Senior Associate QA

Join Amgen’s Mission of Serving PatientsAt 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 QAWhat you will doLet’s do this. Let’s change the world. In this role as Senior Associate QA, you will be working in a shift system; you will be mainly responsible for providing QA guidance and support to ATO Drug Substance production. Next to that, you will provide support in different QA related projects/systems. In this role, you will be in direct contact with a wide range of partners, and you will be accountable for establishing effective working relationships with production operators, production line leads, production shift supervisors, warehouse, facilities, maintenance and engineering. This role will require local presence at the ATO site.Responsibilities:

Provide daily guidance and support to Production staff regarding compliance with Standard Operating Procedures and Work Instructions.

Ensure purposeful presence in drug substance areas to provide oversight to GMP operations and quality systems.

Act as a first point of contact in case of production queries (quality related) during DS operations.

Lead, mentor, and coach Operations and support personnel on quality matters, while driving the site Quality culture.

Review and approve batch production record and other GMP documentation in support of daily operations. data entries before production activities take place

Compile and review batch records for lots manufactured in preparation for batch disposition.

Own, review, and approve controlled documents, including Standard Operating Procedures (SOPs), Work Instructions and Forms

What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The professional we seek is a go getter with these qualifications.Basic Qualifications:

High school/GED + 4 years of Quality experience OR

Associate’s + 2 years of Quality experience OR

Bachelor’s + 6 months of Quality experience

Master's

Preferred Qualifications:

Quality and manufacturing experience in biotech or pharmaceutical industry

Bachelor’s Degree in a Science Field

Ability to successfully manage workload to timelines

Familiarity with basic project management tools

Demonstrated ability to consistently deliver on-time, and high-quality results

Ability to operate in a matrixed or team environment

What you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll 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 sales-based incentive plan

Stock-based long-term incentives

Award-winning time-off plans

Flexible work models, including remote and hybrid work arrangements, where possible

Apply nowfor a career that defies imaginationObjects in your future are closer than they appear. Join us.careers.amgen.comIn any materials you submit, you may redact or remove age-identifying 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 deadlineExternal/Internal postings: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.