Discover Remedica’s world of career opportunities. Working at Remedica means being employed by a leading Cypriot pharmaceutical company.

We are amongst Cyprus’s fastest growing companies and we are committed to developing innovative solutions for the production of high-quality, safe and efficacious pharmaceutical products for human use. For this reason, we are looking to recruit the most talented people from across the world, who bring a diverse range of experience and capabilities to our existing team of experts.

Pharmaceutical production has been on a steady incline in Cyprus for the past 40 years and shows no sign of slowing down. As a matter of fact, this segment represents a top export category of the Cypriot manufacturing industry with a whopping €300+ million in revenues. For the past 60 years, Remedica has not only been amongst the biggest revenue generators of the island, but it is also one of its biggest employers, employing more than 800 people. We currently have 5 manufacturing plants and facilities located in the heart of Limassol’s Industrial Area, scattered across a massive area of 50000 sqm2.

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Open positions at Remedica

Check out all the open positions at Remedica, apply for a job position and join our talent pool for future opportunities.


Why REMEDICA

Remedica is a leading pharmaceutical company with a vision for a healthier world through high quality, safe and efficacious products at affordable prices.

Quality and Compliance

  • Job Posted: 17 March 2024
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Perform the worldwide literature search
  • Review the EV website and other relevant websites for any information regarding new regulations, laws etc.
  • Update the Pharmacovigilance System Master File (PSMF)
  • Manage Remedica’s Pharmacovigilance System to ensure that all information on suspected ADRs, is collected, evaluated and reported to the National Competent Authorities
  • Prepares and submits PSURs and RMPs
  • Have an overview of medicinal product safety profile (including management of signals)
  • Prepare and revise agreements with other organizations for the exchange of relevant information
  • Submit 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
  • Participate in Safety Review Meetings, in audits etc.
  • Participate in educational seminars
  • Be 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
  • Be a 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

Remuneration Package

  • 13th and 14th salary
  • Provident Fund
  • Group Medical Plan
  • Discount scheme
  • Gym access

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    • Job Posted: 17 March 2024
    • Location: Limassol, Cyprus
    • Working Hours: Full-Time

    Duties and Responsibilities

    • Conducts internal and external Compliance Assessments of Actives/Excipients and Packaging Materials supplier facilities based on the EU cGMP
    • Develops audit plans, conducts quality audits, prepares audit reports and communicates findings, including compliance risk
    • Reviews and evaluates Suppliers audit responses against current regulations and guidelines to assure compliance
    • Follows-up on corrective and preventative actions to ensure implementation, compliance and continuing efficacy
    • Maintains supplier database and determine final supplier approval status
    • Revises, reviews, and writes SOPs and checklists, as needed in order to complete required audit tasks
    • Reviews, approves or rejects 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 Chemistry or Chemical Engineering)
    • Ability to interpret regulatory guidelines/legislation
    • High level of integrity & ethical standards
    • Excellent time management skills
    • Ability to travel both domestically and internationally
    • Strong analytical and communication skills
    • Problem-solving abilities
    • Excellent command of the English language
    • Computer literacy with working knowledge of MS Office applications
    • Minimum of 2 years of QA/QC experience
    • Experience in the pharmaceutical industry and especially in pharmaceutical quality audit will be

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      • Job Posted: 17 March 2024
      • 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 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

      Remuneration Package

      • 13th and 14th salary
      • Provident Fund
      • Group Medical Plan
      • Discount scheme
      • Gym access

      Apply Online

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        • Job Posted: 17 March 2024
        • 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 about 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

        Remuneration Package

        • 13th and 14th salary
        • Provident Fund
        • Group Medical Plan
        • Discount scheme
        • Gym access

        Apply Online

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          • Job Posted: 17 March 2024
          • Location: Limassol, Cyprus
          • Working Hours: Full-Time

          Duties and Responsibilities

          • Performing the necessary tests for raw materials, intermediates, and finished products to ensure compliance with specifications and then complete the required documentation according to the relevant specifications.
          • Checking the documentation and results of the analysis to ensure the validity of the analysis and its conformity with specifications. Preparing laboratory documents such as reports and analytical protocols
          • Providing guidance and supervision to Junior Analysts and Assistants in conducting their work as and when needed
          • Evaluating new and updated analytical methods and procedures
          • Monitoring equipment maintenance needs, keeping the working area clean and tidy and promptly informing of any equipment troubleshooting needed
          • Reporting updates as regards the status of analysis to supervisors and conduct the relevant investigation when necessary
          • Ensuring that tasks and analysis are completed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and the current Good Manufacturing Practices (cGMP)

          Qualifications, Skills and Experience

          • University degree in Chemistry, Chemical Engineering or any other relevant field
          • Previous experience in Junior Analyst position
          • Excellent knowledge of English language
          • Good command of Microsoft Office
          • 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 as part of a team and individually
          • Excellent time management and prioritization skills

          Remuneration Package

          • 13th and 14th salary
          • Provident Fund
          • Group Medical Plan
          • Discount scheme
          • Gym access

          Apply Online

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            Registration

            • Job Posted: 17 March 2024
            • Location: Limassol, Cyprus
            • Working Hours: Full-Time

