## QC Specialist申请: Burnaby, BC: 全职: 今天发布: R50791**我们提供** 在赢创(Evonik),您将成为一家活跃于全球的化工企业的一员,并在各大关键技术与行业的交汇处开展工作。无论是健康营养、低碳出行还是绿色能源——我们的产品正在改善人们的生活,惠及当下与未来。 根据我们的理念,成功并非单打独斗,而是源于多元化的思想和团队合作。无论是在自然科学还是工程领域,无论是职场新人还是拥有丰富经验的专业人士,无论是在业务、生产还是其他任何领域——我们彼此激励,不论挑战多么艰巨。加入我们,成为“特别的一部分(Part of Something Special)”! **欢迎了解我们丰富多样的福利待遇:** https://www.evonik.com/en/careers/why.html **在这里,您可以直接通过我们的员工了解更多关于赢创的信息:** https://www.evonik.com/en/news/meet-the-team.html**RESPONSIBILITIES**Leadership/ Functional:* Proactively collaborate with stakeholders of various functional groups to prioritize the work for QC to meet the business needs to achieve the best-in-class operation for a Contract Development and Manufacturing Organization (CDMO)* Be able to effectively influence QC team members to optimize the planning, daily and weekly QC schedules, and operational activities* Identify gaps and define implementation strategies to achieve operational efficiencies and improvementsOperational Excellence & Planning:* Act as a QC representative to provide operational input for clients' projects* Attend routine operational and project meetings; provide QC progress updates to Project Management and the site operational team* Bring strategic/ tactical plans into attainable QC actions to achieve on-time delivery of tasks and projects* Communicate status of QC activities to external stakeholders and project-related updated to QC Manager* -Prepare/revise and manage the QC master schedule / plans (including QC resource allocation and planning)



to ensure proper alignment with business plan and delivery schedules* Support the leading of the QC team to ensure all sample management and testing activities are performed efficiently and effectively, in accordance with approved SOPs, GxP requirements and expectations and EHSS requirements. Sample management includes cross-functional collaboration for RM sampling, arrangement of external testing, Utilities and Environmental Monitoring as well as proactive communication with those external labs regarding testing requirements and timelines for batch disposition.* Draft drug product specification & sampling plans* Ensure all stability projects are captured and maintained accurately in the QC system, which includes but is not limited to the following:* Prepare stability protocols accurately in accordance with the project requirements for internal and external review and approval in a timely manner* Ensure all stability samples are pulled and scheduled for testing within the defined timeframe* Support periodic inventory count of all stability samples performed by the assigned QC analyst(s)* Perform peer review and approval of QC data related to testing of raw material, in-process, release and stability materials* Support the team to assure all reference standards are received and managed accurately in accordance with site procedure,



includes but is not limited to:* Coordinate with Project Management to receive the reference standards from Clients* Coordinate the purchasing of the required reference standards* Accurately maintain the master list of reference standards; proactively manage the expiry/ re-test dating to assure adequate supply of standards are available for testing as per defined schedule* Participate in project(s) and temporary assignment(s) as assigned**REQUIREMENTS*** BSc. Or MSc. in Chemistry, Biochemistry, Microbiology, applied sciences or equivalent* Approximately 5 to 8 years of experience in the parenteral pharmaceutical or biopharmaceutical industry* Experience working in Quality Control is strongly preferred, with experience in project management, resource planning, and a CDMO workplace as assets* Proficient in real-life application of various program management/ resource planning tools (e.g., LEAN processes, Six Sigma, *etc.)* to drive operational excellence/ efficiencies* Proven time management and organizational skills to work in a fast-paced, regulated environment and manage multiple projects concurrently.* Demonstrated ability to think critically within applicable regulations for regulatory compliance and operational excellence* Excellent technical writing, problem-solving, and communication skills.* Detail oriented to assure accuracy of data and information.* Effective and professional interpersonal skills with abilities to collaborate with others across multiple functions.* Self-motivated with abilities to work in an undefined environment.* Flexibility in work hours may be required* Proficient in computing (e.g., Microsoft Word, Excel, PowerPoint, Visio, *etc.)* and performing appropriate data analysis and risk assessment**您的申请** 为了确保尽快处理您的申请以及保护环境,请您通过我们的职业门户在线申请。作为雇主,您可以在www.evonik.com/en/careers找到有关赢创的更多信息。 请将您的申请发送给 Talent Acquisition Manager,说明您的最早入职日期和薪资期望。如有疑问或需要更多信息,可拨打Evonik Candidate Support 的电话:+49201 177 4200。
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📌 QC Specialist (British Columbia)
🏢 Evonik group
📍 British Columbia