10 Manufacturing Technicians jobs in Puerto Rico

Job Description

Job Description

Descripción de PuestoQuality Control Cordinator – Facturación y Registros (Puesto Exento)

Departamento: Oficina Administrativa
Reporta a: Presidente
Ubicación: Oficina Central

Propósito del Puesto

Garantizar la exactitud y consistencia de los registros y documentación utilizada para la facturación de servicios de transporte en ambulancia, verificando que cumplan con los requisitos internos, contractuales y regulatorios. Auditar y evaluar tanto los reportes de choferes y paramédicos como la facturación generada por el personal de Facturación, supervisar el cumplimiento de funciones clave del personal de Despacho en relación con el cierre de casos y documentación en el sistema Pockets, y contribuir a la eficiencia operativa y la transparencia de los procesos.

Responsabilidades Principales

- Verificar que las facturas emitidas por el personal de Facturación estén correctas y basadas en datos completos y validados.

- Auditar y revisar los registros de transporte realizados por choferes y paramédicos para asegurar que la información esté completa, precisa y conforme a las políticas de la empresa.

- Confirmar que Despacho monitoree diariamente, por turno, que no queden casos abiertos en sistema y, de ser necesario, que proceda a cerrarlos.

- Identificar errores, omisiones o inconsistencias y canalizar las correcciones, según los protocolos establecidos. Deberá reportar a la gerencia cualquier incumplimiento.

- Preparar informes periódicos de hallazgos y recomendaciones dirigidos al Presidente de la Empresa.

- Mantener actualizados los formatos y procedimientos para la captura de datos y facturación.

- Coordinar con las distintas áreas para asegurar el cumplimiento de estándares de calidad.

- Manejar información confidencial con el más alto nivel de integridad.

- Cumplir con otras tareas afines que le sean asignadas por el Presidente.

Requisitos del Puesto

- Educación: Grado Asociado o Bachillerato en Administración de Empresas, Contabilidad, Facturación Médica o área relacionada (preferible).

- Experiencia: Mínimo 1 año en funciones administrativas, facturación médica, auditorías o control de calidad.

- Conocimientos Técnicos: Dominio de Microsoft Word, Excel y Google Sheets; manejo de sistemas administrativos y herramientas de análisis de datos.

- Competencias Clave: Atención rigurosa al detalle, habilidad para analizar información y proponer mejoras, organización y manejo eficiente del tiempo, comunicación escrita y verbal efectiva, discreción y manejo de información confidencial.

Condiciones del Puesto

- Clasificación: Exento, bajo criterios administrativos y de confianza.

- Modalidad: Presencial en Oficina Central y a distancia de ser requerido.

- Reporta directamente al Presidente de la Empresa y sigue sus instrucciones directas.

- Jornada: Tiempo completo, con disponibilidad para atender situaciones urgentes según sea requerido.

