Manufacturing Engineer Jobs in San Juan, PR

Job Description We are seeking an experienced and innovative Senior Process Engineer to independently lead and contribute to complex engineering initiatives, including process optimization, troubleshooting, and major system modifications within a manufacturing or capital projects environment. Key Responsibilities: Lead complex or novel engineering assignments requiring new and/or improved techniques and procedures. Develop policies and SOPs that impact multiple departments or units. Supervise and coordinate the work of engineers, associates, or technicians on both project and day-to-day basis. Apply expertise across various engineering disciplines and serve as a subject matter expert in at least one specialized area. Provide technical leadership in planning, executing, and reporting on large-scale engineering or capital projects. Generate innovative technical solutions for challenging problems using scientific and engineering principles. Collaborate with R&D, Manufacturing, Facilities, QA, and Validation to develop and implement complex system or process changes. Participate in and/or manage design development efforts with consultants, architects, or engineering partners. Develop and manage project and departmental budgets, timelines, and scopes. Support or lead process validation efforts including protocol development, test runs, data collection, and technical report authoring. Apply in-depth knowledge of cGMP, GLP, and validation protocol execution. Ensure documentation complies with regulatory standards and internal quality systems. Competencies & Skills: Familiarity with pharmaceutical manufacturing processes (e.g., filling, formulation). Equipment-specific technical knowledge. Skilled in protocol/test run writing and technical report authoring. Ability to manage multiple projects simultaneously. Schedule and budget development. Vendor and contractor coordination. Strong collaboration and facilitation skills. Conflict resolution and cross-functional communication. Ability to lead and mentor junior team members. Requirements Education: PhD in Engineering; OR Master’s in Engineering + 2 years’ experience; OR Bachelor’s in Engineering + 4 years’ experience. Experience: Proven experience in a biotech/pharmaceutical environment. Strong understanding of validation, equipment qualification, and manufacturing systems. Hands-on knowledge in process optimization and troubleshooting. Preferred Qualifications: Expertise in process validation, protocol development, and execution. Demonstrated success in managing filling line operations or technical transfers. Working knowledge of Oracle, PeopleSoft, or similar ERP systems. Proficient in Microsoft Office, especially Excel and PowerPoint. Strong written and verbal communication skills, including technical documentation. Benefits Administrative Shift 1-year contract

Job Title: Bilingual Industrial Engineer with Process Optimization Experience Position Overview: We are seeking a highly skilled and experienced Bilingual Industrial Engineer with Process Optimization Experience. As an Industrial Engineer, you will apply your expertise in business improvement processes, overcoming resistance to change, and understanding of technical equipment and networks to drive efficiency enhancements and operational excellence. Responsibilities: Analyzing Current Processes: Conduct comprehensive analysis of existing business processes across various functional areas to identify inefficiencies and areas for improvement. Designing and Implementing Process Improvements: Develop and implement innovative solutions to optimize workflows, reduce waste, and enhance overall efficiency. Leading Change Management Efforts: Overcome resistance to change by effectively communicating the benefits of process improvements and fostering a culture of continuous improvement. Collaborating with Cross-Functional Teams: Work closely with teams from different departments to gather insights, address challenges, and ensure successful implementation of process enhancements. Performance Measurement and Data Analysis: Utilize data analysis tools and techniques to measure the performance of optimized processes, identify trends, and drive data-driven decision-making. Project Management: Lead and participate in cross-functional projects aimed at driving business improvement initiatives and achieving operational excellence. Communication: Maintain excellent communication with both internal teams and external stakeholders to ensure alignment, share progress, and address any concerns or feedback effectively. Requirements: Bachelor's degree in industrial engineering. 6 to 8 years of experience in industrial engineering, business improvement processes, or related roles. Strong understanding of process optimization principles and methodologies (Waterfall, Hybrid and Agile). Proven experience in overcoming resistance to change and fostering a culture of continuous improvement. Fully bilingual in Spanish and English. Excellent analytical, communication, and presentation skills. Ability to work independently, adapt to changing project requirements, and thrive in a fast-paced environment. Demonstrated ability to work effectively under pressure and meet deadlines. Preferred Qualifications: Experience with change management methodologies. Strong problem-solving skills and attention to detail.

Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are in compliance with regulations. Other may be assigned. * Requirements 1 to 3 years of engineering experience in the Medical Device industry. Problem Solving knowledge. Yellow or Green Belt knowledge Bachelor Degree in Engineering Completed. Willing to work 100% On-site in Juncos. 2nd Shift (MF 1pm - 9:30pm)

