Associate Manufacturing- Manufacturing Services (Nights)

Amgen SA

West Greenwich (RI)

On-site

USD 70,000 - 90,000

Full time

4 days ago
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Benefits offered by this job

Total Rewards Plan
Retirement & Savings Plan
Stock-based long-term incentives
Flexible work models
Award-winning time-off plans

Job summary

Amgen seeks a dedicated Associate Manufacturing professional to operate on the Night shift within Manufacturing Services. You will lead critical processes, validate procedures, and ensure SOP adherence while drafting and updating technical documents.

The role requires GMP knowledge, troubleshooting skills, and experience with process equipment; a strong quality mindset and teamwork are essential. 12-hour shifts on a rotating schedule with added shift differential.

Qualifications

  • High school/GED + 2 years of manufacturing or operations work experience
  • Associate’s + 6 months of manufacturing or operations work experience
  • Bachelor’s degree

Responsibilities

  • Perform and monitor critical processes, complete routine validation protocols, and review documents such as Manufacturing Procedures and SOPs.
  • Perform basic troubleshooting and assist in the review of documentation for assigned functions.
  • May own area Deviations, revise SOPs and perform LEAN functions.

Skills

LEAN principles
GMP knowledge
Technical writing
Troubleshooting
Power Industrial Vehicles

Education

High school diploma or GED
Associate’s degree + 6 months exp.
Bachelor’s degree

Tools

Washers and Autoclaves
Process equipment
LIMS and access
MES and SAP
DeltaV, RDS, PI system

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.

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 Manufacturing Services on Night shift. Associate Manufacturing will provide technical leadership to the team under the direction of the Manufacturing Services manager. 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. All operations will be performed according to Standard Operating Procedures (SOPs). Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent Manufacturing Services group. Associate may also have the responsibility of owning minor deviations. In addition, Associate may identify, recommend and implement improvements related to routine functions.

Responsibilities Include:

  • Perform and monitor critical processes, complete routine validation protocols, and review documents such as Manufacturing Procedures and SOPs.

  • Perform 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.

In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (C or D Shift). This includes extra benefits such asreceiving 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).

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

Preferred Qualifications:
  • Knowledge of Washers and Autoclaves

  • Prior experience with process equipment, computers, and intermediate mathematical skills

  • Prior experience working in a clean room setting.

  • Knowledge of LIMS and access

  • CFR and Regulatory knowledge

  • Mechanical ability/expertise

  • Experience and Knowledge of Weigh Dispensing

  • Strong understanding of BDS equipment and CIP and SIP processes

  • Basic statistical mathematical skills

  • Ability to interpret and apply GMP knowledge

  • Ability to follow Standard Operating Procedures

  • Understanding of analytical methods for the manufacturing area

  • Ability to demonstrate technical writing capability with TrackWise access

  • Knowledge of MES and SAP systems

  • Independently collaborate with outside resources

  • Ability to understand, apply and evaluate basic chemistry, biology and physical principles

  • Strong troubleshooting skills on Manufacturing Services equipment

  • Ability to use Power Industrial Vehicles

  • Experience with Delta V, RDs, and the PI system

  • Demonstrate ability to lead teams

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

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.

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.

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