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Qc Associate Jobs in Rhode Island (NOW HIRING)

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 ...

New

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 ...

Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ...

Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ...

Specialist QC

West Greenwich, RI · On-site

$95 - $125/hr

Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Associate's degree and 8 years of directly related experience OR * Bachelor's degree and 4 years of ...

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

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Qc Associate information

See Rhode Island salary details

$11

$24

$37

How much do qc associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for qc associate in Rhode Island is $24.94, according to ZipRecruiter salary data. Most workers in this role earn between $18.12 and $30.38 per hour, depending on experience, location, and employer.

What is a QC associate?

A QC (Quality Control) Associate is a professional responsible for performing tests and inspections on products, materials, or processes to ensure they meet established quality standards. They work primarily in manufacturing, pharmaceutical, biotechnology, or food industries, helping to identify defects and maintain compliance with regulatory requirements. QC Associates document their findings, report issues, and may assist in implementing corrective actions to improve product quality. Their work is critical in ensuring that only safe and effective products reach customers.

What skills and qualifications are needed to be a QC associate?

To thrive as a QC Associate, you need a background in chemistry, biology, or a related scientific field, often supported by a relevant degree or laboratory experience. Familiarity with laboratory equipment, analytical instruments (like HPLC or GC), and quality management systems (such as GMP or ISO standards) is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring accuracy and collaborating with team members. These competencies are essential for maintaining product quality, regulatory compliance, and operational efficiency in quality control environments.

What challenges do QC associates face when ensuring product quality, and how can they be addressed?

QC Associates often encounter challenges such as tight production deadlines, handling multiple testing protocols, and maintaining accuracy under pressure. Adapting to new technologies or updated regulatory standards can also present difficulties. To address these, strong organizational skills, continuous training, and effective communication with cross-functional teams are essential. Additionally, maintaining thorough documentation and proactively identifying potential issues can help ensure consistent product quality and compliance.

What are the most commonly searched types of Qc jobs in Rhode Island?

The most popular types of Qc jobs in Rhode Island are:

What are popular job titles related to Qc Associate jobs in Rhode Island?

For Qc Associate jobs in Rhode Island, the most frequently searched job titles are:

What cities in Rhode Island are hiring for Qc Associate jobs?

Cities in Rhode Island with the most Qc Associate job openings:

Infographic showing various Qc Associate job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $51,867 per year, or $24.9 per hour.

Quality Control Associate

Initial Therapeutics, Inc.

West Greenwich, RI • On-site

$65 - $82/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

New


Job description

Join Amgens Mission of Serving Patients

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds 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, youll 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, youll 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

Lets do this. Lets 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 Codes Discipline and/or Sub-Discipline] work experience OR
  • Associates + 6 months [Job Codes Discipline and/or Sub-Discipline] work experience OR
  • Bachelors
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, well 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.

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.

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