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).

Medochemie Ltd invites applications from career-oriented professionals for the position of Financial Manager for our offices in Prague, Czech Republic. 

Duties:

General responsibilities:
Provide support to the company, through maintaining the financial records and information analyses (e.g. current processes, actual performance vs budget and prior year, etc.), preparation of operational data/analyses for publication to various constituents throughout company (Management, Sales, Product Management, Operations, etc.) who rely on/benefit from the information to make informed business decisions. Primary responsibilities will include preparation and maintenance of financial records, assisting Operations team in the Monthly Operations Review, identification of areas for cost reductions and operational improvements, annual budget process, periodic forecasting, and periodic analysis of operations performance. 

Specific Responsibilities:
• The successful candidate will report to HQ Finance team and to the Country Manager.
• Key responsibilities of the positon include amongst other to: 
• Prepare, maintain, examine, and analyse accounting records, financial statements, and other financial reports to assess accuracy, completeness, and conformance to reporting and procedural standards. 
• Prepare monthly analysis of sales and operational expenses against prior year and budget, providing explanations and business solutions to help manage business risks. 
• Analyse financial performance against key business metrics and document pertinent financial highlights that will enable management to determine progress against budgets. 
• Identify, investigate, and analyse potential operational improvement. As appropriate, based on findings make proposals for operational changes (policy, procedures, processes, controls etc.) 
• Participate in the strategic review and implementation of operational structure of Medochemie in Czech Republic.
• Manage, safeguard and control company’s financial resources ensuring that they are properly used for company’s purposes. 
• Understand and follow company policies and procedures. 
• Perform all other duties as assigned and required. 
• Maintain accurate cash flow management. 
• Coordinate the annual external audit. 
• Liaise with banks, customers and external advisors.  

Qualifications:

• Bachelor’s/ Master degree in business, accounting or related discipline.   
• 3-5 years of experience in a similar position, experience with operations preferred. 
• Preparation and submission of VAT forms and comply with any other tax requirement. 
• Strong experience in income statement analysis. 
• Experience in working with ERP system and Business Intelligence systems will be a plus. 
• Self- motivated with strong analytical, problem solving skills and initiative to achieve desired outcomes. 
• Strong prioritization skills handling multiple priorities. 
• Excellent verbal and written communication skills. 
• English language proficient (both written and verbal). 
• Have a flare for numbers, work well with people, and aggressively anticipate impacts of workload/issues. 
• Adherence to team deadlines. 
• Proficiency in Microsoft office. 

Location: Prague, Czech Republic

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 Φύλακα - Θυρωρού:

Ωράριο: Πρωινό/ Απογευματινό/ Νυκτερινό:         
Δευτέρα- Κυριακή: 07:00-15:00/ 15:00-23:00/ 23:00-07:00 

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: 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.

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 Computerized System Validation Manager for our offices in Limassol, CYPRUS. 

Duties:

• Provides oversight to assure that computerized systems are selected, implemented and maintained in compliance with applicable quality procedures, regulations and guidelines. 
• Promote compliance, quality and best practice-oriented culture regarding computerized systems.
• Manage validation deliverables produced for computerized system projects, including operational procedures, maintenance procedures and change requests. 
• Support the development of Computerized Systems QA related procedures. 
• Conduct audits of computerized system vendors and 3rd party software providers.
• Provide expertise and support during audits and inspections. 
• Proactively identify risks and issues. Drive implementation of pragmatic, compliant, quality based solutions. 
• Lead on-going initiatives and improvement projects in areas related to computerized systems and regulated data, as assigned. 
• Support the response and remediation of corrective actions.
• Collaborate with key business partners including IT, Vendors, Quality SMEs and Business System Owners to ensure activities are performed in line with regulatory requirements and industry standards.
• Responsible for all activities related to computerized system validation Follow cGMP related guidelines and GAMPv5 methodology.
• Monitor the lifecycle of the validated software.
• Secure data integrity.

Qualifications:

• University degree in Computer Science or BIS or other relate field.
• Minimum 5 years of work experience.
• Experience with software testing, preparation and execution of UAT is a must.
• Knowledge cof GMP Annex 11 or  GAMPv5 would be consider as an advantage.
• Excellent command of the English language, both written and verbal.
• Excellent communication and interpersonal skills.
• Ability to travel abroad.

