Intellex Acquires Expert by Big Village

We're thrilled to announce that Intellex has acquired Expert by Big Village, effective March 22, 2024. This strategic move enhances our capabilities and strengthens our commitment to delivering exceptional solutions to our customers.

Stay tuned for more updates on how this acquisition will benefit our clients and experts.

For inquiries or more information, please contact us at info@intellex.com.

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ID: 726156 Florida, USA

UV Inkjet Printers

Dynamic background includes developing and implementing products as well as directing large projects to on-time and within-budget completion. Resourceful and cost-conscious leader with a comprehensive knowledge base; track record of fueling growth while ensuring quality levels. Adept in profit &…

ID: 725858 India

Regulatory Affairs, Technology Management, Pharmaceutical Industry, Turnaround Management

Expert has experience in applying 21 CFR Part 11 to the manufacturing of pharmaceuticals and preparing and facing FDA inspections. He has more than 20 years of experience in various facets of API industry ranging from research to manufacturing, projects,…

ID: 725431 Nevada, USA

Quality Control, Quality Assurance, ISO9000, Forensic Pathology, Products Liability

Expert has over 40 years of progressively increasing experience in business beginning as an electronics technician, production planner, quality control engineer, quality manager, manufacturing manager, director of training and finally as a consultant, senior consultant, expert witness and now a…

ID: 724893 Virginia, USA

Nondestructive Testing including Radiography, Ultrasonic, Liquid Penetrant, Magnetic Particle

Expert is an ASNT (American Society for Nondestructive Testing) Level III certificate holder in UT (ultrasonic testing), RT (radiographic testing), MT (magnetic particle testing), and PT (liquid penetrant testing). He has held these certifications for 23 years and has recertified…

ID: 724439 Canada

ERP and Software Package Contract Negotiation for Customers, SLA\’s and Quality Assurance

Expert helped implement ISI9001:2000 in many software organizations. He also teaches graduate students and conduct research in this field. He is a member of the ISO committee that updates the international standards (TC 156). His specialty is software so he…

ID: 724356 United Kingdom

Automotive Supplier Development Engineer

He has experience of Continuous improvement activities at automotive and general product supplier sites has achieved Problem resolution using global 8D to address both plant and customer satisfaction issues. He is experienced in Problem prevention by the implementation of APQP,…

ID: 724172 South Carolina, USA

Textile Flammability and Dyes, QC for Color, Textile Environmental, Training

Expert has over 25 years experience with bleaching textile materials composed of cotton, flax, wool, polyester and viscose on a full range of equipment including continuous steaming(roller and flatbed), jiggers, pad-batch, jets yarn package, skein and garment laundry. He is…

ID: 724023 New York, USA

Global Strategic Sourcing and Supply Chain Management; Cost Reduction; International Trade Dispute Resolution; New Product Development; U.S. Harmonized Tariff Schedule

Expert manages the global supply chain for a $200 million U.S. consumer goods company. Expert excels at solving complex and unusual international supply chain problems, particularly those involving suppliers in Asia, and especially in China. Expert speaks, reads, and writes…

ID: 723910 Massachusetts, USA

Software Development, Technical Writing, and Project Management

Expert has experience with Software development tools for embedded systems engineers, marketing, project management, and technical publishing. The technical publications Expert develops show three essential qualities: close attention to the needs of the audience, correct content, and a clean look…

ID: 723891 India

Pharmaceutical Quality Assurance

He possess thorough knowledge of GMP / GLP regulations like US FDA, WHO GMP, ICH, MHRA, ANVISA, requirements of cGMP documents (SOP’s/ Change controls/ Deviations) as per various regulatory agencies. He had actively participated in various international regulatory inspections (USFDA…

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