Regulatory Jobs in Manama

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 Zahrawi’s products comply with the regulations of the NHRA. Keep up to date with the latest changes in regulatory legislation and guidelines. Liaise and negotiate with regulatory authority to ensure a smooth registration process. Provide advice about regulations More...

Ensure that new and existing products meet regulatory requirements within the assigned region. Ensures that the department is appropriately resourced and organised. Manages the day-to-day activities of the regulatory affairs department and ensures that the department is appropriat More...

Elixir Associates will be hiring Regulatory Affairs Associate roles exclusively across the EMEA region through out the rest of 2024 with our various CRO, Biotech & Biopharma clients. If these roles are of an interest to you, please follow our company page on LinkedIn for regul More...

About the company: At Biocon Biologics, we are creating a model for the future of healthcare for all. We are a leading company in the biosimilars revolution where patients come first. Our ambition is to impact a billion lives and we do this by fostering a culture of affordable innova 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...

Company Intro Booking Holdings (NASDAQ: BKNG) is the world leader in online travel and related services, provided to customers and partners in over 220 countries and territories through six primary consumer-facing brands - Booking.com, KAYAK, priceline, agoda.com, Rentalcars.com, and More...

POSITION TITLE: Regulatory Operations Specialist II DEPARTMENT: Ora Europe LOCATION: UK or Europe Ora Values the Daily Practice of... Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor The Role: The Regulatory Operations Specialist is responsible 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.

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology More...

The candidate will be supporting the Head of Compliance & MLRO in developing, managing, executing the compliance, implementation of the compliance program, policies and procedures across the group. Moreover, responsible in conducting robust oversight of regulatory compliance unive More...

The opportunity Regulatory compliance and financial crime risks related to money laundering and terrorist financing, bribery, sanctions compliance and fraud as well as the many other facets of risk management are a high focus for the regulated environment in which EY works. Currently More...

Minimum 15 years relevant experience out of which more than 10 years of people manager role Responsible for all aspects of the EU regulatory strategy for approved products and products under development. Lead the development and execution of a regulatory intelligencestrategy for E 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...

Overseeing Accounting Operations: Manage all aspects, including Billing, A/R, A/P, GL, Cost Accounting, Inventory Accounting, and Revenue Recognition. Leading Budget and Financial Forecasts: Direct the preparation of our budget and financial forecasts, reporting on variances. Publ More...

VAM Systems is currently looking for GRC Specialist for our Bahrain operations with the following skillsets & terms and conditions:Requirements: Bachelors degree in Information systems or any other related field Strong interest in governance risk and compliance management Familiarity More...

. Minimum 4 year post qualification work experience in external audit . Plan effective auditing processes . Audit financial statements and assess accounts for accuracy and regulatory compliance . Inspect internal systems and controls . Assess risk management tactics . Repor 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...

Act as the LRPPV (Local Responsible Person for Pharmacovigilance). Perform regulatory intelligence by screening the NHRA websites on a weekly basis. Screen all scientific and medical literature to stay up to date with the latest regulations. Comply with local regulatory requireme More...