Ritsa Pharma is a global pharmaceutical contract development and manufacturing organization providing services for commercialization of drug products by applying scientific principles and process controls for consistently delivering products of highest quality meeting the regulatory requirements cost effectively and timely.

Job Title: Accounts Manager / Assistant ManagerExperience: 10 yearsQualification: CA-Inter or Graduate (may or may not be CA qualified)Location: Madhapur - HyderabadWe are seeking a skilled Accounts Manager/Asst. Manager with 10 years of experience in books closure and taxation. The role involves overseeing monthly/annual books close, managing GST, Income Tax, and TDS compliance, and preparing financial reports like P&amp;L, balance sheet, and cash flow statements. The ideal candidate will ensure timely tax filings, handle audits, and supervise junior staff. Proficiency in accounting software (Tally, SAP) and Excel is required. The candidate should be detail-oriented, flexible, and capable of managing multiple tasks under pressure. Experience in budgeting and forecasting is a plus.

Job OverviewRitsa Pharma is seeking a dedicated Analytical Quality Assurance Specialist to join our Hyderabad office in a full-time, mid-level position. The ideal candidate will have 4 to 6 years of work experience in quality assurance and be skilled in API testing, which is a mandatory skill for this position. The candidate will thrive in a collaborative environment and contribute to ensuring the consistent quality of our drug products. Qualifications and Skills<ul><li>Proven experience of 4 to 6 years in quality assurance, demonstrating a solid understanding of testing methodologies and best practices.</li><li>Experience with API Testing (Mandatory skill) and a thorough knowledge of software testing principles and processes.</li><li>Proficient in Selenium with practical experience in designing and implementing test automation frameworks.</li><li>Strong working knowledge of JIRA for test management and issue tracking in a collaborative team environment.</li><li>Experience using Postman for efficient API testing and validation of project requirements.</li><li>Sound knowledge of Python for scripting and automating daily testing tasks to enhance productivity.</li><li>Ability to perform Regression Testing efficiently, ensuring no defects following major modifications.</li><li>Familiarity with TestNG and its application in organizing complex test cases effectively.</li><li>Experience in Agile Methodologies, adapting to the fast-paced environment while maintaining quality standards.</li></ul> Roles and Responsibilities<ul><li>Conduct thorough quality assurance on newly developed product lines to ensure they meet high-quality standards and regulatory compliance.</li><li>Design, develop, and execute test plans and cases for integration and system testing, prioritizing API testing.</li><li>Collaborate with cross-functional teams to identify, analyze, and troubleshoot issues, ensuring timely resolution.</li><li>Monitor and document testing results, providing analysis and insights to stakeholders for process improvements.</li><li>Continuously improve existing testing methodologies and automation practices to enhance the quality of output.</li><li>Stay updated with industry trends related to quality assurance practices and implement best practices at Ritsa Pharma.</li><li>Work collaboratively with development teams to integrate advanced testing techniques and tools seamlessly into the product lifecycle.</li><li>Participate in the lifecycle of project developments from requirements gathering through post-release, ensuring quality control at every step.</li></ul>

