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: 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: 21 May, 2018
  • 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.
  • Builds and maintains excellent relationship with customers under his/her supervision.
  • Suggests marketing plans for the assigned countries of responsibility.
  • Possess good knowledge of the performance, potential and characteristics of his/her assigned countries so as to facilitate planning and development of business.
  • Make effective application of the data in all related sales activities and systems to ensure good maintenance of records.

Qualifications, Skills and Experience

  • Bachelor’s degree in Business Administration or relevant degree.
  • MBA will be considered as an advantage.
  • Minimum 5 years of relevant experience in Sales roles.
  • Experience in the Pharmaceutical industry will be considered as an advantage.
  • Demonstrated understanding of customer segments and regional market dynamics.

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

Duties and Responsibilities

  • Propose a strategic plan to the Managing Director to maximize the sales revenue.
  • Manage alignment of resources within the Sales team to ensure sales forecasts and operational budgets are met or exceeded.
  • Manage a successful sales team and ensure that the team consistently meets or exceed sales targets. Coordinate regular effective sales meetings to drive strategy and results.
  • Identify opportunities to maximize the commercial potential.
  • Analyse performance metrics and leverage data to effectively coach sales teams. Create reports for staff based on metrics gathered from internal systems.
  • Actively manage the identification and sourcing prospective future business and bring new and reputable clients and sales in strategic growth areas.
  • Participate in appropriate expos and industries conferences. Participate and collaborate on sales and prospecting trips and missions as appropriate.
  • Identify, hire, develop and retain talents in the departments reporting to him/her; Work with sales leaders of National Sales, Export Sales and Business Development to make decisions about promoting or dismissing existing team members.

Qualifications, Skills and Experience

  • Bachelor’s degree in Business Administration or relevant degree.
  • MBA will be considered as an advantage.
  • Minimum 10 years of relevant experience in the Pharmaceutical industry.
  • Experience in multiple commercial functional business areas is preferred.
  • Demonstrated understanding of customer segments and regional market dynamics within the pharmaceutical industry.

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

Duties and Responsibilities

  • Proposes a plan for the development/upgrading/in-licensing/out-licensing of Remedica’s product portfolio strategy, which is based on certain criteria.
  • Analyses information from various sources and converts them into compelling facts (technical & commercial) that enable correct decision making in portfolio management.
  • Suggests to the Managing Director the focus areas, allocations, pipeline gaps, in/out-licensing and inter alia, identifies new product opportunities (short and long-term) and manages the cross-functional evaluation of these candidates including patent reviews, technical evaluations, and commercial assessments.

Qualifications, Skills and Experience

  • Bachelor’s degree in Business Administration or relevant degree.
  • Minimum 10 years of relevant experience in Pharmaceutical industry.

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  • Job Posted: 04 May, 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Role

  • Title: Registration Scientist – Regulatory Affairs.

Duties and Responsibilities

  • Prepares regulatory dossiers according to the requirements of each country.
  • Replies to deficiency letters after submission until a marketing license for the product is issued.
  • Prepares regulatory dossiers for renewals and variations on marketing authorizations (MA).
  • Reviews Drug Master Files.
  • Communicates with Regulatory Authorities or representatives about regulatory matters.
  • 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 are required according to the guidelines for dossier preparation and that the company decides to implement.
  • Keeps databases with regulatory information updated at all times.
  • Makes sure that correct information is passed to people within the department and within the company in regards to product registration.
  • Prepares departmental SOPs.
  • Keeps records updated accurately and in an organized manner.
  • Reviews and remains up to date with the regulatory landscape that governs the territories at which Remedica’s products are or are to be marketed

Qualifications and Experience

  • University degree in Pharmacy, Pharmacology or relevant field.
  • Previous relevant experience of at least 2 years in the field of Regulatory Affairs or in the pharmaceutical industry.
  • Knowledge of the regulatory framework of the industry.
  • Very good knowledge of English language.
  • Strong analytical, communication, organisational skills.
  • Computer literacy.

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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

Apply Online

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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