Regulatory documentation affairs

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...

Candidate should be M.Pharmacy with 12 to 15 years of experience inRegulatory Affairs department from a reputed injectable manufacturing company,Manage regulatory affairs for injectable products, ensuring compliance with global regulations and guidelines.Develop and implement effective strategies to maintain product registrations, variations, and renewals...

About the Role:We are looking for a passionate and detail-orientedRegulatory Affairs Internto support our Regulatory team at Wellbeing Nutrition. This role offers a great opportunity to gain hands-on experience inNutraceutical and Nutrition regulatory processes.Key Responsibilities:Assist in ensuring all FSSAI licenses (NLPL, APOB) are up to dateSupport in...

Company DescriptionOlive PharmaScience Ltd, an Indian pharmaceutical manufacturer with over five decades of experience, specializes in developing and manufacturing high-quality pharmaceuticals, OTC products, and dietary supplements. Renowned for its focus on advanced soft gelatin dosage forms, the company leverages its expertise in research and development...

Regulatory Affairs Specialist duties and responsibilitiesEnsuring compliance with all regulatory requirementsMaintaining regulatory documentation databaseAssisting with the preparation and submission of all regulatory reportsProviding accurate reviews of data and reportsEnsuring accurate and timely submissions to regulatory agenciesAdvising others on...

Company OverviewCelogen Pharma Pvt. Ltd. is a leading pharmaceutical formulations exporter & manufacturer based in India. The company provides it products and services in multiple countries globally including West Africa, East Africa, South Asia, South East Asia, the Middle East, South America & Europe. Apart from promoting our branded products in the retail...

Job Title: Associate Regulatory Affairs SpecialistExperience: 5+ YearsLocation: Mumbai(Hybrid mode)Job Type: 12 months contractREQUIREMENTS:5+ years supporting a regulatory or compliance organization.Experience in Regulatory Affairs or a related field, particularly within a compliance function.Hands-on experience with ETQ, RIMS, and document management...

Dear Candidates,We have job opportunity for the position of Regulatory Affairs Executive & QMR in our leading manufacturing Medical Devices companies.Position:-Regulatory Affairs Executive & Quality Management RepresentativeExperience:-2 to 4 yrsGender:-Male/FemaleThe JD as follows:-· Maintain regulatory files. Maintain and update regulatory authorizations,...

Dear Candidates,We have job opportunity for the position of Regulatory Affairs Executive & QMR in our leading manufacturing Medical Devices companies.Position:-Regulatory Affairs Executive & Quality Management RepresentativeExperience:-1 to 3 yrsGender:-Male/FemaleThe JD as follows:-· Maintain regulatory files. Maintain and update regulatory authorizations,...

Licensing & Approvals:Obtain product permissions from relevant regulatory authorities.Prepare and submit applications for new manufacturing licenses.Liaise with government agencies to ensure timely approvals and renewalsDossier Compilation:Compile, review, and submit regulatory dossiers in CTD (Common Technical Document) and ACTD (ASEAN Common Technical...