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are in compliance with regulations. Qualifications: Bachelor degree in Engineering One (1) to (2) two years of relevant experience. Root Cause Analysis Process Validation (IQ/PD/OQ/PQ) Technical Writing Availability for 2nd shift (2pm-11pm) Tuesday to Saturday or Sunday to Thursday. Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

div class="main__left col-lg-8 px-md-0 px-lg-0 d-flex flex-column" div class="main__img-container-mobile" /div div class="main__description bg-white p-4" h6 class="commonstxt hrc-green d-flex hrc-fs-16 font-weight-bold mb-3" i class="commonstxt hr-File hrc-green hrc-fs-16"/i Descripción del puesto /h6 p class="hrc-fs-14 m-0 hrc-black"pPara trabajar en Juncos Puerto Rico/p pstrong style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"Description:/strongbr/ br/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"In a full automation role the Sr. Associate Mfg Systems will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards./spanbr/ br/ strong style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"Functions:/strongbr/ br/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- 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./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Ensure the maintenance team training program, standard operating procedures and equipment/system operational standards are consistent throughout the team./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Participate in the coordination of technical support to the maintenance team on engineering issues, regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues and process maintenance issues./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Assist the maintenance team during FDA and other regulatory agency inspections. Provide technical support to the maintenance team in response to the FDA and other regulatory agencies./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Assist the maintenance team when responding to high purity water systems and environmental monitoring alert/action notifications. Assist with the investigation on all alert/action notifications./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Assist with the development and maintenance of an audit program for the maintenance team and facilitate routine audits of activities, documentation, operations and related areas to ensure a continued state of compliance./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Assist plant engineering in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"- Assist with the testing of proposed sanitization and maintenance procedure changes and modifications for process, utility and clean room systems./spanbr/ span style="-webkit-text-stroke-width:0px; background-color:#fcfcfd; color:#333333; display:inline !important; float:none; letter-spacing:normal; orphans:2; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; text-indent:0px; text-transform:none; white-space:normal; widows:2; word-spacing:0px"**Other functions that may be assigned/span/p /p h6 class="commonstxt hrc-green d-flex align-items-center hrc-fs-16 mt-4 mb-3 font-weight-bold" i class="commonstxt hr-Required hrc-green hrc-fs-16"/i Requisitos /h6 p class="hrc-fs-14 m-0 hrc-black"ul style="background-color:#ffffff; color:#222222; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; white-space:normal" li style="margin-left:15px"Trabajo presencial en Juncos; Puerto Rico/li li style="margin-left:15px"span Los candidatos deben tener conocimiento en /spanspan PLC (el proceso de conectarse a PLC), conocer a profundidad sobre Troubleshooting (cómo identificar la señal que está llegando), sistemas de inspección, el funcionamiento del sistema de /span Visiónspan y resolver problemas técnicos./span/li li style="margin-left:15px"span style="background-color:#ffffff"Un "plus" en evaluaciones: conocimiento en escala, sistemas de inspección, sistemas de mantenimiento (ej. Maximo), disponibilidad completa, habilidad de trabajar en equipo y trabajar con mínima supervisión./span/li li style="margin-left:15px"Requiere que la persona domine idiomas inglés y español - oral y escrito./li li style="margin-left:15px" pstrong Education:/strongbr/ br/ strong Master's degree or Bachelor's degree and 2 years of Engineering experience or Associate's degree and 6 years of Engineering experience or High school diploma / GED and 8 years of Engineering experience./strongbr/ br/ strong Preferred Qualifications:/strong/p /li listrong Automation Background in programming, installation of manufacturing process controls, automation and field instrumentation technologies./strong/li listrong Knowledge on Rockwell Automation Platform and Allen-Bradley PLCs./strong/li listrong Working knowledge of pharmaceutical/biotech processes./strong/li listrong Familiarity with validation processes and documentation in a highly regulated environment./strong/li listrong Strong verbal communication skills in English and Spanish./strong/li listrong Skills in the following areas:/strong ul listrong Problem solving and root cause analysis/strong./li listrong Basic technical report writing./strong/li listrong Basic technical presentations./strong/li listrong Personal Organization./strong/li listrong Dealing with and managing change./strong/li listrong Technical (Equipment Specific)./strong/li listrong Analytical Problem Solving./strong/li listrong Computer Literacy/strong/li listrong Knowledgeable on Rockwell Automation Factory Talk amp; ControlLogix PLC Platform./strong/li listrong Knowledgeable on Rockwell SLC500 PLC families Controllers./strong/li listrong Knowledgeable on Rockwell Automation FTView SE and FTBatch systems./strong/li listrong Knowledgeable on DeviceNet technologies./strong/li /ul /li listrong Work schedule flexibility to support 24/7 operations./strong/li listrong Knowledge in programming language (e.g. VBA, SQL)./strong/li listrong Knowledge in vision system technology./strong/li listrong Knowledge in serialization process./strong/li listrong Basic Knowledge in robot or cobot programming./strong/li li style="margin-left:15px" pstrong Skills:/strongbr/ br/ - Leadership and teambuildingbr/ - Verbal communicationbr/ - Written Communication/Technical Writingbr/ - Organizationbr/ - Facilitationbr/ - Dealing with and managing changebr/ - Comprehensive understanding of validation protocol requirementsbr/ - Technical (Equipment Specific)br/ - Analytical Problem Solvingbr/ - Project Management amp; Planningbr/ - Schedulingbr/ - Computer Literacybr/ br/ strong Work Methodology:/strong/p /li listrong100% on-site job/strong/li listrong Full time opportunity/strong/li listrong Shift: 5:00 am to 5:30 pm or 5:00pm to 5:00am; including alternate weekend/strong/li listrong Professional services or Temporary contract/strong/li /ul /p h6 class="commonstxt hrc-green d-flex align-items-center hrc-fs-16 mt-4 mb-3 font-weight-bold" i class="commonstxt hr-Heart hrc-green hrc-fs-16"/i Beneficios /h6 p class="hrc-black font-weight-bold hrc-fs-14"ul style="background-color:#ffffff; color:#222222; text-align:start; text-decoration-color:initial; text-decoration-style:initial; text-decoration-thickness:initial; white-space:normal" li style="margin-left:15px"Rango de salario disponible $35-40 por hora - servicios profesionales./li /ul /p /div div class="main__details bg-white p-4" h6 class="commonstxt hrc-green d-flex hrc-fs-16 font-weight-bold mb-3" i class="commonstxt hr-Open-answer hrc-green hrc-fs-16"/i Detalles /h6 div p class="hrc-fs-14 m-0 hrc-black"span class="commonstxt font-weight-semibold"Nivel mínimo de educación:/span Universitario (Graduado)/p /div /div div class="main__button-container" /div /div

