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 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).   We ‘re on a mission to find the best talent out there. We are now looking for a talented Production 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, Industrial Pharmacy, Pharmacy or other related field Any previous experience in Pharmaceutical Industry will be considered an advantage Experience in Production in an industrial environment is a must Excellent analytical and technical skills related to this discipline Ability to work under pressure Accountable and responsible An enthusiastic team player with a strong drive to create a positive and collaborative work environment Proficient in the English language with excellent written and verbal communication skills

 

Location: Limassol,Cyprus

Benefits:
 

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

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

Duties:

• Be responsible for the CMC compilation of dossiers and dossier updates for existing products, in eCTD format and in compliance with the global regulations in force
• Be responsible for the CMC dossier compilation of new products in a timely and accurate manner
• Compilation and monitoring the progress of scientific responses to deficiencies in a timely and accurate manner
• Be responsible of data evaluation and review of CMC relevant documentation in line with internal procedures and relevant guidelines for the dossier submission fulfilling key milestones and being accountable for the quality and compliance of submissions
• Evaluate deviations to the relevant documentation, identifying regulatory actions required for the marketed products. Have a key role representing Regulatory Affairs team in the Interdepartmental discussions on the issues affecting Medochemie’s projects
• Successfully maintain dossiers’s lifecycle
• Be able to monitor, coordinate and supervise a team of people for the successful handling of CMC tasks

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an advantage
• At least 5 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs or QA
• 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
• Ability to be adaptive to change, to multitask and give attention to detail.
• Very good interpersonal skills, analytical thinking and result orientation.
• Fluency in Greek and English (written and spoken) and computer literacy.  Knowledge of any other languages will be considered an asset
• Ability to travel abroad if requested

Location: Athens,Greece

Benefits: A unique opportunity for a career in a fast-growing company Competitive remuneration package based on qualifications and experience 13th and 14th Salary Paid Vacation Modern & Proffesional Work Environment Participation on the Company's Medical Scheme Opportunities to learn and develop yourself through our 'Employee Training & Development Plan' 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 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).
 
We ‘re on a mission to find the best talent out there. We are now looking for a talented students to join our summer internship programme.

Qualifications:

• Final or Third Year of an Undergraduate degree in Chemistry, Biology, Pharmacy, or Chemical Engineering
• Excellent interpersonal and comunnication skills
• Excellent verbal and written communication skills in English
• Excellent computer literacy (MS Office)

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.

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).   We ‘re on a mission to find the best talent out there. We are now looking for a talented Messenger to join our team for executing work in Nicosia.

Duties:

Execute tasks inside and outside of the office Handle mail (receipt and delivery of correspondence letters) Transport letters and parcels inside and outside the Company Handle the photocopiers, office equipment and other technical equipment Handling any work assigned to him by the Company

 

Qualifications:

Graduate of High School or Technical School Good knowledge of Greek and English language Excellent communication and interpersonal skills Strong organization skills Holder of Clean Criminal Record and no previous road safety convictions Strong work ethics Ability to handle confidential information

 

Location: Limassol,Cyprus

Βenefits: 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 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 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).
 
We ‘re on a mission to find the best talent out there. We are now looking for a talented Junior IT Technician to join our IT team in our offices in Limassol,Cyprus .

Duties:

• Install, configure, and maintain software and hardware components
• Install, configure, and support copiers, fax machines, printers, scanners and miscellaneous peripheral hardware
• Provide 1st level support to users for all computer hardware and software issues or queries
• Troubleshoot software and hardware systems, such as computers/laptops, telephony systems and network devices
• Repair and or replace damaged computer and/or network components
• Maintain the up-to-date technical documentation
• Desktop OS administration/ network operating systems
• Carries out any further duties assigned

Qualifications:

• Relevant certificates or College Diploma in Computer Engineering/Computer Science
• Previous experience in a relevant role will be considered as an advantage
• Experience with Active directory, Exchange and Windows Infrastructure, Cisco Technologies will be considered as an advantage
• Very good interpersonal skills and customer-oriented attitude
• Fluency in both written and spoken English and Greek
 

Location: Limassol,Cyprus

Benefits: 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 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 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 Hellas, affiliate company of Medochemie Ltd, is looking for a talented and career-oriented Medical Sales Representative for the area of Thessaloniki, Greece.
 

