Quality Processes and Validation Associate
Job Description
Medochemie Ltd 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 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 Process and Validation will have the opportunity to:
· Support and coordinate the needed actions for the implementation of guideline as per cGMP requirements for Cleaning Validation as well as internal quality procedures
· Prepare and assist in the preparation of Cleaning Validation Protocols
· Collaborate with Production, Quality Control, and other departments to join efforts for a Cleaning Validation run
· Supervise and/or assist sampling for Cleaning Validation by checking that sampling is performed according to the protocol and that the sampling forms are filled in correctly
· Compile and evaluate the results after execution of the protocols as well as prepare reports on the validation tasks undertaken
· Prepare and review the necessary documents for ensuring compliance with the company’s policies
· Follow the change management procedure relevant to the Cleaning Validation process
What does it take to do the job?
· A University degree in a relevant scientific discipline such as Chemical Engineering, Pharmacy, Chemistry, Biochemistry, Biology
· Ability to clearly and concisely communicate technical information
· Ability to research, analyse and report independently across a range of topics
· Strong organisational skills and an eye for detail.
· Multi project handling
· Ability to work under strict deadlines
· Good collaboration skills and team spirit
· Fluency in Greek and English language
· Strong IT Strong computer literacy skills
Ιt would be considered a plus if you have:
· A postgraduate degree
· Experience in the field of pharmaceutical
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 and 14th 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.
Department: Quality Process and Validation
Location: Limassol
Employment Status: Full Time
All applications will be treated with strict confidentiality. Only shortlisted candidates will be contacted.
How to Apply
Interested candidates are kindly requested to send their CV to the HR Manager at HR.Cyprus@medochemie.com.
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About Company
Medochemie Ltd
MEDOCHEMIE was established in 1976 in Cyprus by Dr. Andreas Pittas and is still driven by the same philosophy: "To provide every human being around the globe with quality and affordable drug treatment".
We develop, license, manufacture, market, and distribute branded generic and super-generic pharmaceutical products as well as our own patented brands.
The journey has seen our active expansion into promising markets across the world – from our base in Europe, to the Middle East & Africa, through to the Far East.
Outside our 20 core offices, we developed a network of trusted agents and partners allowing us to operate in more than 100 countries. Today, Medochemie Ltd has eleven manufacturing plants and facilities.
Nine are in Cyprus, one in the Netherlands, and one in Vietnam. We have acquired and maintain 3,800 marketing authorization licenses for 630 different pharmaceutical products, classified in over 10 therapeutic categories.
We operate in accordance with the strictest quality standards and in full compliance with European guidelines. The driving force behind Medochemie is our 1,250 multinational, talented, quality-focused employees, who work in our manufacturing plants and offices worldwide.
Medochemie is a founding member of the European Generic Medicines Association (EGA).