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Senior Qa Associate Jobs in Oregon (NOW HIRING)

A-dec, Inc.

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

Overview The Senior Quality Assurance Specialist is responsible for coordinating, organizing, and maintaining aspects of A-dec's Quality Management System (QMS) in a state of audit readiness and ...

A-dec, Inc.

Quality Assurance Specialist, Sr

Newberg, OR · On-site

$86K - $119K/yr

Overview The Senior Quality Assurance Specialist is responsible for coordinating, organizing, and maintaining aspects of A-dec's Quality Management System (QMS) in a state of audit readiness and ...

Smarsh

Sr. QA Automation Engineer

Portland, OR · On-site

We're looking for a Sr. Automation Engineer to join our QA team and help bring our automation up to speed. We're less interested in a list of your skills and acronyms, and more interested in how you ...

Smarsh

Sr. QA Automation Engineer

Portland, OR · On-site

We're looking for a Sr. Automation Engineer to join our QA team and help bring our automation up to speed. We're less interested in a list of your skills and acronyms, and more interested in how you ...

CLEAResult

Senior Residential QA & QC Specialist

OR · On-site +1

$55K - $83K/yr

The Senior QA & QC Specialist will be accountable for conducting technical quality assurance inspections of HVAC and weatherization installations, as well as educating contractors and community based ...

OMIC, USA

Quality Assurance Manager

Portland, OR · On-site

SUPERVISORY RESPONSIBILITIES Manages the QA Associate/Assistant position(s). Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.

Lonza

Associate Director, Quality Assurance

Bend, OR · On-site

This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance ...

Lonza

Associate Director, Quality Assurance

Bend, OR · On-site

This role offers an exciting opportunity to lead a high-performing Quality Assurance team in a regulated pharmaceutical environment. You will play a critical role in ensuring compliance ...

GT Independence

Quality Assurance Manager - OR

Salem, OR · On-site

$75K - $85K/hr

Reporting to the Director of Quality Assurance, this role provides direct supervision to Quality Assurance Associates and is responsible for ensuring organizational adherence to regulatory ...

Arcus Biosciences

Summary The Senior Manager, Clinical Quality Assurance is responsible for working with study management teams to facilitate internal and external adherence to Quality and Regulatory Compliance by ...

Care Access

Specialist, Quality Assurance

OR · On-site +1

Working in support of the Associate Director of Quality Assurance, the Quality Assurance Specialist will ensure that Care Access maintains a high level of quality while executing clinical trials ...

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Showing results 21-40

All JobsQa Associate JobsSenior Qa Associate JobsSenior Qa Associate Jobs in Oregon

Senior Qa Associate information

See Oregon salary details

$30.7K

$78.4K

$140.6K

How much do senior qa associate jobs pay per year?

As of Sep 1, 2026, the average yearly pay for senior qa associate in Oregon is $78,449.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,000.00 and $100,400.00 per year, depending on experience, location, and employer.

What does a Senior QA Associate do?

A Senior QA (Quality Assurance) Associate is responsible for overseeing and executing quality control processes to ensure that products or services meet established standards and regulatory requirements. They design and implement test plans, conduct inspections, analyze data, and collaborate with cross-functional teams to identify and resolve quality issues. Additionally, Senior QA Associates often mentor junior team members and help improve overall quality systems and procedures within an organization.

What are the key skills and qualifications needed to thrive as a Senior QA Associate?

To thrive as a Senior QA Associate, you need a solid background in quality assurance methodologies, process validation, and regulatory compliance, typically supported by a relevant degree and several years of industry experience. Familiarity with quality management systems (QMS), electronic documentation tools, and regulatory standards like GMP or ISO is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These competencies are crucial to ensure product quality, regulatory adherence, and continuous process improvement in highly regulated environments.

What are some typical challenges faced by Senior QA Associates when managing multiple testing projects simultaneously?

Senior QA Associates often juggle several testing projects at once, which requires excellent organizational and prioritization skills. Common challenges include balancing tight deadlines, ensuring thorough test coverage, and coordinating with cross-functional teams such as development, product management, and regulatory affairs. Proactively communicating and setting clear expectations with stakeholders is key to managing these challenges. Additionally, Senior QA Associates often mentor junior team members, adding another layer of responsibility to their role.

What is the difference between Senior Qa Associate vs Quality Assurance Tester?

