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Biotech Manufacturing Associate Jobs in Rhode Island

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 ...

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 ...

Associate's degree and 6 years of Manufacturing and Operations experience OR * Bachelor's degree ... Experience working in a GMP pharmaceutical or biotechnology manufacturing environment, with ...

Associate's degree and 6 years of Manufacturing and Operations experience OR * Bachelor's degree ... Experience working in a GMP pharmaceutical or biotechnology manufacturing environment, with ...

Sr. Specialist Manufacturing

West Greenwich, RI ยท On-site

$89K - $123K/yr

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 and/or Manufacturing experience OR * Bachelor's degree ...

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 and/or Manufacturing experience OR * Bachelor's degree ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Exposure to Operational Excellence initiatives including Lean Manufacturing and 5S * Demonstrated ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Exposure to Operational Excellence initiatives including Lean Manufacturing and 5S * Demonstrated ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree Preferred Qualifications: * Experience in a GMP/ other regulated environment.

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate's degree Preferred Qualifications: * Experience in a GMP/ other regulated environment.

Showing results 21-40

Biotech Manufacturing Associate information

See Rhode Island salary details

$12

$20

$32

How much do biotech manufacturing associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for biotech manufacturing associate in Rhode Island is $20.41, according to ZipRecruiter salary data. Most workers in this role earn between $16.01 and $22.84 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

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

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

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

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

What job categories do people searching Biotech Manufacturing Associate jobs in Rhode Island look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Rhode Island are:

Infographic showing various Biotech Manufacturing Associate job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $42,445 per year, or $20.4 per hour.

Associate Manufacturing - Days

Amgen, Inc.

West Greenwich, RI โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 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.
Associate Manufacturing - Days
What you will do
Let's do this. Let's change the world. In this vital role you will perform operations within the Manufacturing area, specifically purification, at Amgen's innovative Rhode Island facility. You will be required to know, comprehend, and apply Good Manufacturing Practices (GMP), as well as understand, follow, and document in batch records.
This role is expected to work a 12-hour shift on a rotating schedule. The shift pattern will be 7AM-7PM (A shift), with a two-week rotation covering 7 days per rotation (A Shift). The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off.
Responsibilities:
  • Efficiently perform and monitor critical GMP manufacturing operations in accordance with Standard Operating Procedures (SOPs).
  • Effectively use and perform basic troubleshooting within the site's electronic systems (e.g., and Manufacturing Execution System (MES), Delta V, and Enterprise Resource Planning (ERP) system).
  • Execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
  • Contribute to the culture of safety and quality by participating in and leading team safety and quality initiatives.
  • Understand and contribute to the team's Lean Manufacturing goals and objectives by identifying improvement opportunities and implementing solutions.
  • Work with diverse teams.
  • Escalate issues appropriately.
  • Ownership of corrective and preventative action and non-conformance records.

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 great teammate with these qualifications.
Basic Qualifications:
  • High school/GED + 2 years of manufacturing or operations work experience OR
  • Associate's + 6 months of manufacturing or operations work experience OR
  • Bachelor's Degree in a related field

Preferred Qualifications:
  • Knowledge of large-scale Purification operations, chromatography, TFF, aseptic processing, etc.
  • Knowledge of large-scale cell culture operations.
  • CFR and Regulatory knowledge.
  • Mechanical ability/expertise on fed-batch manufacturing equipment.
  • Knowledge of WIP lab equipment and computers, with LIMS access.
  • Demonstrated strong work ethic and positive attitude.
  • Basic statistical mathematical skills.
  • Ability to interpret and apply GMP knowledge.
  • Understanding of analytical methods for manufacturing area.
  • Ability to demonstrate technical writing capability with Trackwise access.
  • Able to demonstrate project management skills and presentation skills.
  • Independently collaborate with outside resources.
  • Ability to understand, apply and evaluate basic chemistry, biology and physical principles.
  • Experience with Delta V, RD's.
  • Experience with lab equipment/testing.

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
70,985.20USD -96,038.80 USD