Grow your IT career with client-focused technology work.

Job Duties

• Collect, clean, and validate data from multiple sources, including ERP systems, CRM platforms, supply chain databases, and flat files (Excel/CSV), ensuring accuracy and consistency.
• Use SQL and relational database tools (such as SQL Server, Oracle, or MySQL) to extract, transform, and analyze large datasets for business reporting and decision-making.
• Develop dashboards and reports using visualization tools such as Power BI and Tableau to monitor KPIs related to procurement, demand forecasting, logistics, and supplier performance.
• Perform statistical and predictive analysis using tools like Python, R, or Excel (PivotTables, Power Query, Macros) to identify trends, patterns, and anomalies in supply chain data.
• Support data integration projects by working with tools such as Azure Data Factory, ETL pipelines, or SSIS packages to consolidate data from multiple systems into a central warehouse.
• Work under supervision.
• Travel and/or Relocation to unanticipated Client sites throughout USA is required.

Education

Master's degree in Computer Science / Information Technology /Engineering (Any)/ Business/ Supply Chain Management or closely related field with Six (6) months of experience in the job offered or as an IT Consultant or Analyst or Programmer or Developer or Engineer or very closely related area.

Experience

Experience of Six (6) months working with Power BI, Tableau and SQL is required. Travel and/or relocation is required to unanticipated client sites within USA. International travel is not required. The frequency of travel is currently not known as it depends on the client and project requirement that cannot be currently anticipated. Employer provides Information technology services to various clients in USA and hence implementing projects will require such travel.

Hiring Contact

Designation: HR Manager

Job Duties

• Create submissions of Advertising and Promotional (Ad/Promo) materials to Office of Prescription and Drug Promotion (OPDP), division of the U.S. Food and Drug Administration (FDA).
• Process and publish submissions for Subpart H and Subpart E to OPDP.
• Prepare, review, and publish Advisory comments, correspondences, and TV commercial submissions to OPDP.
• Work on different simple, medium, and complex level submissions of various products promotional material types like Websites, Videos, Exhibits, Formulary Kits, Direct Mail, Print Ads, Slides, Electronic Detail Ads etc.
• Maintain promotional document and submission metrics; archive OPDP pieces and submissions.
• Participate in cross-functional Alignment meetings with Marketing and Ad/Promo teams and analyze the current workflow processes to improve and develop the overall 2253 promotional materials submission process.
• Compile the dossier in the required format of submission to the relevant agencies.
• Bookmark and hyperlink pdf documents using ISI Publisher tool.
• Prepare and submit 1571, 356h, 2252 submissions as per the requirements in association with the Regulatory team.
• Support with IND, NDA and BLA submissions for various health agencies (US and Canada).
• Work under supervision.
• Travel and/or relocation to unanticipated client sites throughout USA is required

Education

Master's degree in Chemistry/Pharmacy or closely related field with Twelve (12) months of experience in the job offered or as a Regulatory Affairs Specialist or very closely related area.

Experience

Experience of Twelve (12) months in Regulatory Affairs is required.

Hiring Contact

Designation: HR Manager