Careers

Duties:

• Search in available patent databases in order to check the status of patent applications, litigations etc in both European and non - European territories
• Review, analyze and inform on patent restrictions and prepare consolidated patent reports with due diligence 
• Search for the patent regulations in force in each country for new or existing products   
• Assess and conclude on active pharmaceutical substances patents pertinent to their synthetic schemes and physical properties, on finished dosage forms compositions, indications, manufacturing processes  etc towards any valid patents
• Prepare high quality and substantiated advices on the new products strategies in terms of patent restrictions and specific issues that need to be taken into consideration. 
 

Qualifications:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Minimum of 5 years’ experience as patent specialist in generic medicines is a must
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment
• Very good interpersonal skills, analytical thinking and result orientation
• Strong computer literacy
• Fluency in English language
• Committed to relocate to Cyprus
 

Location: LIMASSOL, CYPRUS

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites applications from career oriented professionals for the position of Quality Assurance Assistant for our offices in Limassol, CYPRUS.

Duties:

• To provide administrative support for tasks related to Quality Assurance
• To review batch documentation
• To carry out clerical work including typing, filing, copying and distribution of documents
• To ensure all procedures are carried out as per defined Standard Operating Procedures
• To undertake other tasks as required by the Quality Operations Senior Manager

Qualifications:

• Τwo or three years Higher Education Degree
• Fluency in Greek and English language
• Proficiency with MS office tools (Word, Excel, PowerPoint, etc)
• Professional approach to work and excellent character
• Ability to work in a team environment and prioritize work in a dynamic and fast-moving environment

Location: LIMASSOL, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
All applications will be treated in strict confidence.

 Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

We invite applications from highly qualified and motivated professionals for the position of R&D Associate based in Limassol, Cyprus. 
 

Duties:

• Be responsible for the raw materials sourcing for under development products, by contacting with a variety of external stakeholders. 
• Conduct a preliminary and limited quality evaluation of the raw material used for R&D purposes in accordance with the current guidelines in force.
• Apply basic regulatory knowledge under which the medical products are governed.
• Compile consolidated summaries and provide required reports throughout the development of each products in support to the R&D team.
• Support other departments related to the R&D functions and operations when this is required. 

Qualifications:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Experience in the pharmaceutical industry it will be considered an advantage. 
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment. 
• Very good interpersonal skills, analytical thinking and result orientation.
• Strong computer literacy
• Fluency in English language 

Location: LIMASSOL, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development. 
​
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. 

All applications will be treated in strict confidence. 
 

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.

Η Medochemie Ltd ζητά να προσλάβει υπεύθυνο και συνεργάσιμο άτομο με έδρα τη Λεμεσό στην Κύπρο, για τη θέση Engineering Associate.
 

Duties:

• Εκπόνηση και υλοποίηση προγραμμάτων προληπτικής συντήρησης
• Υπεύθυνος για την συντήρηση των μηχανήματων παραγωγής , συσκευασίας και βοηθητικών εγκαταστάσεων  
• Επίλυση προβλημάτων που προκύπτουν κατά τη λειτουργία των μηχανών (βλάβες, ρυθμίσεις κλπ)
• Δημιουργία και εφαρμογή διαδικασιών λειτουργίας και συντήρησης εξοπλισμού
• Διαχείριση του προσωπικού

Qualifications:

• Κάτοχος πτυχίου Μηχανολόγου Μηχανικού ή Ηλεκτρολόγου Μηχανικού
• Προηγούμενη πείρα στη συντήρηση τεχνικού εξοπλισμού και βιομηχανικών εγκαταστάσεων θα θεωρηθεί επιπρόσθετο προσόν 
• Καλή γνώση της Αγγλική γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.
• Πιθανή εργασία σε πρόγραμμα βάρδιας

Location: LIMASSOL

Προσφέρεται ελκυστικό πακέτο απολαβών ανάλογα με τα προσόντα και την πείρα.

Εάν διαθέτετε τα πιο πάνω προσόντα και επιθυμείτε να εργασθείτε σε ένα ευχάριστο, σύγχρονο, επαγγελματικό περιβάλλον με άριστες προοπτικές αποστείλετε την αίτηση σας πατώντας Υποβολή Βιογραφικού Σημειώματος ή Συμπληρώστε την Ηλεκτρονική Αίτηση.

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.
 

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.
 