Responsible for accessing the processes productivity challenges, generate and execute solutions following the procedures of and quality regulations of the client to assure improvement and sustainability of the results. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Assist process development activities. Performs root-cause analysis, define and implement corrective/preventive actions. Mitigate product failures at all stages of the client's manufacturing process. Identifies opportunities or the need for equipment, material or process changes or improvements. Provides product design reviews and feedback for manufacturability guidance. Responsible for developing process documentation and training materials for new processes, materials, and equipment process engineering and controls support. Requirements BS Degree in Engineering. One (1)) to five (5) years of work experience in a similar role. Strong customer service skills are necessary. - Proven experience working with Six Sigma/Process Excellence Tools and Methodologies (i.e. DMAIC, Lean Manufacturing, Process Mapping, Cause & Effect, FMEA, DOE)

div class="col col-xs-7 description" id="job-description" span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:11pt;"span style="line-height:normal;"span style="font-size:10pt;"For engineering services in/span/span/spanspan style="font-size:13.3333px;" the Manufacturing area./spanbr/br/ span style="font-size:18px;"bWHAT MAKES YOU A FIT: bspan style="font-size:18px;"bb/b/b/span/b/b/spanbr/span style="font-size:18px;"bThe Technical Part:/b/span/spanullispan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Bachelor's degree in Engineering amp; two (2) years of relevant experience within the Medical Devices or Pharmaceutical industry./span/span/lilispan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Bilingual (Spanish amp; English)./span/span/lilispan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Shift: 1st and according to business needs. /span/span/lilispan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Experience in:/span/spanullispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Equipment installation, set up, and installation qualification./span/span/lilispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Technical writing of reports and procedures./span/span/lilispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Manufacturing process validatio/spannstrong./strong/span/li/ul/li/ulspan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:18px;"bThe Personality Part: /b/span/spanullispan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Our Next Piece treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?/span/span/li/ulspan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:18px;"bAS A PIECE OF FITS, YOU WILL: /bb(The day-to-day on the job)/b/span/spanulli style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Designs manufacturing processes, procedures, and production layouts for assemblies, equipment installation, processing, machining, and materials. /span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Designs the arrangement of machines within plant facilities to ensure the most efficient and productive layout./span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Designs the sequence of operations and specifies procedures for fabricating tools and equipment, and other functions that affect product performance./span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Adapts machine or equipment design to factory and production conditions./span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"May incorporate inspection and test requirements into the production plan./span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective actions. /span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Develops manufacturing processes that apply to statistical process control, and may develop those techniques./span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques./span/span/lili style="text-align:justify;margin-left:8px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"Ensures processes and procedures comply with regulations. /span/span/li/ulspan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:18px;"bWHO WE ARE:/b/spanbr/span style="font-size:16px;"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. bWe're FITS! /b/spanbr/span style="font-size:18px;"strong Are you the Next Piece?/strong/span/spanp style="text-align:center;"/pbr/span style="font-family:Arial, Helvetica, sans-serif;" /span /div

For engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering and two (2) year of exposure within the Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Excellent teamwork skills Shift: Administrative and according to business needs. Experience in: Equipment installation, setup, and Installation Qualification. Technical Writing of reports and procedures. Manufacturing Process Validations. The Personality Part: Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to Be The Piece? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Designs manufacturing processes, procedures, and production layouts for assemblies, equipment installation, machining, and material handling. Design arrangement of machines within plant facilities to ensure the most efficient and productive layout. Designs the sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action. Develops manufacturing processes that apply to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures comply with regulations. WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves on 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 Devic,e and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the Next Piece?

