Kenvue 目前正在招聘 a:
我們做什麼
在 Kenvue,我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎,植根於科學,是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成,他們的職場文化中,每個聲音都很重要,每一個貢獻都受到讚賞。 我們熱衷於洞察, 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心,成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本,熱切關懷,以科學贏得信任,以勇氣解決——有絕佳的機會等著您!加入我們,塑造我們和您的未來。有關更多資訊,請按兩下 here.
Role reports to:
Operations Manager位置:
North America, United States, Puerto Rico, Las Piedras工作地點:
完全現場你會做什麼
The Manufacturing Supervisor coordinates the activities necessary for the completion of all production plans. Supervise, train, coordinate, and distribute tasks among all employees for the operation. Assure proper maintenance of facilities manufacturing equipment, in a compliance environment of a 24 hours / 7 days operation. Support the development of special projects and initiatives established by the company’s business plan. Review (when required) and approve the manufacturing and packaging records. Support employee development, and coaching and assure proper weekly employee communication and recognition.
This role requires a Second Shift (1:15PM to 9:45PM) or Third Shift (9:45PM to 5:45AM) availability
Key Responsibilities
Quality & Compliance
- Ensure strict adherence to cGMP, SOPs, and regulatory requirements.
- Complete all required GMP and job-specific training; ensure team members do the same.
- Promote a culture of integrity, Right‑First‑Time execution, and proactive deviation reporting.
- Discuss job descriptions with employees within required timelines and ensure training is completed prior to task execution.
- Model and enforce ethical conduct in all internal and external business activities.
Environmental, Health & Safety (EHS)
- Comply with all EHS policies, procedures, and ISO 14001 requirements.
- Promote safe behaviors and ensure proper use of PPE, fire protection protocols, spill reporting, and LockOut/TagOut compliance.
- Participate in EHS initiatives, waste reduction, recycling, and energy conservation activities.
- Identify and correct unsafe conditions; report incidents immediately and ensure timely incident documentation.
- Support ergonomic programs and ensure the timely completion of safety-related tasks.
- Monitor and improve EHS performance within the assigned area.
Area / Operations Responsibilities
- Lead daily operations, assigning tasks to operators and mechanics to execute the production plan.
- Coordinate equipment maintenance, materials, and resources to ensure operational efficiency.
- Conduct daily shift meetings and participate in tactical meetings to optimize production, manage costs, and maximize efficiencies.
- Ensure compliance with all GMP, Safety, and Environmental requirements.
- Drive timely resolution of operational and quality incidents through accurate documentation and work order generation.
- Oversee housekeeping standards and ensure accurate, timely completion of documentation and transactions.
- Support internal and external audits, CAPA execution, and cross-department coordination.
- Manage subcontracted work to ensure compliance with policies and procedures.
- Handle personnel management activities (hiring, evaluations, training, corrective actions, rewards, vacation planning).
- Respond to emergency medical situations when necessary.
- Ensure preventive and corrective maintenance is executed effectively.
- Support operators and promote Operator Asset Care principles.
- Perform yearly Efficiency Assessments using FMECA and Reliability Engineering tools.
- For Packaging Supervisors: perform line/area confirmation following cleaning and before QA clearance.
- Promote environmental responsibility and ensure proper disposal of recyclable materials.
- Participate in cross‑training initiatives and provide support across operations as needed.
Qualifications
Education
- Bachelor’s degree preferred in Engineering, Administration, or Natural Sciences.
Experience
- 1–3 years of experience in the pharmaceutical industry preferred.
- Prior experience in a supervisory or leadership role required.
Knowledge, Skills & Abilities
- Bilingual (English/Spanish).
- Knowledge of cGMPs and applicable pharmaceutical regulations.
- Strong communication, documentation, and organizational skills.
- Computer proficient.
- Ability to lead teams, resolve issues, and manage shifting priorities.
Physical Requirements
- Ability to perform sedentary work with occasional climbing, kneeling, stooping, lifting, or moving materials.
- Must be able to use PPE, including respiratory protection.
- Requires adequate visual acuity and hearing.
Other Requirements
- Ability to travel within and outside Puerto Rico.
- Must be able to work overtime, respond to emergency call‑backs, and work alternate shifts.
- Flexibility to support other operational areas based on business needs.
對您有什麼好處
本職位新員工年薪底薪範圍:
這考慮了許多因素,包括工作地點、候選人的技能、經驗、教育水準和其他與工作相關的因素
有競爭力的福利待遇**
帶薪公司假期, 帶薪休假、志願者時間 &更多!
學習 &發展機會
Kenvuer Impact Networks
此列表可能因位置/地區而異
*注意:Kenvue 的總薪酬包括薪水、獎金(如適用)和福利。您的 Talent Access 合作夥伴將能夠在招聘期間分享更多關於我們的整體薪酬產品以及相關地點的具體薪酬範圍的資訊。招聘流程.
Kenvue 很自豪能成為一個機會均等的雇主。所有合格的申請人都將根據業績獲得就業考慮,不分種族、膚色、宗教、性別、性取向、性別認同、年齡、國籍或受保護的退伍軍人身份,並且不會因殘疾而受到歧視。
如果您是殘障人士,請查看我們的 殘障人士援助頁面瞭解如何申請便利