168 Manufacturing jobs in Harrisville

Anduril Industries is a defense technology company with a mission to transform U.S. and allied military capabilities with advanced technology. By bringing the expertise, technology, and business model of the 21st century's most innovative companies to the defense industry, Anduril is changing how military systems are designed, built and sold. Anduril's family of systems is powered by Lattice OS, an AI-powered operating system that turns thousands of data streams into a realtime, 3D command and control center. As the world enters an era of strategic competition, Anduril is committed to bringing cutting-edge autonomy, AI, computer vision, sensor fusion, and networking technology to the military in months, not years.

ABOUT THE TEAM

Anduril is fielding the next generation of Autonomous Underwater Vehicles (AUVs) to tackle the extremely challenging industry demands of seabed exploration. Anduril has brought to the market a unique, ultra-long-range, full-ocean-depth platform, and a completely refreshed maritime vehicle and flexible manufacturing architecture that scales from "large" to "extra-large" vehicle sizes. Today, Anduril is executing on multi-million-dollar contracts while simultaneously performing Robot-as-a-Service (RaaS) AUV operations.
ABOUT THE JOB

We are looking for a Manufacturing Technician to join our growing team in Quincy, MA. In this role, you will play be responsible for working hands-on with our engineering team on a multi-disciplinary workflow to deliver world class AUVs. This will require building complex electromechanical assemblies and integrating them into the final product!

Please note: This role will be based in our Quincy, MA location until Q4 of 2025. Following this period, the successful candidate will be expected to work out of our new Quonset, RI facility. Based on eligibility, relocation assistance may be available.
WHAT YOU'LL DO:

• Work within a team of multidisciplinary engineers and specialists on AUV assembly and integration efforts
• Build, integrate, and test complex electro-mechanical assemblies into our world class AUVs
• Routing and servicing high-reliability cabling and wiring harnesses
• Design, prototype, and scale manufacturing jigs and fixtures to improve build and test efficiency
• Fabricate and modify machined parts and COTS components
• Contribute to all stages of the vehicle product development and manufacturing life cycle and provide feedback to the engineering team
• Help develop, document, and improve our workflows
• Help organize and establish our on-site manufacturing workflow
• Potential of traveling offshore to support our operations team

REQUIRED QUALIFICATIONS:

• 3+ years of relevant experience in a mechanical field (automotive/marine, aerospace, industrial equipment)
• Familiar with simple fabrication processes, basic hand tools, and both plastic/metal part manufacturing
• A sincere commitment to a positive, inclusive, and collaborative culture
• A full understanding of the manufacturing life cycle
• Experience working off of technical documentation and engineering drawings
• Commitment to a high-quality product and strong sense of personal accountability
• Familiarity with building and maintaining electromechanical systems
• Extremely organized and detail-oriented
• Excellent verbal & written communication skills
• Has a never-ending sense of urgency and enthusiasm
• Eligible to obtain and maintain an active U.S. Secret security clearance

PREFERRED QUALIFICATIONS:

• Experience in sub-sea robotics (AUVs, UUVs, underwater equipment)
• Previous experience hoisting equipment or MA state hoisting license (overhead gantry, rigging)
• Experience working with electrical components up to 400VDc
• Proficiency with electrical debug including use of tools such as a digital multimeter
• Machining and/or 3D printing experience

US Hourly Range

$26.92-$40.38 USD

The salary range for this role is an estimate based on a wide range of compensation factors, inclusive of base salary only. Actual salary offer may vary based on (but not limited to) work experience, education and/or training, critical skills, and/or business considerations. Highly competitive equity grants are included in the majority of full time offers; and are considered part of Anduril's total compensation package. Additionally, Anduril offers top-tier benefits for full-time employees, including:

