Jobs at HealthMinds Consulting Private Limited

Develop and maintain full-stack .NET applications supporting warehousing, transportation, dangerous goods, and trade compliance. Modernize applications by migrating servers, upgrading .NET and SQL Server versions, refactoring or decommissioning systems, and improving performance and reliability. Write optimized SQL and T-SQL, manage Git repositories and CI/CD pipelines in Azure DevOps and Octopus Deploy, collaborate with global stakeholders, conduct code reviews, and write unit tests.

Own brand positioning, content, campaigns, social media, influencer partnerships, media planning, external communications, events, and marketing performance. Serve as a strategic partner to the CEO/MD by managing priorities, preparing briefings, coordinating cross-functional initiatives, tracking follow-through, supporting special projects, and coordinating key engagements. Represent leadership externally while handling sensitive information and shifting priorities.

Develop and maintain mobile applications integrating medical device hardware and cloud services. Responsibilities include architecture, design, coding, code reviews, debugging, testing, documentation, deployment, and product support. The role participates throughout the product lifecycle, applies Agile methodologies and software design patterns, coordinates work with others, and supports regulatory and business requirements for medical products.

Create digital marketing advertisements, promotions, comps, and final artwork within brand guidelines. Apply strong design aesthetics, typography, color theory, visual identity, and illustration skills. Collaborate with peers, clients, and management, solve increasingly complex design problems, and deliver high-quality work with limited supervision. The role may involve overseeing small work efforts and working rotational US shifts.

Manage supplier quality processes for medical device or pharmaceutical suppliers, including supplier qualification, performance monitoring, quality agreements, SCARs, audits, requalification, and corrective actions. Maintain accurate supplier master data in SAP and ensure documentation is audit-ready and compliant with FDA, ISO, EU MDR, GMP, GDP, and internal quality requirements. Collaborate with Procurement, R&D, Operations, and IT to resolve supplier issues and drive continuous improvement.

Technically lead product security engineers; create and maintain SBOMs; analyze, triage, and track vulnerabilities; assess risk and prioritize remediation; automate vulnerability management with Python; document findings and support audit readiness, regulatory compliance, and medical device cybersecurity initiatives.

Develops and oversees product quality plans across the medical device lifecycle. Leads risk management, design quality reviews, verification and validation, design transfer, post-market quality analysis, and regulatory compliance. Applies FMEA, robust design, root cause analysis, statistical methods, and reliability practices. Evaluates design inputs including usability, performance, manufacturability, security, privacy, and serviceability, while reporting field quality performance and supporting corrective actions.

Lead end-to-end QA and proofing for creative and digital assets across multiple channels. Responsibilities include functional, cross-browser, responsive, accessibility, regulatory, and brand-compliance testing; validating content, links, forms, tracking, and metadata; managing defects; developing QA documentation; mentoring QA staff; monitoring quality KPIs; supporting audits; and identifying automation and AI-enabled quality improvements.

Develops and maintains automated test suites and frameworks for enterprise software supporting navigation and imaging systems. Owns module testing strategy, creates test protocols, performs code reviews, conducts functional, API, performance, load, and regression testing, and analyzes results for defect reporting. Guides teams on automation, deployment bottlenecks, engineering practices, and quality improvements while collaborating with product, development, and DevOps teams.

Supports global regulatory strategies for medical devices and combination products. Prepares FDA, EU MDR, and international submissions; maintains registrations and technical documentation; assesses product, manufacturing, software, supplier, process, and labeling changes; supports lifecycle management, audits, inspections, and regulatory research; and collaborates with R&D, Quality, Clinical, Manufacturing, Supply Chain, and Marketing teams.

Develops full-stack AI and machine learning applications using web technologies, statistical modeling, deep learning, databases, cloud platforms, and APIs. Designs algorithms, translates technical specifications into code, performs testing and debugging, documents solutions, and improves product and system performance. Works independently on complex initiatives, collaborates with stakeholders, mentors colleagues, and may manage projects or review others’ work.

Design digital and print assets for pharmaceutical and technology clients, including websites, brochures, banners, interactive PDFs, e-learning modules, and mobile experiences. Apply branding, typography, layout, responsive design, and basic web technologies across omnichannel deliverables. Maintain brand consistency, develop artwork and visual styles, review work, provide creative direction, and support timeline-driven projects. The role also involves collaboration, multitasking, and occasional use of video and motion graphics tools.