?

A successful Quality Assurance professional in pharmaceuticals needs a solid background in life sciences or pharmacy, understanding of GMP regulations, and relevant QA experience. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for excelling in this role. These skills ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceutical products.

What does quality assurance do in the pharmaceutical industry?

Quality assurance professionals in the pharmaceutical industry ensure that products meet safety, quality, and regulatory standards throughout the manufacturing process. They develop and implement procedures, conduct audits, and review documentation to prevent defects and ensure compliance with Good Manufacturing Practices (GMP).

What does a quality assurance professional do in the pharmaceutical industry?

A Quality Assurance (QA) professional in the pharmaceutical industry is responsible for ensuring that all products meet established standards of quality, safety, and efficacy. They develop, maintain, and monitor procedures and systems that comply with regulatory requirements such as Good Manufacturing Practices (GMP). QA professionals conduct audits, review documentation, manage deviations, and support continuous improvement to ensure that medications are safe for patients. Their work is critical in preventing errors, ensuring product consistency, and maintaining the trust of regulatory agencies and consumers.

What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?

AspectQuality Assurance In PharmaceuticalQuality Control In Pharmaceutical
FocusProcesses, compliance, and preventing defectsTesting and inspecting products for defects
ResponsibilitiesDeveloping quality systems, audits, documentationSampling, testing, and analyzing products
CredentialsGMP certifications, quality management trainingLab certifications, analytical testing skills
Work EnvironmentOffice-based, quality departments, manufacturing sitesLaboratories, manufacturing facilities

Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.

What are popular job titles related to Quality Assurance In Pharmaceutical jobs in Renton, WA? For Quality Assurance In Pharmaceutical jobs in Renton, WA, the most frequently searched job titles are:
What cities near Renton, WA are hiring for Quality Assurance In Pharmaceutical jobs? Cities near Renton, WA with the most Quality Assurance In Pharmaceutical job openings:
Quality Assurance In Pharmaceutical jobs near you
Infographic showing various Quality Assurance In Pharmaceutical job openings in Renton, WA as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 1% Temporary, 5% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $54,258 per year, or $26.1 per hour.

Quality Assurance Specialist

Probi AB

Redmond, WA • On-site

$23 - $26/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

Job description

COMPANY INFORMATION
Probi® is a global leader in biotic solutions, dedicated to researching, manufacturing, and delivering high-quality biotics for dietary supplements and functional food and beverage applications. Rooted in science, and working closely with customers and research partners, Probi aims to empower people worldwide to take control of their gut microbiome, helping them live healthier, longer lives.
Founded in 1991 in Sweden, Probi has grown to serve more than 40 markets and holds numerous global patents. As part of Symrise AG, the company benefits from expanded capabilities, resources, and worldwide reach, further strengthening its position as an innovation leader in the biotics category.
Why Us? Because We're Not Just a Company; We're a Community:
  • People Focus: Probi isn't just about products; it's about the people behind them. Join a community that values collaboration, diversity, and the unique contributions each team member brings.
  • Own It Culture: At Probi, we believe in empowerment. Our 'Own It' culture means you're not just following a script; you're part of shaping it.
  • Sustainability Matters: We're committed to a sustainable future. Join a team that cares about the environment, values responsible practices, and is dedicated to making a positive impact.

