• Vehicle and Bus Washer

    First Vehicle Services
    Vehicle Washer Job in Guaynabo, PR
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    F irst things First: Who are we? First Vehicle Services is a leading provider of diverse fleet management and maintenance services in North America. Since 1981, First Vehicle Services has been providing efficient and cost-effective vehicle management and maintenance services at governments, school districts, petrochemical companies, transit agencies, airports, universities, and private organizations throughout the United States. Why join First as a Lot Attendant? Tremendous career advancement opportunities Benefits include medical, dental, vision, & 401(k) Paid holidays & vacation Discounts on cell phone plans, cars, and more through the Perk Spot program! About the Position As a Lot Attendant with First, you will have an important role in keeping vehicles clean and operational for our customers. Lot Attendant job duties include: Wash all vehicles and busses Check and add fluids to vehicles as needed Clean and detail facility and the interiors and exteriors of vehicles Complete other maintenance tasks assigned by the supervisor. Qualifications Valid driver's license Vehicle fueling, cleaning, and detailing experience a plus Ability to work outdoors in all weather conditions Subject to DOT drug testing. DOT Regulation 49 CFR Part 40 does not authorize the use of Schedule I drugs, including marijuana, for any reason. Apply today and get your career on the road with First Vehicle Services! We aspire to have a culture where all people are First. We strive to attract and retain a diverse workforce therefore all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. First is also committed to providing a drug-free workplace. For candidates applying to positions in San Francisco or Los Angeles California, First will consider for employment qualified applicants with criminal histories consistent with the requirements of the San Francisco Fair Chance Ordinance or Los Angeles Fair Chance Ordinance. First is an equal opportunity employer and by doing so we will sustain and promote an inclusive culture that supports future growth for all.
    Entry Level
    Offers Benefits
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  • 4.8

    Senior Retail Sales Associate (Full-Time)

    Autozone
    Sales Associate Job in San Juan, PR
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    Maintains product knowledge and current promotions through AutoZone systems and information sources While assisting customers, the Senior Retail Sales Associate will perform daily assigned duties and remain compliant with company procedures in accordance to AutoZone expectations by Living the Pledge every day. AutoZone's Full-Time Senior Retail Sales Associate drives sales through superior customer service by exceeding customer expectations and providing a WOW!
    Full Time
    Senior Level
    High School Diploma Preferred
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  • Diesel and Automotive Mechanic

    First Vehicle Services
    Automotive Mechanic Job in Guaynabo, PR
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    First Vehicle Services is now hiring an Automotive and Diesel Mechanic for our shop serving Municipio Autonomo de Guaynabo! Why join First as an Automotive and Diesel Mechanic? About the Automotive and Diesel Mechanic Position First Vehicle Services is a leading provider of diverse fleet management and maintenance services in North America. Get your career on the road with First Vehicle Services! As a Diesel Mechanic with First Vehicle Services, you will help maintain and repair light, medium, and heavy-duty vehicles, including police cars, pickups, vans, trucks, refuse trucks, emergency vehicles, firetrucks, school buses, transit buses, motorcycles, heavy equipment, pavement, lawnmowers, tractors, and concrete mixers to ensure vehicle readiness & safety. Since 1981, First Vehicle Services has provided efficient and cost-effective vehicle management and maintenance services to governments, school districts, petrochemical companies, transit agencies, airports, universities, and private organizations throughout the United States. Possess a mechanic s tool set
    Full Time
    Junior Level
    Mid Level
    Offers Benefits
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  • WAREHOUSE EMPLOYEE

    Luis Garraton LLC
    Warehouse Employee Job in San Juan, PR
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    Empleado de Almacen. Varios puestos disponibles: Despacho Verificador Loaders Replenishment Putaway Returns
    Entry Level
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  • EMPACADOR DE CARNES

    Plaza Loiza Corp
    Chef De Partie Job in San Juan, PR
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    Encargado de garantizar que todos los productos se coloquen en el área de ventas y estén aptos para el consumo de nuestros clientes. Conocimiento en los cortes de carnes para manejo efectivo. Mantiene abastecida todas las frescas y congelados según requerido por la empresa.
    Entry Level
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  • QA Supervisor

    Invid
    Quality Assurance Supervisor Job in San Juan, PR
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    The QA Supervisor position is for the employee with expert knowledge, skills, and experience for software testing and validating and for managing one or multiple QA teams. Also, QA Supervisor constantly provides suggestions and performs research for the betterment of QA testing processes, standards, and techniques. QA Supervisor must have the necessary experience to perform manual and automated tests to web and mobile applications and manage QA teams for professional development.
    Senior Level
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  • Regulatory Compliance Officer

    Innovative Emergency Mgmt
    Regulatory Compliance Officer Job, Remote or San Juan, PR
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    Candidate must live a commutable distance to San Juan, PR IEM believes in the greater good and it is our commitment to attract those who have excellent technical skills, creative minds and innovative ideas to keep propelling us forward.
    Full Time
    Mid Level
    Bachelors Required
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  • 4.7

    Advisor, Business Development (Sales)

