The Role:
To undertake the duties of a Qualified Person as defined in Article 51 of 2001/83/EC Directive, This role is instrumental in managing the release activities of the company, leading batch assessments to ensure releases are carried out efficiently, in a timely manner and meeting relevant regulatory standards. It is vital that a quality management system is properly maintained and that any customers’ complaints are dealt with effectively. Coordination and efficacious management of any product recalls is essential.
Responsible for managing the Quality Assurance activities with nominated third parties and internal operating units, in order to ensure compliance with the Life Cycle Management of the pharmaceutical products as defined by the corporate GMP Quality Manual and all the relevant EU regulatory and legislative requirements.
Profile:
- University Degree in pharmacy, or medicine, or alternatively other health science degree with good evidence of development in the competencies mentioned above.
- Holder of a diploma, certificate or other evidence of formal qualifications awarded on completion of a university course of study, or a course recognized as equivalent, extending over a period of at least four years of theoretical and practical study in one of the following scientific disciplines: pharmacy, medicine, veterinary medicine, chemistry, pharmaceutical chemistry and technology, biology. Alternative qualifications as defined by the Directive 2001/83 (Article 49) may be considered.
- Minimum of two years of work experience as a Qualified Person.
- High sense of responsibility and professionalism coupled with the ability to work with tight deadlines,
- Strong organizational, analytical and communication skills.
- Excellent command of Greek and English languages, both verbal and written.
- Experience in working with a multicultural environment will be considered an advantage.
A competitive remuneration package will be offered to the successful candidate.
Interested applicants are required to submit their curriculum vitae to Marinos Kokkinis at mkokkins@pharmascience-intl.com
by Wednesday, 5 December 2012.