NA Cleaning Validation Principal

NA Cleaning Validation Principal

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:

Tech Ops Process Science Leader - NA

Location:

North America, United States, Pennsylvania, Fort Washington

勤務地:

ハイブリッド

あなたがすること

The NA Cleaning Validation Principal is the NA leader for the oversight of cleaning and sanitization (C&S) procedures, development and validation across all segments for the NA Kenvue portfolio including cosmetic, nutritional, and drug product, as applicable.  This role is responsible for monitoring the cleaning and sanitization processes at our Internal Manufacturing sites, act as a SME (subject matter expert) and consultant for cleaning across our external manufacturing network and to ensure continued maintenance of the validated state.  In addition, this role will have global responsibility for all cleaning and sanitization procedures across all segments of the business. The person in this role is expected to provide a high degree of scientific expertise and leadership across the region. The individual provides departmental technical expertise and company leadership for cleaning activities while collaborating with Technical Operations, R&D, Quality and Operations to identify and address overall needs.

Key Responsibilities

• Provides oversight to the development and execution of cleaning and sanitization strategies for the NA internal manufacturing sites. Responsibilities include driving efficiencies, understanding existing limitations and developing technical solutions to address challenges and eliminate roadblocks.
• Leads the development of policy and procedures for the overall strategy for cleaning and sanitization for all segments and franchises globally
• Leads a global C&S Community of Practice to drive continuous improvement and enhancement of the C&S program
• Applies scientific principles to resolve technical challenges of high complexity while being able to articulate complex subject matter in clear, concise terms. Serves as a primary technical lead, on cross functional teams and sets technical direction, leads, and coordinates complex project activities and resources.
• Develop, plan, implement and/or coordinate major project activities in collaboration with other SME's, site and platform leadership or department management. Proposes and reviews program technical directions, benefits, costs, resource needs, schedules, risks, and risk mitigations.
• Identifies and stays abreast of emerging industry guidance related to cleaning and sanitization. Investigates and communicates innovation and trends.
• Develop recommendations on general validation guidelines and standards for processes and functional requirements.
• Oversee, write, review, and/or approve technical documentation, including but not limited to, validation documents, SOPs, Product Impact Assessments, Technical Justifications, manufacturing work instructions, and investigation (INV) reports. Contributes to defining department, project and / or program goals, tactics, and priorities. Defines objectives to achieve department, team, and individual goals/targets.
• Provides direction and mentorship to scientists, co-ops, and interns, as applicable.

What we are looking for

Required Qualifications

• Bachelor’s Degree is preferred in Pharmacy, Chemistry, Engineering, or related scientific field.
• 8+ years of industry experience is required.  Process knowledge related to all aspects of cleaning and sanitization is required.
• Previous experience in a healthcare manufacturing environment highly desired. GMP experience is preferred.

Desired Qualifications

• Proficient knowledge in cleaning and sanitization for liquid/semi-solid formulation development (i.e., solution, suspension, semi-solid), solid dosage development (i.e., immediate, and delayed release), and other formulation development (i.e., Nasal Spray, Eye drops, Lozenges, and sterile products), as applicable.
• Has a proven track record of meeting project objectives by successfully managing, tracking and implementing successful strategies in regard to scope, quality, time and cost.
• Communicates effectively to all levels of the organization, including effectively presenting information and responding to questions or complex inquiries.
• In-depth understanding of the consumer goods manufacturing.
• Proficient knowledge and understanding of equipment design, cleaning procedures, analytical methods, sampling requirements, and in the collection and evaluation of data, from the cleaning design stage through commercial production.
• Proficient knowledge and understanding of the Root Cause Analysis tools such as brainstorming, cause and effect analysis, fishbone diagrams, 5 why's, failure mode, effect analysis, RATIO, and others as applicable.
• Proficient in regulatory requirements in the development, validation, and manufacture of consumer cosmetic, nutritional, engineered and OTC drug products (regulatory agencies such as, FDA, MHRA, Health Canada, AIFA etc.).

それは何ですか

$0.00 - $0.00

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。