    Target Human Resources Solutions
    Business Advisor Job in San Juan, PR
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    Job DescriptionLo que antes se conocía como un "Business Banker" ahora es Advisor, Business Development (Sales). Se encarga de las ventas de prestamos comerciales a pequeños y grandes negocios. (PYMES).El vendedor estara en la calle , realizando ventas en los comercios y empresas. Requisitos: Debe conocer y tener experiencia en prestamos comerciales (por lo menos mas de 5 años de experiencia. Tenga cartera de cliente y dedicarse a la ventas para hacer crecer esa cartera de clientes. Conocer de Ventas, una persona que conozca el proceso completo de la documentación que se necesita, y requisitos de un préstamo comercial. Conocer como se maneja los pequeños y grandes negocios. Servicio al cliente. Educacion: Preferiblemente Bachillerato en Administración de Empresa. (pero podría ser en cualquier área, después que cumpla con la experiencia) Beneficios: Salario dentro del rango de 70k-90k depende de sus experiencia Incentivos tales como; comisión hasta un tope de 15k Car allowance Pago de Conectividad
    Mid Level
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  • 4.0

    Loader PT San Juan, PR

    Air Cargo Carriers
    Loader Job in Carolina, PR
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    Aircraft loaders are responsible for loading and unloading cargo for commercial aircraft. ROLE AND RESPONSIBILITIES • Take work orders from pilots or supervisors and determine which aircraft have been assigned. • Conduct a survey of assigned cargo to determine the time that will be required to conduct loading or unloading work. • Lift and carry all cargo items from dollies to the airplane cargo area and ensure that all items are properly stacked and secured. • Unload airplane cargo areas and move to staging areas. • Ensure that cargo is distributed/stacked in a manner that maximizes space and balance the weight of the load. • Determine both quantity and orientation of assigned cargo Qualifications and Education Requirements Ability to work under pressure and adapt quickly to suit client needs Good attention to detail Previous warehouse, shipping/ receiving or aircraft loading experience would be highly beneficial Ability to lift 50-75 pounds
    Entry Level
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  • 4.2

    Specialist Manufacturing (rotative shifts)

    FITS LLC
    Manufacturing Technician Job in Manat, PR
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    For Quality services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science (Chemistry, Biology or Microbiology) or Engineering and three (3) years of experience within the pharmaceutical industry. A minimum of one (1) year of experience in Quality Assurance responsibilities is required. Shift: 1st shift (8:00am- 5:00pm) Experience in: Manufacturing operations of Oral Solid Dosage and Parenteral Products Batch Record, Protocol and Investigation Review CAPA, Change Control, Annual Product Review. GMP, FDA, EU regulations Computer systems: Microsoft Office, TrackWise and SAP The Personality Part: If you have a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, you might just be what we are looking for! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Support manufacturing operations areas (OSD) such as Compounding, Filling, preparation, capping, inspection, compression, and packaging to comply with appropriate cGMPs. Manage audit observations, investigations and CAPAs records in Track Wise, participate in the investigation management process to identify RCA, evaluate, approve CAPA’s, and provide appropriate recommendations for the lot disposition. Review and approve the investigations occurred in the manufacturing process, facility and utilities, microbiology and warehouse areas. Review and approve the master documentation related to manufacturing and support areas such as CR’s, SOP’s, WPP’s, BOM’s, qualification and validation protocols. Provide technical guidance and compliance support in the transfer of new products and process to maintain quality standards. Manage audit observations, investigations and CAPAs records in TrackWise on timely manner. Maintain management informed (via frequent written reports) of any problem that might affect the quality and/or timely release of materials. Assure that electronic systems are aligned and in compliance with cGMP’s, Regulatory Standards and requirements for domestic and international markets. Provide support and training to other departments as required. Participate in the risk analysis process when a quality event has happened that cannot be solved immediately and assesses the needs to be completed to continue. BEING A FITS PIECE COMES WITH PERKS: One of these is the excellent, unmatched, never-before-seen customer service of our team (trust us, you’ll be amazed). However, that’s not all we have to offer. Talk with us to find out! WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the Next Piece? Powered by JazzHR vtp YNQjO9m
    Mid Level
    Bachelors Required
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  • 4.6

    Full-Time Technology, Services, Furniture Retail Solutions Advisor

    Office Depot
    Technical Service Advisor Job in San Juan, PR
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    Provides exceptional customer service by educating customers about Office Depot products and services. At Office Depot Inc., the Solutions Advisor is a full-time role, providing total solutions to our customers encompassing Technology, Services, Furniture and Print offerings. The Solutions Advisor will utilize Office Depot Inc. s proven sales principles to proactively engage customers, drive the sales of our total offerings, and properly assess customer needs to ensure satisfaction in every interaction.
    Full Time
    Junior Level
    High School Diploma Preferred
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  • MF04-112022 QA Resource for Packaging Equipment Qualification Documents

    Validation & Engineering Group
    Quality Assurance Job in Manat, PR
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    Validation & Engineering Group, Inc.
    Mid Level
    Bachelors Required
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  • 3.8

