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: 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: 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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  • 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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  • Job Posted: 3 March, 2019
  • 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 pharmaceutical quality audit will be considered as an advantage.
  • Excellent command of the English language

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  • Job Posted: 3 March, 2019
  • 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 Chemical Engineering or another related field.
  • Masters’ degree will be considered as an advantage.
  • Experience in the Pharmaceutical industry will be considered an advantage.
  • Good command of the English language

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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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  • 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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  • 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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