Job Openings

Duties:

Qualifications:

Benefits:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path'

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

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.

Medochemie is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.
 
We ‘re on a mission to find the best talent out there. We are now looking for a motivated and experienced QP to join our dynamic team in our offices in Limassol, Cyprus.

Duties:

• Certify that each batch of medicinal product complies with its marketing authorization, Good Manufacturing Practices (GMP), and other relevant legal requirements

• Ensure that testing, and manufacturing processes have been properly completed, and the relevant documentation has been reviewed before release for sale or use

• Ensure that any deviations or planned changes in production or quality control have been authorized by Quality Assurance, and their impact on the quality, safety and efficacy of the product and on the compliance with GMP and the marketing authorization, has been evaluated.

• Ensure that any changes requiring variation to the marketing or manufacturing authorization have been notified to and authorized by Regulatory Affairs as required

• Ensure that the manufacturing and testing processes have been validated

• Ensure that all necessary checks and tests have been performed, including any additional sampling, inspection, tests or checks initiated because of deviations or planned changes

Qualifications:

• Registered Qualified Person in Cyprus or another EU Member State

• Previous experience in the pharma industry as a qualified person

• Ability to interpret regulatory guidelines/legislation

• Highly organized; ability to multitask and process excellent time management skills

• Problem solving abilities

• Strong analytical and communication skills

• Proficient in the English language with excellent written and verbal communication skills

• Excellent computer literacy (MS Office)

Benefits:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

 
If you believe that you have the above qualifications and this 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.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Supply Chain Specialist to join our Supply Chain team in our offices in Limassol, Cyprus.

Duties:

• Coordinate the production workflow for one or multiple products

• Create and maintain a constrained production schedule and ensure raw material availability

• Create efficient scheduling processes or methods to attain production goals

• Handle all production issues in a way that it doesn’t hinder production and delivery

• Identify issues or areas of improvement and suggest alternative ways to improve the existing processes

• Collect and analyse data and use software to generate production reports

• Ensure that company deadlines are met

Qualifications:

• Bachelor’s degree in Chemical Engineering, Mathematics, or any other related field

• Ability to handle and prioritize multiple tasks

• Excellent organisational and numeracy skills

• Strong knowledge of Excel and any other Microsoft Office tools

• Strong computer literacy

• Fluency in Greek and English language

It would be considered a plus if you have:

• Previous experience in the supply chain in the pharmaceutical sector

• Knowledge of MS Project

Benefits:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this 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.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Production Shift Associate to join our Production Admin team in our offices in Limassol, Cyprus.

• 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 
• Supervise, coach, develop and monitor of the production personnel to ensure productivity and product quality 
• Follow and apply the requirements of the Good Manufacturing Practice (GMP)

• Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Pharmacy or other related field 
• Any previous experience in the pharmaceutical industry or in the specific field is desired; the position level will be defined based on experience
• Fluent in English language with excellent written and verbal communication skills 
• Excellent analytical and technical skills related to this discipline 
• Excellent problem-solving and analytical skills 
• Ability to work under pressure Accountable and responsible 
• An enthusiastic team player with a strong drive to create a positive and collaborative work environment 

It would be considered a plus if you have: 

• Any previous experience in the Pharmaceutical Industry or industrial environment 

• A unique opportunity for a career in a fast-growing company 
• Competitive remuneration package based on qualifications and experience  
• 13th Salary and 14th Salary
• Paid Vacation 
• Modern & Professional Work Environment 
• Multiple events to bond with the team 
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary  
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme 
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ 

Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτό το άνοιγμα ακούγεται ενδιαφέρον, κάντε αίτηση τώρα ανεβάζοντας το βιογραφικό σας παρακάτω ή συμπληρώνοντας την ηλεκτρονική αίτηση.

Εάν πιστεύετε ότι έχετε τα παραπάνω προσόντα και αυτή η θέση ακούγεται πρόκληση, υποβάλετε την αίτησή σας μέσω του παρακάτω συνδέσμου: (for portals)

http://www.medochemie.com/MainMenu/Careers.aspx

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.

Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Η Medochemie Ltd είναι μια διεθνής Φαρμακευτική εταιρεία, εξάγει τα προϊόντα σε122 χώρες, έχοντας το 29% των συνολικών εξαγωγών τις Κύπρου. Η Medochemie λειτουργεί σε 15 υπερσύγχρονες εγκαταστάσεις, 9 στη Κύπρο, 5 στο Βιετνάμ και 1 στην Ολλανδία, όλα σχεδιασμένα με τα πρότυπα καλής πρακτικής GMP της Ευρωπαϊκής Ένωσης και του ΠΟΥ (Παγκόσμιος Οργανισμός Υγείας). Η Medochemie έχει γραφεία σε 19 χώρες και εργοδοτεί πέραν των 2000 υπαλλήλων.

Ποια θα είναι τα καθήκοντα σου;

 
• Υπεύθυνος /η για τον έλεγχο των αποθεμάτων πρώτων υλών και υλικών συσκευασίας, καθώς και ημιέτοιμου και έτοιμου προϊόντος στην αποθήκη.
• Βέλτιστη διαχείριση των πόρων που διαχειρίζεται.
• Διασφαλίζει τη σωστή διεξαγωγή των διαδικασιών όπως αυτές περιγράφονται στα Standard Operating Procedures (SOP’s) σύμφωνα με τους Κανόνες Καλής Παρασκευής (GMP).
• Μεριμνά για την ασφάλεια τόσο του προσωπικού όσο και των υλικών/προϊόντων της Εταιρείας.
• Βέλτιστη επικοινωνία με τα τμήματα παραγωγής και συσκευασίας για να διασφαλίζεται η συνεχής ροή προϊόντων.
• Ικανότητα να διαχειρίζεται πολλές παραγγελίες ή διαδικασίες ταυτόχρονα, χωρίς λάθη.
• Γρήγορη και αποτελεσματική αντιμετώπιση προβλημάτων.
• Δεξιότητες στη χρήση λογισμικών διαχείρισης αποθήκης και συστημάτων παρακολούθησης (π.χ. barcode scanners).
• Κατανόηση ηλεκτρονικών αρχείων και διαδικασιών εισαγωγής/εξαγωγής δεδομένων.
• Κατανόηση της χρήσης ειδικών συστημάτων για τη διαχείριση αποθεμάτων, όπως τα ERP συστήματα.
• Διασφαλίζει ότι το σύστημα ERP είναι πάντοτε σωστά ενημερωμένο και ανταποκρίνεται στη πραγματικότητα
• Διασφαλίζει αποτελεσματικές και αποδοτικές συνθήκες αποθήκευσης για όλα τα υλικά/προϊόντα στην αποθήκη.           
• Διασφαλίζει τη σωστή παρακολούθηση και έγκαιρη ενημέρωση στον ηλεκτρονικό υπολογιστή όλων των λογισμικών πράξεων που διεξάγονται στην αποθήκη.
• Εκδίδει έγκαιρα οποιαδήποτε έντυπα χρειάζονται από το Document Management System (DMS)
• Είναι υπεύθυνος και ενημερώνει τον Διευθυντή Αποθηκών για την κυκλική απογραφή αποθεμάτων
• Λαμβάνει μέρος στη Διαδικασία Καταγραφής των Αποθεμάτων.
• Συμπληρώνει έγκαιρα και έγκυρα όλα τα ημερολόγια καταγραφής (logbook)
• Λαμβάνει μέρος στη Διαδικασία Παραγγελιών υλικών/προϊόντων
• Εισηγείται σκέψεις/τρόπους για καλυτέρευση των διαδικασιών της Αποθήκης και της Εταιρείας γενικότερα.
• Αναλαμβάνει νέα ή αναπροσαρμοσμένα καθήκοντα σύμφωνα πάντα με τις ειδικές ανάγκες του Τμήματος Αποθηκών και της Εταιρείας γενικότερα.
• Εξασφαλίζει την ιχνηλασιμότητα των υλικών/προϊόντων και ακολουθεί το FEFO
• Εντοπίζει και αξιολογεί κίνδυνους που σχετίζονται με το χώρο που εποπτεύει 

Ποιες δεξιότητες είναι απαραίτητες για να κάνεις αυτή την δουλειά;

• Δίπλωμα σε Διοίκηση Εφοδιαστικής Αλυσίδας (Supply Chain Management), Διοίκηση Επιχειρήσεων, Οργάνωση, Διοίκηση Αποθηκών ή αλλον συναφή τομέα.
• Προηγούμενη τριετής εμπειρία σε Διαχείριση Λειτουργίας Αποθήκης.
• Πολύ καλή γνώση συστημάτων ERP και RF Scanner
• Πολύ καλή γνώση ηλεκτρονικών υπολογιστών και MS Office.
• Πολύ καλή γνώση της ελληνικής και αγγλικής γλώσσας.
• Πρωτοβουλία, ενδιαφέρον για προσωπική ανάπτυξη και διάθεση για συνεχή μάθηση.
• Ακεραιότητα χαρακτήρα, ομαδικό πνεύμα, υψηλό αίσθημα ευθύνης και προσοχή στη λεπτομέρεια.

