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Quality Control Associate Ii Jobs in Bothell, WA

Associate, Quality Control

Bothell, WA · On-site +1

$35.29 - $42.77/hr

Associate degree with equivalent combination of education and work experience may be considered. * 0-2+ years of relevant microbiological or QC experience or equivalent combination of education and ...

Associate, Quality Control

Bothell, WA · On-site

$35.29 - $42.77/hr

Associate degree with equivalent combination of education and work experience may be considered. 0-2+ years of relevant microbiological or QC experience or equivalent combination of education and ...

Associate, Quality Control

Bothell, WA · On-site +1

$35.29 - $42.77/hr

Associate degree with equivalent combination of education and work experience may be considered. 0-2+ years of relevant microbiological or QC experience or equivalent combination of education and ...

Quality Control Supervisor

Monroe, WA · On-site

$32.08 - $38.81/hr

Quality Control (QC) Supervisor Pay: $32.08 - $38.81/hour Schedule: Monday to Friday 8:00am-4:30pm ... Prior supervisory or leadership experience required, 2+ years preferred * Completion of a bachelor ...

Quality Control Supervisor

Monroe, WA · On-site

$32.08 - $38.81/hr

Quality Control (QC) Supervisor Pay: $32.08 - $38.81/hour Schedule: Monday to Friday 8:00am-4:30pm ... Prior supervisory or leadership experience required, 2+ years preferred * Completion of a bachelor ...

OMS1029, Omeros' long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

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Quality Control Manager

Bremerton, WA · On-site

$120K - $170K/yr

Minimum ten (10) years of construction experience, with at least two (2) years serving as the Primary Quality Control Manager on federal construction projects. * Demonstrated experience on federal ...

OMS1029, Omeros' long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

QC Reviewer

Everett, WA · On-site

$25 - $30/hr

About the Role The QC Reviewer is responsible for performing the quality control reviews of data ... Two years of experience in the medical and/or pharmaceutical fields, a plus * Technical Skills: MS ...

Quality Control Supervisor FLSA STATUS: Non-Exempt PAY RANGE: $35.00-$45.00 per hour DOE FT / PT ... High School diploma or equivalent * 2+ years experience in the Maritime Industry * Formal or ...

Shift 2: 3:00 PM - 3:00 AM * Extended hours and weekend work may be required during peak production ... Basic understanding of quality control principles and practices * Ability to use equipment and ...

Quality Control Supervisor FLSA STATUS: Non-Exempt PAY RANGE: $35.00-$45.00 per hour DOE FT / PT ... High School diploma or equivalent * 2+ years experience in the Maritime Industry * Formal or ...

Shift 2: 3:00 PM - 3:00 AM * Extended hours and weekend work may be required during peak production ... Basic understanding of quality control principles and practices * Ability to use equipment and ...

Title Quality Control Inspector About the Organization IMIA,LLC is the only national marine surface ... High School diploma or equivalent * 2+ years experience in the Maritime Industry * Formal or ...

Title Quality Control Inspector About the Organization IMIA,LLC is the only national marine surface ... High School diploma or equivalent * 2+ years experience in the Maritime Industry * Formal or ...

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Showing results 1-20

Quality Control Associate Ii information

See Bothell, WA salary details

$12

$28

$42

How much do quality control associate ii jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for quality control associate ii in Bothell, WA is $28.46, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $34.66 per hour, depending on experience, location, and employer.

What is a quality control associate ii?

Quality Control Associate IIs are professionals responsible for performing intermediate-level testing and inspections in laboratories or manufacturing environments to ensure products meet established quality standards. They analyze samples, document test results, and help maintain compliance with regulatory requirements. These associates may also assist in troubleshooting issues, calibrating equipment, and training junior staff. Typically, they report to Quality Control Supervisors or Managers and play a key role in ensuring product safety and reliability.

What skills and qualifications are needed to be a quality control associate ii?

