Quality and Regulatory Intern

**AM- Regulatory Affairs-International**: **Domnic Lewis has been Mandated to hire for AM- Regulatory Affairs-International** **Function / Department**: Regulatory Affairs - International Markets **Direct Reports**: None **Primary Purpose of the Role**: To ensure the timely preparation, review, and submission of high-quality regulatory dossiers for...

Dear Candidates,We have job opportunity for the position of Regulatory Affairs Executive & QMR in our leading manufacturing Medical Devices companies.Position:-Regulatory Affairs Executive & Quality Management RepresentativeExperience:-2 to 4 yrsGender:-Male/FemaleThe JD as follows:-· Maintain regulatory files. Maintain and update regulatory authorizations,...

Job Overview:We are seeking an experienced and visionary Head of Quality and Regulatory Compliance (QRC) to lead and oversee all aspects of Quality Assurance and Regulatory Affairs in India. This senior leadership role is responsible for ensuring compliance with Medical Devices Rules 2017 and global quality standards, while building and executing a long-term...

Job Purpose:To lead and support regulatory operations for agrochemical products across the Asia Pacific region, ensuring compliance with local regulations, facilitating product registrations, and enabling market access. This role is critical in aligning regional regulatory strategies with global business objectives.Regulatory Compliance & StrategyMonitor and...

Job OverviewThe Director of Quality and Regulatory Compliance will serve as a key member of the Global Sales leadership team. The incumbent is responsible for providing regulatory and quality leadership for the region.A comprehensive list of responsibilities includes:Ensuring compliance with global quality management systems and local regulations.Leading...

Research and interpret complex technical regulations and standards.Translate regulatory language into actionable guidance for internal teams.Design and implement policies, procedures, and systems to ensure regulatory compliance across the product lifecycle.Collaborate with cross-functional teams to embed compliance into operations.Compile and submit...

**Role & responsibilities** - ensure that a company's products comply with the regulations of the regions where they want to distribute them - keep up to date with national and international legislation, guidelines and customer practices - respond to queries from medical bodies like the Medicines and Healthcare products Regulatory Agency (MHRA) - collect,...

**Summary**: **About the Role**: **Major accountabilities**: - To author and review high quality clinical and safety documents: non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Risk Management Plans (RMP). 2. Lead for outsourced Narrative projects. Coordinate other outsourced activities in RWS. 3. Core member of...

Role & responsibilitiesDossier Preparation and Submission:Compile and review regulatory submissions in ACTD, CTD and formats.Ensure all regulatory documents are accurate, complete, and compliant with regulatory requirements.Review of Plant and R&D Data:Review R&D data to confirm compliance with regulatory expectations and assist in developing effective...

Our organization seeks a Quality Systems Manager to join our team. This is a pivotal role that requires a high level of expertise and leadership.Job DescriptionThe Quality Systems Manager will be responsible for establishing, implementing, and maintaining quality systems across the API manufacturing unit. This involves leading and participating in...