    Sales

    HCOA Fitness
    Sales/Marketing Job in San Juan, PR
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    Job DescriptionHCOA Fitness es el líder en la industria del acondicionamiento físico en Puerto Rico con 13 gimnasios alrededor de toda la Isla. Nos enfocamos en ofrecer a nuestros miembros las herramientas necesarias para el logro de sus metas y la obtención de resultados de por vida. El/la vendedor(a) contribuye en promover el club y la empresa mediante la promoción los beneficios del ejercicio, consistentemente alcanzar y superar los objetivos de ventas, y garantizar de una experiencia positiva para nuestros socios. DEBERES Y RESPONSABILIDADES Trabajar para establecer y lograr meta de ventas. Prospectaje de clientes potenciales a través de diversos métodos de colectar leads. Participación de eventos promocionales del gimnasio. Asistir a los eventos y reuniones de capacitación, según sea necesario. Buscar oportunidades para elevar los niveles de servicio de los clientes y aumentar la retención de socios. Estar bien informado de todos los productos, programas y servicios ofrecidos en el gimnasio. EDUCACIÓN / EXPERIENCIA Debe poseer un diploma de escuela secundaria o GED. 1 año de experiencia previa en ventas y servicio al cliente (preferido). Experiencia y/o pasión por la industria del fitness. HABILIDADES Alto grado de iniciativa; persona altamente motivado/a y dinámico/a. Horario flexible - puede incluir fines de semana y/o noches. Método de transportación confiable. Excelente servicio al cliente y comunicación profesional. BENEFICIOS Membresia gratis para ti y un familiar Comunidad divertida y energetica, orientada al equipo Ambiente de trabajo eficiente con la energia que incluye sistemas purificadores de aire y agua Descuento para entrenamiento personal Oportunidades de crecimiento dentro de la compañia Alto potencial de comisiones y bonos Bono de Inicio*
    Junior Level
    High School Diploma Required
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  • 3.4

