Vacancy Notice N° e32/2015
CEP Scientific Assistants (Revisions’ Team) (Grade B4)
Directorate General of Democracy and Human Dignity (DG II)
European Directorate for the Quality of Medicines & HealthCare (EDQM)

Certification of Substances Division (DCEP)
Closing date: 07 April 2015
Location : Strasbourg

Fixed-term contract: The total length of employment under fixed-term contracts will not exceed five years.

Job mission

Turnover Profile 

 

Turnover profiles are specific roles where it is considered to be in the best interests of the Organisation to have a consistent rotation of staff. Turnover profiles offer once-only opportunities under this scheme  and the total duration of employment cannot exceed five years.  

Staff members or former staff members who are or have previously been employed in the framework of the Junior Professional Programme or Turnover Profiles will not be eligible again for any of the profiles under these schemes. The Council of Europe reserves the right to assess the admissibility of candidates who are or have previously been employed with the Organisation according to their contractual situation at the closing date of this competition.

Job mission 

 

Under the authority of the Director of the European Directorate for the Quality of Medicines & Healthcare (EDQM) and the Head of Certification Division, the incumbent shall provide professional scientific assistance to the procedure for the Certification of Suitability to the monographs of the European Pharmacopoeia (CEP) in accordance with procedures, guidelines and priorities with a concern for quality, efficiency, and accuracy and in compliance with the Council of Europe’s values and regulations.

Key activities

The incumbent performs all or a combination of the following duties:

 

·         Participates in the scientific evaluation of dossiers submitted for revision in respect of existing certificates of suitability to the monographs of the European Pharmacopoeia in accordance with technical rules and guidelines (general and specific monographs of the European Pharmacopoeia, guidelines adopted by the Steering Committee and the Technical Advisory Boards of the Certification procedure, guidelines of the European Medicines Agency);

·         Manages assigned dossiers in accordance with established rules and procedures;  reports to the supervisor on the status and progress of activities and if and when problems occur;

·         Ensures consistency of assessment reports for similar products and consistency of the reports with the policy of the procedure, if necessary analysing and reporting any discrepancies and proposing solutions;

·         Prepares reports for review by supervisors or external experts, drafts correspondence and certificates, and communicates with applicants;

·         Participates in the maintenance and improvement of the EDQM’s quality management system and the maintenance of the ISO 9001 certificate for Certification related activities.

 

Please note that the incumbent may be required to perform other duties not listed in the vacancy notice.

Eligibility Requirements

Only applicants who best meet the following criteria will be considered for shortlisting.

·      Qualifications: completed higher education degree or qualification in pharmacy, chemistry, biochemistry or other relevant discipline. 

·      Experience: short professional experience (minimum 6 months) in the evaluation or in the preparation of dossiers on the quality of substances for pharmaceutical use (CTD Module 3.2.S), either in a licensing authority or in the industry. 

·      Language requirements: very good knowledge of one of the official languages (English) in oral and written communication; basic knowledge of the other official language (French).

·      Nationality: nationality of one of the 47 Council of Europe member states. 

·      Age: under 65 years of age, at the closing date of the vacancy notice. 

Employee Core Values

Competencies

Essential:

·      Professional and technical competencies:

-       knowledge of the European regulatory requirements in the field of pharmaceuticals;

-       planning and work organisation;

-       analytical thinking; problem-solving; judgement skills; concern for quality, efficiency and accuracy.

·      Interpersonal skills: service and client orientation, team-work and co-operation.

·      ICT skills : sound computer skills of standard tools in office applications. 

 

Desirable:

·      ICT skills: knowledge and experience of electronic Common Technical Document (eCTD) tools would be an advantage. 

·      Professional Competencies: information-seeking.

·      Personal attitudes: initiative and responsibility; results orientation and sense of continuous improvement; self-management and development.

·      Personal values: discretion. 

 

For more information, please refer to the competency inventory of the Council of Europe.

