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 lie within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Be part of Amgen’s newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen’s plan to be a carbon-neutral company by 2027.
**Specialist Manufacturing** **New Product Introduction (NPI)**
**Live**
**What you will do**
Let’s do this. Let’s change the world. In this vital role you will communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance Manufacturing plant and Process Development scientific groups. As part of ANC’s Manufacturing Support team, this position is responsible for ensuring new products are successfully introduced into ANC’s biologics manufacturing facility. It is a highly visible role across the site with the core responsibility of hosting cross-functional meetings to drive to timelines to support the tech transfer of the program into the facility. This role will also offer the opportunity to propose, participate, and lead team improvement initiatives to drive improved productivity and scheduling accuracy.
+ New Product Introduction lead coordinating withManufacturing, Process Development,Supply Chain, Planning, Facilities and Engineering,as well asQuality to introduce new Drug Substance products and/or advanced technologies into the plantusingproject management tools(i.e.Smartsheet).
+ Technical expert who leads orparticipatesin projects, ensuring that production documents areaccurateand up to date.
+ Support Manufacturing in troubleshooting, problemsolvingand RCAs. Support CAPA development to prevent error recurrence.
+ Owns New Product Introduction Change Controlsand collaborateswithstakeholders to drive on-time completion. Respondsto regulatory questions and/or audit findings.
+ Champions Lean Transformation and OEinitiatives,facilitatesthe drive towards continuous improvement in the plant and tracks progress on a plant level.
**Win**
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The manufacturing professional we seek has a biologics DS manufacturing background with strong cross-functional project management and communication skills as well as the below qualifications.
**Basic Qualifications:**
+ High school diploma / GED & 10 years of biotechnology operations experience OR
+ Associate’s degree & 8 years of biotechnology operations experience OR
+ Bachelor’s degree and 4 years of biotechnology operations experience OR
+ Master’s degree in chemistry, biology, or engineering & 2 years of biotechnology operations experience OR
+ Doctorate degree
**Preferred Qualifications:**
+ Degree in Chemical Engineering, Industrial Engineering, Biology, or Biochemistry
+ Excellentcross-functionalproject management, meeting facilitation, andtechnical writing skills
+ Experience in GMPmanufacturingoperations
+ Strong technical knowledge of drug substance processing (chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing (cell culture, harvest)
+ Ability to organize,analyzeand interpret technical data through trend analysis, forecasting, modeling, etc.
+ Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writingforms
+ Ability to coach,mentorand/or cross train colleagues within core technical areas
+ Background in lean manufacturing methodologies and operational excellence
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
The annual base salary range for this opportunity in the U.S. is provided below.
In addition to the base salary, Amgen offers a Total Rewards Plan comprising 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 including:
+ 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 forfield sales representatives, a sales-based incentive plan.
+ Stock-based long-term incentives.
+ Award-winning time-off plans and bi-annual company-wide shutdowns.
+ Flexible work models, including remote work arrangements, where possible.
**Apply** **now** **for a career that defies imagination**
Objects in your future are closer than they appear. Join us.
**careers.amgen.com**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
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.
**#AmgenNorthCarolina**
