Careers

Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 3800 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (cGMP).
We invite applications from highly qualified and motivated professionals for the position of R&D Senior Specialist based in Limassol, Cyprus.  
 

Duties:

•    Act as Coordinator for the assigned new products under development.
•    Apply the stipulated R&D procedure during coordination of the new products development and follow the respective timelines prescribed in the R&D procedure.
•    Compile consolidated documents and summaries throughout the development of each products, such as literature searches, overall summaries etc. 
•    Review analytical data generated from other departments (e.g stability data, quality control analysis etc), provide constructive comments and make suggestions on the actions to be followed.
•    Work together with other teams in the preparation of the necessary documents, review and comment of the documents created by other departments (e.g  SOPs, process validation protocols and reports, NPD reports, Project reports, analytical validation reports etc). 
•    Read and interpret patent claims and patent reports and provide suggestions related to the overall strategy to be followed. 
•    Take into consideration clinical aspects of the products and propose further actions. 
•    Maintain up to date status of all guidelines covering the medical products. 
•    Prepare and justify the quality specifications of both drug substances and drug product
 

Qualifications:

•    University degree in Chemistry, Pharmacy or other relevant science degree. 
•    At least three years experience in R&D senior role or five years experience in the field.
•    Advanced knowledge of IP environments. 
•    Sufficient knowledge on clinical aspects. 
•    Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment.
•    Very good interpersonal skills, analytical thinking and result orientation.
•    Strong computer literacy.
•    Fluency in Greek & English language. 

Location: Limassol, Cyprus

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 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 based in Limassol, Cyprus.  
 

Duties:

•    Acts as first point of contact for HR requests
•    Assists in the development and implementation of policies and procedures
•    Maintains human resource information system records 
•    Performs data analysis and report preparation-incorporating determinations into recommendations
•    Performs compensation and benefits administration and reporting. 
•    Assists in talent acquisition and recruitment processes 
•    Provides HR project support for internal projects
•    Coordinates employee development plans and performance management
•    Provides efficient and effective HR assistance and service to overseas offices  
•    Assists with all internal and external HR-related matters
 

Qualifications:

•    University Degree in Human Resources Management or any other related discipline
•    Minimum 3 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 labor 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

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. 
 

Duties:

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

 

Qualifications:

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

 

Location: Limassol, Cyprus

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 R&D Specialist based in Limassol, Cyprus.  

Duties:

• Act as Coordinator throughout the development of a new product Compile consolidated documents and summaries throughout the development of each products, such as literature searches, overall summaries etc 
• Review analytical data generated from other departments and provide constructive comments (e.g stability data, quality control analysis etc)
• Review and comment of the documents created by other departments (e.g SOPs, process validation protocols and reports, NPD reports, Project reports, analytical validation reports etc) 
• Read and interpret patent claims and patent reports 
• Maintain up to date status of all guidelines covering the medical products 

Qualifications:

•   University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as advantage.
• Minimum of 3 years’ experience in the pharmaceutical industry. 
• 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

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 Formulation Development Specialist/Senior Specialist for our offices in Limassol, CYPRUS.
 

Duties:

• To study the literature of the product and know its pharmaceutical characteristics.
• To study the reference product and be able to develop a generic formulation of Injectables (Solutions, Pre-filled cartridges, Lyophilized formulations).
• To study the reference product and be able to develop a generic formulation of Dry Powder Inhalers.
• To prepare the formulation(s) proposal for patent clearance.
• To apply knowledge in the QbD based product development.
• To perform the formulation development trials in the formulation development laboratory, possibly without any errors.
• To transfer the manufacturing process from trials to scale up and coordinate in the execution of production scale batches in production facilities.
• To follow Regulatory Affairs requirements and current European and WHO guidelines related to the development pharmaceutics section and stability guidelines.
Qualifications:
• University Post graduate 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
• 8-10 years industrial experience in a similar position involving the above duties
• Committed to relocate to Cyprus
Location: Limassol, 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 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 Pharmacovigilance Associate in our offices in Limassol, CYPRUS. Pharmacovigilance is the scientific department of the Company that  deals with the safety of pharmaceutical products.

Duties:

•  To collect and manage information on adverse events from various sources and report them to Eudravigilance according to current EU legislation. 
•  To regularly perform signal detection activities, as per the Pharmacovigilance system of Medochemie and current EU legislation.
•  To maintain the Drug safety information and the Pharmacovigilance system as per internal procedures.
•  To execute a number of task relating to the Quality of the Pharmacovigilance system, including but not limited to trainings, audits, contractual agreements, deviations and quality reviews, as per internal procedures. 
 

Qualifications:

•  University degree in Pharmacy degree. A post graduate degree will be considered an asset.
•  Previous experience within the pharmaceutical industry in the field of drug safety and Regulatory Affairs (for generics) will be considered an asset.
•  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 Greek and English language.
 