Additional information

Applications must be made in English or French using the Council of Europe on-line application system.  By connecting to our website www.coe.int/jobs you can create and submit your on-line application.  Applications must be submitted at the latest 7 April 2015 (midnight Central European Time).  

 

The selection procedure consists of a shortlisting based on candidates’ applications and may include ability tests, behavioural questionnaires, a job related written exam, situational exercises, language tests, interviews and full assessment centres.

 

Only candidates who best match the requirements of the job vacancy will be shortlisted and invited to test or a written exam. Tests or written exams may be eliminatory, in which case only candidates who succeed in the tests will be invited for interview. Depending on the number of applicants, the length of the professional experience considered for shortlisting may be increased from that indicated in the vacancy notice.  

 

Following this competition, a list of eligible candidates, in order of merit, may be established. This list will be valid for two years with the possibility of extending it to a maximum of four years. During the period of validity of the list, candidates on the list may be offered employment of fixed term duration. It should be noted that placement on this list does not give candidates the right to an appointment within the Council of Europe. The choice of candidates from a reserve list is not made solely according to the order of merit, but also takes into account the requirements of the position to be filled and the qualifications of the candidates.

 

For the moment, the duration of the position is limited to 31 December 2015, but may be prolonged.

 

The first two years of employment will constitute a probationary period. Provided the staff members’ work is considered satisfactory, he/she may be offered a contract of fixed term duration. However, the total length of employment will not exceed five years. The staff member so recruited shall not be eligible for any subsequent internal competition, promotion or transfer to a post, or for secondment.

 

Details on conditions of employment including salaries, allowances, pension scheme and social insurance can be consulted on our recruitment website. 

 

Under its equal opportunities policy, the Council of Europe is aiming to achieve parity in the number of women and men employed in each category and grade. In the event of equal merit, preference will therefore be given to the applicant belonging to the under-represented sex. 

 

The Council of Europe welcomes applications from all suitably qualified candidates, irrespective of gender, disability, marital or parental status, racial, ethnic or social origin, colour, religion, belief or sexual orientation.

 

During the different stages of the recruitment procedure, specific measures may be taken to ensure equal opportunities for candidates with disabilities. 

 

The Organisation 

 

The Council of Europe is the continent’s leading organisation in the protection of human rights, democracy and rule of law. It was founded in 1949 in order to promote greater unity between its members  and  now includes 47 member states, all having signed up to the European Convention on Human Rights.

 

By Statute, the Council of Europe has two constituent organs: the Committee of Ministers, composed of the member States’ Ministers for Foreign Affairs, and the Parliamentary Assembly, comprising delegations from the national parliaments. The Congress of Local and Regional Authorities of Europe represents the entities of local and regional self-government within the member States. The Commissioner for Human Rights is an independent and impartial institution within the Council of Europe mandated to promote the awareness of and respect for human rights in member states.

 

The European Court of Human Rights is the judicial body which oversees the implementation of the Convention in the member states. Individuals can bring complaints of human rights violations to the Strasbourg Court once all possibilities of appeal have been exhausted in the member state concerned.

The Council of Europe has its permanent headquarters in Strasbourg (France) and in addition it maintains external presence in more than twenty countries. More information about Council of Europe external presence.

 

The European Directorate for the Quality of Medicines & HealthCare (http://www.edqm.eu) is a leading organisation that protects public health by enabling the development, supporting the implementation and monitoring the application of quality standards for safe medicines and their safe use. Its standards are recognised as a scientific benchmark world-wide. The European Pharmacopoeia is legally binding in European member states.  Similarly, the EDQM develops guidance and standards in the areas of blood transfusion, organ transplantations and consumer health issues.  Its mission is to contribute to the basic human right of access to good quality medicines and healthcare and to promote and protect human and animal health 

External recruitment procedure organised in accordance with Article 16 of the Regulations on Appointments