QC Specialist
Amgen
This listing was originally posted on Amgen's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moAt 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.
QC Specialist
Let’s do this. Let’s change the world. In this vital role you will serve as the Quality Assurance (QA) Specialist supporting Quality Control (QC) laboratory systems, with primary responsibility for the Laboratory Information Management System (LIMS) and other laboratory computerized systems. You will ensure QC systems remain compliant with GMP regulations, Data Integrity requirements, Computer System Validation (CSV) expectations, and Amgen's Quality Management System while supporting the design, configuration, validation, implementation, maintenance, and continuous improvement of laboratory systems as applicable.
Serve as the Quality Control Systems Subject Matter Expert (SME) and Business Process Owner as applicable for Sample Manager LIMS and associated laboratory computerized systems.
Support the lifecycle management of laboratory systems, including design, configuration, implementation, validation, maintenance, upgrades, and retirement.
Maintain laboratory computerized systems in compliance with GMP, 21 CFR Part 11 and Amgen Quality Management System requirements.
Configure, maintain and approve LIMS templates related to sample plans and specifications.
Support implementation of new functionality and deployment of QC systems in alignment with Amgen network initiatives as applicable.
Support laboratory data retrieval through query execution and reporting tools.
Provide technical support to QC laboratories to ensure laboratory operations meet regulatory requirements and business needs.
Provide technical and critical systems support as applicable across multiple shifts when required.
Support laboratory processes through the LIMS system associated with raw materials, utilities, in-process testing, stability, environmental monitoring, cleaning validation, and finished product testing.
Serve as a SME for revisions and LIMS templating related to sample plans, laboratory metrics and trending program queries.
Support LIMS templating related to new product introductions and product re-introductions in addition to source document revisions on a routine basis.
Assist with planning and coordination of laboratory system enhancements and process improvements.
Ensure laboratory systems remain inspection ready through proactive monitoring, periodic reviews and change management.
Support deviations and investigations from a systems perspective as applicable.
Author and review SOPs, Work Instructions, Forms, validation documentation and assessments supporting QC systems as applicable.
Support internal audits and represent QC Systems during regulatory inspections.
Partner with cross-functional teams including Manufacturing, Process Development, Engineering, Information Systems, Supply Chain, and Global Quality.
Provide technical guidance and mentoring to laboratory users and QC personnel on laboratory systems and best practices.
Develop and deliver training materials related to QC systems and computerized system processes as applicable.
Work closely with the QC network to support global harmonization of QC systems and laboratory business processes across manufacturing sites and support implementation at the site level.
Utilize laboratory metrics and data analytics to identify trends and drive continuous improvement.
Evaluate and implement innovative technologies that enhance compliance, reduce manual effort, and improve the user experience while ensuring adherence to regulatory and data integrity requirements.
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.
Basic Qualifications:
Doctorate degree
OR
Master’s degree and 2 years of quality, quality systems, or quality control experience
OR
Bachelor’s degree and 4 years of quality, quality systems, or quality control experience
OR
Associate’s degree and 8 years of quality, quality systems, or quality control experience
OR
High school diploma / GED and 10 years of quality, quality systems, or quality control experience
Preferred Qualifications:
5+ years of experience in pharmaceutical or biotechnology Quality Control, Quality Assurance, or Quality Systems.
Experience supporting Laboratory Information Management Systems (LIMS), preferably Sample Manager LIMS.
Strong understanding of laboratory operations, analytical testing, sample management, and QC workflows.
Experience supporting computerized laboratory systems including Empower, Electronic Laboratory Notebook (ELN/LMES), Veeva, Kneat, ALM, or similar platforms.
Demonstrated knowledge of GMP regulations, 21 CFR Part 11, Data Integrity principles, and regulatory inspection expectations.
Experience supporting system implementation and system lifecycle management.
Experience authoring SOPs, sample plans, validation documentation, and Work Instructions
Strong technical writing, collaboration, innovation, communication, and presentation skills.
Demonstrated ability to work effectively across global, cross-functional teams.
Strong analytical, organizational, and problem-solving skills with the ability to manage multiple priorities in a fast-paced environment.
Experience supporting regulatory inspections and audit readiness activities.
Experience with SQL, reporting tools, or laboratory data analytics is preferred.
Demonstrated commitment to continuous improvement and operational excellence.
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.
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:
careers.amgen.com
In 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.
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.
Sponsorship for this role is not guaranteed.
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. 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.
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