Cardinal Health Sonexus Access and Patient Support helps specialty pharmaceutical manufacturers remove barriers to care so that patients can access, afford and remain on the therapy they need for a better quality of life. Our diverse expertise in pharma, payer and hub services allows us to deliver best-in-class solutions-driving brand and patient markers of success. We're continuously integrating advanced and emerging technologies to streamline patient onboarding, qualification, and adherence. Our non-commercial specialty pharmacy is centralized at our custom-designed facility outside of Dallas, Texas, empowering manufacturers to rethink the reach and impact of their products.
**Together, we can get life-changing therapies to patients who need them-faster.**
**What Performance Monitoring contributes to Cardinal Health:**
Performance Monitoring is responsible for establishing, maintaining, and enhancing customer business through contract administration, customer orders, and problem resolution. Performance Monitoring is responsible for monitoring, analyzing, and reviewing customer contact quality.
**Responsibilities:**
+ Evaluate calls and cases to assess performance based on a standard set of criteria, providing constructive feedback and recognition to employees to ensure high performance and continuous improvement.
+ Accurately score transactions to gauge employee's quality performance based on organizational and departmental policies and requirements.
+ Monitor and evaluate team performance, whether voice or non-voice, of assigned entity and team, ensuring adherence to company quality standards, and compliance with industry regulations.
+ Track and report any trends from the customer experience that can be improved or celebrated.
+ Analyze and provide weekly & monthly trend analysis to leadership.
+ Provide support to leadership by participating in and hosting internal/external client calibration sessions.
+ Engage in and lead projects to promote quality enhancements and/or broaden services for the team.
+ Maintain a comprehensive understanding of quality systems and methodologies as well as knowledge of applicable regulations, standards, and operating procedures.
+ Conduct investigations/root cause analysis and formulate corrective action recommendations.
+ Show an understanding of the program requirements and be capable of conducting gap assessments based on those requirements.
+ Uphold quality standards that adhere to company, regulatory, and HIPAA policies and procedures.
+ Collaborate across various functions, interpret requirements, educate and influence others regarding those requirements.
+ Identify training needs or potential disciplinary actions which will be reported to leadership.
+ Build strong customer relationships and deliver customer-centric solutions.
+ Optimize work processes by identifying effective and efficient methods to complete tasks, with an emphasis on continuous improvement.
+ Develop strategic alliances and cooperate with stakeholders to achieve mutual goals.
+ Demonstrate resourcefulness by adeptly securing and efficiently deploying resources.
+ Analyze complex and high-quality, sometimes contradictory, information to solve problems effectively.
+ Hold oneself and others accountable for meeting commitments and objectives.
+ Exhibit situational adaptability by adjusting approach and demeanor in real time to meet the changing demands of various situations.
+ Create and implement diverse communication strategies that clearly address the specific requirements of various target audiences.
**Qualifications:**
+ HS Diploma, GED or technical certification in related field or equivalent experience, preferred. Diploma or degree in relevant field desirable.
+ 3+ years' call quality audit experience strongly preferred.
+ 3+ years' experience in a patient support program or hub field would be an asset.
+ Adverse Event reporting and reconciliation experience strongly preferred.
+ Data collection and trend reporting experience is essential for this role.
+ Proficiency in MS Office applications required - Outlook, Excel, PowerPoint, and Word.
+ Excellent verbal and written communication skills.
+ High regard for superior quality of service.
+ Ability to prioritize and manage multiple responsibilities.
+ Experience handling tasks where attention to detail is critical to success.
+ Bilingual Spanish would be an asset.
**What is expected of you and others at this level:**
+ Demonstrates strong leadership and collaboration skills with a proven ability to develop and execute effective quality assurance programs.
+ Works independently within established procedures; may receive general guidance on new assignments.
+ May provide general guidance or technical assistance to less experienced team members.
+ Excellent attention to detail and problem-solving skills.
+ Strong communication and interpersonal skills.
+ Ability to analyze data and generate reports.
+ Ability to drive process improvements and implement quality assurance procedures.
**TRAINING AND WORK SCHEDULES** : Your new hire training will take place 8:00am-5:00pm CST, mandatory attendance is required.
This position is full-time (8-hour shifts, 40 hours/week). Employees are required to have flexibility to work any of our shift schedules during our normal business hours of Monday-Friday, 7:00am- 8:00pm CST.
**REMOTE DETAILS:** You will work remotely, full-time. It will require a dedicated, quiet, private, distraction free environment with access to high-speed internet. We will provide you with the computer, technology and equipment needed to successfully perform your job. You will be responsible for providing high-speed internet. Internet requirements include the following:
+ Maintain a secure, high-speed, broadband internet connection (DSL, Cable, or Fiber) at the remote location. Dial-up, satellite, WIFI, Cellular connections are NOT acceptable.
+ Download speed of 15Mbps (megabyte per second)
+ Upload speed of 5Mbps (megabyte per second)
+ Ping Rate Maximum of 30ms (milliseconds)
+ Hardwired to the router
+ Surge protector with Network Line Protection for CAH issued equipment
**Anticipated hourly range:** $21.90 per hour - $31.40 per hour
**Bonus eligible:** No
**Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage
+ Paid time off plan
+ Health savings account (HSA)
+ 401k savings plan
+ Access to wages before pay day with myFlexPay
+ Flexible spending accounts (FSAs)
+ Short- and long-term disability coverage
+ Work-Life resources
+ Paid parental leave
+ Healthy lifestyle programs
**Application window anticipated to close:** 10/10/2025. If interested in opportunity, please submit application as soon as possible.
The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
+ Works independently within established procedures; may receive general guidance on new assignments
+ May provide general guidance or technical assistance to less experienced team members
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
_Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._
_To read and review this privacy notice click_ here (

