Jobs at SAVA HEALTHCARE

Execute primary and secondary tablet packaging using blister, alu-alu, strip, and bottle packaging lines. Operate packaging equipment, perform line clearance and in-process quality checks, maintain packaging documentation and electronic records, ensure material accountability, and follow cGMP, SOP, data integrity, safety, hygiene, and regulatory requirements.

Coordinates sales order processing, fulfillment, billing, and communication across sales, supply chain, and finance teams. Maintains sales data, dashboards, customer and distributor records, and territory mappings. Generates performance reports, monitors distributor stock and secondary sales, supports incentives, budgeting, expense tracking, meetings, training, campaigns, and travel claims. Resolves customer and distributor queries while ensuring accurate, timely administrative support.

Leads the pharmaceutical Quality Control department at the Surendranagar site, overseeing chemical, instrumental, and microbiology laboratories. Ensures cGMP, GLP, ICH, and regulatory compliance; approves specifications and analytical reports; manages sampling, testing, stability studies, method validation, deviations, OOS investigations, CAPAs, documentation, product release, audits, and QC staff development. Collaborates with QA, Production, Regulatory Affairs, and other departments to maintain quality standards and support inspections.

Supports engineering operations at a pharmaceutical/API plant across electrical, instrumentation, control systems, mechanical maintenance, HVAC, utilities, stores, and equipment validation. Responsibilities include troubleshooting, preventive and breakdown maintenance, calibration, utility management, spare-parts inventory, installation and commissioning, qualification protocols, documentation, CAPA, change control, and audit support. The role requires GMP-compliant practices, technical coordination, SAP/ERP familiarity, and willingness to work rotational shifts.

Entry-level trainee role for graduates in pharmaceutical, life sciences, chemistry, biotech, microbiology, or engineering disciplines. Provides structured hands-on training across quality control, quality assurance, engineering, and production in a regulated pharmaceutical manufacturing environment. Responsibilities include developing documentation, observation, communication, teamwork, GMP, regulatory compliance, and operational excellence skills, followed by assessment-based progression to Officer or Executive.

Leads engineering and maintenance operations for a manufacturing plant, ensuring equipment reliability, plant uptime, utility continuity, safety compliance, cost control, and continuous improvement. Oversees preventive and predictive maintenance, breakdown reduction, RCA, CAPA, utilities, spare inventory, maintenance budgets, CMMS digitization, TPM, Lean Maintenance, and team capability development.

Perform quality control testing of raw materials, finished products, stability samples, and microbiological parameters in a regulated pharmaceutical manufacturing plant. Operate and calibrate analytical instruments, conduct method and process validation testing, maintain compliant documentation, support audits and inspections, investigate OOS/OOT results, and coordinate with QA, production, and regulatory teams to support product release.

Leads quality assurance for a regulated pharmaceutical manufacturing site, ensuring cGMP compliance, regulatory inspection readiness, QMS effectiveness, batch documentation, and product release. Oversees deviations, CAPA, change control, risk management, audits, vendor qualification, validation, and regulatory responses. Partners with production, QC, engineering, regulatory, and R&D teams while developing QA personnel and promoting a culture of quality. Requires extensive pharmaceutical experience and senior leadership in globally regulated environments.

Supports Regulatory Affairs by preparing and submitting CTD/eCTD dossiers for EU and ROW markets. Manages variations, renewals, deficiency responses, regulatory trackers, submission databases, document archiving, and audit support. Coordinates with QA, QC, Production, R&D, and other departments to ensure complete and compliant documentation. Requires knowledge of EU and international regulatory guidelines, strong documentation skills, attention to detail, and timeline management.

Manage receipt, storage, dispensing, issuance, and inventory control of pharmaceutical raw and packaging materials. Maintain accurate movement records, conduct stock verification, monitor inventory levels, and ensure Good Storage Practices, hygiene, safety, and regulatory compliance. Coordinate with Quality Assurance on material clearance, support audits and inspections, investigate discrepancies, and contribute to continuous improvement in warehouse and stores operations.

Provides first-level IT support across the organization, troubleshooting hardware, software, network, peripheral, account, email, and connectivity issues. Installs and maintains operating systems and business applications, supports backups and cybersecurity protocols, manages IT assets and documentation, coordinates with vendors, assists with video conferencing, and escalates unresolved issues to senior IT staff.

Manage day-to-day stores operations, including receiving, storage, issuance, labeling, inventory control, documentation, and stock reconciliation. Maintain FIFO/FEFO practices and accurate SAP/ERP records while supporting replenishment, audits, GMP compliance, safety, and housekeeping. Coordinate with QA, Purchase, Production, and Logistics teams to ensure efficient material flow and adherence to company procedures.

Coordinates pharmaceutical projects across R&D, QA/QC, Regulatory Affairs, manufacturing, and business functions. Tracks project progress, risks, issues, actions, and management reporting. Facilitates project meetings, governance dashboards, technology transfers, commercial batch manufacturing, and product lifecycle activities while supporting cross-functional stakeholders and ensuring timely completion.

Leads engineering and maintenance operations in a pharmaceutical manufacturing plant, ensuring equipment reliability, utilities availability, production uptime, safety, compliance, and cost optimization. Oversees preventive and predictive maintenance, plant utilities, CAPEX/OPEX budgets, installations, commissioning, qualification, validation, audits, vendors, contractors, spare parts, and regulatory compliance. Drives RCA, CAPA, TPM, Kaizen, energy efficiency, and continuous improvement while managing and developing the engineering team.

Supports companion animal product portfolio management, marketing strategy, market research, product lifecycle activities, promotional content, brand campaigns, sales training, and field-force coordination. Analyzes market and sales data, supports portfolio optimization, coordinates regulatory documentation and label approvals, and ensures compliance with internal SOPs and industry standards. The role helps drive brand growth and customer engagement across the companion animal health and nutrition segment.