Aν γίνεις μέλος της ομάδας μας θα έχεις τα πιο κάτω ωφελήματα:

• Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία
• Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας
• Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία
• 13ος και 14^ος μισθός
• Πληρωμένη Ετήσια Άδεια
• Πολλαπλές Δραστηριότητες με την ομάδα
• Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού
• Προαιρετική συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον 

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.
 
Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie is an International Pharmaceutical Company, one of the top 200 producers of generic drugs globally, exporting its products to 110 countries, thus holding the 29% of the total industrial exports of Cyprus.  Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization, operates in 22 countries and employs a global workforce of 1880 employees of 19 ethnicities.

We ‘re on a mission to find the best talent out there. We are now looking for a motivated and skilled Laboratory Technician to join our Labs in our offices in Limassol, Cyprus.

What the job looks like?

The laboratory technician will have the opportunity to:

• Undertake administration work related to Labs

• Be responsible for Sample management (receipt and destruction)

• Undertake sampling of  Packing Materials

• Perform In-Process Control checks during packing

• Be trained and  follow  Laboratory Hygiene and Safety Guidelines

What does it take to do the job?

• High school certificate

• A certificate or bachelor’s degree would be considered as advantage

• Strong organization skills with a high attention to detail

• Proficient in the English and Greek language with excellent written and verbal communication skills

• Ability to work in Lab environment

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

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

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.
 
We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Control Specialist to join our Quality Control team in our offices in Limassol, Cyprus.

What the job looks like?

• Prepare SOPs and WINs for primary and secondary packaging materials

• Prepare specifications for primary and secondary packaging materials

• Review documentation related to packaging materials

What does it take to do the job?

• University degree in Chemistry, Biochemistry, or another relevant field

• Ability to work under pressure

• Accountable and responsible

• Strong organization skills with a high attention to detail

• Εxcellent communication, interpersonal and teamworking skills

• High levels of ethics and integrity

• Proficient in the English and Greek language with excellent written and verbal communication skills

• Good working knowledge of the Microsoft Office tools

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path'

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

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.

Η Medochemie Ltd είναι μια διεθνής Φαρμακευτική εταιρεία, εξάγει τα προϊόντα σε122 χώρες, έχοντας το 29% των συνολικών εξαγωγών τις Κύπρου. Η Medochemie λειτουργεί σε 15 υπερσύγχρονες εγκαταστάσεις, 9 στη Κύπρο, 5 στο Βιετνάμ και 1 στην Ολλανδία, όλα σχεδιασμένα με τα πρότυπα καλής πρακτικής GMP της Ευρωπαϊκής Ένωσης και του ΠΟΥ (Παγκόσμιος Οργανισμός Υγείας). Η Medochemie έχει γραφεία σε 19 χώρες και εργοδοτεί πέραν των 2000 υπαλλήλων.

Είμαστε σε αποστολή να βρούμε Φύλακα/Θυρωρό για να ενταχθεί στην ομάδα μας στα γραφεία μας στην Λεμεσό, Κύπρο.

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

Ποιες δεξιότητες είναι απαραίτητες για να κάνεις αυτή την δουλειά;

• 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
• Δυνατότητα εργασίας σε βάρδια Πρωινό / Απογευματινό / Νυχτερινό : Δευτέρα- Κυριακή: 07:00-15:00/ 15:00-23:00/ 23:00-07:00

• Προηγούμενη εμπειρία σε φαρακοβιομηχανία.

• Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία
• Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας
• Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία
• 13ος και 14ος Μισθός
• Πληρωμένη Άδεια
• Πολλαπλές Δραστηριότητες με την ομάδα
• Προαιρετική Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού
• Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

Graphic Designer (Packaging)

 Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

 We ‘re on a mission to find the best talent out there. We are now looking for a talented Graphic Designer to join our Marketing team in our offices in Limassol, Cyprus.

