Associate Manufacturing- Manufacturing Services; Nights

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. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.

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.

Let’s do this. Let’s change the world. In this vital role you will perform operations in Manufacturing Services on Night shift. Associate Manufacturing will provide technical leadership to the team under the direction of the Manufacturing Services manager. Associate will perform and monitor critical processes, execute routine validation protocols and regularly draft and revise documents, such as Manufacturing Procedures, SOPs, and technical reports.

All operations will be performed according to Standard Operating Procedures (SOPs). Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent Manufacturing Services group. Associate may also have the responsibility of owning minor deviations. In addition, Associate may identify, recommend and implement improvements related to routine functions.

Responsibilities Include:

• Perform and monitor critical processes, complete routine validation protocols, and review documents such as Manufacturing Procedures and SOPs.

• Perform basic troubleshooting and assist in the review of documentation for assigned functions.

• May also have the responsibility of initiating and owning area Deviations, revising SOP's and performing LEAN functions.

In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (C or D Shift). This includes extra benefits such as
receiving an added 15% shift differential, and also getting premium pay for any Sundays worked.The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a great teammate with these qualifications.

• High school/GED + 2 years of manufacturing or operations work experience OR

• Associate’s + 6 months of manufacturing or operations work experience OR

• Bachelor’s degree

• Knowledge of Washers and Autoclaves

• Prior experience with process equipment, computers, and intermediate mathematical skills

• Prior experience working in a clean room setting.

• Knowledge of LIMS and access

• CFR and Regulatory knowledge

• Mechanical ability/expertise

• Experience and Knowledge of Weigh Dispensing

• Strong understanding of BDS equipment and CIP and SIP processes

• Basic statistical mathematical skills

• Ability to interpret and apply GMP knowledge

• Ability to follow Standard Operating Procedures

• Understanding of…