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Associate Director Quality Control Microbiology Jobs

Cellectis

Director, Quality Control

Raleigh, NC · On-site

The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures ...

Cellectis Group

Director, Quality Control

Raleigh, NC · On-site

$120 - $150/hr

The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures ...

Eagle Labs, Inc

QC Microbiologist

Seminole, FL · On-site

$85K - $87K/yr

Quality Control Microbiology Supervisor Overview: Quality Control (QC) Microbiology Supervisor ... Control Manager, Director of Laboratory Operations, or Executive leadership. * Scheduling ...

Neogen

Lead QC Microbiologist

Lexington, KY

$25.25 - $33.25/hr

Lead daily QC microbiology laboratory operations, ensuring testing is performed accurately and in compliance with GLP, cGMP, and regulatory requirements. * Perform and oversee microbiological testing ...

Neogen Corporation

Lead QC Microbiologist

Lexington, KY · On-site

$25.25 - $33.25/hr

Lead daily QC microbiology laboratory operations, ensuring testing is performed accurately and in compliance with GLP, cGMP, and regulatory requirements. * Perform and oversee microbiological testing ...

Neogen

QC Microbiology Technician

Lexington, KY

$18.75 - $23.75/hr

We are seeking a detail-oriented QC Microbiology Technician to support validation activities that help ensure products are manufactured in accordance with applicable regulatory requirements, internal ...

Neogen Corporation

QC Microbiology Technician

Lexington, KY · On-site

$18.75 - $23.75/hr

We are seeking a detail-oriented QC Microbiology Technician to support validation activities that help ensure products are manufactured in accordance with applicable regulatory requirements, internal ...

WuXi AppTec

QC Analyst, Microbial

Middletown, DE · On-site

$22.50 - $30.50/hr

Associate or bachelor's degree in Microbiology, Biology, or related scientific discipline. * 1-3 years of QC microbiology experience in a GMP-regulated pharmaceutical or biotechnology environment ...

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$31K

$125.6K

$213.5K

How much do associate director quality control microbiology jobs pay per year?

As of Aug 14, 2026, the average yearly pay for associate director quality control microbiology in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced by an associate director quality control microbiology, and how can they be addressed?

As an Associate Director of Quality Control Microbiology, one common challenge is ensuring compliance with evolving regulatory standards while maintaining efficiency in testing workflows. Balancing the demands of rapid product turnaround with rigorous quality standards often requires strong leadership and problem-solving skills. Additionally, managing and mentoring a multidisciplinary team can present challenges in communication and training, particularly as new technologies and methods are introduced. Addressing these issues involves staying updated on industry best practices, fostering a culture of continuous improvement, and promoting open collaboration across departments.

What are the key skills and qualifications needed to thrive as an associate director quality control microbiology?

To thrive as an Associate Director Quality Control Microbiology, you need deep expertise in microbiology, quality control practices, regulatory requirements, and typically a relevant advanced degree such as an MS or PhD. Familiarity with laboratory information management systems (LIMS), GMP/GLP regulations, and certifications like ASQ or Six Sigma are highly valuable. Leadership, problem-solving, and strong communication skills set top candidates apart in managing diverse teams and collaborating across departments. These competencies ensure rigorous microbial quality standards, regulatory compliance, and efficient team performance in highly regulated environments.

What does an associate director quality control microbiology do?

An Associate Director of Quality Control Microbiology oversees the microbiology laboratory operations within pharmaceutical, biotechnology, or related industries. They are responsible for ensuring all microbiological testing, procedures, and documentation meet regulatory standards and company policies. This role includes managing a team of scientists and technicians, developing and validating test methods, troubleshooting laboratory issues, and ensuring the safety and quality of products. The Associate Director also collaborates with other departments to support investigations, audits, and compliance initiatives.
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Associate Director Quality Control Microbiology jobs near you
Infographic showing various Associate Director Quality Control Microbiology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Director, Quality Control

Cellectis

Raleigh, NC • On-site

Full-time

Re-posted 10 days ago

Job description


POSITION SUMMARY
The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and dug product (DP) manufacturing at the site. This role is accountable for ensuing the generation of accurate, reliable, and compliant analytical data to support product release, stability, and lifecycle management in accordance with global GMP requirements.
The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures inspection readiness data integrity, and continuous improvement of QC systems and processes. As a member of the site Quality Leadership Team, the Director partners cross-functionally with Manufacturing m QA, MSAT, AS&T, and Regulatory to support clinical and commercial manufacturing while advancing quality culture and operational excellence.
POSITION RESPONSIBILITIES
  • Provide strategic leadership and oversight of all QC activities supporting DS and DP manufacturing, including release testing, stability programs, and in-process testing.
  • Partner with AS&T to ensure the robustness and lifecycle management of the analytical control strategy including method qualification, validation, transfer, and performance monitoring.
  • Oversee analytical, microbiological, and environmental monitoring programs, ensuring compliance with GMP requirements and site contamination control strategy
  • Ensure data integrity, accuracy, and reliability of all QC data in accordance with regulatory expectations.
  • Establish and maintain inspection readiness, including hosting regulatory inspections and responding to health authority inquiries.
  • Drive timely and thorough investigations of OOS, OOT, and atypical results, ensuring appropriate root cause identification and effective CAPA implementation.
  • Ensure appropriate specifications, test methods, and acceptance criteria are established and maintained throughout the product lifecycle.
  • Oversee QC laboratory operations including resource planning, capacity management, and organizational capability development
  • Partner cross-functionally with Manufacturing, QA, MSAT, AS&T, and Regulatory Affairs to support batch release, process improvements, and regulatory submissions.
  • Lead continuous improvement initiatives to enhance laboratory efficiency, compliance, and right-first-time performance.
  • Develop and monitor QC performance metrics, identifying trends and driving actions to improve performance and compliance.
  • Build and develop a high performing QC organization, fostering a strong quality culture and technical excellence.
  • Participates in business sub-teams as a Subject Matter Expert (SME) to provide input on timeliness and to address analytical/microbiological related issues
  • Other responsibilities and duties as the company may from time-to-time assign

EDUCATION AND EXPERIENCE
  • Bachelor's degree in chemistry, Biology or related scientific discipline required, advanced degree preferred.
  • Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership roles.
  • Strong leadership skills with experience building and leading high-performing technical teams.
  • Experience managing environmental monitoring and contamination control strategies in GMP manufacturing environments.
  • Experience supporting DS & DP manufacturing in GMP environments.
  • Proven track record of regulatory inspection success and audit management.
  • Proven experience with laboratory method lifecycle management.
  • Experience implementing or optimizing laboratory systems and processes preferred.

TECHNICAL SKILLS / CORE COMPETENCIES
  • Deep expertise in GMP regulations applicable to QC laboratories supporting ATMPs.
  • Strong knowledge of analytical techniques (e.g. q/rt/ddPCR, flow cytometry, ELISA, cell-based assays, microbiological methods) and their application tin DS/DP testing.
  • Strong understanding of data integrity principles and regulatory expectations (ALCOA+).
  • Ability to operate effectively in a matrixed, cross-functional environment.
  • Strong problem-solving skills with a risk-based and science-driven approach.
  • Excellent communication skills with the ability to influence at site and executive levels.
  • Strong project management skills.

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