72 Regulatory Inspections Jobs

As a Regulatory Compliance Specialist at the Bank, you will be responsible for ensuring compliance with various regulations such as SEBI, IRDA, and AMFI for the third-party products distribution business. Your key responsibilities include: - Handling Regulatory Compliance for the Bank, including regulations from SEBI, IRDA, and AMFI. - Ensuring compliance with regulations related to Mutual Fund & Insurance Distribution Business. - Circulating action points from regulatory circulars/notifications and following up with stakeholders for timely implementation. - Reviewing processes, corresponding with regulators on compliance matters, and handling Onsite Regulatory Inspections. - Providing clari...

Location: Hyderabad Company: Early Bootstrap Startup Industry: Stock Broking / Financial Services Type: Full-time About the Client Our client is a new-age stock broking startup building a technology-driven investment and trading platform. The firm is in the process of obtaining SEBI registration and related regulatory approvals and is looking for a seasoned professional to lead and oversee all compliance functions. Key Responsibilities Lead and manage all regulatory and compliance activities for the stock broking business in accordance with SEBI, NSE, BSE, and other statutory bodies. Ensure the companys adherence to all applicable laws, circulars, notifications, and guidelines issued by SEBI...

As a Compliance Officer-AIF at our company, your main role will be to ensure end-to-end compliance with IFSC regulations, corporate laws, and other regulatory frameworks. Your responsibilities will include: - Ensuring full compliance with all regulatory requirements under SEBI and/or IFSCA jurisdictions. - Supervising investor onboarding, KYC/AML checks, due diligence of portfolio companies, and reporting. - Monitoring, interpreting, and implementing regulatory changes in internal policies and procedures. - Coordinating with trustees, auditors, valuers, fund administrators, and other stakeholders. - Tracking and maintaining compliance with SEBI AIF / IFSCA FME regulations, PMLA / AML-CFT rul...

As a Material Management Specialist, your role involves planning and controlling inventories of raw materials and packaging materials according to production requirements. You will coordinate with the Purchase and Quality Control teams to ensure timely availability and release of materials. It is essential to oversee the receipt, storage, and dispensing of materials following SOPs, MSDS, and safety requirements. Additionally, you will be responsible for managing return, rejection, and destruction of non-conforming materials in compliance with procedures. Your key responsibilities include: - Plan and control inventories of raw materials and packaging materials - Coordinate with Purchase and Q...

Key Responsibilities JOB DESCRIPTION Material Management Plan and control inventories of raw materials and packaging materials as per production requirements. Coordinate with Purchase and Quality Control teams to ensure timely availability and release of materials. Ensure receipt, storage, and dispensing of materials are conducted as per SOPs, MSDS, and safety requirements. Oversee return, rejection, and destruction of non-conforming materials in compliance with procedures. Compliance & Documentation Prepare, review, implement, and update departmental SOPs. Train and develop warehouse team members on SOPs and cGMP compliance. Ensure integrity and accuracy of cGMP and statutory records. Lead ...

Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accord...

Location: Hyderabad Company: Early Bootstrap Startup Industry: Stock Broking / Financial Services Type: Full-time About the Client Our client is a new-age stock broking startup building a technology-driven investment and trading platform. The firm is in the process of obtaining SEBI registration and related regulatory approvals and is looking for a seasoned professional to lead and oversee all compliance functions. Key Responsibilities Lead and manage all regulatory and compliance activities for the stock broking business in accordance with SEBI, NSE, BSE, and other statutory bodies. Ensure the companys adherence to all applicable laws, circulars, notifications, and guidelines issued by SEBI...

As a Drug Regulatory Affairs Specialist at Medyur Pharmaceuticals Limited, you will be responsible for ensuring compliance with regulatory requirements for our products and driving successful product launches. You will collaborate with cross-functional teams to maintain regulatory compliance and facilitate smooth communication with regulatory bodies. Key Responsibilities: - Prepare and submit regulatory documentation such as dossiers for pre-market submissions to obtain necessary approvals. - Stay up to date on current regulatory requirements, guidelines, and industry trends in global markets. - Develop and maintain strong relationships with regulatory bodies to support approvals. - Review c...

