28 Manufacturing jobs in Jewett City

Description
The Associate of Manufacturing will work in a dynamic production environment at the plant supporting commercial clinical and launch activities. Under general supervision employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures SOPs.
Responsibilities include:
-Hands-on operations: set-up cleaning and sanitization of various manufacturing equipment
-Weighing out buffers/media per defined manufacturing procedures MPs and standard operating procedures SOPs
-Following GMP documents SOPs MPs with strict adherence to safety and compliance
-Performing and monitoring critical processes with the ability to perform basic troubleshooting
-Performing in-process sampling of equipment and operating analytical equipment
-Performing parts washing and sterilization activities
-Maintaining an organized and clean workspace
-Working in a clean room environment wearing steel toe shoes full clean room gowning hairnet and gloves when performing all work
-Initiating and being involved quality deviation reports as required
-Drafting and revising documents SOPs MPs
-Identifying recommending and implementing improvements related to routine functions
-Assisting in the review of documentation for assigned functions equipment logs batch records
-Working around high-pressure systems occasionally work around/moving heavy equipment with powered industrial vehicles
-Available to work various shifts day/nights as dictated by the production schedule Able to work in teams to complete operational tasks
-Ability to take direction well follow documents and policies at all times Ability to take initiative
-Champion Lean Transformation and OE initiatives facilitate the drive towards continuous improvement in all Manufacturing areas.
-Develop relationships and connections within the Manufacturing department and with key site stakeholders
-Support DIB initiatives to increase inclusion connectivity and engagement within the team
-Create a positive work environment through interactions with team members Able to regularly lift up to 35lbs push and pull objects that require up to 50lbs of force and work on your feet for long durations Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending reaching above the head climbing kneeling squatting stooping walking upstairs and standing on portable stairs or ladders up to 6 feet off of the ground
Pay and Benefits
The pay range for this position is $25.00 - $33.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in West Greenwich,RI.
Application Deadline
This position is anticipated to close on Aug 18, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

**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.

**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.
**Specialist Manufacturing**
**What you will do**
Let's do this. Let's change the world. ARI has three openings for a manufacturing Specialist. In this vital role you will be part of the Manufacturing Product Lifecycle management team. You will report to the manager responsible for New Product Introductions/Product Reintroductions and various Manufacturing support activities necessary for the success of the site production deliverables.
Specific strategic product and process implementations will be led from this position. Examples include cross functional initiatives at site and network, support of product teams for NPIs. Support may include evaluation of processes and capabilities for yield improvement, implementation of new equipment, technology changes aligned with Long Range Plan and support of alternate sourcing activities from a technical perspective to enable supply chain agility.
Key Responsibilities Include:
+ Lead and support planning and execution of key initiatives with cross functional teams at the production floor
+ Liaison at the floor and with cross function teams to assure program (NPI/PRI) preparation, implementation, sustainment and capture and share lessons learned.
+ Provide and analyzes data to support management evaluation of process performance trends
+ Provide subject matter expertise for area of responsibility
+ Own quality records (change control, CAPA, deviations) and deliver to timelines
+ Support AR5/AR30 manufacturing organizations in the prioritization and execution of these activities to maximize plant performance and plant capacity.
+ Collaborate with Quality, Process Engineering, Regulatory, and Process Development to implement process improvements
+ Support of front-line managers through on the floor presence
+ Own and author critical standard operating procedures and supporting documentation/training.
+ Anticipate risk and builds contingencies to help mitigate impact
**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 an expert problem solver with these qualifications.
**Basic Qualifications:**
+ High school diploma / GED and 10 years of Manufacturing or Operations experience OR
+ Associate's degree and 8 years of Manufacturing or Operations experience OR
+ Bachelor's degree and 4 years of Manufacturing or Operations experience OR
+ Master's degree and 2 years of Manufacturing or Operations experience OR
+ Doctorate degree
**Preferred Qualifications:**
+ Hands on experience facilitating problem solving and root cause investigations in a biotechnology environment
+ Strong project management skills with ability to multi-task and function in a dynamic environment
+ Excellent communication skills, drive, and sense of urgency
+ Demonstrated ability to forge and maintain strong relationships within other functional areas
+ Previous experience in manufacturing, quality systems, implementation of new equipment and processes (Harvest, Chromatography, Supply Chain).
+ Ability to recommend, judge, and make good decisions in complex situations
+ Ability to tactfully and effectively negotiate and influence
**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.

Great opportunity for a recent graduate with a engineering or life sciences degree to join a world class leader in the biotechnology industry.

Overview:

• Supports various biomanufacturing areas within a cGMP environment
• Routine tasks include equipment preparation such as Clean-In-Place and Steam-In-Place, compounding media and buffer solutions, aseptic operations, and in-process sampling using laboratory analyzers.
• Utilizes scientific principles in execution of experiments and analysis of experimental data.
• Carries out laboratory tasks per plan and procedure in a team environment.
• Complete cross training in both upstream and downstream operations

Qualifications:

• B.S. in Biology, Engineering or Life Science
• Interest in Biotech Manufacturing

Pay: $23-24/hr

#INDBH

Job Title: Manufacturing Process Technician (JP12208)
Location: West Greenwich , RI 02817
Business Unit: Cell Culture
Employment Type: Contract
Duration: Initial 4 month with possible extensions.
Rate : $20 - $25/hour W2
Posting Date: 01/29/2024
Notes : Day Shift

3 Key Consulting is recruiting an Manufacturing Process Technician for a consulting engagement with our direct client, a leading global biotechnology company.