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
Ensures quality control and quality assurance compliance across the manufacturing site. Serves as an integral member of QC leadership team with a focus on ensuring quality system requirements are achieved. Leads the site quality control unit and serves as the primary backup to the QC Head.
Responsibilities:
+ Lead the biologics site Raw Materials and Incoming Materials laboratory processes and programs for a high volume, high level of product complexity including multi products to ensure compliance with regulations including EU Annex 1, FDA Guidalines, EMA, ANSI, among others. Ensure robustness and approves investigations Raw Materials & Incoming, quality and process excursions or incident.
+ Direct RM & Incoming laboratory operations and programs such as RM & Incoming methods for materials, excipients, API, commodities. Testing of raw materials, commodities, USP water and cleaning samples.
+ Responsible for elevating to the appropriate levels of management within Quality Operations Senior Management of significant quality issues in a timely fashion. Reviews and approves laboratory instrumentation, utilities, and facilities qualification and labs system life cycle documentation.
+ Responsible for all raw and incoming materials and commodities (including ERP approval) in the Quality Control (QC) laboratory including direct reports and budgetary responsibilities.
+ Serves as the standalone laboratory systems and site Maximo administrator. Comply with AbbVie policies, ABL plant procedures, Food and Drug Administration (FDA), EMA, and other applicable regulatory agencies cGMP regulations and requirements.
+ Responsible for end results of the Incoming Quality Assurance area. Assures that all incoming materials received at ABL are inspected, sampled, tested, and disposition according to established policies and procedures. Provides strategic direction for area of operation and ensures tactical objectives are met.
+ Responsible for front- and back-room support activities for the RM and Incoming Lab during internal audits, Periodic Validation Review, Annual Product Reviews, and process data reviews and inspections.
+ Represents the decision-making authority on change related to compendia, supplier/service provider notifications, material specifications, analytical test methods, test method validation, SOPs, batch records, and site service requests. Leads the implementation of Quality-related projects, including metrics.
+ Manages a team of quality professionals. Directly responsible for the effective organization, administration, training, and supervision of their functional area.
+ Exception Report (ER) investigation, writing, review, and approval including ensuring effective CAPAs; qualification and validation protocol writing, review, and approval.
Significant Work Activities:
+ Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
+ Continuous walking for prolonged periods (more than 2 consecutive hours in an 8 hr. day) is required
+ Frequent to continuous computer usage (greater or equal to 50% of the workday) is required
Qualifications
+ Bachelor's degree Science (Chemistry or Biology) with 10 years of pharmaceutical (parenteral biologics preferred) Quality experience (preferably in QC) or an equivalent combination of education and experience.
+ Experience managing raw and incoming materials.
+ Knowledge in raw materials /Incoming Materials programs under ANSI guidelines is required.
+ Supplier Quality Programs knowledge and experience.
+ The selected candidate must be fully bilingual written and verbal, both in English and Spanish.
+ Experience with SmartQC, LIMS (Sample Manager), Empower is desired.
+ Previous experience leading teams.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
+ This job is eligible to participate in our long-term incentive programs
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

