Careers

Duties:

Prepare Cleaning Validation Protocols Follow up cleaning validation master plan Prepare in advance any necessary validation tasks Ensure that sampling for cleaning validation is performed based on the relevant protocols Ensure that any possible deviations have been reported Prepare reports for all undertaken validations tasks Prepare and review Standard Operating Procedures and other documents. Prepare and assist in Risk Assessments

 

Qualifications:

Bachelor's degree in Pharmacy or Chemistry (with specialization in organic chemistry).  A post graduate degree will be considered an asset. Related experience in a pharmaceutical industry is a plus Fluency in Greek and English language Proficiency with MS office tools (Word, Excel, PowerPoint, etc) Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment Ability to work in multiple projects

 

Location: Limassol, Cyprus

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

Duties:

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

Qualifications:

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

Location: Limassol, Cyprus

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

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

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

Medochemie Ltd invites applications from career-oriented Regulatory Affairs Associate.
 

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. asset.
• Ability to work both individually and as part of a team, as well as prioritise work in a dynamic and fast-moving environment. 
• Excellent interpersonal skills, analytical thinking and ability to work under pressure.
• Competency in Microsoft Office applications.
• Fluency in both written and spoken English.
 
Preferred:
 
• At least 2 years of experience within the pharmaceutical industry in the Field of Generic Regulatory affairs.
• Solid knowledge of Eur.Ph., EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs.
• Competency in e-CTD preparation. 

Location: LIMASSOL, CYPRUS

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

All applications will be treated in strict confidence.

Duties:

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

 

Qualifications:

University degree in Chemistry, Biochemistry or other relevant field. Post Graduate diploma will be considered as asset. Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, will be considered as an additional asset. Effective verbal and written communication skills Fluency in  Greek and English language Computer literacy sufficient to use standard software (MS Office) as well as the ability to learn specific software and instrumentation.

 

Location: LIMASSOL,CYPRUS

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).

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

Duties:

• Supervise and coordinate a team of specialists for the CMC dossier compilation and  dossier updates for existing products, in eCTD format in compliance with the global regulations in force.
• Supervise the submission and follow up till approval of Marketing Authorisation Applications (MAAs) mainly for European Registration Procedures (DCP/MRP) but also non-EU national procedures according to the company’s strategy, considering the different country specific requirements. 
• Ensure the successful maintenance of dossiers’ and MAs’ lifecycle (variations & renewals) in all territories as necessary so that the MAs are up to date.
• Establish regulatory priorities and ensure the team’s milestones/goals are met and adhering to departmental objectives and corporate strategies.
• Implement departmental policies and procedures to ensure that regulatory compliance is maintained and enhanced.
• Participate in developing Regulatory strategies within the department, interact and negotiate with competent Authorities and maintain close working relationship with internal stakeholders ( e.g. QA, QC, production, commercial) for the preparation review and compilation of regulatory documentation
• Participate in cross functional teams within the company for the implementation, follow up and completion of cross functional projects
• Provide regulatory guidance and communicate regulatory information to different departments

Qualifications:

An adaptive to change, ability to multitask and attention to detail personality with good communication, interpersonal, influencing and problem resolution skills.
• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• Previous Regulatory Affairs/CMC/ product development  experience as a Supervisor/Manager within generic Pharmaceutical industry  
• Extended Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines and competency with e-CTD preparation
• Ability to lead collaboration  in a team, delegate responsibilities  and prioritize work in a dynamic and fast changing  environment. 
• Organizational, planning, problem-solving analytical thinking  and cross functional skills
• Fluency in Greek and English (written and spoken) and computer literacy. Knowledge of any other languages will be considered an asset Ability to travel abroad if requested

Location: ATHENS, GREECE

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

Duties:

Receive, label and store samples to be tested. Perform microbiological testing of raw materials and finished products for product approval and release. Perform water and steam sampling from Production facilities. Perform Environmental Monitoring including settle plates, air sampling and particle monitoring from Production facilities. Record all data and results in raw data forms with accuracy and responsibility. Maintaining equipment and assist in ordering laboratory supplies.

 

Qualifications:

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

Location: LIMASSOL, CYPRUS

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

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

Duties:

IT Support (1st level) Respond to IT issues as they arise; help build, test, and maintain new servers as needed. Perform routine/scheduled procedures and audits of the systems, including all backups and ensure the smooth day-to-day functioning of the IT infrastructure. Carry out server, storage and system updates on a regular basis and provide 1st-level support for all issues under your responsibility for office. Servicing computers, and other IT-related hardware, as well as accessibility HW/SW. Assist with the maintenance of the IT infrastructure throughout the business Perform well defined server administration tasks (following clear procedures from HQs). Keep a complete documentation of the IT infrastructure of our clients. Monitor and maintain acceptable system performance. Investigate bottlenecks and optimization solutions. Train users on supported hardware, software and office automation solutions. Participate in various company IT projects   IT Procurement Is responsible for the procurement done for the various IT Projects (HW/SW) and in contact with the departments expressing the need Contract Management is also necessary for these projects (i.e. ensure that service reception is performed in due time, KPIs are met, follow-up the Invoice validation & Cost Centers etc). Supports IT Budget and its follow-up process with Managers Applies a consistent procurement procedure, including deployment of the following sub processes: specification requirements, supplier identification, proposal analysis, evaluation of suppliers and their processes, contract negotiation, supplier selection and contract placement. Ensures that the entire purchasing process is fit for purpose, adds business value to the organization and is compliant to internal rules, legal and regulatory requirements. Provides insight to the IT leadership team (HQs)

 

Qualifications:

At least 2-3 years of relevant working experience Strong work ethic and team spirit High degree of professionalism and strong interpersonal (verbal and written) communication skills Ability to deal sensitively with confidential material and communicate with various levels of management Decision-making, problem-solving, and analytical skills Organizational, multi-tasking, and prioritizing skills Excellent communication and collaboration skills Organizational, multi-tasking, and prioritizing skills Result & quality oriented Experience with Microsoft products (O365, Exchange, AD, SQL) University Degree in Computer Sciences or relevant discipline Experience with Storages, Advance Endpoint Protection software, VOIP, Firewalls and network administration / installation and Software deployment

 

Location: ATHENS, GREECE

Duties:

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

Qualifications:

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

Location: LIMASSOL, CYPRUS

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

• Ωράριο: Πρωινό/ Απογευματινό/ Νυκτερινό:         

Duties:

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

Qualifications:

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

Location: ΛΕΜΕΣΟΣ, ΚΥΠΡΟΣ

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

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

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

Duties:

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

Qualifications:

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

Location: LIMASSOL, CYPRUS

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

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

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

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

Duties:

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

Qualifications:

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

Location: Limassol, Cyprus

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

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

Duties:

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

 

Qualifications:

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

Location: CYPRUS

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

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

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

Duties:

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

Qualifications:

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

Location: CYPRUS

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

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

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

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

Duties:

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

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

All applications will be treated in strict confidence

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

Medochemie Ltd invites applications from career-oriented professionals for the position of Software Engineer Specialist / Senior Specialist for our offices in Limassol, CYPRUS. 
 

Duties:

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

All applications will be treated in strict confidence

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

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

Duties:

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

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

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

Duties:

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

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

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

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

Duties:

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

Qualifications:

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

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

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

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

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

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

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

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

Duties:

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

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

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

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

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

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

Duties:

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

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

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

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

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

Duties:

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

Qualifications:

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

Location: Limassol, CYPRUS

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

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

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

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.