Categoria:
Healthcare / PharmaceuticalLuogo di lavoro:
Lodi e provinciaFor our client company
Main responsibilitiesEnsure that the organization is operating in compliance with regulatory requirements and industry guidelines, including the review of applicable quality assurance policies, QMS documents and global regulatory guidance to ensure alignment with regulatory requirements and harmonization with QA policies of clients, other recognized institutions and Regulatory Agencies.Ensure the preparation and maintenance of regulatory submissions and files worldwide.Conducting regulatory communications with FDA, under appropriate supervision and direction, for assigned products and activitiesManage electronic submissions in eCTD formatMaintain and improve working knowledge of current/pending regulations and guidance for generic drugs and new drugs to ensure compliance with Regulatory Agency requirementsLead and manage activities concerned with the submission and approval of products and product transfers to government regulatory agencies including US and EU regulatory agenciesBuild and maintain client relationships on regulatory matters with appropriate internal and external stakeholders.Provide technical assistance and consultationon regulatory matters to all the company units, as requestedContribute to the company business development efforts as requested.Requisiti:
QUALIFICATIONS Professional and Technical Knowledge
experience with API registration, authorization and certification requirements.
Knowledge of pharmaceutical and regulatory requirements for international markets such as but not limited to United States and European Union
Experience with pharmaceutical product dossier compilation and review.
Experience in pharmaceutical laboratory commodities, tests, equipment, and techniques.
Knowledge of FDA, WHO, in-country regulations, and stringent regulatory authorities with previous Good Manufacturing Practice (GMP) inspection experience.
Advanced computing skills in standard software systems, such as Microsoft Office suite.
Strong interpersonal skills and an ability to work across disciplines and in diverse locations internationally.
Excellent written and oral communication skills.
English fluency required, additional international business language fluency is preferable.
Salary commensurate with experience.The Senior Regulatory Expert can devolop a career as a Regulatory Manager.