Regulatory Affairs Jobs in Kuwait City

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...

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...

Collaborate with cross-functional teams including engineering, operations, and regulatory affairs to integrate environmental considerations into project planning and execution. Liaise with regulatory agencies and stakeholders to obtain permits, approvals, and ensure adherence to en More...

Prepare and maintain regulatory documentation, such as Product Information Files (PIFs) and Safety Data Sheets (SDS). Collaborate with Research & Development, marketing, and quality assurance teams to offer regulatory guidance throughout the product development cycle. Keep abr More...

Do you crave flexibility and a work environment with new surprises every day? Check out our Teacher job, where you can maintain a work-life balance while guiding and shaping young minds. By joining our school family, you can build strong connections, teach children new skills, and g More...

Roles and responsibilities YOUR ROLE Exchange of scientific information with KOLs, HA and other clients Plan and execute scientific experts (KOLs) engagement Providing medical insight and input to cross-functional team Providing medical and scientific support to all functions a More...

Opening new accounts and market network expansion is key. Build relationship with dealers to improvise sales. Improvise on stocks availability and cross selling on schemes. Market information and detail reporting on day to day affairs in market. Requirements Minimum 3 to 5 years& More...

Reports directly to and communicates with the General Manager on all administrative matters Maintains the utmost confidentiality and discretion when handling business affairs Cooperates, coordinates and communicates with Department Heads and other inter-departmental secretaries as More...

Timely recording of transactions in General Ledger and various sub-ledgers and special modules like HRMS, Telephone Module etc. Responsible for Costing of inventory. Preparation of documents related to banks (Daily deposit Slips, LCs, Payments, cheques etc.) Timely recording of e 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...

Roles and responsibilities We are excited to announce a vacancy for a talented and experienced Content Writer with a specialization in political writing to join our dynamic team remotely. This role is perfect for someone with a passion for politics and a proven ability to produce hig 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...

Roles and responsibilities We are seeking a motivated and detail-oriented individual to support Clinical Trial Managers in the coordination and archiving of clinical trials. This role is pivotal in ensuring that all essential documents are managed effectively within our Clinical Tria More...

Roles and responsibilities Biomedical engineers combine principles of engineering and biological sciences to design, develop, and maintain medical devices and equipment that improve patient care and health outcomes. They work at the intersection of medicine and technology, playing a 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...

Roles and responsibilities Lead the programming aspects of clinical trials, including the development of datasets (SDTM, ADaM) and statistical outputs (tables, listings, and figures). Provide technical expertise and leadership in developing and validating SAS programs in support o More...

Roles and responsibilities The role of the assistant to the Dean is vital for ensuring the efficient functioning of the College of Business. Key responsibilities include the preparation and organization of presentations, predominantly utilizing PowerPoint, to effectively communicate 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 As a Clinical Trial Manager, you will lead and manage clinical trials from initiation through to completion, ensuring all project aspects are executed effectively. This involves overseeing timelines, budgets, and resources to ensure that trials are conducte 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...