• Platinum Healthcare Benefits:For U.S. roles, we offer comprehensive medical, dental, and vision plans at little to no cost to you.
  • For UK roles, Private Medical Insurance (PMI): Anduril will cover the full cost of the insurance premium for an employee and dependents.
  • For AUS roles, Private health plan through Bupa: Coverage is fully subsidized by Anduril.
• Basic Life/AD&D and long-term disability insurance 100% covered by Anduril, plus the option to purchase additional life insurance for you and your dependents.
• Extremely generous company holiday calendar including a holiday hiatus in December, and highly competitive PTO plans.
• 16 weeks of paid Caregiver & Wellness Leave to care for a family member, bond with your baby, or tend to your own medical condition.
• Family Planning & Parenting Support: Fertility (eg, IVF, preservation), adoption, and gestational carrier coverage with additional benefits and resources to provide support from planning to parenting.
• Mental Health Resources: We provide free mental health resources 24/7 including therapy, life coaching, and more. Additional work-life services, such as free legal and financial support, available to you as well.
• A professional development stipend is available to all Andurilians.
• Daily Meals and Provisions: For many of our offices this means breakfast, lunch and fully stocked micro-kitchens.
• Company-funded commuter benefits available based on your region.
• Relocation assistance (depending on role eligibility).
• 401(k) retirement savings plan - both a traditional and Roth 401(k). (US roles only)

The recruiter assigned to this role can share more information about the specific compensation and benefit details associated with this role during the hiring process.

Anduril is an equal-opportunity employer committed to creating a diverse and inclusive workplace. The Anduril team is made up of incredibly talented and unique individuals, who together are disrupting industry norms by creating new paths towards the future of defense technology. All qualified applicants will be treated with respect and receive equal consideration for employment without regard to race, color, creed, religion, sex, gender identity, sexual orientation, national origin, disability, uniform service, Veteran status, age, or any other protected characteristic per federal, state, or local law, including those with a criminal history, in a manner consistent with the requirements of applicable state and local laws, including the CA Fair Chance Initiative for Hiring Ordinance. We actively encourage members of recognized minorities, women, Veterans, and those with disabilities to apply, and we work to create a welcoming and supportive environment for all applicants throughout the interview process. If you are someone passionate about working on problems that have a real-world impact, we'd love to hear from you!

To view Anduril's candidate data privacy policy, please visit

**Manufacturing Associate**
Manufacturing
West Greenwich, RI, US
Pay Rate Low: 21.00 | Pay Rate High: 25.00
+ Added - 21/07/2025
Apply for Job
Our client, a renowned leader in biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement.
We are excited to announce a fantastic opportunity to join their team as a Manufacturing Tech!
Let's connect and get started-apply today!
**Position: Manufacturing Tech**
**Location: West Greenwich, RI**
**Shifts:** Night Shift 6:45PM - 6:45AM
C and D Rotation - Swing Shift - Week 1 is 5 working days Week 2 is 2 working days.
**Position Overview:**
The Associate of Manufacturing will support commercial, clinical, and product launch activities in a regulated, high-performance production environment. This role involves hands-on manufacturing responsibilities, with a strong emphasis on safety, compliance, and teamwork.
**Responsibilities:**
+ Set up, clean, and sanitize manufacturing equipment
+ Accurately weigh and prepare buffers/media per manufacturing procedures
+ Operate within GMP-compliant guidelines and maintain strict adherence to safety
+ Conduct in-process sampling and operate basic analytical equipment
+ Perform parts washing and sterilization
+ Maintain a clean, organized workspace in a controlled cleanroom setting
+ Wear appropriate PPE, including full gowning, gloves, and steel-toe footwear
+ Participate in documentation updates and quality deviation reporting
+ Review and maintain accurate records (equipment logs, batch records)
+ Operate near high-pressure systems and use powered industrial vehicles safely
+ Support Lean Transformation and Operational Excellence initiatives
+ Promote a positive, inclusive, and collaborative team culture
+ Support Diversity, Inclusion & Belonging (DI&B) initiatives
**Minimum Qualifications:**
+ Associate Degree OR High School Diploma/GED and 1+ year of manufacturing or operations experience
+ Proven ability to follow Standard Operating Procedures (SOPs)
+ Experience in technical or production-based environments
+ Familiarity with advanced computer systems
+ Proficient in Microsoft Office Suite
+ Strong written communication skills
+ Collaborative, team-oriented mindset
+ Previous experience in lab or safety-focused environments
+ Understanding of chemical batch processing or similar technical processes
+ No prior biotech experience required-open to candidates from related industries
**Physical Requirements:**
+ Regularly lift up to **35 lbs** and push/pull up to **50 lbs of force**
+ Stand for long periods and perform physical tasks (bending, squatting, reaching, using ladders)
Want to take the next step in your career with a global biotech leader?
Let's connect today-this could be the opportunity you've been waiting for!
**_This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_**
INDBH
#LI-DNP
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

