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.

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

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Available Positions

  • Job Posted: 21 June, 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Reviews the literature and identifies updates on the clinical and non-clinical data of the product.
  • Prepares the clinical and non-clinical overviews for the initial dossier compilation.
  • Prepares the clinical and non-clinical addendums needed for the renewals and variations of Marketing authorizations in the EU and the rest of the world.
  • Assesses the risk-benefit balance and concludes on the product’s efficacy and safety.
  • Prepares registration dossiers according to the requirements of each country.
  • Replies to deficiency letters after submission until a marketing authorisation for the product is issued.
  • Responsible for renewals and variations of marketing authorisations.
  • Reviews of Drug Master Files.
  • Checks newly prepared or modified labelling.
  • Liaises with other departments and collects information.
  • Replies to correspondence and follows up pending matters.
  • Keeps informed of new regulations and guidelines relating to product and company registration.
  • Learns and works with new programs/software that is required according to the guidelines for dossier preparation and that the company decides to implement.
  • Informs Ministries of Health or representatives about registration matters.

Qualifications, Skills and Experience

  • University degree in Pharmacy, Pharmacology or relevant field.
  • Previous relevant experience of at least 3 years in the field of Regulatory Affairs or in relevant departments (Medical Writing, Research, Publication, etc.)
  • Knowledge of the regulatory framework of the industry.
  • Familiarized with platforms for Scientific Articles.
  • Very good knowledge of English language.
  • Strong analytical, communication, organisational skills.
  • Computer literacy.

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  • Job Posted: 30 May, 2018
  • 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.
  • Relevant experience as software developer and DMS workflow developing will be considered as an advantage
  • Experience in Asp.NET, C#, JavaScript, Angular

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  • Job Posted: 15 March, 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Supervise a group of analysts during their daily work to ensure all quality and goals are met and evaluation of their work.
  • Testing materials and products under development.
  • Performing Analytical method development and validation.
  • Design stability protocols as per the ICH guideline, manage stability analysis, establish the specifications of the impurities for new products and determine the shelf life.
  • Processing / generating of the standard operating procedures (SOP’s) and methods of analysis.
  • Reviewing of drug master files (DMF) and technical packages

Qualifications, Skills and Experience

  • University degree in Pharmacy or Chemistry
  • Previous relevant experience of at least 3 years
  • Very good knowledge of English language
  • Computer literacy

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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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  • Job Posted: 15 September, 2017
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Releases finished product batch the product for customer dispatch or to the market
  • Ensures compliance with Good Manufacturing Practice (GMP)
  • Ensures that each batch is in accordance with the requirements of the relevant Marketing Authorisation (MA)
  • Initiates and reviews Standard Operating Procedures (SOPs)
  • Supports and leads audits from customers and authorities
  • Certifies suppliers of Active Pharmaceutical Ingredients (APIs)
  • Ensures that the Quality System of the company follows the current regulations

Qualifications, Skills and Experience

  • Registered Qualified Person for Finished Product Certification
  • A minimum of 5 years’ experience within the Pharmaceutical industry
  • Detailed knowledge of current GMP requirements
  • Ability to interpret regulatory guidelines/legislation
  • Experience of effectively leading and managing technical teams
  • Ability to apply and communicate scientific and risk based rational in day to day operations
  • Excellent oral and written communication skills in Greek and English
  • Computer literacy with working knowledge of MS Office applications and web browsers

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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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