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: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). Responsibilities: Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are in compliance with regulations. Shift: Administrative Location: Villalba, PR Education: BS in Engineering Years' Experience Required: 2 years relevant experience minimum Preferred Qualifications: Equipment installation, set up, and installation qualification. Technical writing of reports and procedures. Manufacturing process validation. Skills Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments. Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments. Contributes to the completion of project milestones . May have some involvement in cross functional assignments. Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex . Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area. Communication and Influence: Communicates primarily and frequently with internal contacts . External interactions are less complex or problem solving in nature. Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making. Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream. Required Knowledge and Experience: Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience. 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

Are you ready to see your future take flight? At GE Aerospace, we are advancing aviation technologies for today and tomorrow. Your work will contribute to the production of advanced jet engines, components, and integrated systems that power commercial and military aircraft. You'll be part of a team that embraces your drive, your curiosity, and your unique ideas and perspectives. Most importantly, you'll share in our pride and purpose that affects the lives of millions around the world! The Product Quality Engineer for Aerospace Investment Casting manufacturing process will drive product qualifications and quality improvements for key performance indicators (KPIs) of suppliers within the Investment Casting supply chain including quality plan implementation. The PQE, will own supplier First Article Inspection results and drive supplier compliance to Source Substantiation Plans or design intent verification. Provide supplier product release direction when part approval cycles are not complete while also being the internal quality focal for those parts. Collaborate with Supplier Quality, Supplier Quality Operations and New Product Introduction / Management of Change teams as required- this collaboration may include onsite visitation. In this role, you will also understand how the team integrates with other teams outside of Quality to meet short term and long term the business objectives. Demonstrate an in-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area. **Job Description** **Roles and Responsibilities** + Role is responsible for supplier processes, from initial qualification, maintenance, and necessary improvement driven by business quality needs. + Product Quality Engineer will have a technical understanding of engineering drawings and will have the ability to manage suppliers and/or quality projects related projects. + Develop in-depth knowledge of a discipline. Use prior experience and acquired expertise to execute functional policy/strategy. + Communication with direct colleagues and the business on the status of First Article Inspection and Source Substantiation Plans. + Provide onsite support at suppliers, as needed ( **approximately 15% travel** ) + Collaboration with other Engineering, Quality, and Sourcing functions to ensure joint success + Impacts projects, processes, and procedures in own field. The role operates with some autonomy but is focused on execution of activities/provision of advice within an enabling discipline covered by standard functional practices and procedures. Activities require professional judgment but may require more senior levels of guidance. + Utilizes technical expertise and judgement to solve problems. Leverages technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions. + Uses high level of judgment to make decisions and handle complex tasks or problems in areas of operational, product management, manufacturing, technology, or engineering. Has ability to assess quality of information given and ask pertinent questions to stakeholders. Able to offer new solutions to problems outside of set parameters and can construct and provide recommendations. Uses multiple internal and some external sources outside of own function to help arrive at a decision. + May lead functional teams or projects with minimal resource requirements, risk, and/or complexity. Communicates difficult concepts and may influence others' options on specific topics. May guide others to consider a different point of view. **Required Qualifications** + Bachelor's Degree accredited college or university in Engineering or Materials Science + Minimum of 4 years of experience in Engineering, Materials Science or Quality related roles. **Desired Characteristics** + Demonstrated experience in manufacturing or supplier quality. + Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills. + Demonstrated history of problem solving, root cause and corrective action methodology, data analysis, statistical analysis and quality experience. + Humble: respectful, receptive, agile, eager to learn + Transparent: shares critical information, speaks with candor, contributes constructively + Focused: quick learner, strategically prioritizes work, committed + Leadership ability: strong communicator, decision-maker, collaborative + Problem solver: analytical-minded, challenges existing processes, critical thinker + Demonstrated Investment Casting manufacturing knowledge and experience is advantageous to the role. GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness. GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual. The base pay range for this position is 100,000.00 - 120,000.00. The specific pay offered may be influenced by a variety of factors, including the candidate's experience, education, and skill set. This position is also eligible for an annual discretionary bonus based on a percentage of your base salary/ commission based on the plan. This posting is expected to close on **June 11** **,** **2025** **.** \#LI-AZ1 _This role requires access to U.S. export-controlled information. Therefore, for applicants who are not asylees, refugees, lawful permanent residents or U.S. Citizens (i.e., not a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3), otherwise known as a U.S. Person), final offers will be contingent on the ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._ **Additional Information** GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** No \#LI-Remote - This is a remote position GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

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: An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies - from design to implementation - while adhering to policies, using specialized knowledge and skills. Responsibilities: * Responsibilities may include the following and other duties may be assigned. * Ensures that suppliers deliver quality parts, materials, and services. * Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. * Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur. * Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. * Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation. * Some individuals may have responsibilities that include Pre-Market Supplier Quality and duties may include: Provides Pre-Market Quality Engineering support to New Product Development (NPD) working in partnership with the Component Engineering and Post-Market Supplier Quality Teams, to deliver quality parts, materials, and services, prevent defects, and allow to provide customers with the highest quality and reliable products. * Provides technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements. * Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products. * Define Receiving Inspection requirements as required and associated test method validation for all internal Test Methods. Shift: Administrative Location: Villalba, PR Education: Bachelors degree in Engineering Preferred Qualifications: * Communication skills * Computer proficiency * Problem-solving techniques Skills: * Autonomy: Entry-level individual contributor on a project or work team.Works with close supervision. * Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities. * Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex.Makes minor changes in systems and processes to solve problems. * Communication and Influence: Communicates primarily with internal contacts within immediate group.Contacts others to gather, confirm and convey information. This position is for a fixed term contract supporting one of ECHO Consulting Group (dba PharmaLex 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

