drjobs Sr Associate Scheduler

Sr Associate Scheduler

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1 Vacancy
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Job Location drjobs

Thousand Oaks, CA - USA

Monthly Salary drjobs

$ 106188 - 106188

Vacancy

1 Vacancy

Job Description

Career Category

Manufacturing

Job Description

Join Amgens Mission of Serving Patients

At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980 weve helped pioneer the world of biotech in our fight against the worlds 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 youll 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 awardwinning culture is collaborative innovative and science based. If you have a passion for challenges and the opportunities that lay within them youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Sr. Associate Scheduler

What you will do

Lets do this. Lets change the world. In this vital role you will responsible for managing the daytoday production schedule for Drug Substance Manufacturing. This is a highly visible role across the site with the core responsibility of supporting manufacturing and EF&R by delivering a detailed schedule of manufacturing maintenance and client activities. This role will also offer the opportunity to propose participate and lead team improvement initiatives to drive improved efficiency and scheduling accuracy. Additionally this role is a key communication and technical interface between the GMP manufacturing teams in the plant and our partner organizations within the global network. This Sr. Associate Scheduling position is within Amgen Thousand Oaks Drug Substance Supply (Manufacturing) organization.

Responsibilities:

  • Build and maintain the Downstream production schedule for Clinical and Commercial manufacturing in a multisuite facility.
  • Lead meetings as needed and update and communicate the schedule to clients.
  • Forecast potential issues and help drive solutions.
  • Schedule EF&R activities validation and project support.
  • Work with the various teams (EBR PTS PD CPE Supply Chain and Purification) on New Product Introduction and Resupply.
  • Requires scientific and technical understanding.
  • Champions Lean Transformation and OE initiatives facilitates the drive towards continuous improvement in the plant and tracks progress on a plant level.
  • May support Manufacturing in troubleshooting Deviation events conducting problem solving and RCAs owning records and works with Quality EF&R EH&S PD CPE etc to develop and own CAPAs to prevent recurrence.
  • May collaborate with Regulatory and Quality partners to manage change control records and respond to regulatory questions and/or audit findings.
  • Technical specialist who leads or participates in projects to introduce new products and/or sophisticated technologies into the plant.
  • Off business hour oncall support as needed.
  • Knowledge of complex excel formulas or background in programming
  • General Knowledge of Smartsheets
  • Experience with Data Visualizations generating reports using power BI Tableau Spotfire or similar programs

What we expect of you

We are all different yet we all use our outstanding contributions to serve patients. The manufacturing scheduling professional we seek is a collaborative teamplayer with these qualifications.

Basic Qualifications:

  • High school/GED 4 years manufacturing and operations experience OR
  • Associates 2 years manufacturing and operations experience OR
  • Bachelors 6 months manufacturing and operations experience OR
  • Masters

Preferred Qualifications:

  • Degree in Chemical Engineering Industrial Engineering or Life Sciences and the following :
  • Experience in GMP Tech Support roles GMP operations process development or scheduling.
  • Technical knowledge of drug substance (upstream and/or downstream) processing and broad understanding of related disciplinary areas
  • Ability to coordinate analyze and interpret technical data through trend analysis forecasting modeling
  • Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms
  • Ability to coach mentor and/or cross train colleagues within core technical areas
  • Background in lean manufacturing methodologies and operational excellence

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 wellbeing. From our competitive benefits to our collaborative culture well 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 salesbased incentive plan
  • Stockbased longterm incentives
  • Awardwinning timeoff plans
  • Flexible work models including remote and hybrid work arrangements where possible

Apply now and make a lasting impact with the Amgen team.

In any materials you submit you may redact or remove ageidentifying 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.

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Salary Range

88378.00 USD 106188.00 USD

Required Experience:

Senior IC

Employment Type

Full-Time

Company Industry

About Company

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