5 Regulatory Affairs jobs in Bahrain

Senior Regulatory Affairs Specialist

20550 Amwaj Islands BHD48 Hourly WhatJobs

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Job Description

full-time
Our client, a dynamic pharmaceutical company, is seeking a highly experienced Senior Regulatory Affairs Specialist to support their product development and registration efforts in **Isa Town, Southern, BH**. This role is essential for navigating the complex regulatory landscape and ensuring timely approvals of pharmaceutical products. The ideal candidate will possess a strong understanding of regulatory submissions, guidelines, and compliance requirements for the pharmaceutical industry. Responsibilities:
  • Prepare, review, and submit regulatory documents for product registrations, variations, and renewals in accordance with global regulatory requirements.
  • Interpret and apply regulatory guidelines (e.g., ICH, FDA, EMA, local health authorities) to ensure compliance.
  • Manage the lifecycle of regulatory submissions, ensuring timely and accurate filing.
  • Liaise with regulatory authorities to facilitate the review process and respond to queries.
  • Provide regulatory guidance and strategic input to cross-functional teams, including R&D, manufacturing, and marketing.
  • Maintain regulatory databases and filing systems to track submission status and approvals.
  • Monitor changes in the regulatory environment and assess their impact on company products and strategies.
  • Conduct regulatory intelligence activities and provide insights on emerging trends and requirements.
  • Review and approve labeling, promotional materials, and advertising to ensure regulatory compliance.
  • Support post-market surveillance activities and ensure compliance with pharmacovigilance requirements.
  • Participate in regulatory audits and inspections.
  • Contribute to the development of regulatory strategies for new product development.
  • Ensure compliance with all company policies and procedures related to regulatory affairs.
  • Collaborate with external partners and consultants on regulatory matters.
  • Train internal stakeholders on regulatory requirements and processes.

Qualifications:
  • Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or a related field. A Master's degree or advanced degree is highly preferred.
  • Minimum of 6 years of experience in regulatory affairs within the pharmaceutical industry.
  • In-depth knowledge of pharmaceutical regulations, guidelines, and submission requirements in key markets.
  • Proven experience in preparing and submitting various types of regulatory filings (e.g., ANDAs, NDAs, variations).
  • Strong understanding of drug development processes and product lifecycle management.
  • Excellent analytical, problem-solving, and critical thinking skills.
  • Proficiency in regulatory information management systems (RIMS).
  • Exceptional written and verbal communication skills, with the ability to articulate complex regulatory information clearly.
  • Strong project management and organizational skills, with the ability to manage multiple submissions simultaneously.
  • Ability to work independently and collaboratively in a team-oriented environment.
  • Detail-oriented with a strong commitment to accuracy and compliance.
  • Experience with specific therapeutic areas is a plus.
  • Familiarity with quality assurance principles.
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Pharmaceutical Regulatory Affairs Manager

123 Riffa, Southern BHD4800 month WhatJobs

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a highly qualified and experienced Pharmaceutical Regulatory Affairs Manager to oversee regulatory compliance and submissions for their product portfolio in Riffa, Southern, BH . This critical role ensures that all products meet the stringent requirements of local and international health authorities. The ideal candidate will possess a deep understanding of pharmaceutical regulations, excellent analytical skills, and a meticulous approach to documentation and compliance. Key responsibilities include developing and implementing regulatory strategies, preparing and submitting regulatory dossiers (e.g., CTD, ANDA, NDA) to health authorities, and managing post-approval regulatory activities. You will also stay abreast of evolving regulatory landscapes, provide regulatory guidance to internal teams (R&D, manufacturing, marketing), and liaise with regulatory agencies. Experience in managing regulatory affairs for generic and/or innovator pharmaceuticals is essential. A proven track record in successfully navigating regulatory approval processes is required. A minimum of 6 years of experience in pharmaceutical regulatory affairs is mandatory. A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required; a Master's or PhD is advantageous. Fluency in English and excellent written and verbal communication skills are essential. Familiarity with GMP, GLP, and GCP is also important. This role offers a significant opportunity to contribute to bringing vital pharmaceutical products to market in compliance with all necessary regulations.
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Regulatory Affairs Executive & Warehouse Pharmacist

Manama, Capital Zahrawi Group

Posted 6 days ago

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Job Description

Regulatory Affairs Executive & Warehouse Pharmacist - (484) About Zahrawi Group

Zahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, & Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, & Analytical Industries.

