Jobs at DAWAR CONSULTING INC

Lead planning, coordination, and hands-on execution of email and lifecycle marketing campaigns. Manage end-to-end production (setup, QA, UAT, approvals, deployment, monitoring), partner with marketing, product, analytics and agencies, maintain workflows and documentation, and ensure compliance and stakeholder alignment.

Onsite, hands-on role supporting enterprise infrastructure across manufacturing facilities: Windows Server administration, VMware virtualization, Active Directory/Group Policy, networking (TCP/IP, LAN/WAN, DNS, DHCP, firewalls), Microsoft SQL Server, backup/disaster recovery, business continuity, and day-to-day operations. Uses ServiceNow for ticketing. Life-sciences or regulated environment experience preferred.

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 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.

Manage planning, delivery, and continuous improvement of leadership development programs for US Commercial teams. Coordinate virtual and in-person training, logistics, vendors, stakeholder communication, tracking of attendance and impact, and program reporting and sustainment.

Manage accurate bi-weekly payroll for a large, multi-state employee population using ADP WorkforceNow and Workday. Audit interfaces, process hires/terminations/LOAs, reconcile reports, resolve discrepancies, and ensure federal and state compliance while partnering with HR, Finance, and Benefits.

Coordinate global clinical labeling implementation, map and validate label content in Bartender, partner with Regulatory Affairs and quality teams, author SOPs and process improvements, and support labeling updates to ensure compliance with FDA, cGMP, and company requirements.

Manage end-to-end commercial labeling projects in a regulated pharmaceutical environment: coordinate artwork review cycles, route workflows in Veeva Vault, proofread artwork, track timelines and approvals, partner with regulatory/quality/supply chain/packaging/manufacturing and external vendors, and support label implementation including phase-in/phase-out and obsolete inventory tracking.

Perform oligonucleotide synthesis, purification, and characterization to support RNAi therapeutic discovery. Run HPLC and mass spectrometry, scale lead candidates for preclinical work, troubleshoot equipment, collaborate cross-functionally, and contribute to experimental design and literature reviews.

Provide expert clinical review and quality oversight of ICSR/AE cases, ensure regulatory-compliant case processing, monitor vendor performance and quality trends, lead process improvements, support inspections/audits, and prepare scientific documentation and training.

Support oligonucleotide therapeutic discovery through hands-on synthesis, purification, and characterization using automated synthesizers, HPLC, and mass spectrometry. Develop and optimize synthesis methods, troubleshoot processes and equipment, analyze data, maintain documentation, and collaborate with cross-functional teams to advance lead molecules and support preclinical scale-up.

Manage day-to-day communications team operations: coordinate calendars and events, support internal engagement, develop processes and documentation, enable cross-functional collaboration, and drive continuous improvement to increase efficiency.

Lead internal communications for the Research organization: build frameworks, governance, and templates; develop executive and employee communications; run engagement programs, change communications, and events; gather employee insights and measure communications effectiveness while partnering closely with senior leaders.

Design, develop, and deploy LLM-powered agentic AI workflows and RAG pipelines to automate pharmacometric and clinical pharmacology processes. Build human-in-the-loop systems, evaluation frameworks, and guardrails; integrate scientific knowledge into AI solutions. Produce production-ready code with engineering best practices, collaborate with cross-functional scientists and engineers, and support cloud deployment and stakeholder presentations.

Provide quality engineering oversight for cGMP maintenance, validation, and equipment monitoring to support commercial and clinical manufacturing. Review work orders, resolve EMS alarms, support CQV/CSV activities, manage quality risks, collaborate with cross-functional teams, monitor quality metrics, and ensure FDA and GMP compliance.

Manage full lifecycle of outgoing Material Transfer Agreements (MTAs): intake, negotiation coordination, execution, recordkeeping, and shipment coordination. Liaise with scientists, legal, tech transfer offices, and operations; ensure compliance, track deadlines, and support contract administration and post-execution activities in a fast-paced research environment.

Hands-on role optimizing and validating single-molecule NGS workflows: perform nucleic acid extraction, library prep, sequencing, run experiments, troubleshoot instruments and assays, apply DoE and statistical analysis, develop test cases, document results, and collaborate across assay, instrumentation, software, and bioinformatics teams.

Design, prototype, integrate, test, and validate robotic and mechatronic automation systems for lab and diagnostic R&D. Lead concept generation, experiments, troubleshooting, and cross-functional collaboration; contribute to IP and present technical results to stakeholders.

Coordinate and manage multiple clinical testing and laboratory services projects from initiation to completion. Develop project plans and timelines, track progress, mitigate risks, oversee sample workflows and reporting, liaise with pharmaceutical clients/CROs/sites, run meetings, maintain study data and reports, and promote continuous improvement in regulated clinical operations.

Maintain and govern SharePoint Online sites, manage permissions and security, improve content discoverability, and build lightweight business solutions using Power Apps, Power Automate, Forms, and Power BI. Partner with stakeholders to automate workflows, monitor adoption and site usage, and drive Microsoft 365 and AI tool adoption.