Biomedical Engineer Jobs in Bahrain

<p><b>Requirements Essential:</b></p><ul><li>PhD or Postgraduate qualification in library and information science</li><li>Minimum of 3 years’ experience in an academic or research library setting, with a focus on research support or scholarly communications.</li><li>Demonstrated knowledge of open access publishing, copyright, and research impact metrics.</li><li>Experience supporting systematic reviews or advanced literature searching in databases such as PubMed, Embase, CINAHL, and Scopus.</li></ul><p><b><br></b></p><p><b>Desirable</b>:</p><ul><li>Familiarity with biomedical or health sciences research environments.</li><li>Experience working with institutional repositories (e.g., DSpace) and current awareness tools (e.g., ORCID, ResearcherID).</li><li>Understanding of research data management practices and policies.</li><li>Knowledge of emerging scholarly communication trends such as preprints, open peer review, and transformative agreements.</li></ul><p><b><br></b></p><p><b>Skills and Attributes:</b></p><ul><li>Excellent communication, interpersonal, and presentation skills.</li><li>Strong analytical and problem-solving abilities.</li><li>Ability to work independently and collaboratively within cross-functional teams.</li><li>Commitment to user-centred service and continuous improvement.</li><li>Awareness of ethical issues in scholarly publishing and research integrity.</li></ul><p><strong>Desired Candidate Profile</strong></p>PhD or Postgraduate qualification in library and information science<br>Minimum of 3 years’ experience in an academic or research library setting, with a focus on research support or scholarly communications.<br>Demonstrated knowledge of open access publishing, copyright, and research impact metrics.<br>Experience supporting systematic reviews or advanced literature searching in databases such as PubMed, Embase, CINAHL, and Scopus.<br>Familiarity with biomedical or health sciences research environments.<br>Experience working with institutional repositories (e.g., DSpace) and current awareness tools (e.g., ORCID, ResearcherID).<br>Understanding of research data management practices and policies.<br>Knowledge of emerging scholarly communication trends such as preprints, open peer review, and transformative agreements.<br>Excellent communication, interpersonal, and presentation skills.<br>Strong analytical and problem-solving abilities.<br>Ability to work independently and collaboratively within cross-functional teams.<br>Commitment to user-centred service and continuous improvement.<br>Awareness of ethical issues in scholarly publishing and research integrity.

<p>Manage regulatory activities related to product registration, renewal, variation, and approval. Prepare, review, and submit regulatory documents to the relevant authorities. Ensure compliance with applicable regulatory requirements, guidelines, and company procedures. Coordinate with regulatory authorities, manufacturers, suppliers, and internal departments. Review product information, labels, artworks, and supporting documents for regulatory compliance. Follow up on regulatory submissions and respond to authority queries when required. Maintain accurate and up-to-date regulatory records and documentation. Monitor product registration status, approvals, licenses, and renewal timelines. Support regulatory documentation related to product importation and other business activities. Assist with Quality Assurance and Pharmacovigilance activities when required. Monitor updates and changes in applicable regulatory requirements and guidelines. Provide regulatory guidance and support to relevant departments. Perform other regulatory and compliance-related duties as assigned. </p><p><strong>Desired Candidate Profile</strong></p><p>Bachelor of Pharmacy (BPharm), Master of Pharmacy (MPharm), or Doctor of Pharmacy (PharmD) from a recognized university. Previous experience in Regulatory Affairs, Quality Assurance, Pharmacovigilance, or a related healthcare field is preferred. Knowledge of regulatory requirements and product registration processes is an advantage. Good understanding of regulatory documentation and compliance requirements. Strong written and verbal communication skills in English. Good organizational and time-management skills. Strong attention to detail and ability to manage multiple tasks and deadlines. Ability to communicate and coordinate effectively with internal and external stakeholders. Proficiency in Microsoft Office and general document management. Ability to work independently and as part of a team.</p><p><br><br></p><p>Preferred Qualifications Experience within the pharmaceutical, healthcare, food supplement, or medical device industry. Familiarity with regulatory authorities and procedures in Bahrain or the GCC is an advantage. Experience in product registration, regulatory submissions, quality documentation, or pharmacovigilance is preferred.</p>