Medochemie is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization). Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We‘re on a mission to find the best talent out there. We are now looking for a motivated Pharmacist to join our dynamic Quality Control team for our offices in Limassol, Cyprus.

What the job looks like?

The Pharmacist will have the opportunity to undertake the required training in view of becoming a Qualified Person. The training will last for 2 years and during these years you will have the opportunity to work in Quality Control and be trained on the full product lifecycle.

• To perform analysis on starting materials and bulk products of different dosage forms using a variety of analytical techniques including separation techniques such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC)
• To carry out stability studies on finished products stored under different climatic control condition
• To be trained and familiarised with all GLP (Good Laboratory Practice), QC (Quality Control) and QA (Quality Assurance) GMP procedures
• To take part in the internal GMP trainings undertaken within the organization

• To take part in any training and required examination in view of becoming a Qualified Person in Medochemie Ltd

Upon obtaining your certificate, your duties will expand to the following:

• To certify that each batch of medicinal product complies with its marketing authorization, Good Manufacturing Practices (GMP), and other relevant legal requirements
• To ensure that testing, documentation, and manufacturing processes have been properly completed and reviewed before release for sale or use
• To ensure that any deviations or planned changes in any related GP (Good Practices) activities have been authorized by Quality Assurance
• To ensure that any changes requiring variation to the marketing or manufacturing authorization have been notified to and authorized by the relevant Regulatory agencies
• To ensure that the required validation and qualification activities have been performed satisfactorily

What does it take to do the job?

• Bachelor’s degree in Pharmacy
• Highly organized; ability to multitask and process excellent time management skills
• Problem solving abilities
• Strong analytical and communication skills
• Proficient in the English language with excellent written and verbal communication skills
• Excellent computer literacy (MS Office)

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience
• 13th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this position sounds challenging, submit your application through the link below:

http://www.medochemie.com/MainMenu/Careers.aspx

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CVs are kept in our database based on the consent period each candidate applied for. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

Location: Limassol

Employment Status: Full Time

All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.