Jobs at DAWAR CONSULTING INC

Manage GMP/GxP change control records from initiation through closure for Global Supply Chain. Track approvals, milestones, risks, and dependencies; coordinate cross-functional stakeholders, maintain trackers, report status, escalate delays, and drive continuous improvement of change control processes to meet QMS and compliance requirements.

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.

Support purification process development, characterization, scale-up, and GMP technology transfer for biologics. Execute lab-scale purification experiments, analyze data, document protocols and ELNs, support manufacturing investigations, mentor junior staff, and collaborate cross-functionally to implement purification platforms and new technologies.

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.

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.

Lead global Phase I/II clinical trial execution within early development. Oversee cross-functional Protocol Execution Teams, manage CROs/vendors, drive study start-up through close-out, ensure compliance with GCP/ICH, control budgets, mitigate operational risks, and mentor junior staff.

Lead configuration and support of SAP SD and MM on S/4HANA across OTC, procurement, billing, intercompany and integrations. Run requirements workshops, fit-gap, solution design, testing, and user support. Create functional specs for integrations and reporting, troubleshoot issues, and coordinate with technical teams while managing multiple projects.

Design, configure, and optimize end-to-end SAP SD Order-to-Cash processes. Run design workshops, translate requirements into functional/technical designs, configure and test SAP SD solutions, support integrations (IDoc, XML, APIs, CIF) with MM/WM, FI/CO, PP and external systems, produce documentation, and support full lifecycle implementations through go-live and hypercare in a regulated global environment.

Support records management and document control for engineering and construction projects: manage project documentation and electronic records, administer Autodesk Forma, upload/scan/archive documents, and ensure compliance with document management standards.

Support scientists and engineers by managing and improving R&D and enterprise tools, fulfill system requests, act as SME for applications, execute core R&D processes, identify and automate repetitive tasks, digitize administrative work, and ensure data integrity, compliance, and audit readiness.

Lead commercial procurement category strategies to optimize cost, quality, and supplier performance. Manage strategic sourcing (RFPs, negotiations, contracts), supplier relationships, spend analysis, forecasts, and cross-functional stakeholder alignment to deliver savings and continuous improvement.

Implement, configure, and maintain Benchling ELN to support process development and analytical teams. Develop integrations, automations, dashboards, and label templates, support Zebra printers, follow SDLC and CSV practices, collaborate with scientists, and produce documentation while participating in Agile processes.