            Duties and Responsibilities

            • Preparing regulatory submissions (new registrations, renewals, variations) according to the requirements of each country
            • Communicating with internal and external stakeholders responding to queries and requests following the approval of Supervisor
            • Updating departmental databases, ensuring regulatory compliance
            • Notifying all departments when approvals and withdrawals are received and when registration/renewal submissions have been sent
            • Compiling and/or assisting in the preparation of dossier sections and the updating of dossier sections and document versions
            • Preparing dispatch of samples, original documents and declarations to customers
            • Ensuring that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs) and the current Good Manufacturing Practices (cGMP)

            Qualifications, Skills and Experience

            • Degree in Pharmacology, Pharmacy, Biology, and any other relevant science field
            • Accuracy and close attention to detail
            • Strong analytical skills
            • Time management skills
            • Problem-solving and organizational 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

            Remuneration Package

            • 13th and 14th salary
            • Provident Fund
            • Group Medical Plan
            • Discount scheme
            • Gym access

            Apply Online

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              • Job Posted: 17 March 2024
              • 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

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                • Job Posted: 17 March 2024
                • 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

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                  Operations

                  • Job Posted: 17 March 2024
                  • Location: Limassol, Cyprus
                  • Working Hours: Full-Time

                  Duties and Responsibilities

                  • Organize and monitor equipment maintenance
                  • Fill in related documents taking into consideration relevant legislation, guidelines, company procedures and regulations
                  • Plan and coordinate engineering processes on daily basis
                  • Execute personally troubleshooting of the equipment and assists his team in this activity
                  • Collaborate to the development of production equipment operating SOPs
                  • Communicate and liaises with any relevant department such as Production, R&D, QA and QC Departments

                  Qualifications, Skills and Experience

                  • Bachelor in Electrical, Mechanical or Chemical Engineering, or any other relevant field
                  • Master Degree will be considered as an advantage
                  • Accuracy and close attention to detail
                  • Demonstrated ability to work in both independent and team environments
                  • Ability to work under pressure with minimum supervision

                  Remuneration Package

                  • 13th and 14th salary
                  • Provident Fund
                  • Group Medical Plan
                  • Discount scheme
                  • Gym access

                  Apply Online

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                    • Job Posted: 17 March 2024
                    • 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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                      Research and Development

                      • Job Posted: 17 March 2024
                      • Location: Limassol, Cyprus
                      • Working Hours: Full-Time

                      Duties and Responsibilities

                      • Executing the development and validation of analytical methods according to ICH guidelines
                      • Executing stability studies
                      • Carrying out of Method Transfer procedures
                      • Carrying out analysis during process validation activities
                      • 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
                      • Previous experience with HPLC mandatory
                      • 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

                      Remuneration Package

                      • 13th and 14th salary
                      • Provident Fund
                      • Group Medical Plan
                      • Discount scheme
                      • Gym access

                      Apply Online

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                        • Job Posted: 17 March 2024
                        • 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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                          • Job Posted: 17 March 2024
                          • 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
                          • 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
                          • Writing and/or assisting in the write-up of documents related to project management timelines and procedures

                          Qualifications, Skills and Experience

                          • Bachelor in Chemical Engineering, Chemistry, Pharmacy or any other relevant field
                          • Master’s degree in pharmaceutical sciences or MBA preferred
                          • Project Management certification preferred
                          • 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)

                          Remuneration Package

                          • 13th and 14th salary
                          • Provident Fund
                          • Group Medical Plan
                          • Discount scheme
                          • Gym access

                          Apply Online

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                            • Job Posted: 17 March 2024
                            • 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
                            • 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
                            • Writing and/or assisting in the write-up of documents related to project management timelines and procedures
                            • Preparing and/or reviewing organizational and departmental documents, reports, policies, and procedures

                            Qualifications, Skills and Experience

                            • Bachelor in Chemical Engineering, Chemistry, Pharmacy or any other relevant field
                            • Master’s degree in pharmaceutical sciences or MBA preferred
                            • Previous experience within an R&D Department 3-4 years’ minimum
                            • Project Management certification preferred
                            • 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
                            • Good leadership skills are essential
                            • 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)

                            Remuneration Package

                            • 13th and 14th salary
                            • Provident Fund
                            • Group Medical Plan
                            • Discount scheme
                            • Gym access

                            Apply Online

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                              • Job Posted: 17 March 2024
                              • 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

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                                • Job Posted: 17 March 2024
                                • 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)

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                                  Commercial

                                  • Job Posted: 17 March 2024
                                  • 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 about 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 communication and organizational skills
                                  • Exceptional customer service skills

                                  Remuneration Package

                                  • 13th and 14th salary
                                  • Provident Fund
                                  • Group Medical Plan
                                  • Discount scheme
                                  • Gym access

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                                    General Applications

                                    If you don’t see a job opening that’s relevant for you, feel free to join our talent pool by submitting your CV. If a suitable career opportunity that matches your skillset and experience is found, we will contact you with company information. Your CV will be stored for 6 months in our internal database in accordance with the General Data Protection Regulation and our HR Team will contact you in case an opportunity arises.

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

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