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

Role

  • Title: Chief Portfolio Officer, reporting directly to the General Manager.
  • Reporting to him/her: Managers of the Registration, Portfolio Development and R&D departments.
  • Key interdependencies: CROs and other co-development parties.

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 General Manager 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 and Experience

  • Bachelor’s degree in Business Administration or relevant degree.
  • Minimum 5 years of relevant experience in Pharmaceutical industry.

Leadership requirements

  • Is perceived leading from the front.
  • High level of integrity & ethical standards.
  • Problem-solving abilities.
  • Great cross functional collaborator who sets the company first.
  • Results-oriented while focusing on the “journey” too.
  • Ability to balance rigour with speed when decisions are to be made.
  • Ability to balance challenge with support when leading/coaching.
  • Strong analytical and communication skills.
  • Commanding, visionary, affiliative, pacesetting, coaching.
  • Self-confident and trustworthy.
  • Doer.

Apply Online

* Indicates a mandatory field

I agree to the Data Protection Notice *

  • 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

* Indicates a mandatory field

I agree to the Data Protection Notice *

  • Job Posted: March 16, 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Identify suitable suppliers that meet pre-set standards.
  • Direct and control the process related to the purchasing activities.
  • Administer bidding processes and tendering procedures with the aim of securing the best possible prices.
  • Agree, establish and monitor contracts with vendors / suppliers.
  • Maintain and update a Master vendor list and process related information.
  • Ensure compliance with company policies and procedures.
  • Manage the operations of the department.

Qualifications, Skills and Experience

  • University degree in a business-related field.
  • Minimum 3 years of relevant experience in a similar position.
  • Excellent oral and written communication skills in Greek and English.

Apply Online

* Indicates a mandatory field

I agree to the Data Protection Notice *

  • 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

* Indicates a mandatory field

I agree to the Data Protection Notice *

  • Job Posted: March 15, 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

Apply Online

* Indicates a mandatory field

I agree to the Data Protection Notice *

  • 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.

* Indicates a mandatory field

I agree to the Data Protection Notice *