Regulatory Affairs Trainer

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**Position : Executive Regulatory Affairs** Qualification : BSc (Life-Sciences/ Biochem /Biotech)/B.Pharmacy Experience : Min.4y,,in Regulatory Affairs Gender : Male Location : Vijayawada Salary : Best in the Market (Based on current Salary ) - Regulations and Compliance Execute tasks as per SOP and work process - Read and understand all regulatory...

Job Description: - CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. - Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for Indian market. - Review of technical...

Job Title: Head of Compliance and Legal Affairs Location: Noida Salary: 40L-60L per annum Experience: 15-15 years Job Description: We are seeking a highly skilled and experienced individual to join our team as the Head of Compliance and Legal Affairs . As a key member of our organization, you will be responsible for ensuring compliance with all relevant...

Job Title: Head of Compliance and Legal AffairsLocation: NoidaSalary: 40L-60L per annumExperience: 15-15 yearsJob Description:We are seeking a highly skilled and experienced individual to join our team as the Head of Compliance and Legal Affairs . As a key member of our organization, you will be responsible for ensuring compliance with all relevant laws,...

**Location: Noida** **Job Title: Executive - Trainer** **Job Summary**: The Trainer Executive in the Contact Center is like the star coach in our team, leading the charge in boosting the skills and performance of our contact center superheroes! They're the masterminds behind crafting, delivering, and fine-tuning our training programs to ensure our squad is...

JOB DESCRIPTION: - Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø A Bachelor’s/ Master degree in B. Pharma / M. Pharma Ø Perform assessments of new or revised products Ø Experienced with 1 Yrs should apply. Ø Good Communication skills Job Type-Fulltime contact no-8810226562 **Salary**: ₹15,000.00 - ₹25,000.00 per...

JOB DESCRIPTION: - Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø A Bachelor’s/ Master degree in B. Pharma / M. Pharma Ø Perform assessments of new or revised products Ø Experienced with 1 Yrs should apply. Ø Good Communication skills Job Type-Fulltime contact no-8810226562 **Salary**: ₹15,000.00 - ₹25,000.00 per...

1. REGULATORY AFFAIRS- FINISHED FORMULATION 2. Preparation and reviewing of administrative documents. 3. Preparation and review of Dossier in CTD, ACTD and ECTD Format. 4. Preparing the SPC/ SMPC as per country guidelines. 5. Preparation of Dossier For CIS, Africa Countries, Gulf Countries and South India Countries 6. Review and making of stability...

About Client:Our client brings together Pharmacovigilance expertise, third party system knowledge and Deep technology to develop well-defined solutions, which address challenges across Medical Affairs, Regulatory and Safety functions. Our client solutions free up responsible personnel within Pharma companies to execute their stated responsibilities while...

We are seeking a dynamic and motivated Green Energy Executive with 1-3 years of experience in the oil & gas industry, specifically in Bio Diesel, renewable energy sectors such as CBG (Compressed Biogas) Plant, CNG/CBG Station, Solar Energy, and Manufacturing of Hydrogen/Ethanol/Methanol plants. As a Green Energy Executive, you will play a pivotal role in...

JOB DETAILS 1 Review & preparation of MES & other GMP Software Qualification Documents.2 Preparation of URS, GxP Risk Assessment, Qualification protocols (OQ, PQ), RTM, VSR.3 Review URS, RA, Design documents, qualification document.4 Handling of post implementation changes documents.5 Execute OQ and PQ.6 To prepare compliance report for internal /...

About the job Key Accountabilities: Project Execution: Works effectively within a team environment Works within broad project guidelines as directed by the Project Lead or Technical SME With the guidance of the project Technical SME, demonstrates the ability to prioritize work to achieve specified project outcomes Capitalizes on opportunities to...

Legal CounselLocal India compliancesCross-border M&As and Due DiligenceCorporate & Commercial transactionsInterjurisdictional legal issues and conflict of lawsAd hoc inhouse workJob Location – NoidaWorkdays - 5 days (Work from Office)Key ResponsibilitiesLegal Counsel will be part of the Office of General Counsel in London and will be responsible for...

Hi Jobseekers, We are looking for executive level Experience - 06 months - 3 years - Hands on experience in quality certification (ISI mark) of different products as per BIS norms. - Working experience in documentation required for quality certification. - Hands on experience in quality testing of various products as per their standards. - Working...

About Testbook : Testbook is the fastest-growing & leading EdTech platform established 10 years ago. We focus on Government & Private Job Exams with an eye to capture UPSC, Banking including Regulatory body, SSC, Railways, Teaching and many more categories. Testbook is poised to revolutionize the industry with a registered user base of over 5 Crore+...

About Testbook : Testbook is the fastest-growing & leading EdTech platform established 10 years ago. We focus on Government & Private Job Exams with an eye to capture UPSC, Banking including Regulatory body, SSC, Railways, Teaching and many more categories. Testbook is poised to revolutionize the industry with a registered user base of over 5 Crore+...