Consulting In Regulatory Affairs, Training Material And Computer Application Development Internship in Vadodara

URGENT OPENING FOR REGULATORY AFFAIRS OFFICER/ SR OFFICER LOCATION VADODARA Position:-Regulatory Affairs Officer/ Sr OfficerLocation:-VadodaraExperience:-1 to 3 Yrs (Formulation)Qualification :- B.Pharm/ M.Pharm Required Candidate profilePreparing dossiers as per country-specific guidelines.Compiling and reviewing documents.Coordinating with QA for...

POST: RA OFFICER/EXECUITVELOCATION: JAROD, VADODARAEXPERIENCE: 2-3 YEARSExperience in handling regulatory affairs for ROW market mainly Latin American, African & Asian countries for Pharma Formulations.Preparation, compilation & Review of Registration documents that include Administrative & Technical.Reviewing the technical documents provided by QA, QC,...

Location: India – Office based in Anand, Vadodara :Salary: Dependent on ExperienceWorking Pattern: Full-time, Monday–Friday 9am – 5.30pm, but would have regular UK communications and other markets, so flexibility is keyReports to: COOAbout UsWe are a UK based Food Supplement Company, who is both UK and export-focused with a growing global footprint. We...

Job Description:Regulatory Affairs Officer (RA)Qualification: B.Pharm/ M.PharmExperience: Minimum 3 years in regulatory affairs for the ROW (Rest of the World) market, with a total of 3 to 5 years of experience.Job Description:Preparing dossiers as per country-specific guidelines.Compiling and reviewing documents.Coordinating with QA for...

Job Description:works to help a company or organization meet all state, local, federal, international, and industrial regulations that apply to their products.They must have excellent organizational, analytical, project management, and communication skills.They work frequently with other employees and team members to coordinate complex activities, often with...

Selected Intern's Day-to-day Responsibilities IncludeConducting experiments under defined conditionsWorking on technical content writingOperating of Scientific Analytical InstrumentsLaboratory Management.Perform QC on Lab DevicesAbout Company: M19-Material Intelligence lab is perhaps the only startup in India developing indigenous scientific lab instruments...

Role & responsibilitiesResponsible for Drug Master Filing submissions to various regulatory agencies like USFDA, European Agencies, Brazil, and other semi-regulatory countries.Review and submission of Response to queries raised on DMF by USFDA, and other agencies.Review and submission of Amendments and revisions of Drug Master Files.Review and ensuring the...

Responsible for Regulatory Affairs functions at Exemed Pharmaceuticals Luna.Responsible for Issues Letter of Access, Letter of commitment and CEP certificate for customer as per specific regulatory requirement.To prepare commitment, Declaration and Statement certificate for customer as per specific regulatory requirement.Responsible for prepare and review...

Scientific Instrumentation is a highly technical industry.As an electronics/electrical engineer, you'll design, develop and test components, devices, systems or equipment. You may be involved at any stage of a project including the initial brief for a concept, the design and development stage, testing of prototypes and the final manufacture and assembly of...

Job TitleExecutive – Regulatory AffairsBusiness UnitR&D1 Regulatory AffairsJob GradeG12ALocationBarodaAt Sun Pharma, we commit to helping you "Create your own sunshine"— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.Are You Ready to Create Your Own Sunshine? As you enter the Sun...