Top 67 Microbiology Jobs in Clayton Nc

Production & Processes Systems Improvement Specialist
Guerbet —Raleigh, NC
- Full-time
- Engineering
- Analysis skills
- Senior level
QC Senior Microbiologist
Guerbet —Raleigh, NC
- Full-time
- 5 years
- Master's degree
- Bachelor's degree
1d
Investigator
Guerbet —Raleigh, NC
- Full-time
- Microsoft Outlook
- Computer literacy
- Mid-level
12d
Medical Laboratory Scientist - Microbiology
Lighthouse Lab Services —Raleigh, NC
- Full-time
- Bachelor's degree
- In-person
- Senior level
- Paid holidays
- Relocation assistance
Quick Apply
QC Laboratory Systems Improvement Specialist
Guerbet —Raleigh, NC
- Full-time
- Senior level
- Radiology
- 10 years
Manufacturing QA Specialist
Guerbet —Raleigh, NC
- Full-time
- Mid-level
- 3 years
- Warehouse
1d
Analyst 1, QC Microbiology
FUJIFILM —Holly Springs, NC
- Call employer
- Bachelor of Science
- Mid-level
- Bachelor's degree
17h
Laboratory Tech (Andrologist)
Carolinas Fertility Institute, P.A. —Cary, NC
- $22 - $25 an hour
- 12 hour shift
- Anatomy knowledge
- Bachelor of Science
- Mid-level
Quick Apply
Supervisor, Environmental Monitoring
Indivior —Raleigh, NC
- $88,000 - $95,731 a year
- Full-time
- Mid-level
- 3 years
- Analysis skills
- Profit sharing
- Employee stock purchase plan
1d
Micro / EM Associate QC I
Amgen —Holly Springs, NC
- $62,571.90 - $84,656.10 a year
- Weekends as needed
- Inventory management
- High school diploma or GED
- In-person
- Disability insurance
- Health insurance
11d
Field Application Scientist- Mid-Atlantic
PerkinElmer —Raleigh, NC
- $90,000 - $110,000 a year
- Full-time
- Remote
- Classroom
- Mid-level
- Master's degree
11d
Environmental Health Specialist (Wastewater)
Johnston County, NC —Johnston County, NC
- $75,354.53 - $137,333.63 a year
- Full-time
- Background check
- Pass drug screening
- Mid-level
- Paid holidays
- Health insurance
BTEC Scientist
North Carolina State University —Raleigh, NC
- $63,000 - $88,000 a year
- Nights as needed
- Google Workspace
- Bachelor of Science
- Engineering
- Paid holidays
- Disability insurance
Clinical Applications Specialist I
bioMérieux —Morrisville, NC
- $67,800 - $86,200 a year
- On call
- Hybrid work
- Microsoft Outlook
- Writing skills
- ERP systems
- Commuter assistance
- Disability insurance
Quick Apply
11d
Material Management Systems Improvement Specialist
Guerbet —Raleigh, NC
- Full-time
- Mid-level
- Warehouse
- Manufacturing
QA Operations Sr. Manager
Guerbet —Raleigh, NC
- Full-time
- Master's degree
- Bachelor's degree
- Mentoring
Infection Prevention Cntrl Offcr LPN
Raleigh Rehabilitation Center —Raleigh, NC
- Weekends as needed
- Nursing
- Skilled nursing facility
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Case Educator - Rare Disease
McKesson —Cary, NC
- $32.78 - $54.64 an hour
- Monday to Friday
- Hybrid work
- Nursing
- RN License
- Word processing
Lab Computing Analyst
Zifo —Raleigh, NC
- $70,000 - $80,000 a year
- Full-time
- Mid-level
- Windows
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Consultant, Scientific and Laboratory Informatics
Accenture —Raleigh, NC
- $59,100 - $205,800 a year
- Full-time
- Computer Science
- Up to 50% travel
- System design
- Paid holidays
- Disability insurance

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Production & Processes Systems Improvement Specialist

Guerbet -
Raleigh, NC

Apply Now

Job Details

Full-time

Qualifications

Data integrity assurance
Chemical process control design
Defect resolution root cause analysis
Environmental monitoring in sterile processing
Document control experience within pharmaceutical industry
Cleanroom environmental monitoring
Contamination control
Cleanroom protocols
Sterile field contamination management
Pharmaceutical company experience
Compliance documentation
Regulatory/legal compliance standards in production
Cleanroom experience
Environmental monitoring
Production batch record review
Cross-functional collaboration
Cross-functional communication
FDA regulations
Failure analysis
Pharmaceutical manufacturing facility experience

Full Job Description

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 100 years, we continuously innovate to improve the diagnosis, prognosis and quality of life of patients.