Duties:

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

Qualifications:

• At least 3 years of experience in sales
• Prior experience in similar position and experience in CNS 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

Location: Thessaloniki, Greece

Benefits:
 

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

Duties:

The Quality Assurance Assistant will have the opportunity to:   Provide administrative support for tasks related to Quality Assurance Review batch documentation Carry out clerical work including typing, filing, copying and distribution of documents Ensure all procedures are carried out as per defined Standard Operating Procedures Undertake other tasks as required by the Quality Operations Senior Manager

 

Qualifications:

High School Certificate or Two/Three years Higher Education Certificate Proficient in the English language with excellent written and verbal communication skills Excellent computer literacy (MS Office) Ability to work in a team environment and prioritize work in a dynamic and fast-moving Highly organized; ability to multitask and process excellent time management skills

 

Location: Limassol,Cyprus

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 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 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).   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.

Duties:

Prepare and review Standard Operating Procedures, Change Proposals, deviations and other documents To review and perform deviation investigations and provide corrective action plans 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

 

Qualifications:

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.

 

Location: Limassol,Cyprus

Benefits

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’

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 4355 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 107 χώρες σε όλο τον κόσμο. Οι δεκατρείς ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.   Είμαστε σε αποστολή να βρούμε ταλαντούχο Τεχνικό Συντήρησης για να ενταχθεί στo τμήμα Engineering Support στα γραφεία μας στην Λεμεσό.

Duties:

Εκτέλεση προληπτικής συντήρησης των μηχανήματων παραγωγής και των συστημάτων υποστήριξης (κλιματισμός, θέρμανση, εξαερισμός, συμπιεσμένος αέρας)  Εκτέλεση επισκευών/ επιδιόρθωση βλαβών  των μηχανήματων παραγωγής και των συστημάτων υποστήριξης υπό την καθοδήγηση του Μηχανολόγου Συντήρησης. Εκτέλεση ελέγχων και παρακολούθηση  των συστημάτων κλιματισμού, θέρμανσης και εξαερισμού Λειτουργία και έλεγχος των συστημάτων επεξεργασίας νερού Λειτουργία και έλεγχος των συστημάτων παραγωγής και διανομής ατμού

 

Qualifications:

Απόφοιτος Τεχνικής Σχολής στον κλάδο Μηχανολογίας, στην κατεύθυνση  Μηχανικής αυτοκινήτων ή άλλων σχετικών προσόντων Προυπηρεσία στην Φαρμακευτική βιομηχανία θα θεωρηθεί επιπρόσθετο προσόν Πολύ καλή γνώση στην εφαρμογή προγραμμάτων συντήρησης καθώς και στην επισκευή και επιδιόρθωση μηχανημάτων και τεχνικού εξοπλισμού Εμπειρία στην επίλυση τεχνικών προβλημάτων Γνώση της Αγγλικής και Ελληνικής γλώσσας Δυνατότητα εργασίας σε βάρδιες είναι απαραίτητη (ωράρια 07:00-15:30/ 14:30-23:00,23:00-07:00)

 

Location: Λεμεσός, Κύπρος

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 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   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.     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.

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

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

Duties:

• Be responsible for the CMC compilation of dossiers and dossier updates for existing products, in eCTD format and in compliance with the global regulations in force.
• Have a key role representing under supervision Regulatory Affairs in the Interdepartmental Team whose aim is to successfully transfer the manufacturing processes and analytical methods between different Medochemie Manufacturing Sites
• Successfully maintain dossiers’s lifecycle.

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• At least 3 years of experience in the pharmaceutical sector, in the field of generic product development, Regulatory Affairs or QA.
• 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
• Ability to be adaptive to change, to multitask and give attention to detail.
• Very good interpersonal skills, analytical thinking and result orientation.
• Fluency in Greek and English (written and spoken) and computer literacy.  Knowledge of any other languages will be considered an asset
• Ability to travel abroad if requested

Location: Athens, Greece

We are offering an attractive remuneration package (including medical insurance) and a 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 wtih strict confidentiality. Only shortlisted candidates will be contacted.
 

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 ‘re on a mission to find the best talent out there. We are now looking for a talented Clinical Manager (Bio Equivalence Expert) to join our team in our offices in Limassol, Cyprus.
 

Duties:

The Clinical Manager (Bio Equivalence Expert) will have the opportunity to:
 
• Evaluate, design, and oversee Bioequivalence clinical studies 
• Reviewing protocols and reports for EU and non-EU applications
• Reviewing and approving relevant sections of clinical protocols, analysis plans, study reports, and regulatory submissions
• Maintaining a high standard for good clinical practice, compliance, and ethics
• Maintaining and establishing relationships and agreements with contract vendors
• Providing detailed clinical input and feedback in support of product registration 
• Providing authoring support for Bioequivalence clinical-related documents 
• Solving problems during clinical trials 
• Analysing and presenting Bioequivalence related data to internal project teams and senior management
• Determining strategy to resolve deficiency questions from the Agenciesand path forward to complete additional activities to support responses

