Regulatory Jobs in Manama
Regulatory Jobs in Manama
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As Senior Technical Writing expert/regulatory affairs expert you will work closely with manufacturers from start-ups to large multinationals to support them in achieving regulatory approval for various products including AI and software solutions! You will work with startups that requ More...
Ensure compliance of all cosmetic products with EU regulations, including Cosmetic Product Regulation (EC) No 1223/2009. Assess product claims to confirm they are substantiated and meet regulatory standards. Perform risk-based evaluations of formulations to guarantee safety and re More...
Regulatory Affairs Executive
his is a full-time Regulatory - NHRA certified executive role at ARAMED Middle East based in Bahrain. The Regulatory executive will be responsible for overseeing NHRA guidelines and ensuring compliance with regulatory requirements. Daily tasks include managing regulatory submissions, More...
Regulatory Affairs Consultant
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...
Senior Regulatory Counsel - Telecoms
A telecoms/IT regulatory organisation with a long standing and excellent reputation is interested in hiring a Senior Counsel to lead part of its legal team. The role is a key position within the wider team and answers directly to the General Counsel with whom you will work with cl More...
Regulatory Affairs Specialist North America
Job Description Preferred Candidate Identified*** Responsibilities RESPONSIBILITIES: Assist with formula reviews and approvals for compliance and associated data. Assist with customer requested information regarding Packaging products; including declarations of complianc More...
Global Regulatory Affairs Project Manager
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...
Roles and responsibilities We are seeking to hire a Regulatory Research Analyst to be based in our EU offices (Markdorf (Germany). If you have more than 2 years of regulatory and/or legal experience, strong writing skills and are fluent in English, share your profile with us. We More...
Location: Bahrain We are looking for a Compliance Manager to join our clients team in Bahrain. As the Compliance Manager you will be responsible for ensuring that the firm complies with all regulatory requirements in Bahrain and global jurisdictions. You will oversee and implement eff More...
Computer Systems Validation Consultant
The Computer Systems Validation (CSV) Consultant will be responsible for ensuring that computerized systems used in the development, manufacturing, and distribution of pharmaceuticals, medical devices, and other healthcare products comply with regulatory requirements and operate effec More...
Public Relation Officer
We are looking for a PRO to join our dynamic team in Bahrain. The PRO will be responsible for the day to day administration and co-ordination of Public Relations with the Regulatory Ministries, LMRA, SIO, MOL, Municipality, Immigration, MOICT, Traffic directorate, etc. Monitor the c More...
Leadership & Management: Provide strategic leadership and direction to the company, ensuring alignment with our vision and goals. Sales Focus: Develop and execute sales strategies to drive revenue growth. Build and maintain relationships with key stakeholders to expand our mark More...
Standard Operating Procedures Specialist
The Standard Operating Procedure (SOP) Specialist is responsible for developing, implementing, and maintaining standard operating procedures across the organization. This role ensures that all procedures align with industry standards, regulatory requirements, and company objectives to More...
Roles and responsibilities Key Responsibilities and Qualifications for a SAS Programmer in Clinical Data Analysis As a SAS Programmer specializing in clinical data analysis, you will play a crucial role in ensuring the integrity and quality of data in clinical trials. Your primary r More...
POSITION TITLE: Clinical Trial Associate II DEPARTMENT: Ora Europe LOCATION: Italy or Spain Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical rese More...
Principal Statistical Programmer
Roles and responsibilities AL Solutions are looking for a highly skilled Senior or Principal Statistical Programmer to join a global, fast-paced organization committed to delivering innovative solutions in the clinical research space. This position offers the opportunity to play a cr More...
Clinical Project Manager
Roles and responsibilities Clements Partners is a leader in connecting top talent with leading pharmaceutical organizations. We are excited to announce an opening for a Clinical Project Manager to join our esteemed client’s team. This fully remote position is open to candidates More...
Supports Finance Compliance program and ensures that policies and procedures are up to date and followed. Serves as Finance liaison on DCAA and DCMA audits and informational requirements as assigned. Assists in the development and compliancy review of the annual Incurred Cost Subm More...
Legal Research and Analysis: To provide comprehensive legal research and in-depth analysis of regulatory requirements, Monitoring changes in legislation that affect our clients, advising on necessary actions to remain compliant, and developing internal compliance guidelines. Docume More...
We are on a mission to deliver solutions that bring life-changing treatments to patients faster. But we can´t do it alone. We are seeking a Principal Medical Writer to lead authoring and development of high complexity clinical regulatory documents that are critical to the strat More...
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