As a Quality Management System (QMS) Specialist, your role will involve establishing, implementing, and continuously improving the company's QMS to support its clinical-stage biopharmaceutical development programs while ensuring compliance with regulatory requirements such as FDA, EMA, ICH, and GxP standards like GMP, GDP, GCP, GLP. Your responsibilities will include: - **QMS Development & Implementation**: - Developing, implementing, and maintaining a phase-appropriate QMS aligned with regulatory requirements. - Establishing, reviewing, and updating Quality System documentation to support GxP operations. - Serving as the system owner for the electronic QMS and ensuring effective document co...

Location: Hyderabad Company: Early Bootstrap Startup Industry: Stock Broking / Financial Services Type: Full-time About the Client Our client is a new-age stock broking startup building a technology-driven investment and trading platform. The firm is in the process of obtaining SEBI registration and related regulatory approvals and is looking for a seasoned professional to lead and oversee all compliance functions. Key Responsibilities Lead and manage all regulatory and compliance activities for the stock broking business in accordance with SEBI, NSE, BSE, and other statutory bodies. Ensure the companys adherence to all applicable laws, circulars, notifications, and guidelines issued by SEBI...

As a Technical Assistant in our company, your role will involve providing technical guidance and support for onsite implementation and inspection readiness activities required for obtaining a Drug Manufacturing Licence. Your responsibilities will include: - Providing technical guidance for onsite implementation as per Schedule M. - Supporting management during regulatory inspections and compliance verification. - Identifying and guiding corrective actions needed for facility and process compliance. - Coordinating with internal teams to ensure all infrastructure and operational compliance measures are in place. The Qualifications required for this role include: - B.Pharmacy or B.Sc. in Analyt...

As an Audit Quality Control and Risk Management Director at Weaver, you will play a crucial role in ensuring the quality of audit engagements for investment fund engagements. Your responsibilities will include: - Performing audit engagement quality reviews for various types of investment funds - Ensuring full compliance with professional standards and firm guidelines - Overseeing and enhancing the firm's audit methodology and tools specific to hedge funds, private equity funds, venture capital funds, mutual funds, and other pooled investment vehicles - Driving continuous improvements in risk assessment, documentation quality, independence, and ethics compliance Qualifications required for th...

As a Senior Quality Auditor at Precision, you will play a crucial role in ensuring compliance with regulations and company procedures for clinical projects. Your responsibilities will include: - Supporting the Quality Management System by managing SOPs, training, and CAPA - Processing and maintaining documentation for controlled documents - Developing and administering training for employees and consultants - Hosting client/sponsor audits and supporting regulatory inspections - Coordinating and conducting assessments of vendors, including vendor audits - Conducting internal audits of quality systems, investigator site audits, and trial master file audits - Participating in computer systems v...

As the Compliance Risk Management Lead in the CCOR team, you will be responsible for implementing the firm's AML and anti-corruption programme in India for the Corporate and Investment Banking businesses. You will collaborate with business, location Compliance, and Line of Business Compliance to ensure programmes are aligned with firm policies, standards, and local laws. **Key Responsibilities:** - Implement the India AML programme, including risk assessments and trainings. - Assist in implementing the local AML investigations and SAR filing program, including local reviews and alerts arising from online and offline scenarios. - Liaise with FIU India and regulators, as the Alternate MLRO, fo...

Job Posting Title India Remote/Ahmedabad/Bengaluru/New Delhi Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accord...

Role Overview: Every day, everything you do will be driven by an unwavering commitment to delivering safe and effective products to patients. The quality culture at the company is both science and risk-based, designed to be flexible, innovative, and customer-oriented. Your role, whether it involves development, maintenance, compliance, or analysis through research programs, will be crucial and have a direct impact on patients. The dedication to quality and safety ensures that the highest standards are consistently met, making a real difference in the lives of those who rely on the products. Key Responsibilities: - Ensure compliance & on-time implementation of corrective actions/preventive ac...

Location: Hyderabad or Mumbai Company: Early Bootstrap Startup Industry: Stock Broking / Financial Services Type: Full-time About the Client Our client is a new-age stock broking startup building a technology-driven investment and trading platform. The firm is in the process of obtaining SEBI registration and related regulatory approvals and is looking for a seasoned professional to lead and oversee all compliance functions. Key Responsibilities Lead and manage all regulatory and compliance activities for the stock broking business in accordance with SEBI, NSE, BSE, and other statutory bodies. Ensure the companys adherence to all applicable laws, circulars, notifications, and guidelines issu...

