Jobs at CORONA Remedies Limited

Supports international pharmaceutical business operations through MIS management, cross-functional coordination, product registration support, client and order management, financial modeling, market intelligence, and international event activities. Coordinates with regulatory, supply chain, production, quality, R&D, project management, and external clients. Requires pharmaceutical lifecycle knowledge, analytical skills, strong communication, and proficiency in Excel, PowerPoint, and SAP/ERP systems.

Manage formulation R&D projects from scope definition through commercialization, including roadmaps, milestones, risks, budgets, resources, technology transfers, validation, regulatory filings, and CMO/CRO coordination. Collaborate with R&D, quality, regulatory, manufacturing, packaging, and supply chain teams to resolve technical issues, manage change controls and CAPAs, and keep project deliverables aligned with regulatory and business timelines.

Manage regulatory documentation and dossiers across Modules 1–5 for new product registrations and renewals in emerging markets. Prepare, review, file, and submit technical dossiers while coordinating with cross-functional teams. Ensure regulatory compliance, product registration, lifecycle management, stakeholder coordination, and effective communication.

Leads electrical engineering, utilities, maintenance, and project execution for pharmaceutical OSD manufacturing facilities. Oversees electrical systems, capacity expansion, greenfield and brownfield projects, vendor management, energy optimization, GMP and EHS compliance, audit readiness, and validation documentation. Manages cross-functional engineering teams and ensures safe, timely, cost-effective project delivery and uninterrupted plant operations.

Leads global regulatory strategy and compliance across international markets, including product registrations, renewals, variations, submissions, dossier and labeling reviews, health authority interactions, inspections, audits, and GMP activities. Coordinates cross-functional stakeholders to support product launches and lifecycle management, resolves regulatory deficiencies, monitors regulatory changes, manages compliance risks, and mentors regulatory team members.

Manage formulation R&D programs from scope definition through technology transfer and commercialization. Develop roadmaps, timelines, budgets, and risk plans; coordinate R&D, quality, regulatory, manufacturing, packaging, supply chain, CRO, and CMO stakeholders. Track milestones, report status, facilitate change controls and CAPAs, support regulatory filings and deficiency responses, and manage vendor contracts and resource allocation.

Develops primary and secondary pharmaceutical packaging for new and existing products. Coordinates packaging material vendors, prepares specifications, artworks, and BOMs, and conducts compatibility and stability studies. Ensures compliance with WHO, USFDA, and EU requirements while managing change controls, deviations, and CAPA. Supports technology transfer and exhibit batches, collaborates with QA, QC, Production, and Regulatory Affairs, and oversees vendor qualification, performance, cost optimization, and alternative material development.

Procurement officer responsible for sourcing machine spares and consumables, developing vendors, evaluating quotations, negotiating prices, issuing purchase orders, tracking deliveries, managing AMCs and service orders, coordinating internal stakeholders, resolving supplier issues, and supporting timely vendor payments. The role is based at the corporate office in Ahmedabad and may require procurement-related travel.

Conducts quality-control analysis of raw materials, in-process and finished products, and stability samples for an OSD formulation plant. Operates and maintains analytical instruments, prepares and reviews COAs, STPs, and SOPs, and ensures cGMP, GLP, regulatory, and data-integrity compliance. Investigates OOS/OOT results and deviations, supports method validation and calibration, and maintains laboratory records and samples.

Supports sales teams by coordinating with internal departments, resolving field complaints and queries, preparing sales performance data, completing administrative tasks, and ensuring organizational compliance.

Performs analytical method development, validation, transfer, and routine testing for oral solid dosage formulations. Uses HPLC, GC, dissolution, UV-Visible, and FTIR instruments; conducts stability studies; prepares protocols, reports, specifications, SOPs, and testing procedures. Ensures cGMP, GLP, data integrity, and regulatory compliance; maintains laboratory and instrument records; investigates OOS, OOT, and deviations; and collaborates with formulation, quality, and regulatory teams during projects, audits, and inspections.

Performs analytical method validation, development, and transfer activities. Calibrates HPLC, GC, IR, UV, and dissolution instruments according to the master calibration schedule. Conducts routine analytical testing and maintains documentation for daily analyses.