Regulatory Affairs Jobs in Kuwait City

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

Join a software dev company top-ranked by and DOU and pump up your skills by working with some of the brightest tech experts across four continents.With us, you canWork in a dream team of A-playersKnow that your opinion mattersEnjoy flexibility by operating remotely or onsite in our More...

A minimum of 3 years of management experience. 7+ Years of experience with global submissions with Class III devices. Strong understanding of MDR regulations. Hebrew speakers are preferred. Start-up experience is preferred.

Bachelor's degree or higher in Pharmacy, Life Sciences, or a related field Minimum of 5 years of experience in regulatory affairs in the pharmaceutical or medical device industry Strong knowledge of local and international regulations governing pharmaceuticals and medical devi More...

Provide strategic leadership and direction for all medical affairs activities, including clinical development, regulatory affairs, and pharmacovigilance for a Phase 2 ALS program Establish and nurture collaborative partnerships with key stakeholders, including, regulatory agencies, More...

Development and execution of global clinical studies in line with corporate objectives. Leadership and direction of a team of clinical operational support personnel including internal and field clinical operations. Close collaboration with Therapy Development and Marketing partner More...

. Responsible for the coordination of submissions to Regulatory Authorities and Ethics Committees in the assigned regions and ensures quality of regulatory documentation . Provides regulatory support regarding start up activities and maintenance in the assigned clinical projects and More...

Lead the creation of top-tier regulatory documents, ensuring compliance with industry standards. Synthesize complex scientific data with precision in documents like clinical study reports, protocols, regulatory submissions, and marketing authorization applications. Collaborate sea 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...

Regulatory Expertise: Leverage your in-depth knowledge of European regulations to contribute to the development of high-quality regulatory documents, including but not limited to clinical study reports, regulatory submissions, protocols, investigator brochures, and marketing authori More...

Strategic Planning: Develop and implement engineering strategies in alignment with the organization's overall goals and objectives. Provide technical leadership in the development of long-term plans and strategies for the engineering department. Project Management: Overse More...

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...

Obtain a degree in human resources, business administration, or a related field. Provides 2-3 years of experience in a related field. Fluency in communication skills in both English and Arabic (reading, writing and speaking). Knowledge of the Kuwaiti Labor Law. Possession of a transfe More...

Weve got immediate openings for well qualified CNC Machinists to join a highly profitable world-class company. They offer great pay, awesome benefits and huge potential for growth. Their facilities and equipment are well maintained and they are constantly reinvesting in the business More...

Experience Operations (XO) is a functional group within Genentech Business Operations (GBO), dedicated to delivering integrated customer experiences across Commercial, Medical Affairs, and Government Affairs (CMG). As a Translation Project Manager, you will play a vital role in facili More...

Develop and execute comprehensive digital advertising strategies aligned with the university's enrollment and brand awareness goals. Collaborate with student affairs team to understand target audiences and campaign objectives. Plan, launch, and manage digital advertising campa More...

1. This position will be required to actively promote our brand, engaging with potential clients such as building owners, consultants, and contractors, presenting our lighting solutions and products, and delivering outstanding customer service. 2. This position reports to the Directo More...

Develop and manage relationships with public relations agencies and other outside companies in the development of programs to meet communications objectives. Promote teamwork and quality service through daily communication and coordination with other departments. Key departmental c More...

JOB DESCRIPTIONJob Title: Legal Advisor & Public RelationsJob Code: Legal Advisor & Public RelationsPosition: Legal Advisor & Public RelationsThe purpose of this position is to oversee all the legal transactions on behalf of the company both locally and internationally inc More...

This role required candidate to permanently relocate at Dhahran Saudi Arabia. About the Company This company engages in the exploration production transportation and sale of crude oil and natural gas. It operates through the following segments: Upstream Downstream and Corporate. The More...