Jobs in an International Pharmaceutical Company in Limassol
The company
An International Pharmaceutical Company with operations in Limassol is looking for:
1. Patent Attorney (508/HRS)
Limassol
ΑΝΑΖΗΤΑΤΕ ΕΡΓΑΣΙΑ; – ΕΚΑΤΟΝΤΑΔΕΣ ΘΕΣΕΙΣ ΕΡΓΑΣΙΑΣ – ΠΑΤΗΣΤΕ ΕΔΩ!!
Responsibilities
This is a great opportunity for a person who seeks a position of challenge in a fast pace, dynamic international environment. The successful candidate will have the responsibility for the coordination and management
• Develop and implement patent strategies
• Identify inventions, organise and participate in patent research
• File and prosecute utility models and patent applications
• Monitor patent applications, prepare and maintain all necessary documentation throughout the application process
• Register and design trademarks
• Evaluate company’s current patenting procedures and propose improvements in order to enhance operational effectiveness
• Deal with patent assignments when a patent is sold or transferred
• Keep abreast of current patent legislation
Profile of the ideal candidate
• University degree in Medicine/Pharmacy/Chemistry or in a related field.
• At least 10 years of solid experience as a Patent Attorney in the pharmaceutical industry is a must. Experience in an international organisation will be considered an advantage
• Certification of Qualified Patent Attorney (CIPA) or possibility to pass the exam in a short time
• Dynamic, results driven with an ability to take own initiative
• High attention to detail and problem solving skills
• Excellent organisational skills with high attention to detail
• Excellent command of English
Benefits
A very attractive remuneration package plus benefits will be offered to the successful candidate according to qualifications and experience.
Apply now online in strict confidence
Deadline: 23rd August 2013
Please note, that only successful candidates will be contacted.
2. Preclinical and Clinical Research Associate (507/HRS)
Limassol
Responsibilities
This is a great opportunity for a person who seeks a position of challenge in a fast pace, dynamic international environment. The successful candidate will have the responsibility for the coordination and management of all aspects associated with the preclinical and clinical research of the pharmaceutical products. Main responsibilities include:
Develop and implement researching strategy and set priorities
Initiate new preclinical and clinical research and maintain existing ones
Identify potential research centres and participate in the negotiations for their selection
Choose the trial design and organise the preclinical and clinical trials
Prepare and maintain all the necessary documentation in accordance to GCP and the local legislation of the research centre
Monitor the progress of trials and ensure compliance with trial protocol and procedures, local regulations and ICH-GCP throughout the whole period of the trials
Keep abreast of current international legislation in the preclinical field
Profile of the ideal candidate
University degree in Medicine/Pharmacy/Chemistry or in a related field
At least 5 years of solid experience in Preclinical and Clinical research in the pharmaceutical industry is a must. Experience in an international organisation will be considered an advantage
Very good knowledge of regulations governing clinical research, ICH/GCP guidelines
Very good knowledge of GLP principles, legislation and methods or preclinical researches
Excellent negotiation skills
Dynamic, self-motivated and results driven with high levels of energy
Strong organisational skills with high attention to detail
Willingness to travel abroad
Excellent command of English
Benefits
A very attractive remuneration package plus benefits will be offered to the successful candidate according to qualifications and experience.
Apply now in strict confidence
Deadline: 23rd August 2013
Please note, that only successful candidates will be contacted.
3. Foreign Regulatory Affairs Manager (506/HRS)
Limassol
Responsibilities
This is a great opportunity for a person who seeks a position of challenge in a fast pace, dynamic international environment. The successful candidate will have the responsibility for the coordination and management of all aspects associated with the registration of the pharmaceutical products in other countries. Main responsibilities include:
Develop registration strategy and define priorities
Initiate new registrations and maintain existing ones
Prepare all necessary Regulatory Documentation (dossier) for submission and variations according to the requirements of each country
Liaise and maintain relationships with governmental agencies in Cyprus and other countries in order to monitor and follow up on the approval process
Provide regulatory support to other departments
Evaluate company’s current regulatory procedures and propose improvements in order to enhance operational effectiveness
Keep abreast of current international regulatory procedures and changes
Profile of the ideal candidate
University degree in Medicine/Biology/Chemistry/Pharmacy or in a related field
At least 5 years of solid experience in Foreign Regulatory Affairs in the pharmaceutical industry is a must. Experience in an international organisation will be considered an advantage
Very good knowledge of Health Care Regulations
Dynamic, self-motivated and results driven with high levels of energy
Excellent organisational skills with high attention to detail
Strong networking and negotiation skills with an ability to communicate with impact and persuade
Excellent command of English
Benefits
A very attractive remuneration package plus benefits will be offered to the successful candidate according to qualifications and experience.
Apply now online in strict confidence
Deadline: 23rd August 2013
Please note, that only successful candidates will be contacted.
ΑΝΑΖΗΤΑΤΕ ΕΡΓΑΣΙΑ; – ΕΚΑΤΟΝΤΑΔΕΣ ΘΕΣΕΙΣ ΕΡΓΑΣΙΑΣ – ΠΑΤΗΣΤΕ ΕΔΩ!!
To apply online visit: http://www.pwc.com.cy/en/careers/jobs-pwc-clients/recruiting_now.jhtml
Email: cyhcd@cy.pwc.com
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