"Alerted.org

Job Title, Industry, Employer
City & State or Zip Code
20 mi
  • 0 mi
  • 5 mi
  • 10 mi
  • 20 mi
  • 50 mi
  • 100 mi
Advanced Search

Advanced Search

Cancel
Remove
+ Add search criteria
City & State or Zip Code
20 mi
  • 0 mi
  • 5 mi
  • 10 mi
  • 20 mi
  • 50 mi
  • 100 mi
Related to

  • Engineer, Quality Assurance

    Revlon (Oxford, NC)



    Apply Now

    Description

    At Revlon, we create beauty innovations for everyone that inspire confidence and ignite joy every day.

     

    Breaking beauty boundaries is in our company’s DNA. Since its game-changing launch of the first opaque nail enamel in 1932 (and later, the first long-wear foundation), Revlon has provided consumers with high-quality product innovation, performance, and sophisticated glamour. Elizabeth Arden made waves as a woman-led beauty company in the 1920s. In 1931, Almay became the original hypoallergenic, fragrance-free beauty brand.

     

    Today, Revlon resiliently continues its legacy as a leading global beauty company. Our diverse portfolio—which consists of some of the world’s most iconic brands and product offerings in color cosmetics, skincare, hair color & care, personal care, and fragrances—is sold around the world through prestige, professional, mass, and direct-to-consumer retail channels. These brands include Revlon, Revlon Professional, Elizabeth Arden, Almay, American Crew, CND, Cutex, Mitchum, Sinful Colors, Creme of Nature, Britney Spears, Christina Aguilera, John Varvatos, Juicy Couture, Ed Hardy and more.

     

    We honor our heritage, embrace change, and applaud diversity. We champion our employees and celebrate our consumers.

     

    We are Revlon, together, transforming beauty.

     

    Overview: 

     

    This role will drive culture change in the organization to that of a harmonized, consistent Quality Unit and expectation.

     

    No Direct reports.

     

    + **People**

    + Develop excellent working relationships with both Oxford peers and management. Mentor and coach team as well as all cross-functional colleagues on process-based root cause problem solving.

    + **Culture**

    + Drive culture change, to one that is data-driven, fact-based, and quality-oriented, without sacrificing plant capacities and output.

    + **Q** **uality**

    + Support New Product Development and Existing Product innovation/launches. (Operations, R&D, QC, etc.) and follow up on plans.

    + Prior experience operating within quality systems as either a user or owner to review or approve GMP documents (change controls, deviations, CAPAs).

    + Assesses the impact of deviations, CAPAs, and associated change request on the validation status of equipment and/or systems.

    + Assess changes via NPD, change controls, deviations, etc. for impact on validated systems (Equipment, Cleaning, Process, etc.).

    + Assist in defining, testing, and implementing comprehensive guidelines and procedures for all manufactured products to ensure products and processes meet all regulatory and customer requirements.

    + Lead, support, review and approve Quality Investigations, Nonconformance(s) and Quality Complaint(s) assigned to the Oxford location.

    + Identify and lead continuous improvement opportunities within quality systems and other areas as appropriate.

    + Establish and perform carryover limit calculations and determine appropriate carryover limits with documented rationale. (As applicable)

    + Support cleaning process development activities for CIP and COP, manual and automated processes.

    + Prepare detailed plans for coordination and execution of validation activities with various stakeholders (Operations, R&D, QC, etc.) and follow up on validation plans.

    + Author Validation Protocols and Reports. (Cleaning, Process, Systems, etc.)

    + Delivery/Innovation New Product Development (NPD) is the driver of our industry’s success. Do what it takes to achieve Ship-to-Trade (STT) dates without sacrificing cGMP compliance, Safety of the end user, and brand Quality expectations.

    + Cost-Support directly all assigned cost reduction initiatives. Be aware of the business impact that quality has on cost reduction and suggest projects to achieve plant goals.

    + Key Partners-Will need to build solid relationships with all functions of the organization, in particular Global QA, plant Quality Control (QC), Regulatory Affairs (RA), R&D Development and Services, Packaging Development and Engineering, Supply Chain, and Revlon-owned plant Production

    + Other duties as assigned.

    + Minimal to no travel required

    Experience: 

    + Minimum of 4 years of relevant experience within the consumer personal care industry and/or pharmaceutical industry.

    + Bachelor of Science degree, such as Engineering, Microbiology, Chemistry or Associate of Science degree with 5 years of experience.

    + Experience working in a cGMP environment and good understanding of regulations and industry guidance including but not limited to FDA, Health Canada, EMA, and ICH.

    Required Knowledge & Skills:

    + Experience working in a cGMP environment and good understanding of regulations and industry guidance including but not limited to FDA, Health Canada, EMA, and ICH

    + Enjoys learning and development and considers self an emerging Subject Matter expert (SME) on the FDA regulations governing OTC and non-OTC products; prefer to also have experience with ISO 9001, ISO 22716, European regulations, and ICH guidelines.

    + Ability to manage time and workload so that the goals and objectives for each role are met, using appropriate prioritization strategies.

    + Proficiency in standard business software (Word, Excel, Outlook, PowerPoint)

    + Excellent oral and written skills coupled with the ability to succeed in a teamwork-oriented atmosphere.

    + Demonstrated, hands-on experience with cleaning validation activities

    + General experience with SAP or other ERP system

    + Engaging and motivational personality that enjoys being a part of the team, so that strong, tight-knit, cross-functional teams are built, and the culture is changed as needed to drive business growth. Communication and relationship-building is critical as needed to drive business growth. Communication and relationship-building is a critical skill for this role.

    + Experience leading or participating in auditing activities for cGMP compliance

     

    The base pay range for this position is $75,000 and $85,000/year]; however base pay offered may vary depending on skills, experience, job-related knowledge, and geographic location. Certain positions may also be eligible for short-term incentives as part of total compensation.

     

    Employees (and their families) are eligible for medical, dental, and vision benefits. Employees are covered by the company-paid basic life insurance policy and company-paid short-term disability insurance (the benefit commences upon hire and allows for a portion of base salary for up to 26 weeks if you are disabled). Other benefits offered to employees include but are not limited to the following: long-term disability, supplemental life insurances, flexible spending accounts, critical illness insurance, group legal, identity theft protection, etc. Employees are also able to enroll in our 401k Retirement Savings Plan.

     

    Employees will also receive 3 weeks of vacation, pro-rated based on date of hire for the 1st year of employment and twelve paid holidays throughout the calendar year. Vacation will depend on role.

    \#LI-AH1

    Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

     

    This employer is required to notify all applicants of their rights pursuant to federal employment laws.

     

    For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

     


    Apply Now



Recent Searches

  • Electrical BIM Designer Design (Washington)
  • patient scheduling specialist (United States)
[X] Clear History

Recent Jobs

  • Engineer, Quality Assurance
    Revlon (Oxford, NC)
  • Sr Configuration Management Analyst
    Leidos (Colorado Springs, CO)
  • Value Stream/Quality Control Technician
    Cytiva (Miami, FL)
[X] Clear History

Account Login

Cancel
 
Forgot your password?

Not a member? Sign up

Sign Up

Cancel
 

Already have an account? Log in
Forgot your password?

Forgot your password?

Cancel
 
Enter the email associated with your account.

Already have an account? Sign in
Not a member? Sign up

© 2025 Alerted.org