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: 24 August 2022
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Establishing and nourishing partnerships with doctors, focusing on the provision of scientific support and readily offering solutions to accommodate their needs
  • Demonstrating/promoting Remedica’s products to doctors Maintaining detailed records, documenting customer calls and business-related metrics
  • Providing detailed reports as/when requested
  • Conducting market and product exploration to develop an in-depth understanding of Remedica’s and competitors’ products
  • Providing support in product launches and participating in relevant scientific and promotional events

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 pharmaceutical companies) for a minimum of 3 years and ideally as a Medical Representative
  • Registered as a Medical Representative of the “Cyprus Medical Representatives Registration Council”, operating under the auspices of the Ministry of Health
  • Excellent communication skills
  • Exceptional customer service skills
  • Strong negotiation skills
  • Effective organizational skills
  • Persuasion and resilience
  • Good level of knowledge of the English language

Apply Online

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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*

    Quality Assurance

    Registration

    • Job Posted: 24 August 2022
    • 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.
    • Updating 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 English language

    Apply Online

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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*

      • Job Posted: 24 August 2022
      • 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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        Quality Control

        • Job Posted: 24 August 2022
        • 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

        Apply Online

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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*

          Operations

          • Job Posted: 24 August 2022
          • 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

          Apply Online

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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*

            Research and Development

            • Job Posted: 16 September 2022
            • Location: Limassol, Cyprus
            • Working Hours: Full-Time

            Duties and Responsibilities

            • Monitoring/participating in the final trials of prototype development in the R&D unit, in order to understand the product’s behaviour.
            • Evaluation of the product technical suitability at Remedica with the guidance of Supervisor/Head
            • Conducting literature research on the originator drug product (RLD)/drug substance prior to the initiation of lab activities including Product & API patent (if applicable) with the consent of Supervisor/Head
            • Technical aspects: Designing of the formula & process as per QbD, evaluate equipment feasibility, API physical characterisation, DEC study, feasibility/prototype trials/scale up trials including the optimization of process and process parameters, stability testing in accordance to the specifications as per the guidance of Supervisor/Head.
            • Planning, organising, follow-ups must be made to achieve target timelines among technical teams as per the guidance from the Supervisor/Head
            • Compiling/reviewing formal documentation required for product registration purposes

            Qualifications, Skills and Experience

            • Bachelor in Chemical Engineering, Chemistry, and Pharmacy
            • Master’s degree in pharmaceutical sciences preferred with minimum 1 – 3 years of experience is preferred.
            • Accuracy and close attention to detail
            • Sufficient analytical skills & mind set to interpret the analytical data in order to decide on the further product formulation activities
            • Strong analytical skills and mind-set
            • Demonstrated ability to work in both independent and team environments
            • Ability to work under pressure with minimum supervision
            • Excellent communication skills
            • Organization skills
            • Time management skills and ability to prioritize and manage multiple tasks
            • Fluency in English writing and speaking
            • Good MS skills (Word, PowerPoint, Excel)

            Apply Online

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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*

              • Job Posted: 16 September 2022
              • Location: Limassol, Cyprus
              • Working Hours: Full-Time

              Duties and Responsibilities

              • Monitoring/participating in the final trials of prototype development in the R&D unit, in order to understand the product’s behaviour.
              • Executing the procedures required to perform the scale up of prototype formulations to the industrial scale, setting up master documents and performing trials at bigger scale if necessary
              • Executing the process validation procedures during the manufacturing of the validation batches and the production of ICH stability samples.
              • Executing process validation required for API changes for older R&D developed products
              • Cooperates with other R&D teams during a certain process
              • Collecting data in order to compile scientific written responses to deficiency letters from authorities
              • Maintaining accurate records of the Technology Transfer / Scale up activities and communicating results to R&D Management
              • Writing and/or assisting in the write up of documents related to Technology Transfer and Scale Up following guidance from Senior Formulation Scientist.

              Qualifications, Skills and Experience

              • Bachelor in Chemical Engineering, Chemistry, and Pharmacy
              • Master’s degree in pharmaceutical technology preferred
              • Accuracy and close attention to detail
              • Strong technology transfer and scale up skills and mindset
              • Demonstrated ability to work in both independent and team environments
              • Ability to work under pressure with minimum supervision
              • Excellent communication skills
              • Organization skills
              • Time management skills and ability to prioritize and manage multiple tasks
              • Fluency in English writing and speaking
              • Good MS skills (Word, PowerPoint, Excel)

              Apply Online

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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*

                • Job Posted: 24 August 2022
                • 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.

