Descubre oportunidades laborales en Juncos, Puerto Rico, un municipio con una economía diversificada. Aunque no se especifica un tipo de trabajo, Juncos ofrece empleos en sectores como manufactura, servicios y comercio minorista. La búsqueda de empleo en esta área puede revelar posiciones en empresas locales y multinacionales que operan en la región.110 Empleos en Juncos
Medical Records Technician (Juncos, PR) 6010
Hoy
Trabajo visto
Descripción Del Trabajo
Advantmed is hiring enthusiastic Medical Records Technicians This is a great "foot-in-the-door" position for those looking to be involved in the emerging Healthcare & Technology industry.
At Advantmed, our mission is to improve the healthcare system by ensuring appropriate, quality care, and eliminating unnecessary costs. Advantmed is a privately held company founded in 2005 and composed of over 1,800 seasoned professionals aligned by one common goal: to meet our clients' evolving needs with accuracy, efficiency, and transparency.
We would love to have you join our team of dedicated professionals We encourage you to visit the details of the role by watching the video available at the following link: Medical Records Technician
Our Medical Records Technicians receive company-provided laptops and portable scanners to travel to various medical facilities and hospitals for scanning patient medical records.
Duties and Responsibilities:
- Maintain a record system for patient information and gathering documents.
- Use electronic systems to properly collect, organize, and manage data.
- Ensure medical records are organized, accurate, and complete.
- Create digital copies of paperwork and store records electronically.
- File paperwork/reports quickly and accurately.
- Ensure HIPAA standards are met.
- Follow all confidentiality guidelines, rules, and procedures.
- Interact with medical staff, healthcare providers, and other medical personnel.
- Ability to lift and carry up to 25 pounds.
Additional Good-to-Have Qualifications:
- Previous work experience in a healthcare setting, such as a hospital, clinic, or medical office dealing with medical charts.
- Proficiency in Electronic Health Records (EHR) / EMR systems such as Epic, Cerner, Meditech, etc.
- Intermediate knowledge of medical chart structure, content, and medical terminologies.
- Familiarity with Word, Excel, and Outlook for documentation and communication.
- Ability to operate and troubleshoot common issues with printers and scanners.
- Strong verbal and written communication skills for interacting with healthcare professionals.
Must-Have Qualifications:
- Valid driver's license and clean motor vehicle record.
- Have a car and active insurance in their name (Candidates must provide registration documentation).
- Willing to drive up to 60-80 miles or more (round-trip).
- Internet access at home.
- Basic PC and office equipment skills.
- Applicants must be available from 08:00 am to 05:00 pm in their respective time zones to visit the required facilities.
- Candidate must be bilingual in English and Spanish.
Pay Rate:
- $10.50-$1 per hour or 1.75 per record, whichever is higher
- Paid semi-monthly based on total hours worked or total records retrieved during the work period (whichever is higher).
- Paid mileage, reimbursement for some travel expenses, paid 50 (daily) Food Allowance, when traveling out of state & paid Flight + Hotel + Rental (if required).
This is a part-time, seasonal position, with the potential for extension based on project requirements and needs
Process Development Scientist
Hoy
Trabajo visto
Descripción Del Trabajo
We are seeking a Process Development Scientist to lead and support scientific experimentation, equipment characterization, and validation activities within a regulated manufacturing or packaging environment. This role involves designing and executing experimental strategies, analyzing data, and developing robust protocols to support equipment implementation and process optimization. The ideal candidate will bring deep technical expertise, strong project management skills, and the ability to collaborate across multidisciplinary teams.
Key Responsibilities
- Conceive, design, and execute scientific experiments under general guidance.
- Analyze and interpret experimental data to assess impact on project goals.
- Develop and implement novel protocols to address specific technical challenges.
- Ensure studies are conducted in compliance with applicable guidelines and regulations.
- Monitor scientific literature and technology trends relevant to the role.
- Lead development and execution of equipment characterization strategies.
- Design and implement testing protocols, including SATs and challenge validations.
- Author technical reports, validation documentation, and risk assessments.
- Apply QRAES methodology to support risk-based decision making.
- Support new equipment installations through validation planning and execution.
- Collaborate with internal departments to support project execution and troubleshooting.
- Represent the department on project teams and contribute to cross-functional initiatives.
- Mentor junior staff and contribute to department-wide efforts such as safety and recruiting.