Η Medochemie Ltd ζητά να προσλάβει υπεύθυνα και συνεργάσιμα άτομα με έδρα την Λεμεσό, για τη θέση Φύλακα:
 

• Ωράριο: Πρωινό/ Απογευματινό/ Νυκτερινό:         

Duties:

• Επιτήρηση και έλεγχος εγκαταστάσεων Εταιρείας
• Έλεγχος πρόσβασης ατόμων και οχημάτων
• Διαχείριση συστήματος πυρανίχνευσης

Qualifications:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης
• Απαραίτητη Άδεια άσκησης του επαγγέλματος Ιδιώτη Φύλακα
• Τουλάχιστον 2 χρόνια προϋπηρεσία
• Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: ΛΕΜΕΣΟΣ, ΚΥΠΡΟΣ

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13^ο μισθό, 14^ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας και άλλα ωφελήματα ανάλογα με προσόντα και πείρα.
 
Εάν διαθέτετε τα πιο πάνω προσόντα και επιθυμείτε να εργασθείτε σε ένα ευχάριστο, σύγχρονο, επαγγελματικό περιβάλλον με άριστες προοπτικές αποστείλετε την αίτηση σας πατώντας Υποβολή Βιογραφικού Σημειώματος ή Συμπληρώστε την Ηλεκτρονική Αίτηση.
 
Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.
 
Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.
 

Duties:

• Maintain local pharmacovigilance (PV) system and fulfill compliance with external requirements in line with the local PV legislation and applicable internal procedures. 
• Ensure conduct of pharmacovigilance and submission of all pharmacovigilance-related documents in accordance with the legal requirements and GVP.
• Responsible of fulfilling the requirements of the Saudi Arabian legislation for pharmacovigilance for all products. 
• Ensure the necessary quality requirements, including the correctness and completeness, of pharmacovigilance data submitted to the relevant authorities. 
• Responsible for ICRS 

Qualifications:

University degree in Pharmacy (Licensed) Valid license by Saudi Commission for Health Specialties At least one year of experience as Local QPPV Strong computer literacy Fluency in English and Arabic Saudi Nationality is a must

 

Location: RIHARD OR JEDDAH, SAUDI ARABIA

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

We invite applications from highly qualified and motivated professionals for the position of HR Specialist/Senior Specialist based in Limassol, Cyprus.

Duties:

• Works closely with management, increasingly in a consultancy role, assisting on all HR issues of the business by identifying problem areas and proposing solutions.
• Develops and implements policies and procedures on essential HR topics and issues
  Acts as point of contact for employees and managers.
• Interprets and advises on employment legislation and practise
• Leads HR global projects in her/his area of responsibility
• Creates and maintains HR metrics and audit controls
• Supports HR administration tasks concerning the full employee cycle
• Performs compensation and benefits administration and reporting
• Assists in talent acquisition and recruitment processes
• Coordinates employee development plans and performance management
• Provides efficient and effective HR assistance and service to overseas offices 

Qualifications:

• University Degree in Human Resources Management or any other related discipline such as occupational psychology, behavioural sciences, organizational development, business, etc.
• Minimum 5 years of experience in a similar role
• Strong knowledge on HR processes and operations
• Hands-on experience with Human Resources Information Systems
• Solid understanding of labour legislation
• Strong computer literacy; advance excel user
• Fluency in Greek and English language
• Maintains confidentiality and professional demeanour
• Very good interpersonal skills and problem-solving abilities
• Desire to work as a team with a results driven approach

Location: LIMASSOL, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. All applications will be treated in strict confidence.

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites applications from career-oriented professionals for the position of Quality Assurance Associate (System Validation) in our offices in Limassol, CYPRUS.

Duties:

•    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 systems.

Qualifications:

•    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.

Location: Limassol, Cyprus

We are offering an attractive remuneration package and challenging opportunity for professional development.

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. 

All applications will be treated in strict confidence.

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites applications for the position of IT Systems Administrator Senior Specialist for our offices in Limassol, CYPRUS. 

