Quality control technician jobs in Carolina, PR

**_Inspector/a de Calidad_** **Turnos:** Disponibilidad para todos los turnos **Tipo de empleo:** Temporero/a Regular después de 6 meses **Descripción del puesto** Buscamos un/a Inspector/a de Calidad responsable de realizar pruebas e inspecciones de productos, materiales y componentes a lo largo del proceso de manufactura. Asegurará el cumplimiento de estándares de calidad, guías de la FDA y buenas prácticas de documentación. **Responsabilidades principales** Seleccionar y analizar muestras en diferentes etapas de producción. Evaluar datos, preparar informes y validar desviaciones. Aprobar o rechazar lotes según criterios de calidad. Documentar información en sistemas QAD y generar reportes. Reportar problemas o desviaciones a su supervisor. Mantener áreas de trabajo limpias (6S) y cumplir con normas de seguridad, FDA y políticas ambientales. Participar en actividades de mejora continua (SBU). **Requisitos** Diploma de Escuela Superior o GED. 1-3 años de experiencia industrial (preferible en ambiente regulado por FDA). Preferible Bachillerato relacionado. Bilingüe (español/inglés). **Habilidades:** atención al detalle, comunicación, análisis, multitareas, manejo del tiempo, adaptabilidad. Capacidad para trabajar con diversas audiencias, pensar críticamente y mantener relaciones efectivas. **Pay Details:** $12.00 per hour Benefit offerings available for our associates include short-term disability and additional voluntary benefits including medical, dental, vision, life insurance, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave and Vacation Leave or any other paid leave required by Federal, State, or local law where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ********************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance

Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, manufacturing operations among other services. Job Description Development and execution of Laboratory Equipment Validation. Development of Validation Plan, Risk Assessment, IOQ, CSV IOQ, Traceability Matrix, Validation Report, Operational and Administrative SOPs. Execution of related validation protocols. Development of documentation packages for all activities, including: Original format documents, approved document and applicable drawings. Qualifications Bachelor Degree in Chemistry or related discipline Experience developing Validation Plans, Risk Assessments, IOQ, CSV IOQ, Traceability Matrix, Validation Report, Operational and Administrative SOPs. Validation Experience in Computer Systems 21 CFR Part 11 practical knowledge Strong knowledge in GMPs regulations Technical Writing Experience Validation expertise in: Sterilization Kaye Validator & Data loggers Process Validation Equipment Qualification Re-qualification Computer System Validation Additional Information Positions available for Puerto Rico. Only candidates that meet the minimum requirements will be considered. Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer.

The Quality Technician will assist in the execution and documentation of quality control activities, focusing on inspection processes, document review, and support for manufacturing area(s). Responsibilities: Review production documentation per batches. Assist in the revision of incoming inspection documentation. Perform quality checks on assembly and inspection lines using established techniques. Document inspection results and escalate non-conformances. Maintain compliance with internal procedures and regulatory requirements. Apply regulatory compliance and quality practices in a regulated manufacturing work environment. Other assigned duties, as assigned. Qualifications: Bachelor´s degree in Science, Administration, Engineering, or related field. Minimum of 3 years of experience in quality assurance for manufacturing industries. Familiarity with validation documentation and inspection protocols. Detail-oriented with strong documentation and communication skills. Bilingual (English/Spanish) preferred. Work Methodology: 100% On-site and Full-time project 13 months (1st Contract) Administrative Shift (if a special validation is required, a second shift may need to be scheduled based on the need). Professional services contract

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide. Currently, one of our clients in the North Region is looking to hire a Process Development Technician. * Associate degree, with at least 3 years of medical devices or pharma experience. * Proven record of working closely and successfully with manufacturing and process development engineers. * Supports development of capable processes and ensures efficient and effective transfer of products into production. * Basic understanding of medical device documentation requirements. * Ability to read electrical prints and schematics. * Technical writing skills * lly bilingual - Spanish & English