**At Corteva Agriscience,** you will help us grow what's next. No matter what your role, you will be part of a team that is building the future of agriculture - solving the world's food problems through innovation, technology, and putting people first.
The **Seed Production Technician** provides hands-on-support for seed production research across multiple crops at the Salinas Research Center. The role spans planning and executing field trials activities from seed receive to harvest, data collection and validation, material flow management, and supervision of short-term crews.
***Please note: there is no visa sponsorship or relocation assistance provided for this role.
**What You'll Do:**
+ Support operations at the Salinas Research Center across multiple crops, including material handling and preparation, data collection, printing and sorting of seed packets/labels, planting activities, pollination, detasseling, plot maintenance, and harvest.
+ Effectively manage assigned field research activities from experimental planning through harvesting.
+ Assist with material movement, including receiving and shipping materials.
+ Collect data and ensure data quality.
+ Supervise short-term, part-time crews to complete material movement and processing, hand harvesting, and field activities according to protocols, accurately and efficiently.
+ Assess and improve safety practices to meet safety goals and environmental standards.
+ Maintain an organized workspace and ensure tools, materials and data are properly stored and accessible.
+ Foster a welcoming and inclusive work environment.
+ Collaborate across process steps as needed.
+ Manage resources successfully under changing circumstances.
+ Ensure all operations are conducted safely.
+ Perform other duties as assigned.
**What Skills You Need:**
+ Bachelor's degree in agronomy, agriculture, or a related field, or an equivalent combination of relevant education and experience.
+ Valid US driver's license
+ Excellent interpersonal communication and teamwork skills, including conflict management.
+ Pride in accuracy, value for timeliness, and adaptability to change.
+ Willing and able to work outdoors in varying conditions (hot/cold, wet/dry. etc)
+ Ability to perform physical tasks, including lifting and working in varying ergonomic environments.
+ Strong self-motivation with the ability to initiate projects, make decisions, and effectively solve problems.
+ Willing and able to learn about various research fields and data collection equipment, as well as the necessary computer and data collection hardware and software.
+ Willing and able to work a daytime schedule with overtime hours, including weekend work during seasonal peaks.
+ Fully Bilingual in English and Spanish, with the ability to communicate fluently in both languages.
**What Makes You Stand Out:**
+ Previous research experience.
+ Mechanical aptitude coupled with computer knowledge to effectively operate sophisticated research equipment.
+ Knowledge of agronomy, crop production, plant development, and experimental field plot design.
**Benefits - How We'll Support You:**
+ Numerous development opportunities offered to build your skills
+ Be part of a company with a higher purpose and contribute to making the world a better place
+ Health benefits for you and your family on your first day of employment
+ Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays
+ Excellent parental leave which includes a minimum of 16 weeks for mother and father
+ Future planning with our competitive retirement savings plan and tuition reimbursement program
+ Learn more about our total rewards package here - Corteva Benefits ( Check out life at Corteva! you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team.
Corteva Agriscience is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.
Corteva Agriscience is an equal opportunity employer. We are committed to boldly embracing the power of inclusion, diversity, and equity to enrich the lives of our employees and strengthen the performance of our company, while advancing equity in agriculture. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. Discrimination, harassment and retaliation are inconsistent with our values and will not be tolerated. If you require a reasonable accommodation to search or apply for a position, please visit:Accessibility Page for Contact Information
For US Applicants: See the 'Equal Employment Opportunity is the Law' poster. To all recruitment agencies: Corteva does not accept unsolicited third party resumes and is not responsible for any fees related to unsolicited resumes.