**Are you a Manufacturing Technician looking for an opportunity to build and improve groundbreaking technologies? We have just the opportunity for you! Under the direction of the Supervisor of Special Projects Assembly, you will assist in the designing, laying out and detailing new developments or modifications to company lines of safety relief valves and line valve products!**
**In this Role, Your Responsibilities Will Be:**
+ Inspect, assemble, and perform production and/or engineering steam, air or water tests on various types of valves, including prototypes for special customer applications and engineering proficiency.
+ Set up and perform engineering test on competitive valves and evaluate data. Perform product testing and test to ASME standards.
+ Advise and assist Manufacturing, Sales, Specifications and other departments concerning technical aspects of the product.
+ Recommend purchase of material or equipment for current projects.
+ As warranted, travel to nuclear facilities to perform field service work as needed.
**Who You Are:**
You identify and build the processes vital to get work done. You build and deliver solutions that meet customer expectations. You learn quickly when facing new situations.
**For This Role, You Will Need:**
+ Minimum of an Associates degree in Engineering, technical military experience, or equivalent work experience.
+ The ability to adapt communication style to suit different audiences and situations, ensuring clear and efficient exchange of information.
+ Highly engineered product experience.
+ Ability to work on call, or travel to service client's needs.
**Preferred Qualifications that Set You Apart:**
+ Experience with safety relief valves and/or line valve products.
+ Advance knowledge in Electrical Engineering.
+ An understanding of the importance of maintaining a safe work environment for oneself and colleagues.
+ Proven track record of working optimally both as part of a team and independently, adapting to the needs of the situation.
**Our Culture & Commitment to You:**
At Emerson, we prioritize a workplace where every employee is valued, respected, and empowered to grow. We foster an environment that encourages innovation, collaboration, and diverse perspectives-because we know that great ideas come from great teams. Our commitment to ongoing career development and growing an inclusive culture ensures you have the support to thrive. Whether through mentorship, training, or leadership opportunities, we invest in your success so you can make a lasting impact. We believe diverse teams, working together are key to driving growth and delivering business results.
We recognize the importance of employee wellbeing. We prioritize providing flexible, competitive benefits plans to meet you and your family's physical, mental, financial, and social needs. We provide a variety of medical insurance plans, with dental and vision coverage, Employee Assistance Program, 401(k), tuition reimbursement, employee resource groups, recognition, and much more. Our culture offers flexible time off plans, including paid parental leave (maternal and paternal), vacation and holiday leave. Learn more about our Culture & Values ( .
**Our Location:**
Mansfield, Massachusetts, offers the charm of a suburban community with the convenience of a prime location in southeastern Massachusetts. Known for its excellent schools and family-friendly atmosphere, Mansfield provides easy access to both Boston and Providence via major highways and a commuter rail station. Residents enjoy a variety of recreational opportunities, including local parks, sports fields, and trails, as well as vibrant community events and concerts at the Xfinity Center, a popular outdoor entertainment venue, as well as proximity to Patriot Place! With its strong sense of community and convenient amenities, Mansfield is an ideal place to call home!
**WHY EMERSON**
**Our Commitment to Our People**
At Emerson, we are motivated by a spirit of collaboration that helps our diverse, multicultural teams across the world drive innovation that makes the world healthier, safer, smarter, and more sustainable. And we want you to join us in our bold aspiration.
We have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world's most complex problems - for our customers, our communities, and the planet. You'll contribute to this vital work while further developing your skills through our award-winning employee development programs. We are a proud corporate citizen in every city where we operate and are committed to our people, our communities, and the world at large. We take this responsibility seriously and strive to make a positive impact through every endeavor.
At Emerson, you'll see firsthand that our people are at the center of everything we do. So, let's go. Let's think differently. Learn, collaborate, and grow. Seek opportunity. Push boundaries. Be empowered to make things better. Speed up to break through. Let's go, together.
**Work Authorization**
Emerson will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas such as E, F-1(including those with OPT or CPT) , H-1, H-2, L-1, B, J or TN, or who need sponsorship for work authorization now or in the future, are not eligible for hire.
**Equal Opportunity Employer**
Emerson is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.
**Accessibility Assistance or Accommodation**
If you have a disability and are having difficulty accessing or using this website to apply for a position, please contact: .
**ABOUT EMERSON**
Emerson is a global leader in automation technology and software. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability.
With global operations and a comprehensive portfolio of software and technology, we are helping companies implement digital transformation to measurably improve their operations, conserve valuable resources and enhance their safety.
We offer equitable opportunities, celebrate diversity, and embrace challenges with confidence that, together, we can make an impact across a broad spectrum of countries and industries. Whether you're an established professional looking for a career change, an undergraduate student exploring possibilities, or a recent graduate with an advanced degree, you'll find your chance to make a difference with Emerson. Join our team - let's go!
**No calls or agencies please.**
**Requisition ID** : 25022432
Emerson is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.