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Summary of Role: Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. Responsibilities: Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot for assays as necessary Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, Lead audit teams May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, Independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. Shift: Administrative Location: Juncos, PR Education: Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience. Preferred Qualifications: Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses Strong knowledge in Microsoft Excel as a Tool for Data Analysis Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experience with quality process management Basic Knowledge on equipment preventive maintenance and troubleshooting Agile on prioritization of critical tasks Ability to develop inspection or qualification protocols in a short timeframe period. Strong negotiation skills Skill: Understand, support and demonstrate the values. Excellent communication skills, facilitation and presentation skills. Excellent technical writing skills. Strong computer operation skills including work processing, presentation, database and spreadsheet application skills. Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion. Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities. Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution. Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility. Knowledge of pharmaceutical processes. Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products. Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products. Extensive knowledge and application of GMPs/CFRs. Ability to evaluate compliance issues. Skill in evaluating and documenting according to Company and various guidelines. Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. Advanced scientific data analysis and interpretation skills. Advanced skills in solving complex problems. Advanced data trending and evaluation. Strong skill in working independently and to effectively interact with various levels. Ability to interact with regulatory agencies both orally and in writing. Initiate, coordinate and lead cross functional teams. Excellent skill in leading, motivating, influencing, and negotiating. This position is for a fixed term contract supporting one of ECHO Consulting Group (a Cencora company) partners on site at their facility. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated CompaniesAffiliated Companies: Echo Consulting Group Inc

As an on -site Solar Quality Inspector, you will be responsible for ensuring that every Prosolar photovoltaic system is built and delivered in full compliance with the current Electrical Code, while keeping the installation clean, orderly, and aligned with the company's internal standards. From the pre -construction stage, you will review electrical drawings, materials, and data sheets to verify that everything meets NEC requirements; during installation, you will check torque values and the proper fastening of structures. You will also handle equipment programming and perform any necessary repairs. With your expertise, you will guarantee optimal project operability and complete customer satisfaction. Key Responsibilities ● Document findings, non -conformities, and opportunities for improvement. ● Perform quality inspections on solar installation projects. ● Develop and update quality procedures and checklists. ● Support design reviews to ensure the constructability and maintainability of the photovoltaic system. Requirements● Minimum of 2 years of experience in quality assurance or technical supervision on electrical, construction, or renewable energy projects. ● Ability to read electrical plans and technical specifications. ● Knowledge of NEC, OSHA, and applicable Puerto Rico building codes. ● Proficiency with computer programs and work tools. ● Valid driver's license in Puerto Rico. ● Bilingual (Spanish and English) ● Electrical knowledge. Benefits Health Insurance 401K Paid Holidays 15 days of vacation 12 sick days

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the LifeThis position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care. Responsibilities may include the following and other duties may be assigned. Shift C: Week 1 Saturday, Sunday, Thursday & Friday (6pm - 6am) Week 2: Monday, Tuesday & Wednesday (6pm - 6am) Shift D: Week 1: Monday, Tuesday & Wednesday (6pm - 6am) Week 2: Saturday, Sunday, Thursday & Friday (6pm - 6am) Provides technical support to engineers to achieve improvements in cycle-time, yield, unit cost, quality, safety and compliance of production and operations processes and products. Monitors instruments and equipment and collects operating data, including calibration, inspection, testing and repair activities, to assist in making on-line adjustments to instruments, equipment, or products. Analyzes and resolves malfunctions and deviations of instruments and control systems to identify and resolve problems. Conducts, analyses and prepares reports using metrics from salvage tracking, trending, reporting and root-cause analyses. Maintains process designs to optimize process, equipment and facility use while conforming to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs). Must Have: Minimum Requirements Requires high school diploma or equivalent (United States), vocational or technical education or certification (all other countries). Requires minimum of 2 years of relevant experience Nice to Have Educational: Electronics, Engineering Technology, Industrial Technology or related field. Experience in medical devices, pharmaceutical or electronic industry Knowledgeable & experience in mechanical, electrical/electronic design. Knowledge in programmable logic controls (PLC) - Allen Bradley, Knowledge in Vision System Cognex. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Operations Incentive Plan (OIP). Medtronic benefits and compensation plans About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people. We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

