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Actavis Ltd Regulatory Affairs Manager, CMC
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Job Description
The Position
The role of the CMC Manager within RA CMC is to oversee all projects handled by the team in Malta, plan all activities in order to ensure that deadlines are maintained and provide technical support and advice. The main activities are responding to queries from regulatory authorities or clients concerning dossiers, keeping the dossier master files fully up to date and preparing the necessary documents as required by the variation process. This position is on full time basis.

The Applicant
The position calls for a person having:
  • Preferably a Degree / Masters level of education in Pharmaceutical Technology / Pharmacy or Chemistry and / or at least 5-7 years’ experience in a related field within the pharmaceutical industry;
  • Excellent technical, verbal and written communication skills and the ability to work effectively with internal / external stakeholders as may be required;
  • Capability in problem-solving and co-ordination of regulatory issues; analytical thought needed to resolve issues in a variety of complex situations;
  • Knowledge of EU regulatory framework;
  • Very good computer skills; excellent organizational skills; must have an eye for detail and a methodical approach to work; must be able to work under pressure and on own initiative.
How To Apply
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