197 fda jobs in India.

... thought partner aligned with the vision of the Medical Writing team. Independently research and authors response documents, reviews compendia, and prepares US FDA Annual reports with minimal guidance or supervision by the global and local Medical Information team. Proficient understanding of Medical Information achieved ...

How You’ll Make an Impact You shall be responsible to lead all the Occupational Safety, Risk mitigation efforts and handling Statutory Norms (MPCB, PESO, DISH, FDA, NMMC, Controller of Rationing, etc) related to government authorities of the site while propagating the corporate goal “Zero error, Zero Harm” at Turbhe and ...

... with Prototyping, writing Business Requirements, Functional Specifications and User Stories Desired Qualifications: - Familiarity with Medical domain standards & FDA requirements - Familiarity with embedded systems, networking, web and mobile platform.. - Familiarity with SW verification and SDLC. - Strong interpersonal skills, ...

... Develop, implement, and maintain GMP (Good Manufacturing Practices) and ISO standards for cosmetics production. o Ensure compliance with regulatory requirements (FDA, EU Cosmetics Regulation, BIS in India, etc.). 2. Raw Material & Supplier Quality Control o Establish and monitor quality standards for incoming raw materials, ...

... excellence in a highly regulated environment. Your key responsibilities Client Responsibilities - Lead global regulatory strategy development, ensuring compliance with FDA, EMA, MHRA, PMDA, and other health authorities - Provide expert guidance on regulatory submissions, dossier preparation, and lifecycle management across multiple ...

... cybersecurity experience. - Strong understanding of mitigating security controls . - Vulnerability Management, Penetration Testing, Code Security. - Good to have - FDA and other medical device regulators experience. Knowledge of cyber security standard frameworks such as HIPAA, FDA, ISO 27001/2, NIST CSF, and OWASP. - Understanding ...

... Apply engineering principles to the design, development, and testing of JD Edwards Human Capital Management. - Build solutions using JDE technologies such as RDA, FDA, TDA, NER, BSFN, OMW, ER Compare, Visual Studio, and data dictionary tools. - Design, support, configure, and maintain JDE application settings, processing options, ...

... impurity qualification, extractables and leachable assessments, and product safety profiles. - Monitor evolving global regulations and guidance documents (ICH, FDA, EMA, WHO, and regional requirements) relevant to toxicology and impurity assessment. Required Experience - 3-5 years of experience in toxicology, safety assessment, ...

... regulated and business critical computerized systems for global pharmaceutical clients. The ideal candidate will ensure compliance with global regulatory standards (FDA, EMA, MHRA) and drive strategic initiatives for business process transformation and operational excellence. Your Key Responsibilities - Lead CSA/CSV strategy ...

... Management Systems (QMS). - Excellent organizational, communication, and problem-solving skills. - Proficiency with Microsoft Office Suite. Preferred Knowledge - FDA 21 CFR Part 11 - 21 CFR Parts 820 - ISO 9001 and/or ISO 13485 - GMP, GDP, Change Control, CAPA, and Risk Management Leadership Responsibilities - Provide day-to-day ...

... powders, natural colors, and many more. With continuous plant machinery advancement to ensure the highest quality of food ingredients, we are also Halal Kosher, US FDA, and organic certified. Activity on Internshala Hiring since May 2026 3 opportunities posted Additional Questions Sign up to continue Candidate sign up Sign up/ ...

... Management Systems (QMS). - Excellent organizational, communication, and problem-solving skills. - Proficiency with Microsoft Office Suite. Preferred Knowledge - FDA 21 CFR Part 11 - 21 CFR Parts 820 - ISO 9001 and/or ISO 13485 - GMP, GDP, Change Control, CAPA, and Risk Management Leadership Responsibilities - Provide day-to-day ...

... Posted 2 days ago Job Be an early applicant About the job Key responsibilities: 1. GMP & Regulatory Compliance: Ensure adherence to Schedule T, applicable AYUSH/FDA requirements, hygiene standards, and approved manufacturing procedures. 2. Raw Material Quality: Verify raw materials, supplier documentation, COAs, and testing ...

... applying editorial standards to medical and pharmaceutical content. - Experience with medical, regulatory, and legal review processes, along with familiarity with FDA requirements related to pharmaceutical and drug promotion. - Strong understanding of medical and pharmaceutical terminology, with the confidence to work accurately ...

... skills - Strong Interpersonal skills with the ability to work collaboratively with others in a team environment - Experience in the medical device industry and FDA Regulations is preferred Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, ...

... microservices, Web APIs) and cloud/database platforms (AWS/Azure, SQL/NoSQL). - Regulatory Rigor & Data Integrity: Adhere to medical device SDLC standards (IEC 62304/FDA compliance) across the full stack, utilizing ALM tools for complete requirements-to-implementation traceability and ensuring HIPAA-compliant patient data security. ...

... IQVIA and clients in the implementation and management of standards. - Ensure that work delivered to clients meets minimum submission requirements as defined by FDA guidance and other applicable regulatory guidance. - Guide clients in the interpretation and application of CDISC standards through governance teams. - Monitor ...

... initiatives - Manage maintenance budgets, supplier relationships, and equipment life cycle costs - Ensure compliance with regulatory requirements including GMP, FDA, and OSHA standards Requirements - Experience managing maintenance engineering teams and technicians - Knowledge of medical device manufacturing and GMP requirements ...

... hardware development lifecycle from concept through release, including verification and risk mitigation - Ensure regulatory compliance with IEC 60601, ISO 13485, and FDA requirements - Conduct root cause analysis and implement corrective actions for product issues - Collaborate with cross-functional teams on manufacturing, field ...

... management experience from protocol review through database lock - Hands-on experience with Medidata RAVE and Oracle Clinical EDC systems - Knowledge of ICH-GCP, FDA guidelines, and clinical trial processes - Demonstrated expertise authoring and reviewing data management documents (DQMP, DVP, DRP, PDRP, eCRF Completion Guidelines) ...