JLL empowers you to shape a brighter way. Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. Técnico de Control de Procesos Resumen del Puesto El Técnico de Control de Procesos es responsable de operar, monitorear y mantener sistemas de control automatizados para optimizar procesos industriales. Garantiza el funcionamiento eficiente y seguro de equipos de control, sistemas SCADA, y dispositivos de instrumentación. Responsabilidades Principales: * Monitorear continuamente sistemas de control de procesos utilizando interfaces HMI y sistemas SCADA para detectar desviaciones operacionales. * Realizar ajustes en controladores PLC, DCS y sistemas de instrumentación para mantener parámetros dentro de especificaciones establecidas. * Ejecutar procedimientos de calibración y mantenimiento preventivo en sensores, transmisores, válvulas de control y otros dispositivos de campo. * Diagnosticar fallas en sistemas de control mediante análisis de alarmas, tendencias de datos y pruebas de componentes. * Documentar todas las actividades de mantenimiento, calibraciones y reparaciones en sistemas de gestión de mantenimiento. * Colaborar con ingenieros de procesos para implementar mejoras y modificaciones en sistemas de control. * Garantizar cumplimiento de protocolos de seguridad y procedimientos operacionales estándar. * Participar en paradas programadas y mantenimientos mayores de planta. * Proporcionar soporte técnico durante emergencias y situaciones críticas fuera del horario regular. Requisitos: * Título técnico en Instrumentación, Control de Procesos, Electrónica o campo relacionado * 2-5 años de experiencia en sistemas de control industrial * Inglés básico a intermedio * Conocimiento de PLCs (Honeywell, Allen Bradley, Siemens, Schneider) * Experiencia con sistemas SCADA/HMI * Comprensión de instrumentación (presión, temperatura, flujo, nivel) * Conocimientos de protocolos de comunicación industrial (Modbus, Ethernet/IP) * Capacidad para leer diagramas P&ID y esquemas eléctricos * Disponibilidad para trabajo por turnos y guardias Competencias Deseadas: * Certificaciones en sistemas PLC específicos * Experiencia con sistemas DCS (DeltaV, Honeywell, ABB) * Conocimiento de seguridad funcional (SIL, SIS) * Habilidades de soldadura y trabajo mecánico básico This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without employer sponsorship. Location: On-site -Gurabo, PR If this job description resonates with you, we encourage you to apply, even if you don't meet all the requirements. We're interested in getting to know you and what you bring to the table! Personalized benefits that support personal well-being and growth: JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits may include: * 401(k) plan with matching company contributions * Comprehensive Medical, Dental & Vision Care * Paid parental leave at 100% of salary * Paid Time Off and Company Holidays * Early access to earned wages through Daily Pay JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely. For more information about how JLL processes your personal data, please view our Candidate Privacy Statement. For additional details please see our career site pages for each country. For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here. Jones Lang LaSalle ("JLL") is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process - including the online application and/or overall selection process - you may email us at ******************. This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page > I want to work for JLL. Accepting applications on an ongoing basis until candidate identified.

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website ************************ to learn more about our services and solutions! Job Description Associate Tech Engineering with experience with pneumatics, automatic control and vision inspection systems required. Duties: Identify, and resolve, all problems related to the process equipment and where possible minimize equipment downtime. Complete advanced maintenance activities, including but not limited to preventive maintenance among other maintenance tasks. Monitor inspection and packaging equipment, with the ability to investigate and troubleshoot advance issues or problems including mechanical, electrical, or automation. Assist the team with maintaining an up-to-date working spare parts inventory system. Ensure that operational log paperwork, daily log files, and work order documentation is completed with accurate information. Develop, revise, and review SOPs or job plans/work plans for work related areas. Evaluate the current maintenance procedures and assist in the changes to optimize the maintenance program. Recognize and report malfunctions and adjust equipment. Provides technical expertise and act as a resource/trainer to others on maintenance support tasks and/or in the use of all the equipment used in the area. Provides customer service to internal and external clients, including ongoing support with detailed technical information and solving technical situations. All work must be guided by team requirements or department objectives and completed in accordance with CFRs, cGMPs, SOPs, job plans and company policies. Qualifications Bachelor's degree or Associate's degree and 4 years of directly related experience or High school diploma / GED and 6 years of directly related experience Availability for 12 hrs shifts Bilingual (Spanish/English)(Write/Speak) Additional Information All your information will be kept confidential according to EEO guidelines.

