Consultez toutes les offres d’emploi disponibles, postulez à des emplois et rejoignez notre base de données des opportunités.

Nous sommes l’une des entreprises à Chypre qui connaît la croissance et nous nous spécialisons dans le développement, la production et la commercialisation de produits pharmaceutiques de haute qualité, sûrs et efficaces à usage humain. Pour cette raison, nous recrutons les personnes les plus talentueuses du monde qui peuvent ajouter de la valeur à notre équipe d’experts existante grâce à leurs connaissances, leur expérience et leurs capacités.

Au cours des 40 dernières années à Chypre et dans le monde, l’industrie pharmaceutique a suivi une trajectoire ascendante régulière sans aucun signe de ralentissement. Au contraire, le secteur est la première catégorie d’exportation de l’industrie manufacturière chypriote avec des bénéfices de 300 millions d’euros +. Depuis sa création, Remedica est non seulement l’un des plus grands générateurs de revenus de l’île, mais aussi l’un des plus grands employeurs, employant plus de 800 personnes. Actuellement, nos installations à Limassol comprennent 12 bâtiments totalisant plus de 45 000 mètres carrés, dont cinq sont des usines de production de pointe comprenant une usine centrale destinée aux produits à usage général et quatre bâtiments utilisés pour la production de produits à base de pénicilline, de céphalosporines, d’hormones spécifiques et de produits anticancéreux.

Prestations d’emploi

Chez Remedica, vous faites partie de notre vision d’un monde plus sain, nous aidant à améliorer la qualité de la vie humaine en fournissant des médicaments sûrs et efficaces de haute qualité à des millions de patients dans le monde. Notre succès dépend de la performance de nos collaborateurs et de leur engagement envers l’entreprise. En conséquence, nous voulons attirer et développer des talents avec créativité et passion pour ce qu’ils font. L’un des moyens d’atteindre cet objectif est de proposer un ensemble des prestations d’emploi compétitif, comprenant les 13e et 14e salaires, une caisse de prévoyance et une couverture d’assurance, ainsi que des ressources pour cultiver le niveau professionnel et personnel des employés.

Développement

Pour avoir un impact positif sur la vie des patients, nous devons d’abord investir dans l’avancement de notre personnel, car grâce à leur développement, nous aidons Remedica à atteindre son objectif et à maintenir sa position de leader sur le marché mondial. Pour cette raison, nous offrons des opportunités de formation et encourageons activement nos employés à améliorer et développer leurs connaissances et compétences. Les possibilités de formation sont souvent fournies sous forme de cours d’emploi ainsi que des ateliers. De plus, il existe un solide système de rétroaction, qui complète les rapports d’étape annuels, facilitant ainsi le développement professionnel de nos employés.

Culture de travail

Chez Remedica, nous voulons créer une culture d’inclusion qui renforce le sentiment que tous les employés font partie du succès de l’entreprise et leur fournit les outils necessaires pour apprendre, et développer leur potentiel. Nous avons commencé nos activités en 1960 en tant qu’entreprise familiale petite, et bien que nous soyons devenus un acteur majeur de l’industrie pharmaceutique générique mondiale, nous maintenons toujours la même atmosphère familiale chaleureuse et éthique qui prévalaient dans l’entreprise et nous agissons en tant que citoyen du monde responsable. En conséquence, nous encourageons activement nos employés à faire du bénévolat, en leur donnant les opportunités et les ressources necessaires pour contribuer au travail caritatif de l’entreprise.

Diversité et intégration

Chez Remedica,  la diversité est notre priorité. Nous nous engageons à travailler sans discrimination en termes d’âge, de handicap, de sexe, d’état matrimonial, de maternité ou de grossesse, de nationalité, de convictions religieuses, d’orientation sexuelle ou d’appartenance à un syndicat.

Nous sommes constamment à la recherche de nouveaux talents, alors consultez tous nos postes vacants et postulez maintenant!

Remedica traite vos données d’employé(e) candidat(e) conformément a la Politique de confidentialité pour les CV des candidats.

