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Perfusion Assistant Jobs in Rhode Island (NOW HIRING)

Lead on-the-floor execution of AR5 PPH upstream manufacturing operations, including perfusion ... * Assist in developing and implementing departmental strategy and plans aligned with broader AR5 ...

OR Support Secretary

Providence, RI · On-site

$21.09 - $22.04/hr

... Anesthesia, Perfusion and the like. * Contacts physician's offices in order to inform them of ... Maintains records of all cases processed and assists in generating activity statistics, assist in ...

OR Support Secretary

Providence, RI · On-site

$21.09 - $22.04/hr

... Anesthesia, Perfusion and the like. Contacts physician's offices in order to inform them of ... Maintains records of all cases processed and assists in generating activity statistics, assist in ...

Perform basic troubleshooting and assist in the review of documentation for assigned functions ... This position is for the AR5 A shift Upstream Cell Culture (Perfusion, Production, Harvest - PPH ...

Perform basic troubleshooting and assist in the review of documentation for assigned functions ... This position is for the AR5 A shift Upstream Cell Culture (Perfusion, Production, Harvest - PPH ...

Perfusion Assistant information

See Rhode Island salary details

$9

$37

$104

How much do perfusion assistant jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for perfusion assistant in Rhode Island is $37.42, according to ZipRecruiter salary data. Most workers in this role earn between $16.57 and $49.95 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to thrive as a perfusion assistant?

To thrive as a Perfusion Assistant, you typically need a background in healthcare or life sciences, familiarity with cardiovascular anatomy, and knowledge of sterile techniques. Experience with perfusion equipment, cardiopulmonary bypass machines, and basic laboratory systems is highly valuable, and some positions may require certification in Basic Life Support (BLS). Strong attention to detail, teamwork, and effective communication skills help you excel in assisting perfusionists and surgical teams under pressure. These competencies are vital to ensure patient safety, precise support during surgeries, and efficient collaboration within the operating room environment.

What does a perfusion assistant do?

As a Perfusion Assistant, your day often begins with equipment checks and preparation for surgical procedures involving cardiopulmonary bypass or other advanced circulatory support. You’ll assist perfusionists in setting up, operating, and maintaining perfusion machines, monitor patient status, and manage disposable supplies in a sterile environment. Expect to work closely with surgeons, anesthesiologists, nurses, and other operating room staff, often in high-stress situations requiring quick thinking and strong teamwork. This dynamic role offers valuable hands-on experience in cardiac surgical care and can be a stepping stone to advanced positions in perfusion or related healthcare specialties.

What is a perfusion assistant?

A Perfusion Assistant supports Perfusionists during cardiovascular surgeries by preparing and maintaining perfusion equipment, monitoring supplies, and ensuring a sterile environment. They help set up heart-lung machines, blood pumps, and other devices critical for bypass procedures. Their role is essential in maintaining patient safety and operational efficiency in the surgical team.

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What job categories do people searching Perfusion Assistant jobs in Rhode Island look for? The top searched job categories for Perfusion Assistant jobs in Rhode Island are:
What cities in Rhode Island are hiring for Perfusion Assistant jobs? Cities in Rhode Island with the most Perfusion Assistant job openings:
Infographic showing various Perfusion Assistant job openings in Rhode Island as of August 2026, with employment types broken down into 76% Full Time, 13% Part Time, and 11% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $77,827 per year, or $37.4 per hour.

Mgr Manufacturing - Nights

Amgen, Inc.

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 13 hours 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.
Manager Manufacturing PPH - Nights
What you will do
Let's do this. Let's change the world. In this vital role, you will lead front-line manufacturing operations within AR5 PPH, supporting upstream cell culture activities including perfusion, production, and harvest operations. You will be accountable for safe, compliant, reliable, and right-first-time execution of the manufacturing plan while building a high-performing team that consistently demonstrates Amgen's "Every Action, Every Time" culture.
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 AR5's commitment to being the best place for talent.
Scope of Responsibility
  • Lead on-the-floor execution of AR5 PPH upstream manufacturing operations, including perfusion, production, and harvest activities.
  • Demonstrate technical mastery of cell culture processes, equipment, systems, and operational requirements.
  • Oversee right-first-time execution of the production plan in alignment with cGMP, safety, quality, and operational standards.
  • Provide daily oversight of cGMP practices and safety programs to reduce human error events and strengthen operational discipline.
  • Ensure adherence to Standard Operating Procedures, batch records, electronic batch records, GMP requirements, safety standards, and site procedures.
  • Ensure the manufacturing area remains inspection-ready at all times through strong housekeeping, audit readiness, and routine area ownership.
  • Drive reduction in housekeeping and inspection-readiness observations by ensuring timely correction of gaps and sustained adherence to standards.
  • Lead or support housekeeping audits, inspection-readiness mock audits, area walkthroughs, and readiness activities.
  • Coach staff on proper use of error-prevention behaviors before, during, and after manufacturing execution.
  • Troubleshoot process deviations, equipment issues, material constraints, and operational challenges in real time.
  • Make sound processing decisions using technical knowledge, procedural requirements, quality expectations, and business priorities.
  • Participate in investigations, deviations, CAPAs, audits, and regulatory inspections as the manufacturing operations owner or representative.
  • Ensure clear, timely, and effective communication across shifts, functions, and levels of the organization.
  • Ensure appropriate scheduling and coordination of production, maintenance, cleaning, turnover, training, and support activities.
  • Collaborate with QA, QC, F&E, Maintenance, PD, Process Engineering, Supply Chain, Regulatory, and other partners to complete production activities and maintain schedule adherence.
  • Monitor area performance and drive improvements in safety, quality, compliance, reliability, throughput, and efficiency

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 Amgen'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.

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 (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 receiving an added 15% shift differential.
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 collaborative leader with these qualifications.
Basic Qualifications:
  • High school diploma / GED and 12 years of Manufacturing and Operations experience OR
  • Associate's degree and 10 years of Manufacturing and Operations experience OR
  • Bachelor's degree and 5 years of Manufacturing and Operations experience OR
  • Master'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:
  • Bachelor's degree 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
  • Strong leadership and teambuilding skills (coaching, mentoring, counseling)
  • Experience with staff capability and team performance improvements
  • Experience with performance management including performance reviews
  • Conflict Resolution skills
  • Analytical problem solving skills
  • Project Management skills
  • Thorough understanding of regulatory requirements
  • Ability to be flexible and manage change
  • Excellent verbal and written communication (technical) skills
  • Excellent computer skills with Microsoft, EBR/MES, Delta V, Electronic quality systems.

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
106,148.00USD -143,612.00 USD