Orthopaedics Jobs in Algeria
27 Jobs Found
<section><p class="heading jdMain">Job Description</p><p class="heading">Roles & Responsibilities</p><div class="paragraph"><p></p><ul> <li><font dir="auto" ><font dir="auto" >Promote the company's products to healthcare professionals (doctors, pharmacists, etc.).</font></font></li> <li><font dir="auto" ><font dir="auto" >Develop and maintain strong relationships with clients and partners.</font></font></li> <li><font dir="auto" ><font dir="auto" >Conduct competitive intelligence and gather field information.</font></font></li> <li><font dir="auto" ><font dir="auto" >Develop action plans to achieve the set business objectives.</font></font></li> <li><font dir="auto" ><font dir="auto" >Provide regular reporting to the sales management.</font></font></li> <li><font dir="auto" ><font dir="auto" >Participate in training sessions and meetings organized by the company.</font></font></li> </ul><p></p></div></section><section><p class="heading">Desired Candidate Profile</p><p class="paragraph"></p><p></p><ul> <li><font dir="auto" ><font dir="auto" >Graduate in Pharmacy, Medicine, Dentistry, Veterinary Medicine or Biology.</font></font></li> <li><font dir="auto" ><font dir="auto" >Excellent command of spoken and written French.</font></font></li> <li><font dir="auto" ><font dir="auto" >Practical knowledge of the Office suite (Word, Excel, PowerPoint).</font></font></li> <li><font dir="auto" ><font dir="auto" >Must have own transportation and be available for travel outside the residence.</font></font></li> <li><font dir="auto" ><font dir="auto" >Dynamism, rigor and a sense of organization.</font></font></li> <li><font dir="auto" ><font dir="auto" >Good interpersonal skills and team spirit.</font></font></li> </ul><p></p><p></p></section>
<p>Ensure nursing care according to medical prescriptions. Welcome, assist and monitor patients. Administer treatments and ensure follow-up of care. Ensure compliance with hygiene and safety rules. Participate in the management of medical equipment and patient records.</p><p><strong>Desired Candidate Profile</strong></p><div>State diploma or recognized nursing diploma. Professional experience of at least 1 year desired. Sense of responsibility, rigor and discretion. Good interpersonal skills and ability to work in a team. Availability and responsiveness.</div>
<section><p class="heading jdMain">Job Description</p><p class="heading">Roles & Responsibilities</p><div class="paragraph"><p>Accueillir et orienter les clients/patients au sein de l officine. Assister le pharmacien dans la pr paration, la d livrance et la gestion des m dicaments. Participer la vente des produits parapharmaceutiques (hygi ne, beaut , nutrition, etc.). Effectuer le suivi des stocks, la r ception et le rangement des livraisons. S assurer du respect des r gles d hygi ne, de s curit et de tra abilit . Bonne connaissance des produits pharmaceutiques et parapharmaceutiques. Sens du service client, rigueur et discr tion professionnelle. S rieuse, organis e et passionn e par le domaine de la sant . Ma trise des outils informatiques et des logiciels de gestion en pharmacie.</p></div></section><section><p class="heading">Desired Candidate Profile</p><p class="paragraph"></p><p>Bonne connaissance des produits pharmaceutiques et parapharmaceutiques. Sens du service client, rigueur et discr tion professionnelle. S rieuse, organis e et passionn e par le domaine de la sant . Ma trise des outils informatiques et des logiciels de gestion en pharmacie.</p><p></p></section>
