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SR QUALITY ANALYST (Fixed Term - 12 months)
Location:
São José dos Campos
Description:
Description Kenvue is currently recruiting for: Sr. Quality Analyst (Fixed Term - 12 months) This position reports into Quality Regional Project Manager and is based at São José dos Campos. Who We Are 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. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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. What You Will Do The Sr, Quality Analyst will be responsible for project coordination to ensure project compliance for Kenvue by ensuring compliance requirements are incorporate it into Kenvue Quality System including product Labels , marketing authorization holder changes, Licenses , Supplier Management, product release and all applicable quality elements. Key Responsibilities • Develop , Execute and monitor action plans for Qualiy to comply with company policies, procedures, and quality standards; as well as applicable regulations by developing and executing quality plans • Quality representative at regional foruns to ensure quality deliverables are met considering cross-fuctional interdependencies , risks and mitigation plans in place • Regularly reports projects status to management , internal and external stakeholders at regional level What We Are Looking For Required Qualifications • Bachelor degree in pharmacy or a related technical field • Experience in regulatory affairs and quality sytems • Project management certification /experience • Regulatory knowledge (regulatory affairs,licensing and inspections) • Advanced English Desired Qualifications /Technical competences • At least four (6) years-experience in the field regulated industry. • Comprehensive knowledge of applicable LATAM regulatory requirements (GMP , product filings, labels) • Strong problem-solving skills • Proven track record of development and implementation quality & compliance processes • Track record of successful cross functional partnership • Experience working with virtual teams • Comfortable and effective at communicating Sr. Leadership • Strong written and verbal communication and technical writing • Data Management and visualization • Must be able to develop and maintain relationships/partnerships and to work collaboratively both internally and externally • Risk management What's In It For You • Competitive Benefit Package • Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More! • Learning & Development Opportunities • Employee Resource Groups • This list could vary based on location/region 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.
Company:
J & J Brazil
Posted:
April 12 on Equest
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