Discover Remedica’s world of career opportunities. Working at Remedica means being employed by a leading Cypriot pharmaceutical company.

We are amongst Cyprus’s fastest growing companies and we are committed to developing innovative solutions for the production of high-quality, safe and efficacious pharmaceutical products for human use. For this reason, we are looking to recruit the most talented people from across the world, who bring a diverse range of experience and capabilities to our existing team of experts.

Pharmaceutical production has been on a steady incline in Cyprus for the past 40 years and shows no sign of slowing down. As a matter of fact, this segment represents a top export category of the Cypriot manufacturing industry with a whopping €300+ million in revenues. For the past 60 years, Remedica has not only been amongst the biggest revenue generators of the island, but it is also one of its biggest employers, employing more than 800 people. We currently have 5 manufacturing plants and facilities located in the heart of Limassol’s Industrial Area, scattered across a massive area of 50000 sqm2.

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Open positions at Remedica

Check out all the open positions at Remedica, apply for a job position and join our talent pool for future opportunities.


Commercial Department

  • Job Posted: 29 May 2020
  • 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.
  • Build and maintain excellent relationship with customers under his/her supervision.
  • Suggest marketing plans for the assigned countries of responsibility.
  • Possess good knowledge of the performance, potential and characteristics of his/her assigned countries to facilitate planning and development of business.
  • Make an effective application of the data in all related sales activities and systems to ensure good maintenance of records.
  • Acquire sales and market intelligence on issues such as competition, price, and project status.

Qualifications, Skills and Experience

  • Bachelor’s Degree in Business Administration, Economics, or relevant Degree
  • MBA will be considered an advantage
  • Knowledge of Pharmaceutical procedures and GMP will be considered as an advantage.
  • Prior experience of 3-5 years in a relevant role is required.
  • Experience in the Pharmaceutical industry will be considered as an advantage.
  • Demonstrated understanding of customer segments and regional market dynamics.

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Operations

  • 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: 26 July, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Test starting materials, intermediate and finished products according to procedures and specifications.
  • Work productively for the completion of each task assigned in a timely and efficient manner, to minimize the running cost of the analysis.
  • Follow Standard operating procedures.
  • Follow GLP, GMP and company regulations on safety, cleanliness, personal hygiene and tidiness.

Qualifications, Skills and Experience

  • University degree in Chemistry, Pharmacy or a related field.
  • Master degree in a relevant field will be considered as an advantage.
  • Previous work experience will be considered as an advantage.

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Quality & Compliance

  • Job Posted: 28 August, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Review the manufacture and testing of the product.
  • Ensures the GMP compliance.
  • Ensures that the product is in accordance with the requirements of the Marketing Authorisations.
  • Releases finished product batch.
  • Generates batch release certificates
  • Performs investigations as required.
  • Initiates and reviews procedures.
  • Supports audits from customers and authorities

Qualifications, Skills and Experience

  • Registered Qualified Person in accordance with EU GMP.
  • If the candidate is not registered as a Qualified Person, then a University degree in Pharmacy is mandatory.
  • Master degree and previous experience within the Pharmaceutical industry will be considered as an advantage.
  • Understands fundamental scientific problems
  • Able to write and review reports with clarity and brevity
  • Fluent in English and Greek language
  • Good knowledge of Microsoft office package

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Portfolio Development

  • Job Posted: 03 April, 2020
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Product formulation and process development including background research on planned new Remedica products
  • Carrying out of experiments in order to obtain stable formulations with a feasible manufacturing process
  • Scale-up of R&D formulations into full-scale production
  • Coordination and supervision of work at Contract Research Organizations for the development of Remedica’s products
  • Carrying out of technology transfer activities to and from Remedica

Qualifications, Skills and Experience

  • University degree in Pharmacy, Chemical Engineering or related science subject, preferably with MSc.
  • Very good spoken and written English required.
  • Ability to communicate in Greek is an advantage.
  • Proficiency in Windows, Word, Excel.
  • Prior knowledge of pharmaceutical research or manufacturing is an advantage but not an absolute requirement.

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  • Job Posted: 15 November, 2019
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Obtain new Marketing Authorizations, Maintain existing MAs and Manage and report regulatory information by:
    • Compiling regulatory documents according to the requirements of each country.
    • Preparing registration dossiers according to CTD or any other relevant format
    • Maintaining product life-cycle and regulatory compliance by submitting MA renewals and variations
    • Keeping up to date with changes in regulatory legislations and guidelines
    • Liaising and negotiating with regulatory authorities and external associates
    • Liaising with Contract Research Organisations for designing and performing in-vivo studies
    • Keeping accurate records and report promptly currently approved information to the relevant departments within the company thus ensuring regulatory compliance

Qualifications, Skills 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: 23 October, 2018
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

• Analytical Method Development and Validation.
• Execution of stability studies.
• Carrying out of Method Transfer procedures.
• Testing materials and products under development
• Preparing quality reports.
• Ensuring data integrity and proper documentation of experimental data.
• Achieve departments’ goals.
• Complying with GMP/GLP.

Qualifications, Skills and Experience

• University degree in Chemistry or Pharmacy.
• Master degree will be considered as an advantage.
• Minimum of 2 years’ experience in Research and Development (Analytical) in Pharmaceutical Industry, handling instrumentation such as HPLC, HPLC-MS, GC.

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General Applications

If you don’t see a job opening that’s relevant for you, feel free to join our talent pool by submitting your CV. If a suitable career opportunity that matches your skillset and experience is found, we will contact you with company information. Your CV will be stored for 6 months in our internal database in accordance with the General Data Protection Regulation and our HR Team will contact you in case an opportunity arises.

  • Location: Limassol, Cyprus
  • Working Hours: Depending on the Position

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Student Opportunities

We offer a dynamic Summer Internship Program, which is designed to enable exemplary students to gain hands-on work experience in an area related to their academic field of study or interest while experiencing the unique environment and culture that Remedica offers. You can apply for Remedica’s internship program between February and April.

  • Location: Limassol, Cyprus
  • Working Hours: Depending on the Position

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