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Associate Director Microbiology Jobs (NOW HIRING)

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

$115K - $125K/yr

Associate Director, Laboratory Operations (GMP) - Oakdale, MN Compensation: $115,000 - $125,000 per ... Bachelor's degree in Chemistry, Biochemistry, Biology/Microbiology, Pharmaceutical Sciences ...

New

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

... or director. * Assure that specimen processing and testing performed are performed in a timely ... Associate's Degree in Medical Technology, Biomedical Science, Biology or Chemistry required

Showing results 41-60

Associate Director Microbiology information

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$34.5K

$70.6K

$126K

How much do associate director microbiology jobs pay per year?

As of Sep 10, 2026, the average yearly pay for associate director microbiology in the United States is $70,647.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,500.00 and $83,000.00 per year, depending on experience, location, and employer.

What does an associate director of microbiology do?

An Associate Director of Microbiology oversees the operations and strategic direction of a microbiology department within an organization, such as a pharmaceutical, biotech, or research institution. Their responsibilities often include managing laboratory staff, ensuring regulatory compliance, developing and implementing scientific protocols, and collaborating with other departments to support product development or quality assurance. They also play a key role in advancing research initiatives, maintaining safety standards, and mentoring junior scientists. This role requires strong leadership, technical expertise in microbiology, and experience in regulatory environments.

How does an associate director of microbiology typically collaborate with cross-functional teams within a pharmaceutical organization?

As an Associate Director of Microbiology, you will regularly collaborate with teams such as Quality Assurance, Manufacturing, Regulatory Affairs, and Research & Development. Your role involves providing scientific guidance on microbiological testing, interpreting regulatory requirements, and ensuring microbiological quality across products and processes. Effective communication and leadership are crucial, as you'll often lead meetings, review protocols, and troubleshoot issues alongside other department leads. This collaborative environment helps drive continuous improvement and ensures compliance with industry standards.

What are the key skills and qualifications needed to thrive as an associate director of microbiology, and why are they important?

An Associate Director of Microbiology typically requires an advanced degree in microbiology or a related field, extensive laboratory experience, and a solid background in regulatory compliance and quality standards. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP), and relevant certifications such as ASCP or similar are highly valuable. Leadership, strong problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies are critical to ensure scientific rigor, regulatory adherence, and successful team management within complex laboratory environments.

What is the difference between Associate Director Microbiology vs Microbiology Manager?

AspectAssociate Director MicrobiologyMicrobiology Manager
Required CredentialsBachelor's or Master's in Microbiology, relevant certifications (e.g., ASCP)Bachelor's or Master's in Microbiology, relevant certifications
Work EnvironmentLeadership role in labs, overseeing multiple projects, strategic planningSupervises daily lab operations, manages microbiology staff
Employer & Industry UsagePharmaceutical, biotech, or healthcare companiesResearch labs, manufacturing facilities, healthcare institutions
Search & Comparison IntentUnderstanding higher-level responsibilities and qualificationsFocus on daily management and operational tasks

The Associate Director Microbiology typically holds a higher strategic and leadership role, overseeing multiple projects and guiding microbiology teams, while the Microbiology Manager focuses on daily lab operations and staff supervision. Both roles require similar educational backgrounds and certifications but differ in scope and responsibilities.

What are popular job titles related to Associate Director Microbiology jobs?

For Associate Director Microbiology jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Microbiology job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $70,647 per year, or $34 per hour.

Associate Director, Laboratory Quality Operations

Morrisville, NC • On-site

Alcami Corporation
Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees

Full-time

Re-posted 17 days ago


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Associate Director, Laboratory Quality Operations is accountable for driving results in a fast-paced environment by continuously challenging the performance of quality standards, systems, and operating procedures. The Associate Director, Laboratory Quality Operations provides leadership to the site Quality team who perform quality review and approval of documents, data, protocols, qualifications, change controls, deviations, investigations, complaints, corrective action activities (CAPAs), and quality audits and inspections. This leader develops short and long-range goals, metrics, and objectives; directs the implementation of quality plans and works with lab management to ensure department goals and objectives are met. The Associate Director, Laboratory Quality Operations interacts with clients and regulatory agencies regarding quality issues, audits, and inspections.
On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.

Responsibilities
  • Ensures and is ultimately responsible for compliance of laboratory operations within established SOPs, FDA regulations as well as compendial requirements.
  • Collaborates with corporate quality functions to ensure site compliance with the company's Quality Management Systems (QMS).
  • Oversees QMS to ensure timely closure of deviations, investigations, corrective actions, etc.
  • Conducts thorough root-cause analysis for investigations.
  • Implements corrective and preventive actions to eliminate repeat observations.
  • Guides, instructs, and coaches members of management in compliance issues.
  • Leads regulatory inspections to ensure minimal observations.
  • Engages in client audits and client interactions.
  • Writes responses to regulatory and client audit reports.
  • Develops and implements systems to aid in efficiency and compliance improvements for the site.
  • Develops short and long-range goals and objectives for the site quality function.
  • Develops, implements, and maintains internal auditing program.
  • Ensures controlled documentation is generated, revised, approved, and maintained per corporate and regulatory agency procedures.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Attracts, develops, and retains a high performing team to meet the current and evolving needs of the business through effective selection, training and development, coaching and mentoring and performance management.
  • Other duties as assigned.

Qualifications
  • Bachelor's degree (Chemistry, Biology, Microbiology) required; master's degree preferred.
  • 10-12 years of related experience required, 12+ years preferred.
  • 10+ years of pharmaceutical quality experience required.
  • 7+ years of management experience required.
  • Prior pharmaceutical experience required; prior CDMO experience preferred.
  • Prior experience with controlled substance reporting and handling, final product release, major equipment validation, validation protocol review, process validation protocol review and APRs preferred.

Knowledge, Skills, and Abilities
  • Expert knowledge of pharmaceutical regulatory requirements and cGMP required.
  • Knowledge of quality systems and processes, change control, CAPA and data integrity required.
  • Knowledge of aseptic processing of commercial or clinical parenteral required for parenteral site(s).
  • Knowledge of auditing preferred.
  • Excellent skills in leadership, coaching and influencing others, strategic planning, critical thinking and problem solving, root-cause analysis and written communication and presentation skills required.
  • Strong computer skills.

Travel Expectations
  • Up to 10% travel required.

Physical Demands and Work Environment
The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 50 pounds and occasionally lift and/or move up to 100 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level is moderate. Occasionally, employee may be exposed to airborne particles and fumes. Occasionally, employee may be exposed to chemicals. Must have the ability to wear PPE including respiratory protection as required. Employee occasionally may be exposed to moving mechanical parts and vibration. Must have a valid drivers license and reliable transportation available to travel between local sites.

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