What the job looks like?

The Graphic Designer will have the opportunity to:

• Design and implementation of the packaging design in accordance with the corporate identity (cartons, leaflets, aluminium foils, labels, tubes), from concept through to production
• Follow corporate branding procedures and country specific regulations for pharmaceutical products
• Time-manage multiple projects and keep stakeholders updated on progress
• Work independently as well as cooperatively with internal and external stakeholders to meet deadlines and schedule project implementation based on workload
• Update and maintain internal databases as per department procedures

What does it take to do the job?

• Bachelor’s degree (or equivalent) in graphic design, art, or related discipline. A post graduate degree will be considered an advantage.
• Minimum 2 years of experience in graphic design. Experience in the pharmaceutical sector will be considered an advantage.
• Expertise with graphic design software such as Corel Draw or Adobe Creative Cloud (Illustrator, Photoshop)
• Ability to clearly and concisely communicate technical information
• Organizational and time-management skills for meeting deadlines in a fast-paced environment as well the ability to handle multiple projects
• Very good knowledge of the English language, both in written and verbal
• Desire to continue building skill set with education and training
• Have a strong drive to create a positive and collaborative work environment

 By joining us you can expect:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th and 14^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Medical Representative

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Medical Representative to join our Sales team for the following areas: Limassol/Paphos, Limassol/Nicosia & Larnaca/Nicosia/Ammochostos.

What the job looks like?

The Medical Representative will have the opportunity to:

·         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

What does it take to do the job?

·         Licensed Medical Representatives with at least two years of experience in a similar position.

·         University degree in Medical Representative, Pharmacy, Biology, Chemistry or related field will be considered an advantage

·         Proficient in the English and Greek language with excellent written and verbal communication skills

·         Very good interpersonal and influence skills, analytical thinking, results orientation.

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th and 14^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Production Shift Associate to join our Production Admin team in our offices in Limassol, Cyprus.

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 
• Supervise, coach, develop and monitor of the production personnel to ensure productivity and product quality 
• Follow and apply the requirements of the Good Manufacturing Practice (GMP)

Qualifications:

• Bachelor’s Degree in Chemical Engineering, Mechanical Engineering, Pharmacy or other related field 
• Any previous experience in the pharmaceutical industry or in the specific field is desired; the position level will be defined based on experience
• Fluent in English language with excellent written and verbal communication skills 
• Excellent analytical and technical skills related to this discipline 
• Excellent problem-solving and analytical skills 
• Ability to work under pressure Accountable and responsible 
• An enthusiastic team player with a strong drive to create a positive and collaborative work environment 

It would be considered a plus if you have: 

• Any previous experience in the Pharmaceutical Industry or industrial environment 

Benefits: 

• A unique opportunity for a career in a fast-growing company 
• Competitive remuneration package based on qualifications and experience  
• 13th Salary & 14th salary
• Paid Vacation 
• Modern & Professional Work Environment 
• Multiple events to bond with the team 
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary  
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme 
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’ 

If you 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/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. 

Pharmaceutical Representative

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a Pharmaceutical Representative to join our Sales team for the areas of Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos.

What the job looks like?

The Pharmaceutical Representative will have the opportunity to:

·         Conduct visits to pharmacies for the proper promotion of the medical products

·         Develop and maintain positive clients’ relationships

·         Inform about the new products and seeks their immediate placement in pharmacies

·         Control the stocks of the products

·         Solve any problems in a reliable way, always acting within the framework of the procedures and the policies of the Company

What does it take to do the job?

·         Licensed Medical/Pharmaceutical Representatives with at least two years of experience in a similar position

·         University degree in Pharmacy, Biology, Chemistry or related field will be considered an advantage

·         Proficient in the English language with excellent written and verbal communication skills

·         Very good interpersonal and influence skills, analytical thinking, results orientation.

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th and 14^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees

We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Assurance to join our QA team in our offices in Limassol, Cyprus.

What the jobs look like?

• Oversee and review change control processes and procedures, making recommendations for changes and/or improvements

• Review Batch records

• Assist in self-inspections and perform the follow up.

• Assist in external inspections

• 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

What does it take to do the job?

•University degree in a relevant scientific discipline such as Pharmacy, Chemistry, Biochemistry, Biology, etc. A postgraduate degree will be considered an advantage

•Experience in the field of pharmaceutical industry will be considered 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

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now 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. Only shortlisted candidates will be contacted.