Company OverviewRitsa Pharma is a global pharmaceutical contract development and manufacturing organization headquartered in Hyderabad. We specialize in the commercialization of drug products, ensuring they meet the highest quality standards and regulatory requirements. Our operations integrate scientific principles and process controls to deliver cost-effective and timely solutions. With a team of 51-200 employees, Ritsa Pharma is a key player in the Pharmaceutical Manufacturing industry. Visit our website at <a href="https://www.ritsapharma.com/" rel="noopener noreferrer" target="_blank">ritsapharma.com</a> for more information. Job OverviewWe are seeking a qualified Document Life Cycle Management professional with a minimum of 4 to 6 years of work experience. This is a full-time, mid-level position based in our Hyderabad office. The selected candidate will play a crucial role in ensuring efficient management of documents throughout their lifecycle in compliance with regulatory standards. Qualifications and Skills<ul><li>Experience in regulatory compliance is mandatory for ensuring all documents adhere to needed standards.</li><li>Proficiency in clinical trial management is mandatory to oversee and document clinical trial processes efficiently.</li><li>Expertise in project management software is mandatory for organizing, controlling, and executing project documentation.</li><li>Proven ability to utilize pharmacovigilance systems to monitor, assess, and prevent adverse effects.</li><li>Understanding of market access strategy to facilitate successful document management for product distribution.</li><li>Knowledge of biostatistics to accurately manage and interpret data-related documents.</li><li>Competence in supply chain optimization for effective documentation in managing supply logistics.</li><li>Familiarity with health economics to document the economic evaluation of healthcare services.</li></ul> Roles and Responsibilities<ul><li>Manage the full lifecycle of documents from creation to disposal while ensuring compliance with regulatory requirements.</li><li>Coordinate with cross-functional teams to ensure the accuracy and completeness of document content.</li><li>Implement and maintain effective document version control processes.</li><li>Ensure timely access to documents for stakeholders to support business operations and decision-making.</li><li>Maintain a document management system that supports efficient storage, retrieval, and sharing of documents.</li><li>Collaborate with the project management and clinical trial teams to support documentation related to trial management.</li><li>Prepare and present reports on document status, ensuring management is informed of any risks or issues.</li><li>Stay updated with industry regulations and best practices to continuously improve document management procedures.</li></ul>

Company OverviewRitsa Pharma is a leading global pharmaceutical contract development and manufacturing organization. Our mission is to provide high-quality drug products, leveraging scientific principles and process controls. Headquartered in Hyderabad, we offer efficient and cost-effective solutions that meet stringent regulatory requirements. For more information, visit our website at <a href="https://www.ritsapharma.com/" rel="noopener noreferrer" target="_blank">https://www.ritsapharma.com/</a>. Job OverviewWe are seeking a talented Analytical Instrument Engineer to join our team at Ritsa Pharma in Hyderabad. This is a full-time, mid-level position that requires a pragmatic approach to managing our state-of-the-art instrumentation systems. The ideal candidate will have 4 to 6 years of related work experience and will be pivotal in maintaining and optimizing our analytical instruments to ensure they meet the highest industry standards. Qualifications and Skills<ul><li>Proficiency in instrumentation calibration to ensure accuracy and reliability of scientific measurements.</li><li>Experience with LabVIEW for developing and maintaining data acquisition systems for research and development processes.</li><li>Strong understanding of data acquisition systems necessary for capturing, analysis, and reporting data accurately.</li><li>In-depth knowledge of spectroscopy equipment used to identify chemical compounds in drug products.</li><li>Expertise in signal processing techniques to filter and interpret data generated by instrumentation systems.</li><li>Practical experience with PLC programming to integrate control systems effectively within laboratory settings.</li><li>Familiarity with HMI software to facilitate seamless human-machine interfaces, ensuring user-friendly operations.</li><li>Capability in using CAD software for instrumentation design, enabling the innovation of efficient drug manufacturing solutions.</li></ul> Roles and Responsibilities<ul><li>Perform regular maintenance and calibration of analytical instruments to ensure optimal performance and data accuracy.</li><li>Evaluate and troubleshoot instrumentation issues to minimize downtime in manufacturing and testing processes.</li><li>Collaborate with cross-functional teams to develop and refine instrumentation specifications for new projects.</li><li>Ensure compliance with all regulatory and safety requirements concerning laboratory equipment and processes.</li><li>Design and implement improvements in instrumentation to enhance data quality and streamline production activities.</li><li>Conduct training sessions for technical staff to familiarize them with new instruments and updated protocols.</li><li>Stay informed of industry advancements to integrate innovative technologies that boost Ritsa Pharma's capabilities.</li><li>Document and maintain accurate records of all inspections, calibrations, and corrective actions undertaken.</li></ul>