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Summary of Role: The Associate Technical Engineering will provide automation support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that supported areas and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards. Responsibilities: * Evaluate and determine if utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards. * Participate in the coordination of TECHSUPPORT on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical and process automation issues. * Assist during FDA and other regulatory agency inspections. Provide TECHSUPPORT in response to the FDA and other regulatory agencies. * Assist in the evaluation and implementation of engineering improvements, policy changes, compliance Improvements and optimization programs. * Other functions that may be assigned Shift: Non-Standard Shift - 12 hours shift Location: Juncos, PR Education: Bachelor's degree or Associate's degree and 4 years of directly related experience or High school diploma / GED and 6 years of directly related experience. Preferred Qualifications: * Experience with pneumatics, automatic control and vision inspection systems required. * Identify, and resolve, all problems related to the process equipment and where possible minimize equipment downtime. Complete advanced maintenance activities, including but not limited to preventive maintenance among other maintenance tasks. * Monitor inspection and packaging equipment, with ability to investigate and troubleshoot advance issues or problems including mechanical, electrical, or automation. * Assist the team with maintaining an up-to-date working spare parts inventory system. * Ensure that operational log paperwork, daily log files, and work order documentation is completed with accurate information. * All work must be guided by team requirements or department objectives and completed in accordance with CFRs, cGMPs, SOPs, job plans and policies. * Develop, revise, and review SOPs or job plans/work plans for work related areas. * Evaluate the current maintenance procedures and assist in the changes to optimize the maintenance program. * Recognize and report malfunctions and adjust equipment. * Provides technical expertise and act as a resource/trainer to others on maintenance support tasks and/or in the use of all the equipment used in the area. * Provides customer service to internal and external clients including ongoing support with detailed technical information and solving technical situations. Skills: * Leadership and teambuilding * Verbal communication * Written Communication/Technical Writing * Organization * Facilitation * Dealing with and managing change * Comprehensive understanding of validation protocol requirements. * Technical (Equipment Specific) * Analytical Problem Solving * Project Management & Planning * Scheduling * Computer Literacy This position is for a fixed term contract supporting one of ECHO Consulting Group (a Cencora company) partners on site at their facility. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated Companies Affiliated Companies: Echo Consulting Group Inc

For mechanical and Troubleshooting services in the Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree or Associate Degree with two (4) years of experience in the regulated industry. Bilingual (English & Spanish). Problem-solving and root cause analysis. Shift: Non-standard and according to business needs. 5:00 AM - 5:00 PM 5:00 PM - 5:00 AM Experience in: PLC, Mechanical Machine. VFD, Writing, and Machine Troubleshooting. Pneumatics, Automation Controls, and Vision Inspection Systems. The Personality Part: Besides being an Automation Pro, you're able to analyze data so that not a single inconsistency gets past you (which allows you to be an amazing problem-solver). You're also a skilled multitasker with an incredible ability to set priorities. Add to this a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, and you might just be what we're looking for! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Evaluate and determine if utility systems, process maintenance, instrumentation/calibration/electrical systems, and technical cleaning systems are required. Maintained in compliance with all applicable industry standards, regulatory standards, and FDA standards. Participate in the coordination of TECHSUPPORT on engineering, regulatory, and compliance. Calibration, quality, microbial/environmental, technical cleaning, validation, electrical, and process automation issues. Assist in the evaluation and implementation of engineering improvements, policy changes, compliance Improvements, and optimization programs. Identify and resolve all problems with process equipment and, where possible, minimize equipment downtime. Complete advanced maintenance activities, including but not limited to preventive maintenance, among other maintenance tasks. Monitor inspection and packaging equipment and investigate and troubleshoot advanced issues, including mechanical, electrical, or automation-related problems. Assist the team with maintaining an up-to-date working spare parts inventory system. Ensure that operational log paperwork, daily log files, and work order documentation are completed with accurate information. All work must be guided by team requirements or department objectives and completed in accordance with CFRs, cGMPs, SOPs, job plans, and clients' policies. Develop, revise, and review SOPs or job plans/work plans for work-related areas. Evaluate current maintenance procedures and assist with changes to optimize the maintenance program. Recognize and report malfunctions and adjust equipment. Provides technical expertise and acts as a resource/trainer to others on maintenance support tasks and/or in the use of all the equipment used in the area. Provides customer service to internal and external clients, including ongoing support with detailed technical information and troubleshooting. WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?

