Quality Processes and Validation Associate

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Job Description - Quality Processes and Validation Associate

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 Quality Processes and Validation Associate to join our Quality Processes and Validation team in our offices in Limassol, Cyprus.

What the job looks like?

The Quality Processes and Validation Associate will have the opportunity to:

  • Collect and evaluate the necessary information for the preparation of risk assessments in pharmaceutical products /materials
  • Prepare / assist the risk assessments preparation
  • Participate in the process of setting mitigation / corrective / preventive actions
  • Handle cleaning validation and cross-contamination activities, including organization, protocol and report preparation, study execution and related deviations handling

What does it take to do the job?

  • Bachelor's degree in Chemical Engineering, Chemistry or Pharmacy
  • Highly organized; ability to multitask and process excellent time management skills
  • Ability to work under pressure
  • Accountable and responsible
  • An enthusiastic team player with a strong drive to create a positive and collaborative work environment
  • Excellent interpersonal and communication skills
  • Proficient in the English language with excellent written and verbal communication skills
  • Excellent computer literacy (MS Office)

It would be considered a plus if you have: 

  • Experience in Pharmaceutical industry

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:

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.

Department: Quality Processes and Validation

Location: Limassol

Employment Status: Full Time

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

Original job Quality Processes and Validation Associate posted on GrabJobs ©. To flag any issues with this job please use the Report Job button on GrabJobs.
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