Ανακαλύψτε τις διάφορες ευκαιρίες σταδιοδρομίας στην Remedica. Οι ευκαιρίες σταδιοδρομίας στη Remedica σημαίνει εργοδότησησε μια κορυφαία κυπριακή φαρμακευτική εταιρεία.

Ανήκουμε στις ταχύτερα αναπτυσσόμενες εταιρείες της Κύπρου και ειδικευόμαστε στην ανάπτυξη, παραγωγή και εμπορία υψηλής ποιότητας, ασφαλών και αποτελεσματικών φαρμακευτικών προϊόντων για ανθρώπινη χρήση. Γι’ αυτό το λόγο στοχεύουμε στο να προσλαμβάνουμε τους πιο ταλαντούχους ανθρώπους από όλο τον κόσμο, οι οποίοι θα προσθέσουν αξία στην υπάρχουσα ομάδα εμπειρογνωμόνων μας με τις γνώσεις, εμπειρίες και δυνατότητες τους, αλλά και την όρεξη για κάνουν τη διαφορά.

Τα τελευταία 40 χρόνια στην Κύπρο και ανά το παγκόσμιο, η φαρμακοβιομηχανία παρουσιάζει μια σταθερή ανοδική πορεία χωρίς κανένα σημάδι καθοδικής πορείας Αντιθέτως, ο τομέας μας συγκαταλέγεται στην κορυφαία κατηγορία εξαγωγών της κυπριακής μεταποιητικής βιομηχανίας με κέρδη ύψους €300 + εκατομμυρίων. Από την αρχή της δημιουργίας της μέχρι και σήμερα, η Remedica δεν είναι μόνο ένας από τους μεγαλύτερους δημιουργούς εσόδων του νησιού, αλλά είναι επίσης και ένας από τους μεγαλύτερους εργοδότες , απασχολώντας περισσότερους από 800 ανθρώπους. Επί του παρόντος, οι εγκαταστάσεις μας στη Λεμεσό αποτελούνται από 12 κτήρια συνολικής έκτασης πέραν των 45.000 τ.μ., εκ των οποίων τα πέντε είναι εγκαταστάσεις παραγωγής τελευταίας τεχνολογίας που αποτελούνται από το κεντρικό εργοστάσιο που προορίζεται για προϊόντα γενικής χρήσης και τέσσερα κτήρια που χρησιμοποιούνται για την παραγωγή προϊόντων πενικιλίνης, κεφαλοσπορίνων, συγκεκριμένων ορμονών και αντικαρκινικών προϊόντων.

Η επεξεργασία του βιογραφικού σημειώματος που μας αποστέλλετε είναι σύμφωνη με τις διατάξεις του περί Επεξεργασίας Προσωπικών Δεδομένων Νόμου του 2001 (Προστασία του Ατόμου).

Ευκαιρίες σταδιοδρομίας στην Remedica

Δείτε όλες τις υπάρχουσες ανοιχτές θέσεις, κάντε αίτηση για θέσεις εργασίας και ενταχθείτε στη βάση δεδομένων μας για μελλοντικές ευκαιρίες.


Commercial Department

  • Job Posted: 06 November 2020
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Visit doctors, dentists and other health professionals to promote (scientifically update) products assigned to him/her according to schedule
  • Develops relationships of trust with health professionals
  • Keeps track of product sample for doctors, dentists and other healthcare professionals
  • Provides a daily report as regards schedule, activities and/or other issues related to his/her duties work done
  • Collects information, data and other material about competitors, conferences and other events of interest for Remedica, including relevant laws / regulations
  • Keeps a record with data of doctors, dentists and other health professionals
  • Actively participates in scientific conferences related to the health sector