¡Únete a nuestro equipo de almacén! ¡DP World se incorpora a la zona! Join Our Warehouse Team - DP World is New to the Area! We're New to the Area! Somos una empresa nueva que se instala en la zona y estamos renovando nuestro equipo de almacén desde cero. We're a new company coming to the area, and we're building our warehouse team from the ground up! Buscamos un Ingeniero de Procesos cualificado para liderar iniciativas de mejora continua y eficiencia en todas nuestras operaciones. Este puesto utilizará herramientas Lean como el balanceo de línea, el mapeo del flujo de valor, el AMEF y los planes de control para analizar y optimizar los sistemas de trabajo. El Ingeniero de Procesos apoyará la planificación del diseño, realizará estudios de tiempos y evaluará el impacto de los cambios de proceso en la mano de obra y la capacidad. Sus responsabilidades también incluyen la gestión de proyectos de ingeniería, la recomendación de compra de equipos y la colaboración con equipos multifuncionales para implementar soluciones sostenibles que impulsen la productividad y reduzcan el desperdicio. We are seeking a skilled Process Engineer to lead continuous improvement and efficiency initiatives across our operations. This role will utilize Lean tools such as line balancing, value stream mapping, FMEA, and control plans to analyze and enhance work systems. The Process Engineer will support layout planning, conduct time studies, and evaluate the impact of process changes on labor and capacity. Responsibilities also include managing engineering projects, recommending equipment purchases, and collaborating with cross-functional teams to implement sustainable solutions that drive productivity and reduce waste. Esta es una oportunidad emocionante para formar parte de un equipo completamente nuevo, ayudarnos a construir una sólida cultura laboral y crecer en una empresa que valora el trabajo duro y el trabajo en equipo. This is an exciting opportunity to be part of a brand-new team, help us build a strong workplace culture, and grow with a company that values hard work and teamwork. Esperamos tu solicitud y esperamos darte la bienvenida pronto. We look forward to your application and hope to welcome you onboard soon! About the Role How you will contribute * Utilize Lean Standards in everyday assignments and analysis including: Line Balancing, PFEP, Value Stream Mapping, Process FMEA's, Control Plans, engineering studies, and resource requirement sheets. * Provide leadership and support to Continuous Improvement initiatives at the plant level including; work studies to analyze work systems, developing standards and/or improvements to existing systems, providing input for the development of functional layouts that minimize space and material transit distance that provides flexibility for expansion, and utilize simulation software to analyze and/or improve work systems. * Develop and update existing headcount analysis tools (direct and indirect labor) in order to analyze the impact of changes on business, and prepare summary reports for and in support of Operations, IT and Business Process Improvement initiatives. * Prepare engineering studies to ensure that continuously changing operational processes are reflected in operational and strategic calculations. * Measure standard time to proactively challenge and support the realization of reductions in standard time, while always striving to eliminate waste. * Serve as the main point of contact for capacity, process improvement tasks, and standard time inquiries. * Work closely with Operations, Account Management, Facilities and Project Management teams to develop and implement solutions to meet the requirements of the business. * Manage the engineering function for assigned projects and activities including; engineering budget, processes, equipment, work standards and facilities. * Make informed recommendations and decisions related to the purchase or lease of capital equipment including; forklifts, tooling, lift assists, generators, compressed air systems, racking, scrubbers, compactors, and miscellaneous items pertaining to specific projects. * Other duties as assigned Your Key Qualifications * Bachelor's or Master's Degree in Industrial Engineering, Supply Chain or Operations Research or related fields with very strong background in engineering redesign and cost savings initiatives. * 3 yrs of Experience in solutions design within a logistics/warehousing/manufacturing facility environment * Experience in supporting warehousing contracts with engineering expertise. * Experience in packaging and/or innovation. * Highly developed computer skills, including Microsoft Excel, Access, Word, Visio or equivalent, and Project Management software are required. Knowledge of Excel should include pivot tables and familiarity with common formulas. Must be proficient in Access, with thorough knowledge of relational database creation, queries, forms, reports, macros, and functions. * Hands on experience with supply chain applications such as WMS, TMS, OMS, and SCM. Compensation DP World offers exciting and challenging roles within a growing international organization. We strive to hire and develop the right people, locally and globally, stimulating personal growth and self-development within an informal atmosphere. We offer a market competitive compensation package. About DP World Trade is the lifeblood of the global economy, creating opportunities and improving the quality of life for people around the world. DP World exists to make the world's trade flow better, changing what's possible for the customers and communities we serve globally. With a dedicated, diverse and professional team of more than 111,000 employees from 159 nationalities, spanning 77 countries on six continents, DP World is pushing trade further and faster towards a seamless supply chain that's fit for the future. We're rapidly transforming and integrating our businesses -- Ports and Terminals, Marine Services, Logistics and Technology - and uniting our global infrastructure with local expertise to create stronger, more efficient end-to-end supply chain solutions that can change the way the world trades. What's more, we're reshaping the future by investing in innovation. From intelligent delivery systems to automated warehouse stacking, we're at the cutting edge of disruptive technology, pushing the sector towards better ways to trade, minimising disruptions from the factory floor to the customer's door. DP World is on a mission to transcend boundaries and bridge the gap between all nations and cultures - not just in what we do but also in how we behave. We are dedicated to creating a culture where everyone feels respected, supported, and empowered to reach their full potential. We believe that embracing inclusion and diversity, drives innovation and growth and helps us connect people, businesses, and societies. Free minds and different perspectives are changing our world, and together we can change what's possible. The DP World family comprises of syncreon, Imperial and P&O. WE MAKE TRADE FLOW TO CHANGE WHAT'S POSSIBLE FOR EVERYONE. Nearest Major Market: Puerto Rico Job Segment: Logistics, Facilities, Supply Chain, Process Engineer, Business Process, Operations, Engineering, Management

