Tech Ops Scientist - Pilot Plant

Tech Ops Scientist - Pilot Plant

O que fazemos

At Kenvue, percebemos o extraordinário poder do cuidado diário. Construída com base em mais de um século de herança e enraizada na ciência, somos a casa de marcas icônicas - incluindo NEUTROGENA®, AVEENO®, TYLENOL,® LISTERINE,® JOHNSON'S® e BAND-AID® que você já conhece e ama. A ciência é a nossa paixão; O cuidado é o nosso talento.

Quem somos

Nossa equipe global é de ~ 22.000 pessoas brilhantes com uma cultura no local de trabalho onde cada voz é importante e cada contribuição é apreciada. Somos apaixonados por insights, inovação e comprometidos em entregar os melhores produtos aos nossos clientes. Com experiência e empatia, ser um Kenvuer significa ter o poder de impactar milhões de pessoas todos os dias. Colocamos as pessoas em primeiro lugar, nos importamos ferozmente, ganhamos confiança com a ciência e resolvemos com coragem - e temos oportunidades brilhantes esperando por você! Junte-se a nós para moldar nosso futuro - e o seu. Para obter mais informações, clique em aqui.

Role reporta para:

Tech Ops Senior Manager Process Science

Location:

North America, United States, Pennsylvania, Lititz

Local de trabalho:

Totalmente no local

O que você fará

The Scientist supports Technical Operations R&D Pilot Plant for a broad range of pilot scale consumer cosmetics, OTC drug products, and OTC monograph drug products. Primary activities require the use of basic scientific knowledge while developing a solid understanding of the principles of manufacturing processes and a passion for innovation and continuous improvement. This individual is expected to implement technical aspects of projects, report metrics, and interact with multi-functional teams to implement projects.

 

Additionally, the Scientist will ensure quality and compliance through GMP training, adhere to strict compliance with procedures and GDP, exercise the highest level of integrity in tasks performed, identify, report, and seek corrections for deviations noted in the workplace and embrace a behavior of employee involvement and commitment to doing the job right the first time.

• Ensure quality and compliance in all actions by:

  • Attending GMP / EHS&S (Environmental, Health, Safety & Sustainability) training

  • Adhering to strict compliance with procedures applicable to the role.

  • Exercising the highest level of integrity in the tasks that they perform.

  • In a timely and prompt manner, identifying, reporting, and seeking correction for deviations noted in the workplace.

  • Accepting the behavior of employee involvement and commitment to doing the job right the first time.

• Uses scientific principles to resolve moderately sophisticated technical challenges while being able to articulate complex subject matter in clear, concise terms.

• Support execution of or lead small to moderately sized project tasks per established timeline, including any activities associated with production of Pilot scale batches and Clinical Supplies operations.

• Work with project teams to manage and execute batch requests in the pilot plant

• Responsible for Clinical Supplies Project Execution and Coordination including repacking and labeling operations for clinical supplies

• Support the execution of the planned experimental design (i.e., sample collection, in-process testing, sample management, etc.).

• Support with report preparation by compiling and analyzing and summarizing data using appropriate analysis techniques.

• Support change control deliverables/documentation, investigations, and corrective/preventative actions.

• Support or lead conducting investigations related to product out of specification or process deviation, stability deviation, consumer complaints, and other investigations as applicable.

• Conduct laboratory experimentation as needed related to investigations and root cause analysis.

• Support or lead in conducting troubleshooting of scale-up issues, root cause analysis, and remediation for technical-related issues. Corrective Action and Preventative Action (CAPA) implementation and follow up to ensure CAPA effectiveness to address investigation and the root causes related to process deviation, stability, out of specification, out of trend, out of expectation, complaints, and others as applicable.

• Support or lead in manufacturing process improvements through data analysis, identification of critical process parameters, the proposal of alternate process modifications, assistance in conducting DOE to determine the best processes.  

• Support in writing technical documentation including but not limited to Manufacturing Work Instructions, Fill Records, Cleaning Procedures, Technical Justifications, and INV reports.

• Works with general/moderate direction. Provide direction and mentorship to contractors.

• Decisions made at this level are limited in scope and authority.

• Support and execute End to End Pilot Tasks including material management, cleaning and sanitization of small-scale equipment, labeling, shipping, document control/closure, etc.

• May assist in process or equipment validation.

O que você ganha com isso

$72,675.00 - $102,600.00

Isso leva em consideração vários fatores, incluindo local de trabalho, habilidades do candidato, experiência, nível de educação e outros fatores relacionados ao trabalho.

A Kenvue tem orgulho de ser um empregador de oportunidades iguais. Todos os candidatos qualificados serão considerados para o emprego com base no mérito, independentemente de raça, cor, religião, sexo, orientação sexual, identidade de gênero, idade, nacionalidade ou status de veterano protegido e não serão discriminados com base na deficiência.