这是你的时刻

这是你的时刻

Senior Technician – BioPhysical

  • 需求编号#: 224628_en_US
  • Wayne, PA, US
  • 1st
  • 全职

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For 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

Perform multiple routine biophysical methods, data interpretation, and reporting independently as specified in standard in house SOPs, Client Test Methods and other written procedures.  Under direct supervision, perform method development work as assigned.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  
•    Independently perform laboratory activities including but not limited to reagent preparation, laboratory maintenance / monitoring of equipment, routine testing of client samples, and the generation of routine GMP and R&D grade reports.
•    Become proficient in performing a minimum of 4 of the below listed BioPhysical department routine testing methods with a high degree of reliability, efficiency and accuracy: 
o    Analytical Ultracentrifugation (AUC)
o    Size Exclusion HPLC-MALLS (SEC-MALLS)
o    Differential Scanning Calorimetry (DSC)
o    Intrinsic Tryptophan Fluorescence (ITF)
o    Fourier Transform Infrared (FTIR)
o    Dynamic Light Scattering (DLS)
o    Protein Binding via SPR-Biacore
o    Circular Dichroism (CD)
•    Maintain excellent laboratory techniques including: 
o    pipetting 
o    weighing material on an analytical balance
o    reagent preparation 
•    Update sample-tracking databases and maintain chemical/consumables inventory for the laboratory.
•    Analyze data and report results of experiments and procedures .
•    Competently perform Technical Review for Routine data generated by staff. This includes Review of reports, raw data, or any other data produced by the group to ensure data packages are complete and compliant.
•    For both cGMP and R&D grade routine testing, generate biophysical data and technical reports on-time with respect to internal and client deadlines.  Maintain a weekly schedule to ensure all timelines are met.
•    Actively participate in laboratory instrumentation and equipment preventative maintenance and qualification programs. 
•    Maintain a safe working environment by adhering to Company policies or procedures. Actively participate in laboratory maintenance.
•    Comply with all pertinent regulatory standards regarding environs, equipment, and testing services.
•    Perform assay and equipment troubleshooting with minimal guidance from senior members of the group. 
•    Make detailed observations and maintain clear, accurate and timely documentation of all laboratory work. 
•    Independently compose high quality written reports such as deviation reports and change control documentation.
•    Create, review and edit SOPs, protocols and testing documentation. 
•    Follow all SOPs, CTMs and cGMPs as they relate to specific tasks
•    Assist in training of junior staff.
•    Participate in transferring and training of analytical technical staff on methodology for which qualification has been successfully completed. 
•    Maintain up to date training records on all procedures and protocols applicable to work duties. 
•    Ability to work in a structured and regulated environment 
•    Work productively in group situations as well as independently 
•    Perform all other related duties as required.

Job Qualifications

•    Education: Bachelor’s degree (B.S.) or equivalent in biochemistry, chemistry or related discipline. 
•    Experience: Minimum 3-5 years related industry experience in a biophysical science area in the Pharmaceutical, Biotech or contract (CRO) laboratory environment.  
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
•    Certification/Licensure: None.
•    Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred.  Knowledge of basic protein /peptide biophysical techniques and ability to operate typical laboratory equipment, specifically HPLC, spectrophotometer, dialysis/buffer exchange via SPE, and other laboratory equipment a plus.  Strong organizational and prioritization skills required. Attention to detail and accuracy a must.  Must possess excellent interpersonal skills to maintain communication across functional groups. Ability to collaborate effectively within a group environment. Able to communicate effectively (verbal and written) in a small group or one on one setting. Basic Microsoft Office skills are required. Ability to understand and use internal software programs such as LIMS required. 
 

Compensation Data

The pay range for this position is $31.25 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs.  Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

 

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.

 

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.

 

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

 

For more information, please visit www.criver.com.

还没准备好申请吗?

接收与您的背景和兴趣相匹配的职位提醒 – 直接发送到您的电子邮件收件箱!

帮助您找到属于您的时刻

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

通过与多元化的面试官会面来参与我们的包容性面试流程,他们将提供有关公司、文化和您的角色的信息,同时还会向您提出问题以评估您的技能、兴趣和专业知识。这也是您提问的好时机。

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。

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

通过与多元化的面试官会面来参与我们的包容性面试流程,他们将提供有关公司、文化和您的角色的信息,同时还会向您提出问题以评估您的技能、兴趣和专业知识。这也是您提问的好时机。 注意: Charles River 根据我们的 DNA(关怀、领导、拥有和协作)利用基于技术和行为的面试问题。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!

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。

  • 运营助理

    帮助跟踪和指导操作改进

  • 项目协调员

    管理关键设施相关项目

  • 采购主管

    管理采购、运输、库存和收货

  • 副经理

    推动持续改进项目和设施建设

  • 萨拉·霍塔奈宁,工商管理硕士
    芬兰库奥皮奥

萨拉·霍塔奈宁,工商管理硕士
芬兰库奥皮奥

运营助理

帮助跟踪和指导操作改进

项目协调员

管理关键设施相关项目

采购主管

管理采购、运输、库存和收货

副经理

推动持续改进项目和设施建设

关于Charles River

Charles River 是一家有着悠久历史的 CRO 公司。在这里,我们热衷于改善人们的生活质量。我们在全球设有 100 个分支机构,战略定位为协调全球资源并运用多学科视角来解决客户的独特挑战。我们的客户群包括全球制药公司、生物技术公司、政府机构、医院和世界各地的学术机构。

查尔斯河实验室的专业人员在最先进的实验室环境的实验台上通过显微镜进行观察。

支持您的福祉

您的奉献和热情为世界各地的人们带来了拯救生命的改变。我们致力于为您提供福利,提高您的生活质量。

财力

  • 收益+激励
  • 退休福利
  • 假期+外出度假
  • 认可
  • 员工援助基金

职业

  • 专业发展机会
  • 职业发展
  • 奖项
  • 教育支持

健康和保健保险

  • 员工福利支持
  • 家庭支持计划
  • 育儿津贴+家庭组建福利
  • 工作与生活平衡的灵活性

社会与社区

  • 包容文化
  • 11 个员工资源小组 (ERG),成员人数超过 3,000 人
  • 带薪志愿者休假的机会
  • 社区外展+配套礼物+参与活动

财力

  • 收益+激励
  • 退休福利
  • 假期+外出度假
  • 认可
  • 员工援助基金

职业

  • 专业发展机会
  • 职业发展
  • 奖项
  • 教育支持

健康和保健保险

  • 员工福利支持
  • 家庭支持计划
  • 育儿津贴+家庭组建福利
  • 工作与生活平衡的灵活性

社会与社区

  • 包容文化
  • 11 个员工资源小组 (ERG),成员人数超过 3,000 人
  • 带薪志愿者休假的机会
  • 社区外展+配套礼物+参与活动
查尔斯河实验室的专业人员在最先进的实验室环境的实验台上通过显微镜进行观察。

关于Charles River

Charles River 是一家有着悠久历史的 CRO 公司。在这里,我们热衷于改善人们的生活质量。我们在全球设有 100 个分支机构,战略定位为协调全球资源并运用多学科视角来解决客户的独特挑战。我们的客户群包括全球制药公司、生物技术公司、政府机构、医院和世界各地的学术机构。