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浏览职位招聘观察购买与订阅
Sigma-Aldrich logo
默克生命科学
Associate Scientist 2
立即应聘

Associate Scientist 2

发布于 5 个月前

普通员工/个人贡献者

Rockville, Maryland, United States
初级经验
全职员工
仅现场办公
硕士
研究与开发 (研发)
实验室操作
数据分析
检测方法开发
生物安全测试
cGMP
GLP
LIMS
SOP

AI 估算 · 35k–54k

该职位为生命科学领域研发岗,技术要求高且需遵守严格法规,市场价值较高。

职位详情

关于这个职位

这是一个在生物安全测试领域的研发岗位,主要负责支持新检测方法的开发并将其应用于商业化服务

您将在实验室中独立或协作完成测试,确保数据的科学性和完整性,并严格遵守行业标准与法规

最低要求

最低任职要求:

科学学科(如生物学、化学、生物化学等)硕士学位,并具有6个月以上的科学/实验室经验
或科学学科学士学位,并具有1年以上的科学/实验室经验
或科学学科副学士学位,并具有2年以上的科学/实验室经验
或高中文凭/GED,并具有5年以上的科学/实验室经验

工作职责

工作职责:

在实验室安排的限制下,以最少的监督进行指定的测试
根据标准操作规程(SOP)和法规(cGMP和GLP)执行测试
为研究的完整性维护完整和全面的记录
进行详细观察并记录结果
始终保持高水平的工作质量
根据SOP和测试程序操作和维护实验室设备
对检测批次/实验室记录进行同行评审,以确保“一次做对”(RFT)
在测试和日常任务中使用适用的计算机程序(如Word、Excel、Oracle、LIMS、BRIQS等)
运用问题解决/故障排除技能
向研究管理部门沟通偏差/事件、进展和中期结果
向主管报告可能影响数据质量和准确性的偏差或因素
保持对实验室程序和检测方法的了解
按要求创建/修订SOP、实验室记录和其他相关文件
根据需要/指派协助培训实验室人员
提出改进标准实验室技术、协议、流程和设备的想法和建议
遵守公司健康和安全规定及程序
执行其他指派的任务

优先资格

优先资质要求:

具备相关实验室实践、技术、设备、材料和数学计算的经验
具备相关计算机程序的基本技能
有效的口头和书面沟通能力
能够在独立和团队环境中良好工作

AI 洞察

优缺点分析

优点

  • Gain valuable, hands-on experience in a critical and regulated field (biosafety testing) within a global life science leader, enhancing your technical resume.
  • Opportunity to work on the commercialization of new services, providing exposure to the intersection of R&D and business applications.
  • Structured environment with clear protocols (SOPs, GMP/GLP) offers excellent training in compliance and quality standards, highly valued in the industry.
  • Potential for skill development in both laboratory techniques and data management software, building a versatile technical profile.
  • The work requires meticulous attention to detail and strict adherence to procedures, which can be repetitive and demand high levels of concentration.
  • Operating under regulatory constraints (cGMP/GLP) adds pressure to maintain flawless documentation and avoid errors, with little room for deviation.
  • As an entry-level scientist role, initial tasks may be routine, requiring patience and initiative to seek out more complex responsibilities and growth.
  • This role is ideal for detail-oriented science graduates seeking to launch their career in a structured, regulatory-driven laboratory environment within the pharmaceutical or life sciences sector.

缺点 / 挑战

暂无明显挑战项

角色解读

  • With experience, you could advance to a Senior Scientist role, taking on more complex project leadership, method optimization, or validation responsibilities.
  • Career paths may branch into specialized areas like Quality Assurance, Regulatory Affairs, or Project Management within the life sciences and pharmaceutical industry.
  • Long-term opportunities include moving into laboratory management, technical training roles, or contributing to innovative research and development initiatives.
  • Conduct biosafety testing and assay development in a laboratory setting, following strict SOPs and regulatory guidelines (cGMP/GLP).
  • Document all experimental procedures, observations, and results meticulously to ensure data integrity and traceability for commercial applications.
  • Operate and maintain specialized lab equipment, and utilize software systems like LIMS and BRIQS for data management and analysis.
  • Participate in quality control through peer review of records and contribute to improving laboratory protocols and processes.
  • Strong foundation in biological or chemical sciences, with hands-on laboratory experience in techniques relevant to biosafety or assay development.
  • Proficiency in adhering to detailed protocols (SOPs) and regulatory standards like GMP/GLP, ensuring compliance and data accuracy.
  • Competence in using laboratory software and tools (e.g., LIMS, Microsoft Office) for documentation, data entry, and basic analysis.
  • Effective communication skills to report findings, deviations, and collaborate within a team-oriented research environment.

申请策略

  • Research MilliporeSigma's specific service offerings in biosafety testing to tailor your application and show how your skills align with their business needs.
  • In your cover letter or interviews, convey your understanding of the importance of data integrity and regulatory compliance in this field.
  • Emphasize any hands-on laboratory experience, specifying the techniques used (e.g., cell culture, ELISA, PCR) and the context (academic projects, prior roles).
  • Detail your experience with documentation, quality control, or working under specific protocols or standards, even from academic settings.
  • Highlight proficiency with relevant software mentioned (Microsoft Office, any LIMS or data analysis tools) and provide concrete examples.
  • Showcase instances of teamwork, problem-solving in a lab, or effectively communicating technical information, as these are key soft skills for the role.
  • Familiarize yourself with Good Laboratory Practice (GLP) and Good Manufacturing Practice (cGMP) principles, as they are central to the job.
  • Brush up on basic data management and analysis skills, particularly using Excel, and explore introductory resources on Laboratory Information Management Systems (LIMS).

面试指南

  • Use the STAR method (Situation, Task, Action, Result) to structure your answers, providing specific, concise examples from past experiences.
  • For technical questions, clearly explain the principle, your hands-on role, and the outcome, emphasizing attention to detail and adherence to methods.
  • When discussing challenges or deviations, focus on your systematic approach to problem-solving, communication with supervisors, and commitment to data integrity.
  • Describe your experience with a specific laboratory technique relevant to biosafety or assay development.
  • Tell us about a time you had to follow a strict protocol or SOP. How did you ensure accuracy and compliance?
  • How do you handle and document an unexpected result or deviation during an experiment?
  • What experience do you have with laboratory software or data management systems?
  • Describe a situation where you had to work effectively as part of a team on a technical project.

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