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 Business Development Manager.

Overview:

The Business Development Manager’s primary role is to evaluate and assess contract manufacturing opportunities with customers to align internal capabilities and services with the customers’ outsourcing needs.
 

Duties:

• Proactively develop business opportunities for contract manufacturing by prospecting for and calling on pharmaceutical companies
• Partner with internal commercial and technical support teams to assess the competitive advantages which can be offered to customers
• Respond to incoming pharmaceutical leads and inquiries from multi-sources, and qualify through business analysis, customer evaluations and strategic fit
• Engage in the preliminary selling stage of the sales cycle—prepare baseline price proposals and scope of work 
• Present the value proposition for the Company’s capabilities and services to customers, and facilitate on-site capabilities presentations and tours
• Increase the financial return of each project by maximizing each lead and guiding the client on all of the solutions available by the Company
• Ensure a successful transition to Project Management when appropriate, while maintaining strong client relationships leading to future business development opportunities

Qualifications:

• Bachelor’s degree 
• 5 years of prior experience in business development for pharmaceutical contract manufacturing
• Over 10 years of experience in the pharmaceutical industry 
• Ability to effectively build strong relationships within all levels/disciplines of a pharmaceutical account—matrix approach involving both functional representation and multiple levels of senior management
• Deep knowledge of the pharmaceutical industry
• Proven leadership skills and the ability to understand financial analytics, prioritize multiple tasks, and drive projects to completion
• Frequent traveling will be required for this position. 
• Fluency in both written and spoken English.

Location: Limassol, Cyprus or Athens, Greece or Duiven, Netherlands

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 Regulatory Affairs Specialist for our office in Athens, Greece. 

Duties:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology,). A post graduate degree will be considered an asset.
• 3-4 years’ experience within the pharmaceutical industry and preferably in the field of Regulatory Affairs.
• Solid knowledge of Ph. Eur., EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs and competency with e-CTD preparation.
• 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.
• Fluency in both written and spoken English and computer literacy.
• Ability to travel abroad.

Qualifications:

• To prepare CTD format dossiers for submission for generic pharmaceutical products in compliance with regulatory, and commercial strategy of Medochemie Ltd.
• To successfully follow dossier submissions for both European Registration Procedures (DCP/MRP) and non-EU national procedures according the requirements
• To successfully maintain dossiers’ and MAs’ lifecycle (variations & renewals) in all territories (EU & non-EU) where the products are registered.

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. 

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 ANALYST for 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.

Qualifications:

• University degree in Chemistry or other relevant discipline.
• Post Graduate or Doctoral degrees will be considered as an additional asset.
• Experience in pharmaceutical analysis or in use of liquid chromatography HPLC, 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 applications from career oriented professionals for the position of Quality Assurance Assistant for our offices in Limassol, CYPRUS.

Duties:

• Assists the team in preparation of reports, presentations and QA materials.

Qualifications:

• Τwo or three years higher education degree
• Good command of the English language, both written and verbal
• Excellent knowledge of Microsoft Office
• Professional approach to work and excellent character

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 Quality Assurance Associate in our offices in Limassol, CYPRUS.

Duties:

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

 

Qualifications:

• University degree in Pharmacy or Chemical Engineering. A post graduate degree will be considered an asset.
• Multi project handling at once under time pressure.
• Excellent command of the English language, both written and oral.
• Advanced project management and technical writing skills is preferred.
• Experience in the field of pharmaceutical industry will be considered as an asset.
• Ability to work in a team environment and proritize 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. 

