9 Empleos en Camuy

Maestro de Computadoras

Aguadilla Colegio Privado

Publicado hace 14 días

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Descripción Del Trabajo

tiempo indefinido
Plaza disponible para Maestro de Computadoras ofreciendo clases a los estudiantes de lunes a viernes en el área noroeste específicamente para el municipio de Aguadilla. Interesados enviar resume al siguiente correo electrónico:

Requisitos

Auto propio

Responsable

Disponibilidad Inmediata
Lo sentimos, este trabajo no está disponible en su región

Coordinador(A) Call Center - Manatí

Manatí Doctors' Center Hospital Manati

Publicado hace 9 días

Trabajo visto

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Descripción Del Trabajo

*Job description*

Planifica, organiza, dirige y coordina todas las actividades del Departamento de Call Center.

*Requisitos Mínimos:*

* Experiencia en supervisión
* Bachillerato o Grado Asociado

Conocimiento y Manejo de MS Office (Word, Excel, Power Point, Outlook). Disponibilidad inmediata.

Si reúnes todos los requisitos favor de enviar tu Resume a: ***. Equal Employment Opportunity.

Job Type: Full-time

Benefits:
* Health insurance
* Life insurance

Work Location: In person

Lo sentimos, este trabajo no está disponible en su región

Ventas-Invasiones $16.36 (P/H)-Aguadilla

Aguadilla Alvacom Employment Solutions

Publicado hace 10 días

Trabajo visto

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Descripción Del Trabajo

Venta puerta a puerta de servicios de internet y televisión y/o atender requerimientos del público en general.
Para solicitar:
Email: ***
Teléfono:
Requisitos:
Cuarto Año de Escuela Superior. Experiencia en el campo de las promociones, funciones de ventas y/o servicio al cliente. Preferiblemente conocimiento sobre productos y servicios de telecomunicaciones. Disponible para trabajar de lunes a sábado de 9am-6pm.
"Patrono con igualdad de oportunidades en el Empleo. Todos los solicitantes cualificados recibirán consideración para empleo sin distinción de raza, color, religión, sexo, embarazo, orientación sexual, identidad de género, origen nacional, edad, estatus como veterano protegido o discapacidad física o mental."

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Buscamos Promotores

Manatí Ci International

Publicado hace 12 días

Trabajo visto

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Descripción Del Trabajo

? ¡Estamos contratando promotores! ? ¿Buscas una oportunidad inmediata y bien remunerada?
¡Únete a nuestro equipo y comienza a crecer con nosotros!

? Ofrecemos:
• Ingredos comienzan desde $2,400 mensuales ?
• Plazas híbridas: 2 días presenciales y el resto remoto
• Comienzo inmediato
• Adiestramiento completo y continuo (¡no necesitas experiencia previa!)
• Oportunidades de crecimiento dentro de la empresa
Requisitos:
? Requisitos básicos: • Ser mayor de 18 años
• Compromiso, responsabilidad y actitud positiva
• Disponibilidad para trabajar modalidad híbrida
• Ganas de aprender y superarse

? Interesados:
Envíanos tu resumé a: ***

¡Da el primer paso hacia tu futuro profesional!

Lo sentimos, este trabajo no está disponible en su región

Project Manager - Electrical

Aguadilla Teksol Integration Group

Publicado hace 13 días

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Descripción Del Trabajo

*Teksol Integration Group, Inc.*

Has an opening available for:

*Project Manager – *_*Electrical*_

Área: Starting in Aguadilla

We are seeking a results-driven *Project Manager* to lead and oversee electrical construction and instrumentation projects. This role ensures timely and efficient execution aligned with client specifications, safety standards, and applicable regulations. While estimating may be required occasionally, the primary focus is on project planning, coordination, and execution.

*Responsibilities*

* Define clear project scope based on proposals, purchase orders, or client contracts, including specific, measurable, and realistic goals within the project timeline.
* Lead and manage electrical and instrumentation projects, including turnkey installations and multidisciplinary efforts.
* Oversee installation and commissioning of electrical systems and equipment such as switchgears, paralleling systems, emergency generators, substations, protective relays, transformers, control panels, and related infrastructure.
* Develop and implement project management tools such as Gantt charts, SWOT analysis, and DMAIC to monitor progress and performance.
* Coordinate with engineering, operations, procurement, and client teams to ensure alignment and successful delivery.
* Provide leadership and direction to project teams, fostering collaboration and accountability.
* Prepare and review project documentation, attend team meetings, manage communications, and handle administrative tasks related to assigned projects.
* Establish and maintain a risk management plan to mitigate potential issues such as design changes, delays, or resource misalignment.
* Support cost estimation efforts for electrical and instrumentation scopes using industry standards and templates.
* Participate in pre-bid meetings and client presentations when required.
* Maintain accurate records of project status, risks, and documentation.
* Build and sustain strong relationships with clients, vendors, and internal stakeholders.
* Ensure compliance with deadlines, safety protocols, and quality standards.
* Other duties may be assigned as needed.