Postes vacants

  • Job Posted: 31 January, 2020
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Analyse a variety of activities including manufacturing, laboratory, and engineering processes and propose efficient improvements with customized applications.
  • Collaborate with a team of IT and non-IT professionals to develop specifications for new applications.
  • Design creative prototypes according to specifications found in a highly regulated environment.
  • Write high-quality source code to program complete applications within deadlines.
  • Perform unit and integration testing before launch.
  • Conduct functional and non-functional testing.
  • Troubleshoot and debug applications.
  • Perform continuous evaluation of existing applications to update and add new features.
  • Develop highly technical documents and handbooks to accurately represent application design and code.

Qualifications, Skills and Experience

    • University degree in Computer Science or related field.
    • Experience across all stages of software development i.e. requirements gathering, design, implementation, testing, deployment.
    • Experience in Asp.NET, C#, VB, JavaScript, SQL, AngularJS, jQuery

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  • Job Posted: 27 January, 2020
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Coordinating Logistics Teams
  • Coordinating the Warehouse and Distribution to improve efficiency and customer service
  • Measuring and monitoring logistics operations through Key Performance Indicators
  • Evaluating logistics practices related to stock management, warehouse management and procurement management through the KPI’s
  • Execute Logistic Projects
  • Lead or follow up basic logistics projects regarding:
    • a) Implementation of Good Distribution Practices
    • b) Upgrade of current logistics tools/software
    • c) Regulatory requirements or European Requirements related to Good Manufacturing Practices (cGMP)
  • Demand Planning

Qualifications, Skills and Experience

  • University degree in Logistics, Supply Chain or any other field related to operations management.
  • Experience similar roles and especially in pharmaceutical industry will be considered as an advantage.
  • Comprehensive knowledge of Warehouse Management Systems (WMS), Enterprise Resource Planning Systems (ERP), Lean Management will be considered as an asset.

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  • Job Posted: 08 January, 2020
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Reviews the EV website and other relevant websites for any information regarding new regulations, laws etc.
  • Performs the worldwide literature search.
  • Updates the Pharmacovigilance System Master File (PSMF).
  • Manages Remedica’s Pharmacovigilance System in order to ensure that all information on suspected ADRs, is collected, evaluated and reported to the National Competent Authorities.
  • Prepares and submits PSURs and RMPs.
  • Has an overview of medicinal product safety profile (including management of signals).
  • Prepares and revises agreements with other organizations for the exchange of relevant information.
  • Submits all information on medicinal products marketed within the European Economic Area in the electronic database (EudraVigilance) of the European Medicines Agency (EMA), and keeps this information up to date.
  • Participates in Safety Review Meetings, in audits etc.
  • Participates in educational seminars.
  • Is aware of any conditions or obligations adopted as part of the marketing authorizations and other commitments relating to safety or the safe use of the medicinal products.
  • Is member of Remedica’s Scientific Advisory Service and performs the duties set out in the relevant Scientific Service internal instructions.

Qualifications, Skills and Experience

  • BS in Pharmacy or Medicine or Chemistry or Biology or Biomedical Science.
  • Excellent knowledge of Microsoft Office i.e. Word, Excel, PowerPoint, etc.
  • Excellent knowledge of the Greek and English languages.
  • Excellent communication skills.
  • Trusted, Hardworking, Organised, Ability to work under pressure with minimum supervision.
  • Experience: For pharmacist or Doctor or Biomedical scientist: Not necessary. For Biologist or Chemist: Minimum 2 years.

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  • Job Posted: 15 November, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Obtain new Marketing Authorizations, Maintain existing MAs and Manage and report regulatory information by:
    • Compiling regulatory documents according to the requirements of each country.
    • Preparing registration dossiers according to CTD or any other relevant format
    • Maintaining product life-cycle and regulatory compliance by submitting MA renewals and variations
    • Keeping up to date with changes in regulatory legislations and guidelines
    • Liaising and negotiating with regulatory authorities and external associates
    • Liaising with Contract Research Organisations for designing and performing in-vivo studies
    • Keeping accurate records and report promptly currently approved information to the relevant departments within the company thus ensuring regulatory compliance

Qualifications, Skills and Experience

  • University degree in Pharmacy, Pharmacology or relevant field.
  • Previous relevant experience of at least 2 years in the field of Regulatory Affairs or in the pharmaceutical industry.
  • Knowledge of the regulatory framework of the industry.
  • Very good knowledge of English language.
  • Strong analytical, communication, organisational skills.
  • Computer literacy. 