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 Sales Operations Manager in our offices in Limassol, Cyprus.
 
The purpose of this role is to provide extensive and collective support to the entire sales operation across the MENA region, ensuring a consistent seamless flow of communication and activities, removing any potential clutter, and ensuring highly efficient yet lean operation. This critical job plays a pivotal role to connect and improve all functions that might affect the sales operation within the leeway from demand to supply, comprising (accurate forecast, robust and strong supply chain process, validated efficient communication process, and valid sales & stock management practices and reporting).

Duties:

The purpose of this role is to provide extensive and collective support to the entire sales operation across the MENA region, ensuring a consistent seamless flow of communication and activities, removing any potential clutter, and ensuring highly efficient yet lean operation. This critical job plays a pivotal role to connect and improve all functions that might affect the sales operation within the leeway from demand to supply, comprising (accurate forecast, robust and strong supply chain process, validated efficient communication process, and valid sales & stock management practices and reporting).
 
Job Responsibilities (Key Result Areas- KRAs)
 
KRA 1: Reporting and operational control
 
• Conduct/ perform thorough timely analysis and strategic planning to support the senior management decision-making process and to ensure mistake-proof sales and stock reporting process.
• Work cross-functionally with sales/country managers, marketing, finance and accounting, and supply chain to ensure a smooth and clutter-free end-to-end (demand-to-supply) process.
• Operationalize all sales and commercial activities and aspects that influence demand and supply communication reporting.
• Ensure that sales forecast, phasing, and shipping requests are exercised effectively with robust planning and understanding of both external and internal factors.
• Analyze sales and other stock management reports that give insights into how the company can make adjustments to improve performance and enhance profitability (contribution) in each market.
• Follow shipping requests, production schedules, supply chain procedures, and channels to ensure that obstacles and problems are solved immediately to avoid any potential delay, towards effective implementation of the supply chain plan.
KRA 2: Achieving Operational Excellence
• Supervise the generation of all sales & stock management proposals. Interface with financial staff, business operations for the purpose of reviewing proposal content and pricing strategy in order to achieve the company’s best interest.
• Assist the Commercial Director/ Area VP-MENA to provide clients, distributors, or agents with supplemental proposals, letters of authorization, and contract amendments as appropriate to guard the company’s rights and achieve its best interest.
• Initialize contact with new clients, technical staff (RA, Attorneys, Accountants, etc.), and division leadership personnel, interacting with these groups until contract closure and project launch/ initiation.
• Implement new approaches and methodologies to streamline, automate or digitize the commercial/sales operations across the region to ensure traceable, mistake-proof, efficient, and effective operation.
• Provide expert advice and coaching support to the sales operations team to ensure continuous development and engagement.
• In collaboration with related functional personnel, design and implement effective operational measures and KPIs to evaluate critical areas for future improvement.
KRA 3: Achieving effective Cross-functional/ management Communication
• Build strong ties and business relationships with MENA operations and sales teams to promote effective cross-selling communication and collaboration whenever possible.
• Provide technical closed-loop feedback to clients, partners, and associates to ensure that critical information is shared concisely and accurately to promote continuous improvement.
• Build & maintain a collaborative network of functional influencers and leaders to ensure prompt response to critical issues and problems along with improving future planning and forecast.
• Assist key stakeholders to use well-thought operational leading indicators to improve future planning and forecast, and the best possibility predict future performance.

Qualifications:

• Education: Bachelor’s degree in relevant major(s).
• At least 5 years of experience in the pharmaceutical industry.
• Knowledge of standard sales operational practices and forecasting
• Experience in Operations Management and using forecasting techniques and methods.
• Excellent computer skills; Forecasting, Analysis & reporting software such as (SAP BPC, ERP systems, and other relevant programs)
• Organizational, verbal and written communication skills and English language knowledge
• Attention to detail and ability to multi-task is a must
• Advanced Analytical skills and experience
• Astounding Executive business writing skills
• Sales Experience: more than 5 years of experience in Sales Management (Managerial role in a matrix organization)
• Experience in dealing with distributors and wholesalers in the MENA region would be advantageous.

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 Regulatory Affairs Specialist in our offices in Athens, GREECE.

Duties:

• Be responsible for the CMC compilation of dossiers for new products and dossier updates for existing products, in eCTD format and in compliance with the global regulations in force.
• Submit Marketing Authorisation Applications (MAAs) and follow up till approval mainly for European Registration Procedures (DCP/MRP) according to the company’s strategy. 
•  Successfully maintain dossiers’ and MA’s lifecycle (variations & renewals) in all territories as necessary so that the MAs are up to date.
• 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). 