Qualifications:

• University degree in Medicine , Pharmacy, or a related field
• A minimum of 5 years’ experience as an expert in monitoring Bioequivalence studies  for generic medicines is a must
• Knowledge of EMA and AESEAN guidelines for Bioequivalence studies
• Ability to work collaboratively in  cross functional groups in a matrix team environment
• Ability to multitask and work under pressure with commitment to timelines
• Excellent interpersonal and communication skills including ability to communicate scientific information clearly and effectively.  
• Excellent computer literacy
• Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills
It would be considered a plus if you have:
• Postgraduate degree in a related field 
• Experience/knowledge in CTIS application is an advantage 
• Familiarity with formulation development is preferred 
• Experience evaluating and selecting vendors for clinical studies will be considered an asset.


 

Location: Limassol, Cyprus

 

 
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 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 Hellas, affiliate company of Medochemie Ltd, is looking for a talented and career-oriented Medical Sales Representative for the area of Athens, Greece
 

Duties:

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

Qualifications:

•  University degree would be considered an advantage
• At least 3 years of experience in sales
• Prior experience in similar position and experience in diabetes products will be considered an advantage
• Very good interpersonal and influence skills, analytical thinking and results orientation
• Business acumen and ability to work under pressure
• Excellent interpersonal and communication skills
• Excellent computer literacy (MSOffice)

Location: Athens, Greece

Benefits:
 

• A unique opportunity for a career in a fast-growing company
• Competitive remuneration package based on qualifications and experience
• Modern & Professional Work Environment
• Optional participation in the Company’s Group Medical Scheme
• Opportunities to learn and develop yourself through our ‘Employee Training & Development Path’
• Company car
• Company mobile

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 (GDPR), all applications/CVs are kept in our databse 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 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  Patent Specialist based in Cairo, Egypt.  
 

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 a related field. A postgraduate degree will be considered an advantage
• Minimum of 5 years’ experience as patent specialist in generic medicines is a must. Experience in European Intellectual Property environment will be considered as an additional asset.
• Ability to work collaboratively in a team 
• Ability to multitask and work under pressure
• Excellent interpersonal and communication skills
•  Analytical thinking and problem-solving skills
• Proficient in the English language with excellent written and verbal communication skills

Location: CAIRO,EGYPT

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. Only shortlisted candidates will be contacted.
 

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).   We ‘re on a mission to find the best talent out there. We are now looking for a talented  Ticketing & Travel Associate to join our Ticketing & Travel team in our offices in Limassol .

Duties:

The Ticketing & Travel Associate  will have the opportunity to:   Plan and arrange itineraries, hotels and transfers for in house travellers and/or associates. Administer and check invoices as per quoted prices. Assist, work and provide 24/7 backup to travellers on a rotational basis. Act as a point of contact for the ticketing needs of internal clients and offers efficient service at all times.

 

Qualifications:

University degree or Diploma in Travel & Tourism or other relevant discipline. At least 2 years of service in a similar role. Knowledge of Galileo and/or Amadeus GDS systems, hotel platforms etc. Ability to work collaboratively in a team and prioritize work in a dynamic and fast moving environment. Excellent command of the English language, both written and oral Excellent communication and interpersonal skills.

 

Location: Limassol,Cyprus

Benefits 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 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.

Η φαρμακευτική εταιρεία MEDOCHEMIE HELLAS A.E. είναι θυγατρική εταιρεία της MEDOCHEMIE Ltd, που
εξειδικεύεται στην παραγωγή/εμπορία γενοσήμων φαρμάκων και συμπληρωμάτων διατροφής.
Η εταιρεία δραστηριοποιείται σε πάνω από 107 χώρες, έχοντας 13 δικές της μονάδες παραγωγής στην Κύπρο,
την Ολλανδία και την Ασία. Διαθέτει στο χαρτοφυλάκιό της 630 εγκεκριμένα προϊόντα και πάνω από
4.355 εγγραφές προϊόντων παγκοσμίως.
 
H MEDOCHEMIE HELLAS A.E. στοχεύοντας στην περαιτέρω ανάπτυξή της ζητά να προσλάβει άμεσα
Επιστημονικό Συνεργάτη με έδρα την Αττική.

