Join Gulf Biotech as a Regulatory Affairs Officer in Bahrain. Open to all nationalities. B.Pharm graduates with 1–2 years of CTD submission experience are encouraged to apply. Email your CV to hr@gulf-biotech.com
🌐 Gulf Biotech Hiring Regulatory Affairs Officer in Bahrain – Apply from Any Country
Are you looking for regulatory affairs jobs in the Gulf with high salaries and international exposure? Gulf Biotech, a pioneering name in sterile injectable and vaccine manufacturing, is actively hiring a Regulatory Affairs Officer at its state-of-the-art facility in Bahrain. This is an exciting opportunity for pharmacy graduates worldwide who are passionate about regulatory documentation and compliance.
✈️ Open to All Nationalities | High Paying Job in Gulf Pharma
Whether you’re a Regulatory Affairs Associate in India, a CTD Dossier Executive in Egypt, or a QA/RA Officer in the Philippines, this opening provides the perfect platform to work in Bahrain’s thriving pharmaceutical ecosystem.
🏢 About Gulf Biotech – Bahrain’s Leading Vaccine Manufacturer
Gulf Biotech is a Bahrain-based pharmaceutical company that specializes in manufacturing vaccines and sterile injectable drugs. The company operates in compliance with GMP, WHO, PIC/S, and EMA standards and is known for its robust quality systems and innovation in pharmaceutical production.
Their facility is a key supplier across the MENA region, Europe, and emerging markets, making it an ideal environment for ambitious professionals to grow.
👨⚕️ Regulatory Affairs Officer – Job Overview
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Position: Regulatory Affairs Officer
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Location: Gulf Biotech, Bahrain
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Department: Regulatory Operations / Compliance
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Industry: Pharmaceuticals, Injectables, Vaccines
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Qualification: Bachelor’s Degree in Pharmacy (B.Pharm mandatory)
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Experience Required: 1–2 years in regulatory operations or CTD submissions
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Nationality: Open to all (Indians, Pakistanis, Filipinos, Egyptians, Sri Lankans, etc. are welcome)
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Mode of Work: Full-time, Onsite
📋 Key Responsibilities
As a Regulatory Affairs Officer, you will play a critical role in ensuring that Gulf Biotech’s pharmaceutical products meet international regulatory requirements. Your core responsibilities include:
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Preparing and reviewing Common Technical Documents (CTDs) for product registration across various global health authorities.
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Managing product dossiers and regulatory documentation for both domestic and international filings.
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Working closely with the Quality Assurance (QA), Research and Development (R&D), and Production teams to ensure regulatory readiness.
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Ensuring timely submission and approval of product registrations.
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Maintaining comprehensive regulatory records, archives, and documentation logs as per GCC, WHO, and ICH standards.
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Supporting post-approval changes and product lifecycle management.
✅ Who Should Apply?
This position is ideal for candidates who meet the following criteria:
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Hold a Bachelor’s degree in Pharmacy (B.Pharm).
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Have 1–2 years of hands-on experience in regulatory operations in a pharmaceutical company.
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Are familiar with CTD module preparation, eCTD tools, and global submission practices.
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Understand international regulatory frameworks such as EMA, US-FDA, MHRA, TGA, and GCC.
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Have excellent organizational skills, attention to detail, and strong verbal/written communication.
💵 Salary & Benefits – Regulatory Affairs Officer in Bahrain
While exact compensation is not disclosed, the role offers:
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Tax-Free Salary – Competitive monthly pay
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Medical insurance
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Annual air ticket to home country
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Visa and work permit sponsorship
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Housing allowance or provided accommodation
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Relocation assistance
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Annual paid leaves and GCC holiday benefits
For a candidate with 1–2 years of experience, you can expect a monthly salary between BHD 500–700, depending on qualifications and performance in the interview.
📧 How to Apply – Direct Email Submission
If you’re interested and meet the eligibility criteria, send your updated CV directly to the HR team using the following official email addresses:
Make sure your subject line is clear, for example:Application for Regulatory Affairs Officer – [Your Full Name]
🧠 Tips to Strengthen Your Application
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Customize your CV with keywords like CTD, regulatory affairs, GMP compliance, dossier submission.
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Mention any experience in QA/QC, eCTD software, or international filings.
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Attach your degree certificates, passport copy, and recent photograph for faster processing.
🌍 Why Choose a Regulatory Career in the Gulf?
The Middle East pharmaceutical market is expanding rapidly, with a growing focus on local manufacturing, exports, and biotech innovation. Bahrain, with its stable economy and government support for the health sector, is emerging as a key destination for pharmaceutical professionals.
Top benefits of working in the Gulf:
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Zero income tax
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Modern infrastructure and safe living
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Multinational work culture
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Higher disposable income
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Opportunities to travel and grow your global network.
📣 The Regulatory Affairs Officer role at Gulf Biotech in Bahrain is an exceptional opportunity for pharmacy graduates aiming to enter the international pharmaceutical arena. With global regulatory exposure, tax-free income, and the prestige of working at one of Bahrain’s top pharma firms, this job is an ideal stepping stone toward a successful global career.
🚀 Apply now and be part of the Gulf’s pharma revolution.