Job Brief

The incumbent is responsible for all Product Classification/Manufacturing Site Registration and Product Registration and to ensure that all documents required are available and are submitted on time.

ACCOUNTABILITIES

Adhere to all Zahrawi Policies & Procedures as applicable.

Regulatory Affairs:

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 to customers/suppliers.

Analyze product complaints and make recommendations to solve the problem and to avoid them in the future.

  • Prepare and apply for the permit document as per the NHRA guidelines and verify the items being imported and the documents required.
  • Apply for the NHRA regulated products permits on the NHRA website as per the specified guidelines.
  • Register and submit the permits for SCE when required.
  • Resubmit any permits that have not been approved and make sure all the information provided is correct and attach any new documents if required.
  • Prepare daily report regarding the rejections/ delays for NHRA importation permits and reasons related to that.
  • Communicate with the existing and new suppliers regarding NHRA importation rules and policies.
  • Upload on the NHRA importation system any new classifications or registration certificates.
  • Ensure that all urgent requests from the Sales team and suppliers are dealt with in a fast manner and ensure that all documents are in place.
  • Report any deviation from NHRA guidelines of imported shipments and take the corrective and preventive action accordingly.
  • Review on a regular basis the NHRA importation process of distribution agreements.
  • Ensure that the NHRA license is renewed before expiry date to avoid importation disturbance.
  • Segregate the imported products as per HS code in coordination with logistic team and confirm if products are NHRA regulated or not.
  • Coordinate with the Procurement & Logistics Team to update all the required documents in time to avoid importation rejections.
  • 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 requirements for reporting adverse drug reactions and submission of safety reports.
  • Responsible for all Pharmacovigilance related work and assigned as the LRPPV (Local Responsible Person for Pharmacovigilance).
  • Report Adverse Drug Reactions (ADRs) for all products by collating the needed information and incorporating customer’s comments.
  • Fill the Council for International Organizations of Medical Sciences (CIOMS) forms with all the information collected from the ADRs.
  • Send all CIOMS forms to the Manufacturers and the relevant authorities.
  • Manage the Pharmacovigilance process of Zahrawi by preparing all SOPs, product safety reviews and literature reviews when needed.
  • Maintain a high level of standard to ensure that all work is moving smoothly and that there are no delays.
  • Prepare and review all SOP’s Pharmacovigilance plans for all Zahrawi Suppliers.
  • Prepare all Registration and Pharmacovigilance forms and communicate the same to the Suppliers and stakeholders.
  • Provide trainings to all internal divisions on the current Pharmacovigilance Policies & Procedures.

Individual Case Study Reports (ICSRs):

  • Report any spontaneous Individual Case Study Reports (ICSRs) to the Supplier and the Health Authority.
  • Maintain a soft and hard copy of all ICSRs for the future.
  • Track and follow up with all active ICSR reconciliation with the respective authorities.
  • Report all Suspected and Unexpected Serious Adverse Reactions to relevant Health Authorities.

Product Classification & Registration:

Ensure that all required documents and actions for Product Classification/Manufacturing Site Registration and Product Registration are available.

Prepare all required documents to be submitted for Product Classification under NHRA.

Prepare all required documents to be submitted for Manufacturing Site registration under NHRA.

Prepare all the Dossiers to be submitted to NHRA for product registration.

Collect all necessary documents from Supplier to submit for Health Authorities.