Duties:

•    Ensure the availability of the systems, addressing the reported issues, both scheduled and unscheduled
•    Monitor performance and maintain systems according to requirements
•    Install and configure software and hardware
•    Upgrade systems with new releases and fixes
•    Manage network servers and technology tools
•    Manage the organization’s compliance to internal / external accreditation regulations and policies
•    Support the Service / Help Desk in day-to-day end-user assistance and event management, including Incident troubleshooting and resolution
•    Ensure security through access controls, backups and firewalls
•    Train staff on new technologies
•    Maintain internal technical documentation, manuals and IT policies when required
•    Implement policies for asset management, including maintenance of related documentation, and technical specifications information

Qualifications:

•    Experience in telecommunications hardware and software and network management functions
•    Experience in Databases Administration (SQL, NoSQL) and/or networks (LAN, WAN)
•    Experience in Windows operating systems and platforms administration. Experience or familiarity with Unix/Linux will be considered as an advantage
•    Able to prioritize work based on pending tasks 
•    BSc/Diploma in Information Technology, Computer Science, Computer Engineering or a related discipline
•    4 or more years of experience in similar position (Systems Administrator, Network Administrator etc.) Experience in Pharmaceutical sector will be considered as an advantage
•    Excellent communication skills

Location: Λεμεσός, Κύπρος

We are offering an attractive remuneration package and challenging opportunity for professional development.
 
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.


Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated in strict confidence

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations, and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
 
Medochemie Ltd invites career-oriented professionals to apply for the full-time position of Administrative Assistant based in Cairo. The successful candidate will be responsible for administrative and other supportive tasks related to the office operations and the Area Commercial Director.
 

Duties:

• Provide general administrative support inclusive and not limited to: scheduling meetings, coordinating staff activities, events, and activations, maintain calendars, collate, and distribute mails, meetings agendas, minutes of meetings, along with maintaining filing systems, both electronic and physical.
• First point of contact for any requests related to office management and administrative tasks.
• Support interoffice communication through preparing reports, memos, invoices, and other correspondence.
• Coordinate travel arrangements either with our local travel office in the HQ, or other vendors across the region.
• Support colleagues during travel and ensure seamless arrangement from travel requests to departure and expenses reconciliation.
• Manage local purchases and procurement activities in cooperation with the finance team in Egypt.
• Respond effectively to other administrative requests and tasks as required by the Area Commercial Director of MENA region.
This position reports to Area Commercial Director of Mena Region.
 

Qualifications:

 
• Education level to bachelor degree in relevant major is essential.
• At least 5 years’ experience in a similar role in a multinational company; regional exposure will be considered as an advantage. 
• Solid administrative experience.
• Previous experience in pharmaceutical industry is necessary.
• High proficiency in Office.
• Excellent business writing skills to compose correspondence or reports.
• Fluency in English language.
• Customer-service mindset and good problem solving skills.

Location: Cairo, Egypt

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
 
Medochemie Ltd invites applications from career-oriented professionals for the position of Quality Assurance Associate in our offices in Limassol, CYPRUS.
 

Duties:

• To prepare and review Standard Operating Procedures, Change Proposals, deviations and other documents.
• To review and perform deviation investigations and provide corrective action plans.
• To oversee and review change control processes and procedures, making recommendations for changes and/or improvements.
• To review Batch records.
• To assist in self-inspections and perform the follow up.
• To assist in external inspections.
• To ensure that the monitoring environment is monitored and controlled by checking the following:
• To ensure that the monitoring environment is monitored and controlled by checking the following:
       • The hygiene rules are followed by the personnel.
       • Training programs are carried out.
       • Gowning procedures are followed.
       • All validations are carried out.
 

Qualifications:

• University degree in a relevant scientific discipline such as Pharmacy, Chemistry, Biochemistry, Biology, etc. A post graduate degree will be considered an asset.
• Experience in the field of pharmaceutical industry will be an advantage.
• Ability to clearly and concisely communicate technical information.
• Ability to research, analyse and report independently across a breadth of topics.
• Strong organisational skills and an eye for detail.
• Multi project handling at once under time pressure.
• Good collaboration skills and team spirit.
• Fluency in Greek and English language.
• Strong IT, Strong computer literacy skills.
 

Location: Limassol, Cyprus

We are offering an attractive remuneration package and challenging opportunity for professional development.
 
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please apply online through our web site:
 
http://www.medochemie.com/MainMenu/Careers.aspx
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
 
Medochemie Ltd invites career-oriented professionals to apply for the position(s) of Pharmaceutical Representative in the following areas:  Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos.
 

Duties:

o Conducts visits to pharmacies for the proper promotion of the medical products
o Develops and maintain positive clients relationships
o Informs about the new products and seeks their immediate placement in pharmacies
o Controls the stocks of the products
o Solves any problems in a reliable way, always acting within the framework of the procedures and the policies of the Company

 

Qualifications:

 o Licensed Medical/Pharmaceutical Representatives with at least two years of experience in a similar position.
o University degree in Pharmacy, Biology, Chemistry, Medical Representative or other relevant disciplines will be considered as an additional asset.
o Excellent level of knowledge of the Greek and the English language.
o Very good interpersonal and influence skills, analytical thinking, results orientation.

