Microbiologist II 503A (2nd shift)

Empower Pharmacy•Houston, TX

15h•Onsite

About The Position

Empower Pharmacy is a visionary healthcare company dedicated to making quality, affordable medication accessible to millions of patients nationwide. As the nation’s most advanced 503A compounding pharmacy and FDA-registered 503B outsourcing facility, we’re redefining what’s possible in personalized medicine and pharmaceutical manufacturing. We’re proud to be recognized as one of Houston’s fastest-growing private companies and ranked #116 in Healthcare & Medical on the Inc. 5000 List for 2025. Our strength is built on four core values: People, Quality, Service, and Innovation. Guided by these principles, we’ve created a uniquely integrated healthcare platform powered by advanced technology, operational excellence, and a relentless commitment to patient care. From manufacturing and quality control to distribution and customer experience, our teams work together to raise industry standards, expand access to critical medications, and improve outcomes for patients and providers across the country. At Empower, joining our team means more than starting a new role. It means becoming part of a mission-driven organization that’s transforming healthcare at scale. We invest deeply in our people, encourage bold thinking, and create opportunities for growth, leadership, and innovation at every level. Your ideas matter here, your development is supported, and the work you do has a direct impact on the lives of millions. If you thrive in a fast-moving, purpose-driven environment where innovation, collaboration, and ambition come together, Empower Pharmacy is the place for you. Let’s transform healthcare together. Position Summary: Microbiologist II 503A safeguards product quality, patient safety, and regulatory readiness by executing microbiological testing, environmental monitoring, investigations, and data analysis supporting Empower’s high-growth 503A and 503B compounding operations. This role owns accurate, timely laboratory execution, deviation identification, and continuous improvement initiatives that strengthen release reliability, compliance performance, and operational scalability. Leveraging AI-enabled analytics, digital workflows, and automation tools as force multipliers, the Microbiologist II accelerates decision-making, improves testing precision, enhances trend visibility, and elevates quality outcomes across the microbiology program. Success requires disciplined execution, learning agility, strategic problem solving, and consistent performance within a fast-paced, highly regulated environment where P80–P90 talent combines technical depth, accountability, collaboration, and proactive risk management to support enterprise growth. The position influences audit readiness, manufacturing continuity, and customer trust through rigorous scientific standards daily.

Requirements

Strong understanding of microbiological testing methodologies, environmental monitoring practices, aseptic processing principles, contamination control strategies, and cGMP requirements supporting regulated pharmaceutical or healthcare manufacturing environments.
Proficiency using laboratory information systems, digital quality platforms, AI-enabled analytics tools, and automated workflows to improve testing accuracy, data visibility, operational efficiency, and compliance execution.
Demonstrated analytical problem-solving capabilities with experience investigating deviations, interpreting microbiological trends, conducting root cause analysis, and implementing effective corrective and preventive actions within regulated environments.
Excellent communication, collaboration, and organizational skills with the ability to manage competing priorities, maintain documentation accuracy, and operate effectively within fast-paced, high-growth operational environments.
Bachelor’s degree in Microbiology, Biology, Chemistry, Biochemistry, or related scientific discipline required.
Minimum 2 years of microbiology laboratory experience within pharmaceutical, biotechnology, healthcare, food manufacturing, or other highly regulated operational environments preferred.
Experience supporting environmental monitoring programs, microbiological testing, investigations, and quality documentation within cGMP or similarly regulated environments preferred.
Familiarity with USP requirements, aseptic processing standards, laboratory investigations, data integrity practices, and digital laboratory systems strongly preferred.
Demonstrated ability to operate independently, execute with precision, adapt quickly to change, and contribute effectively within collaborative, high-performance teams.

Responsibilities

Performs microbiological testing, environmental monitoring, growth promotion, and sample analysis supporting 503A compounding operations while maintaining data integrity, procedural compliance, and operational efficiency.
Utilizes AI-enabled laboratory systems, automated trending tools, and digital workflows to accelerate result interpretation, strengthen testing accuracy, improve documentation quality, and support timely product disposition decisions within a highly regulated manufacturing environment.
Maintains laboratory readiness through disciplined execution of equipment monitoring, media preparation, inventory management, calibration coordination, and documentation review activities.
Applies analytical thinking and AI-supported data insights to identify process variation, reduce operational risk, improve testing throughput, and strengthen compliance performance while consistently meeting quality standards, production timelines, and departmental objectives in a fast-paced growth environment.
Coordinates sample receipt, tracking, testing prioritization, and workflow execution to support manufacturing schedules, stability programs, and release timelines.
Partners cross-functionally with Quality, Production, and Validation teams while leveraging digital systems and AI-assisted analytics to improve visibility, enhance communication, accelerate issue resolution, and maintain accurate microbiological records supporting operational continuity and regulatory compliance expectations.
Investigates microbiological deviations, environmental excursions, out-of-trend results, and contamination risks using structured root cause methodologies and scientific analysis.
Integrates AI-enabled trend monitoring, historical data evaluation, and risk assessment tools to improve decision-making quality, strengthen corrective actions, reduce recurrence potential, and support audit-ready documentation aligned with FDA, USP, and internal quality requirements.
Executes microbiology activities in accordance with cGMP requirements, standard operating procedures, aseptic processing standards, and regulatory expectations supporting Empower’s 503A and 503B operations.
Maintains precise documentation practices while using digital quality systems, automated workflows, and AI-supported review capabilities to improve accuracy, streamline compliance processes, and strengthen inspection readiness across laboratory operations.
Supports internal audits, regulatory inspections, and quality assessments through organized documentation, accurate record management, and responsive issue resolution.
Demonstrates execution rigor and learning agility by identifying compliance gaps, escalating operational risks appropriately, and applying AI-assisted reporting and data analysis tools to strengthen transparency, accelerate remediation activities, and sustain operational excellence within a hyper-growth environment.
Identifies opportunities to improve microbiological workflows, laboratory efficiency, environmental monitoring effectiveness, and testing reliability through data-driven analysis and operational collaboration.
Utilizes AI-powered analytics, automation technologies, and performance metrics to increase scalability, reduce manual inefficiencies, improve turnaround times, and support continuous improvement initiatives aligned with enterprise growth and evolving regulatory expectations.
Partners with Quality Assurance, Manufacturing, Engineering, and Validation teams to support investigations, process changes, new equipment implementation, and operational improvements.
Applies scientific expertise, strategic thinking, and AI-enabled insights to evaluate microbiological risks, optimize laboratory processes, and improve cross-functional decision-making supporting product quality, patient safety, and sustainable operational performance.
Continuously expands technical expertise in microbiology, aseptic processing, contamination control, and regulatory expectations through training, research, and operational experience.
Demonstrates P80–P90 talent expectations by rapidly adapting to evolving technologies, leveraging AI as a force multiplier for learning and execution, and contributing innovative ideas that improve quality, compliance, and laboratory performance outcomes.