32 Remote fda jobs in India.

... and analytical skills and high attention to detail; - Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines. [{"name": "permanent_employment", "text": "Permanent employment", "categoryName": "Type of employment"}, {"name": "full_time", "text": ...

... pharmaceutical or biotechnology industry. - Advanced Proficiency in CDISC (Clinical Data Interchange Standards Consortium) standards and relevant regulations (e.g., FDA, EMA). - Excellent analytical and problem-solving skills with a keen attention to detail. - Excellent communication and collaboration abilities to work effectively ...

... standards. Write and review group SOP and WPD. Evaluates compliance with SOP/WPD on an ongoing basis. Stays updated on the guidelines and requirements of the ICH, FDA and other relevant agencies. • Gives marketing presentations to potential clients on the capabilities of the Medical Writing department. Interacts with Bids and ...

... acument and knowledge of budgeting, forecasting and fiscal management • Strong attention to detail • Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc. • Good computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc. Working Conditions ...

... Responsibilities • Responsible to assess customers requests for Letters of Authorization (LOA) to reference Drug Master Files (DMFs) • Issue LOA drafts for US-FDA, Health Canada and NMPA China. • Maintain LOA data base, prepare analysis and share with the sales teams as required • Prepare weekly data packages for DMFs & ...

... life sciences environments are preferred. Preferred Pharma candidates should possess a practical understanding of: - Current Good Manufacturing Practice (cGMP) - FDA 21 CFR Parts 210 and 211 - Good Documentation Practices (GDP) - Change control processes - Deviation management - Risk-based quality management - Inspection readiness ...

... helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based ...

... service teams to improve product usability. 5. Gather customer feedback and relay it to the product development team. 6. Ensure compliance with medical standards (FDA/CE/ISO) during deployments. 7. Maintain documentation of service reports, training sessions, and issue resolutions. Skill(s) required Biology Business Development ...

... detailed grading rubrics and technical documentation. Preferred Experience - Experience preparing submission-ready deliverables for regulatory agencies such as the FDA or EMA . Compensation & Engagement This is a remote contractor opportunity with output-based compensation. Experts are paid per task that meets project specifications. ...

... detailed grading rubrics and technical documentation. Preferred Experience - Experience preparing submission-ready deliverables for regulatory agencies such as the FDA or EMA . Compensation & Engagement This is a remote contractor opportunity with output-based compensation. Experts are paid per task that meets project specifications. ...

... fleet operations, and preparing operational data and reports. - Agency Hub: Checking port agency costs, including proforma and final disbursement accounts (PDA/FDA), and clearing backlog items. - Vessel IT: Logging tickets, handling user access requests, and maintaining IT documentation for ship and shore users. - Digital ...

... Risk mitigation strategies - Dust and solvent flammability assessment for pharmaceutical powder handling and solvent-based processes. Preferred experience: - FDA-regulated manufacturing - API or chemical pharmaceutical manufacturing - Hazardous materials storage and processing - Ambitious, energetic, self-motivated, self-managed, ...