Location: CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites career-oriented professionals to apply for the position(s) of Medical Representative in the following areas: Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos.

Duties:

• Conducts visits to doctors for the proper promotion of the medical products
• Maintains existing business and presents new products
• Develops and maintain positive clients relationships
• Organizes and participates in medical events
• Solves any problems in a reliable way, always acting within the framework of the procedures and the policies of the Company

Qualifications:

• Licensed Medical Representatives with at least two years of experience in a similar position.
• University degree in Pharmacy, Biology, Chemistry, Medical Representative or other relevant disciplines will be considered as an additional asset.
• Excellent level of knowledge of the Greek and the English language.
• Very good interpersonal and influence skills, analytical thinking, results orientation.

Location: CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
 
Medochemie Ltd invites applications from career oriented professionals for the position of Quality Control Associate in our offices in Limassol, CYPRUS.
 

Duties:

• To perform chemical analysis to raw materials and finished pharmaceutical dosage forms using a variety of analytical and separation techniques such as High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC).
• To carry out stability studies to pharmaceutical products stored under different climatic control conditions following the appropriate monitoring software, using the required analytical & separation technique and implementing analytical chemistry statistics.
• Use of statistical tools to monitor trends will be considered as an asset
• To follow all the guideline’s on Good Laboratory Practice (GLP)
 

Qualifications:

• University degree in Chemistry
• Post Graduate diploma will be considered as asset.
• Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, will be considered as an additional asset.
• Effective verbal and written communication skills
• Fluency in  Greek and English language

Computer literacy sufficient to use standard software (MS Office) as well as the ability to learn specific software and instrumentation.

Location: Limassol, Cyprus

We are offering an attractive remuneration package based on the candidate’s experience and relevant qualifications as well as great opportunities for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
 
All applications will be treated in strict confidence.
 
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
Medochemie Ltd invites applications from career-oriented professionals for the position of R&D Formulation Development Specialist/Senior Specialist for our offices in Limassol, CYPRUS.
 

Duties:

• To study the literature of the product and know its pharmaceutical characteristics.
• To study the reference product and be able to develop a generic formulation of Injectables (Solutions, Pre-filled cartridges, Lyophilized formulations).
• To study the reference product and be able to develop a generic formulation of Dry Powder Inhalers.
• To prepare the formulation(s) proposal for patent clearance.
• To apply knowledge in the QbD based product development.
• To perform the formulation development trials in the formulation development laboratory, possibly without any errors.
• To transfer the manufacturing process from trials to scale up and coordinate in the execution of production scale batches in production facilities.
• To follow Regulatory Affairs requirements and current European and WHO guidelines related to the development pharmaceutics section and stability guidelines.

Qualifications:

• University Post graduate Degree in Pharmacy or related field
• Excellent Pharmaceutical and Technology skills related to this discipline
• Multi project handling at once under time pressure
• Excellent command of the English language, both written and oral
• 8-10 years industrial experience in a similar position involving the above duties
• Committed to relocate to Cyprus

Location: Limassol, Cyprus

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please apply online.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites applications from career oriented professionals for the position of Regulatory Affairs Specialist in our offices in Athens, GREECE.

Duties:

• Be responsible for the CMC compilation of dossiers for new products and dossier updates for existing products, in eCTD format and in compliance with the global regulations in force.
• Submit Marketing Authorisation Applications (MAAs) and follow up till approval mainly for European Registration Procedures (DCP/MRP) according to the company’s strategy. 
•  Successfully maintain dossiers’ and MA’s lifecycle (variations & renewals) in all territories as necessary so that the MAs are up to date.
• Participate in developing Regulatory strategies within the department, interact and negotiate with competent Authorities and maintain close working relationship with internal stakeholders (e.g. QA, QC, production, commercial). 

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• 3 to 5 years experience in the pharmaceutical sector, in the field of generic product development and Regulatory Affairs.
• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines and competency with e-CTD preparation
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment.
• Strong communication, influencing and problem resolution skills.
• Ability to be adaptive to change, to multitask and give attention to detail.
• Very good interpersonal skills, analytical thinking and result orientation.
• Fluency in Greek and English (written and spoken) and computer literacy.  Knowledge of any other languages will be considered an asset
• Ability to travel abroad if requested

Location: Athens, Greece

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

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

All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP)

Medochemie Ltd invites applications from career-oriented professionals for the position of Quality Control (QC) Technician for our offices in Limassol, Cyprus.