To thrive as a Quality Control Associate II, you generally need a background in life sciences or chemistry, experience with laboratory testing, and knowledge of GMP or GLP regulations. Familiarity with analytical instruments such as HPLC, GC, and LIMS software, as well as relevant certifications, is typically required. Strong attention to detail, analytical thinking, and effective communication are standout soft skills in this position. These skills and qualifications are essential for ensuring product quality, regulatory compliance, and the reliability of laboratory results.

What are common challenges faced by a quality control associate ii, and how can they be addressed?

Quality Control Associate II professionals often encounter challenges such as managing tight deadlines for testing and documentation, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. To address these challenges, it is important to develop strong organizational skills, maintain up-to-date knowledge of industry regulations, and communicate effectively with both production and laboratory teams. Proactively participating in training sessions and collaborating with colleagues can also help ensure consistent quality and foster a supportive work environment.

What is the difference between Quality Control Associate Ii vs Quality Control Associate I?

AspectQuality Control Associate IiQuality Control Associate I
CredentialsTypically requires an associate degree or equivalent; some roles may prefer certifications like CQEHigh school diploma or equivalent; entry-level position
Work EnvironmentLaboratory or manufacturing settings, performing inspections and testsSimilar environments, often with less complex testing responsibilities
ResponsibilitiesPerforming routine quality checks, documenting results, assisting in investigationsAssisting with basic inspections and data collection
Experience LevelUsually 1-3 years of related experienceEntry-level, minimal experience required

In summary, the Quality Control Associate II typically has more experience and may hold certifications, performing more complex testing and analysis compared to the Quality Control Associate I, which is an entry-level role with basic inspection duties.

What does a quality control associate do?

A Quality Control Associate II is responsible for inspecting products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and collaborate with production teams to address quality issues, often using tools like measurement instruments and quality management systems. Attention to detail and adherence to safety protocols are essential in this role.
Infographic showing various Quality Control Associate Ii job openings in Bothell, WA as of September 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 100% In-person job distribution, with an average salary of $59,206 per year, or $28.5 per hour.

Associate, Quality Control

Bothell, WA • On-site, Remote

Bristol Myers Squibb
Scientific Research and Development Services • 10K+ employees

$35.29 - $42.77/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz


Job description

At Bristol Myers Squibb, our employees often ask, "Who are you working for?"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.


Position Summary


The primary focus of the Quality Control Associate is to support QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation updates, deviations, investigations and continuous improvement efforts.

Duties/Responsibilities

Key Responsibilities

  • Perform routine testing of in-process, final product and stability samples.
  • Perform environmental/facilities monitoring and microbiological testing.
  • May review GMP documentation and perform data verification.
  • Perform document revision.
  • Identify opportunities for continuous improvement.
  • Support document revision, deviations, CAPA's and investigations.
  • May train analysts on general job duties.
  • Perform other tasks as assigned.

Reporting Relationship

Report to shift 3 QC Manager, Microbiology.

Qualifications

Education and Experience

  • Bachelor's degree preferred in science. Associate degree with equivalent combination of education and work experience may be considered.
  • 0-2+ years of relevant microbiological or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
  • Demonstrated experience in microbiological techniques and basic laboratory safety procedures.
  • Prior experience with microbiological techniques is preferred.

Knowledge, Skills, and Abilities

  • Ability to accurately and completely understand and follow procedures.
  • Apply scientific principles to QC testing and the proper use of laboratory equipment.
  • Ability to communicate effectively with peers and management about task status, roadblocks, and needs.
  • Attention to detail and demonstrated organizational skills.
  • Ability to work in a fast-paced environment, meet deadlines, and prioritize work.

Shift is Wed-Sat 0600-1630


We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Bothell - WA - US: $35.29 - $42.77per hour

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.


Benefits:


Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).


U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.


Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.


Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.


U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits


How We Work

Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.


Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries toadastaffingsupport@bms.com. Visitcareers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/


Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself athttps://careers.bms.com/fraud-protection.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


If this posting is missing required information required by local law or incorrect, contact BMS atTAEnablement@bms.comwith the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.


R1605812 : Associate, Quality Control

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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US