Reference 2500020E Responsibilities DEPARTMENT DESCRIPTION GLOBAL BANKING AND ADVISORY (GLBA) /Credit Portfolio Management Financial Assets and Insurance (GLBA/CPM/FAI) The mission of GLBA/CPM/FAI is to provide credit analysi...

About Antier SolutionsAntier Solutions is a global leader in blockchain, DeFi, and tokenization, driving regulatory-compliant Web3 innovations. As the industry evolves, ensuringlegal and regulatorycompliance is critical for s...

About Antier SolutionsAntier Solutions is a global leader in blockchain, DeFi, and tokenization, driving regulatory-compliant Web3 innovations. As the industry evolves, ensuringlegal and regulatorycompliance is critical for s...

About Antier SolutionsAntier Solutions is a global leader in blockchain, DeFi, and tokenization, driving regulatory-compliant Web3 innovations. As the industry evolves, ensuringlegal and regulatorycompliance is critical for s...

About Antier SolutionsAntier Solutions is a global leader in blockchain, DeFi, and tokenization, driving regulatory-compliant Web3 innovations. As the industry evolves, ensuringlegal and regulatorycompliance is critical for s...

A Regulatory Affairs Specialist ensures a company complies with all applicable regulations for its products, working with regulatory agencies to obtain approvals and maintain compliance throughout the product lifecycle. They ...

About the Role:We are looking for Government Relations professional based out of Chandigarh and will look after Haryana, Punjab, Himachal Pradesh and Jammu & Kashmir. He should be strong in stakeholder managemen...

Why join AliveCor ?At AliveCor, we imagine a healthier world powered by access to personalised intelligent information. Were on a mission to be the world s heart health partner by enabling access to quality heart care for eve...

Hiring for Manager Public Affairs, Communication & Sustainability (PACS) Location- Lotte Exp- 7-10 Years (5 Years in Manufacturing ) Key Responsibilities: Collaborate to design and develop plans to mitigate and mana...

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration.Dossier compilation as per guidelines.Compilation and review the product dossiers for submission in CTD, ACTD.Gap analysi...

Ensure ComplianceCommunication with Regulatory AgenciesDrug Development SupportSubmitting product registration dossiers, clinical trial documentationCOPP product wise approvalAuditRequired Candidate profileQualification B. Ph...

We are seeking a young and driven professional with prior hands-on experience working with the Ministry of New and Renewable Energy (MNRE). The ideal candidate will support the Corporate Affairs team in driving policy advocac...

Job Summary:We are seeking a highly motivated and detail-oriented Clinical Affairs Specialist with strong experience in post-market surveillance, Post-market Clinical Follow-up (PMCF), Periodic Safety Update Reports (PSUR), c...

Role & responsibilities Independent variation submission to UK Artwork/PIQ/Safety Submission to EU/UK Renewal submission to EU/UK Sunset Exemption to EU/UK Independent change control assessment EU CTD dossier understandi...

Educational Qualification:Degree in Mechanical Engineering, Electrical Engineering, Applied Sciences, or a related discipline. Professional Experience:10+ years of experience in Medical Device Regulatory Affairs with expertis...

Job Summary: The Assistant Product Manager/Product Manager is responsible for the strategic and operational management of diagnostic testing products. This includes managing the product lifecycle from concept to commercializ...

Degree in mechanical engineering, electrical engineering, applied sciences or a related discipline;10+ years of professional experience in medical device regulatory affairs EU MDR, US FDA 510(k) and closely working R&D, Q...

Immediate Joining | Remote | | Part Time - Visiting Faculty Impart Training Sessions for the students of Drug Regulatory Affairs Weekend Training SessionsPrepare presentationsDeliver Training SessionsJob ClassificationIndustr...

We need Regulatory Affairs Officer for a Reputed Life Science Company of Ahmedabad.Job ClassificationIndustry: Pharmaceutical & Life SciencesFunctional Area / Department: Legal & RegulatoryRole Category: Corporate Aff...

Preparation of DMFs for different markets in CTD and eCTD formats.Coordination with cross-functional dept to manage the documents.Supporting marketing team & QC/QA/R&D in various capacity.Preparation of Declarations a...

Deputy General Manager/ General Manager-Design & EngineeringLocation: AnandReporting to: Director Design & EngineeringAbout the role:The DGM/GM Design & Engineering will be responsible for overseeing product deve...

Title: Regulatory Affairs-CMC (Junior-Senior level)Location: 100% REMOTEExperience: 4-14 YearsIndustry: Pharmaceuticals / Life SciencesJob OverviewJoin our team as a Regulatory Affairs Specialist with 4-14 years of experience...

Exp.: Min 4 to 5 yearsDesignation: Executive- Regulatory AffairsLocation: MumbaiMust have Key Skills: CTD/ ACTD/ CMC/ technical review/ Dossier/ MOH queries/ Variations/ RenewalsOther essential skills: LATAM/ GCC/ MENA/ SEA/A...

8-10 yrs of expPrepare and Revise Architectural DrawingsCoordinate with Architects and EngineersConduct Site VisitsDevelop and Maintain Drawing StandardsEnsure Compliance with Industry Standards and RegulationsCAD & Revit...

1. Extensive experience in the pharmaceutical industry with a strong understanding of drug regulatory requirements and processes.2. Strong project management skills and the ability to lead cross-functional teams.3. Strong att...

Preparation of Sweets & Snacks:Assist in the preparation of traditional Indian sweets such as laddoos, barfis, jalebis, halwas, gulab jamuns, and other festive itemsHelp in making popular savory snacks like samosas, kacho...

Government and Public Affairs lead for the LEGOGroup in India; responsible for anticipating, analyzing and providing regulatory advice to the business. Driving strategic government engagement and enabling operating stabilit...

Core Responsibilities Government and Public Affairs lead for the LEGO Group in India; responsible for anticipating, analyzing and providing regulatory advice to the business. Driving strategic government engagemen...

1. Preparation of documentation for submission to FDA for medical device approval and/or response to FDA inquiries2. Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO14971:2012 & ...

(2 -4) Years of Work Experience in regulatory.WHO Collaborative countries having knowledge of Regulatory guideline viz ICH, EMEA , PIC.Job ClassificationIndustry: Pharmaceutical & Life SciencesFunctional Area / Department...