Duties:

• Receive, label and store samples to be tested
• Perform analysis and testing of products for product approval and release
• Report data and primary results; gather all necessary documentation
• Maintain equipment and assist in ordering laboratory supplies.
• Keep the working area clean and tidy, as per the Laboratory Hygiene and Safety Guidelines

Qualifications:

• School leaving certificate; college diploma will be considered as advantage
• Excellent command of the Greek and English language, both written and oral
• Excellent knowledge of Microsoft Office
• Excellent communication and interpersonal skills
• Multi project handling at once under time pressure
• Experience in the field of pharmaceutical industry will be considered as advantage

Location: Limassol, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated in strict confidence

Medochemie Ltd is a Cypriot pharmaceutical company with international exposure offering quality pharmaceutical products to patients in more than 100 countries worldwide. Medochemie manufactures and licenses a wide range of products produced at its 13, GMP-certified manufacturing facilities around the world and divided into more than 10 therapeutic categories.
Medochemie Ltd invites applications from career-oriented Regulatory Affairs Professionals.

Duties:

• To prepare CTD as well as eCTD format dossiers for new products and update the ones for existing products in compliance with the global regulations in force.
• To submit and oversee the attainment of Marketing Authorisations according to the company’s commercial strategy and considering the different country-specific requirements. 
• To submit the necessary lifecycle management activities (renewals and variations) in all territories as necessary to maintain the company’s Marketing Authorisations while enabling the materialisation of the company’s evolving strategy.

Qualifications:

Required:
• University degree in sciences (e.g. Chemistry, Biochemistry, Biology). A postgraduate degree will be considered an advantage. asset.
• Ability to work both individually and as part of a team, as well as prioritise work in a dynamic and fast-moving environment. 
• Excellent interpersonal skills, analytical thinking and ability to work under pressure.
• Competency in Microsoft Office applications.
• Fluency in both written and spoken English.
Preferred:
• At least 3 years of experience within the pharmaceutical industry in the Field of Generic Regulatory affairs.
• Solid knowledge of Eur.Ph., EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs.
• Competency in e-CTD preparation. 

Location: Limassol, CYPRUS

We are offering an attractive remuneration package based on the candidate’s experience and relevant qualifications as well as great opportunities for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
We invite applications from highly qualified and motivated professionals for the position of R&D Senior Patent Specialist based in Limassol, Cyprus.  

Duties:

• Search in available patent databases in order to check the status of patent applications, litigations etc in both European and non- European territories
• Review, analyze and inform on patent restrictions and prepare consolidated patent reports with due diligence 
• Search for the patent regulations in force in each country for new or existing products   
• Assess and conclude on active pharmaceutical substances patents pertinent to their synthetic schemes and physical properties, on finished dosage forms compositions, indications, manufacturing processes  etc towards any valid patents
• Prepare high quality and substantiated advices on the new products strategies in terms of patent restrictions and specific issues that need to be taken into consideration. 

Qualifications:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Minimum of 4 years’ experience as patent specialist in generic medicines is a must
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment
• Very good interpersonal skills, analytical thinking and result orientation
• Strong computer literacy
• Fluency in English language
• Committed to relocate to Cyprus

Location: Limassol, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development. 
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. 
All applications will be treated in strict confidence. 
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP)

Medochemie Ltd invites applications from career-oriented professionals for the position of Marketing Senior Manager for our offices in Limassol, Cyprus. 

Duties:

The Responsibilities include but are not limited to: 

•    Be responsible for executing global marketing initiatives to drive business growth including innovation in the way we conduct business, customer/patient connections, path to purchase strategies, insight development & deployment, brand positioning, pricing strategy, expansion strategy, retail facing category vision and strategy for the Company’s OTC/ Consumer Healthcare brands.
•    Collaborate with Area Sales Leads around the globe to develop multiple marketing programmes. 
•    Develop commercial business development programs for all regions. Create and foster strong strategic partnerships with Sales and other business leaders.
•     Coordinate and proactively facilitate the identification of new business opportunities, strategic and operational analysis of opportunities, including leading the vetting and validation of ideas and opportunities. 
•    To act as single point of contact for our global regions helping to maximise their potential growth.
•    Adapt a central multi-channel communications programme ensuring high cultural resonance for all regions and the probable addition of alternative copy for any specific local challenges. 
•    Partner with R&D, Regulatory, Sales, Regional Marketing, Finance and key customers in planning, coordinating and sequencing product launches and customer targeting. 
•    Support business financial objectives and ensure applicable company compliance with all relevant country and regional requirements, company regulations, policies and procedures.

