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28 Medasource Systems Analyst Jobs Hiring Near You

Medasource

GMP Compliance Investigator

Durham, NC · On-site

Experience with electronic Quality Management Systems (QMS). * Project management experience. * Strong analytical and root cause investigation skills. * Excellent written and verbal communication ...

Medasource

$100 - $125/hr

Review project documents, Request for Information (RFI) submittals, and Hazardous Monitoring System (HMS) program documents * Perform waste analysis and design waste management programs to ensure ...

Medasource

R&D Formulation Scientist

Summit, NJ · On-site

$25 - $32/hr

Analyze consumer insights and contribute to innovation pipeline development * Maintain accurate ... Strong foundation in formulated systems (emulsions, surfactants, suspensions, structured liquids)

Medasource

CE-IT Engineer

Omaha, NE · On-site

$60 - $80/hr

Perform system validation, testing, and documentation for new device integrations or upgrades ... Strong troubleshooting and analytical skills across hardware and software environments. * Excellent ...

Medasource

Complaint Handling Specialist

Madison, WI · On-site

... cause analysis and corrective/preventive action documentation. * Support investigations and ... Experience working with electronic Quality Management Systems ( eQMS ). * Experience with ...

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Medasource Jobs Information

What is it like to work at Medasource?

Medasource is a healthcare IT staffing and consulting company that values collaboration, innovation, and customer satisfaction, fostering a dynamic and supportive work environment.

The company's team structure is designed to promote open communication and knowledge sharing, with a flat organizational hierarchy that encourages employee growth and development. Medasource's mission is to deliver exceptional service and expertise to its clients, while also providing opportunities for employees to make a meaningful impact in the healthcare industry.

Working at Medasource may appeal to candidates who are passionate about healthcare technology and enjoy a fast-paced, results-driven work environment, with opportunities for professional growth and development in a company that prioritizes employee satisfaction and well-being.

What makes Medasource an attractive place to work?

Medasource is a leading provider of healthcare workforce solutions, known for its expertise in staffing and recruitment services. The company offers a dynamic work environment that values collaboration, innovation, and employee growth, with opportunities for professional development and advancement. By joining Medasource, individuals can contribute to the company's mission of delivering exceptional healthcare staffing solutions and enjoy a stable and rewarding career in a rapidly evolving industry.

What other companies are hiring for Systems Analyst jobs?

What are the most popular jobs at Medasource?

What are the most popular categories at Medasource?

Infographic showing various Systems Analyst job openings at Medasource in the United States as of September 2026, with employment types broken down into 13% Full Time, and 87% Contract. Highlights an 97% Physical, and 3% Remote job distribution.

GMP Compliance Investigator

Durham, NC • On-site

Medasource
Health Care and Social Assistance • 201 - 500 employees
Learn more about Medasourceexternal

Contractor

Posted 28 days ago

Job description

GMP Compliance Investigator - Equipment & Facilities
Overview
Our client is seeking a GMP Compliance Investigator - Equipment & Facilities to support a GMP manufacturing laboratory focused on advanced cellular therapies. This individual will play a key role in maintaining compliance with FDA regulations and applicable accreditation standards by leading investigations, authoring quality documentation, and partnering closely with Manufacturing and Quality teams.
This is a highly collaborative role for someone with strong GMP quality experience, exceptional technical writing skills, and the ability to manage complex investigations from initiation through closure.
Responsibilities
  • Develop, revise, and maintain Standard Operating Procedures (SOPs) to ensure compliance with FDA and applicable regulatory requirements.
  • Author and manage change controls related to SOP updates and manufacturing process improvements.
  • Edit batch records and manufacturing documentation as needed.
  • Initiate, investigate, author, and close deviations, CAPAs, investigations, and quality memos.
  • Partner with Manufacturing and Quality teams to investigate manufacturing events and drive timely closure of quality records.
  • Serve as the primary author for equipment and facility-related deviation investigations.
  • Attend meetings with equipment vendors and internal stakeholders to gather information supporting investigations.
  • Author validation documentation, including IQ, OQ, and PQ protocols, equipment assessments, and validation reports.
  • Manage deviation, CAPA, and change control timelines to support on-time batch release.
  • Perform failure mode analysis and root cause investigations.
  • Support batch release activities from a compliance perspective.
  • Ensure compliance with FDA regulations and applicable accreditation standards.
  • Train and educate personnel on updated procedures, SOPs, quality systems, and compliance requirements.
  • Assist during FDA, accreditation, sponsor, and regulatory inspections, including responses to audit observations.
  • Monitor Quality Agreements to ensure sponsor notification requirements are met.
  • Participate in continuous improvement initiatives to optimize quality systems and documentation processes.
Preferred Qualifications
  • Experience working in a Quality Assurance or GMP Compliance function within an FDA-regulated manufacturing environment.
  • Experience supporting deviations, investigations, CAPAs, and change controls.
  • Strong technical writing skills with experience authoring investigation reports and SOPs.
  • Experience participating in FDA inspections, regulatory audits, and sponsor audits.
  • Experience with electronic Quality Management Systems (QMS).
  • Project management experience.
  • Strong analytical and root cause investigation skills.
  • Excellent written and verbal communication skills.
  • Strong organizational skills with exceptional attention to detail.
  • Ability to work independently while collaborating effectively across cross-functional teams.
Minimum Qualifications
Education
  • Bachelor's degree in Biology, Life Sciences, or a related scientific discipline.

Experience
  • Minimum of 6 years of Quality Assurance, Quality Systems, or GMP Compliance experience within a regulated manufacturing environment.
  • A Master's degree in a related field may substitute for two years of experience.

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