Regulatory 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 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...

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...

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...

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...

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...

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...

Drive continuous improvement initiatives to enhance supply chain performance, including inventory management and cost optimization. Analyze market trends and supplier capabilities to identify strategic opportunities and mitigate risks. Ensure compliance with regulatory requirements an More...

Proactively prepare for governmental investigations and audits, ensuring readiness and compliance before they occur. For that purpose: Develop and implement the Export Control assessment methodology taking into consideration the EMEA regulatory requirements.

Lead strategic planning and marketing efforts to grow international presence. Oversee user interface design to ensure an engaging and intuitive user experience. Manage and update our service offerings, focusing on innovation and quality. Ensure compliance with regulatory standard More...

Ensure compliance with local regulatory requirements and corporate governance standards. Lead financial planning, risk management, and cost control initiatives. Collaborate with senior leadership to provide financial insights and guide decision-making. Oversee tax planning, audit More...

Roles and responsibilities At Clements Partners, we specialize in connecting top talent with leading pharmaceutical organizations. We are currently working with a renowned pharmaceutical client who is looking to add a highly skilled Statistical Programmer to their team. This is a ful More...

Target or buyer identification – Identify businesses to be acquired or assets to be sold and find the buyers or sellers Transaction structuring – Advise on transaction terms and pricing and on structuring of the transaction Arranging financing – Advise on financi More...