Qualifications:

    Bachelor’s degree is required with science expertise as preferred.  Master’s Degree in business or marketing will be preferred.  
•    15+ years of marketing or related function experience in the pharmaceutical industry with 5 years in management-level positions with increasing responsibilities. A demonstrated record of accomplishments regarding business development strategies, brand marketing and portfolio management.
•    Deep understanding of the pharmaceutical industry across a range of lenses (e.g. Marketing, Sales, Medical Affairs, Market Access, etc.)
•    People management experience and high propensity for people development. Experience in leading cross-functional teams will be considered as advantage. 
•    Experience in leading business growth in complex global framework.
•    Ability to travel.
•    Fluency in English language both verbal and writing. 

Location: Limassol, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.
 
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated in strict confidence

Medochemie Ltd is an International pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites career-oriented professionals to apply for the position of Medical Representative, for the following provinces/governorates:

1. Baghdad
2. Basra
3. Mousel
4. Najaf
5. Wasit & Maysan

Duties:

• Conducts visits to doctors, pharmacies and other HCPS for the proper detailing and promotion of our medical products, anchored by the patient needs & safety
• Delivers sales presentations to multiple decision-makers in order to promote the Company’s portfolio of products, within the entrusted/ assigned territory
• Achieves the sales targets in light of operational & promotional indicators
• Establishes and nurtures strong productive client relationships
• Develops strong relationships with key decision makers and key stakeholders
• Maintains existing business and presents new products

Qualifications:

• University degree in Pharmacy (Registered member of the Pharmacist Syndicate in Iraq)
• At least two years of experience in a similar position with an international company
• Excellent level of knowledge of the English language
• Very good interpersonal and influence skills, analytical thinking, results orientation
• Iraqi National 

Location: Baghdad, Wasit & Maysan, Najaf, Basra and Mousel

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
 
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites applications from career oriented Chemical Engineer Professionals. We will employee candidates on the positions of Specialist, Senior Specialist or Assistant Manager based on the level of experience.   

Duties:

• Coordinate, supervise and control production processes to ensure that products are produced according to the appropriate procedures in order to obtain the required quality.
• Monitor the compliance of the department with the requirements of Good Manufacturing Practice (GMP).
• Carry out the production plan according to the production schedule.
• Effective supervision, coaching, development and monitoring of all production personnel in order to ensure productivity and product quality. 
• Follow and apply the requirements of the Good Manufacturing Practice (GMP). 

Qualifications:

• University Degree in Chemical Engineering, Industrial Pharmacy, Pharmacy or other related field
• Experience specific in Production in an industrial environment is required. Any previous experience in the Pharmaceutical Industry will be considered an important asset
• Good command of the English and Greek language, both written and verbal
• Excellent analytical and technical skills related to this discipline

Location: Limassol, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.
 

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites applications from career oriented Chemist to join our team based in Company’s offices in Limassol, CYPRUS. We will employee candidates for the levels of Associate or Specialist (based on experience) for our Quality Control and R&D Departments.   

Duties:

Duties for QC:
• To perform physical and chemical analysis on starting materials and finished pharmaceutical dosage forms using a variety of analytical and separation techniques such as High Performance Liquid Chromatography (HPLC),Gas Chromatography (GC), UV/VIS Spectrophotometry, Thin-layer Chromatography (TLC) and IR.
• To carry out stability studies on pharmaceutical products stored under different climatic control conditions  
• Use of statistical tools to monitor trends will be considered as an asset
• To follow all the guideline’s on Good Laboratory Practice (GLP)

Duties for R&D:
• Strong Method development, Method Validation and Method transfer of new analytical methods.
• Experienced in operational knowledge of analytical instrumentation like HPLC, GC, LC/MS, UPLC, TLC, Dissolution apparatus(manual and automated), FTIR and UV-VIS spectrophotometer
• To perform detailed literature searches and review all available literature data for the development of analytical methods and to design new method development if no available procedure can be found in the literature.

Qualifications:

• University degree in Chemistry. 
• Post Graduate or Doctoral degrees will be considered as an additional asset.
• Excellent command of the English language, both written and oral.
• Excellent communication and interpersonal skills.

Location: Limassol, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Medochemie Ltd is an international pharmaceutical company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).

