Job Openings
Job Opening for Validation Specialist
The following website advertisement will be posted from
04/14/2025 – 05/08/2025
Validation Specialist needed w/Master’s degree or Foreign Equivalent in Biomedical Sciences or Biomedical Engineering or Pharmaceutical Engineering or Pharmacy and one (1) year experience as Validation Specialist or CQV Specialist performing following job duties:
Write and execute commissioning, qualification protocols (IQ, OQ and PQ), requalification, deviation resolution, traceability matrices and final reports. Use Met One Particle Counter, Haemonetics Cell Saver, Cell Washer, Centrifuges, Filter Integrity Tester, Pass through Boxes, -20°C Freezer, -75°C Freezer, Liquid Nitrogen Storage Freezer, Brooks Automatic LN2 Freezer, Controlled Rate Freezer, Walk-in Cold Rooms, -20°C & -25°C Trailers, CryoPods, Cryo Carts, CO2 Incubator, Refrigerator, Biological Safety Cabinets, Thawing Device and Spinning Rotator. Perform calibration verification, program temperature mapping study and create temperature mapping report for controlled temperature units using Kaye AVS, Kaye Validator, Kaye Val probes and MadgeTech loggers. Maintain all temperature mapping equipment and tools. Perform technical study to verify Grade C/ISO 8 conditions for production support area. Perform Temperature and Humidity profile study in Dispensary and production support area. Assist in closing the oldest CAPA by performing Requalification, decommissioning of -20°C 20ft Cold room, generating mapping report, final Summary Report and Deviations.
Job Locations:
Tampa, FL or unanticipated client sites within the U.S.
Must be available to travel and relocate to unanticipated client sites for temporary projects.
Benefits: Health Insurance & PTO.
Mail Resumes to:
ND Global Consulting Services, Inc.
Job Opening for Validation Engineer
The following website advertisement will be posted from
04/14/2025 – 05/08/2025
Validation Engineer needed w/Master’s degree or Foreign Equivalent in Chemistry or Pharmacy or Pharmaceuticals Engineering and one (1) year experience as Validation Engineer performing following job duties:
Responsible for all respects of validation processes like- documenting commissioning activities, establishing the process and developing and performing qualification studies to provide a high degree of assurance that equipment and processes will consistently produce a drug product meeting its predetermined specifications along with quality attributes. Generate change control, CAPA and perform investigation for process deviations. Draft related protocols, develop validation strategies to maintain continuous improvement in cleaning and aseptic site environments. Execute development study and validation protocols which involves mock soiling of product contact surfaces, operation of equipment for cleaning procedure, collection of rinse water samples for bioburden, endotoxin, TOC testing, visual inspection and collection of swab samples. Draft summary report for various validation studies includes clean-in-place, clean hold study and sanitization-in-place performed for manufacturing equipment. Develop IOQ protocols for Water systems, HVAC, Clean air, Nitrogen, portable tanks, filtration systems, temperature control units and CIP. Prepare deviation reports and coordinate with the QA department for approval of deviation reports.
Job Locations:
Tampa, FL or unanticipated client sites within the U.S.
Must be available to travel and relocate to unanticipated client sites for temporary projects.
Benefits: Health Insurance & PTO.
Mail Resumes to:
ND Global Consulting Services, Inc.
Job Opening for Computer Systems Validation Engineer
The following website advertisement will be posted from
04/14/2025 – 05/08/2025
Computer Systems Validation Engineer needed w/Master’s degree or Foreign Equivalent in Data Analytics & Business Statistic or Computer Engineering or Computer Science and one (1) year experience as Computer Systems Validation Engineer or Software Validation Engineer or performing following job duties:
Draft, review and approve Validation Life Cycle (VLC) documents such as Validation Master Plan (VMP), specifying requirements (URS/ FRS), Develop Risk Analysis, Gap Analysis and Risk Management Procedures. Perform QA auditing and methodologies, Test Cases, Test Plans and Test Documentation. Design Specifications (DS), create protocols – Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and write Validation Summary Report (VSR). Review and approve Installation Qualification protocols (IQ) and Operational Qualification protocols (OQ). Implement Change Management/ Control and Corrective Action and Preventive Action (CAPA) procedures. Author and review Standard Operating Procedures (SOPs) and User Manuals. Use Integrated and data acquisition systems application for final review and approval of protocols. Resolve data integrity issues in qualification protocol to comply with company standards.
Job Locations:
Tampa, FL or unanticipated client sites within the U.S.
Must be available to travel and relocate to unanticipated client sites for temporary projects.
The occupation is only required to travel to National which is Tampa, FL or unanticipated client sites within the U.S for temporary projects based on the project length.
Benefits: Health Insurance and PTO.
Mail Resumes to:
ND Global Consulting Services, Inc.