    Quality - Manager, Compliance

    Weil Group, Inc.
    Quality Manager Job in Manat, PR
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    Job DescriptionPRINCIPAL OBJECTIVE OF POSITION This position is responsible for maintaining several elements within the Quality Systems frame work to ensure the Site compliance with current and forthcoming Biopharmaceutical and Medical Devices industries Good Manufacturing practices regulations and Client policies. Incumbent must comply with Corporate and HR Policies, FDA, GMP, internal/external audit, and any other regulatory requirements. Environmental Health and Safety regulations and the current Good Manufacturing Practices required by the job function. MAJOR DUTIES AND RESPONSIBILITIES State the most important activities and accountabilities of this position. The achievement of company or business goals. (Attach additional sheets if needed): 1. Acknowledge conducts and/or approve investigations for Customer Complaints, External Complaints, approve Regulatory Corrective Actions and Preventive Actions (CAPA), Vendor Certification, Quality Agreements, Annual Product Review/Report for Finished Product and Systems and site licenses. 2. Supports readiness of the facility for Regulatory Inspection. Assists the Associate Director Compliance and auditing during regulatory agencies inspections such as FDA / EMEA and/or during internal company audits. Documents any FDA communication between Site and agency. 3. Conducts internal / external audits following annual site plan with respective reports and actions items from areas impacted during the audit. Ensures the site has an internal audit program and that all system audits are conducted at a specified frequency. Create, review approves and track corrective actions related to internal and external audits. 4. Prepares, submit and discuss reports of assigned Quality Systems status for trending and evaluation to the site management. 5. Provides site GMP training based on annual requirements and support and training to other departments to ensure quality compliance as needed. 6. Generates, reviews and implements departmental procedure and forms to assure compliance with current practices or GMP’s trends. 7. Assures that site complies with Corporate Systems by evaluating, implementing and enforcing the company policies and guidelines. 8. Ensures that Quality and Compliance is implemented in laboratory and operational areas and maintains it according with regulatory agencies expectations. 9. Manages document including record retention program, compliance and custody of SOP’s, and review / approval / issuance of master documentation related to operational areas and; evaluates compliance of all procedure(SOP’s) and master documentation with regulations and Client Policies. 10. Provides guidance and support on the transfer and introduction of new products and processes to the site to maintain quality and compliance. 11. Support the Site Master File (SMF) and assists our regulatory section to handle and update documentation as part of our filing. 12. Coordinates Fact Findings documentation following Worldwide Quality and Compliance Directive and conducts root cause analysis to guarantee that underlying problems are identified and resolved. 13. Support Field Alert Report/Biological License Application (FAR/BLA) and Recall investigations and provides tracking to any Site Planned deviation. Ensures that recall operations are capable of being initiated promptly and at any time. This includes that lists are maintained of customers of all batches distributed and of distribution information. 14. Supports the Quality Risk Management program at the site participating in multidisciplinary teams. 15. Provides support to the Associate Director Compliance and Auditing in the preparation of monthly Quality Council meeting and presentations. 16. Develops impact assessments related to Policies and Directives implementation. Ensures corporate policies and directives are implemented in a timely fashion, following pre-establish schedule. 17. Ensures that all current vendors are qualified and conduct audits of approved Third Party Manufacturers and other vendors at defined frequencies as part of the vendor monitoring process as part of the Supplier Management Program. 18. Support the Inspection Readiness Program. 19. Provides support to Site Projects. 20. Provides compliance oversight and verifying compliance with Client and WWQ&C Policies and Guidelines and site cGMP compliance policies and procedures are addressed. 21. Provides compliance oversight and verifying compliance with Client Policies, guidelines and regulations 22. Liaison for regulatory initiatives 23. Manages Licenses renewals 24. Supports product submissions. 25. Manages the Records Retention program 26. Creates, evaluates, follows up and approves Change controls for the site, including interaction with corporate support areas, other Client sites and third parties. 27. Ensures Change controls are created according to local SOPs and corporate directives with all the appropriate requirements in placed for each change control. 28. Ensures the site has an internal audit program and that all system audits are conducted at a specified frequency. 29. Enforces critical analytical thinking in the Change Control management process. 30. Provides scientific input into change controls program management to assure all requirements to complete a change control are properly established and that no requirements are missing 31. Supports actively the engineering, laboratories and Supply chain areas for Quality and Compliance documentation and site oversight providing coaching from Quality perspective. 32. Provides guidance on gaps identified from the review and actively participates to determine potential remediation activities. 33. Provides technical guidance and quality assurance support in the transfer of new products and process to maintain quality standards. 34. Participates in Manufacturing Alignment Teams (MAT) and Project Alignment Teams (PAT), department staff, planning and change control board meetings as required. 35. Maintains communication with internal and external customers to ensure compliance and timely completion of the assigned activities. 36. Evaluates OP’s, BR’s, BOM’s, WPP’s, qualification and validation Protocols, according with government regulations and Client Policies. DECISION MAKING A. Describe the position's responsibility for taking action, making final decisions and developing recommendations. Limiting factors might include existing policies, procedures, laws, regulations, internal controls, etc.: • Notify immediate supervisor of any inconsistencies or violations to Company operation procedures and policies. • The incumbent is responsible of the compliance of the facility in terms of implementation, maintenance and challenge of the regulatory requirements which applied to GMP regulations in pharmaceutical, biopharmaceutical and medical devices industries. • The incumbent takes actions as deemed necessary and/or to communicate management in a promptly manner the actions required to ensure full compliance of the quality systems previously listed and to set priorities and meet deadlines within a complex and changing environment. • Inappropriate decision or action regarding a situation may result in regulatory action. • Unjustified delays in tasks execution may result in regulatory actions. • Position is expected to meet with the necessary areas to assure prompt solution of Quality and Compliance issues. B. Describe the nature of supervision received, the degree to which procedures, methods and goals are outlined by the supervisor, and the immediacy of supervision: On emergency situations, the incumbent may be required to make immediate decisions on the course of action of a lot without direct consultation. The incumbents must be able to work with minimum supervision as must be able to make compliance oriented decision taking in consideration the site procedures, cGMP’s, regulatory agencies , Client policies and guidelines. Must interact with governmental agencies, especially in the regulatory field, such as Food and Drug Administration, European agencies and others and must have the ability to provide back-up support to the Associate Director Compliance and Auditing during absence. CONTACTS Describe the most important working relationships of this position. Include the frequency, level, and the purpose of contacts necessary for effective performance: The incumbent will have interaction with personnel at all levels. Daily contact with Supply Chain Department, QC Laboratories, Warehouse, Technical Services, Manufacturing, Engineer and QA departments. Frequent communication with Management and Corporate Quality Unit is required. Continuous communication with external suppliers, external customers and headquarters are required. KNOWLEDGE / SKILL Describe the type and extent to which knowledge of a specific type is required to perform this job in a satisfactory manner. Where skills can be obtained through formal training / education and experience, list the type and amount of education and experience that would typically prepare an individual for this position:  Bachelor Degree in Chemical, Engineering, Biology or Microbiology Science.  Five 5 years of experience in Quality Unit responsibilities in the pharmaceutical industry.  Fully Bilingual (Spanish/English) communication skills, both written and verbal are required.  Strong knowledge of relevant GMP, FDA, EU regulations.  Expert in the interpretation and application of regulations according with the intended use.  Self-motivated, creative and team work oriented.  Excellent interpersonal skills and the ability to interact with people at all levels.  Strong Technical Writing Skills to prepare trends analysis, investigation reports and regulatory and internal audits responses.  Self-motivated, creative and team work oriented.  Self starter and good organizing and planning skills  Excellent knowledge of computer systems (Microsoft Office, etc.) and tracking system like QCIS and Trackwise.  Strong knowledge and experience in statistical tools  Strong presentation skills  Able to exercise good judgment  Able to work under pressure  Willing to work irregular hours, rotation shifts, weekends and holidays, when necessary.  Sense of urgency and analytical thinking are some of the critical competencies required for this position. WORKING CONDITIONS Describe the extent to which the job must be performed under working conditions that are considered undesirable, potentially hazardous, require travel, or require absence from home overnight: A. Describe exposure to any hazards / disagreeable conditions in the work environment: • Minimum exposure to hazardous areas. B. Travel required (describe nature and frequency): • No significant travel required. Less than 15% of the normal work time. C. Overnight absences required(per typical month) • No significant absence in a typical month required. Use this space to provide any additional information that you believe would help in evaluating this job: • Demands of 40% of the time sit, 30% stand and 30% walk. • Ability to keep work pace and or meet deadlines. • Frequent writing in English and Spanish • Extreme attention to documentation nomenclature details, retention policy applicable and coordination are considered critical due to the variety and regulation of documents being handled. • Special gowning as defined and required in the manufacturing and required areas. Frequent material handling between 21-35 pounds (lifting) *Weil Group is proud to be an Equal Employment Opportunity Employer.*
    Management
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  • Spa Attendant

