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.


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 samples 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

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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

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        Registration

        • 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

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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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              Engineering

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

              Duties and Responsibilities

              • Executing assigned tasks regarding the maintenance and minor repair needs of equipment/facilities promptly, reporting any discrepancies to the Deputy Packing Engineer and/or Packing Engineer.
              • Conducting visual and other kind of inspections to packing department equipment, reporting any discrepancies to the Deputy Packing Engineer and/or Packing Engineer.
              • Preparing and changing machine forming tools/parts. Ensuring that after their use, the cleaned and labelled forming tools/parts are stored accordingly in the store room.
              • Ensuring that there is adequate quantity of consumables used for the purposes of the department, reporting needs to Deputy Packing Engineer and/or Packing Engineer.

              Qualifications, Skills and Experience

              • Relevant certificate (i.e. Electrician) will be considered as an advantage
              • Experience in manufacturing or related field is preferred
              • Ability to follow verbal and written instructions
              • Strong communication skills and desire to work with other team members
              • Attention to detail
              • Demonstrated ability to work in both independent and team environments
              • Ability to work 2nd and 3rd shift between 14:00-22:00 and 22:00-06:00

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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

                    • 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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                      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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                        Student Opportunities

                        We offer a dynamic Summer Internship Program, which is designed to enable exemplary students to gain hands-on work experience in an area related to their academic field of study or interest while experiencing the unique environment and culture that Remedica offers. You can apply for Remedica’s internship program between February and April.

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

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