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Associate Director Quality Control Microbiology Jobs

The QC MicrobiologySupervisor is responsible for the following: * Overseeing daily Quality Control Microbiology activities * Ensuring all testing/data review is completed within appropriate ...

$140 - $190/hr

Principal Scientist- Quality Control Microbiology Lead Date: 2 Aug 2026 Location: Baltimore, MD, US, 21224 Division: Manufacturing Services Job Title: Principal Specialist - Quality Control ...

$108 - $150/hr

Ensure proper oversight and guidance for direct reports in the areas of protocol development ... Own QC Microbiology performance metrics (e.g., turnaround time, right-first-time, on‑time testing ...

Job Title: QC Microbiology Specialist Location: Mahwah, NJ Type: Contract Compensation: $45/hr Work Model: Onsite Hours: 8am - 4pm or 9am - 5pm Responsibilities * Support onsite manufacturing of ...

Job Title: QC Microbiology Specialist Location: Mahwah, NJ Type: Contract Compensation: $45/hr Work Model: Onsite Hours: 8am - 4pm or 9am - 5pm Responsibilities * Support onsite manufacturing of ...

Job Title: QC Microbiology Specialist Location: Mahwah, NJ Type: Contract Compensation: $45/hr Work Model: Onsite Hours: 8am - 4pm or 9am - 5pm Responsibilities * Support onsite manufacturing of ...

Job Title: QC Microbiology Specialist Location: Mahwah, NJ Type: Contract Compensation: $45/hr Work Model: Onsite Hours: 8am - 4pm or 9am - 5pm Responsibilities * Support onsite manufacturing of ...

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 ...

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Associate Director Quality Control Microbiology information

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$31K

$125.6K

$213.5K

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

As of Sep 5, 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 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.

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 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.
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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, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

QC Microbiology Supervisor

INCOG

Fishers, IN

Full-time

Posted 12 days ago


Job description

The QC MicrobiologySupervisor is responsible for the following:

  • Overseeing daily Quality Control Microbiology activities

  • Ensuring all testing/data review is completed within appropriate timeframes

  • Delivering daily expectations and assignments

  • Providing in-lab support, as needed, and oversight of routine/on-demand testing

  • Providing coaching and feedback to Quality Control microbiology team


The QC Microbiology Supervisor will be involved in Quality Control deviation investigations, laboratory investigations and CAPA implementation. They will also influence the accomplishments of companywide and team goals and objectives as well as inspire team members while consistently modeling ALP values in all interactions.


This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) The Quality Control Supervisor will constantly evaluate the internal processes and procedures and work to create a productive space while maintaining the highest possible quality standards.


Essential Job Functions:

  • Provide technical support, oversite and team leadership for Quality Control Microbiology

  • Assist in the development of individual team members by providing mentorship to analysts/data reviewers and communicating with Quality Control Leadership on team performance.

  • Develop and improve current processes to maintain and control the general functions of INCOG Quality Control.

  • Assure compliance with cGMP requirements (current good manufacturing practices).

  • Perform laboratory walk-throughs and ensure laboratory spaces maintain inspection readiness and control.


Special Job Requirements:

  • This position will support primarily first shift (7 am to 4:30 pm).

  • Knowledge of Quality Control Microbiology, GxP principles, CAPA/Investigation management, and data/document review.

  • Familiarity with relevant quality and regulatory requirements and trends and cGMP's.

  • Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders.

  • Knowledge of Aseptic techniques and processing.


Additional Preferences:

  • 3-5 years demonstrated working knowledge of GMP laboratory operations.

  • 1-2 years in a people leadership role.


Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.


If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.


INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.


Qualified applicants must be authorized to work in the United States on a full-time basis. INCOG will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.


By submitting your resume and details, you are declaring that the information is correct and accurate.

Employment Type: Full-Time

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About INCOG

Sourced by ZipRecruiter

Industry

Public administration

Company size

51 - 200 Employees

Headquarters location

Tulsa, OK, US

Year founded

1967