**Job Description Summary**
The Manufacturing Technician is responsible for following established instructions for the execution of specific tasks in a biotechnology manufacturing setting, including the execution of manufacturing orders. The Manufacturing Technician should identify potential problems and bring them to the attention of the supervisor. He/she participates in continuous improvement projects.
**Job Description**
We are **the makers of possible**
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a **maker of possible** with us.
**RESPONSIBILITIES**
+ Material Preparation per established procedures.
+ Perform inspection, verification for calibration and maintenance of equipment.
+ Maintains related logs and manufacturing records.
+ Performs area in-process testing as requested.
+ Reclaim and re-test of resins.
+ Performs daily working area cleaning tasks.
+ Performs packing, cleaning and equilibration of chromatography columns as requested and scheduled.
+ Maintains inventory of chemicals and lab supplies required for manufacture. Completes material order transactions in SAP system and performs the required inventory control activities to maintain accuracy.
+ Support set up and manufacturing activities for the following areas: tissue culture, purification and conjugation.
+ Processes cell supernatant to remove debris and to concentrate product before purification.
+ Formulates monoclonal antibody reagents using established documentation.
+ Manufactures buffers and solutions using established procedures.
+ Uses equipment such as pipettes, micro-pipettes, balances, pH and conductivity meters, and UV/Visible spectrophotometers.
+ Performs assigned manufacturing tasks.
+ Complete Filling & Packaging process by scheduling, filling, labeling, bagging, pouching and vialing for: pellets, purified and conjugated materials, as required.
+ Promotes a safe work environment by providing recommendations on maintaining the safety of the work environment, following safety procedures, participating in Environment Health and Safety (EH&S) programs, initiating a corrective action whenever a hazard is identified, notifying supervisor of all observed hazardous conditions or unsafe work practices.
+ Supports Quality Assurance by keeping abreast of the basic requirements for compliance in own area of work and follows those requirements, participating as required in training on regulatory issues affecting own area of work, bringing regulatory compliance questions/issues to next level of management.
+ Maintain good housekeeping practices.
+ Provide recommendations to support systems that continuously improve product/process quality and product availability, reduce cost, and increase production capability.
+ Participates in Continuous Improvement initiatives.
+ Performs other related duties and assignments as required.
**MINIMUM QUALIFICATIONS**
**KNOWLEDGE AND SKILLS**
+ Knowledge of aseptic techniques.
+ Knowledge of methods required to perform in process testing.
+ Knowledge of the operation of related instrumentation such as Spectrophotometers, centrifuges, balances, conductivity meters, micropipettes, CO2 Incubators, Microscopes Micro plate readers, centrifuges, pipettes and Biosafety Hoods
+ Knowledge in the manufacture of dilutions, buffers and solutions.
+ Strong Mathematics skills.
+ Knowledge of GMP, FDA, ISO and OSHA requirements highly desirable.
+ Solid understanding on MS Windows environment software such as MS Office.
+ Effective skills on interpersonal relationships, written and oral communication, and planning/organization.
+ Demonstrated ability to follow established policies and procedures.
+ Bilingual in English - Spanish (read write, speak).
+ Attendance and punctuality are important functions of the job position.
**EDUCATION AND EXPERIENCE**
+ Requires an Associate Degree in a related field
+ 1+ year(s) of experience in a laboratory or pharmaceutical/medical device/biotechnology environment or equivalent combination of related education and experience.
**PHYSICAL DEMAND**
+ Frequently, the work requires carrying, lifting and pushing heavy level objects.
+ In addition, frequently requires pulling medium level objects.
+ Constantly, the job requires standing, walking, sitting, climbing, balancing, stooping, reaching, handling, fingering, talking, hearing and seeing (near/far/depth perception/visual color discrimination). Occasionally, the work requires kneeling.
**WORKING ENVIRONMENT**
+ The work is performed constantly inside the building.
+ The work requires exposure to extreme cold with or without temperature changes.
+ Also, requires the exposure to wet and/or humid conditions.
+ The work environment has hazards exposures (mechanical-equipment, electrical and burns) and atmospheric conditions (fumes and odors).
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
**Why Join Us?**
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit  Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.
#earlycareer
Required Skills
Optional Skills
.
**Primary Work Location**
USA PR Cayey - Vicks Drive (BDB)
**Additional Locations**
**Work Shift**
US BD 2nd Shift 2pm-1030pm (United States of America)
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Supply Chain Manufacturing
**Job Sub** **Function:**
Production Equipment Repair & Maintenance
**Job Category:**
Professional
**All Job Posting Locations:**
Gurabo, Puerto Rico, United States of America
**Job Description:**
**Sobre Medicina Innovadora**
Nuestra experiencia en Medicina Innovadora está informada e inspirada por pacientes, cuyas ideas alimentan nuestros avances científicos. Personas visionarias como tú trabajan en equipos que salvan vidas desarrollando medicamentos del mañana.
Únete a nuestro equipo en el desarrollo de tratamientos, encontrar curas y ser pioneros en el camino desde el laboratorio a la vida mientras alentamos pacientes en cada paso del camino.
