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Sap Gxp Jobs (NOW HIRING)

Spruce Infotech

SAP EWM Consultant

Dallas, TX · On-site

Lead large, complex SAP EWM implementations as part of broader S/4HANA and digital transformation ... Tailor EWM solutions to comply with Life Sciences GxP / validated environments including FDA / EMA ...

E*Pro, Inc.

SAP PP/QM Lead

Montgomery, NJ

SAP PP/QM Lead Ability to map the user requirements Ability to understand SAP manufacturing ... Knowledge of GXP Processes is required. Ability to collaborate in a cross-functional team ...

H R PUNDITS INC

SAP Project Manager

Carnegie, PA

SAP Project Manager Location: Remote Position: Fulltime Primary skills : SAP PM, S/4 HANA ... Experience in the pharma industry, including knowledge of FDA and GxP compliance for plant ...

Judge Group, Inc.

SAP Configuration Analyst

Lakewood, CO · On-site

$135K - $150K/yr

Develop and execute test scripts aligned to GxP/GAMP5/CSV standards. * Provide support during ... Hands-on SAP ECC configuration plus experience with S/4HANA transformations . * Practical exposure ...

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How much do sap gxp jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for sap gxp in the United States is $60.90, according to ZipRecruiter salary data. Most workers in this role earn between $54.09 and $69.71 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals working in SAP GxP compliance roles, and how can they be effectively managed?

Professionals in SAP GxP compliance roles often face challenges such as ensuring system configurations meet strict regulatory requirements, maintaining thorough documentation, and keeping up with changing compliance standards. Balancing the need for robust validation with the fast pace of system updates can also be demanding. Effective management involves collaborating closely with IT, quality assurance, and regulatory teams, as well as staying up-to-date with industry best practices and participating in ongoing training. Utilizing automated validation tools and maintaining clear communication across departments can further streamline compliance efforts.

What are SAP GxP jobs?

SAP GxP jobs refer to positions that involve implementing, managing, or supporting SAP software systems in environments regulated by GxP guidelines. GxP stands for 'Good Practice' quality guidelines and regulations, such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP), which are essential in industries like pharmaceuticals and life sciences. Professionals in these roles ensure that SAP systems comply with regulatory standards, support validation processes, and maintain data integrity. They often collaborate with quality assurance teams and regulatory bodies to ensure seamless compliance. These roles are critical for companies that must meet strict regulatory requirements while leveraging SAP's enterprise resource planning capabilities.

What is the difference between Sap Gxp vs SAP PP?

AspectSap GxpSAP PP
Primary FocusManufacturing execution, quality management, and shop floor operationsProduction planning, scheduling, and control
Required CertificationsSAP GXP compliance, SAP certificationsSAP PP certifications, SAP certifications
Work EnvironmentManufacturing plants, quality assurance labsManufacturing plants, production departments
Industry UsagePharmaceutical, biotech, regulated industriesManufacturing, process industries

While both roles involve SAP modules, Sap Gxp focuses on manufacturing execution and quality compliance, especially in regulated industries, whereas SAP PP centers on production planning and scheduling. Understanding these differences helps organizations assign the right SAP professionals for specific manufacturing needs.

What are the key skills and qualifications needed to thrive as an SAP GxP professional, and why are they important?

To thrive as an SAP GxP professional, you need in-depth knowledge of SAP systems, GxP (Good Practice) regulatory standards, and experience in compliance within regulated industries like pharmaceuticals or life sciences. Familiarity with SAP modules (such as SAP ECC or S/4HANA), validation tools, and regulatory frameworks like FDA 21 CFR Part 11 is typically required, and certifications in SAP or regulatory compliance are highly valued. Strong analytical thinking, attention to detail, and effective communication skills set candidates apart in ensuring compliant system operations. These competencies are critical for maintaining regulatory adherence, reducing business risk, and ensuring product quality and patient safety.

QMS & SAP Validation Analyst (Contract)

Kashiv Biosciences LLC

Piscataway, NJ • On-site

$65 - $75/hr

Contractor

Posted 22 days ago

Job description

Job Type
Contract
Description
Position Type: Contractor / Consultant - FTC (6-9 Months with possible extension)
Location: Piscataway, NJ (onsite - physical presence required) - OR - Chicago, IL (onsite - physical presence required)
Reports To: Sr. Director of IT
Rate: $65-$75/hour, not overtime eligible
Work Authorization: Must be authorized to work in the U.S. without sponsorship, now or in the future
Position Summary
We are seeking a Validation Analyst to support validation of our Quality Management System (MasterControl) and SAP implementation (QM, Materials Management, Production modules). This role works under the direction of a senior validation lead and partners with Quality, IT, and business functions to deliver validation artifacts in compliance with 21 CFR Part 11, GxP, and EMA expectations.
Essential Duties & Responsibilities
  • Support validation of MasterControl QMS - authoring and executing IQ/OQ/PQ protocols, traceability matrices, and validation summary reports
  • Support SAP implementation and validation activities across QM, MM, and PP modules, including test script authoring and execution under senior oversight
  • Contribute to risk assessments, data integrity assessments, and change control documentation
  • Liaise with QA, IT, business process owners, and external SAP implementation partners
  • Support periodic review and maintenance of validated state for assigned systems
  • Assist in audit and inspection readiness for MasterControl and SAP

Requirements
Position Requirements and Qualifications
  • Bachelor's degree in Life Sciences, Engineering, IT, or a lab-based role in life sciences with 3+ years of relevant experience; OR Master's degree with 1-2 years of relevant experience
  • Prior exposure to CSV activities in a GxP-regulated environment
  • Working understanding of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Experience authoring or executing validation protocols

Experience:
  • Exposure to MasterControl QMS (validation, administration, or end-user)
  • Exposure to SAP (any module, ideally QM, MM, or PP) in a GxP environment
  • Familiarity with GAMP 5 principles
  • Experience with ALCOA+ data integrity principles
  • Prior experience supporting enterprise system implementations in pharma, biotech, or medical device

Specialized Knowledge and Skills: •
  • Familiarity with GAMP 5 principles and risk-based validation
  • Exposure to Caliber LIMS
  • Exposure to SAP (QM, MM, PP) in a GxP context
  • Prior experience and acting as a liaison across IT, Quality, Lab, and ERP (SAP Preferred) and related systems.

Work Environment & Physical Demands: •
  • This is an on-site position at our Piscataway, NJ location - OR - Chicago, IL location•
  • Must be able to work extended hours or weekend hours, as may be required.

Noise: •
  • No extraordinary noise levels.

Standing/Lifting: •
  • Very unlikely, but can be able to lift at least 20 lbs.

Visual: •
  • No extraordinary requirements.

Stress: •
  • High-paced demanding environment to meet ambitious project goals.

Travel: •
  • Moderate domestic travel may be required.

Apply