<section><p class="heading jdMain">Job Description</p><p class="heading">Roles & Responsibilities</p><div class="paragraph"><p></p><ul> <li><font dir="auto" ><font dir="auto" >Present pharmaceutical or medical products to healthcare professionals during individual visits or group meetings.</font></font></li> <li><font dir="auto" ><font dir="auto" >Explain the characteristics, indications, contraindications and benefits of the products clearly and precisely.</font></font></li> <li><font dir="auto" ><font dir="auto" >To provide up-to-date information on clinical data and relevant study results to support product use.</font></font></li> <li><font dir="auto" ><font dir="auto" >establish and maintain professional relationships with doctors, pharmacists and other health professionals in the assigned region.</font></font></li> <li><font dir="auto" ><font dir="auto" >Identify the needs of healthcare professionals and offer personalized support based on their preferences and clinical practices.</font></font></li> <li><font dir="auto" ><font dir="auto" >To respond to the questions and concerns of healthcare professionals in an effective and professional manner.</font></font></li> </ul><p></p> <p></p><ul> <li><font dir="auto" ><font dir="auto" >Excellent communication skills and ability to build interpersonal relationships.</font></font></li> <li><font dir="auto" ><font dir="auto" >In-depth understanding of pharmaceutical or medical products, as well as associated medical and scientific concepts.</font></font></li> <li><font dir="auto" ><font dir="auto" >Ability to present complex information in a clear and convincing manner.</font></font></li> <li><font dir="auto" ><font dir="auto" >Sense of organization and ability to manage time and resources effectively.</font></font></li> <li><font dir="auto" ><font dir="auto" >Workplace: Constantine / Stif. </font></font></li> </ul><p></p></div></section><section><p class="heading">Desired Candidate Profile</p><p class="paragraph"></p><p><font dir="auto" ><font dir="auto" >If you match this profile, please send your CV by clicking</font></font></p> <p><font dir="auto" ><font dir="auto" >on the apply tab</font></font></p><p></p></section>
<section><p class="heading jdMain">Job Description</p><p class="heading">Roles & Responsibilities</p><div class="paragraph"><p></p><ul> <li><font dir="auto" ><font dir="auto" >Ensure the processing and follow-up of pharmacovigilance, technovigilance and other vigilance cases in accordance with the regulations and procedures in force.</font></font></li> <li><font dir="auto" ><font dir="auto" >Receive, analyze, enter and control the quality of cases in dedicated databases.</font></font></li> <li><font dir="auto" ><font dir="auto" >Ensure compliance with regulatory laws on the transmission and reporting of cases.</font></font></li> <li><font dir="auto" ><font dir="auto" >Participate in monitoring pharmacovigilance data sources and reconciliation activities.</font></font></li> <li><font dir="auto" ><font dir="auto" >Contribute to the continuous improvement of processes and to the monitoring of compliance of PV/TV activities.</font></font></li> <li><font dir="auto" ><font dir="auto" >Participate in the management of deviations, CAPAs, audits and inspections.</font></font></li> <li><font dir="auto" ><font dir="auto" >Ensure the continuity of service activities and collaborate with local and global teams.</font></font></li> </ul><p></p> <p></p><ul> <li><font dir="auto" ><font dir="auto" >Degree in the field of health, life sciences or medical sciences.</font></font></li> <li><font dir="auto" ><font dir="auto" >Minimum 2 years of experience in pharmacovigilance.</font></font></li> <li><font dir="auto" ><font dir="auto" >Good knowledge of PV/TV regulations and case management processes.</font></font></li> <li><font dir="auto" ><font dir="auto" >Excellent organizational, prioritization, and problem-solving skills.</font></font></li> <li><font dir="auto" ><font dir="auto" >Good oral and written communication skills.</font></font></li> <li><font dir="auto" ><font dir="auto" >My required mastery of written and spoken English.</font></font></li> <li><font dir="auto" ><font dir="auto" >Ability to work in a team and in a constantly changing environment.</font></font></li> <li><font dir="auto" ><font dir="auto" >Rigour, adaptability and a sense of confidentiality.</font></font></li> </ul><p></p></div></section><section><p class="heading">Desired Candidate Profile</p><p class="paragraph"></p><p><font dir="auto" ><font dir="auto" >Degree in the field of health, life sciences or medical sciences.</font></font></p> <p><font dir="auto" ><font dir="auto" >Minimum 2 years of experience in pharmacovigilance.</font></font></p> <p><font dir="auto" ><font dir="auto" >Good knowledge of PV/TV regulations and case management processes.