Remedica offers career development and opportunities and understands that competitive advantage and success is only achieved through the investment in its employees. For this reason, Remedica is looking to recruit the best people from all over the world, who are experts in their field, enthusiastic, energetic, creative and ready to contribute to its development in a professional way.

Why choose Remedica?

When you join Remedica you become a part of our vision “For a Healthier World” helping us improve the quality of human life by providing high quality, safe and efficacious pharmaceuticals to millions of people around the world. We invite you to be a part of something that is positively impacting people globally while enjoying a competitive remuneration and benefits package.

We are looking for people who love a challenge and are ready to grow, learn and innovate together with us. As part of our team, you will have the opportunity to create and contribute to large-scale manufacturing and operational solutions and entirely new platforms used to optimize and enhance Remedica’s ever-developing technological landscape.

Join us and help us continue driving innovation in the global Generic Pharmaceutical Industry.

If you are interested in working with us, please apply online through this website.

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Available Positions

  • Job Posted: 7 August, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Analyse a variety of activities including manufacturing, laboratory, and engineering processes and propose efficient improvements with customized applications.
  • Collaborate with a team of IT and non-IT professionals to develop specifications for new applications.
  • Design creative prototypes according to specifications found in a highly regulated environment.
  • Write high quality source code to program complete applications within deadlines.
  • Perform unit and integration testing before launch.
  • Conduct functional and non-functional testing.
  • Troubleshoot and debug applications.
  • Perform continuous evaluation of existing applications to update and add new features.
  • Develop highly technical documents and handbooks to accurately represent application design and code.

Qualifications, Skills and Experience

  • University degree in Computer Science or related field.
  • Experience across all stages of software development i.e. requirements gathering, design, implementation, testing, deployment.
  • Experience in Asp.NET, C#, JavaScript, Angular, SQL server, AngularJS, jQuery

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  • Job Posted: 6 August, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Reviews the EV website and other relevant websites for any information regarding new regulations, laws etc.
  • Performs the worldwide literature search.
  • Updates the Pharmacovigilance System Master File (PSMF).
  • Manages Remedica’s Pharmacovigilance System in order to ensure that all information on suspected ADRs, is collected, evaluated and reported to the National Competent Authorities.
  • Prepares and submits PSURs and RMPs.
  • Has an overview of medicinal product safety profile (including management of signals).
  • Prepares and revises agreements with other organizations for the exchange of relevant information.
  • Submits 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.
  • Participates in Safety Review Meetings, in audits etc.
  • Participates in educational seminars.
  • Is 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.
  • Is member of Remedica’s Scientific Advisory Service and performs the duties set out in the relevant Scientific Service internal instructions.

Qualifications, Skills and Experience

  • BSc 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.
  • Experience: For pharmacist or Doctor or Biomedical scientist: Not necessary. For Biologist or Chemist: Minimum 2 years.

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  • Job Posted: 26 July, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Test starting materials, intermediate and finished products according to procedures and specifications.
  • Work productively for the completion of each task assigned in a timely and efficient manner, to minimize the running cost of the analysis.
  • Follow Standard operating procedures.
  • Follow GLP, GMP and company regulations on safety, cleanliness, personal hygiene and tidiness.

Qualifications, Skills and Experience

  • University degree in Chemistry, Pharmacy or a related field.
  • Master degree in a relevant field will be considered as an advantage.
  • Previous work experience will be considered as an advantage.

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  • Job Posted: 3 March, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Ensure Compliance of Raw material manufacturers.
  • Handle Deviations for incoming raw material.
  • Handle raw material change controls.
  • Handle raw material complaints.
  • Handle supplier evaluation documentation.
  • Perform annual supplier review.
  • Maintains supplier database.
  • Revise, review, and write SOPs and checklists, as needed in order to complete required evaluation tasks.
  • Review, approve or reject 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 Chemical Engineering).
  • Minimum of 2 years of QA/QC experience.
  • Experience in the pharmaceutical industry and especially in pharmaceutical quality audit will be considered as an advantage.
  • Excellent command of the English language

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  • Job Posted: 3 March, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Responsible to execute daily production schedule.
  • Provide daily supervision of line production personnel.
  • Review executed batch records and insure cGMP is maintained in production operations.
  • Perform process investigations, initiate CAPAs and change controls.
  • Develop and apply a strategy for production improvement.
  • Identify and solve production problems.
  • Apply policies and procedures.
  • Manage people effectively.
  • Perform internal production checks.
  • Responsible to train personnel.

Qualifications, Skills and Experience

  • Bachelor’s degree in Chemical Engineering or another related field.
  • Masters’ degree will be considered as an advantage.
  • Experience in the Pharmaceutical industry will be considered an advantage.
  • Good command of the English language

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  • Job Posted: 23 January 2019
  • 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).
  • Minimum of 2 years of QA/QC experience.
  • Experience in the pharmaceutical industry and especially in pharmaceutical quality audit will be considered as an advantage.

Apply Online

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  • Job Posted: 20 November 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Releases finished product batch to the market.
  • Ensures the GMP compliance.
  • Ensures that the product is in accordance with the requirements of the Marketing Authorisations.
  • Initiates and reviews SOPs.
  • Supports and lead audits from customers and authorities.
  • Certifies suppliers of APIs.
  • Ensures that the Quality System of the company follows the current regulations.

Qualifications, Skills and Experience

  • Registered Qualified Person in accordance with EU GMP.
  • University degree in a scientific field (Pharmacy, Chemistry, Chemical Engineering or any relevant degree).
  • Master degree will be considered as an advantage.
  • A minimum of 5 years’ experience within the Pharmaceutical industry.
  • Detailed knowledge of the current GMP requirements.

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  • Job Posted: 23 October, 2018
  • 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: 15 September, 2017
  • 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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  • Location: Limassol, Cyprus
  • Working Hours: Depending on the Position

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Always looking to expand our team, we encourage you to apply at Remedica even if a vacancy that suits you might not currently be open.

In such a case, use the form below to send us your CV which will be saved for 6 months in our internal database based on the data protection regulation and our HR Team will contact you as soon as possible if an opportunity arises.

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