    Well & Being Spa at Fairmont El San Juan Hotel
    Spa Attendant Job in Carolina, PR
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    Clean and maintain all fixtures, woodwork, walls, and windows, as well as additional parking lot cleanup, as needed. The Spa Attendant is responsible for providing guests with comprehensive and professional guidance regarding spa & fitness procedures and services.
    Full Time
    Junior Level
    Offers Benefits
    High School Diploma Preferred
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  • Supervisor de Ruta (Industria de Salud)

    Prime Janitorial Service
    Supervisor Job in Catao, PR
    Destrezas de liderazgo y organización. Habilidad para trabajar bajo supervisión. Habilidad para mantener excelentes relaciones interpersonales. Habilidad para trabajar en equipo. Destrezas de comunicación. Orientado (a) al servicio al cliente, calidad y seguridad. Manejo del tiempo. Iniciativa, seguir instrucciones orales y escritas. Interesados enviar resume para evaluacion. drosario@primejanitorial.com Powered by JazzHR DDLSjiHyEz
    Senior Level
    Easy Apply
  • 4.7

    Field Service Technician II

    Toshiba America Business Solutions
    Field Service Technician Job in Guaynabo, PR
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    Toshiba America Business Solutions, a leader in digital technology, is seeking a Field Service Technician II working in the Guaynabo, Puerto Rico marketplace.
    Junior Level
    High School Diploma Required
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  • 4.5

    05009 Inside Sales

    Sally Beauty Holdings
    Director, Inside Sales Job in Carolina, PR
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    At Sally Beauty Holdings, we find beauty in diversity.
    Entry Level
    Offers Benefits
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  • Representantes de Ventas

    Firma de Reclutamiento En Pr
    Representative Job in Caguas, PR
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    Requisitos: Diploma de escuela secundaria. 1 a 2 años de experiencia en ventas. Experiencia en atención al cliente, venta de productos y marketing. Debe tener una licencia de conducir válida. Debe tener su propio auto en buenas condiciones. Altamente motivado y orientado a objetivos con un historial probado en ventas. Capacidad para crear y entregar presentaciones adaptadas a las necesidades de la audiencia. Conocimientos básicos de los programas de Microsoft Office. Bilingüe (español e inglés). Excelentes habilidades de comunicación verbal y escrita. Disponibilidad para trabajar de lunes a sábados. Igualdad de Oportunidades en el Empleo. Esta oportunidad podría requerir vacunación completa para Covid-19 y/o presentar la exención debidamente documentada. Las personas exentas están sujetas a pruebas de COVID semanales para mantener el empleo.
    Entry Level
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  • 4.9

    Medical Director, Caribbean

    Bristol Myers Squibb
    Medical Director Job in Guaynabo, PR
    The Country Medical Director, Puerto Rico acts with the highest standards of integrity, providing critical strategic leadership. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. But working at Bristol Myers Squibb is anything but usual.
    Senior Level
    Professional
    Executive
    Offers Benefits
    Doctorate Preferred
    Easy Apply
  • Counter Sales

    Jobtracks, Inc.
    Counter Sales Person Job in San Juan, PR
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    Job Description *El horario regular de trabajo es de 7:00am a 4:00pm de lunes a viernes. "Counter Sales un (1) empleado - $10.00 mas incentivos en ventas Servicio al Cliente Conocimiento en tuberas, valvulas, "fittings, plomeria y Ferreteria Contestar llamadas telefonicas Despacho de mercancia si es necesario Cobrar en caja y manejo de tarjetas de credito Trabajar bajo presion
    Entry Level
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  • Specialist QA

    Paciv
    Quality Assurance Specialist Job in San Juan, PR
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    PACIV, a global leader in industrial automation solutions servicing the Life Sciences sector, is looking for a Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision.
    Senior Level
    Associate Required
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  • 4.4

    Store Associate

    Vitamin World USA Corporation
    Store Associate Job in Bayamn, PR
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    Maintain a professional attitude with sincerity and enthusiasm reflecting Vitamin World s commitment to our customer. Since we opened our first door in 1976 with a single kiosk in Williamsville, New York, Vitamin World has been passionate about good nutrition. Collaborate with the store team to support and achieve the goals of Vitamin World. Vitamin World is looking for Part-Time Store Associates for our retail store located at Plaza Rio Hondo in Bayamon, PR. All Vitamin World Employees will be vaccinated by September 20.
    Part Time
    Junior Level
    Offers Benefits
    High School Diploma Required
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  • 4.7

    Insurance Agent

    Mutual of Omaha
    Insurance Agent Job in Guaynabo, PR
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    At Mutual of Omaha Advisors, we're not afraid to step outside the box, challenge the status-quo and equip our team with all the tools necessary to unleash their full potential, and we are looking for individuals with the same mindset. This role at Mutual of Omaha may be the right fit for you. Mutual of Omaha has been a certified Great Place to Work for three years in row, ranked in Fortune magazine's 100 Best Companies to Work For, and rated by Forbes as one of America's Best Employers for Diversity. About Mutual of Omaha Advisors is a division of Mutual of Omaha Insurance Company. Mutual of Omaha is committed to fostering an inclusive and competitive culture and we've won the awards to back up our statements. Being part of our award-winning team at Mutual of Omaha Advisors, you can expect to make a difference in the lives of others every day. Help clients reach their financial goals by utilizing the award-winning products and services offered through Mutual of Omaha or its affiliates.
    Junior Level
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  • 3.4

    Quality - Quality Assurance Scientist

    Weil Group, Inc.
    Quality Assurance Scientist Job in Manat, PR
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    Job DescriptionMAJOR DUTIES AND RESPONSIBILITIES: 1. Supports manufacturing operations areas (OSD and Parenteral product) such as Compounding, Filling, preparation, capping, Inspection, compression and packaging to assure that appropriate cGMPs are in place through frequent operations audit. 2. Manages audit observations, investigations and CAPAs records in Trackwise on timely manner and participates in the investigations management process to identify root cause, evaluate and approves Corrective and Preventive actions (CAPA’s).and provides appropriate recommendations for the lot disposition. 3. Reviews and approves the investigations occurred in the manufacturing process (OSD and Parenteral products), facility and utilities, microbiology and warehouse areas. 4. Reviews and approves the master documentation related to manufacturing and support areas such as CR’s, SOP’s, WPP’s, BOM’s, qualification and validation Protocols with government regulations and Client Policies. 5. Provides technical guidance and compliance support in the transfer of new products and process to maintain quality standards. 6. Manages audit observations, investigations and CAPAs records in Trackwise on timely manner. 7. Maintains management informed (via frequent written reports) of any problem that might affect the quality and/or timely release of materials. 8. Assures that electronic systems (PMS, Syncade, Maximo, Quasar etc) are aligned and in compliance with cGMP’s, Regulatory Standards and requirements for domestic and international markets. 9. Provides support and training to other departments as required. 10. Participates in the risk analysis process when a quality event has happened that cannot be solved immediately and assesses the needs to be completed to continue or prior to resumption of manufacturing process. 11. Keeps track of the Department performance and attainment to deadlines and goals by means of the QC/QA Metric System. 12. Performs product Acceptance Quality Level (AQL) during inspection (parenteral products) stage and distribute reserve and/or stability samples to the appropriate area. 13. Supports Media Fill activities in order to assure that typical and atypical interventions are performed as established. 14. Reviews and approves the instrumentation and equipment Calibration records and engineering drawings ensuring there are effective systems for the maintenance and calibration of critical equipment and, approves calibration requests.. 15. Participates in PAT, department staff and planning meetings as required. 16. Reviews and approves equipment, utilities and facilities qualification and system life cycle documentation. 17. Reviews and approves all executed batch production records and laboratory testing records before release of the product for distribution to assure that no deviations have occurred, or if deviations have occurred, that they have been fully investigated. 18. Reviews and approves all process, product and computer systems validation protocols and reports, change control documentation, redressing / reprocessing / rework operations, investigation reports related to manufacturing process and microbiology laboratory, and Annual Product Quality Review (APQR’s) elements. 19. Supports the resolution of product and process issues associated to Quality Events. 20. Reviews supporting data for compliance with cGMP documentation practices. 21. Approves or reject procedures and specifications impacting drug products, raw material or packaging components. 22. Verifies compliance with Client Policies and Guidelines. 23. Participates as quality representative or liaison in site projects 24. Assures that the manufacturing and packaging procedures are properly followed and adequate for their use. 25. Verifies consistency with other site procedures and/or specifications. . 26. Ensures the designation and monitoring of storage conditions for quarantine materials and products. KNOWLEDGE / SKILL: • Bachelor Degree in Science, Chemical Engineering, Biology, Pharmacy or Microbiology. • 3 years of experience in the pharmaceutical industry. • Minimum 1 year of experience in Quality Assurance responsibilities in a pharmaceutical industry. • Knowledge of manufacturing operations of Solid Dosage and Parenteral Products Manufacturing. • Strong knowledge of relevant GMP, FDA, EU regulations and the ability to interpret and apply them for intended use. • Fully bilingual (Spanish/English) communication skills, both written and verbal are required. • Self-motivated, creative and team work oriented. • Excellent interpersonal skills and the ability to interact with people at all levels. • Proficient knowledge of computer systems (Microsoft Office, etc.) and applications like Trackwise and SAP. • Solid ability for analyzing data detecting deviations, inconsistencies and interpret sampling test results. • Knowledge of problem solving and root cause analysis methodologies (i.e. Kepner Tregoe)
    Mid Level
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  • Registered Nurse (GI Interventional)

    Veterans Affairs, Veterans Health Administration
    Registered Nurse Job in San Juan, PR
    The incumbent will be responsible for the set-up and pre cleaning of scopes and or /reusable medical equipment used in the section, in accordance with the Veterans Caribbean Healthcare system established SOP's and manufacturer's instructions manual.
    Junior Level
  • Project Analyst I (MRT)