Duties:

Collaborating with Quality, Engineering and Manufacturing to ensure robust process/methods transfer. Provide technical leadership for the tech transfer of new products and processes to ensure smooth transition from process development into GMP manufacturing at all locations. The following tasks are supported from this function: Directs and supports activities related to New Products introduction as it relates to Site issues, capacities, and capabilities. Directs and supports activities related to successful manufacture of new product or existing product stability and validation batches through coordination and communication of the involved departments. Plans work schedules and personnel to accomplish the required duties in a timely manner according to approved schedules. Participates in various new product team meetings and committee meetings as required to support the process and or project. Develops and recommends the product validation matrix. Cooperate with QC excellence to assure the needed analytical method transfer. Cooperate with Regulatory department to assure the provision of needed documentation for registration. Identifies risk involved in manufacturing a product and develop/review the validation protocol to qualify the new product or modified existing product. Keeps abreast of cGMP requirements. Identifies and implements process improvements designed to improve efficiency and enhance product quality.

Qualifications:

University degree in a relevant science (Pharmacy, Chemical Engineering, etc). A postgraduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Ability to work with cross-functional team and global team. Good knowledge in Project management. Excellent command of the English language, both written and oral. Committed to relocate to Cyprus.

Location: LIMASSOL, CYPRUS

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

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

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

Medochemie Ltd invites career-oriented professionals to apply for the position of Manufacturing Continuous Improvement Manager for our offices in Limassol, CYPRUS.

Duties:

Continuous improvement Provides Continuous Improvement support to the sites. These are larger individual projects to improve OEE, Deviations, Yield, etc. Provides Project support. This position will be the primary interface for technical transfers, engineering projects and similar activities. This role will provide support for the projects, especially for time intensive and major projects. Ensure efficient and effective operation by creating a proactive environment, developing & monitoring metrics, and communicating with both team members and support functions about operations performance. Ensure the compliance with all regulatory requirements and good documentation practices to provide a safe, quality, and effective product. Leads root cause analysis for Continuous improvement and definition of solutions for key defects. Evaluates diagnose and resolves technical issues and/or process problems based on data analysis. Bring together cross-disciplinary teams when working on complex or recurring problems or pursuing business opportunities. Access and uses other experts when appropriate. Quality management review process support​   Organize periodic management review per region and at group level, with the involvement of senior management, of the operation of the Pharmaceutical Quality System to identify opportunities for continual improvement of products, processes and the system itself.  Establish the right KPIs for an effective QMR. Coordinate Heads of departments to participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement”. Ensure continuing suitability and effectiveness of the Quality Management System and GMP compliance through participation in Management Review.

Qualifications:

University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Chemical Engineering, etc). A post graduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Understanding of cGMP requirements and other FDA/EU regulatory requirements associated with manufacture of pharmaceutical products and associated equipment and facilities is essential. Familiarity with electronic QA systems /database Excellent command of the English language, both written and oral. Committed to relocate to Cyprus.

Location: LIMASSOL, CYPRUS

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

Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. 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 for the position of Process Engineering & Statistics Expert for our offices in Limassol, CYPRUS.
 

Duties:

Working with site process owners, assure the proper transfer of technical knowledge and documentation to support new products, process changes and manufacturing sites. Collaborating with Quality, Engineering and Manufacturing to ensure robust process/validation protocols and reports. Provide process engineering expertise to assure the manufacturing process remains fully validated through process change evaluations and implementations. Provide technical leadership as required during start-up efforts of new equipment or processes in manufacturing. Provide technical leadership for the tech transfer of new products and processes to ensure smooth transition from process development into GMP manufacturing at all locations. Identify opportunities to implement operational excellence and continuous improvement. Assist the technical operations team to resolve any issues related to production. The following tasks are supported from this function: Support organization, implementation and maintenance of production process flow. Develop working instructions, working standards and process documents, and ensure they are followed. Improve continually existing operation, for increased quality, productivity, efficiency and cost savings. Investigate operational problems affecting production and reporting and recommending solutions. Provide manufacturing data i.e. production control charts, calculate process capability, to improve the process and monitor and measure progress to target. Identify ways to reduce production costs through recommendations – i.e. new process equipment.