Qualifications, Skills and Experience

  • Medical Representative Diploma or Bachelor’s degree in Pharmacy, Biology, Chemistry or related field
  • Proven experience in the health sector (preferably in a pharmaceutical company) for a minimum of 3 years and ideally as a Medical Representative
  • Registered to the Registry of Medical Representatives of the Cyprus Medical Representatives Registration Council, operating under the auspices of the Ministry of Health
  • Excellent level of knowledge of the Greek and the English language
  • Strong negotiation skills
  • Excellent organizational skills
  • Effective communication skills
  • Exceptional customer service skills
  • Persuasive and resilient

Apply Online

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    • Job Posted: 29 May 2020
    • Location: Limassol, Cyprus
    • Working Hours: Full-Time

    Duties and Responsibilities

    • Manage alignment of resources within the assigned countries of responsibility to ensure sales forecasts and operational budgets are met or exceeded.
    • Explore, identify, analyse and recommend new business opportunities.
    • Build and maintain excellent relationship with customers under his/her supervision.
    • Suggest marketing plans for the assigned countries of responsibility.
    • Possess good knowledge of the performance, potential and characteristics of his/her assigned countries to facilitate planning and development of business.
    • Make an effective application of the data in all related sales activities and systems to ensure good maintenance of records.
    • Acquire sales and market intelligence on issues such as competition, price, and project status.

    Qualifications, Skills and Experience

    • Bachelor’s Degree in Business Administration, Economics, or relevant Degree
    • MBA will be considered an advantage
    • Knowledge of Pharmaceutical procedures and GMP will be considered as an advantage.
    • Prior experience of 3-5 years in a relevant role is required.
    • Experience in the Pharmaceutical industry will be considered as an advantage.
    • Demonstrated understanding of customer segments and regional market dynamics.

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      Quality Assurance

      • Job Posted: 05 July 2021
      • Location: Limassol, Cyprus
      • Working Hours: Full-Time

      Duties and Responsibilities

      • Initiating change requests impacting the GMP of the manufacturing facility
      • Evaluating and monitoring change requests
      • Preparing or assisting in the preparation of technical reports, documents and reports
      • Providing training to new employees on how to submit CRFs (Change Request Form) requests through the electronic system.
      • Communicating with relevant internal stakeholders in order to collect feedback needed for the potential implementation of changes to specific products
      • Ensuring that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), Good Documentation Practices (cGDP) and the current Good Manufacturing Practices (cGMP)

      Qualifications, Skills and Experience

      • Degree in Pharmacy, Chemical Engineering or any other relevant field
      • Any relevant experience will be considered an advantage
      • High attention to detail
      • Organized and methodical way of thinking
      • Ability to work collaboratively in a team
      • Excellent written and verbal communication skills
      • Excellent command of the English Language
      • Knowledge of Microsoft Office

      Apply Online

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        Registration

        • Job Posted: 11 October 2021
        • Location: Limassol, Cyprus
        • Working Hours: Full-Time

        Duties and Responsibilities

        • Preparing regulatory submissions (new registrations, renewals, variations) according to the requirements of each country following guidance from Supervisor
        • Communicating with internal and external stakeholders responding to queries and requests following guidance from Supervisor.
        • Upd0ating departmental databases and reviewing of RIM records to ensure regulatory compliance.
        • Assessing Change Requests following feedback from Supervisor for potential regulatory impact
        • Informing all departments when approvals and withdrawals are received, registration/ renewal submissions have been sent.
        • Compiling and/or preparing dossier sections, updating dossier sections and document versions, ensuring the validity of information to be submitted for all regulatory submissions.
        • Monitoring regulations and guidelines relating to products and registration procedures, informing the relevant departments when necessary
        • Assisting in the preparation of departmental documents such as procedures and/or SOPs

        Qualifications, Skills and Experience

        • University degree in, Pharmacology, Pharmacy, Biology and any other relevant science field
        • Previous experience as a Junior RA Officer considered an advantage
        • Accuracy and close attention to detail
          – Time management skills
          – Organisation skills
          – Strong written communication skills to provide concise and clear documentation
          – Must be able to work in a fast-paced environment.
          – Good computer skills
          – Excellent knowledge of the English language

