Regulatory Jobs in Riyadh

. 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...

Education: Bachelor's degree in business administration or related field, specialized certifications in project management or organization may be beneficial. Previous experience: Experience working in the field of organization or management for a specific period of time, preferab 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...

This individual will be a dynamic, go-getter with Corporate Communications experience who can self-manage, loves to collaborate and ideate, and thrives off of carrying a lot of responsibilityManage and collaborate with public relations agency; set PR strategy and manage to outcomes.Ma More...

Compiling and submitting in a timely manner, all regulatory documents on behalf of Baxter Company Limited in line with regulatory requirements. Respond to any regulatory queries within strictly provided deadlines. Maintain regulatory files in a format consistent with company and SFD More...

As a Principal Regulatory Writer, you will play a pivotal role in translating complex scientific and clinical data into compelling regulatory documents. Your expertise will be crucial in ensuring compliance with European regulations and industry standards. Key Responsibilities: More...

Due to increasing demand for metal roofing systems in Atlantic Canada, Maritime Permanent Roofing is looking to immediately expand our installation team. Be your own boss!Join one of the top installers of metal roofing systems in North America. Maritime Permanent Roofing is looking fo More...

Recommends changes for labelling , manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking/control systems. Keeps abreast of regulatory procedures and changes. May direct interaction with regulatory agencies on defined matters. Re More...

In alignment with the Hiring Manager, is responsible for developing and implementing regulatory strategic plans for product registration and lifecycle management. Lead the preparation of regulatory submissions including New Drug Submissions (NDSs). Provide regulatory inputs and g More...

Bachelor’s degree in Life Sciences, Engineering, Technical Writing, or a related field; advanced degree preferred Minimum of 6 years of experience in regulatory writing, preferably within the medical device industry Strong understanding of regulatory requirements and guideli More...

Identifies information sources and resources for local regulations. Collects and coordinates information on regulatory requirements for in vitro diagnostic devices, quality, preclinical and clinical data to meet applicable regulations. Assist in device registration activities - ag More...

About Zahrawi GroupZahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE KSA Qatar Bahrain & Oman markets. The company supplies and distributes highquality products and services to Hospitals Clinics Laboratories & Analytical Industries. job More...

Develop a phased transition plan for each department function to reach end-state model Support the implementation of policies and procedures, ensuring internal and external guidance is up to date Track and communicate progress of delivery Ensure fair, quick and transparent admini More...

ideal candidate for EU regulatory affairs should have Proven EU regulatory affairs experience Excellent leadership and communication skills, Negotiation & liaising experience with EU FDA. Works with Biocon Biologics head of RA to derive the global development strategy partne More...

Bachelor's degree in a relevant field such as civil or chemical engineering, business administration or equivalent. Knowledge of local and international licensing and regulatory laws and regulations. Ability to deal with regulatory and governmental authorities, submit applications 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...

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...

Responsibility for generating, interpreting and communicating internal and external research and trials data in support of registration submissions and products claims throughout Europe and Africa. Overviewing the supporting detail as necessary for regulatory submissions, variation More...

Lead the development of Carrier & Wholesale services regulatory requirements document Develop/Update the business, commercial views and products elements and impact related to any regulatory reference offers/documents in alignment with related stakeholders. Review regulations More...

. Develop and implement governance frameworks based on NCA (National Cybersecurity Authority) and regulatory authorities: You will design and implement governance frameworks that align with industry best practices and regulatory requirements. This includes establishing policies, proce More...