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry, Biochemistry, Biology, etc). A post graduate degree will be considered an asset.
• 3 to 5 years experience in the pharmaceutical sector, in the field of generic product development and Regulatory Affairs.
• Knowledge and practical understanding of EU and non-EU pharmaceutical legislation, EMA & ICH relevant guidelines and competency with e-CTD preparation
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast changing environment.
• Strong communication, influencing and problem resolution skills.
• Ability to be adaptive to change, to multitask and give attention to detail.
• Very good interpersonal skills, analytical thinking and result orientation.
• Fluency in Greek and English (written and spoken) and computer literacy.  Knowledge of any other languages will be considered an asset
• Ability to travel abroad if requested

Location: Athens, Greece

We are offering an attractive remuneration package 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 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 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 Professionals.

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:

Required:
• 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 3 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.
 

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¨
• 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 Pharmacy or Chemical Engineering. A postgraduate degree will be considered an asset.
• Experience in the field of pharmaceutical industry will be considered as an asset.
• Advanced project management and technical writing skills is preferred.
• Multi project handling at once under time pressure.
• Excellent command of the English language, both written and oral.
• Strong IT  Strong computer literacy skills
• 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 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 R&D Associate based in Limassol, Cyprus. 

Duties:

• Be responsible for the raw materials sourcing for under development products, by contacting with a variety of external stakeholders. 
• Conduct a preliminary and limited quality evaluation of the raw material used for R&D purposes in accordance with the current guidelines in force.
• Apply basic regulatory knowledge under which the medical products are governed.
• Compile consolidated summaries and provide required reports throughout the development of each products in support to the R&D team.
• Support other departments related to the R&D functions and operations when this is required. 

Qualifications:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Experience in the pharmaceutical industry it will be considered an advantage. 
• Ability to work collaboratively in a team, and prioritize work in a dynamic and fast moving environment. 
• Very good interpersonal skills, analytical thinking and result orientation.
• Strong computer literacy
• Fluency in English language 

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 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 R&D Senior Patent Specialist based in Limassol, Cyprus.  

Duties:

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

Qualifications:

• University degree in Chemistry, Pharmacy or other relevant science degree. A postgraduate degree will be considered as an asset.
• Minimum of 4 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

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 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
• Prepare the specifications and determine operational feasibility
• Integrate software components into a fully functional software system
• Document and maintain software functionality
• Troubleshoot, debug and upgrade existing systems
• Deploy software and evaluate user feedback
• Manage projects and coordinate with vendors to ensure the on-time delivery and quality of technology projects
• Track and monitor project progress and escalate issues to appropriate stakeholders
• Continually identify, prioritize and mitigate project risks and issues
• Manage procurement and contract management processes when applicable
• Forecast internal resource capacity by tracking the progress of projects across the portfolio
• Estimate project costs and manage the project budget 

Qualifications:

• BSc degree in Computer Science, Engineering or relevant field
• 5+ 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. Experience in designing and developing Application Programming Interfaces (API) will be considered as an advantage
• Ability to develop software in Java, ASP.NET, C++ or other programming languages
• Excellent knowledge of relational databases, SQL and NoSQL technologies
• Experience developing web applications (PHP, Python)
• Experience with test-driven development
• 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.

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 Group Marketing Senior Manager for our offices in Limassol, Cyprus. 

Duties:

The Responsibilities include but are not limited to:
• Be responsible for executing global marketing initiatives to drive business growth including innovation in the way we conduct business, customer/patient connections, path to purchase strategies, insight development & deployment, brand positioning, pricing strategy, expansion strategy, retail facing category vision and strategy for the Company’s OTC/ Consumer Healthcare brands.
• Collaborate with Area Sales Leads around the globe to develop multiple marketing programmes. 
• Develop commercial business development programs for all regions. Create and foster strong strategic partnerships with Sales and other business leaders.
• Coordinate and proactively facilitate the identification of new business opportunities, strategic and operational analysis of opportunities, including leading the vetting and validation of ideas and opportunities. 
• To act as single point of contact for our global regions helping to maximise their potential growth.
• Adapt a central multi-channel communications programme ensuring high cultural resonance for all regions and the probable addition of alternative copy for any specific local challenges. 
• Partner with R&D, Regulatory, Sales, Regional Marketing, Finance and key customers in planning, coordinating and sequencing product launches and customer targeting. 
• Support business financial objectives and ensure applicable company compliance with all relevant country and regional requirements, company regulations, policies and procedures.

Qualifications:

• Bachelor’s degree is required with science expertise as preferred.  Master’s Degree in business or marketing will be preferred.  
• 15+ years of marketing or related function experience in the pharmaceutical industry with 5 years in management-level positions with increasing responsibilities. A demonstrated record of accomplishments regarding business development strategies, brand marketing and portfolio management.
• Deep understanding of the pharmaceutical industry across a range of lenses (e.g. Marketing, Sales, Medical Affairs, Market Access, etc.)
• People management experience and high propensity for people development. Experience in leading cross-functional teams will be considered as advantage. 
• Experience in leading business growth in complex global framework.
• Ability to travel.
• Fluency in English language both verbal and writing. 

