This Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidance s and defined regulatory strategies. He would even be responsible f...

Key Responsibilities:- Develop and implement global regulatory strategies to ensure product approvals.- Market access across multiple regions (FDA, EMA, MHRA, TGA, and Health Canada). - CMC expert in handling the Initial...

Key Responsibilities:Requirements gathering and regulatory analysisSupport with staffing strategy, screening, and interviewsRequired Expertise:Hands-on experience with ISO 13485 QMS, CDSCO dossiers, and/or FDA/...

Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desir...

• 4-7 years experiences for RA role in medical device and or pharmaceutical industry• Good understanding for regulations and policies issued by India, US FDA and EU, and ability to interpret international regulatory requireme...

Role & responsibilities We are hiring for the role of Executive - Regulatory Affairs department (API Industry )Preferred candidate profile Candidate with 3 to 6 years experience in the Regulatory Affairs (API Industry) ca...

Prepare, review, and file global premarket documents, collaborate with teams, develop regulatory strategies, and ensure compliance with India, US FDA, and EU regulations for medical devices or pharmaceuticals.Job Classificati...

JD for Position Sales manger 2. Location - mumbai Main responsibilities –a. Develop and manage relationships with government agencies involved in theprocurement of medical equipment, providing technical expertise, and delive...

Company Name - FairGaze Skill Pvt LimitedLocation - Noida Sector 81Designation - Sub EditorSkills -Creative Writing, Public Speaking, Marketing, Sales, Management, Communication Skills, Leadership, Journalism, EventsExperienc...

UMEDICA is a vertically integrated company engaged in the manufacturing and export of a wide range of finished formulations i.e., Tablets, Capsules, Suspensions, Dry Syrups and SVP, at UMEDICA's manufacturing facility, locate...

UMEDICA is a vertically integrated company engaged in the manufacturing and export of a wide range of finished formulations i.e., Tablets, Capsules, Suspensions, Dry Syrups and SVP, at UMEDICA's manufacturing facility, loca...

Educational Qualification-Post-graduate degree in Pharmacology or other Medical speciality/ Graduate degree in Medicine Minimum work experience- 6-12 years of relevant experience as Medical Advisor with a minimum of 3 years ...

Skills :FAINet inspectAPQPPPAPAerospaceJob ClassificationIndustry: Defence & AerospaceFunctional Area / Department: Production, Manufacturing & EngineeringRole Category: EngineeringRole: Engineering - OtherEmployemen...

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...