Tech Ops Scientist-Process

Tech Ops Scientist-Process

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 Regional Cluster Lead NA EM SH

Location:

North America, United States, New Jersey, Summit

Local de trabalho:

Híbrido

O que você fará

The Technical Operations Scientist is responsible for providing support in Technical Operations for a broad range of consumer cosmetics, OTC drug products, and OTC monograph drug products while developing deeper knowledge and benchmarking with other sites.  The Scientist possesses a passion for innovation and continuous improvement.  Working under moderate direction, this individual collaborates cross-functionally as needed to provide technical support in the design, development, and implementation of technical solutions for new product introductions, cost reduction and critical initiatives. This individual is expected to implement technical aspects of projects, and interact with multi-functional teams to implement projects.

Key Responsibilities

• Support execution of or lead small to moderately sized project tasks per established timeline, including but not limited to the technology transfer process for New Products Introduction, Product Improvements, and new raw material qualification
• Uses scientific principles to resolve technical challenges while being able to articulate complex subject matter in clear, concise terms. Seeks guidance on more complex technical challenges. 
• Support the execution of the planned experimental design (i.e., sample collection, in-process testing, sample management, etc.).
• Prepares technical memos, reports, analyzes and summarizes data, and recommends conclusions based on scientific rationale.
• Support or lead in conducting troubleshooting supply issues, global change control (GCC), root cause analysis, and remediation for technical-related issues]
• Collaborate and work closely with Quality, Operations and R&D teams to ensure seamless transitions through the new product and project development lifecycle.
• Effectively execute technical transfer and life cycle management initiatives

What we are looking for

Required Qualifications

• Bachelor’s Degree is preferred in Pharmacy, Chemistry, Engineering, or related scientific field.
• 2+ years of industry experience related to process development is required.
• Experience within the Consumer, OTC, or Pharmaceutical industry is preferred. GMP experience is preferred.

Desired Qualifications

• General knowledge of product characteristics and their correlation with product/raw material performance and performance requirements of specific products or raw materials and the customer needs.
• General knowledge of scientific principles 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), engineered products and devices as applicable.
• General understanding of the process equipment and in-process control instruments.
• General process knowledge in a few of the processes such as Mixing, Filling, Liquid dosage, Solid dosage, Liquid Packaging, Scale-up, Technology Transfer, Continued Process Verification, Process Development, as applicable.
• General knowledge of regulatory requirements in the development, validation, and manufacture of consumer cosmetic and OTC monograph drug products (regulatory agencies such as, FDA, MHRA, Health Canada, AIFA etc.).
• Strong analytical skills are required. Excellent technical writing skills are required. Experience with MS Word, Excel and Project software packages is required. Excellent interpersonal, influencing, communication, listening, negotiating and problem-solving/decision-making skills are preferred.

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.