Regulatory Affairs Jobs in Saudi Arabia

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...

Open and maintain client Details on stand out.business new & existing shoppers (Lead Generation) and changing potential leads into customers/Clients.Maintain and update shopper database in electronic database system.Resolve product or service issues by elucidative the clients comp More...

Education and experience: Hold a bachelor's degree in business administration, office administration, or a related field. At least 3-5 years of experience in regulatory affairs or management. Organization skills: Strong organizational skills with the ability to manage time and r More...

Compile and submit, in a timely manner, regulatory documents according to regulatory requirements and regular follow up on the submitted files. Ensure timely submissions as well tightly manage deficiency responses. Work with market regulatory manager to develop a detailed understa More...

Education and experience: Hold a bachelor's degree in business administration, office administration, or a related field. At least 3-5 years of experience in regulatory affairs or management. Organization skills: Strong organizational skills with the ability to manage time and r More...

Education and experience: Hold a bachelor's degree in business administration, office administration, or a related field. At least 3-5 years of experience in regulatory affairs or management. Organization skills: Strong organizational skills with the ability to manage time and r 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...

Providing local regulatory affairs services including lifecycle management and document review Preparing renewals, variations, RTQs, MA withdrawals and PSURs Supporting the team with regulatory intel across Benelux and/ or Nordics Regulatory assessments and CCDS compliance checks 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...

Responsible for products registration, renewals, and ensuring approvals via GHAD systems and other SFDA systems, including reimbursement follow up if any. Responsible for the post-market surveillance of medical devices for all related reports in accordance with the regulatory agenc 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...

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...

Maintain company documents including but not limited to company’s SOPs, practices and relevant standards and guidelines. Review and maintain company’s regulatory Affairs to ensure compliance with the government regulatory requirements (ISO 9K, SFDA, MOH etc.) Support th 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...

Qualification: Any degreeExperience: 0 to 1 yearSalary: 10000 to 12000Location ; KarurEvent planning, design and production while managing all project delivery elements within time limitsLiaise with clients to identify their needs and to ensure customer satisfactionConduct market rese 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...

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...

Provide leadership and develop strategies for internal and external communications. Create and execute multifaceted plans with initiatives and programs that each contribute to advancing the strategy and are effective vehicles to drive clearly defined messages across all channels re More...

Establish communication mechanisms with relevant international departments and represent the company in the participation and revision process of policies related to cross-border e-commerce logistics. Advocate for company business development in the construction and operation of lo More...