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 Group Senior Product Manager for our offices in Limassol, CYPRUS. 

Duties:

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

Qualifications:

• Bachelor’s degree with at least 5 year of pharmaceutical marketing and/or sales experience. Academic education in life sciences (medicine, pharmacy, chemistry or relevant) will be considered as additional asset.
• Proven analytical & strategic thinking.
• Excellent internal and external communicator across multidisciplinary team.
• Strong project management orientation with the ability to plan, prioritize and manage complex list of projects to completion.
• Hands-on and can-do mentality, enjoys working in a team, but can also work autonomously and remotely as an individual.
• Excellent communication & presentation skills.
• Committed to relocate to Cyprus.
• 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 (GMP).

Medochemie Ltd invites applications from career-oriented professionals for the position of Quality Assurance Specialist (Risk Assessment) in our offices in Limassol, CYPRUS.

Duties:

• Coordinate the Risk Management process/ function within the company 
• Perform risk assessments
• 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
• Regular follow up on the progress of the mitigation plans and update the status
• Support risk management process for projects in co-ordination with project manager / leader.

Qualifications:

• Bachelor's degree in a science discipline
• Minimum of 3+ years experience in the Pharmaceutical Industry 
• Knowledge and understanding of Quality Assurance, GxP requirements and Quality Management Systems
• Hands on risk management experience within pharmaceuticals will be considered as advantage 
• Excellent command of the English language, both written and oral
• Strong computer literacy skills
• 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 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 Medical Representative, for the following provinces/governorates:

1. Baghdad
2. Basra
3. Mousel
4. Najaf
5. Wasit & Maysan

Duties:

• Conducts visits to doctors, pharmacies and other HCPS for the proper detailing and promotion of our medical products, anchored by the patient needs & safety
• Delivers sales presentations to multiple decision-makers in order to promote the Company’s portfolio of products, within the entrusted/ assigned territory
• Achieves the sales targets in light of operational & promotional indicators
• Establishes and nurtures strong productive client relationships
• Develops strong relationships with key decision makers and key stakeholders
• Maintains existing business and presents new products

Qualifications:

• University degree in Pharmacy (Registered member of the Pharmacist Syndicate in Iraq)
• At least two years of experience in a similar position with an international company
• Excellent level of knowledge of the English language
• Very good interpersonal and influence skills, analytical thinking, results orientation
• Iraqi National 

Location: Baghdad, Wasit & Maysan, Najaf, Basra and Mousel

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.

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 following positions:

Medical Representatives to cover Limassol/ Paphos, Limassol/ Nicosia & Larnaca/ Nicosia/Ammochostos, for medical promotion
Pharmaceutical Representatives to cover Larnaca/ Ammochostos 

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.

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.

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 Technology Transfer Manager for our offices in Limassol, CYPRUS.  

Duties:

• Perform technology transfers of pharmaceutical drug product processes among R&D and Medochemie Production sites, or between Medochemie sites.  
• Manage and mentor the team of experts performing technology transfers.
• Assess processes for gaps, design experiments, write pilot/ batch protocols and batch records, supervise manufacturing batches, assess experimental data, draw scientifically sound conclusions, and write technology transfer reports.
• Perform manufacturing process reviews of processes intended for technology transfer with an eye towards manufacturability, robustness, and validation success.
• Assist in the completion and review of sections of documents needed to complete such transfers.
• Provide scientific trouble shooting having always in mind the quality of products.
• Managing projects to meet Company timelines.

Qualifications:

• University Degree in Pharmacy, Chemistry or Chemical Engineering. 
• Minimum 8 years of experience in cGMP Environment.
• Minimum 8 years industrial experience in a similar position.
• Experience in R&D and production areas will be considered as an additional asset. 
• Good Communication skills.
• Multi project handling at once under time pressure.
• Excellent command of the English language, both written and oral.
• The position will require frequent travelling.
• 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 applications from career-oriented professionals for the position of Patent Specialist for our offices in Limassol, CYPRUS.  

Duties:

• To be able to search in available patent data bases in order to explore the status of patent applications, litigations etc in European and non- European territories.
• To be able to review, analyze and advice on patents and prepare consolidated patent reports. 
• To be in a position to assess and conclude on finished dosage formulations and active substances’ synthetic schemes towards any valid patents for a specific product.

Qualifications:

• University degree in a relevant science (Pharmacy, Chemistry). A post graduate degree will be considered an asset.
• 10 years of experience within the pharmaceutical industry and specifically as patent officer/ expert in generics.
• Ability to work collaboratively in a team.
• Excellent level of knowledge in written and spoken English and computer literacy.
• Willingness to travel frequently or preferably 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.