Manufacturing Supervisor

Kenvue Inc.; Las Piedras (PR); On-site; USD 74,000 - 104,000; Full time

Benefits offered by this job

Competitive Benefits Package

Paid Company Holidays

Paid Vacation

Learning & Development Opportunities

Kenvue Impact Networks

Job summary

Kenvue is seeking a Manufacturing Supervisor for its Puerto Rico facility. The role involves coordinating production plans, supervising staff, and ensuring GMP compliance during 1st/2nd/3rd shifts.

The position requires leadership, strong documentation, and the ability to manage multiple priorities in a fast-paced manufacturing environment. Responsibilities include oversight of safety, quality, and environmental protocols, along with participation in audits and continuous improvement

Qualifications

• Bilingual (English/Spanish) required.
• Knowledge of cGMPs and pharmaceutical regulations.
• Strong communication and documentation skills are essential.
• Organizational skills and ability to manage shifting priorities.
• Experience leading teams in a production/pharma environment preferred.

Responsibilities

• Lead daily operations and assign tasks to operators and mechanics.
• Coordinate maintenance, materials and resources for production.
• Conduct daily shift meetings and optimize production and costs.
• Ensure compliance with GMP, Safety and Environmental requirements.
• Support audits, CAPA and cross‑department coordination.

Skills

Bilingual English/Spanish

cGMP knowledge

Documentation skills

Communication skills

Team leadership

Education

Bachelor’s degree preferred in Engineering/Administration/Natural Sciences

Job description

Kenvue is currently recruiting for a:

Manufacturing Supervisor

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:

Operations Manager

Location:

North America, United States, Puerto Rico, Las Piedras

Work Location:

Fully Onsite

What you will do

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

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.

What’s in it for you

Annual base salary for new hires in this position ranges:

$73,950.00 - $104,400.00

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

• 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.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.