Quality Assurance:

  • Monitor all Cold Products from point of receiving until delivery of products to customers along with Data Logger results within the set temperature limits.
  • Examine the packing of goods from the cold storage and monitor the Data Logger Report to ensure consistency.
  • Check the quality of the vehicles, warehouse cleanliness, temperature control mechanism, storage conditions and validity of goods on shelves on a regular basis.
  • Ensure all Zahrawi Cold Vans/Delivery Vehicles, Data Loggers are calibrated regularly and update the temperature mapping of the Warehouse.
  • Ensure all required licenses and registrations as well as calibration renewals are updated before their expiry dates.
  • Review all technical and quality agreements with suppliers and customers on a regular basis.

Warehouse Quality Check:

Ensure that the Warehouse & Service Room are kept clean and organized.

Ensure that the temperature control mechanism and hygiene standards are maintained in the Warehouse.

Ensure a quick and accurate release of shipments from NHRA to avoid any delays in transporting the products to the customer.

Ensure that all stock areas are segregated properly into: Dispatching, Receiving, Returns, Hold and Expired and that no mix-up could happen at any time.

Product Quality Check:

Ensure that a sample of each batch of products is secured from the WH Assistants and provide the samples along with a progress report and supplier invoice to the Warehouse Operation, QA & RA Manager for NHRA release approval.

Check all shipments leaving the Warehouse are sealed and packed properly and if the vehicle is fit for transporting the products.

Compile all Quality Inspection Forms prepared by the Sr. Driver & Fleet Coordinator and prepare a monthly report.

Generate a discrepancy report to the Warehouse Operation, QA & RA Manager for MOH release approval for any late findings (excess, damaged or expired goods) in the shipment.

Audit:

  • Prepare any documentation needed for internal and external audits.
  • File all documents in the corresponding files to ensure all are available and are correct.
  • Evaluate the suggestions after the audit and implement them when possible.

Admin:

  • Develop a professional relationship with the NHRA staff and proactively monitor relevant governmental bodies to identify changes in legislation/regulations.
  • Represent Zahrawi in NHRA and different authorities.
  • Negotiate with regulatory authorities for marketing authorization.
  • Attend and respond to calls and emails from customers, the Sales team and other support staff.
  • Assist the Warehouse Coordinators with relevant documents when requested.
  • Coordinate with the Procurement team and assist them with any question they or the Suppliers may have related to NHRA importation.
  • Keep track of all registration application on Zahrawi’s tracking system.
  • Record all active Zahrawi licenses on the Shared folder and ensure they are updated.
REQUIREMENTS
  • Education: Bachelors Degree in Pharmacy
  • Candidates must be based in Bahrain.
  • Bahraini national is preferred.
  • Candidates must have a valid Pharmacist license.
  • RAO license is a plus.
  • Experience: Fresh graduates or 1+ years of relevant experience in regulatory affairs within Bahrain is preferred.
  • Job Specific Skills: Excellent Interpersonal Skills & Good English – Good computer skills in Ms. Office (Excel– ERP/Oracle system) - Knowledge about Regulatory Affairs, Product Classification and Importation Regulations as per NHRA.
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Aviation Safety Inspector - Regulatory Compliance