Quality Control Associate

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the best talent out there. We are now looking for a talented Quality Control Associate to join our Quality Control team in our offices in Limassol, Cyprus.

What the job looks like?

The Quality Control Associate will have the opportunity to:

·         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 guidelines on Good Laboratory Practice (GLP)

What does it take to do the job?

·         University degree in Chemistry, Biochemistry or another relevant field.

·         Post Graduate diploma will be considered an advantage

·         Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, will be considered as an additional asset

·         Effective verbal and written communication skills

·         Proficient in the English and Greek language with excellent written and verbal communication skills

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th and 14^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Quality Processes and Validation Technician

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Quality Processes and Validation Technician to join our Quality Processes and Validation team in our offices in Limassol, Cyprus.

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

• Prepare Process Validation Protocols and Reports

• Monitor the manufacturing process and prepare process observation reports

• Perform sampling

• Assist during process validation execution sampling by checking that sampling is performed according to the protocol and that the sampling forms are filled in correctly

• To label and gather all samples according to the protocols

• Assist in the preparation GAPs Analysis of the manufacturing process and equipment’s

• To compile and process data for Product Quality Review Report

What does it take to do the job?

• A High School leaving Certificate or a diploma graduate

• Ability to clearly and concisely communicate technical information

• Ability to work in production environment 

• Strong organisational skills and an eye for detail.

• Multi project handling

• Ability to work under strict deadlines

• Good collaboration skills and team spirit

• Fluency in Greek and English language

• Strong IT Strong computer literacy skills

Ιt would be considered a plus if you have:

• Experience in the field of pharmaceutical

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th and 14^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Regulatory Affairs Specialist

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the best talent out there. We are now looking for a talented Regulatory Affairs Specialist to join our offices in Limassol, Cyprus.

What the job looks like?

The Regulatory Affairs Specialist will have the opportunity to:

• Responsible for the compilation of dossier sections and sourcing of relevant documentation for modules 2-5 of Medochemie dossiers intended for registration for Medochemie or clients at global scale in eCTD format

• Compilation of responses and scientific documentation at correspondences with authorities or clients related to initial submissions, and the lifecycle of submissions i.e. variations, renewals, upgrades and new developments. Monitoring the progress of responses related to Modules 2-5 deficiencies raised by the regulatory authorities

• Review of quality documentation related to Modules 2-5 for the applications in line with the appropriate guidelines and timelines

• CMC regulatory directions provision at the various company departments, external parties and suppliers for the projects which have been assigned

• Liaise with the appropriate departments within the company and external parties to collect all necessary information for the submission of pharmaceutical dossiers and product registration

• Assist in keeping the dossier core files (Modules 2-5 and corresponding QoS) fully up to date during registration procedures and variations

• Continuous follow up of the regulatory affairs activities of all projects that have been assigned. Update of the regulatory database in collaboration with the regulatory partners. • Understand and use the EU and International Regulatory guidelines

• Participate in the change control system and variation process according to the established internal workflow

• Participate in regulatory affairs internal projects of digital transformation, namely Regulatory Information management system and Submission Document Core Model

• Act as a member of responsible Regulatory team who is responsible for the submission of assigned regulatory projects

• Liaise with external Regulatory authorities and/or clients if required for the successful completion of projects

• Ensure policies and procedures are properly evaluated, implemented and carried out, safeguarding the compliance of company

• Support internal activities of Regulatory department in order to ensure regulatory compliance

• Monitoring the progress of the assigned projects and their finalization in a timely and accurate manner

What does it take to do the job?

• Post graduate degree will be considered an asset.

• At least 2-3 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs/CMC

• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines

• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment

• Strong communication, influencing and problem resolution skills.

• Strong organization skills and able to meet deadlines

• 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

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company

• Competitive remuneration package based on qualifications and experience

• 13^th and 14^th Salary

• Paid Vacation

• Modern & Professional Work Environment

• Multiple events to bond with the team

• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary

• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme

• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Research and Development Associate/Specialist

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We invite applications from highly motivated professionals for the position of Research and Development Associate/Specialist based in Limassol, Cyprus. 

What the job looks like?

