Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Manufacturing Lead Excellence位置：
Europe/Middle East/Africa, South Africa, Gauteng, Johannesburg工作地点：
完全现场你会做什么
Four different pillars to achieve the above goal;
Day-to-Day Support: The Production Intern (PI) is responsible for the provision of support to the assigned production area to ensure compliance with current Good Manufacturing Practices and company standard operating procedures.
Process Knowledge: The PI must understand the production processes for which he/she is responsible. This scopes scientific understanding of the process, know-how on production equipment within the process and identifying risks to ensure execution in compliance to cGMP and company policies.
Product Stewardship: This pillar scopes the ownership of the product end-to-end in the area of responsibility. The PI will monitor the processes to ensure they are capable and in control, will participate in any changes (change controls, product transfers, etc) and will facilitate root cause investigation in case deviations happen.
Continuous Improvement: The PI should identify opportunities for process improvement and participate in activities that contribute to leaner and efficient processes in the assigned department. The PI will identify improvement areas, evaluate risks and execute following Good Documentation Practices e.g. Change Control.
Duties / Responsibilities:
Based on the four pillars;
Ensure that production processes within area of responsibility are performed in accordance with relevant Standard Operating Procedures, Work Instructions and current Good Manufacturing Practices.
Drive and support close out of all relevant compliance related audit findings.
Responsible for performing line-openings, line closures, and in process checks according to legislative and company requirements.
Responsible for the supervision of manufacturing processes (dispensing, raw material additions, compression SOR etc.)
Update GMP documents (SOP, WI, PPI and PI etc), as required and train accordingly.
Ensure effective communication to all relevant parties.
Ensure all production documentation and processes are completed as per cGMP guidelines.
Process Knowledge
Understand process flow
Understand process controls as well as risks
Understand technically the product and its composition
Understand process/product cost structure
Support training to operators
Product Stewardship
Ensure compliance with GMP, EHS and Quality policies during execution of the production plan and all related tasks. Ensures compliance with work instructions and relevant SOP's during execution of production processes.
Perform departmental GMP self-inspection audits – both planned and ad hoc to ensure that GMP standards are met and maintained.
Support regulatory with technical documents
Continuous Improvement:
Drive, contribute and support continuous improvement initiatives within the assigned department.
Assist Production Pharmacist and departmental led in the planning and implementation of improvement projects within the assigned department
Implementation of improvement projects within the assigned department
Perform internal assessments in production areas and develop corrective actions to strengthen cGMP
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