Medochemie Ltd invites career-oriented professionals to apply for the position(s) of Medical Representative in the following areas:

• Western and Southern provinces, based in Jeddah
• Central province, based in Riyadh 
• Eastern Province, based in Dammam or Khobar 

Duties:

• Conducts visits to doctors and pharmacists (Hospitals and polyclinics) for the proper promotion of the medical products
• Makes sales presentations to multiple decision-makers in order to promote the company’s portfolio of products, within the entrusted territory
• Achieves the sales targets and statutory performance indicators
• Establishes and nurtures client relationships 
• Develops strong relationships with key decision makers and influencers 
• Maintains existing business and presents new products

Qualifications:

• University degree in Pharmacy (Licensed) 
• Valid specialties accreditation (Practitioner)
• 0- to two years of experience in a similar position.
• Excellent level of knowledge of the English language.
• Very good interpersonal and influence skills, analytical thinking, results orientation.
• Saudi Nationals only

Location: Jeddah, or Riyadh, or Eastern Province, Saudi Arabia

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click Submit your CV or Fill in the online Form buttons below.

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.
All applications will be treated in strict confidence.

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.

Η Medochemie Ltd ζητά να προσλάβει υπεύθυνα και συνεργάσιμα άτομα με έδρα την Λεμεσό, για τη θέση Προσωπικό Παραγωγής, για τα ακόλουθα συστήματα βάρδιας:

Κυλιόμενο ωράριο: Πρωινό/Απογευματινό/ Νυκτερινό:
Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00/ 23:00-07:00 (εκ περιτροπής ανά εβδομάδα)

Μεταβαλλόμενο ωράριο: προγραμματισμός 8ωρης εργασίας καθόλη τη διάρκεια του 24ωρου:
π.χ. 6:00 – 14:15 ή 8:00 – 16:15 ή 11:00 – 19:15 ή 19:00 – 03:15 ή 05:00 – 13:15 κ.α.

Duties:

• Ρύθμιση, επίβλεψη λειτουργίας και καθαρισμός μηχανών παραγωγής φαρμακευτικών σκευασμάτων
• Τήρηση των Κανόνων Καλής Παρασκευής Φαρμάκων (GMP) κατά τη διαδικασία παραγωγής
• Καταχώρηση δεδομένων στις εντολές παρτίδας παραγωγής, στα απαιτούμενα έντυπα και ημερολόγια

Qualifications:

• Απόφοιτος Τεχνικής Σχολής ή Τεχνικού κολλεγίου 
• Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
• Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση, θα θεωρηθεί επιπρόσθετο προσόν
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας και άλλα ωφελήματα ανάλογα με προσόντα και πείρα.

Εάν διαθέτετε τα πιο πάνω προσόντα και επιθυμείτε να εργασθείτε σε ένα ευχάριστο, σύγχρονο, επαγγελματικό περιβάλλον με άριστες προοπτικές αποστείλετε την αίτηση σας πατώντας Υποβολή Βιογραφικού Σημειώματος ή Συμπληρώστε την Ηλεκτρονική Αίτηση.

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.

Η Medochemie Ltd ζητά να προσλάβει υπεύθυνα και συνεργάσιμα άτομα με έδρα την Λεμεσό, για τη θέση Προσωπικό Συσκευασίας, για το ακόλουθο σύστημα βάρδιας:

Κυλιόμενη: Πρωινή/ Απογευματινή/ Νυκτερινή:         
Δευτέρα- Παρασκευή: 07:00-15:30/ 14:30-23:00/ 23:00-07:00 (εκ περιτροπής ανά εβδομάδα)

Duties:

• Συναρμολόγηση, συσκευασία και αποθήκευση φαρμακευτικών σκευασμάτων
• Χειρισμός και επίβλεψη λειτουργίας μηχανών συσκευασίας φαρμακευτικών σκευασμάτων σύμφωνα με τους Κανόνες Καλής Παρασκευής Φαρμάκων (GMP)
• Καταχώρηση δεδομένων στις εντολές παρτίδας παραγωγής, στα απαιτούμενα έντυπα και ημερολόγια 

Qualifications:

• Απόφοιτος Τεχνικής Σχολής ή Τεχνικού κολλεγίου 
• Βασικές γνώσεις της Αγγλικής γλώσσας και Ηλεκτρονικών Υπολογιστών
• Προϋπηρεσία σε βιομηχανία ή σε παρόμοια θέση, θα θεωρηθεί επιπρόσθετο προσόν
• Ευχάριστη προσωπικότητα με ακεραιότητα χαρακτήρα

Location: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας και άλλα ωφελήματα ανάλογα με προσόντα και πείρα.

