{"id":3842088,"url":"https://alion.io/job/curia-senior-microbiologist","title":"Senior Microbiologist","company":{"id":2070902,"name":"Curia","domain":"curiaglobal.com","url":"https://alion.io/company/curiaglobal","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Oracle","truth_index":{"grade":"A","score":89,"open_postings":18,"ghost_share":0,"stale_share":0.444,"repost_share":0,"time_to_fill_p50_days":56,"computed_at":"2026-11-08T05:47:12Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Albuquerque, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GLP","optional":false},{"name":"GMP","optional":false},{"name":"Matter","optional":false}],"status":"live","first_seen_at":"2026-11-05T22:51:09Z","employer_posted_date":"2026-11-05","last_verified_at":"2026-11-08T03:46:36Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Senior Microbiologist, NPI in Albuquerque, NM\nBuild your future at Curia, where our work has the power to save lives\nCuria is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.\nWe proudly offer\nGenerous benefit options (eligible first day of employment)\nPaid training, vacation and holidays (vacation accrual begins on first day of employment)\nCareer advancement opportunities\nEducation reimbursement\n401K program with matching contributions\nLearning platform\nAnd more!\nAs a member of the NPI Tech Transfer Team, this position is responsible for supporting New Product Introduction (NPI) and technology transfer activities within their assigned functional area (e.g., Quality, Technical Operations, Validation, Microbiology, Analytical Sciences, Manufacturing, etc.). This role serves as the primary Subject Matter Expert (SME) for the functional area throughout the NPI lifecycle, providing technical leadership, risk assessment, planning, execution support, and operational readiness to ensure successful transfer and efficient commercialization of new products.\nWorking as a core member of the NPI Tech Transfer Team, the SME collaborates closely with Program Management, Operations, Quality, Regulatory, as a member of the customer-facing team, working to drive project execution through Tech Transfer stage gates, facilitate knowledge transfer, identify and mitigate risks, and ensure compliance with site procedures, regulatory requirements, and customer expectations. The position is dedicated to NPI activities and serves as the functional customer-facing point of contact for multiple concurrent tech transfer programs.\nThe NPI, Microbiologist IV provides advanced microbiological expertise and technical leadership in support of new product introduction (NPI), routine manufacturing, product release, contamination control, and external customer programs. This role leads microbiological workstreams for new products, including method and specification assessment, analytical strategy, protocol development, scientifically justified acceptance criteria, protocol execution, data interpretation, and report preparation. The NPI, Microbiologist IV serves as a customer-facing technical representative for microbiology activities and communicates project status, technical risks, investigation outcomes, and recommendations in coordination with Quality and Project Management. The role leads or supports microbiological method transfer, verification, validation, qualification, suitability, recovery, hold-time, disinfectant effectiveness, and laboratory readiness activities; authors and reviews controlled technical documents; coordinates internal and external laboratory testing; mentors laboratory personnel; and ensures microbiological documentation is accurate, complete, data-integrity compliant, and inspection ready.\nEssential Duties and Responsibilities:\nAct as the designated functional SME for all assigned NPI and technology transfer projects.\nParticipate in cross-functional Tech Transfer teams from project initiation through commercial launch.\nLead discipline-specific assessments, gap analyses, risk evaluations, and readiness reviews.\nSupport development and execution of project plans, timelines, and deliverables required for Tech Transfer stage gates.\nProvide technical expertise during customer meetings, technical discussions, audits, and governance reviews.\nPartner with Program Managers to identify project risks, mitigation plans, and escalation pathways.\nEnsure functional deliverables, documentation, and approvals are completed in accordance with established procedures and project timelines.\nDrive operational readiness activities necessary to support development, validation, and commercial manufacturing.\nSupport knowledge transfer activities between sending and receiving organizations, ensuring effective and efficient transfer of process, product, analytical, and operational knowledge.\nParticipate in Technical Review Boards (TRBs), stage gate reviews, and leadership governance meetings.\nCollaborate with cross-functional departments to resolve technical challenges and remove execution barriers.\nContribute to continuous improvement of NPI and Tech Transfer processes, tools, templates, and best practices.\nLead and perform NPI microbiological testing, including endotoxin, sterility, bioburden, microbial limits, growth promotion, biological indicators, utilities, environmental monitoring, and applicable product-specific assays.\nAnalyze, trend, and interpret microbiological data; evaluate method performance and product or facility risks; and communicate findings and recommendations to management, customers, and cross-functional teams.\nProvide technical leadership for microbial identification, organism trending, environmental and personnel monitoring, media fill support, line clearance, start-up verification, and assessment of isolates or recoveries.\nLead microbiological method and laboratory readiness assessments for new products, including methods, specifications, sample plans, materials, equipment, software, capacity, external laboratory support, and analyst qualification requirements.\nOwn the microbiological technical assessment and strategy for assigned NPI programs, including applicable regulatory, compendial, product, facility, contamination-control, and customer requirements.\nAuthor, review, approve where delegated, and execute protocols and reports for microbiological method development, transfer, verification, validation, qualification, suitability, recovery, neutralization, hold-time, disinfectant effectiveness, environmental monitoring, and new product laboratory implementation.\nDevelop scientifically justified protocol objectives, study designs, sample plans, challenge conditions, and acceptance criteria aligned with applicable specifications, regulatory, compendial, contamination-control, and customer requirements.\nLead protocol execution, ensuring requirements are followed, deviations are assessed, data is reviewed, and conclusions are supported by objective evidence.\nCollaborate with NPI, Manufacturing, Quality, Validation, Engineering, Project Management, and other cross-functional teams to support product onboarding, testing requirements, technical issue resolution, and project schedules.\nCoordinate microbiological activities performed internally and by external laboratories, including technical transfer, sample and material requirements, scheduling, data review, issue escalation, and project commitments.\nProvide technical mentorship, training, and coaching to microbiology personnel on methods, protocol execution, investigations, data integrity, aseptic practices, and regulatory expectations.\nLead or provide technical direction for OOS, sterility, bioburden, endotoxin, environmental monitoring, contamination, and method-performance investigations using root cause analysis, risk assessment, and CAPA.\nSupport lifecycle management and implementation of microbiology laboratory equipment, technologies, methods, materials, supplies, and inventory while maintaining laboratory organization, housekeeping, and audit readiness.\nEducation and/or Experience:\nBachelor’s degree in microbiology, Biology, or a related scientific discipline.\nMinimum of eight (8) years’ relevant professional experience in a pharmaceutical GMP or GLP environment.\nProficient in the validation/qualification of lab microbiological techniques, preferred.\nKnowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485, and 17025 a plus.\nSupervisory Responsibilities:\nThis role does not have supervisory responsibilities, yet it may involve mentoring, guiding, and advising.\nOther Skills and Abilities:\nProvides guidance and mentorship to team members\nFosters a collaborative and positive work environment\nChampions change\nPromotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.\nDemonstrates strong attention to detail\nFacilitate the revision and release of all controlled documents. Facilitate mandatory reviews of SOPs and month-end reports.\nProvide oversight for projects to update/maintain official document templates. Direct and manage the Change Control System\nStrong organizational skills and ability to prioritize and multi-task in a fast-paced environment.\nOther Qualifications:\nMust pass a background check\nMust pass a drug screen\nMay be required to obtain and maintain gowning certification\nMay be required to obtain and maintain media qualification\nMust be able to wear a respirator\nEducation, experience, location and tenure may be considered along with internal equity when job offers are extended.\nWe do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.\nAll interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. 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