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Full Time Gxp Systems Jobs (NOW HIRING)

Product Operations Lead

OR ยท On-site +1

$100K - $125K/yr

Review QA findings to determine whether issues are system defects, requirement gaps, or usability ... GxP Alignment: Ensure requirements and final release packages adhere to GxP compliance standards ...

... | Full-Time Join a growing field service team supporting critical environmental monitoring systems ... Maintain compliance with GMP, GxP, FDA, ISO, and regulatory standards * Travel to customer sites ...

... | Full-Time Join a growing field service team supporting critical environmental monitoring systems ... Maintain compliance with GMP, GxP, FDA, ISO, and regulatory standards * Travel to customer sites ...

PLS Scientist III

Oakdale, MN ยท On-site

$85K - $95K/yr

This is a full-time, onsite, Scientist 3 position located in Oakdale, MN, Monday through Friday, 8 ... Ensure compliance with all safety regulations, GxP standards, and internal quality policies.

Showing results 41-60

Full Time Gxp Systems information

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$46K

$102.1K

$153K

How much do full time gxp systems jobs pay per year?

As of Sep 2, 2026, the average yearly pay for full time gxp systems in the United States is $102,067.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What are GxP systems?

GxP systems are specialized software and processes used in industries like pharmaceuticals, biotechnology, and healthcare to ensure compliance with regulatory standards such as Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Good Manufacturing Practice (GMP). A full-time GxP systems role typically involves maintaining, validating, and supporting these systems to ensure they meet strict quality and compliance requirements. Professionals in this role work closely with quality assurance, IT, and regulatory teams to ensure data integrity and regulatory compliance throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as a full time GxP Systems professional?

To thrive as a Full Time GxP Systems professional, you need a solid background in computer science or life sciences, experience with regulatory compliance (such as FDA, EMA), and knowledge of Good Practice (GxP) guidelines. Familiarity with validated systems, electronic records management tools, and common industry software like Veeva Vault or SAP is typically required. Attention to detail, strong problem-solving skills, and the ability to communicate effectively with cross-functional teams set top candidates apart. These competencies ensure systems are compliant, reliable, and support the integrity of regulated processes within the life sciences industry.

What are some common challenges faced by professionals working in full time GxP Systems roles, and how can they be addressed?

Professionals in full-time GxP Systems roles often face challenges related to maintaining regulatory compliance in a constantly evolving landscape. Staying current with global regulations, ensuring data integrity, and managing system validation can be demanding. Collaboration with quality assurance, IT, and business stakeholders is crucial to anticipate compliance risks and implement effective controls. Regular training, robust documentation practices, and proactive system monitoring are key strategies to overcome these challenges and support successful audits and inspections.

What is the difference between Full Time Gxp Systems vs Gxp Compliance Specialist?

AspectFull Time Gxp SystemsGxp Compliance Specialist
CertificationsGxP-related certifications, Good Practice trainingGxP certifications, regulatory compliance training
Work EnvironmentPharmaceutical or biotech manufacturing facilities, laboratoriesRegulatory departments, quality assurance teams
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsRegulatory agencies, pharmaceutical companies

Full Time Gxp Systems roles focus on managing and maintaining GxP systems within manufacturing or laboratory environments, ensuring compliance and system integrity. Gxp Compliance Specialists primarily handle regulatory adherence, audits, and documentation. Both roles require similar certifications and work in related settings, but their core responsibilities differ in scope and focus.

What cities are hiring for Full Time Gxp Systems jobs?

Cities with the most Full Time Gxp Systems job openings:

What are the most commonly searched types of Gxp Systems jobs?

The most popular types of Gxp Systems jobs are:

What states have the most Full Time Gxp Systems jobs?