- Communicate project status and findings effectively to stakeholders.
Education & Experience
- Doctorate degree
OR - Master's degree with 5 years of scientific experience
OR - Bachelor's degree with 6 years of scientific experience
Technical & Software Requirements
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong knowledge of cGMP regulations and validation processes
- Experience with vision system technologies and inspection/packaging concepts
- Fully bilingual in English and Spanish
Preferred Qualifications
- Expertise in equipment and process characterization
- Experience developing testing strategies and validation protocols
- Strong technical writing and documentation skills
- Familiarity with risk assessment methodologies (e.g., QRAES)
- Ability to solve routine technical problems and manage change effectively
- Strong verbal communication, negotiation, and conflict resolution skills
- Project management experience in a regulated environment
- 5-month contract
- Administrative Shift
Operador de Produccion
Hoy
Trabajo visto
Descripción Del Trabajo
Pan American Grain es una empresa que se desempeña desde hace 45 años en el negocio de importación, procesamiento, manufactura y distribución de alimentos y otros productos (Arroz Rico, Café Mami, Gasolina Party Pouch, Pan American Wine and Spirits, Harina Rico, Café del Patio, fertilizantes). En Pan American Grain nos encontramos en la búsqueda de recursos para nuestra División de Arroz Rico. Como operador de produccion debe mantener el buen funcionamiento de la línea de producción diaria de la empresa para evitar los desperdicios y los errores de planta. Planta localizada en Cataño.
Disponibilidad para 3er turno (10:00 pm - 6:30 am), turno de noche a madrugada.
Como Operador de Producción realizarás las siguientes funciones:
- Realizar las asignaciones otorgadas dentro de la cadena de producción.
- Asistir a los compañeros en el ciclo de producción.
- Documentar las fallas de la maquinaria o de los productos hechos durante el turno de trabajo.
- Revisar la calidad de los productos que esté elaborando la cadena de producción y detectar los errores antes de finalizar el producto.
- Revisar diariamente que el equipo y materiales que utiliza se encuentren en buen estado.
- Reportar cualquier defecto o problema inmediatamente.
- Encargarse de los desechos de materiales utilizados durante el turno depositándolos donde corresponda.
- Controlar y revisar las medidas de seguridad de la planta periódicamente y reportar cualquier problema inmediatamente.
- Corroborar que los detectores e imanes de metales están funcionando antes de comenzar la producción.
- Realizar la verificación del funcionamiento correcto del detector cada tres (3) horas, y registrar la misma en la hoja provista.
- Si durante una de las verificaciones detecta que el detector o los imanes no están funcionando, deberá notificar al Supervisor y al personal de Control de Calidad.
- Cualquier otra tarea que asigne el supervisor o la gerencia.
- Documentacion de trabajos realizados.
Limpiar maquinaria y/ equipo de los procesos de manufactura de las áreas a la que este asignado, de acuerdo a los procedimientos establecidos. - Mantener las áreas y/o cuartos asignados limpios, ordenados y segregados, de acuerdo a los procedimientos.
● Disponibilidad para 3er turno (10:00pm - 6:30 am), turno de noche a madrugada
● Educación – Cuarto Año Escuela Secundaria.
● Experiencia – Indispensable que sepa manejar maquinaria de producción y que conozca términos técnicos de la maquinaria. 1 a 2 años de experiencia preferible.
● Debe ser ordenado y enfocado a resultados y a seguir procedimientos de producción.
● Destrezas de Lenguaje – Habilidad para leer e interpretar documentos como manuales de procedimientos.
● Otros Requisitos – Responsable y Puntual.
● Debe poder cargar un peso de por lo menos 50 libras.
● Licencia de conducir vigente
● Debe hacerse Certificado de Salud y Cultivo de Garganta para comenzar el empleo
● Debe tener Zapatos de Seguridad, el resto del equipo se provee.
BenefitsPlan médico, 401k, días de vacaciones, enfermedad, feriados, Bono de Navidad entre otros.
Engineer-Process/Operations
Hoy
Trabajo visto
Descripción Del Trabajo
Under general supervision, the Process/Operations Engineer provides characterization of process optimization strategies and/or troubleshooting of operational issues in operations, manufacturing, pilot plant, or capital project environments. This role applies fundamental engineering principles to design and implement system modifications, experiments, and/or capital projects. The engineer organizes, analyzes, and interprets results to address operational challenges or engineering projects of moderate scope and complexity.
