NA Cleaning Validation Principal

NA Cleaning Validation Principal

Cosa facciamo

A Kenvue, ci rendiamo conto dello straordinario potere della cura quotidiana. Costruiti su oltre un secolo di tradizione e radicati nella scienza, siamo la casa di marchi iconici, tra cui NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® e BAND-AID® che già conosci e ami. La scienza è la nostra passione; la cura è il nostro talento.

Chi siamo

Il nostro team globale è composto da ~ 22.000 persone brillanti con una cultura del posto di lavoro in cui ogni voce conta e ogni contributo è apprezzato. Siamo appassionati di intuizioni, innovazione e impegno a fornire i migliori prodotti ai nostri clienti. Con competenza ed empatia, essere un Kenvuer significa avere il potere di avere un impatto su milioni di persone ogni giorno. Mettiamo le persone al primo posto, ci prendiamo cura di noi, ci guadagniamo la fiducia della scienza e risolviamo con coraggio - e abbiamo brillanti opportunità che ti aspettano! Unisciti a noi per plasmare il nostro futuro e il tuo. Per ulteriori informazioni, fare clic su here.

Role riporta a:

Tech Ops Process Science Leader - NA

Posizione:

North America, United States, Pennsylvania, Fort Washington

Luogo di lavoro:

Ibrido

Cosa farai

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.).

Cosa c'è per te

$0.00 - $0.00

Questo tiene conto di una serie di fattori tra cui il luogo di lavoro, le competenze del candidato, l'esperienza, il livello di istruzione e altri fattori legati al lavoro.

Kenvue è orgogliosa di essere un datore di lavoro per le pari opportunità. Tutti i candidati qualificati saranno presi in considerazione per l'impiego in base al merito, indipendentemente da razza, colore, religione, sesso, orientamento sessuale, identità di genere, età, origine nazionale o stato di veterano protetto e non saranno discriminati sulla base della disabilità.