9 Regulatory Agencies Jobs

In this role as a Senior Financial Controls Analyst at Wells Fargo, you will have the opportunity to consult with the line of business and enterprise functions on financial reporting or information technology governance, controls, and oversight matters. Your key responsibilities will include identifying compliance and risk management requirements for the supported area, supporting the implementation of key risk initiatives, planning, executing, or providing oversight for testing and monitoring involving complex subject matter or control areas, providing technical interpretation on various matters, and communicating and consulting regularly with stakeholders throughout the enterprise. Additio...

As a Product Content Specialist III on the Digital Content Platforms team at Thermo Fisher Scientific, you will play a crucial role in handling new product content and content updates, supporting SOP documentation and training, prioritizing and managing content error requests, and collaborating with internal and external partners to enhance content health and ensure top-notch quality. Your exceptional communication and project management skills, along with a keen eye for detail, will be key to your success in this role. **Key Responsibilities:** - Partner with collaborators to collect product specifications and relevant data/metadata for highly structured product descriptions - Create SOPs, ...

As a Regulatory Affairs Specialist, you will be responsible for maintaining accurate records of regulatory submissions, approvals, and correspondence with regulatory agencies. You will have the following key responsibilities: - Prepare, review, and submit regulatory documents, including applications, reports, and renewals, to relevant regulatory agencies. - Determine the types of regulatory submissions or internal documentation required for situations such as proposed device changes. - Develop and implement regulatory strategies to ensure compliance with domestic and international regulatory requirements. - Monitor regulatory changes and updates closely, assess their impact on current and fu...

Role Overview: You will work as an experienced professional individual contributor in the area of Medical Affairs with limited supervision. Your role will involve applying subject matter knowledge to meet specific needs or requirements. Key Responsibilities: - Possess well-developed skills in overseeing direction, planning, execution, clinical trials/research, and data collection activities in the Medical Affairs Sub-Function. - Contribute to the implementation of clinical protocols and facilitate the completion of final reports. - Recruit clinical investigators, negotiate study design and costs. - Direct human clinical trials, phases III & IV for company products under development. - Partic...

You will be joining our Clinical Operations team in India, Mumbai as a full-time Experienced Study Start-Up Submissions Coordinator. Your role will be crucial in completing tasks and projects essential to our company's success. If you are looking for a rewarding career where you can utilize your expertise and further develop professionally, this opportunity is for you. At our company, we value expertise and empower our teams to leverage their unique skills and experience in research, problem-solving, and supporting our business partners. Our employees embody our values, work diligently, meet high expectations, and are rewarded with engaging projects, career progression, and exposure to globa...

As a Treasury Analyst at Wells Fargo, you will play a crucial role in managing and supporting global treasury activities. This includes overseeing funding, liquidity risk management, asset and liability management, capital management, financial performance management, and related activities. You will be responsible for monitoring and evaluating global market conditions to provide valuable advisory on treasury finance risk. Additionally, you will be in charge of complex reporting and analytics on treasury finance metrics, ensuring accurate recurring deliverables are completed and compliant with various treasury risk management regulatory requirements. Your role will also involve maintaining d...

Intas is a leading global pharmaceutical company dedicated to the development, manufacturing, and marketing of pharmaceutical formulations. Our mission is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain that spans across the world. With a presence in over 85 countries, including major global markets like North America, Europe, Latin America, and the Asia-Pacific under the brand name Accord Healthcare, Intas has achieved rapid expansion through organic growth and strategic acquisitions. We uphold high standards of quality, with products approved by leading global regulatory agencies such as USFDA, MHRA, and EMA. Our substantial in-house R&D ca...

The main purpose of your role as an experienced professional individual contributor in Medical Affairs is to work under limited supervision and apply your subject matter knowledge effectively. Your capacity to apply skills and knowledge should meet specific needs or requirements within the field. As an experienced professional in the Medical Affairs Sub-Function, you will be responsible for overseeing the direction, planning, and execution of clinical trials and research activities. You will play a key role in data collection, implementation of clinical protocols, and ensuring completion of final reports. Additionally, you will be involved in recruiting clinical investigators, negotiating st...

You should have 8-10 years of experience and a B.Sc./M.Sc. (Agri) or equivalent education with proven experience in certifications. Experience working in a commercial organization of scale and in the field of organic certifications with different agencies is required. Your key responsibilities will include spearheading and delivering end-to-end organic certification requirements of the company, collaborating closely with agriculture, processing, and finished goods teams. You will interact with regulatory agencies, respond to inquiries and submissions, and represent the company during inspections and audits. Experience in implementing Quality Management System (QMS), Vendor due diligence, str...