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.
Senior Associate Manufacturing - Night Shift
What you will
Let's do this. Let's change the world. In this vital role you will support the Downstream Manufacturing Operations according to Standard Operating Procedures (SOPs). Will perform and supervise critical processes, execute routine protocols, and regularly draft and revise documents such as Manufacturing Procedures and SOPs. Perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams. May identify, recommend, and implement improvements related to routine functions in a Non-Standard Shift environment. Multiple Positions Available.
Specific responsibilities include but are not limited to:
Lead the execution of complex manufacturing processes and systems, developing non-routine procedures and documentation as needed to support production efficiency.
Serve as a subject matter expert and trainer for Operators and Associates, sharing knowledge and best practices to build team capability.
Accurately and promptly enter data into systems such as LIMS, LMES, and SAP, ensuring compliance with Good Documentation Practices and cGMP standards.
Revise SOPs and batch records to improve clarity, efficiency, and compliance, while maintaining a high standard for detail and accuracy.
Collaborate with cross-functional teams to support process improvements, share insights, and align on production goals and timelines.
Respond quickly to production issues, conduct root cause analyses, and propose corrective actions to minimize disruptions and prevent recurrence.
Monitor safety conditions on the floor and model adherence to safety protocols, promoting a culture of accountability and compliance.
Analyze process data and critical parameters to assess quality impact and support decision-making during deviations or CAPAs
Inspire team performance by connecting daily work to broader organizational goals, setting high standards, and encouraging continuous improvement.
Actively seek and implement feedback from peers and team members to enhance line performance and develop a culture of learning and innovation.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The Senior Associate Manufacturing professional we seek is an individual contributor with these qualifications:
Basic Qualifications:
Master's Degree
Or
Bachelor's Degree + 6 months Manufacturing work experience
Or
Associate's degree + 2 years Manufacturing work experience
Or
High school/GED + 4 years Manufacturing work experience
Preferred Qualifications:
Experience with purification, buffer and component preparation process.
Availability to the Third Shift including rotative weekdays and weekends.
Proficient experience of performing basic operations and understanding equipment per procedures.
Knowledge of basic computer systems including Microsoft Office, SAP, MES, LIMS.
Educational background in Life Sciences, Biotechnology or Engineering.
Experience working in a GMP regulated environment within the biotechnology, pharmaceutical or medical device industry.
Excellent communication, organization, attention to detail and technical writing skills.
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.
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:
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
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 an annual site shutdown
Flexible work models where possible. Refer to the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
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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 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 with 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.