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Senior Manufacturing Associate Jobs in Rhode Island

Sr Specialist QA - Compliance

West Greenwich, RI ยท On-site

$89K - $123K/yr

... we research, manufacture, and deliver innovative medicines to help people live longer, fuller ... Associate's degree and 10 years of regulatory compliance experience OR * Bachelor's degree and 6 ...

... we research, manufacture, and deliver innovative medicines to help people live longer, fuller ... Associate's degree and 10 years of regulatory compliance experience OR * Bachelor's degree and 6 ...

Senior Associate, Product Training

Warwick, RI ยท On-site

$64K - $129K/yr

About the role Viessmann has long been known as a leading manufacturer in the Hot Water Heating Industry. We are currently expanding into the HVAC industry by offering hot water and chilled water ...

Senior Associate, Product Training

Warwick, RI ยท On-site

$64K - $129K/yr

About the role Viessmann has long been known as a leading manufacturer in the Hot Water Heating Industry. We are currently expanding into the HVAC industry by offering hot water and chilled water ...

Showing results 21-40

Senior Manufacturing Associate information

See Rhode Island salary details

$9

$18

$38

How much do senior manufacturing associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for senior manufacturing associate in Rhode Island is $18.05, according to ZipRecruiter salary data. Most workers in this role earn between $14.13 and $16.97 per hour, depending on experience, location, and employer.

What is the difference between Senior Manufacturing Associate vs Manufacturing Associate?

AspectSenior Manufacturing AssociateManufacturing Associate
CredentialsTypically requires 2+ years of experience, relevant certifications (e.g., GMP, OSHA)Entry-level or 1+ year experience, basic certifications often sufficient
ResponsibilitiesSupervising processes, troubleshooting, quality checks, mentoringPerforming manufacturing tasks, operating equipment, following procedures
Work EnvironmentManufacturing floors, quality control labs, team leadership rolesProduction lines, assembly areas, routine manufacturing tasks
Usage in IndustryUsed for experienced roles with additional responsibilitiesEntry to mid-level manufacturing roles

The main difference between a Senior Manufacturing Associate and a Manufacturing Associate lies in experience, responsibilities, and level of supervision. Senior Manufacturing Associates typically have more experience, take on supervisory or troubleshooting roles, and may mentor junior staff, whereas Manufacturing Associates focus on executing manufacturing tasks under supervision.

What does a senior manufacturing associate do?

A Senior Manufacturing Associate is responsible for overseeing and executing complex manufacturing processes in industries such as pharmaceuticals, biotechnology, or electronics. They ensure that production runs smoothly and efficiently, maintaining quality standards and troubleshooting any issues that arise. Additionally, they often provide training and guidance to junior team members and help implement process improvements. Their role may also involve documentation, compliance with safety regulations, and collaborating with other departments to meet production goals.

How does a senior manufacturing associate typically collaborate with cross-functional teams during production processes?

A Senior Manufacturing Associate frequently works alongside quality assurance, engineering, and supply chain teams to ensure smooth and efficient production workflows. They are often responsible for communicating production issues, facilitating process improvements, and ensuring compliance with safety and regulatory standards. This collaboration is essential for troubleshooting equipment problems, implementing new protocols, and maintaining high product quality. The role requires strong interpersonal skills and the ability to coordinate with diverse teams to meet production goals and deadlines.

What are the key skills and qualifications needed to thrive as a senior manufacturing associate, and why are they important?

To thrive as a Senior Manufacturing Associate, you need in-depth knowledge of manufacturing processes, quality control, and production standards, usually supported by experience in a similar environment and relevant technical training. Familiarity with manufacturing software (such as ERP systems), lean manufacturing methodologies, and compliance certifications like GMP are typically expected. Leadership, problem-solving, and effective communication are vital soft skills for guiding teams and addressing production challenges. These skills and qualifications are crucial to ensuring efficient operations, maintaining high product quality, and driving continuous improvement on the production floor.
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Infographic showing various Senior Manufacturing Associate job openings in Rhode Island 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 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $37,541 per year, or $18 per hour.

Manager Manufacturing Environmental and Contamination Control

Amgen, Inc.

West Greenwich, RI โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday


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 Environmental & Contamination Control
What you will do
Let's do this. Let's change the world. In this vital role you will be responsible for day-to-day delivery of deviation records and investigations, ensuring Deviation Owners and FAOs execute with rigor, speed, and compliance, particularly for microbial and EM-related events. This role shall report to the Senior Manager of the Environmental and Contamination Control (ECC) team.
Responsibilities
The Front-Line Manager
Direct Management of Deviation Owners & FAO's
  • Lead and coordinate:
    • Deviation Owners (execution)
    • Process Specialists (technical oversight)
  • Ensure:
    • Clear ownership assignment and appropriate planning and distribution of workload
    • Timely movement of records
Deviation Lifecycle Execution
  • Oversee: Initiation โ†’ triage โ†’ investigation โ†’ closure
  • Ensure records are complete, accurate, and audit-ready
  • Remove barriers to timely closure and escalation
Investigation Quality Oversight
  • Ensure:
    • Robust root cause analysis (RCA)
    • Appropriate scoping and impact assessment
  • Challenge teams to avoid superficial or convenience-based conclusions
Microbial Event Execution (Critical Focus)
  • Ensure microbial deviations receive appropriate SME engagement (QC Micro, aseptic SMEs)
  • Verify:
    • Investigations reflect true contamination risks
    • Classification reflects risk (not bias or precedent)
Decision Facilitation & Alignment
  • Facilitate alignment between:
    • FAO
    • QA
    • Deviation Owner
  • Ensure decisions (classification, disposition) are clearly documented
CAPA Execution & Follow-Through
  • Ensure CAPAs are:
    • Assigned
    • Owned
    • Completed effectively
  • Confirm clear linkage between root cause and actions
Triage & Prioritization
  • Lead daily deviation triage for environmental and contamination control-related events
  • Prioritize high-risk (e.g., microbial, major deviations)
  • Ensure effective tools and business processes are in place for tracking and reporting record progress
  • Allocate resources appropriately
Inspection Readiness Support
  • Prepare team to:
    • Speak to deviations directly
    • Defend scientific rationale
  • Ensure records are inspection-ready at all times
Continuous Improvement
  • Create a culture of continuous improvement among the ECC team and facilitate implementation of tools and processes that streamline the investigation process, making appropriate use of AI and other digital tools.
Key Performance Metrics
  • On-time closure (OTD)
  • Aging backlog
  • Investigation effectiveness
  • CAPA cycle time
  • Audit/inspection observations

All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.
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 self-starter with these qualifications.
Basic Qualifications
  • High school diploma/GED and 12 years of manufacturing or operations experience OR
  • Associates degree and 10 years of manufacturing or operations experience OR
  • Bachelor's degree and 5 years of manufacturing or operations experience OR
  • Master's degree and 3 years of manufacturing or 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, prograns, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications
  • The knowledge and skills necessary to perform the duties of this position are typically acquired through the following combination of education and experience or the equivalent
  • BS/BA or equivalent (science/engineering/psychology preferred)
  • 8+ years of experience in the pharmaceutical industry
  • Experience applying AI or other digital tools to generate insights and streamline workflows
  • Strong understanding of deviation management process, root cause analysis & GMP compliance
  • Ability to drive execution through others, manage multiple competing priorities, influence cross-functional teams & provide performance management and coaching for a team of professionals

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