Responsibilities
- Provide solutions to a variety of technical problems of moderate scope and complexity.
- Evaluate, select, and apply standard engineering techniques and procedures under general supervision (with guidance for unusual problems).
- Perform assignments with clear and specific objectives requiring investigation of limited variables.
- Initiate and complete routine technical tasks.
- Act as a technical expert for equipment or systems regarding troubleshooting and daily operations support.
- Actively engage in operations when required to meet schedules or resolve complex problems.
- Routinely audit operational performance and regulatory compliance of equipment or systems of moderate complexity.
- Collaborate with cross-functional groups (research, manufacturing, maintenance, process development, utilities, facilities, QA, validation) to develop requirements and recommendations for system modifications.
- Support project managers in completing design, engineering, and construction projects within schedule and budget.
- Work with consultants, architects, and engineering firms on the development of standard design documents.
- Obtain and critique vendor quotes for equipment modifications or installations.
- Generate basic project cost estimates and schedules.
Education Requirements
- Master's degree in Engineering, OR
- Bachelor's degree in Engineering + 2 years of engineering experience.
Preferred Qualifications
- Experience in the purification process of proteins.
- Familiarity with pharmaceutical/biotech processes.
- Knowledge of validation processes and documentation in highly regulated environments.
- Experience in investigations, troubleshooting, process improvements, and technical writing.
- Ability to operate specialized laboratory equipment and relevant computer systems.
- Understanding and application of GLPs and GMPs.
- Strong problem-solving and applied engineering skills.
- Ability to write technical reports and validation protocols.
- Effective verbal and written communication skills, including technical presentations.
- Skills in personal organization, analytical problem solving, computer literacy, and managing change.
- 1 year contract with possible extension
- Administrative Shift
Engineer
Hoy
Trabajo visto
Descripción Del Trabajo
Under general supervision, the Engineer provides technical support to manufacturing operations by applying engineering principles to troubleshoot, optimize, and improve processes and equipment. This role involves implementing process optimization strategies, equipment/system modifications, upgrades, replacements, and troubleshooting activities in a regulated pharmaceutical/biotech environment. The engineer ensures compliance with corporate policies, industry standards, GMP requirements, and regulatory guidelines. This position requires flexibility to support non-standard shifts, including nights and weekends, depending on business needs.
Key Responsibilities
- Provide solutions to a variety of technical problems of moderate scope and complexity.
- Evaluate, select, and apply standard engineering techniques and principles with limited supervision.
- Function as a technical expert for process, equipment, and/or systems during troubleshooting and cross-functional discussions.
- Frequently participate in daily operations to resolve complex issues or ensure schedules are met.
- Monitor manufacturing processes and equipment performance; identify and recommend corrective actions and process optimizations.
- Collaborate with Manufacturing, Maintenance, Utilities, Facilities, QA, Validation, and Process Development teams to define requirements and recommend system modifications.
- Support manufacturing/quality systems such as deviations, CAPAs, equipment qualifications, and process validations.
- Apply scientific expertise, compliance knowledge, and troubleshooting skills to manufacturing operations.
- Organize, analyze, and present interpretation of data and results for operational issues or projects.
- Apply engineering principles to support design and execution of experiments, system modifications, and capital projects.
- Lead or support the implementation of equipment improvement projects.
- Act as SME (Subject Matter Expert) for designated systems regarding design, maintenance, and compliance operations.
- Drive Environmental, Health, and Safety (EHS) compliance within area of responsibility.
- Support deviation investigations, define and implement CAPAs, and ensure equipment reliability within assigned area.
- Develop and track equipment performance metrics (availability, downtime, PM effectiveness, etc.), with focus on improvement opportunities.
- Manage equipment ownership responsibilities in CMMS (approving/closing work orders, PM strategy, spare parts updates, and reliability assessments).
Education & Experience Requirements
- Master's degree in Engineering OR
- Bachelor's degree in Engineering with 2+ years of engineering experience.
- Educational background in Mechanical, Electrical, and/or Chemical Engineering.
Required Skills & Competencies
- Experience with equipment and/or process troubleshooting in a regulated (pharma/biotech) environment.
- Knowledge of pharmaceutical/biotech processes, GMP production operations, and regulatory compliance.
- Strong organizational and technical writing skills.
- Proficient presentation and communication skills in English and Spanish.