Qualifications:

University degree in a relevant science (Pharmacy, Chemical Engineering, etc). A postgraduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Ability to work with cross-functional team and global team. Good knowledge in Project management Excellent command of the English language, both written and oral. Committed to relocate to Cyprus

Location: LIMASSOL, CYPRUS

Duties:

Establish the Risk Management process/ function within the Company. Coordinate risk management process as needed. Ensure overall effectiveness of risk management process at site. Update / administer the Risk Management database. Develop and implement various techniques for proactive risk identification. Ensure good risk description and scoring as per standards. Ensure risk owners & mitigation leaders are assigned for all risks. Ensure availability of mitigation plans for the identified risks. Ensure training is imparted to all the relevant stakeholders on Risk Management process by providing training materials and actual trainings. Support risk management process for projects in co-ordination with project manager / leader.

Qualifications:

University degree in a relevant science (Pharmacy, Chemistry, Chemical Engineering, etc). A postgraduate degree will be considered an asset. At least 5 years of experience in a relevant field. At least 10 years of experience in cGMP Environment. Knowledge on basics of risk management and ICH Q9 principles. Knowledge on risk management tools & templates. Deployment of an appropriate methodology to conduct risk assessments. Ability to work with cross-functional team and global team. Basic knowledge in Project management. Experience in handle tasks independently. Excellent command of the English language, both written and oral. Committed to relocate to Cyprus.

Location: LIMASSOL, CYPRUS

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

Medochemie Ltd invites applications from career-oriented professionals for the position of Medical Representative (Number of the positions: 3)

Duties:

• Conducts visits to doctors and pharmacies 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 promotional indicators
• Establishes and nurtures client relationships
• Develops strong relationships with key decision makers
• Maintains existing business and presents new products

Qualifications:

• University degree in Pharmacy (Licensed as a practitioner)
• 0 to 2 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 National.

Location: Jeddah & Al-Madinah, Saudi Arabia Riyadh (central Province), Saudi Arabia Al-Qassim, 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. 

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 Pharmacovigilance Specialist in our offices in Limassol, CYPRUS. Pharmacovigilance is the scientific department of the Company that takes care of the safety of pharmaceutical products.

Duties:

• To collect and manage information on adverse events from various sources and report them to authorities according to current EU legislation. 
• To perform a number of duties related to Pharmacovigilance, including but not limited to update of drug safety information and signal management, as these are defined by the Pharmacovigilance System of Medochemie and current EU legislation.
• To execute administrative tasks relating to the maintenance of the Pharmacovigilance system and its Quality System, according to written procedures.

Qualifications:

• University degree in Pharmacy or Medicine. A post graduate degree will be considered an asset.
• Minimum ten years of clinical experience.
• 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.
• Fluency in both written and spoken English.
• Committed to relocate to Cyprus.

Location: Limassol, CYPRUS

We are offering an attractive remuneration package and challenging opportunity for professional development.
If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click the APPLY button below and fill in the application form.
 
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 Senior Formulation Technologist for our offices in Limassol, CYPRUS

Duties:

• To prepare trial batches and to determine the formulation percentage composition of pharmaceuticaldosage forms at the Production Formulation Development Laboratory (PFDL).
• To develop new formulations following the company’s new product portfolio and development plans.
• To prepare as many formulations as necessary to obtain a stable product essentially similar in vitro with the reference product.
• To study the reference product and be able to reproduce a generic with similar in vitro behavior.
• To study the literature of the product and know its pharmaceutical characteristics.
• To follow Regulatory Affairs requirements and current European guidelines and WHO related to the development pharmaceutics section and stability guidelines.
• To develop products which will be easy to produce in the company’s premises with current equipment.
• To produce scale up batches that compare to the newly developed product.
• To be able to co-ordinate a team of scientists in order to achieve the company targets.

Qualifications:

• University Degree in Pharmacy or related field
• Excellent Pharmaceutical and Technology skills related to this discipline
• Multi project handling at once under time pressure
• Excellent command of the English language, both written and oral
• Minimum 7 years’ industrial experience in a similar position involving the above duties
• Proven record of leading scientific teams comprised of highly specialised individuals
• Committed to relocate to Cyprus

Location: Limassol, Cyprus

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

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities,please apply online.

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

All applications will be treated in strict confidence.

