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Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.

Your unique talents will help patients on their journey to wellness. Learn more at

Directs and coordinates the activities of production personnel in a designated manufacturing area, applying knowledge of production methods, processes, machine and equipment, and production capacities. Proactively meets corporate/divisional and organizational requirements for regulatory compliance with all local and federal agencies. Adheres to environmental policy, procedures, and supports department environmental objectives.

Duties and Responsibilities

• Obtains maximum productivity and efficiency in the designated area of responsibility by creatively coordinating and supervising the work of hourly manufacturing personnel.

• Monitors processes and determined actions to assure costs, productivity, yields, lead time, service levels, and inventory control activities are in line with business goals.

• Supports/executes validation activities to assure proposals are in line with manufacturing expectations.

• Provides administrative support to business and quality systems representing the process area being supervised.

• Executes production operations, establishing priorities and sequences for manufacturing products, utilizing knowledge of production process and methods, machine and equipment capabilities, and human resources requirements. Maintains adequate floor control.

• Responsible for goal setting and developmental activity of employees under their responsibilities. Monitors and provides continuous feedback on employee’s performance and determines required actions.

• Promotes and assures a safety and teamwork environment according to the organizations values.

• Coordinates activities with other production supervisors to ensure consistency in employee relations

• Interfaces with all plant management, engineering, quality, tool-room, maintenance, materials and H.R. personnel in order to meet production requirements

• Provides input for operational budget and procedures

• Coordinates new product introductions ensuring operators are trained and new product introduction dates are met

• Conducts weekly audits within production areas to ensure continued GMP compliance

• Responsible for pro-active people management

• Facilitates communication to associates and create a Credo based environment

• Ensures correct policies and guidelines are followed to maintain compliance with all regulatory and corporate policies (Health, Safety, and Environmental Standards, etc.).

• Other miscellaneous duties as assigned by supervisor.

Qualifications

• Bachelors Degree is required. Bachelors degree in Science, Engineering or related field is preferred.

• A minimum of 2 years of related experience is required.

• Availability to work all shifts, weekends and nights is required.

• Experience in a manufacturing regulated industry is required.

• Able to read, speak, and write Spanish and English is required.

• Strong leadership skills.

• Demonstrated experience as a lead or supervisor is required.

• Knowledge of FDA regulations is required.

• Must be computer literate in Microsoft Office, E-Mail, word processing and spread sheets is required.

• Knowledge in SAP is preferred.

• Must be detailed oriented and have the ability to develop and meet deadlines, and be able to delegate and follow-up.

• Strong verbal and written communication skills required as well as skills in the following areas: Conflict Resolution, Managing for Performance/Accountability and documenting issues, as well as developing leadership and ownership in individuals.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.