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Quality Control Associate Two Jobs in Coventry, RI

Amgen

Quality Control Associate

West Greenwich, RI · On-site

Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... High school/GED + 2 years [Job Code's Discipline and/or Sub-Discipline] work experience OR

Whirlpool

Quality Control

Fall River, MA · On-site

Writes and distributes quality control reports and educational material, utilizing internal systems ... In 1-2 sentences, provide an overview of the purpose, priorities, deliverables and expected ...

Rust-Oleum

Mgr/Quality Control

Attleboro, MA

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

Kop-Coat, Inc.

Mgr/Quality Control

Attleboro, MA

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

Rust-Oleum

Mgr/Quality Control

Attleboro, MA · On-site

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

Tremco Construction

Mgr/Quality Control

Attleboro, MA · On-site

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

Amgen, Inc.

Specialist QC

West Greenwich, RI · On-site

Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ... Master's degree and 2 years of directly related experience OR * Doctorate degree Preferred ...

Amgen

Specialist QC

West Greenwich, RI · On-site

Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ... Master's degree and 2 years of directly related experience OR * Doctorate degree Preferred ...

Balfour Beatty

Quality Control Technician

Groton, CT · On-site

$18.75 - $23.75/hr

Robust PTO to include, sick, floating holidays, vacation, and personal days * 2 Volunteer Days per ... About the role The Quality Control Technician (QCT) is responsible for the oversight of quality ...

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Quality Control Associate Two information

See Coventry, RI salary details

$11

$24

$37

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

As of Sep 4, 2026, the average hourly pay for quality control associate two in Coventry, RI is $24.81, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $30.19 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Associate Two vs Quality Control Associate One?

AspectQuality Control Associate TwoQuality Control Associate One
Required CredentialsHigh school diploma or equivalent; some roles may require certifications in GMP or ISO standardsHigh school diploma or equivalent; basic understanding of quality standards
Work EnvironmentManufacturing or laboratory settings, often in regulated industriesSimilar environments, typically in labs or production areas
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing companiesCommonly used in similar industries, often as entry-level roles
Common Search & Comparison IntentYes, often compared to associate level roles to understand responsibilities and requirementsNo, usually the starting point for quality roles

Quality Control Associate Two typically requires more experience or certifications than Quality Control Associate One. It involves more responsibilities in quality inspections and compliance, making it suitable for those with some industry experience. Both roles are common in manufacturing and laboratory environments within regulated industries.

Is quality control a good career path?

Quality Control Associate Two is a role focused on inspecting products, ensuring standards are met, and documenting quality issues. It offers opportunities for skill development in inspection techniques, attention to detail, and familiarity with quality management systems, making it a stable career choice in manufacturing and production industries.

What does a quality control associate do?

A Quality Control Associate is responsible for inspecting products and materials to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or laboratory environments. Attention to detail and knowledge of quality procedures are essential for this role.
Quality Control Associate Two jobs near you

Quality Control Associate

Amgen, Inc.

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

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.
Associate Quality Control
What you will do
Let's do this. Let's change the world. In this vital role you will be responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a highly dynamic, team environment.
This role is expected to work a 10-hour shift Saturday - Tuesday, from 6:45AM-5:15PM.
Responsibilities include:
  • 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 to support GMP operations
  • Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory procedures
  • Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
  • Operate and maintain specialized laboratory equipment and instrumentation
  • Participate in laboratory investigations and audits as necessary
  • Perform general laboratory housekeeping activities
  • Maintain training compliance and proficiency
  • At all times, comply with safety guidelines, cGMPs and other applicable regulatory requirements

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 good teammate with these qualifications.
Basic Qualifications:
  • High school/GED + 2 years [Job Code's Discipline and/or Sub-Discipline] work experience OR
  • Associate's + 6 months [Job Code's Discipline and/or Sub-Discipline] work experience OR
  • Bachelor's

Preferred Qualifications:
  • Experience in a regulated biotechnology/pharmaceutical lab environment
  • Professional work experience in a fast-paced, flexible GxP Microbiology Laboratory
  • Experience executing microbiological test methods (ie. Endotoxin, PCR, Growth Promotion Testing)
  • Experience supporting Environmental and Clean Utility monitoring programs
  • Demonstrated written and oral communication skills with ability to write effective science-based quality and compliance documents
  • Demonstrated ability to be flexible and adaptable to support business needs
  • Experience executing endotoxin, media qualification and sterility testing
  • Demonstrated proficiency with electronic systems (LIMS, LMES, Trackwise, etc.)
  • Exposure to Operational Excellence initiatives including Lean Manufacturing and 5S
  • Demonstrated project management and presentation skills, and proven ability to manage priorities effectively

What you can expect of 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.
Salary Range
62,571.90USD -84,656.10 USD

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