                Apply Online

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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*

                  • Job Posted: 24 August 2022
                  • Location: Limassol, Cyprus
                  • Working Hours: Full-Time

                  Duties and Responsibilities

                  • Assisting in the development and validation of analytical methods according to ICH guidelines
                  • Assisting in the execution of stability studies
                  • Assisting in the execution of Method Transfer/Process validation procedures
                  • Testing materials and products under development
                  • Assisting in the preparation of quality reports and other analytical documents
                  • Ensuring data integrity and proper documentation of experimental data
                  • Executing calibration activities for pH metres and balances
                  • Executing cleaning activities of instruments used during analysis

                  Qualifications, Skills and Experience

                  • Degree in Chemistry, Pharmacy or any other relevant field
                  • HPLC hands on experience is preferred and considered an advantage
                  • Excellent attention to detail
                  • Verbal and written communication skills
                  • Good teamwork skills
                  • Ability to keep detailed records
                  • Ability to work under pressure
                  • Willingness to adjust on a full schedule
                  • Good command of English language and computer

                  Apply Online

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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*

                    • Job Posted: 16 September 2022
                    • Location: Limassol, Cyprus
                    • Working Hours: Full-Time

                    Duties and Responsibilities

                    • Defining the scope of the project and communicating it within R&D and to other stakeholders
                    • Setting up the project plan
                    • Following-up with R&D scientists for day to day tasks and project milestones
                    • Ensuring that the projects run on time and within budget
                    • Monitoring Contract Research Organisations’ (CRO) progress, have a constant update on the process and raising flags where necessary
                    • Monitoring the progress of analytical method development and method transfer activities in order to ensure that these are executed within the timelines given
                    • Maintaining accurate records of the development evolvement and communicating results to Head of R&D Project Management
                    • Compiling project progress reports
                    • Maintaining/updating departmental databases and project management software
                    • Identifying risks/opportunities involved in each project and managing them

                    Qualifications, Skills and Experience

                    • Bachelor in Chemical Engineering, Chemistry, Pharmacy or any other relevant field
                    • Project Management training and certification would be considered an advantage
                    • Knowledge and certification on Microsoft Project an added benefit
                    • Accuracy and close attention to detail
                    • Strong analytical skills and mind-set
                    • Demonstrated ability to work in both independent and team environments
                    • Ability to work under pressure with minimum supervision
                    • Excellent communication skills
                    • Organization skills
                    • Time management skills and ability to prioritize and manage multiple tasks
                    • Fluency in English writing and speaking
                    • Good MS skills (Word, PowerPoint, Excel)

                    Apply Online

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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*

                      • Job Posted: 24 August 2022
                      • 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

                      • Degree Chemistry, Pharmacy or any other relevant field
                      • 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
                      • 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

                      Apply Online

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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*

                        • Job Posted: 16 September 2022
                        • Location: Limassol, Cyprus
                        • Working Hours: Full-Time

                        Duties and Responsibilities

                        • Evaluation of the product technical suitability at Remedica, especially for the critical and complex molecule/product
                        • Conducting literature research on the originator drug product (RLD)/drug substance prior to the initiation of lab activities, including Product & API patents (if applicable)
                        • Technical aspects: Designing of the formula & process as per QbD, evaluate equipment feasibility, API physical characterisation, DEC study, feasibility/prototype trials/scale up trials including the optimization of process and process parameters, stability testing in accordance to the specifications
                        • Works closely with IP and reviews patents and proposes non-infringing strategies for active pharmaceutical ingredients, compositions and manufacturing processes.
                        • Planning, organising, follow-ups must be made to achieve target timelines among technical teams as per the guidance from the supervisor/Head
                        • Compiling/reviewing formal documentation required for product registration purposes

                        Qualifications, Skills and Experience

                        • Bachelor in Chemical Engineering, Chemistry and Pharmacy
                        • Master’s degree in pharmaceutical sciences preferred
                        • Minimum 5 – 7 years of previous Job experience in pharma sector
                        • Attention to detail, accurate and precise in recording data and batch information
                        • Strong analytical skills and mindset
                        • Good leadership skills are of essence.
                        • Timely decision making to avoid delays
                        • Demonstrated ability to work in both independent and team environments
                        • Ability to work under pressure with minimum supervision. Multi-tasking as per departmental requirement with minimum supervision
                        • Excellent communication skills
                        • Good organization skills
                        • Fluency in English writing and speaking
                        • Good MS skills (Word, PowerPoint, Excel)

                        Apply Online

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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*

                          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

                          Υποβάλετε Αίτηση

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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*