Permanent About Heraeus Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead. About Heraeus Medevio Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds. To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today. Position Summary The Continuous Improvement Engineer II will play a crucial role in developing and implementing global operational excellence standards and continuous improvement activities across various operational or business areas. The position involves supporting the embedding of HPS Operational Excellence principles into product and process development, training and mentoring teams, and identifying operational improvement opportunities using lean principles and 6-sigma methodology. The Continuous Improvement Engineer II also oversees IT Systems activities through coordination of HSY and is the site ERP SuperUser. Your Role and Responsibilities: * Demonstrating leadership in conveying operational excellence principles and developing global operational excellence standards. * Implementing continuous improvement activities for various operational or business areas. * Supporting the embedding of HPS Operational Excellence principles into product and process development activities and ongoing operations. * Participating in the definition of HPS Global Operational Excellence standards as a member of the CI Team. * Rolling out HPS Operational Excellence standards in coordination with operational leaders. * Training, mentoring, and coaching engineering and operations teams on HPS Operational Excellence principles and methods. * Identifying, evaluating, supporting prioritization, and implementing operational improvement opportunities using lean principles and/or 6-sigma methodology. * Conducting cost/benefit analysis for changes to processes and/or equipment. * Supporting the optimization of process flows, line layouts, staffing, and workstation design to improve product scalability. * Leading value stream mapping exercises to identify waste and areas for improvement. * Other duties as assigned. What is Required for This Role: * Bachelor's degree in Engineering (Industrial preferred). * Minimum 4 years of experience in Medical Device or component manufacturing as Black Belt certified (preferably). * Knowledge of medical device regulations, Statistical analysis, design and manufacturing. Basic understanding of manufacturing equipment and computer programming * Proficiency in reading, writing and speaking English with the ability to interface and influence at all organization levels. * Must be able to create legible, accurate, and detailed documents that clearly communicate product and manufacturing expectations. * Proficient in the use of project management tools, data analytic, statistical tools, and application of continuous improvement methodologies such Lean, Six Sigma or equivalent. * Ability to train, lead, mentor, coach and inspire teams to significantly impact the business. * Demonstrated proficiency in strategic thinking, change management, facilitation, and interpersonal effectiveness. * Proven leadership skills and business acumen; performance driven. * Distinguished through consistent display of leadership by example in accordance with Heraeus' Ethics Statement. * Works with positive attitude and acts within the principle of Heraeus Core Values and Code of Conduct as applicable for position. Curious? Apply now! We are interested in finding the best candidates, and they may come from a nontraditional background. So please don't hesitate to apply, even if you aren't an exact fit. We look forward to getting you started on your employment journey with Heraeus Medevio! Any further questions? Our Recruiting Team, Heraeus Medevio, is happy to assist you by email: [[cust_RecTeam]]. Or visit us at jobs.heraeus.com. ReqID: 57820

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: We are seeking a Process Engineer with strong experience in validations, including Master Validation Plans, IQ, OQ, MSA, PQ, and related activities. The candidate must be fully bilingual and have at least two years of experience in validation within a medical device company. Validation lifecycle knowledge / Hands on experience (Writing and executing IQ/OQ/PQ protocols among others) Troubleshooting equipment / process failures Analyzing test data and statistical trends Qualifications Requirements/Knowledge/Education/Skills: BBA in Enigneering At least two years of hands-on experience in validations within the medical device industry. Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley. Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

