Process Engineer

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. For more information, click here.

Role reports to:

Location:

Work Location:

What you will do

Key Responsibilities

• Responsible for the development and implementation plan to support the production and new product implementation, including machine and process improvement
• Lead development/improvement, machine efficiency optimization, change over and waste reduction.
• Lead continuous improvement projects in key Production Performance include Productivity, Safety, Quality, Reliability and Cost
• Lead / co-operate with concerning department both inside and outside in order to ensure the new projects finished and deliver the Project Goals
• Conduct detail analysis and evaluation of existing manufacturing processes, identifying areas for improvement and appropriate solutions with the shopfloor and cross functional team as needed.
• Ensure machine is commissioned to meet process requirements and product specification
• Collaborate with production team member, Technical Operations and quality assurance teams to develop and implement process instructions (master batch records), standard operating procedures (SOPs) and work instructions.
• Initiates new or revisions of protocols/operating instructions specific to the project.
• Monitor and analyse daily, weekly and monthly performance metrics, such as OEE, OPE, cycle time, yield and scrap rate to manage production to meet the overall target.
• Identify and implement process control measures to ensure consistent quality and reduce process variation.
• Provide technical support and troubleshooting expertise to resolve process-related issues and improve overall equipment effectiveness (OEE).
• Follow and participate in process development (trial), process validation activities with the Technical Operations team
• Participate with cross-functional teams to drive root cause analysis, corrective actions and preventive measures.
• Provide training and guidance to production teams on new processes, procedures and equipment to ensure successful implementation and operation.
• Stay up-to-date with the latest advancements in process engineering technologies, methodologies and best practices.
• Coaches and mentors other Engineers in the development of solutions to problems specific or project
• Manage and provide coaching to operation team

What We Are Looking For

Required Qualifications

• Bachelor’s degree in Pharmacist & Engineering (Chemical, mechantron, mechanical)
• Knowledge and experience in wet and dry granulation, coated tablet, oral liquid, suspension, and packaging technology
• 3+ years of experience as a process engineer in a pharmaceutical or consumer healthcare manufacturing environment.
• Strong knowledge of process optimisation techniques, lean manufacturing principles, Six Sigma methodologies and statistical analysis.
• Proficient in process analysis, statistical analysis and simulation software is preferable.
• Excellent problem-solving and analytical skills with the ability to identify and resolve process issues.
• Working knowledge of process safety, risk assessment and compliance with regulatory standards.
• Effective communication skills to collaborate with cross-functional teams and stakeholders.
• Ability to manage multiple projects simultaneously and meet project targets.
• Project management skills is preferable.

Desired Qualifications

• Minimum 3 years of relevant work experience
• Experience in Manufacturing, Engineering, and Quality for OTC pharmaceutical products
• Experience with production/ packaging machines, automation (preferred), solid and liquid process technology
• Excellent communication and interpersonal skills
• Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook)
• Technical writing skills in English
• Operations experience within a cGMP environment in the pharmaceutical
• Ability to work during weekend working schedule, when required
• Project management certification (preferred)

What’s In It For You

• Competitive Benefit Package
• Learning & Development Opportunities

Kenvue is proud to be an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment 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.