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  • Job Posted: 28 August, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Review the manufacture and testing of the product.
  • Ensures the GMP compliance.
  • Ensures that the product is in accordance with the requirements of the Marketing Authorisations.
  • Releases finished product batch.
  • Generates batch release certificates
  • Performs investigations as required.
  • Initiates and reviews procedures.
  • Supports audits from customers and authorities

Qualifications, Skills and Experience

  • Registered Qualified Person in accordance with EU GMP.
  • If the candidate is not registered as a Qualified Person, then a University degree in Pharmacy is mandatory.
  • Master degree and previous experience within the Pharmaceutical industry will be considered as an advantage.
  • Understands fundamental scientific problems
  • Able to write and review reports with clarity and brevity
  • Fluent in English and Greek language
  • Good knowledge of Microsoft office package

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  • Job Posted: 26 July, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Test starting materials, intermediate and finished products according to procedures and specifications.
  • Work productively for the completion of each task assigned in a timely and efficient manner, to minimize the running cost of the analysis.
  • Follow Standard operating procedures.
  • Follow GLP, GMP and company regulations on safety, cleanliness, personal hygiene and tidiness.

Qualifications, Skills and Experience

  • University degree in Chemistry, Pharmacy or a related field.
  • Master degree in a relevant field will be considered as an advantage.
  • Previous work experience will be considered as an advantage.

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  • Job Posted: 3 March, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Ensure Compliance of Raw material manufacturers.
  • Handle Deviations for incoming raw material.
  • Handle raw material change controls.
  • Handle raw material complaints.
  • Handle supplier evaluation documentation.
  • Perform annual supplier review.
  • Maintains supplier database.
  • Revise, review, and write SOPs and checklists, as needed in order to complete required evaluation tasks.
  • Review, approve or reject DMF and other documents needed to be submitted to the competent authorities in order to obtain or renew the Marketing License of company’s products.

Qualifications, Skills and Experience

  • University degree in a scientific field (preferably Chemical Engineering).
  • Minimum of 2 years of QA/QC experience.
  • Experience in the pharmaceutical industry and especially in pharmaceutical quality audit will be considered as an advantage.
  • Excellent command of the English language

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  • Job Posted: 3 March, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Responsible to execute daily production schedule.
  • Provide daily supervision of line production personnel.
  • Review executed batch records and insure cGMP is maintained in production operations.
  • Perform process investigations, initiate CAPAs and change controls.
  • Develop and apply a strategy for production improvement.
  • Identify and solve production problems.
  • Apply policies and procedures.
  • Manage people effectively.
  • Perform internal production checks.
  • Responsible to train personnel.

Qualifications, Skills and Experience

  • Bachelor’s degree in Chemical Engineering or another related field.
  • Masters’ degree will be considered as an advantage.
  • Experience in the Pharmaceutical industry will be considered an advantage.
  • Good command of the English language

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  • Job Posted: 23 October, 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

• Analytical Method Development and Validation.
• Execution of stability studies.
• Carrying out of Method Transfer procedures.
• Testing materials and products under development
• Preparing quality reports.
• Ensuring data integrity and proper documentation of experimental data.
• Achieve departments’ goals.
• Complying with GMP/GLP.

Qualifications, Skills and Experience

• University degree in Chemistry or Pharmacy.
• Master degree will be considered as an advantage.
• Minimum of 2 years’ experience in Research and Development (Analytical) in Pharmaceutical Industry, handling instrumentation such as HPLC, HPLC-MS, GC.

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  • Job Posted: 15 September, 2017
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Operates production machinery to produce a variety of pharmaceutical products
  • Checks and ensures product compliance to established standards
  • Cleans production machinery and equipment
  • Executes machine changeovers
  • Identifies and reports processing related issues

Qualifications, Skills and Experience

  • High School or Technical School leaving certificate
  • 1 year of relevant experience will be considered as an asset
  • Good command of the Greek and English language

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  • Location: Limassol, Cyprus
  • Working Hours: Depending on the Position

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Always looking to expand our team, we encourage you to apply at Remedica even if a vacancy that suits you might not currently be open.

In such a case, use the form below to send us your CV which will be saved for 6 months in our internal database based on the data protection regulation and our HR Team will contact you as soon as possible if an opportunity arises.

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