Job Description:
Routinely perform moderately-complex to complex processes according to Standard Operating Procedure (SOP). Specific responsibilities include bioreactor sampling activities, cleaning equipment, steaming equipment, and prepping equipment. Skills: Biotech US/DS manufacturing experience, preferably cell culture; understanding of measurements, calculations and the metric system ; basic GMP knowledge. Understanding of Electric Batch Records, DeltaV, and LIMS .

Basic Qualifications:
Associate degree OR High school diploma / GED and 1 year of Manufacturing or Operations experience

Top Must Have Skill Sets:

1. Safety first mindset.
2. GMP experience
3. Biotech experience / cell culture experience specifically will highly stand out

Day to Day Responsibilities:
sampling, cleaning, steaming, and prepping bioreactors. Additionally, strict adherence to SOPs and GMP regulations.
Employee Value Proposition:
Unique industry experience and career opportunity

Why is the Position Open?
Supplement additional workload on team

Interview Process:
One with the hiring manager and another with team members.

We invite qualified candidates to send your resume to . If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.

Regards,

3KC Talent Acquisition Team

**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.
**Manufacturing Associate - Days**
**What you will do**
Let's do this. Let's change the world. In this vital role you will perform operations within the Manufacturing area, specifically cell culture, at Amgen's innovative Rhode Island facility. You will be required to know, comprehend, and apply Good Manufacturing Practices (GMP), as well as understand, follow, and document in batch records.
Additional Responsibilities:
+ Follow and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
+ Conduct basic troubleshooting and assist in the review of documentation for assigned functions.
+ May also have the responsibility of initiating and owning area Deviations, revising SOP's and performing LEAN functions.
+ Identify, recommend, and implement improvements related to routine functions.
This role is expected to work a 12-hour shift on a rotating schedule. The shift pattern will be 7AM-7PM, with a two-week rotation covering 7 days per rotation (B Shift). 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. The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).
**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 an excellent 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
**Preferred Qualifications:**
+ Bachelor's degree in Science or Engineering
+ Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc.
+ Knowledge of Single-use-Systems
+ CFR and Regulatory knowledge
+ Mechanical ability/expertise
+ Basic statistical mathematical skills
+ Ability to interpret and apply GMP knowledge
+ Understanding of analytical methods for manufacturing area
+ Demonstrated technical writing capability
+ Able to demonstrate project management skills and presentation skills
+ Ability to understand, apply and evaluate basic chemistry, biology and physical principles
+ Basic troubleshooting skills on production equipment
+ Experience with Delta V
+ Experience with lab equipment/testing
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
+ A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
+ A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
+ Stock-based long-term incentives
+ Award-winning time-off plans
+ Flexible work models, 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 Process Technician**
Manufacturing
West Greenwich, RI, US
Pay Rate Low: 23 | Pay Rate High: 24
+ Added - 07/01/2025
Apply for Job
Great opportunity for a recent graduate with a engineering or life sciences degree to join a world class leader in the biotechnology industry.
**Overview:**
+ Supports various biomanufacturing areas within a cGMP environment
+ Routine tasks include equipment preparation such as Clean-In-Place and Steam-In-Place, compounding media and buffer solutions, aseptic operations, and in-process sampling using laboratory analyzers.
+ Utilizes scientific principles in execution of experiments and analysis of experimental data.
+ Carries out laboratory tasks per plan and procedure in a team environment.
+ Complete cross training in both upstream and downstream operations
**Qualifications:**
+ B.S. in Biology, Engineering or Life Science
+ Interest in Biotech Manufacturing
Pay: $23-24/hr
#INDBH
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.

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.

**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 perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs), these can include Media/Buffer Preparations along with Weigh & Dispense operations.
In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (C Shift). This includes extra benefits such as **receiving an added 15% shift differential, and also getting premium pay for any Sundays worked.** The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).
Responsibilities include:
+ Associate will perform and monitor critical processes, execute routine validation protocols, and
+ Regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
+ Perform basic troubleshooting and assist in the review of documentation for assigned functions.
+ Participate on cross-functional teams and represent the manufacturing teams.
+ May also have the responsibility of owning deviations/CAPAs.
**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/GED + 2 years of manufacturing or operations work experience OR
+ Associate's + 6 months of manufacturing or operations work experience OR
+ Bachelor's degree
**Preferred Qualifications:**
+ Bachelor's degree in Science or Engineering
+ Large Scale Media/Buffer Preparations Experience
+ Weigh & Dispense operations experience
+ Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc
+ Knowledge of Single-use-Systems
+ CFR and Regulatory knowledge
+ Mechanical ability/expertise
+ Basic statistical mathematical skills
+ Ability to interpret and apply GMP knowledge
+ Understanding of analytical methods for manufacturing area
+ Demonstrated technical writing capability
+ Able to demonstrate project management skills and presentation skills
+ Ability to understand, apply and evaluate basic chemistry, biology and physical principles
+ Basic troubleshooting skills on production equipment
+ Experience with Delta V
+ Experience with lab equipment/testing
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
+ A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
+ A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
+ Stock-based long-term incentives
+ Award-winning time-off plans
+ Flexible work models, 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.