</font></font></p> <p><font dir="auto" ><font dir="auto" >Excellent organizational, prioritization, and problem-solving skills.</font></font></p> <p><font dir="auto" ><font dir="auto" >Good oral and written communication skills.</font></font></p> <p><font dir="auto" ><font dir="auto" >My required mastery of written and spoken English.</font></font></p> <p><font dir="auto" ><font dir="auto" >Ability to work in a team and in a constantly changing environment.</font></font></p> <p><font dir="auto" ><font dir="auto" >Rigour, adaptability and a sense of confidentiality.</font></font></p><p></p></section>
<section><p class="heading jdMain">Job Description</p><p class="heading">Roles & Responsibilities</p><div class="paragraph"><p><strong>Assistant Pharmacist to the Technical Director</strong></p>
<p><strong>1. Job description and role</strong></p>
<p>The Assistant Pharmacist supports the Pharmacist Technical Director in executing all technical and regulatory activities for locally manufactured AstraZeneca products in Algeria, ensuring alignment with Algerian Health Authority laws and AstraZeneca global codes, standards, and procedures.</p>
<p>The role coordinates regulatory submissions, regulatory documentation review and batch release notification , and Health Authority (HA) interactions; and ensures timely reporting.</p>
<p>During the Technical Director s absence, the Assistant Pharmacist acts as the designated Back-Up, with the same powers and responsibilities for the duration of the replacement.</p>
<p>The position is based at the Algiers Head Office, operates within Algeria, reports to the AAPI General manager,</p>
<p>Key interfaces include Regulatory Affairs, Head of Quality, EHS/EQ & ESM, Project Leads, the General Manager, local CMOs, and authorities such as ANPP and the Ministry of the Pharmaceutical Industry.</p>
<p><strong>2. Accountability</strong></p>
<ul>
<li><strong>Regulatory declarations and reporting</strong>: Declare batch releases to the National Agency of Pharmaceutical Products; submit weekly, monthly, and annual stock level reports to the Ministry of the Pharmaceutical Industry; declare expired products, incinerated products, and production schedules to the Ministry; submit the annual inventory of pharmaceutical products as per ministerial procedures.</li>
<li><strong>Regulatory documentation review</strong>: Review and verify completeness, accuracy, and consistency of regulatory documents and dossiers (e.g., registration/approval files, variations, import programs, batch release packages, HA responses), ensuring alignment with approved data, GMP, and internal quality systems prior to submission or release.</li>
<li><strong>Product quality </strong>;Pre-notify the Ministry of any modification affecting quality, safety, or efficacy relative to the approved registration/approval dossier.</li>
<li><strong>Import program</strong>: Prepare and submit the provisional import program for API, raw materials and packaging items to the Ministry responsible for the pharmaceutical industry.</li>
<li><strong>Health Authority interactions and follow up </strong>: HA interactions and respond to HA queries consistently, within required timelines, and in accordance with internal guidelines.</li>
<li><strong>Acting Technical Director (Back-Up)</strong>: Assume the responsibilities of the Pharmacist Technical Director during periods of absence.</li>
<li><strong>Stakeholder collaboration</strong>: Work closely with internal stakeholders (Regulatory Affairs, Quality, EHS/EQ & ESM, Project Leads, General Manager) and external partners (ANPP, Ministry of the Pharmaceutical Industry, local CMOs) to ensure compliant, timely delivery of regulatory and operational obligations.</li>
</ul>
<p><strong>3. Required qualification</strong></p></div></section><section><p class="heading">Desired Candidate Profile</p><p class="paragraph"></p><p><strong>Education</strong>: University degree in Pharmacy.</p>
<p><strong>Experience</strong>: 2 3 years in the pharmaceutical industry within a manufacturing environment, ideally covering quality and/or regulatory functions; desirable minimum of 1 year of dedicated regulatory experience.</p>