*Requirements*

* Bachelor's Degree in Electrical Engineering or a related field.
* Minimum of 5 years of experience in project management, with a strong focus on electrical and instrumentation construction.
* Proven experience in installation and commissioning of electrical systems including switchgears, paralleling systems, emergency generators, substations, protective devices, transformers, and control systems.
* Familiarity with mechanical and civil construction projects is a plus.
* Proficiency in MS Office Suite (Outlook, Word, Excel, PowerPoint).
* Excellent interpersonal, leadership, and communication skills in both English and Spanish.
* Ability to interpret technical drawings and specifications.
* Strong organizational and time management skills with the ability to prioritize tasks effectively.
* Analytical and mathematical proficiency for basic calculations and data interpretation.
* Ability to work independently and collaboratively in a fast-paced environment.

*Benefits*

* Competitive compensation in the industry
* Cellular Allowance
* Health Insurance
* 401K Retirement plan
* 15 Vacation Days
* 12 Sick Days
* Paid Holidays
* Christmas Bonus

_This position requires traveling and working non-regular hours, such as weekends and holidays, if necessary._

_*Teksol Integration Group, Inc. *__is an Equal Employment Opportunity Employer, E-verify participant and we take affirmative action to recruit protected veterans and individuals with disabilities. _

_If reasonable accommodation is required to fully participate in the job application or interview process, to perform the essential functions of the position, and/or to receive all other benefits and privileges of employment, please contact *** *__or call at ._

Job Type: Full-time

Benefits:
* 401(k)
* 401(k) matching
* Dental insurance
* Health insurance
* Paid time off
* Vision insurance

Experience:
* electrical projects: 5 years (Required)

Ability to Commute:
* Aguadilla, PR 00603 (Required)

Willingness to travel:
* 50% (Preferred)

Work Location: In person

Lo sentimos, este trabajo no está disponible en su región

Quality Inspector 1

Añasco Integra Lifesciences

Publicado hace 13 días

Trabajo visto

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Descripción Del Trabajo

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

Inspect labels, pid's and pouches visually to approve packing operations or other operations. Obtains samples, inspect samples to specifications, record inspection data and makes accept/reject decisions based on inspection findings with respect to specifications. Verifies dimensions, cavity measures, pressure, and other specifications of products, using measuring gauges and testing equipment such as optical comparator, micrometer, calipers, go-no-go gauges, pin gauges, microscope, air pressure gauges, and other testing instruments. Follows quality controls inspection criteria in order to release acceptable lots to store or reject lots prior operations for re-work. Reads written specifications, drawings, and procedures such as the Quality Control Inspection Procedures. Fill quality control records, information on shop orders, and maintains other control reports and documentation. Assists in training of new Q.A. Inspectors. Provides G.M.P/ Quality Manual reinforcement and conducts spot audits to manufacturing areas in order to assist production to achieve established goals. May be assigned to different workstations as product needs require. May use forklift or jack pallets for handling raw material incoming inspection area. Sets up and performs destructive and non-destructive test on material, parts, or product to measure performance, material characteristics, etc. Maintains quality control records, blueprints, procedures, and other documentation's accurate, updated, and properly organized in files. Assures all control documentation are prepared and attached to the corresponding lots. Assures that all equipment are adequately calibrated and informs Supervisor of any discrepancy. Assures raw material or products released to stores or for sterilization fulfill quality standards. maintains work area clean and in orderly conditions. Follow Clean Room Rules and Gowning Practices. Must use safety shoes in areas that require it or the required protective equipment of the assigned workstations. This applies to all area where safety shies area required. Maintains control of raw material quarantine area and printed materials, and discrepant materials in store. Works on priority orders when released before others to assure compliance with productions schedules.

Qualifications

High School graduate or equivalent.
One (1) year experience in a similar position in an FDA regulated manufacturing environment preferred.
Driver's license on heavy vehicles highly preferred.
Knowledge of basic math concepts, graph interpretation, and use of procedure, and inspection methods.
Knowledge of statistical process control techniques.
Ability to read, understand drawings and written documents in English.
Ability to work using testing instruments and manual equipment.
Ability to be in a standing position for long periods of time.

