Kenvueは現在、a:
私たちがしていること
Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。ケアは私たちの才能です.
Who We Are
私たちのグローバルチームは~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。 私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々に影響を与える力を持つことを意味します。私たちは人を第一に考え、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細についてはをクリックしてくださいhere.
Role reports to:
Processing Supervisor場所:
North America, Canada, Ontario, Guelph勤務地:
フルオンサイトあなたがすること
Kenvue is currently recruiting for:
Processing Operator 1-Night Shift
This position reports to Processing Supervisor and is based at Guelph.
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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, 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 the 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.
Role reports to: Processing Supervisor
Location: Guelph
Travel %: none
What you will do
The Processing Operator is responsible for all necessary duties associated with the manufacturing of bulk pharmaceutical products and the accurate documentation of these activities in a regulated manufacturing environment. The core manufacturing functions include Weigh & Dispense, Granulation, Compression, Finishing (Coating & Printing) and Liquids.
Key Responsibilities
- Successfully execute all manufacturing steps associated with cleaning/sanitation, set-up and manufacturing operations associated with the work center the operator has been assigned to.
- Processes raw materials according to the validated process identified on the batch record, cleaning record, and SOPs, and follows all steps/instructions in batch records, cleaning records, and SOPs
- Monitor and record all processing parameters and maintain all necessary processing and cleaning/sanitation documentation.
- Performs appropriate SAP/MES transactions in accordance with the SOP. Ensures accurate, timely and complete data recording of progress and downtime events in the Plant Cockpit system. Department goal of 95% completion of downtime events.
- Maintains an updated and current training record and adheres to training timelines.
- Ensure a safety working environment in all actions by:
- Identifying and acting to remedy any potential safety concerns or issues.
- Completing 100% of safety training on time.
- Maintain a safe working environment.
- Report all unsafe conditions and adhere to “See Something, Say Something, Do Something.”
- Ensure quality and compliance in all actions by:
- Identifying and acting to remedy any potential quality concerns or issues.
- Maintaining a sound understanding of GMPs and GDPs.
- Attend GMP training on the schedule designated for my role and as appropriate for the role.
- Adhere to strict compliance with procedures applicable to the role.
- Exercise the highest level of integrity in the tasks performed.
- In a timely and prompt manner, identify, report and seek correction for deviations noted.
- Embrace a behavior of employee involvement and commitment to doing the job right the first time.
What we are looking for
Required Qualifications
- Minimum of a High School Diploma
- Understanding of GMP Compliance is required
- Mechanical aptitude is essential
- Proficiency in MS Word, Excel, and SAP is required
Desired Qualifications
- Completion of Post Secondary Education in Chemistry, Biology or Biochemistry
- Preferred 2-3 years of experience in a regulated (food or Phama) manufacturing environment
- Preferred experience in solid dose manufacturing in an OTC or Pharmaceutical facility.
What’s in it for you
- Competitive Total Rewards Package*
- Paid Company Holidays, Paid Vacation, Volunteer Time & More!
- Learning & Development Opportunities
- Employee Resource Groups
- 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 business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。
