NEW 外資系製薬メーカー Principal Scientist Quality Auditor

ブックマーク一覧

勤務地	東京都港区、兵庫県神戸市
想定年収	1200～1600万円
仕事内容	This job position is for a GCP medical auditor. The position is office-based located at the Kobe affiliate office. ●Position Brand Description: The Quality Auditor is part of the Global Quality Auditing and Compliance (GQAAC) division and provides quality assurance through the execution of internal and external audits in support of pharmaceutical development, non-clinical and clinical research, product commercialization, pharmacovigilance and consumer information quality (CIQ) for this company. Through auditing, the Global Quality Auditor assures that GXP operations conducted or sponsored by this company are performed in accordance with company standards, policies, procedures and practices and are compliant with current regulatory requirements and expectations, applicable guidelines and industry standards. GQAAC is operating as a valued business partner and taking a proactive approach to further enhancing the quality status of business operations and regulatory compliance. The Quality Auditor plays a key part in contributing to the implementation of this strategic approach to quality auditing oversight. ●Key Objectives/Deliverables: The following activities will be performed according to current GQAAC procedures, guidelines and tools. These responsibilities are not intended to be all-inclusive: ●Auditing: Scheduling, preparing, conducting and reporting GQAAC audits and assessments of GXP operations, both internally and externally (contracted) to assess the level of compliance with company standards, policies, practices and procedures and current regulations and guidelines. Participate in or lead the risk assessment of GXP operations in support of generating the GQAAC risk-based annual audit plan. Appropriately escalate any compliance issues. Meet the requirements outlined in quality standards, quality manuals, policies, procedures, and tools. This implies establishment and maintenance of a comprehensive knowledge of all applicable regulations, technical knowledge, and training to meet these responsibilities. ●Global Quality ? Business Related Responsibilities: Participate in or lead the preparation and/or review of standards, policies, procedures and guidelines that are used to establish quality requirements, when needed. Participate in or lead the preparation of organizational metrics and trending of audit findings, when required. Provide audit-related advice to GXP operations on the interpretation of corporate and regulatory GxP requirements (standards/policies/procedures) related to quality management, when required. Establish and maintain relationships with relevant business areas and regulatory authorities, including support for regulatory inspections, when required. Provide technical expertise in identifying, formulating, assembling and delivering quality and compliance education to customers, as required. ●Personnel Development: Maintain good interpersonal and communication skills with auditees and business areas with particular emphasis on verbal and technical writing skills. Complete required training for the roles identified in the Individual Training Plan (ITP) Be continually aware of current industry trends and regulatory agency interpretation of GxP requirements. Seek self-development in GxP areas (e.g. attend training courses, conferences or association meetings) and share such information and knowledge with other members of the group or company to increase internal intelligence. Participate or lead divisional improvement efforts, including Six Sigma projects and departmental teams. Support training and qualification of other auditors.
経験・資格	※求人情報の応募要件全てに該当しなくても、企業様に対して内々に打診したり相談することが可能な場合もございます。一つでも当てはまる方は前向きにご検討下さい。 ●Minimum Requirements: ・Relevant experience(s)within the GCP medical area at this company or within the pharmaceutical environment. ・Good oral and written communication skills in English. Ability to communicate effectively in Japanese language. ・Experience working with Third Party Organizations. ・The ability to understand detailed scientific information, while remaining anchored in the “Big Picture”. ・Ability to interpret and apply regulations, regulatory guidance, codes and public expectations and identify and recommend compliance changes as appropriate. ・Excellent interpersonal skills, ability to remain constructive and civil in difficult situations. ・Ability to deliver timely and professional communications (oral and written) with precision and clarity to all levels of the organization. ・Experience working on a global team and sharing knowledge. ・Experience with computers and entering data into databases. ・Good analytical/problem-solving skills. ・Education Requirements:Bachelors Degree (or equivalent work experience) in physical or biological sciences, engineering or other technical area. ●Additional Preferences: Experience in technical report writing. Work under pressure on multiple tasks concurrently and meet deadlines in a fast-paced work environment with frequent interruptions and changing priorities. Proven ability to think and analyze from a process perspective. Project management skills. Process information to identify linkages and trends and apply findings to compliance strategies as well as to individual assignments. Work independently as well as collaboratively within a global team environment. Deliver constructive feedback to customers while providing a high level of customer service. Ability to influence and manage change/conflict. Establish and maintain effective working relationships at all levels internal and external to this company. Ability to think on your feet and be pragmatic in decision making. ※更なる詳細事項は、カウンセリング（面談）時にお伝えします。
企業データ	会社名 外資系製薬メーカー 資本金 100億円以上 従業員数 1000名以上 事業内容 医薬品・畜産薬の製造、輸入、販売、研究開発
Recruiting No.	02000692000979
ひとことコメント	創業時から研究開発に注力。特化した分野で確かな地位を築く。学閥なし、プロパー優遇なし、職位による差別なし。人物をフェアに見る社風。