Job Description The Associate Technical Engineer (Automation) provides hands-on automation and technical support for system and equipment optimization, upgrades, replacements, and modifications. This role ensures that all supported areas operate in compliance with corporate policies, industry standards, regulatory requirements, and FDA guidelines. The position supports production, utilities, and maintenance teams by troubleshooting issues, driving process improvements, and maintaining reliable automated operations. KEY RESPONSIBILITIES Evaluate utility systems, process maintenance activities, instrumentation/calibration/electrical systems, and technical cleaning systems to ensure compliance with industry, regulatory, and FDA standards. Assist in the assessment and implementation of engineering improvements, policy changes, compliance enhancements, and optimization initiatives. Provide technical support (TECHSUPPORT) on engineering, compliance, calibration, validation, quality, microbial/environmental, electrical, and process automation issues. Troubleshoot advanced equipment-related issues including mechanical, electrical, pneumatic, and automation failures. Identify and resolve process equipment problems to minimize downtime and ensure operational reliability. Monitor inspection and packaging equipment, investigating and resolving issues in automation, controls, and vision systems. Assist during FDA and other regulatory inspections. Support the preparation and response to inquiries from regulatory agencies. Support preventive and corrective maintenance activities as needed. Maintain accurate operational logs, daily log files, work orders, and documentation according to CFRs, cGMPs, SOPs, and internal policies. Assist with maintaining an up-to-date spare parts inventory system. Develop, revise, and review SOPs, job plans, and work instructions for related areas. Evaluate existing maintenance procedures and support revisions to optimize the maintenance program. Act as a technical resource to the team, providing training and guidance on equipment, maintenance practices, and troubleshooting. Provide professional customer service to internal and external partners, including technical support and issue resolution. COMPETENCIES & SKILLS Leadership and team-building Strong verbal communication Technical writing and documentation skills Organizational and facilitation abilities Adaptability and change management Thorough understanding of validation protocol requirements Equipment-specific technical expertise Analytical problem solving Project management, planning, and scheduling High computer literacy Requirements EDUCATION & EXPERIENCE Bachelor's degree, OR Associate's degree + 4 years of directly related experience, OR High school diploma/GED + 6 years of directly related experience. PREFERRED QUALIFICATIONS Experience with pneumatics, automatic control systems, and vision inspection systems (e.g., Cognex, Keyence). Strong troubleshooting skills across mechanical, electrical, and automation disciplines. Demonstrated ability to reduce equipment downtime through proactive and advanced maintenance techniques. Experience monitoring and maintaining inspection and packaging equipment. Ability to recognize, report, and correct equipment malfunctions. Experience maintaining spare parts inventory systems. Ability to revise and optimize SOPs, maintenance procedures, and job plans. Experience providing technical training and support to multidisciplinary teams. Strong customer service orientation with the ability to communicate complex technical issues clearly. Benefits 2-year contract 12 hours shifts 48 hours a week

The Associate Technical Engineering will provide automation support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that supported areas and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards. FUNCTIONS 1. Evaluate and determine if utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards. 2. Participate in the coordination of TECHSUPPORT on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical and process automation issues. 3. Assist during FDA and other regulatory agency inspections. Provide TECHSUPPORT in response to the FDA and other regulatory agencies. 4. Assist in the evaluation and implementation of engineering improvements, policy changes, compliance Improvements and optimization programs. * Other functions that may be assigned EDUCATION/LICENSES - Bachelor's degree or Associate's degree and 4 years of directly related experience or High school diploma / GED and 6 years of directly related experience. COMPETENCIES/SKILLS 1. Leadership and teambuilding 2. Verbal communication 3. Written Communication/Technical Writing 4. Organization 5. Facilitation 6. Dealing with and managing change 7. Comprehensive understanding of validation protocol requirements. 8. Technical (Equipment Specific) 9. Analytical Problem Solving 10. Project Management & Planning 11. Scheduling 12. Computer Literacy **Weil Group is proud to be an Equal Employment Opportunity Employer.*

