Quality Control Specialist, Microbiology

BioSpace; Thousand Oaks (CA); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Competitive benefits package

Flexible work models

Retirement plan with company match

Job summary

Amgen in Thousand Oaks seeks a Quality Control Specialist, Microbiology to lead QC microbiology and environmental monitoring operations. You will guide microbial ID activities, investigations, and regulatory readiness in a fast-paced GMP lab environment.

You will supervise staff, coordinate priorities, author documentation, and collaborate with global teams on process improvements and quality events.

Qualifications

• Education aligned with Quality, Microbiology or Operations expectations.
• Strong documentation writing and technical communication.
• Experience with GMP laboratories and environmental monitoring.

Responsibilities

• Lead microbial identification and testing activities.
• Coordinate daily lab priorities and supervise staff.
• Manage investigations, CAPAs and deviations.
• Support regulatory inspections and audit readiness.
• Maintain inspection-ready electronic documentation.

Skills

Quality experience

Microbiology

Operations experience

Leadership

Documentation

Veeva

GMP

Regulatory inspections

Education

High school diploma / GED

Associate degree

Bachelor’s degree

Master’s degree

Doctorate degree

Tools

LIMS

CIMS

LMES

SAP

Maximo

Job description

Quality Control Specialist, Microbiology

What You Will Do

Lets do this. Lets change the world. In this vital role, you will provide technical and operational leadership for the QC Microbiology and Environmental Monitoring laboratories, leading microbial identification activities, environmental monitoring investigations, and laboratory operations in a highly dynamic, team-oriented environment.

In This Role, You Will Be Responsible For

• Lead microbial identification activities, organism assessments, and support routine and non-routine microbiological testing.
• Provide leadership for microbiology laboratory operations, coordinate daily priorities, supervise laboratory staff, and support weekend laboratory operations.
• Own and lead complex microbiological investigations, deviations, environmental monitoring excursions, and contamination events, including root cause analysis, risk assessments, and product impact assessments.
• Provide technical expertise for environmental monitoring, bioburden control, microbial identification, contamination control strategies, and laboratory controls.
• Author and drive CAPAs, microbial risk assessments, and change controls to ensure compliant resolution of quality events.
• Coordinate contract laboratory activities, including testing support, data review, investigation collaboration, and approval of associated documentation.
• Generate and maintain complete, accurate, and inspection-ready documentation using electronic laboratory and quality systems (e.g., LMES, LIMS, CIMS, and Veeva).
• Partner with Quality, Manufacturing, Engineering, and global microbiology teams to support process improvements, operational excellence initiatives, regulatory inspections, and strategic microbiology projects.

What We Expect Of You

We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a self-starter with these qualifications

Basic Qualifications

• High school diploma / GED and 10 years of Quality, Microbiology or Operations experience OR
• Associates degree and 8 years of Quality, Microbiology or Operations experience OR
• Bachelors degree and 4 years of Quality, Microbiology or Operations experience OR
• Masters degree and 2 years of Quality, Microbiology or Operations experience OR
• Doctorate degree

Preferred Qualifications

• Microbiology degree and/ormicrobiology laboratory experience associated with microbial identification.
• Demonstrated leadership experience, including coaching and developing staff, prioritizing laboratory workloads, and supporting routine and non-routine microbiological testing.
• Understanding of manufacturing processes associated with contamination control.
• Experience supporting regulatory inspections and audit readiness activities.
• Advanced technical writer who can articulate complex events into concise, clear, and contemporaneous documentation that is inspection ready.
• Professional work experience in a fast-paced, flexible GMP laboratory.
• Ability to generate, investigate, triage and close deviations and analytical test result assessments in Veeva.
• Ability to generate and document validation protocols and reports.
• Experience performing aliquoting of samples aseptically.
• Operation, maintenance experience with laboratory equipment.
• Ability to generate and revise methods and SOPs within CDOCs.
• Demonstrated proficiency with electronic systems capturing consumables, testing procedures, results, and investigations (SAP, LIMS, LMES, CIMS, Veeva, etc.).
• Demonstrated understanding and use of Maximo (Work Order System)
• Ability to manage and lead Operational Excellence initiatives including 5S and Standard Work associated with the testing labs.
• Demonstrated written and oral communication skills, project management and presentation skills, and proven ability to manage priorities effectively.
• Demonstrated ability to be flexible and adaptable to support business needs.

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

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.

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.

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.