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Biotech Manufacturing Jobs in Rhode Island (NOW HIRING)

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 ... Lead complex, cross-functional problem-solving efforts involving Manufacturing, Engineering ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Lead complex, cross-functional problem-solving efforts involving Manufacturing, Engineering ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Manufacturing Process Technician - Days What you will do Let's do this! Let's change the world! In ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Manufacturing Process Technician - Days What you will do Let's do this! Let's change the world! In ...

Familiarity with pharmaceutical manufacturing processes and how facilities infrastructure supports ... biotech client portfolio. This position does not provide visa sponsorship. Candidates must be ...

Showing results 41-60

Biotech Manufacturing information

See Rhode Island salary details

$12

$20

$32

How much do biotech manufacturing jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for biotech manufacturing 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 biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

What are the key skills and qualifications needed to thrive in biotech manufacturing?

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

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

The most popular types of Biotech Manufacturing jobs in Rhode Island are:

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

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

What cities in Rhode Island are hiring for Biotech Manufacturing jobs?

Cities in Rhode Island with the most Biotech Manufacturing job openings:

Infographic showing various Biotech Manufacturing job openings in Rhode Island as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, 3% Contract, and 2% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $42,445 per year, or $20.4 per hour.

Manager Manufacturing Solution Prep - Nights

Amgen SA

West Greenwich, RI โ€ข On-site

$110 - $140/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago


Job description

Join Amgenโ€™s Mission of Serving Patients

At Amgen, if you feel like youโ€™re part of something bigger, itโ€™s because you are. Our shared missionโ€”to serve patients living with serious illnessesโ€”drives all that we do.

Since 1980, weโ€™ve helped pioneer the world of biotech in our fight against the worldโ€™s toughest diseases. With our focus on four therapeutic areas โ€“Oncology, Inflammation, General Medicine, and Rare Diseaseโ€“ 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, youโ€™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, youโ€™ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Manager Manufacturing Solution Prep - Nights What you will do

Letโ€™s do this. Letโ€™s change the world. In this vital role you will champion a safe and compliant production environment through structured on-the-floor presence. This role will also be well positioned to champion problem solving and continuous improvement among the team and in collaboration with cross-functional partners in Quality, EHSS, F&E, and Process Development. The manager will be an active player in our OnePlant operating model, building reliability, agility, and efficiency through our I-530 pathway and Agile Workforce.

The Front-Line Manager will collaborate routinely with Quality Assurance, Quality Control, Engineering, Facilities and Engineering, Maintenance, Process Development, Process Engineering, Supply Chain, Regulatory Compliance, and other site functions. This role requires strong technical ownership of manufacturing operations, disciplined execution of cGMP and safety expectations, and the ability to make timely decisions in a dynamic production environment.

With minimal direction, the Manager is responsible for leading on-the-floor operations and staff in manufacturing. The Manager will supervise, coach, hire, onboard, and develop manufacturing staff while ensuring that team members are trained, capable, engaged, and prepared to meet production requirements. The Front-Line Manager will help define area objectives, identify improvement opportunities, lead change efforts, and deliver against short- and long-term AR5 manufacturing goals.

This leader will be expected to strengthen reliability, improve operational efficiency, enable agility for future business needs, and support AR5โ€™s commitment to being the best place for talent.

The on-boarding phase for this role will last 2-6 weeks, during which time successful incumbents will be on an administrative schedule (Monday through Friday, approximately 8am to 5pm). Following the on-boarding phase, the successful incumbent will be expected to join a shift team working a 12-hour shift. The shift pattern will be 7pm -7am (C or D shift) with a two-week rotation covering 7 days per week. The rotating shift offers several benefits such as, an average of 14 days on shift per month with every other weekend off and 15% shift differential.

Scope of Responsibilities:
  • Safety and Quality Oversight: The cornerstone of our operations are safe and compliant execution by the manufacturing team - own and reinforce the strong safety and quality culture within the shift and ensure standards are upheld through active engagement and coaching.

