For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
The Junior Analyst is responsible for performing or managing technical laboratory activities in support of client studies or procedures. He/She will perform or oversee analysis of data for quality and completeness and determines if results are as expected. In addition, this individual is responsible for recording data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.
Roles & Responsibilities:
- Performs all laboratory functions as tasked with high degree of accuracy and strict adherence to Company’s quality requirements.
- Maintains proper records that are compliant with good documentation practices (GDP) and data integrity requirements, for all testing and test-related activities (e.g. raw data sheets, usage log books, and all other records).
- Generates reports for all tests performed in an accurate and timely manner, ensuring that targets are met for accuracy and turnaround time.
- To prepare media and other materials used for test services, including washing of glassware and depyrogenation
- To perform Environment monitoring as required
- To perform QC of media and lab consumables as required
- Performs good housekeeping and maintenance of the laboratory, especially in the area of responsibility.
- Prepares client test protocols, facilitates training of other analysts for the approved client test protocols, and updates protocol database.
- Generates or revises standard operating procedures (SOPs) relating to area of responsibility during routine document review or when there is a regulatory update.
- Participates in investigations (e.g. root cause analysis, impact analysis, risk assessment, corrective action, etc.)
- Contributes significantly to the activities of the assigned technical committee, as per the duties and responsibilities designated to the committee.
- Provides support during external and internal audits for the areas of responsibility.
- Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements.
- Participate in method development and validation of routine and customised testing services.
- Participate in the establishment of customised routine testing services and validations that are in compliance with the latest regulatory and/or customer requirements.
- Conducts test demonstrations to clients during site visit or when necessary.
- Documents and reports to immediate superior any event that has occurred at the laboratory which could, in his/her reasonable opinion, potentially result in a hazardous, litigious or quality-compromising situation.
- Adheres to Company Policies and Procedures.
- Ensures relevant Health and Safety requirements are adhered to, including undertaking any mandatory training as required.
- Undertakes any other duty or responsibility, at the request of your manager that may be required within reason within the remit of your role.
Job Qualifications
- Diploma / Bachelor of Science or any related field
- Preferred minimum 1 year of working experience in an ISO17025 / cGMP laboratory environment
- Meticulous, self-starter and motivator
- Good technical understanding and judgement
- Good interpersonal and communication skills across cultures
- Team player with ability to work in cross-functional teams as well as independently depending on requirement of task on hand
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
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当您向我们申请工作时,您会非常小心和努力。请放心,我们将同样努力寻找适合您的职位。我们的招聘流程如下:
职位搜索
了解 CRL、我们的文化以及我们为何开展我们的工作,同时寻找与您的兴趣和专业知识相匹配的职位。
申请
创建个人资料并申请您感兴趣的多个角色。
注意:根据职位的不同,您可能需要在申请中包含简历。评估和申请审查
如果需要,请完成评估,以确定该职位是否适合您,反之亦然。招聘人员将根据职位要求审查您的简历和资格,并确定后续步骤。
注意:在此过程中的任何时候,您都可以登录您的个人资料以查看您的申请状态。面试
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注意:Charles River 根据我们的 DNA(关注、领导力、责任心和团队合作)利用基于技术和行为的方法来提问。请熟悉 DNA 并准备好将您的经历与它们联系起来。工作机会和入职
通过电话或电子邮件从 Charles River 招聘人员或招聘经理处接收有竞争力的录用通知书。录用通知书将包括您的头衔、工资、地点和其他相关信息。
注意: 接受后,您将与招聘人员一起确认入职日期,并在入职之前收到需要以电子方式完成的文件。对于美国的职位,一旦您接受,您将需要进行就业前药物筛查并通过犯罪背景调查。特色职位
Charles River每时每刻都在发生重要的事情。这意味着您可以探索令人兴奋的新职业机会。今天就申请吧!
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每时每刻
在 Charles River,您将能够为令人难以置信的突破做出贡献,同时体验令人兴奋的成长和发展机会。
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运营助理
帮助跟踪和指导操作改进
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项目协调员
管理关键设施相关项目
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采购主管
管理采购、运输、库存和收货
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副经理
推动持续改进项目和设施建设
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萨拉·霍塔奈宁,工商管理硕士
芬兰库奥皮奥
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