Senior Level Microbiology Jobs
Senior level microbiology jobs put experienced scientists in charge of research direction, quality systems, and the laboratory teams or projects that deliver results. Roles are concentrated across Education, Manufacturing, and Medical Devices, with a mix of on-site, hybrid, and remote positions available and employers like Genentech, Regeneron, and Danaher Corporation hiring at this level now.
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Showing 5 of 7+ Senior Level Microbiology jobs
The Position
Welcome to Holly Springs, North Carolina— home to Roche/Genentech's largest-ever investment: a $2B greenfield start-up where next-generation technology, high-performing teams and Operational Excellence converge to create the global standard for high-volume, highly-efficient Drug Product manufacturing.
The facility's core is defined by Innovation - leveraging advanced automation, robotics, digital tools, real-time data analytics, and simple, streamlined processes to produce the highest quality medicines. This plant meets today’s demand for CVRM (Cardiovascular, Renal, and Metabolism) medicines and is scalable to grow with the portfolio, which focuses on next-generation metabolic medicines specifically targeting the global obesity epidemic and Type 2 diabetes. This is a fast-paced, entrepreneurial environment with a high-level of accountability, with planned launch in 2028.
Are you a problem-solver and change-agent who thrives in a Team environment, eager to tackle the most complex manufacturing challenges? If so, this is a once-in-a-lifetime opportunity to launch a state-of-the-art facility from the ground-up and shape the culture of our organization for the next generation.
Join us in Holly Springs, where you won't just build a plant—you will build the future of medicine.
The Opportunity:
The Holly Springs Quality Control Team is seeking an experienced and dynamic leader to establish and head our QC Microbiology team.
In this critical role, you will build a highly effective and engaged organization capable of delivering safe, compliant, and efficient testing for our CVRM (Cardiovascular, Renal, and Metabolism) products manufactured at the Holly Springs site. Initially, you will focus on laboratory start-up activities—establishing core QC capabilities to support facility, utility, and process qualifications—before pivoting to routine commercial operations following site licensure.
Leadership:
- You will champion a proactive quality culture built on psychological safety and transparent communication—empowering your team to speak up, simplify processes, and take personal accountability for owning quality.
- You will drive a proactive safety culture by fostering Behavior-Based Safety (BBS) principles and ensuring strict compliance with site safety processes and regulatory standards.
- You will foster a high-performing, engaged lab culture by practicing Lean Leadership, providing active coaching, and embedding continuous improvement into daily operations.
- You will ensure appropriate staffing, resource allocation, and workload balancing to support business priorities and changing operational demands.
- You will partner with the global network to harmonize QC standards and ensure seamless execution and compliance across site operations.
Technical and functional tasks:
- You will establish key operational performance measures (KPIs) with a focus on Compliance, Right-First-Time (RFT) execution and continuous improvement to meet business objectives.
- You will author, review, and approve critical technical, scientific, and compliance documents (e.g., test methods, validation protocols, SOPs).
- You will own Quality Management System (QMS) records, including investigations, deviations, CAPAs, and change controls.
- You will participate in the identification, evaluation, and implementation of new technologies in alignment with business objectives or regulatory requirements.
- You will use data-driven decision making to identify trends, mitigate risks, and improve operational performance.
- You will have responsibility for strategic projects to support execution of QC network strategy.
- You are experienced in presenting Microbiology topics during regulatory inspections and maintaining a continuous state of audit readiness across QC operations.
Who you are:
- You hold a B.S. or M.S. degree (Science related discipline) with a minimum of 8 years of experience in pharmaceutical or biopharmaceutical manufacturing. This includes at least 3 years of direct experience in QC operations at a finished drug product commercial manufacturing site.
- You have extensive technical knowledge of Microbiology methods, laboratory instrumentation, and analytical method validation, qualification, and transfer within the pharmaceutical or biopharmaceutical industry.
- You have extensive experience in contamination control strategies, environmental and utility system monitoring.
- You have in-depth working knowledge of cGMP operations, ICH guidelines, and global Health Authority regulatory requirements (FDA, EMA, etc.).
- You have proven technical leadership capabilities and demonstrated project management skills, with a track record of effectively managing workload distribution, timelines, and competing priorities.
- You have exceptional communication skills with the demonstrated ability to inspire, motivate, and coach a team while collaborating effectively with internal cross-functional groups, global partners, suppliers, and external customers.
- You have proven experience managing operational and capital budgets (OpEx/CapEx), with a track record of driving cost-efficient laboratory operations and resource optimization.
Preferred:
- Experience in a greenfield project.
- Formal Operational Excellence certification (e.g., Lean Six Sigma Green/Black Belt, 5S, Kaizen).
Relocation assistance is available for this role.
The expected salary range for this position based on the primary location for this position of Holly Springs, North Carolina is $120,100 - $223,100. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
The Position
Welcome to Holly Springs, North Carolina— home to Roche/Genentech's largest-ever investment: a $2B greenfield start-up where next-generation technology, high-performing teams and Operational Excellence converge to create the global standard for high-volume, highly-efficient Drug Product manufacturing.
The facility's core is defined by Innovation - leveraging advanced automation, robotics, digital tools, real-time data analytics, and simple, streamlined processes to produce the highest quality medicines. This plant meets today’s demand for CVRM (Cardiovascular, Renal, and Metabolism) medicines and is scalable to grow with the portfolio, which focuses on next-generation metabolic medicines specifically targeting the global obesity epidemic and Type 2 diabetes. This is a fast-paced, entrepreneurial environment with a high-level of accountability, with planned launch in 2028.
