QC Specialist

Amgen; West Greenwich (RI); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Stock-based long-term incentives

Award-winning time-off plans

Flexible work models

Retirement and savings plan

Job summary

Amgen is seeking a QC Specialist to support Quality Control laboratory systems, with primary responsibility for LIMS and related systems. You will ensure compliance with GMP, data integrity, and CSV expectations while aiding design, validation, and maintenance across the QC tech stack.

The role requires strong technical writing, cross‑functional collaboration, and experience with LIMS and validated lab systems. Amgen offers robust benefits and opportunities for professional growth.

Qualifications

• Doctorate, or equivalent, required for this QC role.
• 5+ years in pharmaceutical/biotech quality systems or QC.
• Experience with LIMS and validated laboratory systems preferred.

Responsibilities

• Serve as SME for QC systems and LIMS templating across labs.
• Support life‑cycle management: design, config, validation, maintenance.
• Ensure GMP, 21 CFR Part 11 compliance and data integrity.
• Configure and approve LIMS templates for samples and specs.
• Collaborate with Manufacturing, Process Development, Engineering, IT, and QA.

Skills

Analytical skills

Technical writing

Cross-functional collaboration

Communication

Presentation skills

Education

Doctorate degree

Master’s degree + 2 years quality experience

Bachelor’s degree + 4 years quality experience

Associate’s degree + 8 years quality experience

High school diploma + 10 years quality experience

Tools

Sample Manager LIMS

Empower

ELN/LMES

Veeva

Kneat

ALM

SQL

Reporting tools

Job description

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.

QC Specialist

What You Will Do

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.

What We Expect Of You

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.

What you can expect from 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.

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.

• 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 where possible. Refer to the Work Location Type in the job posting to see if this applies.

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.

Application deadline

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

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.