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：
Operations Director位置：
Asia Pacific, Indonesia, Jawa, Jakarta Raya工作地点：
完全现场你会做什么
Key Responsibilities
- Responsible for the development and implementation plan to support the production and new product implementation, including machine and process improvement
- Lead development/improvement, machine efficiency optimization, change over and waste reduction.
- Lead continuous improvement projects in key Production Performance include Productivity, Safety, Quality, Reliability and Cost
- Lead / co-operate with concerning department both inside and outside in order to ensure the new projects finished and deliver the Project Goals
- Conduct detail analysis and evaluation of existing manufacturing processes, identifying areas for improvement and appropriate solutions with the shopfloor and cross functional team as needed.
- Ensure machine is commissioned to meet process requirements and product specification
- Collaborate with production team member, Technical Operations and quality assurance teams to develop and implement process instructions (master batch records), standard operating procedures (SOPs) and work instructions.
- Initiates new or revisions of protocols/operating instructions specific to the project.
- Monitor and analyse daily, weekly and monthly performance metrics, such as OEE, OPE, cycle time, yield and scrap rate to manage production to meet the overall target.
- Identify and implement process control measures to ensure consistent quality and reduce process variation.
- Provide technical support and troubleshooting expertise to resolve process-related issues and improve overall equipment effectiveness (OEE).
- Follow and participate in process development (trial), process validation activities with the Technical Operations team
- Participate with cross-functional teams to drive root cause analysis, corrective actions and preventive measures.
- Provide training and guidance to production teams on new processes, procedures and equipment to ensure successful implementation and operation.
- Stay up-to-date with the latest advancements in process engineering technologies, methodologies and best practices.
- Coaches and mentors other Engineers in the development of solutions to problems specific or project
- Manage and provide coaching to operation team
What We Are Looking For
Required Qualifications
- Bachelor’s degree in Pharmacist & Engineering (Chemical, mechantron, mechanical)
- Knowledge and experience in wet and dry granulation, coated tablet, oral liquid, suspension, and packaging technology
- 3+ years of experience as a process engineer in a pharmaceutical or consumer healthcare manufacturing environment.
- Strong knowledge of process optimisation techniques, lean manufacturing principles, Six Sigma methodologies and statistical analysis.
- Proficient in process analysis, statistical analysis and simulation software is preferable.
- Excellent problem-solving and analytical skills with the ability to identify and resolve process issues.
- Working knowledge of process safety, risk assessment and compliance with regulatory standards.
- Effective communication skills to collaborate with cross-functional teams and stakeholders.
- Ability to manage multiple projects simultaneously and meet project targets.
- Project management skills is preferable.
Desired Qualifications
- Minimum 3 years of relevant work experience
- Experience in Manufacturing, Engineering, and Quality for OTC pharmaceutical products
- Experience with production/ packaging machines, automation (preferred), solid and liquid process technology
- Excellent communication and interpersonal skills
- Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook)
- Technical writing skills in English
- Operations experience within a cGMP environment in the pharmaceutical
- Ability to work during weekend working schedule, when required
- Project management certification (preferred)
What’s In It For You
- Competitive Benefit Package
- Learning & Development Opportunities
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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