501 Busaiteen, Muharraq BHD65000 Annually WhatJobs

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Job Description

full-time
Aviation regulatory authority is seeking a meticulous and experienced Aviation Safety Inspector to ensure compliance with national and international aviation standards in Busaiteen, Muharraq, BH . This critical role involves conducting thorough inspections of aircraft, aviation facilities, and operational procedures to guarantee the highest levels of safety and security within the aviation sector. The successful candidate will possess a comprehensive understanding of aviation regulations, aircraft systems, and safety management principles. Your expertise will be instrumental in maintaining the integrity of air travel operations. Key responsibilities include:
  • Conducting regular and unscheduled inspections of aircraft, airports, maintenance organizations, and flight operations to ensure compliance with aviation regulations.
  • Evaluating aircraft airworthiness, maintenance records, and operational procedures.
  • Assessing the safety management systems (SMS) of aviation stakeholders.
  • Investigating aviation incidents and accidents to determine causes and recommend preventive measures.
  • Reviewing and approving aviation safety programs and documentation.
  • Providing technical guidance and training to aviation personnel on safety regulations and best practices.
  • Developing and implementing safety audit programs.
  • Staying current with evolving aviation regulations, technologies, and safety trends.
  • Preparing detailed inspection reports, findings, and corrective action plans.
  • Collaborating with national and international aviation authorities and organizations.
  • The ideal candidate will possess:
    • A Bachelor's degree in Aerospace Engineering, Aviation Management, Aeronautical Science, or a related field.
    • A minimum of 5 years of experience in aviation safety, aircraft maintenance, flight operations, or regulatory compliance.
    • In-depth knowledge of international aviation regulations (e.g., ICAO Annexes, EASA, FAA standards) and national aviation laws.
    • Strong understanding of aircraft systems, principles of flight, and airworthiness requirements.
    • Experience with Safety Management Systems (SMS) and risk assessment methodologies.
    • Excellent analytical, observational, and problem-solving skills.
    • Strong report writing and communication abilities.
    • The ability to work independently and make critical safety decisions.
    • A strong commitment to aviation safety and security.
    • Relevant aviation certifications (e.g., A&P mechanic license, pilot license, safety auditor certification) are highly desirable.
    • This is a vital role that contributes directly to the safety and reliability of air transport. If you are a dedicated aviation professional with a passion for safety, we encourage you to apply.
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Aviation Safety Inspector, Regulatory Compliance

BH007 Hamad Town, Northern BHD70000 Annually WhatJobs

Posted 6 days ago

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Job Description

full-time
Our client, a prominent entity within the aviation sector, is actively seeking a diligent and detail-oriented Aviation Safety Inspector to ensure adherence to stringent safety regulations and standards. This crucial position is located in Hamad Town, Northern, BH , and plays a vital role in maintaining the highest levels of safety within the aviation industry. The successful candidate will be responsible for conducting thorough inspections of aircraft, operational procedures, and maintenance facilities, identifying potential safety hazards, and ensuring corrective actions are implemented effectively. The ideal candidate possesses a deep understanding of aviation regulations and a commitment to aviation safety excellence.

Responsibilities:
  • Conduct comprehensive safety inspections of aircraft, airports, and aviation-related facilities.
  • Verify compliance with national and international aviation safety regulations and standards.
  • Investigate aviation accidents, incidents, and occurrences, identifying root causes and recommending preventive measures.
  • Evaluate aviation operators' safety management systems (SMS) and ensure their effectiveness.
  • Review and approve aviation safety documentation, including manuals and procedures.
  • Provide guidance and training to aviation stakeholders on safety matters.
  • Perform audits of maintenance organizations and flight operations.
  • Prepare detailed inspection reports and maintain accurate records.
  • Collaborate with aviation authorities and industry partners to promote safety initiatives.

Qualifications:
  • Bachelor's degree in Aviation Management, Aerospace Engineering, or a related field.
  • Minimum of 5 years of experience in aviation safety, operations, or maintenance.
  • Possession of a valid aviation license or certification relevant to the role is highly preferred.
  • In-depth knowledge of ICAO, EASA, FAA, or relevant national aviation regulations.
  • Proven experience in conducting safety audits and inspections.
  • Strong analytical and problem-solving skills, with meticulous attention to detail.
  • Excellent written and verbal communication skills.
  • Ability to work independently and manage time effectively.
  • Proficiency in using relevant safety management software and tools.
  • Commitment to maintaining the highest standards of aviation safety.

This is a critical role for an individual passionate about aviation safety, offering the opportunity to contribute significantly to the integrity and security of air travel.
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