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Senior Quality Control Analyst Jobs in Rhode Island

Amgen, Inc.

Specialist QC

West Greenwich, RI · On-site

Analytical Investigation Ownership * Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results. * Perform ...

Amgen SA

Specialist QC

West Greenwich, RI · On-site

$95 - $125/hr

Analytical Investigation Ownership * Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results. * Perform ...

Amgen

Specialist QC

West Greenwich, RI

Analytical Investigation Ownership * Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results. * Perform ...

Revvity

Senior Quality Inspector

Hopkinton, RI · On-site

$46K - $58K/yr

Senior Quality Control Inspector plays a vital role in maintaining product excellence by performing comprehensive inspection activities to support production operations. This position reports ...

Fujifilm

QC Chemist

North Kingstown, RI · On-site

Coordinate and perform analysis on incoming, in-process, and final product samples. Testing is conducted in designated Quality Control (QC) laboratories and serves as critical quality checkpoints ...

Amgen, Inc.

QC Specialist

West Greenwich, RI · On-site

QC Specialist What you will do Let's do this. Let's change the world. In this vital role you will ... Utilize laboratory metrics and data analytics to identify trends and drive continuous improvement.

Amgen

QC Specialist

West Greenwich, RI · On-site

QC Specialist What you will do Let's do this. Let's change the world. In this vital role you will ... Utilize laboratory metrics and data analytics to identify trends and drive continuous improvement.

Alloy Fasteners

Quality Control Manager

Cranston, RI · On-site

As the Quality Control Manager, * You will ensure that processes for the ISO 9001:2015 certified ... You will be reporting to senior leaders on the performance of the quality management system and any ...

Nordsonhcm

Senior Quality Engineer

East Providence, RI · On-site

$89K - $120K/yr

... analysis and implementing effective long-term corrective actions to prevent recurrence of quality ... Industrial statistics (Cpk, MSA, SPC) * QA Tools (PPAP, FMEA, Control Plans) * Design of ...

Amgen

Quality Control Associate

West Greenwich, RI · On-site

Responsible for one or more of the following activities in Quality Control including analytical testing, characterization, sample and data management * Perform sample collection and sample handling ...

New

Vicor Corporation

Sr Quality Engineer

Lincoln, RI · On-site

$105K - $130K/yr

Job Summary The Senior Product Quality Engineer will be responsible for monitoring supplier ... Work closely with failure analysis and reliability functions to support their activities and ...

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How much do senior quality control analyst jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for senior quality control analyst in Rhode Island is $47.51, according to ZipRecruiter salary data. Most workers in this role earn between $41.44 and $53.22 per hour, depending on experience, location, and employer.

What does a senior quality control analyst do?

A Senior Quality Control Analyst is responsible for overseeing and ensuring the quality of products or processes within a company, typically in industries like pharmaceuticals, manufacturing, or food production. They design and implement testing procedures, analyze data, identify defects or inconsistencies, and ensure compliance with regulatory standards. Additionally, they mentor junior analysts, prepare reports, and collaborate with other departments to improve quality systems. Their expertise helps maintain product integrity and supports continuous improvement initiatives.

What are some common challenges faced by senior quality control analysts, and how are they typically addressed?

Senior Quality Control Analysts often encounter challenges such as managing tight deadlines while maintaining high accuracy, adapting to evolving regulatory standards, and troubleshooting unexpected deviations in product quality. These challenges are typically addressed through effective collaboration with cross-functional teams, ongoing professional development to stay updated with industry regulations, and implementing robust standard operating procedures. Additionally, strong analytical and communication skills help in swiftly resolving issues and ensuring continuous improvement within the quality control process.

What are the key skills and qualifications needed to thrive as a senior quality control analyst, and why are they important?

