Gulf Biotech, a leading pharmaceutical manufacturer, is seeking a Regulatory Affairs Officer to join their vaccine and injectable drugs manufacturing plant in Bahrain. The selected candidate will play a crucial role in ensuring compliance with regulatory standards and managing documentation for product registrations.
Key Responsibilities:
- Prepare and submit Common Technical Document (CTD) dossiers for product registrations.
- Maintain accurate regulatory documentation and ensure adherence to quality standards.
- Collaborate with cross-functional teams to streamline regulatory processes.
This is an excellent opportunity for professionals looking to advance their careers in the pharmaceutical regulatory sector.
About the Hiring Company
Gulf Biotech is a well-established pharmaceutical company specializing in vaccines and injectable drugs. With a strong presence in Bahrain, the company is known for its commitment to quality, innovation, and compliance with global regulatory standards.
For more details, visit their official website: www.gulf-biotech.com
Eligibility Criteria
Educational Qualification:
- Bachelor’s degree in Pharmacy (B.Pharm) or equivalent.
Experience Required:
- 1-2 years of experience in Regulatory Operations within the pharmaceutical industry.
Additional Requirements:
- Strong understanding of regulatory submissions and documentation.
- Attention to detail and ability to work in a compliance-driven environment.
Note: Candidates of any nationality are eligible to apply.
How to Apply
Interested candidates should follow these steps:
- Prepare an updated CV/resume.
- Email the CV to:
Subject Line: “Application for Regulatory Affairs Officer – [Your Name]”
Ensure all details are accurate before submission.
