Specialist Manufacturing I

Amgen Inc.; West Greenwich (RI); Presencial; USD 113 000 - 146 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Stock-based incentives

Retirement plan

Comprehensive medical coverage

Disability insurance

Annual bonus eligibility

Flexible work model

Resumo da oferta

Amgen Inc. is seeking a Specialist Manufacturing I in Rhode Island to lead and support key manufacturing initiatives on the production floor, liaise with cross-functional teams, and ensure on-time delivery.

The role emphasizes data-driven process improvements and regulatory adherence. You will own quality records, support AR5 and AR30 ops, and collaborate with Quality, Process Engineering, Regulatory, and Process Development to optimize plant performance and capacity.

Qualificações

• Master’s degree in Regulatory Affairs and Quality Assurance, Bioengineering, Chemical Engineering, or related field.

Responsabilidades

• Lead and support planning and execution of key initiatives with cross-functional teams on the production floor.

Conhecimentos

Lean manufacturing

Six Sigma

GMP

Data analysis

Project management

Cross-functional collaboration

Formação académica

Master's degree in Regulatory Affairs and Quality Assurance, Bioengineering, Chemical Engineering or related field

Ferramentas

SAP

MES (PAS-X)

PI System

TrackWise

Veeva

Descrição da oferta de emprego

Career Category

Manufacturing

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.

Specialist Manufacturing I

Duties: 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 including change control, CAPA, deviations, and deliver to timelines; Support AR5 and 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 and training; and Anticipate risk and builds contingencies to help mitigate impact.

Requirements: Master’s degree (or foreign equivalent) in Regulatory Affairs and Quality Assurance, Bioengineering, Chemical Engineering or related field & 2 years of experience in the job offered or a manufacturing-related occupation. The position requires 2 years of experience the following:

Implementing Lean manufacturing to optimize inventory, reduce waste and drive continuous improvement methodologies; Applying six sigma principles to lower defect rates for process or raw materials; Continuous Improvement and Operation Excellence Tools including: 5S, Fish Bone, Poke Yoke, and Build Standard work; Good Manufacturing Practice (GMP) production operations; Project management methodology and tools including: Spotfire (Data analytics), MES (PAS-X), PI System (data historian), TrackWise, Veeva, and SAP (ERP); Safety programs including Job Safety Risk Assessment, Ergonomic Job Measurement System, and identification of risks; Data analysis and control charting; and Project management skills including collaborating with cross-functional teams to validate the manufacturing line layout according to equipment and process requirements.

Job type: Full-Time position. The annual salary range for this position in the U.S. is $113,173.00 - $145,503.00 per year. Also, this position offers stock, retirement, medical, life and disability insurance and eligibility for an annual bonus or for sales roles, other incentive compensation. For more details visit https://careers.amgen.com/life-at-amgen/benefits/.

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.

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.

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.

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.

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.

careers.amgen.com