Jobs at DAWAR CONSULTING INC

Lead system-level design, testing, and troubleshooting of electro-mechanical devices. Develop and validate test methods, design test beds, analyze sensor data (Python preferred), author technical reports, support manufacturing process development, and manage defect lifecycle while collaborating with cross-functional teams.

Lead design, implementation, and optimization of filling and packaging equipment in a cGMP diagnostics environment. Manage cross-functional projects, support equipment qualification (IQ/OQ/PQ), maintain manufacturing documentation, drive automation and process improvements, and ensure compliance with ISO and FDA requirements.

Support development and manufacturing of consumable fluidic flowcells for DNA sequencing. Perform SolidWorks design support, dimensional and surface metrology, component testing and quality inspections, inventory and lab support, and collaborate with cross-functional teams on process development and assembly.

Coordinate interview lifecycle and candidate travel, support new-hire onboarding and IT/site access, manage calendars and virtual meetings, process POs/invoices and vendor requests, support office operations and shipping, and act as liaison among candidates, internal teams, and external stakeholders.

Manage end-to-end biospecimen acquisition and data workflows, ensuring accurate sample fulfillment and high data quality. Coordinate with R&D stakeholders and cross-functional teams (Procurement, Legal, Safety, Quality, Logistics), interact with external vendors/CROs, and meet project deadlines while maintaining regulatory compliance and complete documentation.

Hands-on Scientist to develop, optimize, and characterize lipid nanoparticle (LNP) formulations for nucleic acid delivery (mRNA/siRNA/DNA). Responsibilities include DoE-driven formulation optimization, DLS/Zeta/Ribogreen characterization, scale-up, stability and downstream processing support, data analysis, documentation, and cross-functional collaboration for in vitro and in vivo studies.

Design and improve learning data reporting and dashboards in Cornerstone, integrate Cornerstone and Workday data, conduct user research and usability testing, create wireframes and prototypes, design accessible reporting interfaces, and collaborate with L&D, HR, product, and technical teams to optimize reporting and UX.

Perform setup, calibration, testing, troubleshooting, and rework of electro-mechanical assemblies at system level in a cleanroom. Develop/interpret procedures from drawings, prepare technical reports, assist with specialized test equipment setup, and use fine measurement tools. Shift work with training on day shift and regular post-training night shift.

Provide strategic regulatory guidance for U.S. commercial pharmaceutical products. Lead Promotional Review Committees, review and approve promotional/marketing materials, advise on advertising claims, support FDA communications and Form 2253 submissions, and partner with Marketing, Medical Affairs, Legal, and Compliance to ensure FDA-compliant communications.

Conduct and design complex laboratory experiments supporting gene therapy projects. Execute bench work, analyze data, prepare technical reports and protocols, maintain GMP/GLP-compliant documentation, troubleshoot, and contribute as an expert team member or principal investigator.

Provide executive-level administrative support to the Wave Lead and leadership team (calendars, travel, expenses, meeting coordination). Manage leadership meetings, events, and stakeholder workshops. Support project management tasks including status reporting, documentation, templates, and change control. Lead or contribute to organizational projects, drive strategic initiatives, and act as a communication bridge between leadership and teams.

Lead design and delivery of end-user training for ASPIRE SAP S/4HANA deployments. Conduct needs analysis, develop role-based content, manage schedules/logistics, supervise coordinators, track training metrics, support hypercare and post-deployment learning.

Support contracting, supplier payment tracking, and Sunshine Act reporting for Clinical Development and Medical Affairs. Manage POs, accruals, and invoices; maintain contract records and CDMA tracking tools; ensure regulatory and process compliance; collaborate with Procurement, Legal, Finance, suppliers, and project teams; and assist on CDMA special projects.

Support daily biospecimen acquisition and management including inventory, processing, storage, distribution, shipment, and chain-of-custody. Use LIMS and maintain accurate records, assist with lab maintenance and process improvements, and follow SOPs and safety practices.

Perform high-throughput wet-lab clinical sample processing (DNA extraction, library prep, target enrichment, NGS). Design and execute experiments, analyze results, document findings and process improvements, and maintain organized electronic records.

Perform whole slide image acquisition and QC on clinical samples; support clinical research studies and trials; collect, analyze, and enter clinical data into LIS; ensure GCP and protocol compliance; maintain documentation; prepare reports and collaborate with pathologists and cross-functional teams.

Prepare and issue customer invoices, corrected invoices, and credit memos; resolve system issues blocking invoicing; follow up for missing documentation; track and escalate third-party system problems; prioritize workloads and deadlines; recommend process improvements and support special projects.

Design, develop, and optimize high-performance C/C++ software for advanced mask inspection systems. Collaborate with cross-functional teams to define and integrate system requirements, maintain and improve codebases, apply best practices in design and testing, and troubleshoot complex issues in Linux environments.

Support contracting, purchase order and invoice tracking, accruals, and Sunshine Act reporting for Clinical Development and Medical Affairs. Maintain contract records, ensure compliance with SOPs and purchasing/finance processes, collaborate with Procurement, Legal, Finance, suppliers, and cross-functional teams, and assist with CDMA projects.

Perform hands-on purification, characterization, and formulation of oligonucleotides using HPLC and UV-VIS. Support production operations under cGMP, OSHA, and SOPs, document data in SAP/LIMS, maintain equipment and supplies, troubleshoot processes, and contribute to scale-up and process improvement efforts.