- Ability to interpret and apply GLPs and GMPs.
- Strong problem-solving and applied engineering skills.
- Basic experience in validation protocols, technical reports, and system documentation.
- Proficiency with computer systems, CMMS, and technical tools.
Preferred Qualifications
- Ownership of manufacturing equipment in CMMS (work orders, PMs, spare parts accuracy, reliability assessments).
- Experience leading equipment performance improvement initiatives.
- Familiarity with validation processes and protocol execution requirements.
- Strong background in equipment reliability engineering and maintenance strategy development.
- Proven ability to lead cross-functional collaboration on equipment/system improvements.
- Demonstrated ability to manage change and drive continuous improvement initiatives.
- Prior experience as SME for equipment/system compliance and design.
- Ability to generate project cost estimates, schedules, and evaluate vendor quotes.
Shift & Work Schedule
- Non-standard shift support required (including nights and weekends on a 2/3/2 day schedule as per business needs).
- Must be flexible to support extended hours when required.
- Administrative shift available
Operador de Molino 3er turno
Hoy
Trabajo visto
Descripción Del Trabajo
Pan American Grain es una empresa que se desempeña desde hace 45 años en el negocio de importación, procesamiento, manufactura y distribución de alimentos y otros productos (Arroz Rico, Café Mami, Gasolina Party Pouch, Pan American Wine and Spirits, Harina Rico, Café del Patio, fertilizantes). En Pan American Grain nos encontramos en la búsqueda de recursos para nuestra División de Arroz Rico.
Disponibilidad para 3er turno (10:00 pm - 6:30 am), turno de noche a madrugada.
El / La operador/a del molino es responsable de controlar la entrada a esta área restringida. Él / Ella será responsable de notificar al Supervisor si alguna persona no autorizada quiere entrar al molino. Él / Ella será responsable de lograr la máxima eficiencia de molienda con la más alta calidad. Él / Ella será responsable de seguir todas las normas de seguridad de los alimentos, incluidas las GMP, HACCP, OSHA, NFPA, etc.
Tareas:
- Controlar equipos de molinos, válvulas desviadoras y compuertas para procesar el producto programado.
- Mantiene la calidad del producto, los estándares de sanidad del molino y los requisitos de producción.
- Informes completos y documentación requerida.
- Opera Montacargas según sea necesario.
- Ser capaz de preparar el arroz que se va a procesar del molino.
- Proporcionar garantía de calidad para el producto.
- Realizar mediciones de Silos.
- Mantener la limpieza de las áreas de trabajo.
- Cualquier otra tarea que asigne el supervisor o la gerencia.
Cualificaciones: Para desempeñar su trabajo exitosamente, la persona debe ser capaz de llevar a cabo las funciones esenciales del puesto. Los requerimientos establecidos a continuación son representativos del conocimiento, destreza y/o habilidad requerida. Acomodo razonable puede ser hecho para permitir a personas con impedimentos llevar a cabo las funciones esenciales del puesto.
- Educación – Cuarto año completado, .
- Disponibilidad para 3er turno (10:00 pm - 6:30 am), turno de noche a madrugada.
- Experiencia –2 a 3 años de experiencia en un entorno de molienda de arroz. Debe ser ordenado y enfocado a resultados y a seguir procedimientos.
- Destrezas de Lenguaje – Habilidad para leer e interpretar documentos como manuales de procedimientos.
- Otros Requisitos – Responsable y Puntual.
- Habilidades – Capaz de operar equipos de molienda de arroz, Puede levantar 40 lbs consistentemente. Debe ser ordenado y enfocado a resultados y a seguir procedimientos.
Plan médico, 401k, días de vacaciones, enfermedad, feriados, Bono de Navidad entre otros.
Specialist Tech Engineering
Hoy
Trabajo visto
Descripción Del Trabajo
The Specialist, Technical Engineering provides technical engineering support for system and equipment optimization, upgrades, replacements, and modifications. This role ensures that maintenance operations are executed in compliance with corporate policies, industry regulations, and FDA standards. The Specialist will serve as a key liaison between the maintenance, engineering, and compliance teams to maintain operational excellence and regulatory readiness.
Key Responsibilities
- Ensure utility systems, process maintenance, instrumentation, calibration, electrical, and technical cleaning systems meet all applicable regulatory and FDA standards.
- Maintain consistency in maintenance team training programs, SOPs, and operational standards.