Customer Centricity, Cooperation, Audacity, Focus, and Responsibility are the values that we share and practice on a daily basis.

Working at Guerbet is not only being part of a multicultural team with nearly 3,000 people across more than 20 countries, but it is above all about playing a unique role in the future of medical imaging.

WHAT WE ARE LOOKING FOR

The Production & Processes Systems Improvement Specialist will be operating in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for.

The Production & Processes Systems Improvement Specialist is responsible for driving CAPA plan deployment. This role ensures that all required improvements are implemented in a timely, compliant, and sustainable manner. The Specialist is accountable for elevating manufacturing procedures, batch documentation, process controls, and operator practices to align with FDA requirements and industry best practices for facilities producing terminally sterilized pharmaceutical products.

YOUR ROLE

Lead, coordinate, and independently oversee CAPAs originating from system assessments and remediation plans.
Ensure CAPAs are implemented on schedule with sustainable corrective and preventive actions.
Verify CAPA effectiveness through structured follow-up, trending, and objective evidence.
Track remediation progress and escalate delays or barriers to senior leadership.
Remediate and redesign manufacturing SOPs, batch records, work instructions, and in-process controls to enhance compliance.
Implement improvements to line clearance, material flow, equipment status control, and segregation practices across production areas.
Enhance shop floor documentation accuracy, real-time data entry practices, and logbook governance.
Ensure manufacturing processes align with regulatory expectations (e.g., FDA guidance for sterilization, environmental control, and cleanroom operations).
Collaborate with Engineering and Validation to develop or revise process control strategies, equipment parameters, and monitoring requirements.
Provide on-the-floor support to ensure operator practices, gowning, material handling, and data recording meet GMP standards.
Partner with Quality to ensure adherence to data integrity, documentation standards, and change control requirements.
Lead or support investigations into deviations, nonconformances, and process-related issues.
Performs other duties as assigned by management

YOUR BACKGROUND

Required Qualifications

Bachelor’s degree in Engineering, Life Sciences, or a related field (or equivalent combination of education and experience).
10+ years of experience in pharmaceutical manufacturing operations within GMP-regulated environments.
Extensive hands-on experience with batch record design, manufacturing controls, and process improvement within GMP facilities.
Strong understanding of cleanroom operations and environmental control principles, including classifications, airflow, and contamination control.
Ability to interpret and apply FDA guidance and global regulatory expectations.
Strong analytical, problem-solving, and root cause analysis skills.
Proven cross-functional collaboration, influencing, and communication abilities.
Strong attention to detail with a commitment to data integrity and compliant operations.

Preferred Qualifications

Experience in aseptic or terminal sterilization manufacturing environments.
Deep knowledge of terminal sterilization processes, including pressure cascade, HEPA filtration, and environmental monitoring strategies.
Hands-on experience with aseptic filling operations and airflow visualization (e.g., smoke studies).
Expertise in cleanroom behaviors, aseptic practices, and intervention minimization.
Background in microbiology, sterile operations engineering, or process engineering.
Experience supporting site remediation efforts, regulatory enforcement actions, consent decree environments, or large-scale compliance recovery programs.

Apply Now

Refine Your Search

microbiology jobs in clayton nc

Production & Processes Systems Improvement Specialist

QC Senior Microbiologist

Investigator

Medical Laboratory Scientist - Microbiology

QC Laboratory Systems Improvement Specialist

Manufacturing QA Specialist

Analyst 1, QC Microbiology

Laboratory Tech (Andrologist)

Supervisor, Environmental Monitoring

Micro / EM Associate QC I

Field Application Scientist- Mid-Atlantic

Environmental Health Specialist (Wastewater)

BTEC Scientist

Clinical Applications Specialist I

Material Management Systems Improvement Specialist

QA Operations Sr. Manager

Infection Prevention Cntrl Offcr LPN

Clinical Case Educator - Rare Disease

Lab Computing Analyst

Consultant, Scientific and Laboratory Informatics

I want to receive the latest job alert for microbiology in clayton nc

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