divdivdivdivdivdivdivdivdivh2 id="is Pasted" style='box-sizing: inherit; font-family: "Indeed Sans", "Noto Sans", "Helvetica Neue", Helvetica, Arial, "Liberation Sans", Roboto, Noto, sans-serif; font-weight: 700; color: rgb(45, 45, 45); margin: 0px; font-size: 1.25rem; line-height: 1.5; margin-block: 0px 0.5rem; margin-inline: 0px; padding-top: 0px; padding-bottom: 0px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;'Job description/h2pbr//pdiv style="box-sizing: border-box; margin-block: 0px; margin-inline: 0px; min-inline-size: 0px;"div style="box-sizing: inherit;"div style="box-sizing: inherit;"div style="box-sizing: inherit;"p style="box-sizing: inherit; font-size: 0.875rem; line-height: 1.5; color: rgb(89, 89, 89); margin: 0px; margin-block-end: 0.75rem;"CMA Architects amp; Engineering LLC is a full-service architecture and engineering firm with 65 years of experience steeped in solving complex architecture and engineering challenges./pp style="box-sizing: inherit; font-size: 0.875rem; line-height: 1.5; color: rgb(89, 89, 89); margin: 0px; margin-block-end: 0.75rem;"Consulting firms, contractors and infrastructure owners count on us when innovative design and intricate architectural and engineering solutions are required. 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Job DescriptionSalary: Are you passionate about building modern, cloud-native applications that scale? Do you love solving complex problems with elegant code and powerful AWS services? Were on the lookout for a skilled and motivated AWS Application Engineer to join our team. In this role, youll be at the forefront of application development on the AWS cloud, designing and deploying secure, scalable, and high-performing solutions for a variety of clients and industries. At our core, were a software development company that values creativity, ownership, and collaboration. If youre ready to build powerful cloud applications and join a forward-thinking tech team with us, wed love to meet you. Duties and Responsibilities: Analyze application architecture and dependencies to determine migration readiness. Work with architects to design migration strategies (Rehost, Replatform, Refactor) for various workloads. Assist in the migration of applications to AWS using tools like AWS Application Migration Service (MGN), AWS Database Migration Service (DMS), and AWS Elastic Beanstalk. Ensure proper deployment, configuration, and performance of applications in AWS environments. Troubleshoot application issues and ensure smooth functioning in the new AWS environment. Optimize applications for performance, scalability, and cost efficiency. Configure applications to utilize AWS services like RDS, S3, Lambda, DynamoDB, and CloudFront. Set up monitoring and logging for applications using AWS CloudWatch, X-Ray, and third-party tools. Collaborate with DevOps engineers to automate application deployments using AWS CodePipeline, CodeDeploy, or Jenkins. Develop scripts for repeatable application setup and provisioning using Infrastructure as Code (IaC) tools like AWS CloudFormation or Terraform. Work closely with architects, QA engineers, and stakeholders to ensure migration objectives are met. Actively participate in Scrum ceremonies, including sprint planning, daily stand-ups, and retrospectives. Document application changes, migration steps, and configurations. Share knowledge with team members to ensure consistent understanding of application and migration processes. Required skills: Minimum of 3+ years of experience in a security engineering role, with experience in network security, application security, and security frameworks. Bachelor's degree in a related area and/or equivalent experience/training. Strong understanding of AWS services like EC2, S3, RDS, Lambda, and VPC configurations. Familiarity with AWS migration tools, such as AWS MGN, DMS, and Migration Hub. Experience in deploying, configuring, and managing applications in cloud environments. Knowledge of microservices architecture and containerization tools like Docker and ECS. Proficiency in scripting languages such as Python, Shell, or PowerShell for automation. Experience with Infrastructure as Code tools like Terraform, AWS CloudFormation, or CDK. Hands-on experience with monitoring tools like AWS CloudWatch, X-Ray, or third-party solutions like Datadog. Strong problem-solving skills for application performance and dependency issues. Experience working in Scrum or Agile teams, adhering to iterative delivery and collaborative practices. Strong analytical and troubleshooting abilities. Excellent communication and teamwork skills. Ability to manage multiple priorities in a fast-paced environment. Excellent computer proficiency, including JIRA. Nice to have skills: Understanding of advanced services like AWS Step Functions, EventBridge, and Aurora. Experience with AWS serverless technologies like API Gateway, Lambda, and DynamoDB. Familiarity with CI/CD tools like GitHub Actions, Jenkins, or AWS CodePipeline. Knowledge of container orchestration tools such as Kubernetes (EKS). Experience in tuning application performance and cost optimization in AWS. Familiarity with caching solutions like ElastiCache or Content Delivery Networks (CDNs). Experience with migration validation, including data integrity, application functionality, and system dependencies. Ability to mentor junior engineers and contribute to team knowledge sharing. Proactive approach to identifying and resolving migration challenges. AWS Certified Developer Associate or AWS Certified Solutions Architect Associate. What sets INVID apart is our collaborative and flexible work environment. We encourage our team to raise the bar in everything they do while maintaining a healthy work-life balance. With our hybrid work model, team members thrive both in the office and remotely. We foster a culture of mutual respect, autonomy, and accountability, where your voice matters and your growth is supported. From structured career paths and paid professional development to access to industry events, were committed to your success. Join us at INVID, where innovation meets support, and together we deliver excellence. Must be a US Citizen, US Resident Fully bilingual (English and Spanish) Location: San Juan, Puerto Rico Background Check Required: Final candidates must be willing to complete a background check as a condition of employment. EEO

Responsibilities may include the following and other duties may be assigned. Analyzes and designs sequence of operations and work flow to improve efficiencies in plant and production facilities and equipment layouts; and establishes methods for maximum utilization of production facilities and personnel. May establish or assist in establishing accident prevention measures and may manage training programs for personnel concerning all phases of production operations. Conducts studies pertaining to cost control, cost reduction, inventory control, and production record systems. On the basis of these studies, develops and implements plans and programs for facility modifications and revisions to operating methods. May assist facilities engineers in the planning and design of facilities. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University). DIFFERENTIATING FACTORS Autonomy: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments. Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments. Contributes to the completion of project milestones . May have some involvement in cross functional assignments. Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex . Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area. Communication and Influence: Communicates primarily and frequently with internal contacts . Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience. Requires a University Degree and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.

EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service. We are looking for a Supplier Quality Engineer (SQE) with Medical Devices manufacturing experience preferred (3+ years). Must possess experience in CAPA, Quality Tools and Suppliers Selections programs. Understanding of SPC and GD&T. Key Responsibilities Ensure suppliers deliver high-quality parts, materials, and services Qualify suppliers based on company standards, administer Certified Supplier Program for receiving inspection Monitor supplier performance from acquisition through manufacturing, address supplier-related issues promptly Develop and prioritize an auditing schedule for regular supplier audits, ensuring GMP and quality standards Evaluate and assess supplier performance, provide feedback for continuous improvement Provide Pre-Market Quality support for New Product Development (NPD), working with Component Engineering and Post-Market teams Offer technical guidance on newly qualified parts, ensuring compliance with regulatory and customer requirements Collaborate with Component Engineers to develop Product Acceptance Sampling, Approved Supplier List, Supplier-Owned Quality programs, and Control Plans Define receiving inspection requirements and validate test methods for internal Medtronic Test Methods What We Are Looking For: Strong communication skills to effectively work with teams and suppliers Proficiency with computer systems for quality management and documentation Solid problem-solving abilities for identifying root causes and implementing corrective actions Qualifications: 3+ years of experience in Supplier Quality Engineering (medical device manufacturing preferred) Strong experience in CAPA, SPC, GD&T, and quality tools Experience in New Product Development (NPD) and supplier quality engagement Bachelor's degree in Engineering Job Types: Full-time, Contract Benefits: Dental insurance Employee discount Health insurance Life insurance Paid time off Professional development assistance Referral program Schedule: 8 hour shift Monday to Friday Weekends as needed Work Location: In person

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Organization Overview: The Process Engineering function is part of the Maintenance and Engineering Department that provides technical expertise and support to Operations ensuring compliance with cGMP, HSE guidelines and regulations, company standards and business practices. The primary areas of support include technical expertise (process and equipment), manufacturing and business process improvements, compliance with business systems, and people development. Responsibilities: Technical leadership - Provide expertise as equipment/asset expert/steward for the areas supported to design, improve and maintain an efficient manufacturing processes. Establish and maintain technical information of the process and unit operations within the manufacturing process. Develop and monitor process and capacity indicators to identify and address performance issues and identify improvement opportunities. Understand process hazards and participate/lead in Process Hazard Reviews (PHR) and assessments. Implement PHR recommendations. Assure safety processes are in place (i.e. LOTO, Line breaking, etc.). Develop specialized technology/unit operations knowledge and provide training to operations as content expert for manufacturing standard operating procedures (SOPs). Perform troubleshooting and investigation on unexpected issues. Own equipment related deviations, CAPAs and changes. Lead or participate in investigations, problem-solving activities such as root cause analysis, FMEA, problem analysis and in development/implementation of countermeasure for quality, safety, environmental events. Lead efforts in design, selection, installation, qualification, operation, maintenance, and reliability of process equipment and facilities. Perform and summarize improvement opportunities in technical reports, investigations, plant/lab trials, data analysis and process modeling. Active participation and engagement in the meetings and activities of the assigned process team and safety/environmental sub teams. Own the qualified state of their equipment and monitor according to the defined strategy. Own Commissioning & Qualification (C&Q) strategy and execution for the assets, including requirements, design, and verification. Have holistic understanding of Process Validation (and associated equipment, facilities, and computer systems), assessment of significant changes, maintenance and other interventions, involvement with PM Plans and spare parts list. Ensure process complies with current industry regulatory expectations, new regulations, and corporate policies and programs for Quality, Health and Safety & Environmental, Process Safety. Basic Requirements: B.S. in Engineering (Chemical or Mechanical) Minimum of five (5) years of experience in pharmaceutical (API/Chemical) operations. Demonstrated Technical knowledge in Process Equipment requirements, specifically those related to Chemical Operations. Experience in PSM (Process Safety Management) process Salary commensurate with experience. Additional Skills/Preferences: Biotech/Chemical Operations; Spray Dispersing Drying Operations. Bilingual (English/Spanish) with strong written and oral communication skills Strong leadership and organizational skills Knowledge in managing multiple project objectives or assignments. Technical Writing Strong customer service focus Strong compliance mindset and sound judgement Additional Information: Available to work or provide support to a 24/7 operation, if necessary Availability to travel within and outside Puerto Rico and U.S. Work as a resource in other strategic areas of the business, based on business needs. Important Notice: In order to maintain the excellent reputation of our company, the quality of our products, and the safety of our working environment, the company will take all reasonable measures to ensure that drug abuse by employees or other persons does not jeopardize the safety of our operations or the quality of our products or adversely affect in any way the company or its employees. The company recognizes that drug use both on and off the job can be detrimental to the company and its efforts to provide a drug-free workplace. Even if prescribed under a state medical marijuana law, marijuana remains illegal under federal law. Marijuana is considered unauthorized by Lilly. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $78,750 - $148,500 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly