Tech Ops Staff Scientist - Process

我們做什麼

在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

我們是誰

我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

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你會做什麼

The Technical Operations Staff Scientist is responsible for providing a significant degree of scientific expertise in Technical Operations for a broad range of consumer cosmetics, OTC drug products, and OTC monograph drug products.  This position can work in either our Summit NJ location or our Fort Washington PA location. Primary activities require possessing a solid understanding of principles of manufacturing processes and material interactions with a passion for innovation and continuous improvement.  Working under minimal direction, this individual collaborates cross-functionally to lead and provide technical support in the design, development, and implementation of technical solutions for cost reduction and critical initiatives. This individual is expected to assess, determine and implement technical aspects of projects, and interact with multi-functional teams to implement projects.  This position plays a role in ensuring robust product development, process optimization, and adherence to quality standards. The ideal candidate will have a strong background in biopharmaceutical process development and cross-functional collaboration.

Key Responsibilities

• Lead moderate to large sized project per established timeline, including but not limited to the technology transfer process for New Products Introduction, Product Improvements, and new raw material qualification . 
• Applies scientific principles to resolve complex technical challenges while being able to articulate complex subject matter in clear, concise terms. 
• Designs, coordinates, and implements project tasks per established timeline including the execution of planned experiments (i.e., sample collection, in-process testing, sample management, etc.).
• Leads the technology transfer process for New Products Introduction, Products Improvements, and new raw material qualification.
• Oversees, writes, reviews, or approves technical documentation.  Reviews and approves reports and confirms conclusions based on scientific analysis and rationale.
• Leads technical aspects for solving critical supply issues, global change control (GCC), root cause analysis, and remediation for technical-related complex issues
• Collaborate and work closely with Supply Chain, R&D, Quality Assurance, Regulatory Affairs, and other departments to ensure seamless transitions through new product and project development lifecycle.
• Advocates and leads initiatives to drive execution excellence and timely realization. Identify and recommend new agile ways and risk-based approaches to accomplish goals and objectives Provide direction and mentorship to scientists and co-ops

What we are looking for

Required Qualifications

• Bachelor’s Degree is preferred in Pharmacy, Chemistry, Engineering, or related scientific field.
• 6+ years of industry experience related to process development is required.
• Experience within the Consumer, OTC, or Pharmaceutical industry is preferred. GMP experience is preferred. Experience in a highly regulated environment is required.
• Strong knowledge related to process/product development is required.  Previous experience overseeing complex projects in a matrixed environment is required.

Desired Qualifications

• Strong 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.
• Strong Knowledge of performance requirements of specific products or raw materials and the customer needs.
• Strong Knowledge of product design, characteristics, the procedure (how the product works, anatomy), and competitive products.
• Strong 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), as applicable.
• Strong Understanding of the process equipment and in-process control instruments.
• Strong Knowledge in 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.
• Strong Knowledge and understanding of equipment design, cleaning procedures, analytical methods, sampling requirements, and in the collection and evaluation of data, from the process design stage through commercial production.
• Strong Knowledge and ability to apply selected lean tools to a situation. Tools include- 5S, Visual Management, Mistake proofing, kanbans/ rhythm wheels, and other Lean principles.
• Strong Knowledge of statistical methods such as Six Sigma, statistical tools for data analysis. (i.e., CpK, Probability of failure), and risk management tools (FMEA, etc.).
• Strong 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.
• Strong 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.

對您有什麼好處

這考慮了許多因素，包括工作地點、候選人的技能、經驗、教育水準和其他與工作相關的因素

Kenvue 很自豪能成為一個機會均等的雇主。所有合格的申請人都將根據業績獲得就業考慮，不分種族、膚色、宗教、性別、性取向、性別認同、年齡、國籍或受保護的退伍軍人身份，並且不會因殘疾而受到歧視。