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 την θέση Shift Production Officer, 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 γενικά 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 την ομάδα Συσκευασίας για την αποτελεσματική και ποιοτική συσκευασία των προϊόντων

Qualifications:

• Πανεπιστημιακό δίπλωμα ή τριετές πτυχίο σε Μηχανολογικούς ή άλλους συναφείς κλάδους (Χημική Μηχανική, Χημεία, Φαρμακευτική, Μηχανολογία, κ.α.).
• Απαραίτητη προϋπηρεσία τουλάχιστον 3 ετών.
• Προϋπηρεσία στη Βιομηχανία ή σε Επιστασία προσωπικού θα θεωρηθεί επιπρόσθετο προσόν.
• Καλή γνώση της Αγγλική γλώσσας.
• Καλή γνώση Ηλεκτρονικών Υπολογιστών.

Location: Λεμεσός, Κύπρος

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

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

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

Όλες οι αιτήσεις θα κρατηθούν αυστηρά εμπιστευτικές.

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

Medochemie Ltd invites applications from career oriented professionals for the position of Formulation Technologist for our offices in Limassol, CYPRUS.

Duties:

• To prepare trial batches and to determine the formulation percentage composition of pharmaceutical dosage forms at the Production Formulation Development Laboratory (PFDL)
• To develop new formulations following the company’s new product portfolio and development plans
• To prepare as many formulations as necessary to obtain a stable product essentially similar in vitro with the reference product
• To study the reference product and be able to develop a generic with similar in vitro behavior
• To study the literature of the product and know its pharmaceutical characteristics
• To follow Regulatory Affairs requirements and current European and WHO guidelines related to the development pharmaceutics section and stability guidelines
• To develop products which will be easy to produce in the company’s premises with current equipment

Qualifications:

• University Degree in Pharmacy or related field
• Excellent Pharmaceutical and Technology skills related to this discipline
• Multi project handling at once under time pressure
• Excellent command of the English language, both written and oral
• 3-5 years industrial experience in a similar position involving the above duties
• Committed to relocate to Cyprus

Location: Limassol, Cyprus

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

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please apply online.
 

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

All applications will be treated in strict confidence.

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

Medochemie Ltd invites applications from career oriented professionals for the position of Regulatory Affairs Associate for our office in Athens, Greece

Duties:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology).
• 2-3 years’ experience within the pharmaceutical industry and especially in the field of generic product development and regulatory affairs.
• Solid knowledge of Ph. Eur., EMA & ICH guidelines related to pharmaceutical product development and regulatory affairs and competency with e-CTD preparation.
• 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.
• Fluency in both written and spoken English and computer literacy.

   

Qualifications:

• To prepare the documentation and compile Module 1 for submissions of product registration (DCP/MRP), in accordance to current EU legislation.
• To coordinate/submit the Deficiency Letter (DL) responses.
• To successfully maintain dossiers’ and MAs’ lifecycle (variations & renewals) in all territories (EU & non-EU) where the products are registered.
• To successfully follow dossier submissions for both European Registration Procedures (DCP/MRP) and non-EU national procedures according the requirements.
• To prepare CTD format dossiers for submission for existing products in compliance with regulatory and commercial strategy of Medochemie Ltd.
• To negotiate with the regulatory authorities within EU for the marketing authorization.

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 apply online.

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 Χειριστή Μηχανών, για τα ακόλουθα συστήματα βάρδιας:

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

Duties:

• Καθαρισμός, ρύθμιση και Χειρισμός μηχανών παραγωγής
• Τήρηση των Κανόνων Καλής Παρασκευής Φαρμάκων (GMP)

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: Λεμεσός, Κύπρος

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας, επιδόματα βάρδιας 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 τα 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 μηχανημάτων συναρμολόγησης και συσκευασίας

Qualifications:

• Απολυτήριο Σχολής Μέσης ή Τεχνικής Εκπαίδευσης ή δίπλωμα/πτυχίο Κολεγίου ή Πανεπιστημίου
  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: Λεμεσός, Κύπρος

Προσφέρεται ελκυστικό πακέτο απολαβών, το οποίο περιλαμβάνει 13ο μισθό, 14ο μισθό, Κοινωνικές Ασφαλίσεις, Ταμείο Προνοίας, Ταμείο Υγείας, επιδόματα βάρδιας 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.