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Senior Quality Engineer

Сфера деятельности: Quality

Тип должности: Permanent

Тип занятости: Full - Time

Место расположения: Clark, NJ

Страна: United States

Job Title Sr. Quality Engineer

Division: Open Manufacturing

Location: The Hub (Clark, NJ)

Reports To: Sr. Manager Quality Assurance

Who We Are:

For more than a century, L’Oréal has devoted its energy, innovation, and scientific excellence solely to one business: Beauty. Our goal is to offer each and every person around the world the best of beautyin terms of quality, efficacy, safety, sincerity and responsibility to satisfy all beauty needs and desires in their infinite diversity.

At L'Oréal Operations, we create innovative, inclusive, and sustainable beauty together with our business partners by designing, developing, sourcing, manufacturing, and distributing over 6 billion products globally every year. We support over 36 brands across four L’Oréal divisions. We are consumer-oriented, and we act responsibly all along the value chain.

What You Will Learn:

Tasks, Duties & Responsibilities

·       Ensure product compliance with L’Oreal’s Standard Procedures and current Good Manufacturing Practices (cGMPs). 

·       Develop and provide training to OMA Team (Open Manufacturing Americas) and our CM (Contract Manufacturers)

·       Issue Nonconformance notices and follow Root Cause Analysis/Corrective Actions and Preventive Actions (CAPA).

·       Work with subcontractors (CM) on status of Quality nonconformities, support investigations and problem solving. Assess risk which may impact product safety or compliance.

·       Provide support to : CM Quality Audit & Internal Audit

·       Ensure that CAPAs are initiated, assigned, thoroughly investigated, documented and effectively resolved when deficiencies are found during development, testing, manufacturing. Request waivers when necessary

·       Provide support to Quality Manager with quality agreement between L’Oreal and Contract Manufacturers (CM)

·       Provide support to Quality Manager in issuing/updating technical dossier (Blue Book- BB) for CM production

·       Assist Quality Manager on new CM on-boarding process

·       Train/Coach/Assist current & new CMs to ensure understanding of quality requirements

·       Participate in CM’s certification program (test delegation, control and process validation)

·       Present Quality result and CC update to CM, OMA MANCOM and Division

·       Perform product inspection and manage the quality release process - block the Finished Product (FG) when needed, release FGs in SAP and manage reworks (at the Distribution or 3rd party facility) - rework instructions traceability list, re-control, release

·       Disposition FGs, PCs, bulk, WIPs in WISE and block in FUSION if necessary

·       Perform the documentation review process to ensure compliance to established quality requirements 

·       Initiate and follow up the corrective action process for nonconforming finished goods and packaging components

·       Manage reworks (at the DC or 3rd party) - rework instructions, Traceability list, re-control, release

·       Coordinate the samples for approval for R&I, Mktg, or other stakeholders as necessary

·       Train/assist new team members on test methods and procedures

·       Create and implement quality procedures

·       Support DGO/Internal audits

·       Tracking and manage of all KPIs (Quality Performance, Consumer Complaint, Blue Book Tracker)

·       Provide technical support to CM with manufacturing challenges (in processes)

·       Responsible of CC investigation and tracking (QA)

·       Review technical equipment and feasibility of our CMs (in processes)

·       Responsible of tracking for OTC ( APR & LTS)

·       Provide technical support to the Sourcing team (in processes)

·       Support the onboarding of new acquisition

·       Driving new technical and IT solutions for Quality team to improve ways of working and management

What We Are Looking For:

Required Qualifications:

  • Bachelor's degree, Science or Engineering.

        + 2 Years experience in Industrial Quality, preferably within cosmetics and consumer goods industry

        Knowledge of ISO Standards 9001 and GMP Standards (ISO 22716)

        Cosmetic Regulation ( Labeling Regulation for Cosmetics), 21 CFR 210 & 21 CFR 211

        Good Manufacturing Practices (GMPs)

        SAP Experience

        Computer Skills with Microsoft ( Excel,word, Power BI,etc…)

        Strong attention to detail and desire to follow procedures

        Good communication and organization skills

        Ability to interpret data and statistics

        Quality Assurance, Quality Controls and Quality System

        Knowledge on OTC products

What’s In It For You:

  • Competitive Benefit Package (Medical, Dental, Vision, 401K, Pension Plan)
  • Hybrid Work Policy (3 Days in Office, 2 Days Work from Home)
  • Flexible Time Off (Paid Company Holidays, Paid Vacation, Vacation Buy Program, Volunteer Time, Summer Fridays & More!)
  • Access to Company Perks (VIP Access to L’Oréal’s Internal Shop for Discounted Products)
  • Learning & Development Opportunities for Career Progression (Unlimited Access to E-learnings, Lunch & Learn Sessions, Mentorship Programs, & More!)
  • Employee Resource Groups (Think Tanks and Innovation Squads)
  • Access to Mental Health & Wellness Programs

Don’t meet every single requirement? At L'Oréal, we are dedicated to building a diverse, inclusive, and innovative workplace. If you’re excited about this role but your past experience doesn’t align perfectly with the qualifications listed in the job description, we encourage you to apply anyways! You may just be the right candidate for this or other roles!

We are an Equal Opportunity Employer and take pride in a diverse environment. We would love to find out more about you as a candidate and do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting [email protected]. If you need assistance to accommodate a disability, you may request an accommodation at any time. 

Our Safe Together Plan: Your safety is our highest priority. We will proceed with caution and adhere to enhanced protection standards to ensure our sites are safe for all employees. We must all operate with the shared responsibility for each other’s health & safety in mind.