Quality Compliance - Associate Director - Microbiology

Quality Compliance Associate Director - Microbiology Let’s do this. Let’s change the world. In this vital role, you will serve as a Quality Compliance microbiology subject matter expert supporting contamination control, QC microbiology, manufacturing microbiology, inspection readiness, and technical consistency across Amgen Operations. This role partners with Quality, Manufacturing, Process Development, Regulatory Affairs‑CMC, Cellular Sciences, site laboratories, and global technical networks to ensure science‑based, compliant, and practical microbiology decisions. This is a full‑time remote position. Specific responsibilities include but are not limited to: Serve as a microbiology and contamination control subject matter expert for Quality Compliance, QC laboratories, manufacturing, and site teams. Support the contamination control program, including site engagement, network participation, metrics review, risk identification, and escalation of significant concerns. Contribute to the development, revision, and implementation of global microbiology and contamination control standards, procedures, technical guidance, and quality intelligence documents. Support periodic contamination control reviews, trend evaluations, and state‑of‑control assessments for in‑scope sites, processes, and products. Provide technical input for environmental monitoring, bioburden control, endotoxin, microbial identification, disinfectant efficacy, cleaning and disinfection, gowning, aseptic practices, utilities, facilities, and laboratory controls. Partner with site Quality, Manufacturing, Engineering, and QC laboratories to promote consistent application of contamination control expectations. Provide technical review and recommendations for microbiology investigations, deviations, CAPAs, risk assessments, change controls, audit observations, and inspection commitments. Support evaluation and implementation of new or improved microbiology methods, technologies, laboratory practices, and contamination control tools. Contribute to Microbiology Center of Excellence activities, technical forums, communities of practice, and network alignment discussions. Support regulatory inspections, internal audits, health authority commitments, and inspection‑readiness activities related to microbiology, contamination control, QC laboratories, and manufacturing controls. Provide technical input to audit responses, regulatory inspection responses, CAPA plans, and effectiveness checks. Review regulatory filings, responses, or technical documents for microbiology‑related content, as assigned. Monitor relevant regulatory, compendial, and industry developments and help translate them into practical expectations for sites and functions. Lead or support cross‑functional projects related to microbiology, contamination control, laboratory practices, inspection readiness, or quality improvement. What we expect of you The Quality Compliance Associate Director – Microbiology we seek is an experienced, collaborative microbiology subject matter expert with the following qualifications. Basic Qualifications: Doctorate degree and 3 years of Quality, Microbiology, Manufacturing, or relevant regulated industry experience OR Master’s degree and 7 years of Quality, Microbiology, Manufacturing, or relevant regulated industry experience OR Bachelor’s degree and 9 years of Quality, Microbiology, Manufacturing, or relevant regulated industry experience Associate’s degree and 12 years of Quality, Microbiology, Manufacturing, or relevant regulated industry experience OR High school diploma / GED and 14 years of Quality, Microbiology, Manufacturing, or relevant regulated industry experience In addition to meeting at least one of the above requirements, you must have a minimum of 3 years’ experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above. Preferred Qualifications: Life Science, Microbiology, Biology, Biological Sciences, Pharmaceutical Sciences, Biotechnology, Engineering, or related scientific academic background. 8+ years of experience in Quality, QC microbiology, Manufacturing, contamination control, sterility assurance, or a related GMP function within the biotechnology or pharmaceutical industry. At least 3 years of experience leading microbiology laboratories, environmental monitoring programs, or contamination control technical workstreams. Strong technical knowledge of microbiology and contamination control practices, including environmental monitoring, bioburden, endotoxin, microbial identification, disinfectant efficacy, cleaning and disinfection, gowning, aseptic practices, utilities, facilities, and laboratory controls. Experience supporting GMP investigations, deviations, CAPAs, change controls, risk assessments, audits, inspection readiness, or regulatory inspection activities. Experience in biologics, sterile manufacturing, aseptic processing, drug substance manufacturing, drug product manufacturing, or QC microbiology laboratory operations. Experience contributing to global or multi‑site standards, procedures, technical guidance, training materials, quality intelligence, or quality system improvements. Ability to interpret and apply GMP, GxP, regulatory, compendial, and industry expectations to microbiology, manufacturing, Quality Control, and contamination control processes. Experience supporting or participating in technical networks, communities of practice, Centers of Excellence, or cross‑site microbiology forums. Experience evaluating or implementing new microbiology technologies, rapid microbiological methods, laboratory automation, data trending tools, or contamination control improvements. Demonstrated ability to lead cross‑functional teams, influence without direct authority, communicate complex technical information clearly, and manage multiple priorities. Ability to work effectively with global and virtual teams across time zones while adapting approaches based on technical complexity, regulatory considerations, and stakeholder needs. Effective English written and verbal communication skills; additional language capability is a plus. Ability to travel domestically and internationally up to 20% of the time. What you can expect of us From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. 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. 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. #J-18808-Ljbffr Amgen SA