Associate Principal Scientist, Microbiology Testing, EM​/Utilities Monitoring Program – Onsite​/F

R4, Associate Principal Scientist – Microbiology Testing, EM /Utilities Monitoring Program – Onsite (First Shift)

Join us and experience our culture first‑hand with strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

In the role of Associate Principal Scientist, you will be a key member of the Analytical Research and Development Microbiology team, supporting a rapidly expanding pipeline through close collaboration with cross‑functional stakeholders. This role is responsible for generating and delivering critical microbiology data within a GMP laboratory setting, including finished product testing, utilities monitoring, and environmental monitoring.

• Lead the execution of microbiology finished product testing, utilities, and environmental monitoring program in GMP environment
• Leverage QC microbiology expertise as a subject matter expert in support of sterile operations within the quality control department including isolator qualifications, sterility testing, biological indicator challenge tests, and method suitability, endotoxin, microbial enumeration, media / reagent quality control testing, mycoplasma.
• Directly contribute to experimental design of special studies in support of aseptic operations, execution, authoring and trend analysis of environmental monitoring and utilities trend reports.
• Strong experiences in risk‑based assessment, Environmental Monitoring Performance Qualification (EMPQ), Clean Utilities Monitoring, DE study and contamination control strategies is essential. These skills ensure robust identification and mitigation of potential risks, as well as the implementation of comprehensive monitoring and preventive measures to maintain product integrity and regulatory compliance.
• Experience with testing in clean room environments and Aseptic process validation preferred
• Analyze EM and water‑system trends; identify hotspots, personnel‑related risks, and systemic issues; recommend and implement risk‑based mitigations on an ongoing basis
• Oversee the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA and data integrity principle.
• Execute test method suitability studies and implement microbiology methods to support release and stability testing of small molecule, biologic, and vaccines finished drug products.
• Troubleshoot and lead investigations, CAPAs, change controls associated with GMP testing/monitoring through active collaboration with cross‑functional project teams and/or Quality stakeholders. Identify appropriate corrective and preventative actions.
• Partner with internal stakeholders and partners including Quality, Pipeline, and Operations.
• Supervise microbiology team, data entry, data review, equipment, lab inventory and author /approve reports and data summaries.
• Conduct project management and/or scientific oversight of studies performed at Contract Laboratories
• Contribute expertise and creativity to the collective knowledge and aid in solving complex problems.
• Participate in internal and external compliance audit activities.
• Perform additional duties as assigned.

• Minimum 4 years of pharmaceutical industry experience for applicants with a PhD degree; 8 years of experience with a MS degree; or 12 years of experience with a BS in Microbiology or related Biological Sciences, or equivalent with microbiological testing experience.

• A proven record of strong technical problem solving and laboratory experience. Excellent written and oral communication skills, as well as interpersonal skills, are necessary to qualify for this role.
• Extensive knowledge and experience of microbiology testing in context of environmental monitoring program leadership – own and continuously improve the site EM program in alignment with EU GMP Annex 1 and internal standards
• Design and justify risk‑based EM strategies (locations, frequencies, methods) and…