Obtén más información en buscando al mejor talento para la posición Senior Manufacturing Technician, Lyo.**
**Propósito:** El Operador de liofilización tiene la responsabilidad de la operación del proceso de
liofilización en todas sus etapas (preparación de equipo, limpieza en sitio, esterilización en sitio, pruebas de fugas, integridad de filtros, carga de producto, ciclo de liofilización, descarga del producto). Monitoreo constante de los parámetros del proceso para identificar cualquier desviación del proceso validado y tomar las acciones correctivas para preservar la calidad del producto. Evaluación constante de toda la documentación (graficas e impresos) de todas las etapas del proceso para asegurar que toda la documentación sea legible, completa y cumpla con los parámetros establecidos. Responsable de la comunicación inmediata a los distintos departamentos requeridos (Mantenimiento, IT, Manufactura, QA de surgir alguna desviación de proceso que requiera la intervención de dichos departamentos. Ejecuta trabajos de mantenimientos preventivos y calibraciones del equipo. Responsable de asegurase que el equipo tiene todos los trabajos preventivos y calibraciones al día antes de utilizar el equipo en procesos de manufactura. Responsable por el orden y limpieza del cuarto de control y área operacional del
proceso de liofilización.
**Responsabilidades Principales:**
+ Ejecuta y domina las actividades del proceso de liofilización en todas sus etapas, también coteja que toda la información de lote, liofilizado a usarse y pruebas requeridas cumplan con las especificaciones antes de comenzar el proceso de liofilización.
+ Asiste en la revisión y actualización de las instrucciones de trabajo y los análisis de seguridad en el trabajo (JSA).
+ Ejecuta tareas de mantenimiento preventivo y/o correctivo.
+ Realiza "troubleshooting" a los equipos de su área funcional.
+ Lleva registro de las operaciones de los equipos y sistemas del área funcional asignada.
+ Documenta, revisa y verifica calibraciones de equipos e instrumentos previos al uso de los mismos de acuerdo a los procedimientos vigentes y se asegura de que todos los componentes y equipos a utilizarse estén aprobados y en cumplimiento con las especificaciones.
+ Ejecuta las actividades de liofilización siguiendo las instrucciones de manufactura y SOP's correspondientes y documenta dichas actividades.
+ Realiza, inspecciona y documenta la limpieza de las maquinas, equipos y el área de proceso asignada antes de comenzar y al concluir una tarea de acuerdo a los procedimientos establecidos.
+ Maneja montacargas y otros equipos para transportar materiales utilizados en la manufactura de lotes, si es requerido.
+ Responsable del monitoreo del sistema de Control Ambiental (Temperatura, Diferencial presión entre áreas, Humedad Relativas) de las áreas clasificadas y la notificación inmediata al personal correspondiente de surgir alguna alarma o desviación.
+ Documenta las actividades que realiza: limpieza, montaje, desmontaje, etc. En los registros o sistemas de documentación correspondientes de acuerdo a las Buenas Prácticas de Manufactura y las Reglas de documentación vigentes.
**Cualificaciones** **/** **R** **equisitos:**
+ Un mínimo de Grado Técnico en Mecánica Industrial, Electricidad, Instrumentación Electrónica u otro campo relacionado es requerido. Bachillerato en Administración, Ciencias, Ingeniería o campo relacionado es preferido.
+ Un mínimo de cuatro a seis (4-6) años de experiencia en la industria farmacéutica o dos (2) años de experiencia ejecutando como Operador de Liofilización es requerido.
+ Adiestramiento en "Train The Trainer" y Lean / Six-Sigma es preferido.
+ Certificación en "Yellow Belt" (Lean/Six-Sigma) es preferido.
+ Licencia de técnico de refrigeración y/o licencia de perito electricista es requerido.
+ Licencia de Montacargas es preferido.
Adiestramiento en el uso de sistemas computarizados de control de inventario y manejo de documentos es requerido.
+ Leer, escribir y entender ambos idiomas Español e Inglés es requerido.
+ Conocimiento y aplicación de regulaciones de Buenas Prácticas de Manufactura, Reglas de Documentación, Seguridad Ocupacional y Ambiental es requerido.
+ Conocimiento de la teoría y conceptos científicos de los procesos de manufactura de su área funcional, desde materia prima hasta producto final, incluyendo sus especificaciones es preferido.
+ Excelentes destrezas de solución de problemas ("troubleshooting"), incluyendo diagramas eléctricos, neumático e hidráulicos es requerido.
+ Buenas destrezas en el uso de sistemas computarizados son requeridas.
+ Disponibilidad para trabajar turnos de 12 horas, los 7 días de la semana es requerido. Adicional, debe tener flexibilidad para cambiar de turno o semana de trabajo, trabajar tiempo extra, fines de semana y días feriados de acuerdo con las necesidades de negocio es requerido.
Johnson & Johnson es un Empleador con Igualdad de Oportunidades. Todos los aplicantes calificados recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, edad, origen nacional, discapacidad, condición de veterano protegido u otras características protegidas por la ley federal, estatal o local. Buscamos activamente candidatos calificados que sean veteranos protegidos e individuos con discapacidades como se define en VEVRAA y la Sección 503 de la Ley de Rehabilitación.
Johnson and Johnson se compromete a proporcionar un proceso de entrevista que sea inclusivo con las necesidades de nuestros aplicantes. Si usted es una persona con una discapacidad y desea solicitar una adaptación, envíe un correo electrónico al Centro de Apoyo Médico para Empleados ( ) o póngase en contacto con AskGS para que le dirijan a su recurso de acomodación.
#LI-Onsite