Duties:

Η επίτευξη του πλάνου πωλήσεων της εταιρείας στις περιοχές ευθύνης του, μέσω της αποτελεσματικής
υλοποίησης της ισχύουσας στρατηγικής και της εφαρμογής των εκάστοτε πολιτικών

Qualifications:

• Εμπειρία μεγαλύτερη των 3 ετών σε πωλήσεις
• Προηγούμενη εμπειρία στις πωλήσεις φαρμακευτικών προϊόντων και εμπειρία στο διαβήτη, θα θεωρηθεί επιπλέον προσόν
• Ικανότητα επικοινωνίας και ανάπτυξης διαπροσωπικών σχέσεων
• Επαγγελματική συνέπεια και ικανότητα εργασίας υπό πίεση
• Εξαιρετική γνώση Η/Υ

Location: Aθήνα, Ελλάδα

Ωφελήματα
 

• Ανταγωνιστικό πακέτο αποδοχών και κινήτρων (bonus)
• Εταιρικό αυτοκίνητο
• Κινητό τηλέφωνο
• Πρόσθετη ιατροφαρμακευτική κάλυψη
• Δυνατότητα συνεχιζόμενης εκπαίδευσης
• Προοπτικές εξέλιξης

Οι ενδιαφερόμενοι/ες μπορούν να αποστείλουν βιογραφικό σημείωμα μέχρι ή να συμπληρώσουν την
online αίτηση παρακάτω
 
 
ΠΡΟΣΟΧΗ:
 
Οι υποψήφιοι να σημειώσουν ότι βασιζόμενοι στον Γενικό Κανονισμό Προστασίας Προσωπικών Δεδομένων (GDPR), όλες οι αιτήσεις/βιογραφικά που είχαν καταχωρηθεί στη βάση μας, έχουν διαγραφεί. Στην περίπτωση που είχατε αποστείλει παλαιότερα το βιογραφικό σας και σας ενδιαφέρει η συγκεκριμένη θέση, παρακαλώ συμπληρώστε
ξανά την αίτηση.
Όλες οι αιτήσεις θα εξεταστούν και θα θεωρηθούν αυστηρά εμπιστευτικές.

 

Η Medochemie Ltd είναι μια Διεθνής Φαρμακευτική Εταιρεία με έδρα την Κύπρο. Η Medochemie κατασκευάζει ένα ευρύ φάσμα προϊόντων που χωρίζονται σε περισσότερες από 10 θεραπευτικές κατηγορίες, κατέχει 4355 άδειες κυκλοφορίας και δραστηριοποιείται σε περισσότερες από 107 χώρες σε όλο τον κόσμο. Οι δεκατρείς ξεχωριστές εγκαταστάσεις παραγωγής μας έχουν σχεδιαστεί για να συμμορφώνονται πλήρως με την τρέχουσα Ορθή Παραγωγική Πρακτική (cGMP) της Ευρωπαϊκής Ένωσης.
 
Είμαστε σε αποστολή να βρούμε βοηθό χημείου για να ενταχθεί στην ομάδα του Χημείου μας στα γραφεία μας στην Λεμεσό.

Duties:

• Οργάνωση και αποθήκευση δειγμάτων σύμφωνα με όλες τις απαιτήσεις ασφάλειας για τη διασφάλιση της ασφάλειας του προσωπικού και της ακεραιότητας του δείγματος
• Προετοιμασία εργαστηριακού εξοπλισμού για   ερευνητικά πειράματα
• Διεξαγωγή αναλύσεων με βάση της απαιτήσεις του    πρωτοκόλλου
• Kαταγραφή δεδομένων στο ηλεκτρονικό αρχείο
• Συντήρηση εργοστασιακού εξοπλισμού
• Τήρηση αρχείων εξοπλισμού και καθημερινών αρχείων καταγραφής εργασιών
• Να ακολουθεί αυστηρά τις διαδικασίες δίνοντας έμφαση στην λεπτομέρια

Qualifications:

• Αποφοιτος/η Λυκείου ή Τεχνικής Σχολής
• Άριστη γνώση ελληνικής και αγγλικής γλώσσας
• Μαθηματικές και μετρητικές δεξιότητες
• Γνώση χειρισμού ηλεκτρονικού υπολογιστή (ms office, email etc)
• Καλές δεξιότητες επικοινωνίας, οργάνωσης και συνεργασίας

Location: Λεμεσός, Κύπρος

Benefits
 

• 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 Μισθός
• Πληρωμένη Άδεια
• Πολλαπλές Δραστηριότητες με την ομάδα
• Συμμετοχή στο Ομαδικό Σχέδιο Tαμείου Προνοίας όπου ο εργοδότης συμβάλλει το 7% του μηνιαίου μισθού
• Συμμετοχή στο Ομαδικό Σχέδιο Ιατροφαρμακευτικής Περίθαλψης εαν το επιθυμεις
•  Συμμετοχή στο Εκπτωτικό Πρόγραμμα της Εταιρείας
• Σύγχρονη και συνεχής εκπαίδευση, ευκαιρίες ανάπτυξης σε ένα ταχέως αναπτυσσόμενο περιβάλλον

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.
 
