Senior Associate Manufacturing

1 month ago


Thousand Oaks, United States Amgen Full time

HOW MIGHT YOU DEFY IMAGINATION?

Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Senior Associate ManufacturingLive

What you will do

Lets do this Lets change the world

The Amgen, Pharma Product Manufacturing facility, in Thousand Oaks, directly supports Amgens pipeline of clinical drug product supply to patients across the globe. The Sr. Associate Manufacturing Drug Product role offers the opportunity to collaborate with multiple functions within the Thousand Oaks site on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility

In this role, you will work with a team responsible for supporting multiple Drug Product manufacturing operations, including formulation, sterile-isolator filling, aseptic filling, and lyophilization activities. The team leads the efforts of maintaining the highest levels of safety, quality, compliance, and efficiency while balancing a dynamic production schedule. The Associate will work to support multiple internal customers and partners including Supply Chain, Quality Assurance, Process Development, and Engineering.

The Senior Associate Manufacturing will be specifically responsible for:

Performing drug product filling and formulation activities, respectively

Performing initial review of manufacturing batch records

Maintaining a safe environment while adhering to compliance standards and by identifying additional preventative measures

Crafting and/or revising standard procedures

Leading continuous improvement initiatives, which may be multi-functional in nature

Performing data analysis (e.g., SPC, CPV) of critical process parameters and making recommendations to Engineering and/or Process Development teams

Developing finite schedule for tasks including, unit operations

Reviewing efficiency and identifying countermeasures for issues impacting cycle time alignment

Elevating critical and impactful events to management

Applying appropriate systems for job duties (SAP, QMTS, and LIMS etc.)

Supporting the introduction of new products and technologies into the facility

Initiating and owning quality records, including but not limited to non-conformances (NC), Corrective/PreventativeActions (CAPA)Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an employee with these qualifications.Basic Qualifications:

High school diploma / GED & 4 years of operations or quality experience OR

Associates degree & 2 years of operations or quality experience OR

Bachelors degree & 6 months of operations or quality experience OR

Masters degreePreferred Qualifications:

At least 5 years of biopharmaceutical experience, including work within drug or pharmaceutical product manufacturing environment, which includes aseptic and sterile filling environments, as well as lyophilization

Bachelor's or Master's degree in Microbiology, Life Sciences, Business or a related field

An understanding of Lean concepts and application within a regulated manufacturing environment

Ability to communicate and collaborate with technical and management staff within the manufacturing, quality and process teams

Basic project management skills

Demonstrates emergent leadership traits and strong cognitive resolution abilitiesThrive

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 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.

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 for field 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 possibleApply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.careers.amgen.comApplication 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.

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.



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