Israel - Vagas de 27 de Fevereiro de 2008

TEL AVIV - GLOBAL QUALITY DIRECTOR
Pharmaceutical QA /QC. Job Description : Reporting to the Vice President, you will be interfacing internally with the Global Operations units, Solids and Sterile Manufacturing, Purchasing, Engineering, Finance, IT Operations, Quality and Distribution, R&D, Regulatory Affairs and Legal. Externally, you will be working with international health authorities, the pharmaceutical industry and scientific groups. The Role: This is a key role within the organization and you will be responsible for: all QA and QC of manufacturing operations worldwide ( all aspect of compliance with GMP and the quality systems approach captured and optimized across supply chain, manufacturing, marketing and distribution to include a harmonizing and cost effective cross organizational structure). providing expertise on product and quality issues, implementing appropriate quality standards and systems based upon current GMP and company requirements across all stages of product manufacturing, control and distribution. providing the tools and metrics to assess company wide quality performance in relations to business objectives, assess compliance to GMP and quality systems across areas of accountability and providing expertise/support for corrective actions, improvement and readiness for inspection. managing, coaching and developing QA professionals within the Global Quality unit and contributing to the growth of quality professionals and to establish, disseminate and monitor application and harmonization of appropriate quality standards for operations and R&D manufacturing. assessing industry trends across all areas of GMP and anticipate the needs of both company and customers. representation at international quality and regulatory compliance organizations and agencies. Skill Required : You possess an interest in relocating to Israel (you have the ability to access a work permit or wish to relocate to your home country) and have: a PhD or University degree in relevant disciplines with solid expertise in Quality Assurance and Regulatory Compliance across all areas of GMP with significant senior managerial level experience in areas of QA, QC, Manufacturing, Technical Support, Regulatory Compliance. 10 to 15 years experience in a senior role in one or more international life science companies and ideally , a pharmaceutical company. a demonstrated success in regulations and inspections resulting in product approvals with particular exposure to the FDA and EU approval processes. the managerial ability to foster quality standards across functions, cultures and managerial levels as well as solid understanding of trends and implications to Quality, GMP and RA areas. a mature attitude and strong team leadership skills with the ability to build and lead a team with drive, energy and demonstrated success in managing an organization toward business goals and quality compliance. Hebrew would be a plus but not requirement. Please send cv to email :
chicago@chronosconsulting.com Ref. USQM26278