Regulatory Affairs Specialist

Description Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek so they can do what they do best: improve the...

Who You Are:You are skilled professional with deep understanding of regulatory frameworks and have a proven track record of managing the entire regulatory life cycle independently. Your ability to manage projects end-to-end makes you a valued contributor in achieving product approvals.How You ContributeManage the full life cycle of regulatory submissions for...

-Full Time Gurgaon Posted 5 days ago Job title Associate - Regulatory Affairs - Reports to Senior Associate/Astt Manager/Manager - Regulatory Affairs - **Job purpose**: To carry out Regulatory Review and Compilation of Technical documentation & dossiers for - Various Markets in compliance to applicable regulations and guidelines. - **Duties and...

**Senior DRA Executive (Regulatory Affairs)** Ø Preparation and reviewing of administrative documents. Ø Preparation and Review of Dossier in CTD,ACTD and ECTD Format. Ø Preparing the SPC and SMPC as per country guidelines. Ø Preparation of Dossier for CIS, Africa countries, Gulf Countries, and south India countries. Ø Review and Making of...

The Opportunity We are seeking a passionate and innovative Manager of NPD and Regulatory Affairs, to lead the development of new health supplement products for the Indian market. You will be responsible for the entire product development lifecycle, from market research and concept generation to product launch and post-launch monitoring. This exciting role...

Who You Are: You are skilled professional with deep understanding of regulatory frameworks and have a proven track record of managing the entire regulatory life cycle independently. Your ability to manage projects end-to-end makes you a valued contributor in achieving product approvals. How You Contribute Manage the full life cycle of regulatory...

Who You Are:You are skilled professional with deep understanding of regulatory frameworks and have a proven track record of managing the entire regulatory life cycle independently. Your ability to manage projects end-to-end makes you a valued contributor in achieving product approvals.How You ContributeManage the full life cycle of regulatory submissions for...

Who You Are: You are skilled professional with deep understanding of regulatory frameworks and have a proven track record of managing the entire regulatory life cycle independently. Your ability to manage projects end-to-end makes you a valued contributor in achieving product approvals. How You Contribute Manage the full life cycle of regulatory...

Preparation and compilation of DMF for US, EU, CEP, Canada, Japan, China, Brazil and other semi-regulated markets. Submission of technical data package and Applicants Part for semi-regulated markets Submission of response to deficiencies received from authorities and customers Periodic DMF updates (annual report for USDMFs and CEP renewal) and DMF amendments...

This position is primarily to support for ensuring pre-market & post-market regulatory compliances for import/ manufacture of Diagnostics/In vitro devices(IVD) and Medical devices under Medical Device Rule 2017 and other applicable requirements in India. This position will also support in fulfilling the regulatory requirements for these devices in zone...

- Ensure end-to-end management and tracking all company licenses, permits and registrations, ensure all are up to date and be responsible for such renewals and/or applications. - Propose, implement and validate timely action plans in response to regulatory changes in the market. - Provide regulatory approval to innovation projects as required. - Help...

**Responsibilities**: - **Regulatory Compliance**: - Stay abreast of current and evolving regulations related to Drug License and FSSAI requirements. - Ensure the organization's adherence to all applicable government regulations and standards. - **Drug License Application**: - Coordinate with regulatory authorities for timely approvals and compliance...

We’re looking for people who are determined to make life better for people around the world. Job summary The MAP is a therapeutically aligned Clinical Scientist who plays a key role within the Medical Affairs organization. The primary focus of this role is to use the individual’s knowledge of specific disease states, available treatments and...

**_Job Descriptions: _** - Â- Prepare and review technical documents, and dossiers in the format of CTD/ACTD. _ - Â- Check the compliance status of the Quality Systems. _ - Â- Evaluate and comment on requirements of Clinical studies. _ - Â- Prepare artwork of packaging materials as per current rules and regulations. _ - Â- Must have worked on ASEAN,...

Quality Systems Management: Develop, implement, and maintain quality systems and processes to ensure compliance with regulatory requirements, including Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP). - Document Control: Manage document control processes, including document creation, review,...

Job Title: SM /AGM-PR and Public AffairsLocation: GurgaonExperience: Minimum 7 to 12 years of experienceJob Summary:Pristyn Care is looking for a Senior Manager/Associate General Manager in PR and Public Affairs to oversee our communications strategy, drive brand reputation, and enhance relationships with key stakeholders. This role requires a seasoned...

We are looking to hire below positions for our "Regulatory and Compliance" team. Number of vacancies: 2Assistant ManagerExecutive/Sr. ExecutiveJob responsibilities : Oversee monitoring and management of regulatory matters related to recipe compliance, labelling, product registration, and food safety in multiple markets {Domestic retails, HORECA, MT, Ecom,...

We are looking to hire below positions for our "Regulatory and Compliance" team. Number of vacancies: 2Assistant ManagerExecutive/Sr. ExecutiveJob responsibilities : Oversee monitoring and management of regulatory matters related to recipe compliance, labelling, product registration, and food safety in multiple markets {Domestic retails, HORECA, MT, Ecom,...

About the role Finding better ways to provide the materials the world needs. The External Affairs (EA) team has accountability for engaging external stakeholders to positively shape Rio Tinto’s policy and regulatory environment, enhance our competitive position and build trusted partnerships in our priority markets around the world. With teams and country...

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a...