    Icon Clinical Research
    Project Analyst Job in San Juan, PR
    Within the Trust and the Client Services team (PROVIDE), the **Project Analyst I** is responsible for supporting the projects by collecting and analyzing data to plan and manage COA (Clinical Outcomes Assessment) licensing projects, from original proposal through final implementation. The Project analyst I is providing experienced administrative support to the teams with emphasis on entering and checking data, ensuring best practices are implemented timely, govern quality of data and seeks remediation of issues. At ICON, it's our people that set us apart.
    Mid Level
  • 4.5

    Financial Crimes Fraud Specialist

    Regions Bank
    Fraud Specialist Job in San Juan, PR
    Regions is dedicated to taking appropriate steps to safeguard and protect private and personally identifiable information you submit. At Regions, the Financial Crimes Fraud Specialist monitors fraud prevention reports and/or reviews and resolves claims to address potentially fraudulent activity and reduce possible losses. Thank you for your interest in a career at Regions. At Regions, we believe associates deserve more than just a job.
    Full Time
    Mid Level
    High School Diploma Required
  • 4.8

    HUMAN RESOURCES ASSISTANT (D1048000)

    Air National Guard Units
    Human Resources Assistant Job in Bayamn, PR
    DUTIES: As a HUMAN RESOURCES ASSISTANT (D1048000), GS-0203-6, you will provide limited technical assistance and clerical support to Human Resources Specialists within the office and to managers, supervisors and technicians of the serviced organizations on of human resources matters. Area 1 = All permanent Technician Enlisted members (NG T32/NG T5) within Puerto Rico Air National Guard. Area 2 = All indefinite Technician Enlisted members (NG T32/NG T5) within Puerto Rico Air National Guard. Area 4 = Enlisted Prior (former) members of the Puerto Rico Air National Guard. Area 3 = Enlisted currently serving members of the Puerto Rico Air National Guard.
    Entry Level
  • 4.8

    Manufacturing Engineer

    Ford Motor Company
    Manufacturing Engineer Job in San Juan, PR
    At Ford Motor Company, we believe freedom of movement drives human progress.
    Junior Level
  • 4.8

    Manager, ServiceNow

    KPMG
    Requirements Manager Job in San Juan, PR
    + ServiceNow System Administration Certification and ITIL Certification is preferred + Ability to customize workflows, Business Rules and UI Scripts using JavaScript to create custom applications and configurations on the ServiceNow platform Responsibilities: + Formulate and define specifications and modifications for the ServiceNow platform in terms of business needs and applying that to Enterprise organizational objectives and provide technical leadership for planning, designing, upgrading, installing, testing, implementing, documenting and maintaining the ServiceNow platform + Provide subject matter knowledge to the ServiceNow application and ability to implement modules and other third-party integrations and applications used within the environment to ServiceNow for SecDevOps KPMG complies with all applicable federal, state and local laws regarding recruitment and hiring. + Transform business needs from the customer to tangible items within ServiceNow, from using modules available to the platform or creating new modules and direct and help complete detailed documentation for workflows and services implemented within ServiceNow The KPMG Advisory practice is currently our fastest growing practice. KPMG is currently seeking a Manager in Technology Enablement for our Consulting (https://advisory.kpmg.us/) practice. + Evaluate ServiceNow platform performance, isolate and debug software problems and make recommendations for problem resolution KPMG LLP (the U.S. member firm of KPMG International) offers a comprehensive compensation and benefits package. KPMG does not currently require partners or employees to be fully vaccinated or test negative for COVID-19 in order to go to KPMG offices, clie Qualifications: + Minimum ten years of recent experience as an analyst or developer with three plus years of hands-on experience developing and maintaining multiple ServiceNow instances At KPMG, our people are our number one priority.
    Senior Level
    Management
    Bachelors Required
  • Senior Application Security Engineer

    Goto
    Senior Applications Engineer Job in San Juan, PR
    At GoTo, we're passionate about growing a diverse and inclusive work ecosystem because unique takes make us a stronger company, and Stronger Together. + Product Technology and Implementation: Develop a deep understanding of the GoTo SaaS product suite; tools and technologies to effectively perform security-focused architecture reviews, assessments, and implementations + Security Champion Program: Expand and lead the GoTo Security Champion program that increases the security of our products, while strengthening the relationships between internal teams and Security. **As a Senior Application Security Engineer, you would be working on** : By building its secure, easy-to-use software, GoTo is committed to ensuring the time at work is well-spent so that time outside of work is better spent. **As a Senior Application Security Engineer, your background will look like:** RPJ GoTo's flexible-work software - including GoTo Connect, GoTo Resolve, Rescue, Central, and more - is built for small and medium-sized business IT departments, but powerful enough for the enterprise.
    Mid Level
    Senior Level
  • 4.9