AspectSenior Qa AssociateQuality Assurance Tester
Required CredentialsBachelor's degree in Computer Science or related field; experience in QAHigh school diploma or equivalent; some technical training or certifications preferred
Work EnvironmentCollaborates with cross-functional teams; involved in planning and oversightPrimarily executes test cases; reports bugs and issues
Employer & Industry UsageUsed in software development, technology companies, and IT servicesCommon in software firms, startups, and quality-focused organizations
Search & Comparison IntentOften compared for experience level and responsibilitiesCompared for entry-level or mid-level QA roles

The Senior Qa Associate typically has more experience, responsibilities in planning, and oversight in quality assurance processes, whereas a Quality Assurance Tester focuses on executing tests and identifying bugs. The senior role often involves collaboration with development teams and strategic planning, making it suitable for professionals with more experience in QA.

What cities in Oregon are hiring for Senior Qa Associate jobs?

Cities in Oregon with the most Senior Qa Associate job openings:

Senior Qa Associate jobs near you

Quality Assurance Associate II/III (Swing Shift)

Serán BioScience

Bend, OR • On-site

Full-time

PTO

Re-posted 15 days ago

Job description

Serán BioScience is searching for an experienced Quality Assurance Associate to aid in regulatory compliance for the manufacturing of oral solid dosage drug products. The primary responsibilities of this role will be to support the daily activities of Serán's Quality Assurance department by ensuring GMP regulations and internal SOPs are followed throughout the clinical manufacturing process. Essential task include reviewing and approving production records, analytical data, and internal QA documentation. Additional responsibilities include conducting risk analyses and investigations and participating in audits and inspections. Quality experience in a GMP Pharmaceutical Manufacturing setting is a requirement for this position with the ability for the title and compensation to commensurate with experience.
This role will support the alternative manufacturing schedule from Monday - Thursday, beginning at 2:00 pm and ending at 1:00 am. Experience specific to Serán's manufacturing capabilities and confidence to make independent decisions in alignment with Company policies and risk mitigation philosophies will be critical to this role.
Duties and Responsibilities
  • Documents authorships, reviews, and approves of SOPs, batch production and quality control (QC) records, certificates of analysis, method validations, and equipment qualifications
  • Applies working knowledge of best practices in GMP and understands how Quality integrates with other business areas
  • Initiates and oversees investigations
  • Manages corrective and preventive actions (CAPA)
  • Supports internal audits, client audits and regulatory inspections, with the potential to host
  • Manages controlled document issuance and archival
  • Performs quality reviews with minimal oversight
  • Communicates quality-related information to internal teams with minimal guidance
  • Responsibilities may increase in scope to align with company initiatives
  • Performs all other related duties as assigned

Required Skills and Abilities
  • Knowledge of GMP and FDA regulations for clinical trial materials; commercial knowledge is desirable but not required
  • Confident understanding of change control procedures, CAPA program, investigation and root cause analysis, and good documentation practices
  • Excellent organizational skills and attention to detail
  • Excellent time management skills with a proven ability to meet deadlines
  • Strong analytical and problem-solving skills
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the company
  • Demonstrates the ability to collaborate and work in cross-functional teams
  • Accepts feedback from a variety of sources and constructively manages conflict
  • Ability to prioritize tasks and to delegate them when appropriate
  • Excellent verbal and written communication skills
  • Ability to function well in a high-paced and at times stressful environment
  • Proficient with Microsoft Office Suite or related software
  • Ability to solve complex problems, take a new perspective on existing solutions, and exercise sound judgment based on the analysis of multiple sources of information to make independent decisions

Education and Experience
  • Bachelor's degree, preferably in a scientific discipline
  • 3 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate II
  • 6 years of GMP experience within a QC or QA role to meet the minimum qualifications for an Associate III
  • Pharmaceutical Manufacturing experience required, Oral Solid Dosage preferred

Physical Requirements
  • Prolonged periods of sitting or standing at a desk and working on a computer
  • Must be able to lift up to 15 pounds at times
  • Ability to wear required personal protective equipment (PPE), including safety glasses, hearing protection, hard hat, and safety shoes
  • Adheres to consistent and predictable in-person attendance

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.
Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Benefits Summary:
Serán employees accrue over four weeks of paid time off annually. Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period. Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions. Serán covers each employee with basic life and long-term disability, giving access to increase or add coverage. An Employee Assistance Program provides support for all things related to our employees' wellbeing, along with access to pet insurance.
The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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