- Provide technical support to the maintenance team on issues related to engineering, regulatory compliance, calibration, quality, environmental monitoring, cleaning, validation, and electrical systems.
- Support maintenance activities and provide technical assistance during FDA and other regulatory inspections.
- Assist in developing responses to FDA and other regulatory agency observations.
- Support investigations and corrective actions for high-purity water systems and environmental monitoring alert/action notifications.
- Develop and maintain an audit program for the maintenance team; conduct routine audits of operations, documentation, and systems to ensure compliance.
- Collaborate with plant engineering to evaluate and implement process improvements, compliance upgrades, and optimization initiatives.
- Evaluate sanitization and maintenance procedures and recommend process or utility system modifications to Plant Engineering.
- Propose and implement departmental improvements and policy updates as needed.
Skills
- Strong leadership and team-building abilities
- Excellent verbal and written communication, including technical writing
- Organizational and facilitation skills
- Ability to manage and adapt to change effectively
- Comprehensive understanding of validation protocol requirements
- Technical expertise in equipment and system operations
- Analytical problem-solving and project management skills
- Proficient in scheduling and computer literacy
Education & Experience
- Doctorate in Engineering, or
- Master's degree with 3 years of Engineering experience, or
- Bachelor's degree with 5 years of Engineering experience, or
- Associate's degree with 10 years of Engineering experience, or
- High school diploma/GED with 12 years of Engineering experience.
Preferred Qualifications
- Experience with MAXIMO data entry and management
- Skilled in data sheets, job plans, and MMP package creation
- Familiarity with technical drawings and schematics
- Highly organized, detail-oriented, and able to manage multiple priorities in a regulated environment
- Contract position
- Administrative Shift
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Mecanico o tecnico Industrial, 3er turno, Cataño
Hoy
Trabajo visto
Descripción Del Trabajo
Pan American Grain es una empresa que se desempeña desde hace 45 años en el negocio de importación, procesamiento, manufactura y distribución de alimentos y otros productos (Arroz Rico, Café Mami, Gasolina Party Pouch, Pan American Wine and Spirits, Harina Rico, Café del Patio, fertilizantes). En Pan American Grain nos encontramos en la búsqueda de recursos para nuestra División de Arroz Rico.
Si te apasiona un ambiente altamente dinámico en el que puedas poner a prueba todos tus conocimientos y destrezas ¿Posees conocimientos y experiencia en el mantenimiento preventivo y reparación de maquinaria de manufactura? En Pan American Grain queremos conocerte. Pan American es una empresa netamente puertorriqueña sólida y en proceso de expansión que desea robustecer el Departamento de Mantenimiento en la planta de Cataño para atender los nuevos retos y exigencias del mercado . Planta localizada en Cataño. Disponibilidad para trabajar 3er turno; lunes - viernes: 10:00 pm - 6:30 am (noche a madrugada)
Como Mecánico o Tecnico llevaras a cabo las siguientes funciones:
- Realizar mantenimiento preventivo.
- Inspeccionar diariamente equipos y maquinaria.
- Trabajar en la reparación y mantenimiento de equipos de proceso.
- Realizar lecturas diarias de funcionamiento de los equipos.
- Validar que los equipos se encuentren operando dentro de los parámetros SOP.
- Documentar diariamente de registros de inspección.
- Revisar el plan de producción.
- Ensamblaje y montaje de piezas y equipos.
- Estudios en mecánica industrial, electromecánica, estudios tecnicos o area relacionada
- Disponibilidad para trabajar 3er turno; lunes - viernes: 10:00 pm - 6:30 am (noche a madrugada)
- Experiencia en mantenimiento preventivo y correctivo
- Experiencia trabajando con motores.
- Capacidad de trabajar horas extras, fines de semana y turnos irregulares, de ser necesario.
- Leer planos electrónicos o esquemáticos
- Conocimiento básico en electricidad
- Disponibilidad de responder a llamadas de emergencia.
- Capacidad de dar soporte a otros departamentos o proyectos según las necesidades del negocio.
Plan médico, 401k, días de vacaciones, enfermedad, feriados, Bono de Navidad entre otros.
Specialist QA
Hoy
Trabajo visto
Descripción Del Trabajo
The Specialist, Quality Assurance will perform a wide range of QA responsibilities under minimal supervision. This role requires strong expertise in validations, commissioning & qualification of manufacturing and laboratory equipment, technical writing, and quality systems. The Specialist will act as a key partner across cross-functional teams to ensure compliance, drive quality improvements, and support regulatory readiness.