Are you a problem-solver and change-agent who thrives in a Team environment, eager to tackle the most complex manufacturing challenges? If so, this is a once-in-a-lifetime opportunity to launch a state-of-the-art facility from the ground-up and shape the culture of our organization for the next generation.
Join us in Holly Springs, where you won't just build a plant—you will build the future of medicine.
The Opportunity:
The Holly Springs Quality Control Team is seeking an experienced and dynamic leader to establish and head our QC Microbiology team.
In this critical role, you will build a highly effective and engaged organization capable of delivering safe, compliant, and efficient testing for our CVRM (Cardiovascular, Renal, and Metabolism) products manufactured at the Holly Springs site. Initially, you will focus on laboratory start-up activities—establishing core QC capabilities to support facility, utility, and process qualifications—before pivoting to routine commercial operations following site licensure.
Leadership:
- You will champion a proactive quality culture built on psychological safety and transparent communication—empowering your team to speak up, simplify processes, and take personal accountability for owning quality.
- You will drive a proactive safety culture by fostering Behavior-Based Safety (BBS) principles and ensuring strict compliance with site safety processes and regulatory standards.
- You will foster a high-performing, engaged lab culture by practicing Lean Leadership, providing active coaching, and embedding continuous improvement into daily operations.
- You will ensure appropriate staffing, resource allocation, and workload balancing to support business priorities and changing operational demands.
- You will partner with the global network to harmonize QC standards and ensure seamless execution and compliance across site operations.
Technical and functional tasks:
- You will establish key operational performance measures (KPIs) with a focus on Compliance, Right-First-Time (RFT) execution and continuous improvement to meet business objectives.
- You will author, review, and approve critical technical, scientific, and compliance documents (e.g., test methods, validation protocols, SOPs).
- You will own Quality Management System (QMS) records, including investigations, deviations, CAPAs, and change controls.
- You will participate in the identification, evaluation, and implementation of new technologies in alignment with business objectives or regulatory requirements.
- You will use data-driven decision making to identify trends, mitigate risks, and improve operational performance.
- You will have responsibility for strategic projects to support execution of QC network strategy.
- You are experienced in presenting Microbiology topics during regulatory inspections and maintaining a continuous state of audit readiness across QC operations.
Who you are:
- You hold a B.S. or M.S. degree (Science related discipline) with a minimum of 8 years of experience in pharmaceutical or biopharmaceutical manufacturing. This includes at least 3 years of direct experience in QC operations at a finished drug product commercial manufacturing site.
- You have extensive technical knowledge of Microbiology methods, laboratory instrumentation, and analytical method validation, qualification, and transfer within the pharmaceutical or biopharmaceutical industry.
- You have extensive experience in contamination control strategies, environmental and utility system monitoring.
- You have in-depth working knowledge of cGMP operations, ICH guidelines, and global Health Authority regulatory requirements (FDA, EMA, etc.).
- You have proven technical leadership capabilities and demonstrated project management skills, with a track record of effectively managing workload distribution, timelines, and competing priorities.
- You have exceptional communication skills with the demonstrated ability to inspire, motivate, and coach a team while collaborating effectively with internal cross-functional groups, global partners, suppliers, and external customers.
- You have proven experience managing operational and capital budgets (OpEx/CapEx), with a track record of driving cost-efficient laboratory operations and resource optimization.
Preferred:
- Experience in a greenfield project.
- Formal Operational Excellence certification (e.g., Lean Six Sigma Green/Black Belt, 5S, Kaizen).
Relocation assistance is available for this role.
The expected salary range for this position based on the primary location for this position of Holly Springs, North Carolina is $120,100 - $223,100. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
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Senior Level Microbiology Jobs: Frequently Asked Questions
How do I get a senior level microbiology job?
Employers at this level look for candidates who have moved beyond bench execution into ownership of outcomes, whether that means leading a method validation project, guiding junior scientists, or interfacing with regulatory teams. A strong publication record, demonstrated expertise in a specific microbial domain such as environmental, clinical, or industrial microbiology, and experience translating data into decisions all give candidates a meaningful edge over equally credentialed peers.
Which companies hire senior level microbiologys?
Companies hiring senior level microbiologys right now include Genentech, Regeneron, and Danaher Corporation, based on current listings on Migrate Mate as of August 2026. Hiring at this level typically comes from pharmaceutical manufacturers, contract research organizations, food safety companies, and government research agencies that need scientists who can lead programs rather than simply staff them.
Are there remote senior level microbiology jobs?
Yes, though availability depends heavily on the role type. About 0% of senior level microbiology openings are remote or hybrid as of August 2026, with remote options more common in regulatory affairs, bioinformatics, and scientific writing than in wet-lab or quality control positions that require hands-on instrument access.
What makes a microbiology role senior level?
A senior level microbiology role is defined by the scope of responsibility rather than task execution alone. Senior scientists own experimental design, interpret complex results with minimal oversight, mentor junior and mid-level staff, and often represent the team in cross-functional or client-facing contexts. The expectation is that you can set the scientific direction for a project, not just carry it out.
Which industries hire the most senior level microbiologys?
Senior Level microbiology roles concentrate in Education, Manufacturing, and Medical Devices, based on current listings on Migrate Mate as of August 2026. These sectors drive demand at the senior level because they require scientists who can manage compliance obligations, lead validation work, or guide research programs with real regulatory or commercial consequences.