Globiox is a different kind of life sciences consulting firm, focused on providing its customers innovation, efficiency and results. We are always looking to add talented people to our team. We often have full time and contract positions available and we encourage contractors to send us their resume to add to our database. Contract opportunities are sent to our preferred network of consultants. If you would like to apply to be a Globiox Preferred Consultant please email us at

Below is a list of jobs that are currently available:

Contact Info

Interested in joining
our team?

(866) 609-7680

Job Title: Senior Consultant

Company: Globiox

Location: Multiple

Type: Full Time

Experience: Senior Level

Industry: Medical Devices, Pharmaceutical, Biologics, Laboratory, Biotech

Job Function: Consulting, Project Management, Auditing, Remediation

Job Description: • Provide consulting services to a variety of Globiox clients, including medical devices, pharmaceuticals, biotechnology, biologics, laboratories, CRO, suppliers, contract manufacturers • Develop relationships with potential customers and customers, and be able to describe how Globiox can help them • Analyze client situations and develop solutions • Provide and develop thought leadership in areas of expertise • Perform consulting services in an efficient, valuable, and communicative manner to the maximum benefit of clients • Perform project management duties, as needed, to ensure in-scope, on-time, within budget deliverables for clients • Mentor junior level staff, as needed • Occasionally produce training materials for staff or clients

Desired Skills & Experience:

  • 10+ years’ experience in life sciences, including a combination of medical devices, biologics, pharmaceuticals, or laboratory.
  • Extensive network of industry professionals
  • Leadership in professional organizations


  • Willingness to travel up to 90%
  • Ability to communicate effectively and successfully manage conflict
  • Excellent oral, written, & interpersonal communication skills
  • Knowledge of FDA and other international Quality System rules and regulations
  • Ability to interpret applicable standards and objectively make decisions
  • Excellent technical writing skills
  • Project management experience

Highly Desirable:

  • BS/BA degree
  • Entrepreneurial spirit
  • Bilingual or Multilingual
  • Project management certification

Send us your resume

Job Title: Computerized Systems Validation Engineer

Company: Globiox

Location: Remote

Type: Contract

Experience: 5+ Years

Industry: Life Sciences

Job Description: Globiox is seeking to add a Computerized Systems Validation Engineer to its team. Globiox is a consultancy headquartered in Austin, TX. We manage numerous validation projects around the country, and specialize in computerized systems validation. With Globiox, you will be working in a team-oriented environment, with priorities focused on generating innovative solutions to aid our clients. Globiox emphasizes constant communication with a team that has members living across the country. The ideal candidate will not only have the technical qualifications, but also be willing to fit within our company culture of team work, communication, and support. Duties include representing Globiox on CSV projects in the FDA regulated life-sciences industry. The candidate needs an excellent understanding of FDA requirements for computer systems in a regulatory environment, change control methodologies, creating and reviewing validation deliverables, and standard operating procedures. Validation of enterprise systems is required, such as ERP Systems, Argus Safety, Learning Management Systems, TrackWise, and Siebel Clinical Trials Management System. The candidate should also have excellent understanding of 21 CFR Part 11, GLP, GCP, GMP regulations, GAMP Methodologies and general Software Development Standards.

Desired Skills & Experience:

  • Over 5+ years of Computer Validation/CSV experience within the Biotech/Biologics/Pharmaceutical/FDA regulated industries
  • Thorough knowledge of cGMP/FDA regulations & work environment
  • Creating and Reviewing SOP's, Validation Master Plan, Traceability Matrix, IQ/OQ/PQ, Testing Documents, Data Migration Plans, Test Plans, Test Cases


  • Must be willing to travel
  • Must have a flexible schedule
  • Strong interpersonal skills, coupled with attention to detail, excellent review skills and analytical skills
  • Must have strong ability to organize and manage multiple tasks in a fast-paced environment

Highly Desirable:

  • Technical degree in related discipline (Computer Engineering, Engineering, Computer Science, etc.)
  • Experience validating TrackWise
  • Worked in small start ups

Send us your resume