The Research and Development Associate/Specialist will have the opportunity to:

• Overlook projects assigned, ensuring timely and effective execution
• Report on the progress of the projects as required
• Take part in cross-functional teams coordinating projects under responsibility

What does it take to do the job?

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an advantage.
• Ability to work collaboratively in a team and prioritize work in a dynamic and fast-paced environment. 
• Very good interpersonal skills, analytical thinking and results orientation.
• Prior, relevant work experience will be a considered a plus but is not a pre-requisite. 
• Strong computer literacy
• Fluency in English (both verbal and written)

By joining us you can expect:

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• 13^th and 14^th Salary
• Paid Vacation
• Modern & Professional Work Environment
• Multiple events to bond with the team
• Participation in the Company’s Provident fund where the employer contributes 7% of the monthly salary
• Optional participation in the Company’s Group Medical Scheme, and Discount Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.  

Η Medochemie Ltd είναι μια διεθνής Φαρμακευτική εταιρεία, εξάγει τα προϊόντα σε122 χώρες, έχοντας το 29% των συνολικών εξαγωγών τις Κύπρου. Η Medochemie λειτουργεί σε 15 υπερσύγχρονες εγκαταστάσεις, 9 στη Κύπρο, 5 στο Βιετνάμ και 1 στην Ολλανδία, όλα σχεδιασμένα με τα πρότυπα καλής πρακτικής GMP της Ευρωπαϊκής Ένωσης και του ΠΟΥ (Παγκόσμιος Οργανισμός Υγείας). Η Medochemie έχει γραφεία σε 19 χώρες και εργοδοτεί πέραν των 2000 υπαλλήλων.

Ποια θα είναι τα καθήκοντα σου;

• Υπεύθυνος /η για τον έλεγχο των αποθεμάτων πρώτων υλών και υλικών συσκευασίας, καθώς και ημιέτοιμου και έτοιμου προϊόντος στην αποθήκη.

• Βέλτιστη διαχείριση των πόρων που διαχειρίζεται.

• Διασφαλίζει τη σωστή διεξαγωγή των διαδικασιών όπως αυτές περιγράφονται στα Standard Operating Procedures (SOP’s) σύμφωνα με τους Κανόνες Καλής Παρασκευής (GMP).
• Μεριμνά για την ασφάλεια τόσο του προσωπικού όσο και των υλικών/προϊόντων της Εταιρείας.
• Βέλτιστη επικοινωνία με τα τμήματα παραγωγής και συσκευασίας για να διασφαλίζεται η συνεχής ροή προϊόντων.
• Ικανότητα να διαχειρίζεται πολλές παραγγελίες ή διαδικασίες ταυτόχρονα, χωρίς λάθη.
• Γρήγορη και αποτελεσματική αντιμετώπιση προβλημάτων.
• Δεξιότητες στη χρήση λογισμικών διαχείρισης αποθήκης και συστημάτων παρακολούθησης (π.χ. barcode scanners).
• Κατανόηση ηλεκτρονικών αρχείων και διαδικασιών εισαγωγής/εξαγωγής δεδομένων.
• Κατανόηση της χρήσης ειδικών συστημάτων για τη διαχείριση αποθεμάτων, όπως τα ERP συστήματα.
• Διασφαλίζει ότι το σύστημα ERP είναι πάντοτε σωστά ενημερωμένο και ανταποκρίνεται στη πραγματικότητα
• Διασφαλίζει αποτελεσματικές και αποδοτικές συνθήκες αποθήκευσης για όλα τα υλικά/προϊόντα στην αποθήκη.           
• Διασφαλίζει τη σωστή παρακολούθηση και έγκαιρη ενημέρωση στον ηλεκτρονικό υπολογιστή όλων των λογισμικών πράξεων που διεξάγονται στην αποθήκη.
• Εκδίδει έγκαιρα οποιαδήποτε έντυπα χρειάζονται από το Document Management System (DMS)
• Είναι υπεύθυνος και ενημερώνει τον Διευθυντή Αποθηκών για την κυκλική απογραφή αποθεμάτων
• Λαμβάνει μέρος στη Διαδικασία Καταγραφής των Αποθεμάτων.
• Συμπληρώνει έγκαιρα και έγκυρα όλα τα ημερολόγια καταγραφής (logbook)
• Λαμβάνει μέρος στη Διαδικασία Παραγγελιών υλικών/προϊόντων
• Εισηγείται σκέψεις/τρόπους για καλυτέρευση των διαδικασιών της Αποθήκης και της Εταιρείας γενικότερα.
• Αναλαμβάνει νέα ή αναπροσαρμοσμένα καθήκοντα σύμφωνα πάντα με τις ειδικές ανάγκες του Τμήματος Αποθηκών και της Εταιρείας γενικότερα.
• Εξασφαλίζει την ιχνηλασιμότητα των υλικών/προϊόντων και ακολουθεί το FEFO
• Εντοπίζει και αξιολογεί κίνδυνους που σχετίζονται με το χώρο που εποπτεύει 

