Regulatory Documents Jobs in Kuwait City

Developing and implementing regulatory strategies to support product development and commercialization. Advising clients on regulatory requirements, including FDA, EMA, and other global regulations. Preparing and reviewing regulatory submissions, including INDs, NDAs, BLAs, and ot More...

We are looking for strong regulatory professionals with medical device experience, who are experienced with writing technical files and have good attention to detail. We would love to hear from you if you have: Minimum 5 years of experience writing technical files in regulatory aff More...

Ensure that a company`s product comply with the regulations. Keep up to date with national and international legislation, guidelines, and customer practices. Monitor and set timelines for license variations and renewal approvals. Write clear, accessible product labels and leaflet More...

Requirements: Medical Device experience CE Marking Conformities Registration in MENA region (must have) Distribution GSPR Experience working with Notified Bodies Experience working with project plans Must speak English fluently

Collaborate with R&D, clinical, quality, and regulatory teams to gather necessary information and data for regulatory submissions Maintain up-to-date knowledge of regulatory requirements and communicate changes and updates to the team Review and provide feedback on documents p More...

Proven experience as a regulatory writer in the life sciences sector (biotech, pharma, or medical devices). Expertise in regulatory submission processes for major markets (FDA, EMA, or other global agencies). Strong ability to write and edit regulatory documents with a high level More...

Provide inspired leadership for the organization.Make important policy planning and strategy decisions.Develop implement and review operational policies and procedures.Assist HR with recruiting when necessary.Help promote a company culture that encourages top performance and high mora More...

Roles and responsibilities 1. Regulatory Research and Analysis Staying Informed: Keep up to date with changes in relevant laws, regulations, and industry standards that affect the organization’s operations. Regulatory Interpretation: Interpret complex legal and regulatory d More...

Serve as liaison and subject matter expert internally and for clients, guiding and advising them on strategies and best practices for achieving approval/agreement from regulatory authorities for all document types that Synchrogenix writes Author documents per client specifications, More...

Bachelor’s degree (minimum) 10+ years of regulatory writing experience with clinical- related documentation Understands regulatory requirements for different phases of development and different regulatory pathways Knowledge of global health authority requirements Collectiv More...

Roles and responsibilities Bachelor Degree in Law Professional legal qualification or certification preferred Excellent English and Arabic language skills (written and spoken) 5 – 7 years similar experience dealing with legal matters in a company of similar size Respo More...

Title: LCV APS5 Kuwait: Deputy Task Order Manager Supply Contingency Belong Connect Grow with KBR! Program Summary KBR leads the government services world contingency market by providing responsive fullservice logistics support to forces deployed around the world under the Logistic More...

Title: LCV APS5 Kuwait: Deputy Task Order Manager Supply Contingency Belong Connect Grow with KBR! Program Summary KBR leads the government services world contingency market by providing responsive fullservice logistics support to forces deployed around the world under the Logistic More...

Title: LCV APS5 Kuwait: Deputy Task Order Manager Supply Contingency Belong Connect Grow with KBR! Program Summary KBR leads the government services world contingency market by providing responsive fullservice logistics support to forces deployed around the world under the Logistic More...

Roles and responsibilities As a key contributor to clinical trial design and execution, you will collaborate closely with clinical teams to ensure robust and statistically sound trial methodologies. This includes working with cross-functional teams to define appropriate endpoints and More...

Title: LCV APS5 Kuwait: Deputy Task Order Manager Supply Contingency Belong Connect Grow with KBR! Program Summary KBR leads the government services world contingency market by providing responsive fullservice logistics support to forces deployed around the world under the Logistic More...

Job DescriptionWe are looking for an experienced Freelance Pharmaceutical Research Specialist who will conduct indepth research and analysis in the pharmaceutical field. This role offers the flexibility to work remotely allowing you to manage your schedule while delivering valuable in More...

Clinical Research: Conduct comprehensive research on clinical trials, drug efficacy, safety profiles, and patient outcomes. Utilize various research methodologies to gather and analyze data from clinical studies and medical literature. Regulatory Compliance: Stay updated on regulat More...

Gathering, collating, and preparing documents, materials, and information for data entry. Conducting research to obtain information for incomplete documents and materials. Creating digital documents from paper or dictation. Reviewing all documents and information for accuracy and i More...

Implements health, safety and environmental policies, procedures and guidelines for the employee and department safety. Creates incident reports and performs inspections to ensure conformity in all areas of HSE. Interacts with services personnel, clients, subcontractors, and regulator More...