Baxter International

LEAD OPERATOR Sub-Assembly Area (Shift D)


PayCompetitivo
LocationAibonito/Puerto Rico
Employment typeFull-Time

This job is now closed

  • Job Description

      Req#: JR - 137469

      This is where you save and sustain lives

      At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

      Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

      Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

      Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.

      TD 5:30 a 7:00pm Sabado y Domingo Sub-Assembly Area

      Your role at Baxter:

      Assists in implementing and supervising daily activities in the manufacturing area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines and any other regulations that apply.

      Your team:

      We develop quality products with the patient in mind, so our marketing efforts are also patient centric. That means you can be proud of our work and the value we provide to people every day.

      As a large, multinational organization, you could expand your knowledge through collaboration with a variety of individuals, exposure to different facets of our portfolio, and an encouraging leadership team that encourages ongoing development.

      What you'll be doing:

      Leads and audit manufacturing employees over daily/weekly/monthly production plans requirements assuring product quality in compliance with company expectations.

      Monitors and control labor efficiency, downtime, scrap, conversion loss and other key performance indicators.

      With the direction of the Supervisor, coordinates the manufacturing activities to accomplish the goals.

      Assigns employees to specific jobs/job rotations and monitors personnel performance. Provides feedback to supervisor/manager and director concerning employee job performance.

      Identifies and supports VIP projects.

      Aids and assists in equipment troubleshooting problems.

      Informs Supervisor/Manager and fills out reports on manufacturing activities (daily, weekly, monthly, annually) on a timely basis as required.

      Audits manufacturing areas assuring compliance with specifications, batch record documentation and procedures.

      Reviews, make changes and supports implementation of changes to specifications and SOP's.

      Audits and implements procedures and policies in all areas under responsibility assuring compliance and training in cGDP's, specifications, SOP's, procedures and/or training manuals.

      Supports and assures compliance with all the Operational Excellence projects implemented in his/her area.

      Available to work any shift when required, with minimum supervision.

      Perform multiples tasks and projects.

      Focus on creating a positive and equitable working environment emphasizing the Baxter Shared Values and Leadership Expectations.

      Performs and coordinates area changeover.

      Assist the Supervisor with the payroll adjustment to Supervisor for approval. Assure that work schedules of manufacturing employees in his/her area of responsibility are correct in Kronos.

      Serves as backup to other Lead Operators

      Conducts periodic meetings with employees as required.

      Collaborates in the investigation and solution of quality issues and complaints.

      Performs other duties as assigned by Supervisor.

      Responsible for conducting EHS inspections to identify and correct safety hazards and environmental aspects. Follow the EHS applicable procedures and analyze EHS incidents (including near misses) to find causes and take corrective action.

      Observes confidentiality and data privacy rules at all time.

      What you'll bring

      EDUCACIÓN Y/O EXPERIENCIA (EDUCATION AND/OR EXPERIENCE):

      Bachelor degree preferably in Science, Engineering or Technology. Minimum of 1 to 3 years of experience in a manufacturing processes, preferably in pharmaceutical/solutions filling manufacturing environment.

      CUALIFICACIONES (QUALIFICATIONS):

      Excellent interpersonal and leadership skills with ability to interface well with other departments, and lead operators effectively and efficiently in a team environment.

      Ability to manage multiple priorities in a manufacturing plant setting.

      Strong writing skills and ability to prepare reports, write business correspondence and procedure manuals in English.

      Able to effectively prepare and present information and respond to questions.

      Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.

      Strong analytical, problem solving and troubleshooting skills.

      Computer literate. Hands-on experience on computer programs, such as MS Word, Excel, Powerpoint.

      IDIOMA (LANGUAGE):

      Domain of the English and Spanish languages.

      Ability to communicate in English/Spanish languages.

      DEMANDA FISICA (PHYSICAL DEMANDS):

      Medium Work: Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects. Physical demands requirements are in excess of those for Light Work.

      The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.

      Equal Employment Opportunity

      Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

      EEO is the Law
      EEO is the law - Poster Supplement
      Pay Transparency Policy

      Reasonable Accommodations

      Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

      Recruitment Fraud Notice

      Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

  • About the company

      Baxter International Inc. is an American multinational health care company with headquarters in Deerfield, Illinois.

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