Ποιες δεξιότητες είναι απαραίτητες για να κάνεις αυτή την δουλειά;

• Δίπλωμα σε Διοίκηση Εφοδιαστικής Αλυσίδας (Supply Chain Management), Διοίκηση Επιχειρήσεων, Οργάνωση, Διοίκηση Αποθηκών ή αλλον συναφή τομέα.
• Προηγούμενη τριετής εμπειρία σε Διαχείριση Λειτουργίας Αποθήκης.
• Πολύ καλή γνώση συστημάτων ERP και RF Scanner
• Πολύ καλή γνώση ηλεκτρονικών υπολογιστών και MS Office.
• Πολύ καλή γνώση της ελληνικής και αγγλικής γλώσσας.
• Πρωτοβουλία, ενδιαφέρον για προσωπική ανάπτυξη και διάθεση για συνεχή μάθηση.
• Ακεραιότητα χαρακτήρα, ομαδικό πνεύμα, υψηλό αίσθημα ευθύνης και προσοχή στη λεπτομέρεια.

Aν γίνεις μέλος της ομάδας μας θα έχεις τα πιο κάτω ωφελήματα:

• Moναδική Ευκαιρία για καριέρα σε μια ταχέως αναπτυσσόμενη εταιρεία
• Σύγχρονο και Μοντέρνο Περιβάλλον εργασίας
• Ανταγωνιστικό πακέτο αποδοχών με βάση τα προσόντα και την εμπειρία
• 13ος και 14^ος μισθός
• Πληρωμένη Ετήσια Άδεια
• Πολλαπλές Δραστηριότητες με την ομάδα
• Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού
• Προαιρετική συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης, και στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον 

Βάσει του Γενικού Κανονισμού Προστασίας Δεδομένων (GDPR), τα βιογραφικά /οι αιτήσεις εργοδότησης των ενδιαφερόμενων αιτητών διατηρούνται στο αρχείο μας σύμφωνα με την περίοδο συγκατάθεσης τους κατά την υποβολή της αίτησης τους. Ως εκ τούτου, σε περίπτωση που έχετε υποβάλει στο παρελθόν το βιογραφικό  σας και σας ενδιαφέρει η εν λόγω θέση, αποστείλετε ξανά το βιογραφικό σας.
 
Όλες οι αιτήσεις θα αντιμετωπίζονται με αυστηρή εμπιστευτικότητα.  Θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We ‘re on a mission to find the best talent out there. We are now looking for a talented Scientific Office Manager to join our  team in our offices in Saudi Arabia. 

Duties:

 
• Ensure company commitment with local regulations and maintain ethical standards in its scientific and medical activities.
• Implement regulations and instructions issued by local authorities.
• Verify marketing information (eg drug indications, safety profiles & dosage instructions) aligns with the approved labelling and promotional guidelines authorized data by regulatory authorities.
• Provide accurate drug information to beneficiaries (patients) and health healthcare providers, pharmacists, and caregivers.
• Promote health awareness and drug education. 
• Support and participate in scientific activities and education programs.
• To contribute to scientific research with specialized centers (as centers carry the bio equivalence studies) when needed.
• Follow up with the Regulatory Affairs (RA) department on the registration of pharmaceutical preparations thorough SFDA and GHC to ensure all required documentation and submissions for registering new pharmaceutical products or renewing existing registrations are completed on time.
• Act as the official representative of Medochemie LTD in dealings with regulatory authorities (SFDA and GHC).
• To organize meetings with SFDA/ GHC to clarify any issues related to new registrations/ renewals/ variations in well-structured, and on timely manner. To work very closely with SFDA/ GHC authority as per direction/ input shared by HQ/Management on various projects.
• Provide and properly store free samples of registered drugs, this involves managing the distribution, storage, and tracking of samples to ensure compliance with local regulations.
• Monitor drug quality, effectiveness, and side effects of the company products and ensure these are communicated to the RA department and regulatory authorities.
• Follow up updating the PIL and packaging to ensure compliance with approved information in coordination with the RA.
• follow up the protection of patents and manufacturing rights of company drugs in coordination with the relevant stakeholders,
• Act as Deputy QPPV in the absence of the local QPPV

Qualifications:

• Applicant should be Saudi national.
• Must be a licensed pharmacist by the Saudi Council of Health Specialties.
• A minimum of two years of experience in the same position is required.

