Senior Process Improver

Senior Process Improver

私たちがしていること

Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。ケアは私たちの才能です.

Who We Are

私たちのグローバルチームは~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。 私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々に影響を与える力を持つことを意味します。私たちは人を第一に考え、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細についてはをクリックしてくださいhere.

Role reports to:

Make Excellence Cont Improvement Mngr

Location:

North America, United States, Puerto Rico, Las Piedras

勤務地:

フルオンサイト

あなたがすること

The Senior Process Improver is responsible for monitoring, analyzing data of business and quality trends to identify improvement opportunities for processes and systems. Lead/Work with champions and with the Make Excellence Continuous Improvement Manager, chartering and scoping high impact process, Process Excellence (PE) Six Sigma, and Lean projects.

Responsibilities:

• Leads and guides cross functional, multilevel diverse technical teams, to assure projects are implemented using PE/Lean tools.
• Applies intensive and diversified knowledge of Six Sigma/DMAI2C/Lean principles and Risk Management practices in broad areas of assignments.
• Provides training and mentoring on tools for process evaluation and enhancement (Lean/Six Sigma, FMEA).
• Able to generate business cases, justify opportunities and present them to different levels of the organization.
• Acts as a change agent across functions.
• Understands business impact of his/her technical actions. Follows and observes all regulatory requirements (GMP's, ISO, FDA, internal policies) applicable to area of responsibility.
• Lead or supports very complex and high impact PE Six Sigma and LEAN Projects
• Monitor and review critical to quality and business measures and present them to the plant staff team.
• Work with champions and with the Make Excellence Continuous Improvement Manager, chartering and scooping high impact projects.
• Review PE Projects to assure the appropriate use of tools.
• Provide resource requirements, prioritization, and project recommendations.
• Reviews, analyze data of quality and business trends to identify improvement opportunities for processes and systems.
• Communicate project status updates to all stakeholders, including executive management, as needed.
• Dispose adequately recycling materials following the environmental, health and safety procedures to avoid increase in non-hazardous waste generation.

Qualifications:

• Bachelor’s degree in science and/or Engineering.
• At least 6 to eight 8 years of experience within the following areas: process engineering, project management, process validation, manufacturing, process excellence and/or quality.
• Experience leading process excellence and/or lean manufacturing projects.
• Experience working with solid dosage manufacturing under a regulated environment.
• Bilingual (English/Spanish-oral and written).
• Knowledgeable in GMP, OSHA and other pharmaceutical industry applicable regulations.
• Project Management negotiation, influencing and presentation skills. Should have basic knowledge in Microsoft Office software applications (Word, Excel, PowerPoint & Outlook).
• Knowledge in Minitab and a Project Management software is required.
• Process Excellence or Lean Green Belt certification required, or Black Belt certifications will be highly desirable.
• Able to travel in and outside of Puerto Rico. Able to work extra hours and to respond to emergency calls that require returning to the company after regular working hours of the business.
• Able to support other departments or projects according to business needs.

それは何ですか

$90,950.00 - $128,400.00

これは、勤務地、候補者のスキル、経験、教育レベルなど、多くの要素を考慮に入れています。その他の仕事関連の要因.

Kenvueは機会均等雇用者であることを誇りに思っています。人種、肌の色、宗教、性別、性的指向、性同一性、年齢、出身国、または保護された退役軍人の地位に関係なく、すべての資格のある応募者は、能力に基づいて雇用の検討を受け、障害に基づいて差別されることはありません。