
Regulatory Affairs Associate
2 days ago
Our leading herb territory is currently in need of a Regulatory Scientist to join our fast-growing team. The ideal candidate will be intricately involved in filing and getting Licences and other supporting documents for herb marketing and will regularly look for other supporting certificates and updates via theoretical approaches for the smooth establishment of products, especially in Canada. This is the perfect opportunity for the successful candidate to become a part of an innovative and energetic team that develops Natural health products which will influence both our products and beneficiaries.
Responsibilities and duties
The candidate with advanced knowledge of Natural health products. Strategic regulatory understanding for registration of drug products & post-market changes. Expert regulatory/medical writing. Regulatory dossier preparation and submission. Assimilation of scientific dossiers for regulatory review. Toxicology, efficacy, quality, and safety study documentation Scientific understanding for analytical, environmental, and human health regulatory documentation. Product label text drafting and revision will be an asset.
Requirements:
- Master's Degree in Biological Science, applied biology or related field.
- 3+ years' practical experience with licenses and certification legal procedures.
- Extensive background in data mining and analysis.
- Able to understand various botanical and pharmacological common methods and specific terminologies.
- Excellent problem-solving and scientific communication skills.
- Basic Experience in computer skills.
Job Type: Full-time
Pay: ₹25, ₹30,000.00 per month
Application Question(s):
- Have you completed the following level of education: Master's Degree?
- Master's Degree?
Ideal answer: Yes
How many years of work experience do you have using Dossier Preparation?
Experience:
- Dossier: 1 year (Preferred)
- Herbal Medicine: 2 years (Required)
- Regulatory: 4 years (Required)
Work Location: Remote
-
Regulatory Affairs Associate
2 weeks ago
Remote, India Parexel Full timeAs part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...
-
Regulatory Affairs Associate
5 days ago
Remote, India Parexel Full timeAs part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...
-
Regulatory Affairs Officer 633
5 days ago
Remote, India ProductLife Group Full timeResponsibilities In the context of a project for one of our top Pharma client, we’re looking for 2 talented Regulatory Affairs Officer to lead the following missions, and much more! Compile, or supervise the compilation of regulatory dossiers Provide on-going regulatory advice to project teams to ensure regulatory concerns are planned and accounted for...
-
Junior Regulatory Affairs Associate
3 days ago
Remote, India Parexel Full timeAs part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...
-
Medical Device Regulatory and Clinical Affairs
2 weeks ago
Remote, India Medidee Full time**Career opportunity** **Consultant - Medical Device Regulatory and Clinical Affairs** **Project Associate - Remote, India **compliance with international regulatory requirements. We serve clients with hands-on support for compliance with applicable regulatory requirements of our clients’ target markets. Our services cover all steps of Medical Device and...
-
Regulatory Affairs Associate
3 days ago
Remote, India Parexel Full timeAs part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...
-
Regulatory Affairs Associate
3 days ago
Remote, India Parexel Full timeAs part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...
-
Regulatory Publisher 638, 641
1 week ago
Remote, India ProductLife Group Full timeWe are looking for an Regulatory Publisher to develop new challenging projects which would include the following responsibilities: - Perform quality control procedures to ensure completion, correctness, navigability, and adherence to regulatory eCTD guidelines. - Perform document management tasks and post-submission activities including file transfer,...
-
Regulatory Project Assistant, India
1 week ago
Remote, India Innovaderm Research Full timeThe Regulatory Project Assistant (RPA) is responsible for providing project administrative support to the regulatory project team members (regulatory affairs, eTMF operations). The RPA also supports activities within the regulatory website Clinical Trial Information System (CTIS) ensuring completeness and timely entry of information for EU submissions. The...
-
Clinical Research
3 days ago
Remote, India IPR LEARNING INSTITUTE Full time**Responsibilities**: - Assist in the planning, execution, and monitoring of clinical research studies. - Ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. - Monitor and report adverse drug reactions (ADRs) and other pharmacovigilance activities. - Conduct literature reviews and safety signal assessments. - Maintain...