Process Engineer | Southampton, PA

Detailed Information

  • Location: Fort Washington, PA

  • Company: Johnson & Johnson Consumer

LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers.

With expertise and empathy, being a Kenvuer means to have the power to impact life of 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. What You Will Do The Process Engineer 2 supports Manufacturing Science and Technology for a broad range of 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.

Working under general/moderate direction, this individual will collaborate cross-functionally with Operations, Marketing, Quality Assurance, Research and Development (R&D), and other function as needed to provide technical support in the design, development, and implementation of technical solutions for cost reduction and critical initiatives. This individual is expected to implement technical aspects of projects, report metrics, and

interact with multi-functional teams to implement projects.

Additionally, the Process Engineer will ensure quality and compliance through GMP training, adhere to strict compliance with procedures, 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. Key Responsibilities: 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 but not limited to the technology transfer process for New Products Introduction, Products Improvements, and new raw material qualification.

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, corrective/preventative actions, and new product release data collection and analysis. 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 supply issues, global change control (GCC), 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, and assistance in conducting scale-up activities including pilot-scale and validation as required. Support in writing technical documentation including but not limited to Product Impact backssment, Technical Justifications, manufacturing work instructions, and INV reports. Works with general/moderate direction. Provide direction and mentorship to co-ops.

Decisions made at this level are limited in scope and authority. May assist in process or equipment validation. Qualifications What We Are Looking For Required Qualifications A minimum of a BS in Science or Equivalent Generally, requires (2-4) years related experience. Previous experience in a healthcare manufacturing environment desired but not required. 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 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. General 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. General knowledge of statistical methods such as Six Sigma, statistical tools for data analysis. (i. e. Cp K, Probability of failure), and risk management tools (FMEA, etc.

). General 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. 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 Competitive Benefit Package Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More! Learning & Development Opportunities Employee Resource Groups Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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