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at no-style="text-align:left;">Job Function:

Supply Chain Manufacturing

Job Sub Function:

Production Equipment Repair & Maintenance

Job Category:

Professional

All Job Posting Locations:

Gurabo, Puerto Rico, United States of America

Job Description:

Sobre Medicina Innovadora

Nuestra experiencia en Medicina Innovadora está informada e inspirada por pacientes, cuyas ideas alimentan nuestros avances científicos. Personas visionarias como tú trabajan en equipos que salvan vidas desarrollando medicamentos del mañana.

Únete a nuestro equipo en el desarrollo de tratamientos, encontrar curas y ser pioneros en el camino desde el laboratorio a la vida mientras alentamos pacientes en cada paso del camino.

Obtén más información en buscando al mejor talento para la posición Senior Manufacturing Technician, Lyo.

Propósito: El Operador de liofilización tiene la responsabilidad de la operación del proceso de

liofilización en todas sus etapas (preparación de equipo, limpieza en sitio, esterilización en sitio, pruebas de fugas, integridad de filtros, carga de producto, ciclo de liofilización, descarga del producto). Monitoreo constante de los parámetros del proceso para identificar cualquier desviación del proceso validado y tomar las acciones correctivas para preservar la calidad del producto. Evaluación constante de toda la documentación (graficas e impresos) de todas las etapas del proceso para asegurar que toda la documentación sea legible, completa y cumpla con los parámetros establecidos. Responsable de la comunicación inmediata a los distintos departamentos requeridos (Mantenimiento, IT, Manufactura, QA de surgir alguna desviación de proceso que requiera la intervención de dichos departamentos. Ejecuta trabajos de mantenimientos preventivos y calibraciones del equipo. Responsable de asegurase que el equipo tiene todos los trabajos preventivos y calibraciones al día antes de utilizar el equipo en procesos de manufactura. Responsable por el orden y limpieza del cuarto de control y área operacional del

proceso de liofilización.

Responsabilidades Principales:

• Ejecuta y domina las actividades del proceso de liofilización en todas sus etapas, también coteja que toda la información de lote, liofilizado a usarse y pruebas requeridas cumplan con las especificaciones antes de comenzar el proceso de liofilización.
• Asiste en la revisión y actualización de las instrucciones de trabajo y los análisis de seguridad en el trabajo (JSA).
• Ejecuta tareas de mantenimiento preventivo y/o correctivo.
• Realiza “troubleshooting” a los equipos de su área funcional.
• Lleva registro de las operaciones de los equipos y sistemas del área funcional asignada.
• Documenta, revisa y verifica calibraciones de equipos e instrumentos previos al uso de los mismos de acuerdo a los procedimientos vigentes y se asegura de que todos los componentes y equipos a utilizarse estén aprobados y en cumplimiento con las especificaciones.
• Ejecuta las actividades de liofilización siguiendo las instrucciones de manufactura y SOP’s correspondientes y documenta dichas actividades.
• Realiza, inspecciona y documenta la limpieza de las maquinas, equipos y el área de proceso asignada antes de comenzar y al concluir una tarea de acuerdo a los procedimientos establecidos.
• Maneja montacargas y otros equipos para transportar materiales utilizados en la manufactura de lotes, si es requerido.
• Responsable del monitoreo del sistema de Control Ambiental (Temperatura, Diferencial presión entre áreas, Humedad Relativas) de las áreas clasificadas y la notificación inmediata al personal correspondiente de surgir alguna alarma o desviación.
• Documenta las actividades que realiza: limpieza, montaje, desmontaje, etc. En los registros o sistemas de documentación correspondientes de acuerdo a las Buenas Prácticas de Manufactura y las Reglas de documentación vigentes.

Cualificaciones / R equisitos:

• Un mínimo de Grado Técnico en Mecánica Industrial, Electricidad, Instrumentación Electrónica u otro campo relacionado es requerido. Bachillerato en Administración, Ciencias, Ingeniería o campo relacionado es preferido.
• Un mínimo de cuatro a seis (4-6) años de experiencia en la industria farmacéutica o dos (2) años de experiencia ejecutando como Operador de Liofilización es requerido.
• Adiestramiento en “Train The Trainer” y Lean / Six-Sigma es preferido.
• Certificación en “Yellow Belt” (Lean/Six-Sigma) es preferido.
• Licencia de técnico de refrigeración y/o licencia de perito electricista es requerido.  
• Licencia de Montacargas es preferido.

