Quality Assurance Associate

  • Medochemie Ltd
  • Limassol, Cyprus
  • 10/07/2024
Full time Engineering Manufacturing - Industrial Pharmaceutical

Job Description

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 13 ultramodern manufacturing plants, 9 in Cyprus, 3 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

We ‘re on a mission to find the best talent out there. We are now looking for a talented QA Associate (System Validation) to join our Computerized Systems team in our offices in Limassol, Cyprus.

What the job looks like?

The Quality Assurance Associate (System Validation) will have the opportunity to:

  • Execute Computerized Systems Validation (CSV) department daily work and duties assigned by the CSV Manager
  • Execute quality related actions of computerized systems used in site facilities to ensure compliance with company policies, procedures, and regulatory expectations
  • Assure all systems, processes and their outcomes comply with quality standards
  • Keeps informed of all existing and new regulatory requirements and helps maintain compliance in the company’s quality systems
  • Evaluate proposed and existing systems, prioritize risks and address data integrity gaps
  • Review processes and supporting documentary evidence to verify that compliance activities related to computerized systems are in place and effective
  • Review software change requests and test scripts
  • Developing and executing the computerized system validation cycle including installation, operation, performance qualification and developing reports
  • Supporting regulatory inspection and audit activities as needed and taking appropriate actions to ensure GMP compliance related to computerized/automated system
  • Execute computerized systems training to end-users and daily support were required

What does it take to do the job?

  • Bachelor's degree in Life science or Information Technology
  • Strong computer literacy skills
  • Working knowledge of computer validation or system testing development and execution will be considered as advantage
  • Related experience in a pharmaceutical industry is a plus
  • Proficiency with MS office tools (Word, Excel, Vision, PowerPoint, Project Plan, etc)
  • Excellent command of the English language, both written and oral
  • Advanced project management and technical writing skills is preferred
  • Ability to work in a team environment and prioritize work in a dynamic and fast-moving environment.

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’