Senior Manager/Director of Regulatory Affairs

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...

Looking for an Enthusiastic, Efficient & Trustworthy Senior Executive - Regulatory Affairs for a Leading MNC “**Ronak Group”** **Company: Ronak Group (MNC)** Position**:Executive / Senior Executive - Regulatory Affairs** Experience: 2 to 7 Years Location: Vadodara, India We are looking for Energetic & Goal Oriented **Executive / Senior Executive -...

Job description **Company Description** Briyosis Soft Caps Pvt. Ltd. is a privately-owned contract manufacturer of custom dietary supplement formulations. Based in Vadodara, India, we are an FDA registered and WHO-GMP certified company. With our high-efficiency encapsulation lines operating 24/7, we have the capability to produce over 3 billion soft-gels...

Job Title Regulatory Affairs Sr ManagerJob Location Ahmedabad Gujarat IndiaJob Location Type On-siteJob Contract Type Full-timeJob Seniority Level DirectorSkills Regulatory Compliance FDA Regulations Quality Assurance Risk Management Project Management Communication Skills Team Leadership Problem Solving Company OverviewBBioMatrix Healthcare...

Responsibilities As a regulatory affairs officer: ensure that a company's products comply with the regulations of the regions where they want to distribute them keep up to date with national and international legislation, guidelines and customer practices respond to queries from medical bodies like the Medicines and Pertaining to that Guidelines. collect,...

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,...

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...

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...

1. Preparation, Review and Submission of the Dossiers as per CTD/ACTD guidelines as well a country specific guidelines. 2. Compilation of Dossiers and quality documents as per checklist in the guidelines. 3. Review of artworks as per the Regulatory requirements 4. Inter Department coordination to arrange and review of documents and samples for Regulatory...

Bachelor's degree in Chemistry, Environmental Science, or related field. Advanced degree (e.g., MS, PhD) preferred. - 4+ years of experience in regulatory affairs within the agrochemical/pesticide. - In-depth knowledge of pesticide regulations (e.g., CIBRC/EPA, EU, other country etc.) and registration requirements. - Experience with regulatory submissions,...