Check out all the open positions at Remedica, apply for a job position and join our talent pool for future 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 45000 sqm2.

Benefits
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. Our success is highly dependent upon the performance and dedication of each of our people. As a result, our goal is to be an employer of choice that attracts, develops and motivates talented and performance-driven people from across the world. One way to achieve this goal is by providing a competitive remuneration and benefits package, which includes the 13th and 14th salaries, provident fund and insurance coverage, as well as the resources to support our employees’ professional achievement and personal well-being.

Development
We understand that to bring positive change in patients’ lives, we must first invest in the development of our people and by fueling their growth, we assist Remedica to achieve its goal and maintain its position in the global market. For this reason, we offer top training opportunities and actively encourage employees to continuously improve and further develop their skill sets. Learning activities are often provided in the form of on-the-job coaching, complemented by both external or internal training sessions and workshops. In addition, we have a robust feedback system, complete with annual performance reviews, thus facilitating our employees’ professional growth and development.

Community & Culture
At Remedica we want to foster a culture where all employees collectively feel part of our success and strive to create a working culture where they are empowered to give their best, learn, relearn and to develop into their full potential. We began our operations 60 years ago as a small & medium family-owned company, and although we have grown into a competitive player in the global Generic Pharmaceutical Industry, we still maintain our family-like culture and atmosphere, while at the same time, we also maintain our commitment to being a responsible global citizen. As a result, we actively encourage our employees to volunteer and give to society, offering many opportunities and resources for them to do so.

Diversity & Inclusion
Diversity in Remedica means that everyone is welcome. That’s why we are committed to operating in a non-discriminatory manner, protecting employees from unequal treatment in the workplace that may include biased behaviour based on age, disability, gender, marriage or civil partnership, maternity or pregnancy, race, religion or belief, sexual orientation, or membership of a trade union.

If you are interested in working with us, please apply online through this website.

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Available Positions

  • Job Posted: 08 January, 2020
  • Location: Limassol, Cyprus
  • Working Hours: Full-Time

Duties and Responsibilities

  • Reviews the EV website and other relevant websites for any information regarding new regulations, laws etc.
  • Performs the worldwide literature search.
  • Updates the Pharmacovigilance System Master File (PSMF).
  • Manages Remedica’s Pharmacovigilance System in order to ensure that all information on suspected ADRs, is collected, evaluated and reported to the National Competent Authorities.
  • Prepares and submits PSURs and RMPs.
  • Has an overview of medicinal product safety profile (including management of signals).
  • Prepares and revises agreements with other organizations for the exchange of relevant information.
  • Submits all information on medicinal products marketed within the European Economic Area in the electronic database (EudraVigilance) of the European Medicines Agency (EMA), and keeps this information up to date.
  • Participates in Safety Review Meetings, in audits etc.
  • Participates in educational seminars.
  • Is aware of any conditions or obligations adopted as part of the marketing authorizations and other commitments relating to safety or the safe use of the medicinal products.
  • Is member of Remedica’s Scientific Advisory Service and performs the duties set out in the relevant Scientific Service internal instructions.

Qualifications, Skills and Experience

  • BS in Pharmacy or Medicine or Chemistry or Biology or Biomedical Science.
  • Excellent knowledge of Microsoft Office i.e. Word, Excel, PowerPoint, etc.
  • Excellent knowledge of the Greek and English languages.
  • Excellent communication skills.
  • Trusted, Hardworking, Organised, Ability to work under pressure with minimum supervision.
  • Experience: For pharmacist or Doctor or Biomedical scientist: Not necessary. For Biologist or Chemist: Minimum 2 years.

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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: 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

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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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