**Job Title: Manufacturing Inspector**
**Company:** Leader in the Electro-Mechanics industry
**Location:** Attleboro, MA (with additional locations in North Attleboro and upcoming in Plainville)
**Pay Rate:** $16.00/hour
**Schedule:** Monday-Friday, 7:00 AM-3:30 PM or 6:30 AM-2:30 PM
**Employment Type:** Full-Time
**Interview Type:** In-person with Production Manager
**About the Role**
We're hiring **11 General Manufacturing Operators** for our growing team! We are seeking individuals who are **mechanically inclined** and eager to learn-we will provide full training. This is an excellent opportunity to start a career in precision manufacturing with a stable and supportive company.
You'll begin in our **Inspection Department** , working with microscopes to visually inspect components. Over time, you'll be trained in various production areas such as laser trimming, solder dipping, and electrical testing.
**Key Responsibilities**
+ Handle small parts and wafers using tweezers
+ Visually inspect chip resistors and wafers using high-power microscopes
+ Follow detailed manufacturing procedures and documentation
+ Report any defective materials or questionable conditions to supervisors
+ Maintain a clean and organized work environment
+ Wear lab coats and follow safety protocols, including chemical handling when necessary
**Requirements**
**Must-Have:**
+ High school diploma or GED
+ Basic computer skills
+ Ability to read and write in English
+ Comfortable working with small parts and tools
+ Mechanically inclined (training will be provided)
**Nice-to-Have (Not Required):**
+ Prior cleanroom or ISO 9000 manufacturing experience
+ Visual inspection experience
+ Experience handling chemicals or working with microscopes
**Additional Details**
+ This role requires wearing lab coats and handling small precision components.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

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. 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 - Nights

What you will do

Let's do this. Let's change the world. In this vital role you will join a team of impactful manufacturing associates that leverage adaptability, agility, teamwork, and curiosity. The Manufacturing Associate I at Amgen supports the production process by operating equipment, maintaining production records, and adhering to safety and quality standards. They contribute to the overall efficiency of the manufacturing process.

The Associate Manufacturing is a hands-on role in one of the two manufacturing facilities on site at Amgen Rhode Island. Successful candidates will join either the AR5 team, focused on ongoing, high-volume production, or the AR30 team, focused on operational readiness and start-up. Qualifications for this role are the same in both facilities. There are multiple openings for this position.

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 with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay.

Responsibilities Include:

* Under general supervision, Associate will perform operations in the manufacturing area.


* Operations will be performed according to Standard Operating Procedures (SOP's)


* Associate will perform and monitor critical processes, complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures, SOP's and technical reports.


* Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions.


* May participate on cross-functional teams and represent the manufacturing teams.


* Associate may also have the responsibility of owning deviations/CAPA's.


* In addition, Associate may identify, recommend and implement improvements related to routine functions.



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:

* Bachelor's degree in Science, Engineering, or a related technical field


* Internship or academic project experience in Manufacturing, Biotech, Medical Devices, or related industries


* Mechanical competence with a willingness to learn equipment operation and troubleshooting


* Familiarity with computerized systems or automation tools (experience with HMIs is a plus)


* Basic understanding of GMP (Good Manufacturing Practices) and regulatory guidelines


* Foundational knowledge of biotechnology processes like cell culture, purification, or aseptic techniques


* Ability to follow written procedures and safety protocols


* Strong interest in learning about manufacturing systems, lab equipment, and quality standards


* Basic data analysis or statistical skills; comfortable working with Excel and other MS Office tools


* Organized, detail-oriented, and able to manage multiple tasks with guidance


* Clear communication skills, both written and verbal


* Positive attitude, eager to contribute, and a team player


* Demonstrated ability to adapt in dynamic environments and take initiative in problem-solving



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, including remote and hybrid work arrangements, where possible



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.

