Careers

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 Supply Chain Specialist based in Limassol, Cyprus 
 

Duties:

Supply Planning ·   Review and manage Sales Orders generated in the system from Sales Team. ·   Minimize manual process fully operating in the ERP system. ·   In cooperation with Master Scheduling provide the first Estimate Delivery date and communicate to the Customers (Internals / Externals). ·   Communicate to the Customers any deviation vs the final confirmation date. ·   Define and maintain material master data planning /supply chain within ERP. ·   Generate Export documents and book shipments to end Customers Inventory Planning and Control ·   Monitor safety stock and reorder points without hampering the customer service levels ·   Monitor and reduce expired stock in line with Affiliates Team. ·   Monitor backorders and assure on time replenishment. ·   Coordinate inventory allocation and/or transfer during times of supply constrain or in excess ·   Drive inventory optimization based on the safety stock agreed levels. Reporting ·   Create reports on sales/demand, inventory, expiry, for Medochemie Affiliates ·   Analyze and evaluate forecasts accuracy in demand planning system

Qualifications:

• University degree in Supply Chain Management, Chemical Engineering, Industrial Pharmacy or related field
• Minimum 2 years of previous experience in the field of production or supply chain 
• Previous experience in analysis and reporting is a must
• Very good interpersonal skills and analytical thinking
• Able to organize and prioritize work.
• Strong computer literacy
• Fluency in Greek and English language

Location: Limassol, Cyprus

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv below or by completing the online application.
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.

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

Duties:

Ensure that policies, and SOPs with reference to the receiving, storage and dispatch conditions of materials/products are strictly and correctly followed, according to GMP Assure on time and correct documentation processing in the ERP system according to the GMP Takes care of smooth transition of current operational warehouse processes to new future warehouse concept processes (phase-in, phase out) Develops and implements appropriate KPIs and tracking tools to monitor process performance and material flows Builds strong partnerships with other operation groups to identify options to improve performance or to achieve higher process stability Organize and assist during annual inventory counting Perform cycle count controls to ensure inventory accuracy on a weekly base Work closely and communicate regularly with Procurement to identify R+P shortage Is responsible for and improves H&S policies and hygiene rules according to the Company’s systems in place Supervises and Control the Local Transportation Activity Leads, manages coordinates and coaches the warehouse team Assess the training needs of the department's personnel and conduct training and evaluate the training effectiveness, keeping training records

 

Qualifications:

University degree in Logistics, Supply Chain management, Business Administration or other related field Minimum 10 years’ experience in Supply Chain management Previous experience in the pharmaceutical industry (GMP) will be considered as an important asset Experience in leading teams of over 20 people is an important requirement Proficient in Microsoft Office Suite, computer-based applications, WMS systems experience Excellent verbal/written communication skills Fluency in both Greek and English is required Ability to adapt to changing organizational and operational needs, ability to successfully lead others through change Ability to handle multiple tasks simultaneously Skill in organization and prioritization, and attention to detail Strong team player and leader with the ability to work across multiple functions and disciplines Ability to select, coach, develop, engage and retain a team of employees

 

Location: Limassol, Cyprus

Duties:

Collect and evaluate the necessary information for the preparation of risk assessments related to impurities assessment in pharmaceutical products /materials Prepare / assist the risk assessments Participate in the process of setting mitigation / corrective / preventive actions Identify possible degradation paths and formation of relevant impurities / degradation products and possible inter-molecules reactions in active pharmaceutical substances, manufacturing processes and finished pharmaceutical products Handle cleaning validation activities, including organization, protocol and report preparation, study execution and related deviations handling

 

Qualifications:

Bachelor's degree in Pharmacy or Chemistry, with specialization in organic chemistry.  A post graduate degree will be considered an advantage Related experience in a pharmaceutical industry would be considered an advantage Experience in nitrosamines and elemental impurities evaluation is necessary Fluency in Greek and English language Proficiency with MS office tools (Word, Excel, PowerPoint, etc) Ability to work collaboratively in a team, and prioritize work in a dynamic and fast-moving environment Ability to work in multiple projects Good communication skills (verbal and written) within the department, between departments and with external partners Strong organisational skills and data analysis skills Multi-project handling at once under time pressure

 

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 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 Associate – Learning/Development & Wellbeing, based in our offices in Limassol, Cyprus.  

