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Associate Director Quality Control Microbiology Jobs in Springfield, NJ

Ferring Pharmaceuticals

Director, Quality Control

Parsippany, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As Director, Quality Control you will be responsible for strategic leadership and oversight of the Quality Control (Analytical and Microbiology) function, including testing at contract labs for drug ...

Novartis

Site QC Head (Associate Director)

Millburn, NJ · On-site

$226K/yr

  • Medical

  • Retirement

  • PTO

Lead the Millburn Site QC function, about 40 associates, and manage resource allocation to ensure ... Prior / advanced experience within microbiology, environmental monitoring, sterility assurance is ...

USPL NUTRITIONALS LLC

Senior, Microbiologist

North Brunswick, NJ · On-site

$80K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Under the supervision of Quality Control Microbiology Manager and Lead Microbiologist, carry out activities in support of developing new methods for enumeration of probiotic strains, methods ...

CYNET SYSTEMS

Micro QC Analyst I

Ridgefield, NJ · On-site

$33 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

BA/BS in Microbiology/Biology with 2+ years' experience in CGMP, pharma or lab environment is ... Have previous quality control microbiology experience. * Experience in bioburden testing, membrane ...

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All JobsAssociate Quality Control Microbiology JobsAssociate Director Quality Control Microbiology JobsAssociate Director Quality Control Microbiology Jobs in Springfield, NJ

Associate Director Quality Control Microbiology information

See Springfield, NJ salary details

$32.3K

$130.8K

$222.3K

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 Springfield, NJ is $130,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,800.00 and $157,200.00 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.
Associate Director Quality Control Microbiology jobs near you
Infographic showing various Associate Director Quality Control Microbiology job openings in Springfield, NJ as of June 2026, with employment types broken down into 86% Full Time, 5% Temporary, 7% Contract, and 2% Nights. Highlights an 98% In-person, and 2% Remote job distribution, with an average salary of $130,792 per year, or $62.9 per hour.

QC Microbiology Engineer(s) I, III

Lynkx Staffing LLC

Saddle Brook, NJ

$25.75 - $34/hr

Full-time

Re-posted 24 days ago

Job description

Quality Control Microbiology Engineer(s) I, II, III Quality Control Microbiology Engineer I The “Quality Control (QC) Microbiology Engineer I” will support two local sites serving as a support role to clinical and/or commercial production. The QC Microbiology Engineer will perform microbiological testing including, but not limited to, growth promotion, microbial identification, sterility testing, Gram stain, and endotoxin. Under the direction of the Associate Manager of QC Microbiology, responsibilities of the QC Microbiology Engineer I will include but are not limited to: Microbiological Testing:
  • Growth Promotion
  • Microbial Identification
  • Sterility Testing
  • Gram Stain
  • Endotoxin
Equipment Monitoring:
  • Ensure equipment is in proper working conditions
  • Ensure all equipment is properly maintained/calibrated
  • Shipping of test samples and equipment to contract laboratories for testing
  • Complete all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
REQUIREMENTS
  • Associates degree in a science or relevant field required
  • Training in GxP/ GDP, Safety
  • Minimum 0-2 years of experience or equivalent experience.
  • Microbiology testing or within the biopharmaceutical industry experience preferred.
  • Proficient with computer software; Microsoft Office
  • Strong written and oral communication skills
  • Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, liquid nitrogen and noise levels
  • Must be able to work during the weekend, holidays and as required by the company
  • Duties, responsibilities, and activities may change at any time with or without notice.
QC Microbiology Engineer II The Quality Control Microbiology Engineer II will support two local sites serving as a support role to clinical and commercial production. The QC Microbiology Engineer II will perform microbiological testing including, but not limited to, growth promotion, microbial identification, sterility testing, Gram stain, and endotoxin. Under the direction of the Associate Manager of Microbiology, responsibilities of the QC Microbiology Engineer II will include but are not limited to: Microbiological Testing:
  • Growth Promotion
  • Microbial Identification
  • Sterility Testing
  • Gram Stain
  • Endotoxin
Equipment Monitoring:
  • Ensure equipment is in proper working conditions
  • Ensure all equipment is properly maintained/calibrated
  • Shipping of test samples and equipment to contract laboratories for testing
  • Produce documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
  • Writing/conducting investigations pertaining to microbiological testing
  • Develop and train QC Microbiology Engineer I personnel on relevant business processes
REQUIREMENTS
  • BA/BS in a science or relevant field required or equivalent experience
  • Minimum 2-4 years of experience with microbiological testing or within the biopharmaceutical industry.
  • Training in GxP/GDP, Safety
  • Proficient with computer software such as; Microsoft Office
  • MODA/LIMS
  • Familiarity with ISO and EU standards
  • Strong written and oral communication skills
  • Technical writing skills
  • Technical training ability
  • Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
  • Supervisory Responsibility
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, liquid nitrogen and noise levels.
  • Employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays, and as required by the company
  • Occasionally personal protective equipment may be required including lab coat, latex gloves, safety glasses and/or respirator.
  • Duties, responsibilities, and activities may change at any time with or without notice.
QC Microbiology Engineer III The Quality Control Microbiology Engineer III will support two local sites. Serving as a support role to clinical and/or commercial production. The QC Microbiology Engineer III will coordinate data for batch release, participate in project/client meetings, and author/revise microbiological testing procedures. Additionally, the incumbent will perform microbiological testing including, but not limited to, growth promotion, microbial identification, sterility testing, Gram stain, and endotoxin. Under the direction of the Associate Manager of Microbiology, responsibilities of the QC Microbiology Engineer III will include but are not limited to:
  • Documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
  • Coordinates microbiological testing data for batch release
  • Participation in project/client meetings and communications, providing scientific and technical expertise
  • Authoring/revising Standard Operating Procedures, Work Instructions, Forms, and Protocols
  • Review of investigations and documentation of non-confirming events and environmental excursions.
  • Apply expertise of compliance requirements to maintain an inspection-ready state.
  • Participate and act as subject matter expert during audits/inspections
  • Develop and train QC Microbiology Engineer II on relevant business processes
  • Processing of purchase orders for outsourced testing and lab supplies
  • Coordinates work orders
  • Other duties as assigned
REQUIREMENTS
  • BA/BS in a science or relevant field required or equivalent experience
  • Minimum 5-7 years of experience with environmental monitoring or within the biopharmaceutical industry
  • Minimum required training; GxP/GDP Training, Safety Training
  • Proficient with computer software such as; Microsoft Office, MODA/LIMS; Microsoft Visio (preferred); Netsuite (preferred); Maximo Asset Management System (preferred)
  • Proficient knowledge of ISO and EU standards
  • Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review.
  • Strong written and oral communication skills
  • Strong technical writing skills
  • Technical training experience
  • Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
  • Supervisory Responsibility; Direct reports
  • While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, liquid nitrogen and noise levels.
  • Must have the ability to work in a team-oriented environment and with clients.
  • Must be able to work during the weekend, holidays and as required by the company