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

73,359.00 USD - 85,625.00 USD

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. 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 - Nights**

**What you will do**

Let's do this. Let's change the world. In this vital role you will join a team of impactful manufacturing associates that leverage adaptability, agility, teamwork, and curiosity. The Manufacturing Associate I at Amgen supports the production process by operating equipment, maintaining production records, and adhering to safety and quality standards. They contribute to the overall efficiency of the manufacturing process.

The Associate Manufacturing is a hands-on role in one of the two manufacturing facilities on site at Amgen Rhode Island. Successful candidates will join either the AR5 team, focused on ongoing, high-volume production, or the AR30 team, focused on operational readiness and start-up. Qualifications for this role are the same in both facilities. There are multiple openings for this position.

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 with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay.

**Responsibilities Include:**

+ Under general supervision, Associate will perform operations in the manufacturing area.

+ Operations will be performed according to Standard Operating Procedures (SOP's)

+ Associate will perform and monitor critical processes, complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures, SOP's and technical reports.

+ Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions.

+ May participate on cross-functional teams and represent the manufacturing teams.

+ Associate may also have the responsibility of owning deviations/CAPA's.

+ In addition, Associate may identify, recommend and implement improvements related to routine functions.

**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:**

+ Bachelor's degree in Science, Engineering, or a related technical field

+ Internship or academic project experience in Manufacturing, Biotech, Medical Devices, or related industries

+ Mechanical competence with a willingness to learn equipment operation and troubleshooting

+ Familiarity with computerized systems or automation tools (experience with HMIs is a plus)

+ Basic understanding of GMP (Good Manufacturing Practices) and regulatory guidelines

+ Foundational knowledge of biotechnology processes like cell culture, purification, or aseptic techniques

+ Ability to follow written procedures and safety protocols

+ Strong interest in learning about manufacturing systems, lab equipment, and quality standards

+ Basic data analysis or statistical skills; comfortable working with Excel and other MS Office tools

+ Organized, detail-oriented, and able to manage multiple tasks with guidance

+ Clear communication skills, both written and verbal

+ Positive attitude, eager to contribute, and a team player

+ Demonstrated ability to adapt in dynamic environments and take initiative in problem-solving

**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, including remote and hybrid work arrangements, where possible

**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.

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.

Job Details

Join Amgens Mission of Serving Patients

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. As a member of the Amgen team, youll 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, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Associate Manufacturing - Nights

What you will do

Lets do this. Lets change the world. In this vital role you will join a team of impactful manufacturing associates that leverage adaptability, agility, teamwork, and curiosity. The Manufacturing Associate I at Amgen supports the production process by operating equipment, maintaining production records, and adhering to safety and quality standards. They contribute to the overall efficiency of the manufacturing process.

The Associate Manufacturing is a hands-on role in one of the two manufacturing facilities on site at Amgen Rhode Island. Successful candidates will join either the AR5 team, focused on ongoing, high-volume production, or the AR30 team, focused on operational readiness and start-up. Qualifications for this role are the same in both facilities. There are multiple openings for this position.

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 with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay.

Responsibilities Include:

• Under general supervision, Associate will perform operations in the manufacturing area.
• Operations will be performed according to Standard Operating Procedures (SOP's)
• Associate will perform and monitor critical processes, complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures, SOP's and technical reports.
• Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions.
• May participate on cross-functional teams and represent the manufacturing teams.
• Associate may also have the responsibility of owning deviations/CAPA's.
• In addition, Associate may identify, recommend and implement improvements related to routine functions.

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
• Associates + 6 months of manufacturing or operations work experience OR
• Bachelors Degree in a related field

Preferred Qualifications:

• Bachelors degree in Science, Engineering, or a related technical field
• Internship or academic project experience in Manufacturing, Biotech, Medical Devices, or related industries
• Mechanical competence with a willingness to learn equipment operation and troubleshooting
• Familiarity with computerized systems or automation tools (experience with HMIs is a plus)
• Basic understanding of GMP (Good Manufacturing Practices) and regulatory guidelines
• Foundational knowledge of biotechnology processes like cell culture, purification, or aseptic techniques
• Ability to follow written procedures and safety protocols
• Strong interest in learning about manufacturing systems, lab equipment, and quality standards
• Basic data analysis or statistical skills; comfortable working with Excel and other MS Office tools
• Organized, detail-oriented, and able to manage multiple tasks with guidance
• Clear communication skills, both written and verbal
• Positive attitude, eager to contribute, and a team player
• Demonstrated ability to adapt in dynamic environments and take initiative in problem-solving

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, well 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

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.

