Pharmaceutical Industry

Cyprus

Medochemie Ltd

Pharmacists

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.&nbsp; Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.&nbsp;We ‘re on a mission to find the best talent out there. We are now looking for a motivated and experienced QP to join our dynamic team in our offices in Limassol, Cyprus.&nbsp;What the job looks like?The Qualified Person will have the opportunity to:<ul><li>Certify that each batch of medicinal product complies with its marketing authorization, Good Manufacturing Practices (GMP), and other relevant legal requirements</li><li>Ensure that testing, and manufacturing processes have been properly completed, and the relevant documentation has been reviewed before release for sale or use</li><li>Ensure that any deviations or planned changes in production or quality control have been authorized by Quality Assurance, and their impact on the quality, safety and efficacy of the product and on the compliance with GMP and the marketing authorization, has been evaluated.</li><li>Ensure that any changes requiring variation to the marketing or manufacturing authorization have been notified to and authorized by Regulatory Affairs as required</li><li>Ensure that the manufacturing and testing processes have been validated</li><li>Ensure that all necessary checks and tests have been performed, including any additional sampling, inspection, tests or checks initiated because of deviations or planned changes</li></ul>What does it take to do the job?<ul><li>Registered Qualified Person in Cyprus or another EU Member State</li><li>Previous experience in the pharma industry as a qualified person</li><li>Ability to interpret regulatory guidelines/legislation</li><li>Highly organized; ability to multitask and process excellent time management skills</li><li>Problem solving abilities</li><li>Strong analytical and communication skills</li><li>Proficient in the English language with excellent written and verbal communication skills</li><li>Excellent computer literacy (MS Office)</li></ul>By joining us you can expect:<ul><li>A unique opportunity for a career in a fast-growing company</li><li>Competitive remuneration package based on qualifications and experience&nbsp;</li><li>13th Salary</li><li>Paid&nbsp;Vacation</li><li>Modern &amp; Professional&nbsp;Work Environment</li><li>Multiple events to&nbsp;bond with the team</li><li>Participation in the&nbsp;Company’s Provident fund where the employer contributes&nbsp;7% of the monthly salary&nbsp;</li><li>Optional participation in the Company’s&nbsp;Group Medical Scheme, and&nbsp;Discount Scheme</li><li>Opportunities to learn and develop yourself through our ‘Employee Training &amp; Development Path’</li></ul>&nbsp;If you believe that you have the above qualifications and this position sounds challenging, submit your application through the link below:&nbsp;<a target="_blank" rel="noopener noreferrer" href="http://www.medochemie.com/MainMenu/Careers.aspx">http://www.medochemie.com/MainMenu/Careers.aspx</a>&nbsp;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.&nbsp;Location: &nbsp;LimassolEmployment Status:&nbsp;Full Time&nbsp;&nbsp;All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.

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