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Supplier Quality Specialist Job (Las Piedras, PR, US)

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Supplier Quality Specialist-3586130718

Description

McNeil Healthcare LLC, a member of Johnson & Johnson's Family of Companies, is recruiting Supplier Quality Specialist, located in Las Piedras, Puerto Rico.

McNeil Consumer Healthcare, Division of McNeil-PPC, Inc., markets a broad range of over-the-counter products, including TYLENOL® acetaminophen products, ZYRTEC® and BENADRYL® allergy medicines, IMODIUM® A-D, MOTRIN® IB, PediaCare® upper respiratory medicines for infants and children, ROLAIDS® antacid products, ST. JOSEPH® Adult Regimen Aspirin, and SUDAFED® nasal decongestants. McNeil-PPC, Inc. entered into a consent decree, or agreement, with the agency that governs certain manufacturing operations to help ensure quality and compliance. Now is an exciting time to join our business, as we focus on reaffirming the integrity of our iconic brands that are staples of households worldwide. Whether you view this opportunity as a potential career accelerator here, within the J&J's Family of Companies or beyond, or whether this is your entry to the J&J's Family of Companies, we invite you to join us?. Creating the future of McNeil.

Responsible and accountable for the successful deployment of the McNeil SQM strategy and implementation of associated policies, procedures, programs and initiatives at the McNeil manufacturing site level. The position works cooperatively with plant level Incoming Inspection and Procurement personnel (Plant Level Supplier Focus Team) to deliver quality/compliance, and/or operating benefits to the plant operation by optimizing the supply of components. Actively partners with stakeholders, individuals, teams, and external suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business results. The position is the first line of contact with site Quality, Operations, Procurement, and Suppliers to remedy component quality, performance, and supplier service gaps and deficiencies. Assures trainings in the assigned tasks have been delivered prior to execution. Acts in accordance to the principles expressed in Our Credo and the Quality Statement in all negotiations and activities within and outside the company, and assures these are met. Supports the Consent Decree Work Plan activities as required.

Executes against SQM objectives, strategies, policies, procedures, programs, initiatives and projects that deliver quality/compliance, costs, and or operating benefits to the supply chain. Partners with and leverages the activities of individuals and teams to successfully develop and implement innovative solutions and continuous improvements with demonstrated and measurable business results. Coordinates the timely completion of site investigations related to component quality, compliance, and performance gaps and deficiencies. Works with site stakeholders and suppliers to develop effective and sustainable CAPA plans. Assists in the development of component specifications and associated supplier quality and service expectations. Assists in the development and execution of quality agreements and supplemental schedules and in the alignment of supplier specifications/expectations to McNeil incoming, in-process and final product specifications, procedures and policies. Collaborates in the monitoring of the on-going quality/compliance and service performance of suppliers by coordinating the timely and accurate collection and reporting of site-level data. Actively works with and leverages the activities of various site functional groups for the continuous improvement of component quality and performance. Assists and actively participates in the alignment and monitoring of the on-going quality, compliance and service performance of contracted services.

Qualifications


A minimum of a Bachelor’s Degree in Science is required. Five (5) or more years of experience with at least two (2) years in quality assurance department in a GMP product manufacturing plant environment are required. Experience and knowledge on nonconformance investigation process is also required. Candidate must be bilingual (English and Spanish) with excellent verbal, writing and technical skills in both languages. Knowledgeable in GMP and industry applicable regulations is a must. Excellent negotiation skills. Demonstrated ability to implement strategy/initiatives based on business needs. Demonstrated analytical skills to comprehend technical data/information and convert them into value-added actionable items is required. Working understanding of basic statistical and problem-solving tools, with the willingness to pursue statistical skills enhancements. It is required that the candidate be knowledgeable in sampling process, audit, and risk management. Ability to conduct root cause investigations and to develop effective and sustainable CAPA plans. Basic computer knowledge (Microsoft Office software) is a must. Knowledgeable in regard to Six Sigma process/techniques. A Six Sigma certification is preferred. Must be able to travel inside and outside of Puerto Rico 10% of the time. Able to work extra hours and support other departments and/or projects according to business needs.

BE VITAL in your career; Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.

J2W: LI

Primary Location:North America-United States-Puerto Rico-Las Piedras
Organization: McNeil Healthcare LLC (7598)
Travel:Yes, 10 % of the Time
Job Function: Quality Assurance

Certain sites within the Johnson & Johnson family of companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.

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