Accept parts per drawing or quality specifications. Audit process compliance with quality records and procedures Inspect material, subassemblies and rejects parts using procedures, specifications engineering drawings, performs audits or JIS, procedures, certified operations. Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Write routine reports. Define problems, collect data, establish facts, and draw valid conclusions Interpret an extensive variety of technical instructions in mathematical or diagram form and deal with abstract and concrete variables. **Associate or Technical Degree** preferred Minimum 1 year **experience** in a manufacturing environment. As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Engineering? Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world's most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we're here to guide you to the next step in your engineering career. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Technical Engineers pen the plans that lead construction crews to success. As a Technical Engineer in the Army National Guard, you will develop the skills necessary to help build, plan, and repair airstrips, docks, barracks, roads, and other projects. Your training will enable you to assume duties that include construction site development, such as technical investigation, surveying, drafting, and the development of construction plans and specifications. Specific duties may include: construction material testing; drawing maps, charts, and making scale drawings of roads, airfields, and buildings; conducting land surveys and computing survey results; preparing structure wiring and plumbing diagrams; building scale models of land areas that show hills, lakes, roads, and buildings; and piecing together aerial photographs to form large photomaps. Job Duties * Draw topographic maps and charts using Computer Aided Drafting systems and software * Conduct geodetic and construction surveys and results utilizing Automated Integrated Survey Instruments and Global Positioning Survey Technology * Provide technical support for vertical and horizontal construction projects Some of the Skills You'll Learn * Aerial photo interpretation * Architectural and structural drawing Helpful Skills * Ability to convert ideas into drawings * Interest in maps and charts * Working with Computer Aided Drafting technology * Interest in algebra, geometry, and trigonometry Through your training, you will develop the skills and experience to enjoy a civilian career with civilian construction, engineering, and architectural firms, as well as government agencies such as a highway department. Earn While You Learn Instead of paying to learn these skills, get paid to train. In the Army National Guard, you will learn these valuable job skills while earning a regular paycheck and qualifying for tuition assistance. Job training for a Technical Engineer consists of 10 weeks of Basic Training, where you'll learn basic Soldiering skills, and 17 weeks of Advanced Individual Training, depending on the specialty. Part of this time is spent in the classroom and part in the field.

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: * Specialist Quality Control SUMMARY Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. FUNCTIONS * Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. * Resolve technical issues and troubleshoot for assays as necessary * Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. * Manage existing and/or develop and implement new programs, processes and methodologies. * Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. * Approve lab investigations, Lead audit teams * May serve as subject matter expert to develop technical training. * May perform routine work in a specific area of responsibility as necessary. * Represents the department/organization on various teams, independently responsible for following through on multi-site action items. * May interact with regulatory agencies regarding area(s) of responsibility including written responses. * May resolve issues with outside resources. * Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. EDUCATION * Doctorate OR * Masters + 2 years of directly related experience OR * Bachelors + 4 years of directly related experience OR COMPETENCIES/SKILLS * Excellent communication skills, facilitation and presentation skills. * Excellent technical writing skills. * Strong computer operation skills including work processing, presentation, database and spreadsheet application skills. * Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion. * Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities. * Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution. * Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility. * Knowledge of pharmaceutical processes. * Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products. * Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products. * Extensive knowledge and application of GMPs/CFRs. * Ability to evaluate compliance issues. * Skill in evaluating and documenting according to Company and various guidelines. * Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. * Advanced scientific data analysis and interpretation skills. * Advanced skills in solving complex problems. * Advanced data trending and evaluation. * Strong skill in working independently and to effectively interact with various levels. * Ability to interact with regulatory agencies both orally and in writing. * Initiate, coordinate and lead cross functional teams. * Excellent skill in leading, motivating, influencing, and negotiating. ATRIBUTES: * Scientific Data Analysis. * Strong Technical Writing (English and Spanish) mainly focuses. * Strong knowledge in Microsoft Excel as a Tool for Data Analysis. * Good Communication skills. * Project Management. * Knowledge in Computer System and Method Validation (Experience preferable). * Strong knowledge and experience with quality process management. * Basic Knowledge on equipment preventive maintenance and troubleshooting. * Agile on prioritization of critical tasks. * Ability to develop inspection or qualification protocols in a short timeframe period. * Strong negotiation skills.

