Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Supervisor II, Validation位置：
North America, Canada, Ontario, Guelph工作地点：
完全现场你会做什么
Kenvue is currently recruiting for:
Quality Specialist II (Validation) – 12 month contract
This position reports to the Supervisor II Validation and is based at Guelph, ON, Canada.
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 II Validation
Location: Guelph, ON, Canada
Travel %: 0
Pay: Level 24
What you will do
The Quality Specialist II (Validation) will support and co-ordinate activities associated with cleaning, manufacturing and packaging processes, computer systems, analytical and microbial method, shipping, facility, utility and equipment qualifications for the Guelph site.
The Quality Specialist II will coordinate the development, creation, review and approval of qualification and validation documents (protocols, reports, validation assessments, technical reports, and user requirements, function and design specifications).
They will ensure that documented evidence exists to provide a high degree of assurance that processes, equipment, computer systems and methods are consistently reproducible and meet Kenvue policies and quality standards, health, safety and environmental regulations, and regulatory requirements (e.g. Health Canada and the United States FDA).
The Quality Specialist II will collaborate with stakeholders to develop and administer validation policies, including the deployment of these policies
Key Responsibilities
Review, revise or approve validation documents (ie. assessments, documents, protocols, reports, etc.) to ensure they are in compliance with relevant SOPs, government regulations, and company policies. This includes documents executed at Kenvue – Guelph Campus and /or specific business partners and contract sites. Validation types may include but are not limited to: packaging validation; cleaning validation; process validation; analytical and microbial method validation; shipping qualification; equipment qualification; and computer validation.
Represent Quality & Compliance on taskforces / committees for base business, new product introduction and capital projects. Connect with SMEs as appropriate to ensure transfer of knowledge and action on key deliverables.
Create, review and/or approve other site documents, such as: GCC assessments, Annual Product Quality Reports (APQR), Master Batch Records, SOPs etc.
What we are looking for
Required Qualifications
Minimum degree in Science/Engineering or related discipline
Minimum 3-5 years of relevant experience in Quality, R&D or Production environment in the pharmaceutical industry.. Validation experience in the pharmaceutical industry an asset.
Ability to evaluate scientific data.
Ability to take ownership for work independently on project activities.
Excellent communication and presentation skills.
Knowledge of and competence in the application of Health Canada GMPs, CFRs and ICH Guidelines.
Must be able to influence and facilitate groups with diverse perspectives and bring teams to consensus / alignment.
Strong leadership, organization, decision making and interaction management skills.
Strong computer skills, specifically in Microsoft Word, Excel, and Adobe Acrobat.
Strong technical writing, verbal communication, interpersonal and problem solving skills.
What’s in it for you
Competitive Benefit Package*
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Kenvuer Impact Networks
This list could vary based on location/region
*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
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.
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