We are currently seeking candidates for our Quality Assurance Specialist position to work in our manufacturing plant in Redmond, Washington. This full-time position(s) reports to the Quality Supervisor.
This role is fully in-person with the following schedule;
Schedule is Monday through Friday, 7:00 AM to 3:30 PM.
POSITION SUMMARY
The Quality Assurance Specialist supports the Quality Assurance team and reports to the Quality Supervisor. Under the guidance of the Quality leadership, the Quality Assurance Specialist is responsible for the issuance and review of dietary supplement specification sheets, procedures, production batch records, production deviations, CAPAs, product complaints and quality release documents as directed by management. They utilize quality skills to help identify and lead continuous improvement initiatives, ensure quality systems are being managed and executed timely, and are responsible for routine day-to-day functions. They are responsible for the CAPA and deviation
management program, conducting change control activities, audit findings, document management, and investigations. This role forms partnerships with production and plant leadership to drive the success of the organization.
KEY JOB DUTIES
  • Support facility certifications (e.g., GRMA, NSF, Kosher, Halal) by maintaining compliant SOPs and records and promoting an "audit-ready" culture.
  • Maintain controlled documents by creating, revising, and issuing SOPs, forms, records, and policies; draft new documents as needed.
  • Manage and complete assigned tasks in the eQMS (e.g., customer cases/requests, audits, CAPA) to ensure timely closure and appropriate root-cause analysis, corrective actions, and effectiveness checks.
  • Create/revise and issue Product and Raw Material Specifications
  • Support deviation management program by ensuring deviations are documented, risk-assessed, and addressed with appropriate actions.
  • Execute change control activities as assigned.
  • Manage calibration and verification programs ensuring testing equipment is properly maintained. (e.g., ATP testers, temperature monitoring devices).
  • Responsible for creating, reviewing, and approving Master Manufacturing Records (MMRs) and batch records.
  • Responsible for reviewing batch records and generating COAs.
  • Coordinate and manage label review, approval, control, and reconciliation programs.
  • Execute assigned customer cases and properly record actions and close records in eQMS system.
  • Execute assigned findings from audits and inspections. Document results, follow-up actions, and closure.
  • Maintain accurate, complete, and readily retrievable quality records in accordance with regulatory and company requirements.
  • Assist with customer complaints and support investigations using systematic methods to determine root cause and define corrective and preventive actions.
  • Act as designated back up for QA Technician/
  • Collaborate and influence stakeholders across Quality, Supply Chain, Product Development & Application, Suppliers, and Customers to resolve findings with fit-for-purpose, sustainable compliance solutions.
  • All other duties as assigned.

COMPANY REQUIREMENTS
  • Must be able to read, write, and converse in the English language.
  • Must be able to pass background check.
  • Maintain good attendance.
  • Perform other projects / duties as assigned.
  • Good knowledge of best practices in the Natural Health Products Industry.
  • Must be able to recognize audible and visual hazards.
  • Must follow GMP, PPE, and company safety policies in the performance of job duties

WORK EXPERIENCE AND EDUCATION REQUIREMENTS
  • Degree (BSc or MSc) or 4 years + equivalent experience in manufacturing quality role.
  • Minimum of 1 years working within a cGMP regulated environment for ingredients, food, and dietary supplements.
  • Ability to influence and collaborate effectively with stakeholders at any level of the organization.
  • Analytical mind, good attention to details and problem-solving skills within a structured process.
  • Demonstrated application of continuous improvement, change control and risk assessment.
  • Fluent in English - spoken and written.

SOME OF OUR US BENEFITS
  • Medical, vision, and dental coverage after 30 days (and first day of the following month). Three (3) plans to choose from.
  • Long-term and short-term disability insurance at no cost to employee.
  • PTO (Paid Time Off) accrues on hire with up to 4 weeks (20 days) for new hire and increases the longer you are with the company.
  • Participation in the company 401(K) and Roth plan after 6 months of employment with up to 4% employer match.
  • Ten (10) paid holidays.
  • 17 hours per calendar year, to go out and volunteer in your community!
  • Employee Assistance Program
  • Yearly Safety shoe vouchers.
  • Learning and Development Opportunities
  • Monthly birthday and anniversary celebrations.
  • Team-building events throughout the year including summer and winter celebrations.

At Probi USA, we believe hiring should be fair, objective, and centered around helping candidates succeed. That's why we have partnered with Alva Labs' to use science-based and fair assessments. The Psychometric Assessments from, Alva Labs help us understand key traits-such as logic and personality-that contribute to success in this role.
Many Candidates tell us they enjoy taking these assessments as it gives them personal insights on how they naturally work and help support why they would fit in a role that is fair and unbiased.
Please watch for an email from Alva Labs with your assessment link. Completing the assessment is required to move forward in our process.
Thank you for taking this important step with us!
Probi USA is an Equal Employment Opportunity (EEO)/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, disability, marital status, veteran status or any other protected factor.
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