Regulatory Issues Jobs in Kuwait City

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...

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...

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...

Roles and responsibilities In this role, you will play a critical part in developing, implementing, and standardizing systems and processes within the supplier quality domain. This will include ensuring that supplier quality strategies align with organizational goals and regulatory r 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...

Risk Assessment: Conduct regular security assessments, audits, and penetration tests to identify and mitigate potential risks. Incident Response: Lead the investigation and response to security incidents, working with stakeholders across the company to ensure issues are resolved wh 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...

Roles and responsibilities As a subject matter expert in Origin of goods and Free Trade Agreements, you will be responsible for understanding, sourcing, collecting, and processing globally updates related to Free Trade Agreements into usable information to ensure compliance and optim More...

Roles and responsibilities As a Subject Matter Expert (SME) in the international Customs and Trade Tariffs regime, you will play a pivotal role in ensuring compliance and optimization of global trade operations for PST.AG clients. Your responsibilities will include sourcing, collecti More...

Identifying, evaluating, and onboarding new suppliers for raw materials, ensuring they meet quality, sustainability, and regulatory standards. Fostering strong relationships with existing suppliers to enhance collaboration, negotiate favourable terms, and resolve any issues that ma More...

Contributing to strategic planning and decision making at the executive level to develop and implement a financial strategy. Managing the group’s liquidity and cash needs astutely and efficiently. Overseeing all accounting functions and preparing reports in compliance with a 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...

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...

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...

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...

Conducts maintenance of the Managed Pressure Drilling Services equipment at the job site and workshop when required At the discretion of product line management (such as the Engineering Manager, Operations Manager, or their designee) will be responsible for working in the shop. Thi 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...

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...