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.

Manufacturing Program Manager

Summary: Manufacturing is a pillar within Meta's Delivery Team supporting data center construction. We exist to support the predictable delivery of capacity at scale through manufactured solutions. The Manufacturing Team's primary focus is supply chain engagement and optimization. We accept Manufacturing Informed Designed (MID) components and orchestrate their detailing and prototyping to optimum manufacturability then work with our partners in Delivery to plan logistics and integration to avoid challenges in construction. This team is comprised of strategic designers, strategic builders, tactical specialists, plus internal and external subject matter experts (SME) including preconstruction managers, contractors, schedulers, equipment reliability engineers, and sourcing specialists. This position will lead program management of all manufactured components in support of Meta's RPL project. This mega-project is of such scale that it requires a high-performing PM to drive strategic and tactical aspects of first-of-kind prototyping, logistics, and integration. Never before have we relied so heavily on offsite construction; a necessity here to deliver a project of this magnitude on an aggressive timeline. The successful candidate will be instrumental in ensuring the timely delivery of this capacity on what will be the largest project in Meta's history and one of a few of the largest data centers in the world.

Required Skills:

• Program Management Lead coordination, document, and anticipate program needs to ensure cost, schedule, and quality in concert with the mega-project construction
• Primary Interface with the Manufacturing CAPs (Component Accountable PMs) to coordinate on Supplier production (manufacturing execution) including configuring supply chain, production, scheduling, strategic inventory, logistics, and integration in collaboration with our delivery and quality teams
• Interface with mega-project MOFE (Manufactured Owner Furnished Equipment) Onsite Logistics PM for logistical planning
• Interface with mega-project MOFE Onsite Integration / Testing PM for planning and coordination
• Manage GC (General Contractor) MOFE Coordinators for logistics, planning, coordination, reporting, lessons learned, etc.
• Risk Matrix development, maintenance, and related reporting
• Cost & Change Coordination with mega-project Meta designees including CM/PCA, ISCE, & MOFE CAPs
• Schedule Development with Engineering/Scheduling, GCs, CAPs, & Suppliers
• Regular Debriefs / Lessons Learned development, summary and communication to Engineering, Leadership, & XFNs (cross-functional partners)
• Partner with cross functional teams on related efforts to ensure alignment and transparency across Design, Engineering, & Construction (DEC)
• Partner closely with Sourcing Team for strategy and deployment of owner furnished equipment
• Partner with Global QA/QC Team to identify and strategically shift to the vendors and manufacturers, appropriate elements of the multi-trade integration and commissioning efforts to reduce onsite efforts. Your objective is to embed as much trade work and commissioning as is appropriate at the optimum points of fabrication from start through to the final point of integration
• Support team learning by bringing lessons learned, vendors, new technology, and other topics to the group for exploration
• Travel approximately 40% Domestic Travel to construction and fabrication sites required (including minimal international travel as required)

Minimum Qualifications:

• Bachelor's degree or equivalent work experience in program management
• 10+ years' experience in construction, manufacturing, and/or project planning
• Experience in large scale construction management and/or scalable manufacturing
• Manufacturing-for-construction background with understanding of lean manufacturing and supply-chain management plus knowledge of production machinery, processes, and standards in the field or industry experience with developing workflows and their associated flowcharts, schedules, and action plans
• Experience building consensus and communicate effectively with a wide range of audiences (stakeholders to executive leadership)
• Proven track record of adaptability and problem-solving in a dynamic work environment
• Proficient working knowledge of Google Workspace and Bluebeam

Preferred Qualifications:

• Experience with off-site fabrication, pre-assembly and/or modularization of complex elements for construction (or off-shore) projects
• Mission Critical, infrastructure, and/or data center construction experience
• Experience working with blended architecture, engineering, manufacturing/assembly and construction teams
• Software experience with eBuilder, Procore, Solidworks, Autodesk modeling software, Primavera P6, and/or BIM 360
• Experience with LEAN tools (such as Choosing by Advantage, Last Planner/Pull Planning, Gemba, Kanban)
• Experience working with Statistical Process Control (SPC), Just In Time (JIT) strategizing, and manufacturing data analytics
• PMP Certification

Public Compensation: $144,000/year to $201,000/year + bonus + equity + benefits

Industry: Internet

Equal Opportunity: Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at