Tech Ops Scientist-Process

Tech Ops Scientist-Process Kenvue - 3.1 Summit, NJ Job Details $72,675 - $102,600 a year 3 hours ago Benefits Paid holidays Qualifications Microsoft Word Technical report writing Project management software Full Job Description Kenvue is currently recruiting for a: Tech Ops Scientist-Process What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including

NEUTROGENA

®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and

BAND-AID

® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours.

Role reports to:

Tech Ops Regional Cluster Lead

NA EM SH

Location:

North America, United States, New Jersey, Summit Work Location:

Hybrid What you will do 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. What's in it for you Annual base salary for new hires in this position ranges: $72,675.00 - $102,600.00 This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors. Competitive Benefit Package• Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region

Note:

Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.