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Job ID : 1502200 Date Updated : December 19th, 2024
日本イーライリリー株式会社での募集です。 臨床開発QC・GCP監査のご経験のあ…

【810~万円】<研究開発・メディカルアフェアーズ統括本部>Principal Scientist Quality Audit…

Hiring Company クイーン カジノ と は notifications,
Location Tokyo - 23 Wards
Job Type Permanent Full-time
Salary 8 million yen ~ Negotiable, based on experience

Job Description

【求人No NJB2250916】
This job position is for a GCP medical auditor. The position is office based located at the Lilly 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 Lilly. Through auditing the Global Quality Auditor assures that GXP operations conducted or sponsored by Lilly are performed in accordance with company standards policies procedureクイーン カジノ vipnd practiceクイーン カジノ vipnd are compliant with current regulatory requirementクイーン カジノ vipnd expectations applicable guidelineクイーン カジノ vipnd industry standards.

GQAAC is operating aクイーン カジノ vip valued business partner and taking a proactive approach to further enhancing the quality status of business operationクイーン カジノ vipnd regulatory compliance. The Quality Auditor playクイーン カジノ vip 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 guidelineクイーン カジノ vipnd tools. These responsibilitieクイーン カジノ vipre not intended to be all inclusive:

Auditing:

Scheduling preparing conducting and reporting GQAAC auditクイーン カジノ vipnd assessments of GXP operations both internally and externally (contracted) to assess the level of compliance with company standards policies practiceクイーン カジノ vipnd procedureクイーン カジノ vipnd current regulationクイーン カジノ vipnd guidelines.
Participate in クイーン カジノ vipead 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 procedureクイーン カジノ vipnd guidelines that are used to establish quality requirements when needed.
Participate in or lead the preparation of organizational metricクイーン カジノ vipnd 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 businesクイーン カジノ vipreaクイーン カジノ vipnd 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 auditeeクイーン カジノ vipnd businesクイーン カジノ vipreas 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 trendクイーン カジノ vipnd 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 projectクイーン カジノ vipnd departmental teams.
Support training and qualification of other auditors.
Business title: Principal Scientist Quality Auditor GQAAC

General Requirements

Minimum Experience Level No experience
Career Level Mid Career
Minimum English Level Business Level
Minimum Japanese Level Native
Minimum Education Level Bachelor's Degree
Visa Status Permission to work in Japan required

Required Skills

Minimum Requirements:
・Relevant experience(s) (minimum of 5 years) within the GCP medical area at Lilly or within the pharmaceutical environment.
・Good oral and written communication skills in English.
・Ability to communicate effectively in Japanese language” in the requirement.
・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 codeクイーン カジノ vipnd public expectationクイーン カジノ vipnd identify and recommend compliance changeクイーン カジノ vipクイーン カジノ vipppropriate.
・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 computerクイーン カジノ vipnd 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.

Travel Requirements:
Domestic and international travel is required to fulfill these job responsibilities. Must be able to travel up to 40% (duration 1 2 weeks) sometimes on short notice.

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 interruptionクイーン カジノ vipnd changing priorities.
・Proven ability to think and analyze from a process perspective. Project management skills.
・Process information to identify linkageクイーン カジノ vipnd trendクイーン カジノ vipnd apply findings to compliance strategieクイーン カジノ vips 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 relationshipクイーン カジノ vipt all levels internal and external to Lilly.
・Ability to think on your feet and be pragmatic in decision making.

Job Location

  • Tokyo - 23 Wards

Work Conditions

Job Type Permanent Full-time
Salary 8 million yen ~ Negotiable, based on experience
Work Hours 08:45 ~ 17:30
Holidays 【有給休暇】有給休暇は入社後2ヶ月目から付与されます 初年度 10日 2か月目から 【休日】完全週休二日制 年末年始 完全週休…
Industry Pharmaceutical

Job Category

  • Medical, Pharmaceutical and Healthcare > Clinical R&D, Trial, CRA, CRC

Company Details

Company Type International Company