Associate Manufacturing I- Day Shift

HOW MIGHT YOU DEFY IMAGINATION?
You’ve 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 mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Responsibilities

Live; What you will do; There are multiple openings for this position, but the following list offers some insight into basic expectations for our manufacturing associates.; Under general supervision, Associate will perform operations in the manufacturing area.; Operations will be performed according to Standard Operating Procedures (SOP's); Associate will perform and monitor critical processes, complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures, SOP's and technical reports.; Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions.; May participate on cross-functional teams and represent the manufacturing teams.; Associate may also have the responsibility of owning deviations/CAPA's.; In addition, Associate may identify, recommend and implement improvements related to routine functions.

Requirements

Win; What we expect of you; We are all different, yet we all use our unique contributions to serve patients. The Associate Manufacturing professional we seek is a committed individual with these qualifications:; Basic 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 in a related field; Preferred Qualifications:; Bachelor's degree in Science or Engineering; Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc.; Knowledge of Single-use Systems; CFR and Regulatory knowledge; Mechanical ability/expertise; Basic statistical mathematical skills; Ability to interpret and apply GMP knowledge; Understanding of analytical methods for manufacturing area; Demonstrated technical writing capability; Able to demonstrate project management skills and presentation skills; Ability to understand, apply and evaluate basic chemistry, biology and physical principles; Basic troubleshooting skills on production equipment; Experience with Delta V; Experience with lab equipment/testing