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.

Processing of personal data is in accordance with the provisions of the Processing of Personal Data (Protection of the Individual) Law 2001. The purpose of processing of your data is to administer and assess your application for employment. The recipients of your personal data will be the authorised employees of Remedica Ltd who are responsible for the processing and assessment of your application. The Controller of Processing is Remedica Ltd in Aharnon Str., Limassol Industrial Estate, 3056 Limassol, Cyprus, Tel. +357 25 55 3000. You have the right to access and amend your personal data by submitting a written application to the Controller of Processing.

Available Positions

  • Job Posted: September 15, 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

Apply Online


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

Duties and Responsibilities

  • Coordinate and supervise production line(s)/unit
  • Responsible to execute daily production scheduling
  • Identify and solve production issues and make improvements where necessary
  • Apply policies and procedures
  • Manage people effectively
  • Perform internal production checks
  • Responsible to train personnel

Qualifications, Skills and Experience

  • University degree in Chemical Engineering or other life-science degrees
  • Previous relevant experience of at least one year
  • Good understanding of production environment
  • Strong organisational, managerial and communication skills
  • Good command of the English language
  • Computer literacy
  • Presentation skills
  • Ability to work effectively in a team-oriented environment

Apply Online


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  • Job Posted: September 15, 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

Apply Online


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

Duties and Responsibilities

  • Testing materials and products under development
  • Execution of stability studies and determination of shelf life
  • Analytical method development and validation

Qualifications, Skills and Experience

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

Apply Online


I agree to the Data Protection Notice