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: 4 October, 2018
  • 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 the pharmaceutical quality audit will be considered as an advantage.
  • Excellent command of the English language

Apply Online

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  • Job Posted: 3 October, 2018
  • 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 in Chemical Engineering or other related field.
  • Masters’ degree will be considered as an advantage.
  • Experience in Pharmaceutical industry will be considered as advantage.
  • Good command of the English language

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  • 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: 3 September, 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 customised applications.
  • Collaborate with a team of IT and non-IT professionals to develop specifications for new applications.
  • Create software applications by following the software development Lifecycle Process, which includes requirements gathering, design, development, testing, release, and maintenance.
  • Participate in software validation process through development, review, and/or execution of test plan/cases/scripts.
  • Perform continuous evaluation of existing applications to update and add new features.
  • Provide end-user support including Setup, Installation, and Maintenance for applications released.
  • Utilize skills in development areas including object-oriented programming (C#), databases (SQL) and web applications (ASP.NET and Angular).
  • 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 JS, MS SQL

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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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