Gulf Biotech is hiring for Regulatory Affairs

About Company:

Gulf Biotech offers a broad range of parenteral fill and finish “Contract Manufacturing Services” and can provide support throughout the entire sterile manufacturing process. Production of commercial batches is the main Goal to build GBC facility, Extensive production services for commercial drug products, from compounding to primary packaging to filling in Vials (Phase-1) will be available on site from 2019. Automated visual inspection to enable the highest quality manufacturing processes will be made available for our products inspection and leak testing. GBC offer Comprehensive menu of parenteral packaging services, including assembly, printing, labelling, blister packing, cartooning, and storage of Vials, Ampoules and Pre-filled syringes. We have purchased all equipment from highly reputed European companies including Vials filling line (with isolator Technology), Water treatment system, Solution manufacturing system, Inspection machine and Autoclaves etc. GBC offer Comprehensive menu of parenteral packaging services, including assembly, printing, labelling, blister packing, cartooning, and storage.

Vacancy Details:

Job description:

Join Gulf Biotech in Bahrain as Regulatory Affairs Officer

Bahrainis are preferred !

If you’re passionate about ensuring compliance in the pharmaceutical industry, we’re looking for a dedicated professional like you.
As part of our team, you’ll handle critical tasks like CTD, new product registrations, and more. Your expertise will be instrumental in meeting regulatory standards. If you have a solid background in pharmaceutical regulatory affairs and want to make a real impact, reach out to us.

Join Gulf Biotech and contribute to our commitment to excellence in sterile manufacturing. Take the next step in your regulatory affairs career with us! Apply now!

We are hiring a Regulatory Affairs Officer

in our vaccine & injectable drugs manufacturing plant in Bahrain

Main Responsibilities:

1.Ensure adherence to local and international regulatory guidelines.

2.Handle CTD submissions for product registrations.

3.Supervise product registration procedures and engage with regulatory bodies.

4.Develop regulatory strategies in coordination with cross-functional teams.

5.Maintain precise regulatory documentation and uphold quality standards.

6.Keep abreast of regulatory modifications and industry best practices.

7.Coordinate with internal departments for regulatory assistance.

8.Conduct training and offer guidance to junior regulatory personnel.

9.Support audits, inspections, and regulatory project management activities.

Requirements:

1.Bachelors in pharmacy

2.1-2 years in Pharma Regulatory Operations section

3.Advanced Regulatory Affairs Certifications are plus.

4.Strong Communication Skills.

5.Languages Proficiency: English and Arabic (Speaking, Reading, Writing).

How to Apply?

Apply with your latest CV
hr@gulf-biotech.com gbc@gulf-biotech.com
Bahrainis are preferred

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