As a Logistics & Compliance Executive, your role will involve overseeing end-to-end logistics operations to ensure the timely and cost-effective movement of goods. Your key responsibilities will include: - Managing daily logistics operations such as dispatch planning, coordination with transporters, and tracking. - Generating and monitoring E-Way Bills and E-Invoices in compliance with GST norms. - Maintaining accurate records for audits and regulatory inspections. - Liaising with cross-functional teams to ensure timely shipments and delivery. - Optimizing logistics processes to reduce costs and improve efficiency. The company is looking for a detail-oriented and proactive individual who can...

Job Title: Compliance Officer AIF/PMS Location: Mumbai (Andheri) Experience Required: 67 years About the Role: We are looking for an experienced Compliance Officer to manage and oversee compliance for our Alternative Investment Fund (AIF) and Portfolio Management Services (PMS) business. The role involves ensuring adherence to SEBI regulations, internal policies, and providing guidance to business teams. Key Responsibilities: Ensure compliance with SEBI (AIF/PMS) regulations, circulars, and reporting requirements. Draft, implement, and update compliance policies and internal controls. Monitor KYC/AML processes and investor onboarding. Handle regulatory inspections, audits, and filings. Liais...

As a Quality Head at Alutech Packaging Private Limited, your role will involve leading and overseeing the entire Quality function of the plant. You will be responsible for ensuring compliance with pharma packaging standards and customer requirements. Your key responsibilities will include: - Lead and oversee the entire Quality function of the plant - Ensure compliance with pharma packaging standards and customer requirements - Develop and implement quality assurance systems and procedures - Handle audits, certifications, and regulatory inspections - Drive continuous improvement in product quality and processes To excel in this role, you are required to have a minimum of 10 years of experienc...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Ho...

Role Overview: You will be responsible for ensuring the establishment, implementation, and maintenance of processes needed for the Quality Management System at the company. Reporting on the quality system's performance to the Head-QA for review and improvement will be a key part of your role. Additionally, you will plan and execute clinical activities, conduct audits, review equipment maintenance, data analysis, and support regulatory inspections. Key Responsibilities: - Ensure establishment, implementation, and maintenance of processes for the Quality Management System. - Report on the performance of the quality system to the Head-QA and suggest improvements. - Plan and execute clinical act...

Job Purpose This role requires a dynamic candidate who shall be pro-active part of second line of defence i.e. compliance function, independently set-up compliance paradigm and work with various stakeholders to ensure compliance culture is ensure. Role Prepare detailed compliance requirements of various circulars and guidelines issued by the regulators, assist in issuing compliance guidelines and verify their compliance on periodic basis, Assist & set-up development and providing clearance to various policies & SOPs of organization and ensure that Policy Compliance is being done on periodic basis, Evaluate various circulars / products / processes across the Company to assess the compliance r...

Job Summary: You will be responsible for overseeing and managing the validation processes of systems, processes, or products to ensure compliance with industry standards and regulations. Your role will involve extensive experience in system validation, quality assurance, and compliance management, with a focus on meeting regulatory requirements and ensuring operational efficiency. Key Responsibilities: - Lead and manage system validation activities for projects to ensure compliance with relevant regulatory standards such as FDA, GMP, ISO, and 21 CFR Part 11. - Develop and execute validation plans, protocols (IQ, OQ, PQ), and reports for systems and processes. - Coordinate with cross-function...

As an experienced candidate with 18 to 20 years of experience, your role will involve the following responsibilities: - Review and approve change controls initiated by plants and send to CQA for approval. - Review and approve vendor qualification documents and ensure effective implementation of the vendor approval system. - Organize and execute internal audits at all plants and corporate departments as per the annual planner. - Ensure audit reports and compliance reports with CAPA plan are prepared and implemented. - Monitor and ensure that all plants comply with cGMP, cGLP requirements and good documentation practices. - Review and approve of CQA guidelines. Update the CQA guidelines in lin...