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Quality Control Associate Ii Jobs in Rhode Island

Under general supervision, this position will perform routine procedures to support testing within Quality Control. Tasks may include but not limited to performing sample collection, sample handling ...

New

Quality Control Inspector

Lincoln, RI ยท On-site

$20 - $22/hr

Ability to 1) read, write, understand and speak basic English, 2) apply basic English literacy to ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Ability to 1) read, write, understand and speak basic English, 2) apply basic English literacy to ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

... 2,700 people across North America. GENERAL PURPOSE OF THE JOB: Supervise the quality process to ... Minimum of 3 years' experience in quality control within a manufacturing environment with a minimum ...

The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards ...

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Quality Control Associate Ii information

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 Rhode Island as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Quality Control Associate

West Greenwich, RI โ€ข On-site

Initial Therapeutics, Inc.
Biotechnology Research and Developmentย โ€ขย 11 - 50 employees

Other

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago


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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