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:
SR MGR QA SYSTEMS & APPLICATIONS場所:
Europe/Middle East/Africa, Sweden, Skane, Helsingborg勤務地:
ハイブリッドあなたがすること
Kenvue is currently recruiting for:
Lab Systems Automation Lead
This position reports to the Senior Manager - QA Systems & Applications and is based at Helsingborg, Sweden.
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 OTC brands such as NICORETTE®, IPREN®, LIVOSTIN®, IMODIUM®, PEPCID® and consumer health brands like NEUTROGENA®, LISTERINE®, NATUSAN®, PIZ BUIN® and o.b. ®. Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers’ hearts and homes.
The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution.
The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here
What you will do
The Lab Systems Automation Lead is responsible for providing site level support for the Kenvue laboratory systems (LIMS, Empower, SDMS, ComplianceBuilder). Primary responsibilities include implementation of solutions in the Kenvue laboratories to automate processes related to instrument data transfer and driving laboratories towards a paperless laboratory environment through electronic lab notebooks and test method execution.
Additionally this role will identify improvement areas, and recommend process changes to correct issues improve lab processes. This role will also support the resolution of system related issues and fixes, master data setup, and automation of lab processes via LIMS system connections and test scripts.
Key Responsibilities
Integration Execution and Support
- Design and implement automation solutions for Kenvue lab systems to ensure seamless integration of laboratory data from standalone instruments.
- Develop and standardize the maintenance of scripts and standard protocols for instrument integration
- Design, implement, and maintain integrations between laboratory instruments and information management systems (LIMS). Ensure that laboratory systems are interconnected to facilitate efficient data flow.
- Lead integration projects from concept through to implementation, ensuring all milestones and deadlines are met.
- Coordinate with IT, laboratory staff, and external vendors to execute integration projects. Provide technical support and troubleshooting for laboratory systems and integration issues.
- Provide support for projects to build electronic lab notebook templates in conjunction with IT
- Ensure all integrations comply with industry standards and local regulatory requirements. Implement security protocols to protect sensitive laboratory data.
- Develop and maintain documentation related to integration SOPs, User Guides, protocols, etc. Ensure the accuracy and integrity of data transferred between systems. Work with data management teams to enhance data quality and reporting capabilities.
- Conduct training sessions for laboratory staff on new systems and integration processes. Keep up-to-date with the latest technologies and best practices in laboratory integration
LIMS Project and Platform support
- Provide support and troubleshooting for Kenvue LIMS system in conjunction with the global business and IT teams
- Support alignment of site/regional requirements for new LIMS system implementations and enhancements that align with Global solution and design.
- Support Global Master data community of practices so that master data requirements are adopted consistently across internal manufacturing sites. Where applicable support updates and implementation of master data objects relevant to the business requirements and processes.
- Recommend changes to methods and procedures to address improvement areas
- Write, review and modify standard test/operational procedures
- Lead and participate on process improvement teams
What we are looking for
Required Qualifications
- Bachelor's degree in Computer Science or related field
- 6-8 years of experience in automation engineering or LIMS/laboratory management systems (including Labware pharma template experience), or any combination thereof
- Experience in Software Development Lifecycle (SDLC) methodologies and computer system validation required
- Programming acumen for LIMS file based integration
- Excellent problem-solving and analytical skills
- 6-8 years related experience in quality control process analysis
- Strong analytical and problem-solving skills
- Ability to work in a team environment
- Strong attention to detail
- Experience in process improvement methodologies
Desired Qualifications
- Experience with automation tools such as Selenium, Jenkins, and Robot Framework
- Excellent communication and interpersonal skills
- Proficiency in data analysis tools and techniques
What’s in it for you
- Competitive Total Rewards Package
- Paid Company Holidays, Paid Vacation, Volunteer Time & More!
- Learning & Development Opportunities
- Employee Resource Groups
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.
Background checks in the recruitment process
As a final candidate in our recruitment process, you may be subject to a background check. This process is important for us to ensure the quality of our recruitment process.
As part of this, it is important that we encourage you to make sure that the information in your CV is correct before submitting your application to us.
To carry out these background checks, we use a background check company. Different checks may be carried depending on the position that you are applying for. This could be, for example:
- Reference checks
- CV-validation
- Financial checks
- Litigation checks, including criminal cases
The background check company is an independent data controller for any personal data that they will process during the check, and if you have any questions about the processing, you may turn to the background check company.
Due to our business activities and daily operations, we may also carry out drug tests as part of our recruitment process.
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