Agnitio Pharma

As a Documentation Officer at our company located in Ecotech-XI, Greater Noida, you will play a crucial role in managing various documentation tasks to ensure compliance with industry standards and maintain the confidentiality of technical and regulatory documents. Key Responsibilities: - Maintain and update inventory records for Impurities, APIs, and Chemicals, ensuring proper filing, placement, and retrieval on the company server. - Upload and manage product information on agnitio.co.in and company social media platforms for effective information management. - Develop and manage product labels, Material Safety Data Sheets (MSDS), and issue Certificates of Analysis (CoA) from raw data as part of technical documentation. - Support internal and external audits by providing accurate documentation and collaborate with QA, Regulatory, and R&D teams to ensure quality and compliance. - Uphold the confidentiality and integrity of all technical and regulatory documents. Qualifications & Skills: - Education: M.Sc. in Organic Chemistry, Biotechnology, Life Sciences, or a related field. - Experience: Minimum of 3 years in documentation, quality, or regulatory roles within the pharmaceutical or chemical industry. Freshers with relevant knowledge are encouraged to apply. Technical Skills: - Knowledge of GMP and GLP regulations and documentation practices. - Proficiency in MS Office (Word, Excel, PowerPoint) and electronic document management systems. - Understanding of APIs, impurities, chemicals, and MSDS. Soft Skills: - Strong organizational skills and attention to detail. - Excellent communication and teamwork abilities. - Ability to work independently and meet deadlines effectively. In addition to these responsibilities and requirements, joining our company offers you: - Professional Growth: Opportunities for learning and professional development in the pharmaceutical and chemical sectors. - Competitive Compensation: A competitive salary based on qualifications and experience. - Industry Exposure: Gain valuable exposure to regulatory, quality, and documentation practices.,