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:

Location:

Work Location:

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

• 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.

• 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.

• 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.

• Bachelor’s degree preferred in Engineering, Administration, or Natural Sciences.

• 1–3 years of experience in the pharmaceutical industry preferred.

• Prior experience in a supervisory or leadership role required.

• 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.

• 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.

• 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

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

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.