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law | EOE including Disability/Protected Veterans

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at ***.

Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

Integra - Employer Branding from Integra LifeSciences on Vimeo

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Laboratory Commissioning & Decommissioning Engineer

00674 Manatí QRC Group, LLC

Hoy

Trabajo visto

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Descripción Del Trabajo

The Laboratory Commissioning & Decommissioning Engineer will lead and execute technical projects involving the safe shutdown (decommissioning) and startup (commissioning) of laboratory facilities. This role is essential for ensuring smooth transitions of scientific infrastructure in compliance with internal and external regulation.  Key Responsibilities• Plan and manage laboratory decommissioning activities, including equipment removal, hazardous waste handling, and technical cleaning.• Oversee commissioning of new laboratory spaces: equipment installation, system validation, functional testing, and regulatory compliance.• Develop project timelines, technical documentation, testing protocols, and compliance reports.• Collaborate with cross-functional teams: maintenance, quality assurance, EHS, IT, and external vendors.• Ensure adherence to FDA, EPA, OSHA, and Puerto Rico-specific regulations, as well as international standards (GMP, ISO, etc.).• Identify and mitigate technical and operational risks during transition phases.• Support internal and external audits related to facilities and processes.Requirements• Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, Biomedical, or related field). • Minimum 3 years of experience in commissioning/decommissioning projects within regulated environments.• Experience in pharmaceutical or medical device environments.• Knowledge of HVAC, BMS, specialty gases, lab equipment, and automation systems.• Familiarity with GMP, ISO 14644, FDA and OSHA.• Project management skills with strong technical leadership and communication abilities.• Fluent in English and Spanish (spoken and written).
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Quality Systems Specialist

00674 Manatí QRC Group, LLC

Publicado hace 4 días

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Descripción Del Trabajo

Quality Systems Specialist with experience in the pharmaceutical industry and strong expertise in Quality Systems and SOPs.

In-depth knowledge of GMP, FDA regulations, 21 CFR Part 11, Data Integrity (including Risk Assessment, Data Mapping), and EU regulatory requirements, with the ability to interpret and apply them effectively.

Proficient in computer systems and data collection tools, including Microsoft Office Suite, SAP, and Infinity.

Skilled in data analysis, identifying deviations and inconsistencies, and interpreting sampling and test results.

Experienced in problem solving and root cause analysis methodologies, including Kepner-Tregoe.

RequirementsBachelor’s degree in science (Chemical, Engineering, Biology, Pharmacy or Microbiology)Six (6) years of experience in project management, investigations or relevant roles and responsibilitiesin the pharmaceutical industry.Fully bilingual (Spanish/English) communication skills, both written and verbal.Technical and scientific capability to make firm decisions and recommendations.Microsoft Office, SAP, Infinity
Lo sentimos, este trabajo no está disponible en su región

CSV Specialist

00674 Manatí QRC Group, LLC

Publicado hace 4 días

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Descripción Del Trabajo

CSV Specialist with experience in Bioprocess Validations.

Technical Skills:

Tech Transfer, Process Design, Commissioning & Qualification.Vision system technologies (Strong).Inspection/packaging Concepts.Development and Execution of Processes/Equipment Characterization

Duties:

Provides data analysis/interpretation and assesses the impact of the data on the project.Establish Testing Strategies.Technical Reports Development.Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies.RequirementsBS or higher in Chemistry/ Biology/ Microbiology/ Computer Science/ Information Systems/Engineering or related discipline.Background in pharmaceutical products manufacturing environment and in manufacturing and laboratories areasMore than five (5) years of experience working with process validation life cycle, experience in commissioning and validating laboratory and manufacturing computerized systems in a manufacturing environment, and training in validation methodologies, technologies, and process control computer systems.Knowledge on computerized system with data collection software (database).Strong knowledge of cGMP, GAMP, SAT, FDA, 21 CFR Part 11 and Data Integrity Regulations.Experience in Automation process and/or Vision Inspection systems development.Knowledge in statistics using Mini-tab, JMP or other statistical software, project management skills and knowledge in development documentation protocols and reports.Knowledge in MS Project Management and MS Vision programs.Advanced scientific analysis and troubleshooting skills.Experienced in Instrument Performance qualification, and method configurationExcellent skills writing commissioning/ validation, and technical documentation in English and using MS Office applications.Bilingual (both English/Spanish)
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