  • Operational Leadership: Lead the shift and collaborate with peer managers to reliably deliver production targets. Coordinate daily task allocation and plan ahead with the scheduling team for short- to mid-term schedule needs. Provide Purposeful Presence on the Floor (Gemba) to monitor overall department performance, provide coaching, and ensure consistency with our core Floor Operating Principles. Coordinate with support functions to troubleshoot, identify and resolve issues as needed while on shift.

  • Talent Development: Mentor and develop talent, fostering an environment of engagement, belonging, continuous learning, and operational excellence. Build a high-performing team, ensuring accountability and advancing technical and leadership capabilities.

  • Continuous Improvement, Innovation, and Process Enhancement: Identify and drive process improvement initiatives to support higher efficiency and eliminate non-value-added activities.

  • Agile Workforce Leadership: Role model ARI Manufacturingโ€™s Agile Workforce behaviors by planning and executing cross-training and dynamic resource allocation across AR5 and AR30 that enhances responsiveness and productivity while increasing opportunities for staff development.

Leading Strategy Development and Execution
  • Assist in developing and implementing departmental strategy and plans aligned with broader AR5, ARI, and site manufacturing objectives.

  • Translate strategic priorities into clear daily, weekly, and shift-level execution plans.

  • Anticipate operational, quality, safety, training, and schedule risks and build contingencies to reduce impact.

  • Deliver strong business results through continuous improvement, standardization, and disciplined execution.

  • Use metrics, audit outcomes, process data, and staff feedback to identify trends and improve performance.

  • Lead change efforts that improve safety, compliance, quality, efficiency, throughput, and reliability.

  • Ensure the team understands how daily execution connects to Amgenโ€™s mission, patient impact, and AR5 business priorities.

Building a Strong Organizational Alignment
  • Be responsible for selection, onboarding, training, evaluation, staff relations, performance management, and development of manufacturing staff.

  • Ensure the right people, skills, and resources are in place and optimally allocated to achieve production, quality, and business goals.

  • Interact with management to optimize organizational structure, roles, responsibilities, and shift performance.

  • Build and develop a diverse, impactful team that can reliably execute complex manufacturing operations.

  • Work across functions to build organizational and individual capability.

  • Develop strong relationships with staff members and provide open, clear, and actionable feedback.

  • Foster a team environment that supports accountability, innovation, continuous improvement, learning, knowledge-sharing, and psychological safety.

  • Promote clear communication across shifts to ensure continuity, alignment, and readiness.

  • Lead with a people-centered approach that supports engagement, retention, empowerment, and development.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a motivated professional with these qualifications.

Basic Qualifications:
  • High school diploma / GED and 12 years of Manufacturing and Operations experience OR

  • Associateโ€™s degree and 10 years of Manufacturing and Operations experience OR

  • Bachelorโ€™s degree and 5 years of Manufacturing and Operations experience OR

  • Masterโ€™s degree and 3 years of Manufacturing and Operations experience OR

  • Doctorate degree

In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications:
  • Background in Life Sciences or Engineering

  • Knowledge and experience within a cGMP or other highly regulated environment including a basic understanding of technical elements across engineering, biological or chemical processing

  • Skilled in change management, team building, and fostering innovation

  • Excellent communication skills, drive, sense of urgency, and analytical problem-solving abilities

  • Demonstrated experience in applying Operational Excellence and Lean Manufacturing

  • Experience with performance management including coaching, conflict resolution and performance reviews

  • Ability to be flexible and manage change

  • Demonstrated ability to forge and maintain strong relationships with other functional areas

  • User-level fluency with digital tools for daily management, data analysis and visualization, and application of Artificial Intelligence (e.g, Copilot, Chat GPT, etc)

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, weโ€™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, including remote and hybrid work arrangements, where possible

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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