Hi Bharat Would you please help us to get resources for below skill set. PRMS Architect 1 x QAD Architect 1 x BPCS Architect 2x RF Functional/Architects.

Below are the JD's: ) PRMS Architect (Pharma Regulatory / RIMS / Product Registration) Role Summary Lead the design and implementation of Product Registration / Regulatory Information Management systems (PRMS/RIMS) supporting global regulatory submissions and lifecycle management.

Key Responsibilities Define solution architecture for regulatory systems aligned to global compliance (FDA, EMA, MHRA, ASEAN) Design and manage product registration lifecycle (submission, approval, renewal, variation) Integrate PRMS with: ERP systems (QAD / SAP / Oracle) Document systems (Veeva Vault / DMS) Ensure compliance with: GxP, 21 CFR Part 11, audit trails, validation processes Drive data governance and master data strategy for regulatory content Lead vendor evaluation, implementation, and global rollout Required Skills Strong experience in RIMS / PRMS / Veeva Vault RIM / similar platforms Deep understanding of CTD, eCTD, regulatory submissions workflows Knowledge of GxP, validation (CSV), data integrity Integration experience across enterprise applications Experience 10 years (with Pharma domain) 2) QAD Architect (Manufacturing ERP – Pharma) Role Summary Define and lead architecture of QAD ERP solutions for Pharma manufacturing, supply chain, and quality processes.

Key Responsibilities Drive end-to-end QAD solution architecture across: Manufacturing (MRP, production planning) Supply chain (procurement, inventory) Quality (batch, compliance) Translate business needs into ERP solution design and configuration [interviewguy.com] Lead integration design with: MES,



LIMS, WMS, Serialization systems Ensure batch control, traceability, expiry and compliance requirements Support ERP transformation, global template and rollout strategy Provide architecture governance & design authority Required Skills Strong experience in QAD (Functional + Technical) Knowledge of Pharma manufacturing & GMP compliance Experience in: Full lifecycle ERP implementation Integration (Boomi, APIs, middleware) Experience 8-10 years 3) BPCS Architect (Infor LX / Legacy ERP) Role Summary Lead architecture, support, and modernization of BPCS / Infor LX ERP environments in manufacturing-heavy Pharma setups.

Key Responsibilities Manage and enhance BPCS / Infor LX architecture Define roadmap for: Legacy modernization / migration to cloud ERP Support modules: Finance, Manufacturing, Distribution, Inventory Ensure integration with: WMS, RF systems, MES, external systems Handle IBM i (AS/400) platform considerations Provide stability, performance optimization, and system upgrades Required Skills Strong experience in: BPCS / Infor LX ERP AS/400 / IBM i ecosystem Knowledge of: Manufacturing planning (MRP, DRP) Finance modules Experience in ERP upgrade / migration programs Experience 10–12 years 4 & 5) RF Functional / Architect (Warehouse Mobility / RFGen)



Role Summary Design and implement RF (Radio Frequency) / mobility solutions for warehouse and shop-floor operations integrated with ERP.

Key Responsibilities Design RF/mobile solutions for: Warehouse operations (receiving, picking, packing, shipping) Inventory transactions and tracking Implement solutions using: RFGen / Telnet / handheld RF devices Integrate RF systems with: ERP (QAD / BPCS / SAP / Oracle) Improve real-time data capture, inventory accuracy, and operational efficiency Define workflows for: Barcode scanning / RFID-based tracking Work with business teams to optimize warehouse processes and mobility solutions Required Skills Experience in: RFGen / WMS RF / warehouse mobility solutions Knowledge of: Supply chain & warehouse workflows Ability to design integration architecture with ERP systems [linkedin.com] Preferred Pharma warehouse exposure: Controlled substances Cold chain logistics Serialized inventory Business Impact Context RF-based mobility solutions improve inventory accuracy, efficiency, and real-time visibility of warehouse operations [rfgen.com] Experience 8–15 years Common Pharma Expectations (Add to All JDs – Highly Recommended) You should include this in your submission to make it client-aligned (Pharma-specific): Regulatory & Compliance Good Manufacturing Practices (GMP) GxP / 21 CFR Part 11 Data integrity & audit trails Functional Exposure Manufacturing, Supply Chain, Quality, Regulatory Batch management, traceability, recall management Delivery Experience Global rollout (multi-country) ERP transformation / digital manufacturing programs Robust stakeholder engagement (business + IT)

📌 1 x QAD Architect (Greater Toronto Area)
🏢 Info Way Solutions
📍 Greater Toronto Area