Key Responsibilities
- Review and approve product Master Plans (MPs).
- Approve validation protocols and reports for manufacturing processes.
- Serve on incident triage teams and approve planned incidents.
- Approve Environmental Characterization reports.
- Release sanitary utility systems.
- Represent QA in New Product Introduction (NPI) teams.
- Lead investigations and site audits.
- Serve as designee for QA Manager on local CCRB.
- Own and maintain site quality program procedures.
- Review and approve risk assessments.
- Support automation, facilities, and environmental programs.
- Review and approve Work Orders, EMS/BMS alarms, nonconformance (NC) investigations, and CAPA records.
- Approve change controls.
- Provide lot disposition and authorize lots for shipment.
Core Competencies & Skills
- Strong knowledge of QA, QAL, validation, manufacturing, and distribution processes.
- Project management and organizational skills with ability to complete assignments independently.
- Proven leadership in cross-functional teams with strong influencing and negotiation skills.
- Experience interacting with regulatory agencies.
- Advanced data trending, evaluation, and compliance issue resolution skills.
- Proficiency with word processing, presentation, database, and spreadsheet applications.
- Strong communication, facilitation, and presentation skills.
- Ability to collaborate effectively across multiple levels of the organization.
- Demonstrated commitment to core values and quality practices.
Doctorate OR
Master's degree + 2 years directly related experience OR
- Bachelor's degree + 4 years directly related experience OR
- Associate's degree + 8 years directly related experience OR
- High school diploma/GED + 10 years directly related experience.
- Background in Sciences or Engineering required.
Preferred Qualifications
- Quality professional with expertise in Validations and Commissioning & Qualification (IOQ, PQ, Functional Test) of manufacturing and laboratory equipment.
- Strong knowledge of Technical Writing, Quality Systems (Deviations, Change Control), and Maintenance processes (PM, Work Orders, Job Plans review/approval).
- Experience reviewing technical documents (Validation Reports, Procedures, Forms).
- 1 year contract with possible extension
- Administrative Shift
Process/Operations Engineer
Hoy
Trabajo visto
Descripción Del Trabajo
Under general supervision, the Process/Operations Engineer provides characterization of process optimization strategies and/or troubleshooting of operational issues in operations, manufacturing, pilot plant, or capital project environments. This role applies fundamental engineering principles to design and implement system modifications, experiments, and/or capital projects. The engineer organizes, analyzes, and interprets results to address operational challenges or engineering projects of moderate scope and complexity.
Responsibilities
- Provide solutions to a variety of technical problems of moderate scope and complexity.
- Evaluate, select, and apply standard engineering techniques and procedures under general supervision (with guidance for unusual problems).
- Perform assignments with clear and specific objectives requiring investigation of limited variables.
- Initiate and complete routine technical tasks.
- Act as a technical expert for equipment or systems regarding troubleshooting and daily operations support.
- Actively engage in operations when required to meet schedules or resolve complex problems.
- Routinely audit operational performance and regulatory compliance of equipment or systems of moderate complexity.
- Collaborate with cross-functional groups (research, manufacturing, maintenance, process development, utilities, facilities, QA, validation) to develop requirements and recommendations for system modifications.
- Support project managers in completing design, engineering, and construction projects within schedule and budget.
- Work with consultants, architects, and engineering firms on the development of standard design documents.
- Obtain and critique vendor quotes for equipment modifications or installations.
- Generate basic project cost estimates and schedules.
Education Requirements
- Master's degree in Engineering, OR
- Bachelor's degree in Engineering + 2 years of engineering experience.
Preferred Qualifications
- Experience in the purification process of proteins.
- Familiarity with pharmaceutical/biotech processes.
- Knowledge of validation processes and documentation in highly regulated environments.
- Experience in investigations, troubleshooting, process improvements, and technical writing.
- Ability to operate specialized laboratory equipment and relevant computer systems.
- Understanding and application of GLPs and GMPs.
- Strong problem-solving and applied engineering skills.
- Ability to write technical reports and validation protocols.
- Effective verbal and written communication skills, including technical presentations.
- Skills in personal organization, analytical problem solving, computer literacy, and managing change.
- 1 year contract with possible extension