Adiestramiento en el uso de sistemas computarizados de control de inventario y manejo de documentos es requerido.

• Leer, escribir y entender ambos idiomas Español e Inglés es requerido.
• Conocimiento y aplicación de regulaciones de Buenas Prácticas de Manufactura, Reglas de Documentación, Seguridad Ocupacional y Ambiental es requerido.
• Conocimiento de la teoría y conceptos científicos de los procesos de manufactura de su área funcional, desde materia prima hasta producto final, incluyendo sus especificaciones es preferido.
• Excelentes destrezas de solución de problemas (“troubleshooting”), incluyendo diagramas eléctricos, neumático e hidráulicos es requerido.
• Buenas destrezas en el uso de sistemas computarizados son requeridas.
• Disponibilidad para trabajar turnos de 12 horas, los 7 días de la semana es requerido. Adicional, debe tener flexibilidad para cambiar de turno o semana de trabajo, trabajar tiempo extra, fines de semana y días feriados de acuerdo con las necesidades de negocio es requerido.

Johnson & Johnson es un Empleador con Igualdad de Oportunidades. Todos los aplicantes calificados recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, edad, origen nacional, discapacidad, condición de veterano protegido u otras características protegidas por la ley federal, estatal o local. Buscamos activamente candidatos calificados que sean veteranos protegidos e individuos con discapacidades como se define en VEVRAA y la Sección 503 de la Ley de Rehabilitación.

Johnson and Johnson se compromete a proporcionar un proceso de entrevista que sea inclusivo con las necesidades de nuestros aplicantes. Si usted es una persona con una discapacidad y desea solicitar una adaptación, envíe un correo electrónico al Centro de Apoyo Médico para Empleados ( ) o póngase en contacto con AskGS para que le dirijan a su recurso de acomodación.

#LI-Onsite 

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**Join Amgen's Mission of Serving Patients**
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**MANUFACTURING PROCESS TECHNICIAN**
**What you will do**
Let's do this. Let's change the world. In this vital role you will support safe and efficient manufacturing processes, ensuring high-quality production through collaboration, precision, and adherence to Good Manufacturing Practices.
**Specific responsibilities include but are not limited to:**
+ Operate, set up, and troubleshoot manufacturing and inspection equipment, ensuring safety, quality, and efficiency.
+ Perform routine inspections and tests to verify compliance with specifications; document results accurately using electronic systems.
+ Identify and resolve basic equipment performance issues; escalate deviations as needed.
+ Support automated and manual inspection and packaging processes in accordance with SOPs and GMP standards.
+ Maintain accurate records through systems such as SAP and EBR; ensure timely and consistent data entry.
+ Follow cGMPs, SOPs, and safety protocols during all manufacturing activities.
+ Maintain a clean, organized workspace to support efficient operations and product integrity.
+ Participate in deviation investigations and assist with data collection and basic troubleshooting.
+ Communicate effectively with team members during shift handoffs, huddles, and daily operations.
+ Seek guidance from peers and leadership to build technical knowledge and adapt to changing priorities.
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The Manufacturing Process Technician professional we seek is an individual contributor with these qualifications.
**Basic Qualifications:**
Associate's degree
Or
High school/GED + 1 year of Manufacturing work or military experience
**Preferred Qualifications:**
+ Technical degree.
+ Experience in GMP manufacturing or another regulated environment.
+ Familiarity with manual inspection and packaging activities.
+ Proficiency in computer systems and electronic batch records.
+ Strong attention to detail, organizational skills, and ability to work independently.
+ Team player with problem-solving skills, capable of troubleshooting issues and implementing corrective actions collaboratively.
+ Quality-driven, diligent, and proactive with a positive attitude.
+ Flexible to work non-standard shifts, including weekends and holidays, as needed.
+ Proficiency in both Spanish and English (written and verbal).
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being.
In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
+ A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
+ A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
+ Stock-based long-term incentives
+ Award-winning time-off plans and an annual site shutdown
+ Flexible work models, including remote work arrangements, where possible
**Apply now and make a lasting impact with the Amgen team.**
**careers.amgen.com**
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.