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.  Κατόπιν αξιολόγησης, θα υπάρξει τηλεφωνική επικοινωνία μόνο με τους υποψηφίους που θα επιλεγούν για προσωπική συνέντευξη.
 

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 Product Manager for our offices in Limassol, Cyprus.

Duties:

Develop deep understanding of all main Therapeutic Area classes of Medochemie portfolio Develop & implement the marketing & communication strategy for each Therapeutic Area. Partner with local marketing teams to collect market and customer insights  for each Therapeutic Area Harmonize value propositions and messaging, clear communication of features and benefits of products Develop pricing strategy and launch sequence plans Create marketing campaigns, marketing materials and customer presentations Responsible to co-ordinate the internal training of teams across regions and ensure readiness for new launches and strategy implementation Create business plans to drive above market growth Generate competitive assessments Key Opinion Leaders management

 

Qualifications:

University degree in a relevant science (Pharmacy, Pharmacology, Chemistry, Biochemistry, Biology, etc) At least 5 years related working experience in the Pharmaceutical Industry Proven analytical & strategic thinking Excellent internal and external communicator across multidisciplinary team Strong project management orientation with the ability to plan, prioritize and manage complex list of projects to completion Hands-on and can-do mentality, enjoys working in a team, but can also work autonomously and remotely as an individual Excellent communication & presentation skills Excellent English and Greek literature both verbal and writing Ability to travel abroad

 

Location: Limassol,Cyprus

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 databse 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 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

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 databse 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 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 highly qualified and motivated professionals for the position of Regulatory Affairs Associate in our offices in Limassol, Cyprus.
 

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 individually and as part of a team
• Ability to multitask 
• Excellent interpersonal and communication skills
• Analytical Thinking 
• Ability to work under pressure.
• Competency in Microsoft Office applications
• Profficient in the English and Greek language with excellent written and verbal communication skills
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

Benefits   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 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. Only shortlisted candidates will be contacted.

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  highly qualified and motivated professionals for the position of Quality Control Associate in our offices in Limassol, Cyprus.

Duties:

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

 
To follow all the guideline’s on Good Laboratory Practice (GLP)

Qualifications:

University degree in Chemistry, Biochemistry or other 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 Profficient in the English and Greek language with excellent written and verbal communication skills

 
 
 

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 a related field. A postgraduate degree will be considered an advantage
• Minimum of 5 years’ experience as patent specialist in generic medicines is a must
• Ability to work collaboratively in a team 
• Ability to multitask and work under pressure
• Excellent interpersonal and communication skills
•  Analytical thinking and problem solving skills
• Profficient in the English language with excellent written and verbal communication skills
• Willingness to relocate to Cyprus

Location: Limassol, Cyprus

Benefits   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 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. Only shortlisted candidates will be contacted.

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 or related field will be considered an advantage
o Profficient in the English language with excellent written and verbal communication skills
o Very good interpersonal and influence skills, analytical thinking, results orientation.

Location: Cyprus

Benefits

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 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. Only shortlisted candidates will be contacted.
 

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 or related field will be considered an advantage
• Profficient in the English and Greek  language with excellent written and verbal communication skills
• Very good interpersonal and influence skills, analytical thinking, results orientation.

Location: Cyprus

Benefits

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 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. Only shortlisted candidates will be contacted.
 

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 Research and Development Associate based in Limassol, Cyprus. 

Duties:

• Perform physical and chemical analysis for analytical and product development and follow all the guidelines on Good Laboratory Practice (GLP).
• Conduct a preliminary and limited quality evaluation of the raw material and Finished product tested for R&D purposes in accordance with the current guidelines in force.
• Apply basic regulatory knowledge under which the medical products are governed.
• Prepare analytical plan and protocol.
• Compile consolidated summaries and provide required reports throughout the development of each product.
• Perform detailed literature searches and review all available literature data for the development of analytical and product development.

Qualifications:

• University degree in pharmaceutical chemistry or Chemistry.
• Post graduate degree will be considered an advantage.
• Experience in the pharmaceutical industry it will be considered an advantage. 
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment. 
• Very good interpersonal skills, analytical thinking and result orientation.
• Strong computer literacy.
• Fluency in Greek & English language.

Location: Limassol, Cyprus

Benefits   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 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. Only shortlisted candidates will be contacted.
 

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)
• Up to two years of experience in a similar position will be considered as a plus
• Profficient in the English language with excellent written and verbal communication skills
• 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/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.