Kenvueは現在、以下求人を募集しております。
C&Q Technician私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、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、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活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、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
SA Engineering and Reliability Campus Leader場所:
Europe/Middle East/Africa, South Africa, Gauteng, Johannesburg勤務地:
フルオンサイトあなたがすること
C & Q technician
This position reports into Engineering & Reliability Leader and is based in Cape Town, South Africa.
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®, 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: SA Engineering Campus Lead
Location: Cape Town, South Africa
Travel %: Minimal
Pay: 24
What you will do
What you will do
The Commissiong & Qualification technician is responsible for generating and maintaining the validation plan in line with GMP and successfully carry out on all Facilities, Utilities (HVAC, Water, Compressed Air and other), Equipment, Systems.
Key Responsibilities:
- Development of User Requirement Specifications
- Development and execution of System Impact Assessments and Component Impact Assessments
- Development and execution of Validation Risk Assessments and Design Reviews
- Development and execution of Design Qualifications, Installation Qualifications, Operational Qualifications and Performance Qualifications taking a System Lifecycle Approach
- Perform Commissioning (includes Factory Acceptance Testing and Site Acceptance Testing) as required and liaise with other departments
- Validation of Automated Systems
- Perform periodic reviews for Equipment, Facilities, Utilities, Systems
- Re-qualification of Equipment, Facilities, Utilities, Systems
- Interact with all areas and levels of the company in addition to regulatory agencies, vendors, consultants, contractors and other intended parties
- Follow and review site validation/qualification SOP’s to ensure they are in line with current compliance requirements from corporate and regulatory authorities
- Participate in corporate, regulatory and internal audits
- Maintain up to date knowledge of corporate and regulatory standards
- Manage and maintain company validation plan and ensure validation/ qualification activities are successfully carried out
- Maintain the Validation Master Plan schedule and Validation System
What we are looking for
Required Qualifications
- Relevant Degree in Life Science/Chemistry/Math (Not necessarily from Biology/Microbiology) or equivalent
- 3-5 years’ experience of qualification/validation in a Pharmaceutical company
- Experience with cGMP, cGEP, cGDP
- Strong problem-solving skills and documentation experience preferred
- Strong organizational and time management skills.
- Qualifications background.
Desired Qualifications
- Very strong Quality Analytics knowledge and understanding (ISO / FMEA / HAZOP etc.)
- Demonstrated knowledge of working within a quality management system and cGMP and regulations 21 CFR 211, EU Annex 11 and 21 CFR Part 11
- Must have knowledge of Deviations, Investigations, Change Control, CAPA and Risk Assessments within the Pharmaceutical Industry quality system
- Must have basic Protocol and execution and Report writing skills
- Ability to work independently and as part of a team
- Proficiency in relevant software and tools
- Proficiency in Microsoft Office, including Word, PowerPoint, and Excel.
What’s in it for you
- Competitive Benefit Package
- Learning & Development Opportunities
- Kenvuer Impact Networks
- 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 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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