Job description
Quality Scientist I
Location of the job: Raeford, NC
12 hr PM Shift: 6:30 pm - 7:00 am
2/2/3 shift pattern
Pay Rate – $24.99 with an additional $1.50 shift differential | Weekly pay period
Overall Benefits:
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These are direct hires, full time position with a full benefits package (*Medical, Dental, Vision, 401K, SHARE purchase, Tuition/Fitness reimbursement, Paid leaves, Hourly Bonus payouts, etc.)
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Benefits are effective the first day of hire (where applicable)
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Employee Referral Bonus Program
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Onsite Company store for discounted product purchases
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Onsite cafeteria
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Uniforms and PPE provided by the company
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Career Advancement Opportunities
Background & Purpose of the Job
At Unilever – Raeford, we believe in developing talent and leading through our autonomous ways of working. As one team, we will achieve endless possibilities! The Raeford facility is a world-class personal care manufacturing site, utilizing digital tools to be a lighthouse factory globally.
Who You Are & What You’ll Do:
As the Quality Scientist I you will perform all duties related to the inspection, testing and analysis of incoming raw materials, packaging materials, compounding batches/neuters and finished goods for the production of Personal Care Liquids and Antiperspirant Deodorants produced in the facility.
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Perform all required testing, monitoring and recording results and information are to be completed in designated secure systems and in compliance with all Unilever requirements and specifications.
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Completes all Unilever required testing, inspection, and analysis of incoming raw materials, packaging materials, compounding batches/neuters and finished goods using GMP’s and GLP.
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Records quality data into designated systems and makes proper usage decisions to release product to the market in timely manner (Excel, SAP, TnT, etc.). Manages quality paperwork including filing.
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Ensures that all applicable test methods are in place, and that all laboratory testing equipment is appropriate, calibrated/verified and operates to the required standard. This includes reviewing and revising all quality SOP’s.
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Supports, participates and leads continuous improvement activities using WCM methodology.
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Supports factory KPI’s and creates/ manages multiple reports including FDA Drug Report, Right First Time, Annual Product Review, Cleaning & Sanitization, Quality Shift Report, etc.
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Follows non-conforming procedures to hold or release in-bound materials, work-in-process and finished product.
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Evaluate QEF’s and create SNCR’s and partners with Supplier’s to resolve open issues. Includes inspection of non-conforming product to recommend disposition.
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Supports requirements related to innovations, VIP projects, trials, validations, data analysis, etc.
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Cross trained in all areas of the quality department and works in each area on a periodic basis as determined by management.
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Supports and updates quality databases (i.e. RCP files, generic shippers, fill weight specifications, Freeweigh, etc.).
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Troubleshoot quality related issues with the operations team, audit and support warehouse quarantine areas, perform hygiene audits, quality waste tracker and other factory quality audits.
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Special projects including maintaining standards, ordering supplies, kaizens
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Models success and fulfillment, achieves satisfaction by helping others to continue developing their skills.
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Ability to drive change and innovation by gathering knowledge and resources to ensure tasks are completed within timelines to a high degree of accuracy and professionalism.
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Ability to navigate the many embedded operational tensions.
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Responsible for following GXP. This includes but is not limited to Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Good Documentation Practice (GDP).
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All other duties as assigned
What You’ll Need To Succeed
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Bachelor of Science Degree required in technical discipline (biology, chemistry, microbiology preferred)
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Strong computer, analytical, written and verbal communication skills
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Prior lab experience preferred
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Exceptional interpersonal skills and the ability to build collaborative relationships with multiple and diverse stakeholders.
Employment is subject to verification of pre-screening tests, which may include drug screening, physical and background check.
- Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.
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Unilever is an organization committed to diversity and inclusion to drive our business results and create a better future every day for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. 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.
Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check.
If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at
NA.Accommodations@unilever.com
. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses.
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