Duties:

• Supports L&D administration tasks concerning the full Learning and Development cycle
• Analyses learning and development needs based on departmental needs and requests
• Organizes and co-ordinates learning, and development programs based on the approved training budget
• Gets feedback and evaluates learning and development programs and their ROI;
• Maintains the L&D management system up to date
• Coordinates subsidy programs ran by the organisation (i.e. HRDA, Department of Labour, KEPA)
• Organises effective induction programs for new colleagues
• Organises and coordinates events and other activities based on the Company’s Wellbeing Strategy
• Administrates the employees’ discount program
• Authors and edits the in-house newsletters

Qualifications:

• University Degree in Human Resources Management, Psychology, Organizational Psychology, Occupational Psychology, Business Administration or any other related discipline
• Minimum 2 years of experience in a similar role
• Good knowledge on HR processes and operations
• Hands-on experience with Human Resources Management Systems
• Strong computer literacy  
• Fluency in both the Greek and English language
• Business Awareness and high motivation
• Maintains confidentiality and professional demeanour
• Very good interpersonal skills and problem-solving abilities
• Desire to work as a team with a result-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 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.

All applications will be treated with strict confidentiality.
 

Duties:

As part of a team and under supervision of Senior Management, responsibilities will include:   Performance of Internal Audits of various departments in Cyprus and abroad. Risk analysing and monitoring of the implementation of mitigation actions. Assisting in the development and monitoring of the Company’s compliance programme. Monitoring of Key performance indicators. Engaging in process improvement projects. Assisting in the development of policies and procedures in certain areas for the strengthening of internal controls. Participating in special projects and investigations. Communicating with various departments and external associates. Data collection and analysis. Articulating and presenting findings clearly both verbally and in written reports to the BoD and Senior Management. Travelling to Countries where the Company has operations.

 

Qualifications:

University degree in fields such as Accounting, Economics, Management, Operational Research, Risk, Engineering. Professional Accounting qualification (ACA, ACCA, CPA) and/ or Certified Internal Auditor qualification (CIA) will be considered as an advantage. Work experience of at least 5 years in areas such as Internal Audit, Risk and Compliance, Process reengineering, External Audit. Work experience in areas such as manufacturing/ production, logistics, commercial will be considered as an advantage. Project Management experience will be considered as an advantage. Proficiency in MS Office including advanced excel skills. Knowledge of data analytics tools will be considered as an advantage. Excellent knowledge of the Greek and English languages. A highly motivated individual who can demonstrate agility, diversity, curiosity, and willingness for continuous learning. A confident individual, able to communicate in a clear and effective manner.

 

Location: LIMASSOL, CYPRUS

Duties:

Promotion, Sales and Marketing of Pharmaceutical products. Strategic planning for existing and future markets. Supporting, Monitoring and Liaising with the local customers, healthcare professionals, importers/distributors, Healthcare authorities and other partners. Sourcing for new Agencies and Distributors, and Business development. Preparation of all the necessary promotional material.

 

Qualifications:

University degree in a relevant science (Pharmacy, Pharmacology, Chemistry, Biochemistry, Biology, etc). At least 5 years related working experience in the Pharmaceutical Industry. Excellent working knowledge (verbal & written) of English Computer Literacy Ability to work on own initiative and as a member of a professional team. Determination to succeed in a challenging environment. Willingness to travel abroad (outside Europe) extensively.

 

Location: Limassol, Cyprus

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 Associates.
 

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:

• University degree in sciences (e.g. Chemistry, Biochemistry, Biology). A postgraduate degree will be considered an advantage. 
• 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 2 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.

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, Biochemistry or other relevant field. 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

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

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.
 

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 Software Engineer Specialist / Senior Specialist for our offices in Limassol, CYPRUS. 
 

Duties:

•    Execute/Monitor the full software development life cycle (SDLC) for new platforms/tools
•    Document and maintain software functionality
•    Troubleshoot, debug and upgrade existing systems
•    Manage projects and coordinate with vendors to ensure the on-time delivery and quality of technology projects, such as Document Management System, ERP etc.
•    Track and monitor project progress and escalate issues to appropriate stakeholders
•    Continually identify, prioritize and mitigate project risks and issues

Qualifications:

•    BSc degree in Computer Science, Engineering or relevant field
•    3+ years of proven work experience as a Software Engineer or Software Developer. Data Analytics experience will be considered as an advantage.
•    Experience in designing and developing interactive applications. Experience in designing and developing interfaces between systems will be considered as an advantage
•    Ability to develop software in Java, ASP.NET, C++ or other programming languages. Experience in developing web applications (PHP, Python) will be considered as an advantage
•    Background on relational databases, SQL and NoSQL technologies
•    Ability to document requirements and specifications

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.