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.
What you will do
Let’s do this. Let’s change the world. In this vital role you will lead the execution of complex or novel assignments requiring strategic planning and development of new and/or improved validation techniques and procedures. In this position you will monitor validation activities through internal audits and conduct risk assessments to identify the need for requalification and establish policies for computer system re-validation.
This individual will supervise staff who actively participate during all phases of qualification/validation: evaluate projects; provide guidance and technical information to others (lead qualification/validation activities); determine and establish requirements for qualification/validation of each individual system/equipment; formulate independent decisions related to qualification/verification activities.
Responsibilities
Supervise a diverse team of Quality Professionals which span multiple time zones. Review validation/qualification packages for completeness and accuracy, sound rationale, Regulatory expectations, compliance with validation policies and procedures, and accurate data analysis. Compare results against acceptance criteria and work with appropriate departments to resolve exceptions and deviations. Bring critical exceptions or deviations to management’s attention and initiate and enforce necessary improvements and corrections to established systems and processes.
Participation and support of regulatory inspections. The following are examples of execution tasks for this position:
Develop, Mentor, and oversee staff and day to day validation activities
Act as reviewer and approver for operational SOP’s and Work Instructions
Review of operational SOP’s and Work Instructions
Review and approve change controls and Deviations/CAPA/CAPA EVs
Initiate and own QA Deviations/CAPA/CAPA EVs as needed.
Review and approve System Life Cycle Documents (i.e. test protocols) before use in production.
Applies analytical skills to evaluate and interpret complex situations/problems using multiple sources of information
Qualitative information
Quantitative research
Trend data
Forecasts, models and applies advanced analytical tools
Anticipates and prevents potential problems
May be responsible for specific programs and/or projects
Independently develops solutions that are thorough, practical and consistent with functional objectives
Maintain budget
Establish/Improve training curriculum
Provide Management Review Updates on Quality activate
Applies analytical skills to evaluate and interpret complex situations/problems using multiple sources of information
Trend data
Anticipate and prevent potential problems
May be responsible for specific programs and/or projects
Independently develop solutions that are thorough, practical and consistent with functional objectives
What we expect of you
We are all different, yet we all use our unique contributions to serve patients.
Basic Qualifications:
Master’s degree and 8 to 10 years of Software and Systems Quality assurance experience OR
Bachelor’s degree and 10 to 14 years of Software and Systems Quality assurance experience OR
Diploma and 14 to 18 years of Software and Systems Quality assurance experience .
Experience owning and serving as QA Contact for Major and Minor Deviations
Ability to interpret and apply GLPs, GCP’s and GMPs
Knowledge of industry and business principles
Strong demonstration of problem-solving abilities
Contributes to work group/team by ensuring quality of tasks/ services provided by self and others
Provides training and guidance to others
Extends capabilities by working closely with senior staff/ experts within and outside the internal organization.
What you can expect of us
As 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.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.careers.amgen.com
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.