States with the most job openings for Full Time Gxp Systems jobs include:

Field Service Manager - BSC & Cleanroom Certification

SOKOL GxP Services

Bensalem, PA โ€ข On-site

$43.27 - $57.69/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago


Job description

Location: Greater Philadelphia, PA (Home-based with regional travel)
Territory: Pennsylvania, New Jersey, and New York 
Employment Type: Full-Time 
Experience: 5+ years of directly relevant technical field-service experience 
Travel: Frequent regional travel with occasional overnight assignments 
Start Date: TBD 
Salary: $90,000–$120,000 annually (based on experience) + performance bonus opportunities

Position Summary 

SOKOL GxP Services is seeking an experienced, hands-on Field Service Manager to lead our controlled-environment certification operations across Pennsylvania, New Jersey, and New York.

This role combines technical field service, team leadership, regional operations, and customer relationship management. The successful candidate will perform and oversee biological safety cabinet and cleanroom certification, HEPA filter integrity testing, airflow studies, environmental monitoring, troubleshooting, repair, and other contamination-control services while leading a regional team of field-service technicians.

The ideal candidate has 5+ years of hands-on experience with biological safety cabinets, cleanrooms, HEPA-filtered systems, airflow testing, and related controlled-environment technologies. Current or former NSF/ANSI 49 Biosafety Cabinet Field Certifier accreditation is strongly preferred.

Key Responsibilities: 

Technical Services

  • Perform and oversee biological safety cabinet (BSC), cleanroom, laminar airflow workbench, and fume hood certifications.
  • Conduct HEPA filter integrity testing, airflow visualization (smoke studies), airflow measurements, room pressurization testing, and environmental monitoring.
  • Perform maintenance, troubleshooting, repair, calibration, and certification of controlled-environment equipment.
  • Ensure all work complies with NSF/ANSI 49, ISO 14644, USP <797>, USP <800>, and company quality standards.

Operations & Leadership

  • Lead, mentor, and develop field-service technicians.
  • Coordinate schedules, travel, workload, and equipment.
  • Maintain calibration records, certifications, inventory, and service documentation.
  • Promote a culture of safety, quality, and continuous improvement.

Customer Relations

  • Serve as the primary technical contact for clients.
  • Resolve technical issues and customer escalations.
  • Review certification reports and ensure timely, accurate deliverables.
  • Build strong client relationships through responsive, high-quality service.

Business Development

  • Support proposal preparation, technical consultations, and project planning.
  • Identify opportunities to expand services with existing and new clients.
  • Assist with recruiting, onboarding, and training new technical staff.

Requirements

Required Qualifications

  • 5+ years of hands-on experience in biological safety cabinet (BSC) certification, cleanroom certification, or controlled-environment testing.
  • Strong knowledge of HEPA filter integrity testing, airflow measurements, environmental monitoring, and calibration.
  • Experience maintaining, troubleshooting, and repairing controlled-environment equipment.
  • Leadership experience with the ability to mentor and develop field-service technicians.
  • Excellent problem-solving, communication, and customer service skills.
  • Ability to travel frequently throughout Pennsylvania, New Jersey, and New York, with occasional overnight travel.
  • Valid driver's license with a clean driving record.

Preferred Qualifications

  • Current or former NSF/ANSI 49 Accredited Biosafety Cabinet Field Certifier.
  • Experience with ISO 14644, USP <797>, USP <800>, and Annex 1.
  • Experience with airflow visualization (smoke studies), laminar airflow workbenches, and fume hoods.
  • Experience in pharmaceutical, biotechnology, healthcare, or other regulated environments.
  • Bachelor's degree in Engineering, Life Sciences, or a related field (or equivalent technical experience).

Benefits

Competitive hourly rate: $43.27 – $57.69/hr

Company vehicle or mileage reimbursement for business travel

Company-provided tools, and testing equipment

Medical, dental, and vision insurance

401(k) retirement plan with employer contributions

Voluntary life insurance, short-term disability, long-term disability, and accident insurance

Paid Time Off and company holidays

Company-paid professional development, including NSF recertification and technical training

Clear career growth opportunities, including advancement to Director of Operations