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.


Quality and Compliance

  • Job Posted: 09 January 2023
  • 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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    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

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      • 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

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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

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          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

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            Research and Development

            • 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.

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              • 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

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                • 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

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                  • 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)

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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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