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          • Job Posted: 14 May 2021
          • Location: Limassol, Cyprus
          • Working Hours: Full-Time

          Duties and Responsibilities

          • Suggest clinical trial designs, provide input to CROs and finalize designs
          • Review and approve the BE/pK study protocols
          • Analyze data, review/evaluate and approve study reports
          • Liaise with pK experts for the assessment of data and reports
          • Collaborate cross-functionally, working closely with R&D for pK data needed for formulation development
          • Provide feedback advice on strategies for establishing IVIVC
          • Manage the BE Study monitoring activities ensuring compliance with Good Clinical Practices (GCP) and applicable regulations
          • Track and obtain approval of clinical operations expenses

          Qualifications, Skills and Experience

          • BSc in Pharmacy, Pharmacology
          • PhD with concentration on Pharmacology or Pharmacokinetics will be considered an advantage
          • At least two years’ experience in the generic pharmaceutical industry, preferably clinical trial experience
          • Knowledge of Pharmaceutical legislation, Knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial management are mandatory
          • High attention to detail
          • Analytical thinking
          • Scientific writing experience
          • Excellent written and verbal communication skills
          • Excellent command of the English Language
          • Strong clinical study management skills

          Apply Online

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            • Job Posted: 11 October 2021
            • Location: Limassol, Cyprus
            • Working Hours: Full-Time

            Duties and Responsibilities

            • Preparing regulatory submissions (new registrations, renewals, variations) according to the requirements of each country following guidance from Supervisor
            • Communicating with internal and external stakeholders responding to queries and requests following guidance from Supervisor.
            • Upd0ating departmental databases and reviewing of RIM records to ensure regulatory compliance.
            • Assessing Change Requests following feedback from Supervisor for potential regulatory impact
            • Informing all departments when approvals and withdrawals are received, registration/ renewal submissions have been sent.
            • Compiling and/or preparing dossier sections, updating dossier sections and document versions, ensuring the validity of information to be submitted for all regulatory submissions.
            • Monitoring regulations and guidelines relating to products and registration procedures, informing the relevant departments when necessary
            • Assisting in the preparation of departmental documents such as procedures and/or SOPs

            Qualifications, Skills and Experience

            • University degree in, Pharmacology, Pharmacy, Biology and any other relevant science field
            • Previous experience as a Junior RA Officer considered an advantage
            • Accuracy and close attention to detail
              – Time management skills
              – Organisation skills
              – Strong written communication skills to provide concise and clear documentation
              – Must be able to work in a fast-paced environment.
              – Good computer skills
              – Excellent knowledge of the English language

            Apply Online

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              Portfolio

              • Job Posted: 14 May 2021
              • Location: Limassol, Cyprus
              • Working Hours: Full-Time

              Duties and Responsibilities

              • Searching in patent databases and identify patents related to the company’s products, recognizing the status of patent applications and proceedings in European and non- European territories.
              • Compiling all related information and designing appropriate repositories and systems for this task.
              • Reviewing, analysing and providing advice/opinion to the Senior Management, R&D, Legal, Regulatory and other departments on patents via the preparation of consolidated patent reports.
              • Collaborating with external experts and partners for patent searches, patent reports and patent filings.
              • Assessing and concluding on patent clearance for Drug Products and Drug Substances synthetic routes against any valid patents in the concerned territories.

