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Biotech Associate Jobs in Barrington, RI (NOW HIRING)

Amgen, Inc.

Validation Engineer

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree and 6 years of Manufacturing and Operations experience OR * Bachelor's degree ...

Amgen, Inc.

Manager QA - Nights

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree and 10 years of Quality or Manufacturing experience OR * Bachelor's degree or ...

Amgen

Validation Engineer

West Greenwich, RI

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree and 6 years of Manufacturing and Operations experience OR * Bachelor's degree ...

Amgen Inc. (IR)

Validation Engineer

West Greenwich, RI · On-site

$86 - $116/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree and 6 years of Manufacturing and Operations experience * Bachelor's degree and 2 ...

New

Amgen SA

Validation Engineer

West Greenwich, RI · On-site

$90 - $130/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree and 6 years of Manufacturing and Operations experience OR * Bachelor's degree ...

Posted today

Amgen

Sr Associate QA - Nights

West Greenwich, RI

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Join us and transform the lives of patients while transforming your career. Sr Associate QA What ...

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Biotech Associate information

See Barrington, RI salary details

$10

$19

$32

How much do biotech associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for biotech associate in Barrington, RI is $19.76, according to ZipRecruiter salary data. Most workers in this role earn between $14.81 and $20.58 per hour, depending on experience, location, and employer.

What is a biotech associate?

Biotech Associates are professionals who support scientific research, development, and production in biotechnology companies or laboratories. They typically assist in conducting experiments, analyzing data, preparing samples, and maintaining laboratory equipment. Their work helps develop new products or processes in areas like pharmaceuticals, agriculture, and environmental science. Biotech Associates often have a background in biology, chemistry, or related fields and work under the supervision of scientists or senior researchers.

What are the key skills and qualifications needed to thrive as a biotech associate?

To thrive as a Biotech Associate, you need a solid background in biology, chemistry, or a related field, usually supported by a bachelor's or master's degree. Familiarity with laboratory techniques, data analysis software, and compliance with regulatory standards like GLP or GMP is essential. Strong attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this position. These skills ensure accurate experimental results, regulatory compliance, and efficient collaboration in fast-paced research environments.

What are some typical challenges faced by biotech associates when working in a laboratory setting?

Biotech Associates often encounter challenges such as troubleshooting complex experiments, maintaining strict adherence to safety protocols, and managing multiple projects simultaneously. Working with sensitive biological materials requires attention to detail and the ability to quickly adapt to unexpected results or equipment malfunctions. Collaboration with scientists and cross-functional teams is frequent, so strong communication skills are essential to ensure experiments are aligned with broader research goals.

What is the difference between Biotech Associate vs Laboratory Technician?

AspectBiotech AssociateLaboratory Technician
Required CredentialsBachelor's degree in biology, biotech, or related field; some roles may require experienceAssociate's degree or relevant certification; less emphasis on advanced degrees
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsAcademic labs, industrial labs, healthcare facilities
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

The main difference between a Biotech Associate and a Laboratory Technician lies in their educational requirements and work scope. Biotech Associates typically hold a bachelor's degree and engage in research and development activities within biotech companies or research institutions. Laboratory Technicians often have an associate's degree and focus on routine lab tasks, testing, and sample processing. Both roles are essential in laboratory settings but differ in responsibilities and qualifications.

What job categories do people searching Biotech Associate jobs in Barrington, RI look for?

The top searched job categories for Biotech Associate jobs in Barrington, RI are:

What cities near Barrington, RI are hiring for Biotech Associate jobs?

Cities near Barrington, RI with the most Biotech Associate job openings:

Biotech Associate jobs near you
Infographic showing various Biotech Associate job openings in Barrington, RI 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 $41,109 per year, or $19.8 per hour.

Validation Engineer

Amgen, Inc.

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 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.
Validation Engineer
What you will do
Let's do this. Let's change the world. In this vital role is within the Product Lifecycle Management organization at Amgen Rhode Island (ARI), a large-scale mammalian cell biotech manufacturing plant that produces multiple commercial and clinical products. The team is responsible for new product introductions (NPI), product re-introductions (PRI) to Amgen Rhode Island's Manufacturing Facilities (AR5 and AR30) and managing the lifecycle of ARI's product portfolio. The schedule for this position is Monday - Friday Admin Day Shift.
Responsibilities:
  • Support validation strategy and execute validation activities for manufacturing equipment, support equipment, and utilities, including validation planning, protocol development and execution, performance qualification, equipment release, and lifecycle documentation.
  • Plan and coordinate and execute equipment and system qualification activities across a range of technologies, including CIP, SIP and autoclave systems, airflow visualization studies, benchtop equipment, and supporting utilities. Apply appropriate risk- and science-based approaches based on the system and intended use.
  • Serve as the validation technical expert during project planning, equipment implementation, design reviews, and change control. Interpret engineering, automation, process, and equipment design documentation to determine validation requirements and appropriate testing approaches in accordance with established procedures and standards. Develop/author Validation plans
  • Generate, review, and approve validation documentation and provide validation impact assessments for changes, projects, and equipment modifications.
  • Investigate technical issues and develop solutions to validation challenges of moderate complexity.
  • Execute and support cleaning validation and continued cleaning verification activities.
  • Maintain site cleaning acceptance criteria, including calculating maximum allowable carryover (MAC) and providing scientific justification for acceptance criteria.
  • Drive continuous improvement of validation programs, procedures, and execution practices, and develop or deliver training to manufacturing staff in support of validation activities.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The adaptable professional we seek is a self-starter with these qualifications.
Basic Qualifications
  • High school diploma / GED and 8 years of Manufacturing and Operations experience OR
  • Associate's degree and 6 years of Manufacturing and Operations experience OR
  • Bachelor's degree and 2 years of Manufacturing and Operations experience OR
  • Master's degree

Preferred Qualifications
  • Experience working in a GMP pharmaceutical or biotechnology manufacturing environment, with exposure to upstream and/or downstream operations.
  • Hands-on validation experience with manufacturing equipment, facility systems, and utilities, including equipment qualification, sterilization/steaming, cleaning validation, and performance studies.
  • Strong technical understanding of pharmaceutical/biotechnology unit operations and manufacturing equipment and processes.
  • Ability to interpret engineering and automation documentation and translate equipment and process requirements into appropriate validation testing.
  • Strong understanding of GMP requirements and applicable CFR/regulatory expectations, with the ability to interpret and apply regulatory principles to validation activities.
  • Strong analytical and experimental design skills, with the ability to evaluate validation data and resolve technical issues.
  • Strong technical writing skills, with the ability to prepare clear, accurate, and compliant validation documentation.
  • Strong verbal communication and project coordination skills, with the ability to work effectively across manufacturing, engineering, automation, and quality functions.
  • Ability to work independently under general direction, manage priorities, and recognize when additional technical or management direction is appropriate.

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
85,878.05USD -116,187.95 USD

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