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)
• two years of experience in a similar position 
• Proficient in the English language with excellent written and verbal communication skills
• Very good interpersonal and influence skills, analytical thinking, results orientation.
• Saudi Nationals only

Medical Sales Representative

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

What the job looks like?

The Medical Sales Representative will have the opportunity to:

·       Achieve company’s sales plan in assigned area by implementing existing strategy and policies

What does it take to do the job?

•At least 3 years of experience in sales

•Prior experience in similar position and experience in diabetes products will be considered an asset

•University degree would be appreciated

•Very good interpersonal and influence skills, analytical thinking and results orientation

•Business acumen and ability to work under pressure

•PC Literacy

By joining us you can expect:

•Competitive remuneration package and bonus

•Company car

•Company mobile

•Group private medical scheme

•Ongoing training

•Career growth opportunities

If you believe that you have the above qualifications and this opening sounds challenging, apply now by uploading your cv 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. Only shortlisted candidates will be contacted.

Regulatory Affairs Specialist

Medochemie Ltd is an International Pharmaceutical Company, exporting its products to 122 countries, thus holding the 29% of the total industrial exports of Cyprus. Medochemie operates 15 ultramodern manufacturing plants, 9 in Cyprus, 5 in Vietnam and 1 in the Netherlands, all designed in accordance with GMP (Good Manufacturing Practice) of the EU and WHO (World Health Organization.  Medochemie has offices in 19 countries and employs a global workforce of 2000 employees.

We're on a mission to find the best talent out there. We are now looking for a talented Regulatory Affairs Specialist to join our offices in Athens, Greece.

What the job looks like?

The Regulatory Affairs Specialist will have the opportunity to:

• Responsible for the compilation of dossier sections and sourcing of relevant documentation for modules 2-5 of Medochemie dossiers intended for registration for Medochemie or clients at global scale in eCTD format

• Compilation of responses and scientific documentation at correspondences with authorities or clients related to initial submissions, and the lifecycle of submissions i.e. variations, renewals, upgrades and new developments. Monitoring the progress of responses related to Modules 2-5 deficiencies raised by the regulatory authorities

• Review of quality documentation related to Modules 2-5 for the applications in line with the appropriate guidelines and timelines

• CMC regulatory directions provision at the various company departments, external parties and suppliers for the projects which have been assigned

• Liaise with the appropriate departments within the company and external parties to collect all necessary information for the submission of pharmaceutical dossiers and product registration

• Assist in keeping the dossier core files (Modules 2-5 and corresponding QoS) fully up to date during registration procedures and variations

• Continuous follow up of the regulatory affairs activities of all projects that have been assigned. Update of the regulatory database in collaboration with the regulatory partners. Understand and use the EU and International Regulatory guidelines

• Participate in the change control system and variation process according to the established internal workflow

• Participate in regulatory affairs internal projects of digital transformation, namely Regulatory Information management system and Submission Document Core Model

• Act as a member of responsible Regulatory team who is responsible for the submission of assigned regulatory projects

• Liaise with external Regulatory authorities and/or clients if required for the successful completion of projects

• Ensure policies and procedures are properly evaluated, implemented and carried out, safeguarding the compliance of company

• Support internal activities of Regulatory department in order to ensure regulatory compliance

• Monitoring the progress of the assigned projects and their finalization in a timely and accurate manner

 What does it take to do the job?

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset

• At least 2-3 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs/CMC

• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines

• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment

• Strong communication, influencing and problem resolution skills

• Strong organization skills and able to meet deadlines

• 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

We are offering an attractive remuneration package (including medical insurance) and a challenging opportunity for professional development. Ability to become part of one of the most dynamic and prospective teams in the International Pharmaceutical industry in Cyprus / Greece.

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.