As an Apprentice at Eugia Pharma Specialties Ltd., a subsidiary of Aurobindo Pharma, you will be a part of the Production department focusing on Injectables Manufacturing. The role is based on-site in Bhiwadi, Delhi NCR, located 60 kms from Delhi. To qualify for this position, you should have completed ITI in Fitter/Electrical. An interest in pharmaceuticals and healthcare is essential along with good communication and interpersonal skills. You should also demonstrate a willingness to learn and take on new challenges. Join us at Eugia Pharma Specialities Limited, located at A-1128, Phase II, RIICO Industrial Area, Bhiwadi, Rajasthan 301019, and be a part of our global presence specializing in general injectables and oncology. Be a part of our journey in building an extensive specialty portfolio and investing in complex injectables and advanced R&D in Hyderabad.,
Company Description Eugia Pharma Specialities Ltd., a fully integrated subsidiary of Aurobindo Pharma, specializes in general injectables and oncology, offering a comprehensive portfolio across various therapeutic areas. The company operates globally, with facilities and teams in the USA, Europe, Brazil, Mexico, Canada, Colombia, ANZ, and other Emerging markets. Role Description This is a full-time on-site role for a Regulatory Affairs Associate, located in Hyderabad. The Regulatory Affairs Associate will be responsible for preparing and reviewing regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, and managing regulatory submissions across Emerging Markets. The position also involves coordinating with internal teams and regulatory bodies to ensure that all processes adhere to regulatory guidelines. Qualifications Skills in preparing and reviewing Regulatory Documentation Knowledge of Regulatory Compliance and understanding of Regulatory Requirements 04 - 08 years of experience in preparation of dossiers for Regulatory Submissions in Emerging Markets (Asia, Africa, CIS, MENA, Brazil, South Africa markets) Excellent analytical and problem-solving abilities Strong written and verbal communication skills Master’s degree in Pharmacy. Ability to work collaboratively in a team and interact with regulatory bodies
Role & responsibilities Ensure compliance with all regulatory requirements and company procedures/policies across microbiology laboratories at all manufacturing facilities sites. Act as SME Microbiology for conducting internal audits and reviewing compliance responses across the company . Initiate, review, and approve Quality Management System (QMS) elements such as Change Controls, Deviations, Exceptions, and PNCs in respective software platforms. Conduct audits for material suppliers, service providers, and contract testing laboratories. Prepare, review, and approve Standard Operating Procedures (SOPs) and Policies related to microbiological operations. Perform gap assessments of CQA procedures against current regulatory requirements and observations related to microbiology. Deliver training sessions on procedures, policies, and regulatory guidance documents. Review all microbiological activities including: Sterility testing, BET, MLT Environmental monitoring Culture handling, media preparation Water sampling and testing Trend analysis, LBPC, bioassay AET/PET, bioburden Cleaning/sanitization/fogging Disinfectant preparation, usage, and efficacy studies Gowning qualifications, hold time studies, method validations Review Aseptic Processes, including Media Fill simulations and associated documentation. Verify Audit Trails related to microbiology software systems. Review Microbiologist qualifications and training records. Oversee Isolate Identification and Library Maintenance for environmental and water isolates. Preferred candidate profile Experience with isolator/RABS technology. Familiarity with rapid microbiological methods (RMM). Proficiency in microbiology software systems and audit trail verification. In-depth knowledge of GMP, FDA, EU, WHO, and PIC/S guidelines. Experience in managing QMS systems and regulatory audits. Strong analytical, documentation, and communication skills.
Company Description Eugia Pharma Specialties Ltd., a subsidiary of Aurobindo Pharma, is a global leader specializing in general injectables and oncology with a diverse portfolio across multiple therapeutic areas. With facilities and teams operating in the USA, Europe, Brazil, Mexico, Canada, Colombia, ANZ, and other regions, Eugia employs over 4,000 professionals, including 150+ scientists driving innovation. Headquartered in Hyderabad, Eugia is committed to advancing healthcare through investments in complex injectables and cutting-edge research, focusing on developing peptides, long-acting injectables, and other advanced pharmaceutical solutions. Role Description This is a full-time, on-site role for a Finance Manager, based in Hyderabad. The Finance Manager will be responsible for overseeing financial planning, budgeting, and forecasting processes, analyzing financial data to provide strategic guidance, and ensuring compliance with regulatory and legal financial requirements. Key responsibilities include managing accounting operations, preparing financial reports, driving cost optimization initiatives, and collaborating with various departments to ensure the organization’s financial health. The role entails leading a team and supporting decision-making processes through solid financial insights. Qualifications Expertise in financial planning, budgeting, and forecasting Strong analytical and problem-solving skills to manage financial reporting and data analysis Proficiency in accounting principles, tax regulations, and compliance standards Experience in team management, leadership, and cross-functional collaboration Proficiency in financial software and tools, with strong knowledge of Microsoft Excel Excellent communication and interpersonal skills to present financial insights and strategies to stakeholders Master's degree in Finance, Accounting, Economics, or a related field (Chartered Accountant or MBA in Finance preferred) Prior experience in the pharmaceutical or healthcare industry is a plus Demonstrated ability to work effectively in a fast-paced, on-site professional environment