    Natural Gas and Industrial Gases Buyer

    Chemours
    Buyer Job, Remote or San Juan, PR
    This full-time position will report to the **Procurement Director - Global Real Estate, Utilities, EMEA and APAC** and is located at Chemours headquarters in **Wilmington, DE** . Chemours is seeking a **Buyer** to devise strategies and buy natural gas, industrial gases as well as contract for onsite production at its plants in the US and around the world. From the frontline to the back office, every Chemours employee is part of something bigger than themselves as together we work to create a better world through the power of our chemistry. Chemours is a $6.3 billion company with a portfolio of products and processes that enable technologies and products that people use every day in their lives.
    Full Time
    Junior Level
    Bachelors Required
  • 4.9

    Chief Technology Officer, Corporate Strategy Office

    Intel
    Chief Technology Officer Job in San Juan, PR
    Intel's Corporate Strategy Office (CSO) is seeking a trusted technical senior leader to partner with both the CSO's leadership team and Intel's top leadership to continue Intel's transformation from a PC centric company, to a data centric company. As a member of the CSO leadership team, this technology leader will be a critical partner in enabling Intel's strategy planning processes to achieve growth aspirations of 100B, while maximizing company performance and long-term shareholder value. Demonstrated results and accountability for broad leadership, building of followership and role modeling of Intel's cultural attributes of :
    Executive
    Masters Preferred
    Bachelors Required
  • 4.2

    Manager, Compliance

    FITS LLC
    Compliance Manager Job in Manat, PR
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    For Compliance services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Chemical, Engineering, Biology or Microbiology Science & five (5) years of exposure in Pharmaceutical Manufacturing industry. Bilingual (English & Spanish) Experience in: GMP, FDA, EU regulations Technical Writing Investigation reports and regulatory and internal audits Computer Systems & Track wise The Personality Part: If you have a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, you might just be what we’re looking for! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Acknowledge conduct and/or approve investigations for Customer Complaints, External Complaints, approve Regulatory CAPA, Vendor Certification, Quality Agreements, APR for Finished Product and Systems and site licenses. Support readiness of the facility for Regulatory Inspection. Assist the Associate Director Compliance and auditing during regulatory agencies inspections such as FDA / EMEA and/or during internal company audits. Conduct internal / external audits following annual site plan with respective reports and actions items from areas impacted during the audit. Ensure the site has an internal audit program and that all system audits are conducted at a specified frequency. Create, review approves and track corrective actions related to internal and external audits and prepare, submit and discuss reports of assigned Quality Systems status for trending and evaluation to the site management. Provide site GMP training based on annual requirements and support and training to other departments to ensure quality compliance as needed. Generate, review and implement departmental procedure and forms to assure compliance with current practices or GMP’s trends. Ensure that Quality and Compliance is implemented in laboratory and operational areas and maintains it according with regulatory agencies expectations. Manage document including record retention program, compliance and custody of SOP’s, and review / approval / issuance of master documentation related to operational areas and evaluate compliance of all procedure (SOP’s) and master documentation with regulations and company policies. Provide guidance and support on the transfer and introduction of new products and processes to the site to maintain quality and compliance. BEING A FITS PIECE COMES WITH PERKS: One of these is the excellent, unmatched, never-before-seen customer service of our team (trust us, you’ll be amazed). However, that’s not all we have to offer. Talk with us to find out! WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the Next Piece? Powered by JazzHR Jz8vH7x4CD
    Entry Level
    Management
    Bachelors Required
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  • 4.1

    Technical Writer I

    Healthedge Software Inc.
    Technical Writer Job in San Juan, PR
    As a technical writer, you will work closely with our subject matter experts and team members to support documentation efforts for products and services. + Collaborate with software developers, analysts, project managers, and technical writer teammates to gather documentation requirements for product release notes.
    Full Time
    Junior Level
    Mid Level
    Bachelors Required
  • 4.0

    Information Systems Security Officer (ISSO) (Secret) (2183)

    SMX
    Information Systems Security Officer Job in San Juan, PR
    SMX is seeking an Information Systems Security Officer to support projects across the Cloud Business Unit focusing in on Defense and National Security Clients. Information Systems Security Officer (ISSO) (Secret) (2183)at SMX(View all jobs) (https://www.smxtech.com/careers/)
    Junior Level
    Bachelors Preferred
  • 4.6

    Utilization Management Specialist (RN required) - 100% REMOTE

    Vanderbilt University Medical Center
    Watershed Management Specialist Job, Remote or San Juan, PR
    Utilization Management Specialist (RN required) - 100% REMOTE - 2300162 **Description** **Utilization Management Specialist (RN required) - 100% REMOTE**
    Management
  • 3.1

    Network Engineer II

    Red River
    Network Engineer Job in San Juan, PR
    The Network Engineer II is primarily responsible for working on a team at the Red River Service Desk at our HQ location in Chantilly, VA. + Act as a mentor to Red River interns and Junior Engineers
    Mid Level
    Bachelors Preferred
  • 4.6

    Product Support Representative 3

    Change Healthcare
    Product Support Representative Job in San Juan, PR
    + Ready, Set, Grow Career Development Center & access to Change Healthcare University for continuous professional learning & development with more than 5,000 training assets Change Healthcare is a leading healthcare technology company with a mission to inspire a better healthcare system. + At Change Healthcare, we include all. The Product Application Support Representative will be responsible for providing second level technical support to Change Healthcare customers using an ASP web application.
    Part Time
    Mid Level
    Bachelors Preferred
    High School Diploma Required

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