Job Description QA/QC Site Inspector- Construction Reports to: TBD The Site Inspector - QA/QC will be responsible for ensuring that all construction and operational activities at generation sites meet the highest quality standards and comply with regulatory requirements. This role involves conducting regular inspections, documenting findings, and collaborating with project teams to address any quality issues. Key Responsibilities: Perform regular inspections of construction and operational activities at generation sites to ensure compliance with quality standards and regulatory requirements. Document inspection findings, prepare comprehensive reports, and recommend corrective actions to address deficiencies. Maintain detailed and accurate records of inspections, findings, and implement corrective actions for quality assurance purposes. Collaborate with project managers, engineers, and contractors to identify, address, and resolve quality-related issues. Verify that materials, equipment, and workmanship adhere to project specifications, industry standards, and quality benchmarks. Ensure strict compliance with safety protocols and environmental regulations throughout all phases of the project. Provide technical expertise and guidance on quality control procedures, standards, and best practices to project teams. Participate in project meetings and deliver updates on quality control status, including identified issues and resolution progress. Qualifications: Education: Bachelor's degree in Engineering, Construction Management, or a related field preferred. Experience: Minimum of 3-5 years of experience in a similar role. Skills: Extensive knowledge of quality assurance and control principles, particularly in construction sites. Proficiency in using quality management tools and software for inspection reporting and documentation. Ability to read and interpret blueprints, technical drawings, and specifications to ensure compliance with standards. Strong attention to detail with excellent problem-solving and organizational skills. Effective communication and interpersonal abilities to collaborate with project teams and stakeholders. Proven experience conducting construction site inspections and documenting findings. Commitment to safety and environmental compliance in all activities. Strong time management skills to prioritize tasks effectively in dynamic environments. Certifications: Required: Valid Driver's License. Preferred: Certified Construction Quality Inspector (CCQI), Certified Quality Auditor (CQA), OSHA 30-Hour Construction Safety Certification. Language: Proficiency in both English and Spanish is mandatory. Working Conditions: Full-time position, with travel to project sites as required. The position may involve working in office and field environments, with a focus on construction sites. Ability to work on-site and in potentially challenging outdoor conditions during installation and construction phases. Primary functions require sufficient physical ability and mobility to work in an office setting; to stand or sit for prolonged periods of time; to occasionally stoop, bend, kneel, crouch, reach, and twist; to lift, carry, push, and/or pull light to moderate amounts of weight; make repetitive hand movement and fine coordination in the performance of daily duties; to travel to other locations using various modes of private and commercial transportation; and to verbally communicate to exchange information. BENEFITS: Comprehensive health insurance, 401K, Paid Time Off (PTO), and bonus incentives. Commitment to Diversity: We are an equal-opportunity employer, dedicated to fostering a diverse and inclusive workplace. For more about DCMC Partners, please visit our website at dcmcpartners.com/careers. Job Posted by ApplicantPro

