QC Microbiology Manager

Yoh Idibu ·jobs.yoh.com

Location Sacramento, California, United States
Salary USD 120,000 - 135,000 / year
Type Full time
Level Mid
Source Shazamme
Life Science
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A rapidly growing specialty pharmaceutical company is seeking an experienced Quality Control Microbiology Manager to lead all microbiological quality control activities and provide strategic oversight of the microbiology laboratory. This position is responsible for ensuring compliance with regulatory requirements, maintaining a state of inspection readiness, and driving continuous improvement across microbiology operations.

Position Summary
The QC Microbiology Manager provides leadership for all microbiological testing, environmental monitoring, contamination control, utility monitoring, and microbiological compliance programs. This role is responsible for laboratory staffing, budgeting, strategic planning, regulatory readiness, and operational excellence.

The successful candidate will serve as the site's microbiology subject matter expert and work cross-functionally to support product quality, patient safety, and business objectives. Position level will be commensurate with experience.

Key Responsibilities
Department Leadership
  • Manage all QC Microbiology laboratory operations and personnel.
  • Develop departmental goals, metrics, and strategic initiatives.
  • Establish staffing plans and oversee hiring, training, performance management, and succession planning.
  • Manage departmental budgets, resources, and laboratory capital projects.
Compliance and Regulatory Oversight
  • Ensure ongoing compliance with FDA, USP, cGMP, and applicable regulatory requirements.
  • Maintain laboratory inspection readiness at all times.
  • Lead microbiology support activities during regulatory inspections and customer audits.
  • Approve microbiology investigations, CAPAs, change controls, and risk assessments.
Technical and Scientific Leadership
  • Serve as site subject matter expert for microbiology and contamination control.
  • Provide oversight for environmental monitoring, utility monitoring, sterility assurance, and contamination control strategies.
  • Review and approve method validations, method transfers, and qualification studies.
  • Provide technical leadership for investigations involving contamination events, microbial recoveries, environmental excursions, and adverse trends.
Continuous Improvement
  • Develop and implement laboratory efficiency and automation initiatives.
  • Evaluate and implement new technologies and rapid microbial methods.
  • Drive continuous improvement and operational excellence programs.
  • Establish and monitor key performance indicators (KPIs) for laboratory performance.
Cross-Functional Collaboration
  • Partner with Manufacturing, Quality Assurance, Validation, Engineering, Regulatory Affairs, and Supply Chain teams.
  • Support new product introductions, process validations, and facility expansion projects.
  • Contribute to quality systems and site-wide compliance initiatives.
Knowledge and Skills
  • Expert knowledge of pharmaceutical microbiology, sterility assurance, and contamination control.
  • Extensive knowledge of USP microbiology requirements, FDA regulations, and cGMP standards.
  • Strong leadership and organizational management skills.
  • Experience leading regulatory inspections and responding to agency observations.
  • Strong project management, budgeting, and strategic planning capabilities.
  • Excellent communication and stakeholder management skills.

Experience and Qualifications
  • Bachelor's degree in Microbiology, Biology, or related scientific discipline required.
  • Master's degree preferred.
  • Minimum 8 years of microbiology laboratory experience.
  • Minimum 3-5 years of laboratory management experience.
  • Demonstrated experience supporting FDA inspections and regulatory audits.
  • Extensive experience with Sterility Testing, BET, MLT, Environmental Monitoring, Water Systems, PET, Method Validation, Disinfectant Qualification, Hold Time Studies, and Container Closure Integrity.
  • Experience in sterile manufacturing, compounding, biologics, or specialty pharmaceutical environments strongly preferred.

Benefits:
  • Competitive Pay
  • Medical, dental and vision coverage
  • Paid time off
  • 401k savings plan

#IND-SPG

Estimated Min Rate: $120000.00
Estimated Max Rate: $135000.00


What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, 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, disability, or status as a protected veteran.

Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice

Frequently asked questions

Who is hiring for the QC Microbiology Manager role?
Yoh Idibu is hiring for the QC Microbiology Manager position, a Shazamme client. Apply directly on the employer's career site.
Where is the QC Microbiology Manager job located?
The QC Microbiology Manager role with Yoh Idibu is based in Sacramento, CA, US.
What does the QC Microbiology Manager role pay?
Yoh Idibu lists the QC Microbiology Manager role at USD 120,000–135,000 per year.
Is the QC Microbiology Manager role full-time or contract?
This is a full time position at Yoh Idibu.
What experience level is the QC Microbiology Manager role?
The QC Microbiology Manager position is aimed at mid-level candidates.
How do I apply for the QC Microbiology Manager role at Yoh Idibu?
Apply directly on Yoh Idibu's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.
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