Sr. Supply Quality Specialist, Day Shift

Sr. Supply Quality Specialist, Day Shift

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:

Supervisor 1, Quality Assurance

Location:

North America, United States, Pennsylvania, Fort Washington

Work Location:

Fully Onsite

What you will do

The Sr. Supply Quality Specialist responsible and accountable for the successful deployment of the Kenvue Supply Quality Management (SQM) strategy and implementation of associated policies, procedures, programs and initiatives at the Kenvue manufacturing site. This position works cooperatively with plant level procurement to deliver quality/compliance, cost and/or operating benefits to the plant operation by optimizing the supply of components.  This position actively partners with stakeholders, individuals, teams and external suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business results.  The incumbent will also be responsible for the qualification and maintenance of GMP Contract Service Providers.

This individual may also provide support for the other elements of the Fort Washington Quality Compliance group as needed.  This individual may also be required to participate in cross functional teams providing support as needed

Key Responsibilities:

• Coordinates timely completion of site investigations related to raw material/component quality, compliance and performance gaps and deficiencies. 

• Actively partner with stakeholders, individuals, teams and external suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business results. 

• Coordinate service provider quality related activities.

• Assists in the development of raw material/component specification and associated supplier quality and service expectations.

• Assists in the development and execution of quality agreements and supplemental schedules.

• Assists in the alignment of supplier specifications/expectations to Kenvue incoming, in-process, and final product specifications, procedure and policies.

• Partner with SQM and procurement to ensure on-going quality/compliance and service performance of suppliers by coordinating the timely and accurate collection and reporting of site-level data.

• Attend GMP training on the schedule designated for my role and as appropriate for my role.

• Adhere to strict compliance with procedures applicable to my role.

• Exercise the highest level of integrity in the tasks that I perform.

• In a timely and prompt manner, identify, report and seek correction for deviations noted in my workplace.

• Embrace the behavior of employee involvement and commitment to doing the job right the first time.

Additional Responsibilities:

• May be required to participate in cross functional teams providing Quality support as needed.

• Author investigations, CAPAs and Change Controls related to supplier quality functions.

• Provide support to other functions within the Compliance group.

• Provide support to multisite teams and meetings.

• Perform other related duties as required.

What we are looking for

Required Qualifications

• Bachelor’s degree is required.  Biology, Chemistry, Microbiology, Engineering or related technical degree is preferred.

• Minimum 4-6 years of Pharmaceutical and/or OTC Industry Quality experience is required

• Knowledge of cGMP requirements and the ability to interpret regulations

• Strong skills and experience in Partnering and Influencing

• Ability to think critically/strategically, act proactively and follow through

• Demonstrated ability to identify and correct gaps

• Highly motivated and driven

• Strong Organizational/Facilitation skills

• Strong verbal, written and presentation skills

• Ability to travel up to 10%

Preferred Qualification

• Investigation skills with Non-conformances and/or CAPAs preferred.

• Experience in electronic systems such as EtQ, SAP, etc. is preferred

What’s in it for you

$90,100.00 - $127,200.00

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

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.