              Qualifications, Skills and Experience

              • BSc in Pharmacy, Chemistry, Pharmacology with a post graduate degree in a relevant field
              • Pharmaceutical Intellectual Property Landscape, Organic Chemistry, Pharmaceutical Industry knowledge is required
              • Experience within the pharmaceutical industry (1-2 years) and preferably as an Intellectual Property or Patent Officer
              • High attention to detail
              • Organized and methodical way of thinking
              • Ability to work collaboratively in a team
              • Excellent written and verbal communication skills
              • Excellent command of the English Language

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                Quality Control

                • Job Posted: 16 April 2021
                • Location: Limassol, Cyprus
                • Working Hours: Full-Time

                Duties and Responsibilities

                • Performing the necessary tests for raw materials, and the products’ intermediate, final and under stability studies, according to written procedures and specifications. Proceeding with the completion of the required documentation.
                • Ensuring that all analysis conducted follow the procedures of the analytical methods.
                • Checking the documentation and results of the analysis prepared by the QC Department, as and when requested to ensure the validity of the analysis/conformity with regulations.
                • Monitoring equipment maintenance needs, keeping the working area clean and tidy and promptly informing Laboratory Engineers of any equipment troubleshooting needed.
                • Reporting updates as regards the status of analysis to Supervisors, conducting relevant investigations when necessary.

                Qualifications, Skills and Experience

                • University degree in Chemistry, Chemical Engineering or any other relevant field
                • MSc will be considered as an advantage
                • Excellent knowledge of English language
                • Previous experience within pharma industry will be considered an advantage (HPLC, GC/MS, ICP, TLC, LC/MS, LC/MS/MS, XRD, PSD)
                • Excellent organizational skills.
                • Ability to work on multiple projects at the same time
                • Ability to work as part of a team and individually
                • Excellent time management and prioritization skills

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                  Operations

                  • Job Posted: -
                  • 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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                    Quality & Compliance

                    • Job Posted: -
                    • 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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                      Portfolio Development

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

                      Duties and Responsibilities

                      • Leading a team of analysts, giving support and guidance during their daily work
                      • Reviewing and evaluating the development and validation of analytical methods and procedures
                      • Reviewing and evaluating stability study results
                      • Designing and/or overviewing dissolution method development experiments
                      • Preparing laboratory documents such as SOPs, protocols and reports.
                      • Reviewing the documentation and results of the analysis to ensure the validity of the analysis and its conformity with specifications and approve the audit trail, managing out of specification/out of trend procedures if and when needed
                      • Evaluating deficiencies received by the registration department and providing scientific explanations.

                      Qualifications, Skills and Experience

                      • A Senior Analyst must be obedient organized, cooperative and willing to adjust on a full schedule
                      •  Good time-task allocation and ability to meet project deadlines
                      •  Good leadership skills are of essence
                      •  Attention to Detail
                      •  Analytical Thinking
                      •  To be able to work under pressure
                      •  Good command of English language
                      Experience
                      •  Previous experience with HPLC systems, GC, UV mandatory, Previous experience with method validation an advantage
                      •  Previous experience on pharmaceutical analysis of 4-6 years in QC or R&D roles mandatory

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                        • Job Posted: -
                        • 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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                          Γενική Αίτηση Εργοδότησης

                          Εάν δεν υπάρχουν θέσεις εργασίας που σας ενδιαφέρουν, μπορείτε να υποβάλετε το βιογραφικό σας στη βάση δεδομένων μας, στην οποία και θα ανατρέξουμε όταν ανοιχθεί νέα αντίστοιχη θέση εργασίας. Το βιογραφικό σας, θα αποθηκευτεί για περίοδο 6 μηνών στην εσωτερική βάση δεδομένων μας, σύμφωνα πάντα με τον Γενικό Κανονισμό Προστασίας Δεδομένων. Η ομάδα Ανθρώπινου Δυναμικού μας θα επικοινωνήσει μαζί σας σε περίπτωση που προκύψει η οποιαδήποτε ευκαιρία η οποία ταιριάζει το προφίλ σας.

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

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                            Συμφωνώ με την επεξεργασία των προσωπικών μου δεδομένων σύμφωνα με την πολιτική προστασίας προσωπικών δεδομένων της Remedica για τα υποψήφια βιογραφικά σημειώματα*