To thrive as a Senior Quality Control Analyst, you need expertise in laboratory testing, analytical methods, and a strong understanding of regulatory standards, often supported by a degree in chemistry, biology, or a related field. Familiarity with laboratory information management systems (LIMS), chromatography software, and relevant certifications such as GMP training are typically required. Attention to detail, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies ensure accurate quality assessments, compliance with regulations, and efficient collaboration across teams to maintain product integrity.

What is the role of a senior quality control analyst?

A senior quality control analyst is responsible for inspecting and testing products or materials to ensure they meet quality standards and regulatory requirements. They analyze data, identify issues, and collaborate with production teams to improve processes, often using tools like laboratory equipment and quality management systems. This role typically requires experience, attention to detail, and knowledge of industry-specific regulations.

What are the most commonly searched types of Quality Control Analyst jobs in Rhode Island?

The most popular types of Quality Control Analyst jobs in Rhode Island are:

What are popular job titles related to Senior Quality Control Analyst jobs in Rhode Island?

For Senior Quality Control Analyst jobs in Rhode Island, the most frequently searched job titles are:

What job categories do people searching Senior Quality Control Analyst jobs in Rhode Island look for?

The top searched job categories for Senior Quality Control Analyst jobs in Rhode Island are:

What cities in Rhode Island are hiring for Senior Quality Control Analyst jobs?

Cities in Rhode Island with the most Senior Quality Control Analyst job openings:

Senior Quality Control Analyst jobs near you
Infographic showing various Senior Quality Control Analyst job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $98,828 per year, or $47.5 per hour.

Specialist QC

Amgen, Inc.

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 11 days ago

Job description

Career Category
Operations
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Specialist QC
What you will do
Let's do this. Let's change the world. In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen.
Responsibilities:
Analytical Investigation Ownership
  • Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results.
  • Perform scientifically sound root cause analysis and develop effective corrective and preventive actions (CAPAs).
  • Ensure investigations are completed accurately, on time, and in compliance with GMP requirements and internal quality standards.

Quality Systems & Risk Assessment
  • Own and support deviations, CAPAs, and effectiveness verifications as assigned.
  • Review and approve equipment-related change controls, as applicable.
  • Partner with Quality Assurance to ensure investigation outcomes are risk-based and inspection-ready.
  • May support additional project-based assignments as required.

Cross-Functional Collaboration
  • Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality Assurance, Supply Chain, and other functional groups to resolve complex quality events.
  • Facilitate effective communication among stakeholders to ensure timely investigation progression and issue resolution.
  • Engage subject matter experts as needed to support technically complex investigations.

Inspection Readiness
  • Support internal and external audits by clearly communicating investigation findings, root cause, and CAPA effectiveness.
  • Maintain complete, accurate, and inspection-ready documentation.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborative teammate with these qualifications.
Basic Qualifications
  • High school diploma/GED and 10 years of directly related experience OR
  • Associate's degree and 8 years of directly related experience OR
  • Bachelor's degree and 4 years of directly related experience OR
  • Master's degree and 2 years of directly related experience OR
  • Doctorate degree

Preferred Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or another Life Science discipline.
  • 5-8+ years of Quality Control or Quality Assurance experience within the biotechnology or pharmaceutical industry.
  • Demonstrated experience leading complex laboratory investigations, including OOS, OOT, atypical results, and laboratory deviations.
  • Strong knowledge of GMP regulations, laboratory quality systems, and deviation management processes.
  • Experience performing root cause analysis using structured problem-solving methodologies.
  • Strong understanding of analytical laboratory techniques, instrumentation, and data integrity principles.
  • Experience authoring and managing deviations, CAPAs, change controls, and effectiveness verifications.
  • Ability to evaluate technical data, assess risk, and make sound, science-based decisions.
  • Strong written and verbal communication skills with the ability to influence cross-functional teams.
  • Experience supporting regulatory inspections and responding to auditor inquiries.
  • Experience utilizing digital tools, data analytics, or AI-enabled technologies to improve laboratory processes is preferred.

What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
100,450.45USD -135,903.55 USD

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