Εάν διαθέτετε τα πιο πάνω προσόντα και επιθυμείτε να εργασθείτε σε ένα ευχάριστο, σύγχρονο, επαγγελματικό περιβάλλον με άριστες προοπτικές αποστείλετε την αίτηση σας πατώντας Υποβολή Βιογραφικού Σημειώματος ή Συμπληρώστε την Ηλεκτρονική Αίτηση.

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

Η Medochemie Ltd διεθνής φαρμακευτική Εταιρεία στην Κύπρο, διαθέτει 13 υπερσύγχρονες παραγωγικές μονάδες και εγκαταστάσεις, εκ των οποίων 9 βρίσκονται στην Κύπρο, μία στη Ολλανδία και τρείς στο Βιετνάμ. Έχει αποκτήσει και διατηρεί 4.355 άδειες κυκλοφορίας για 630 διαφορετικά φαρμακευτικά προϊόντα, τα οποία κατατάσσονται σε περισσότερες από 10 θεραπευτικές κατηγορίες και δραστηριοποιείται σε 107 χώρες σε όλον τον κόσμο. Λειτουργεί σύμφωνα με τις πλέον αυστηρές προδιαγραφές υψηλής ποιότητας και σε πλήρη συμφωνία με τις Ευρωπαϊκές οδηγίες.

Η Medochemie Ltd ζητά να προσλάβει υπεύθυνο και συνεργάσιμο άτομο με έδρα τη Λεμεσό στην Κύπρο, για τη θέση Production Shift Associate για εργασία σε πρόγραμμα βάρδιας. 

Duties:

• Να εφαρμόζει πλήρως το πρόγραμμα της παραγωγής σύμφωνα με τις οδηγίες του Δ/ντή Παραγωγής.
• Να παρακολουθεί και να διασφαλίζει την τήρηση των Κανόνων Ασφάλειας καθώς επίσης και των απαιτήσεων των Κανόνων Ορθής Παρασκευαστικής Πρακτικής (GMP), για την διασφάλιση της ποιότητας των προϊόντων.
• Χειρισμός,  ρύθμιση και  αλλαγή σετ των μηχανών της μονάδας.
• Να προγραμματίζει, συντονίζει, επιβλέπει και να διοικεί αποτελεσματικά το προσωπικό που εργάζεται στην γραμμή Παραγωγής.
• Να διασφαλίζει  την παραγωγικότητα, την ποιότητα, την υγιεινή και την σωστή συμπεριφορά του προσωπικού.
• Να εντοπίζει και να αναφέρει έγκαιρα στο τεχνικό τμήμα τυχών μηχανικές βλάβες και να συντονίζει για την έγκαιρη διόρθωση τους.
• Έγκαιρη και σωστή εισαγωγή των απαιτούμενων δεδομένων στα έντυπα και ημερολόγια της παραγωγής.
• Να συνεργάζεται με τα υπόλοιπα τμήματα για τη διασφάλιση της εύρυθμής λειτουργίας του τμήματος.  

Qualifications:

• Κάτοχος πτυχίου Μηχανολόγου Μηχανικού, Μηχανικού Παραγωγής, Ηλεκτρολόγου Μηχανικού, Χημικού Μηχανικού ή άλλες συναφή σπουδές.
• Απαραίτητη εργασιακή εμπειρία τουλάχιστο ενός χρόνου   
• Προϋπηρεσία στη Βιομηχανία ή σε Επιστασία προσωπικού θα θεωρηθεί επιπρόσθετο προσόν. 
• Καλή γνώση της Αγγλική γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.

Location: Limassol, CYPRUS

Προσφέρεται ελκυστικό πακέτο απολαβών ανάλογα με τα προσόντα και την πείρα.

Εάν διαθέτετε τα πιο πάνω προσόντα και επιθυμείτε να εργασθείτε σε ένα ευχάριστο, σύγχρονο, επαγγελματικό περιβάλλον με άριστες προοπτικές αποστείλετε την αίτηση σας πατώντας Υποβολή Βιογραφικού Σημειώματος ή Συμπληρώστε την Ηλεκτρονική Αίτηση.

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR) όλα τα βιογραφικά που διατηρούσαμε στη βάση δεδομένων της Εταιρείας έχουν διαγραφεί. Ως εκ τούτου, αποστείλετε ξανά το βιογραφικό σας εάν ενδιαφέρεστε για την εν λόγω θέση.

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.