<p><strong>Skills and competencies</strong>: Working knowledge of Microsoft Office; good knowledge of the pharmaceutical industry requirement; organized and accurate, with strong stakeholder management / proficiency in English</p>
<p><strong>Mobility:</strong> autonomous for frequent travel to authorities and potentially to the CMO sites.</p><p></p></section>
<section><p class="heading jdMain">Job Description</p><p class="heading">Roles & Responsibilities</p><div class="paragraph"><ul> <li><font dir="auto" ><font dir="auto" ><font dir="auto" ><font dir="auto" >Microbiologist Analyst</font></font></font></font></li><li><font dir="auto" ><font dir="auto" ><br></font></font></li><li><font dir="auto" ><font dir="auto" >to study, analyze, classify and identify the structure and functions of microorganisms (viruses, fungi, bacteria, algae, etc.) as well as their relationships with the environment, their reproduction, their actions, in order to optimize their use in the manufacture of pharmaceutical products.</font></font></li> <li><font dir="auto" ><font dir="auto" >Perform technical tests and microbiological analyses to identify and count microorganisms (bacteria, viruses, fungi, parasites, etc.) present in various environments.</font></font></li> <li><font dir="auto" ><font dir="auto" >to study the action of microorganisms and to develop ways to counteract their harmful effects or exploit their beneficial effects.</font></font></li> <li><font dir="auto" ><font dir="auto" >Complete the documents relating to the batch files.</font></font></li> <li><font dir="auto" ><font dir="auto" >Perform the various laboratory analysis procedures.</font></font></li> <li><font dir="auto" ><font dir="auto" >Perform bacteriological checks and evaluate the performance of packaging items (tubes, P sorting boxes, bottles, leaflets, cases, etc.).</font></font></li> <li><font dir="auto" ><font dir="auto" >assess the chemical and biological risks of the products used; possess good visual acuity and be able to distinguish colors.</font></font></li> <li><font dir="auto" ><font dir="auto" >Carry out microbiological sampling and analysis (environmental controls, membrane filtration, microbial counts) on raw materials, semi-finished products and finished products, in accordance with procedures, in compliance with GLP and GMP.</font></font></li> <li><font dir="auto" ><font dir="auto" >Prepare the analysis files within the given deadlines.</font></font></li> <li><font dir="auto" ><font dir="auto" >Supply your workstation and ensure that the equipment is functioning properly.</font></font></li> <li><font dir="auto" ><font dir="auto" >Alert management in case of anomalies and contribute to the resulting investigations.</font></font></li> <li><font dir="auto" ><font dir="auto" >Ensure traceability of all operations carried out.</font></font></li> <li><font dir="auto" ><font dir="auto" >Participate in updating procedures related to methods or equipment.</font></font></li> <li><font dir="auto" ><font dir="auto" >Participate in the qualification of equipment and carry out periodic checks.</font></font></li> <li><font dir="auto" ><font dir="auto" >Verify the analysis results related to its activity and update trend monitoring.</font></font></li> <li><font dir="auto" ><font dir="auto" >Participate in the drafting of protocols, procedures, instruction sheets, operating procedures, raw data and safety data sheets.</font></font></li> <li><font dir="auto" ><font dir="auto" >Verify the raw data from routine microbiological analyses.</font></font></li> </ul> <ul> <li> <b><font dir="auto" ><font dir="auto" >Basic education</font></font></b><font dir="auto" ><font dir="auto" > : Bachelor's or Master's degree in chemistry, biology or process engineering or equivalent.</font></font><br></li> <li> <b><font dir="auto" ><font dir="auto" >Professional training</font></font></b><font dir="auto" ><font dir="auto" > : GMP and GLP standards and basic concepts in metrology.</font></font><br></li> <li><font dir="auto" ><font dir="auto" >3-4 years of experience.</font></font></li></ul></div></section>