Specialist Manufacturing I

Amgen•West Greenwich, RI
•$113,173 - $145,503

About The Position

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.

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.
  • 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
  • Project management skills including collaborating with cross-functional teams to validate the manufacturing line layout according to equipment and process requirements

Responsibilities

  • 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
  • Anticipate risk and builds contingencies to help mitigate impact

Benefits

  • stock
  • retirement
  • medical
  • life and disability insurance
  • eligibility for an annual bonus or for sales roles, other incentive compensation
  • health and welfare plans for staff and eligible dependents
  • financial plans with opportunities to save towards retirement or other goals
  • work/life balance
  • career development opportunities
  • Retirement and Savings Plan with generous company contributions
  • group medical, dental and vision coverage
  • 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
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