JLL empowers you to shape a brighter way. Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients. We are committed to hiring the best, most talented people and empowering them to thrive, grow meaningful careers and to find a place where they belong. Whether you've got deep experience in commercial real estate, skilled trades or technology, or you're looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. Técnico de Control de Procesos Resumen del Puesto El Técnico de Control de Procesos es responsable de operar, monitorear y mantener sistemas de control automatizados para optimizar procesos industriales. Garantiza el funcionamiento eficiente y seguro de equipos de control, sistemas SCADA, y dispositivos de instrumentación. Responsabilidades Principales: Monitorear continuamente sistemas de control de procesos utilizando interfaces HMI y sistemas SCADA para detectar desviaciones operacionales. Realizar ajustes en controladores PLC, DCS y sistemas de instrumentación para mantener parámetros dentro de especificaciones establecidas. Ejecutar procedimientos de calibración y mantenimiento preventivo en sensores, transmisores, válvulas de control y otros dispositivos de campo. Diagnosticar fallas en sistemas de control mediante análisis de alarmas, tendencias de datos y pruebas de componentes. Documentar todas las actividades de mantenimiento, calibraciones y reparaciones en sistemas de gestión de mantenimiento. Colaborar con ingenieros de procesos para implementar mejoras y modificaciones en sistemas de control. Garantizar cumplimiento de protocolos de seguridad y procedimientos operacionales estándar. Participar en paradas programadas y mantenimientos mayores de planta. Proporcionar soporte técnico durante emergencias y situaciones críticas fuera del horario regular. Requisitos: Título técnico en Instrumentación, Control de Procesos, Electrónica o campo relacionado 2-5 años de experiencia en sistemas de control industrial Inglés básico a intermedio Conocimiento de PLCs (Honeywell, Allen Bradley, Siemens, Schneider) Experiencia con sistemas SCADA/HMI Comprensión de instrumentación (presión, temperatura, flujo, nivel) Conocimientos de protocolos de comunicación industrial (Modbus, Ethernet/IP) Capacidad para leer diagramas P&ID y esquemas eléctricos Disponibilidad para trabajo por turnos y guardias Competencias Deseadas: Certificaciones en sistemas PLC específicos Experiencia con sistemas DCS (DeltaV, Honeywell, ABB) Conocimiento de seguridad funcional (SIL, SIS) Habilidades de soldadura y trabajo mecánico básico This position does not provide visa sponsorship. Candidates must be authorized to work in the United States without employer sponsorship. Location: On-site -Gurabo, PR If this job description resonates with you, we encourage you to apply, even if you don't meet all the requirements. We're interested in getting to know you and what you bring to the table! Personalized benefits that support personal well-being and growth: JLL recognizes the impact that the workplace can have on your wellness, so we offer a supportive culture and comprehensive benefits package that prioritizes mental, physical and emotional health. Some of these benefits may include: 401(k) plan with matching company contributions Comprehensive Medical, Dental & Vision Care Paid parental leave at 100% of salary Paid Time Off and Company Holidays Early access to earned wages through Daily Pay JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL's recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely. For more information about how JLL processes your personal data, please view our Candidate Privacy Statement. For additional details please see our career site pages for each country. For candidates in the United States, please see a full copy of our Equal Employment Opportunity policy here. Jones Lang LaSalle (“JLL”) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process - including the online application and/or overall selection process - you may email us at ******************. This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page > I want to work for JLL. Accepting applications on an ongoing basis until candidate identified.

The Associate Technical Engineering will provide automation support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that supported areas and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards. FUNCTIONS: Evaluate and determine if utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards. Participate in the coordination of TECHSUPPORT on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical and process automation issues. Assist during FDA and other regulatory agency inspections. Provide TECHSUPPORT in response to the FDA and other regulatory agencies. Assist in the evaluation and implementation of engineering improvements, policy changes, compliance Improvements and optimization programs. * Other functions that may be assigned EDUCATION: Bachelor's degree or Associate's degree and 4 years of directly related experience. PREFERRED QUALIFICATIONS: Experience with pneumatics, automatic control and vision inspection systems required. Identify, and resolve, all problems related to the process equipment and where possible minimize equipment downtime. Complete advanced maintenance activities, including but not limited to preventive maintenance among other maintenance tasks. Monitor inspection and packaging equipment, with ability to investigate and troubleshoot advance issues or problems including mechanical, electrical, or automation. Assist the team with maintaining an up-to-date working spare parts inventory system. Ensure that operational log paperwork, daily log files, and work order documentation is completed with accurate information. All work must be guided by team requirements or department objectives and completed in accordance with CFRs, cGMPs, SOPs, job plans and Amgen policies. Develop, revise, and review SOPs or job plans/work plans for work related areas. Evaluate the current maintenance procedures and assist in the changes to optimize the maintenance program. Recognize and report malfunctions and adjust equipment. Provides technical expertise and act as a resource/trainer to others on maintenance support tasks and/or in the use of all the equipment used in the area. Provides customer service to internal and external clients including ongoing support with detailed technical information and solving technical situations. SKILLS: Leadership and teambuilding Verbal communication Written Communication/Technical Writing Organization Facilitation Dealing with and managing change Comprehensive understanding of validation protocol requirements. Technical (Equipment Specific) Analytical Problem Solving Project Management & Planning Scheduling Computer Literacy WORK METHODOLOGY: Full on site job in Juncos, PR Full time job Expected project duration: 29 months for the first contract Non Standard (12 hrs shift | Day & Night Shift). Weekends and overtime may also be required. Professional services contract with potential extension based on performance and budget Expected hiring date: January 2026