Engineering Associate Jobs in Carolina, PR

A Mechanical Design Engineer is responsible for designing, developing, and testing mechanical systems and components in various industries. The role requires an individual who has a solid understanding of mechanical engineering principles and can apply this knowledge to real-world design problems. The engineer will work closely with cross-functional teams and be involved in all aspects of the design process from concept development to product launch. Responsibility: Prepare calculations on the proposed machine before completing technical drawings Sketch and draw up designs using input from engineers and architects on the team Calculate factors like tolerance, dimensions, and thermal and structural analysis Create designs in line with company procedure, regulations and client standards Submit drawings to upper management and construction teams Use customer feedback and data to upgrade, improve or repair the company's existing machines Provide support during the building and installation process, ensuring that the machine is built properly and according to design specifications Finalize designs and send prints to the production department Requirements/Education: Bachelor's Degree with 5-10 years experience Professional Engineer (P.E.) License or Engineer In Training (EIT) License preferred Previous experience in mechanical engineering, such as HVAC Systems, Plumbing Systems & Pump and water systems. Familiarity with manufacturing designs or schematics Strong problem solving and critical thinking skills Ability to prioritize and multitask Experience and/or knowledge in AutoCAD, REVIT and Trane TRACE Others Qualifications: Experience in Siemens NX, Visio, Solidworks software. Experience in ANSYS, ABAQUS FEA software. Experience in design and analysis of heat exchangers. Desirable experience in CNC Manufacturing, Mechanical Design. Experience interacting with Mechanical Computer Aided Design Resources (MCAD). Project Engineering experience is a plus. Experience interacting with configuration management (CM). Knowledge and experience working Geometric Dimensioning and Tolerancing (GD&T), Tolerance Stack up Calculation, Weight Analysis, etc. Teamcenter (or other collaborational space) knowledge is a plus. Project management /MS Project is valuable. "Drug Free Workplace Policy: In accordance with our commitment to maintaining a safe and productive work environment, all applicants for employment with our company are required to affirm their commitment to a drug-free workplace and consent to pre-employment drug testing as a condition of employment." Share Tech Group is committed to being an equal opportunity employer, fostering a diverse and inclusive workplace where all individuals are treated with respect and provided with equal opportunities for employment and advancement.

Designs and plans layout for such activities as machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling. Adapts machine or equipment design to factory and production conditions. 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. 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. Ensure compliance with company programs procedures and applicable quality system regulations and standards.

Validation & Engineering Group (VEG) is a leading services supplier 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. Job Description Responsible and accountable for the Reliability and Maintainability initiatives for new and modified installations. Assist efforts to ensure reliability and maintainability of equipment, processes, utilities, facilities, controls and safety/security systems. Supports the definition, design, development, monitoring and refining of an asset maintenance plan that includes: Value-added preventive maintenance tasks Effective utilization of predictive and other non-destructive testing methodologies designed to identify and isolate inherent reliability problems Provides input to a risk management plan that will anticipate reliability-related and non-reliability-related risks that could adversely impact plant operations. Assists in the development of engineering solutions to repetitive failures and all other problems that adversely affect plant operations. These problems include capacity, quality, cost or regulatory compliance issues. Perform Root Cause Analysis (RCA) and root cause failure analysis (RCFA). Perform failure reporting, analysis and corrective action system (FRACAS). Works with Production and Engineering to perform analyses of assets including: Asset utilization Overall equipment effectiveness Remaining useful life Other parameters that define operating condition, reliability and costs of assets Provides technical support to production, maintenance management and technical personnel. Qualifications Bachelor Degree in Engineering Five (5) years' experience in maintenance related field with at least three (3) years' experience in the equipment reliability function Experience with Predictive Technologies, Root Cause Failure Analysis and Failure Mode & Effect Analysis. Must have experience in data analysis techniques including: Statistical process control, reliability modeling and prediction, Fault tree and weibull analysis. Experience using Six Sigma methodology Advanced computer and excellent technical skills Demonstrated outstanding technical expertise in mechanical and electrical failures. Demonstrated leadership and team oriented skills Excellent oral and written communication skills in English and Spanish. Additional Information Positions available for Puerto Rico. Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer.

Senior Electrical Engineering Technologist On-site in PUERTO RICO ***Must be a Canadian Citizen*** $110K-$135K, based on experience + Benefits Rotation shift work. 3 weeks on 2 weeks off + LOA We are currently hiring a highly motivated and experienced Senior Electrical Engineering Technologist, PSE, or Engineer to join our client's field services team on a full time basis. If you are an excellent communicator and skilled problem-solver with strong attention to detail, our client offers a dynamic work environment where you will be continuously challenged in all aspects of the testing and commissioning process. Responsibilities: Manage and lead a commissioning crew of workers. Testing and commissioning of MV/HV power system protection & control schemes in the utility, power generation, and oil & gas industry. Read and interpret drawings and troubleshoot / resolve technical issues. Train/develop employees to ensure highest performance standards are met. Report preparation and submission. Assist with generation of commissioning startup procedures or work instructions. Ensure compliance with all safety practices as per corporate, client, and industry standards. Initiate and/or respond to customer inquiries, discuss trouble details and confirm resolutions. Qualifications: Bachelor's Degree in Electrical Engineering, Power Systems Electrician Journeyman Ticket, or an Electrical Engineering Technologist Diploma from a recognized institute. Eligible for registration with professional association. Comprehensive understanding of electrical power system protection and controls including SCADA, relay protection, metering, equipment functionals, and telecom networks. Minimum 5+ years of proven experience in the medium voltage and/or high voltage utility substations and power generation industry with experience in a supervisory role leading and running projects in greenfield and BROWNFIELD substations IS A MUST. Relay testing of microprocessor-based protection IED's (SEL, ABB, Siemens, GE, etc.) with fully automated test equipment (Omicron CMC356) and test data management. Experienced in high voltage primary equipment testing and commissioning involving power transformers, reactors, circuit breakers, CT's, PT's, surge arrestors, disconnect switches, cap and reactor Banks, etc. Testing and commissioning as per NETA/IEEE/IEC standards. Strong understanding of CSA Z462 safety standards. Strong interpersonal and communication skills and an extreme attention to detail are essential. Knowledge of the Microsoft office software suite of programs coupled with strong computer skills. Excellent organizational skills and ability to manage a wide variety of issues simultaneously. Strong analytical, risk assessment and problem solving skills. NETA Testing Certification an asset. Background checks and Drug and Alcohol Pre-Access Testing will be required as part of employment. Thank you for your interest in this job posting. We look forward to hearing from you. TalentSphere Staffing Solutions talentsphere.ca Canada Toronto: 416.900.3435 Calgary: 403.910.9222 Edmonton: 587.333.7929 Halifax: 902.800.7808 Kelowna: 250.448.8880 Montreal: 438.448.4300 Mississauga: 905.919.3688 Ottawa: 613.783.1441 Vancouver: 778.807.9777 Victoria: 250.294.8095 Winnipeg: 204.285.3905 United States USA Toll-Free: 1855.900.3435 Dallas 469.498.2002 Los Angeles 213.290.4030

Designs and plans layout for activities such as machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling. Adapts machine or equipment design to factory and production conditions. 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. 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. Complies with company programs, procedures and applicable quality system regulations and standards. Leverages technical expertise and knowledge of Medtronic's standard engineering approaches, design concepts and specification requirements to best utilize equipment and manufacturing techniques. The candidate will be working on the introduction on a new product that may include: Process Development and documentation Equipment validation SOP Development Line layout and infrastructure and development MES (Manufacturing Execution System) Special Build Documentation and Line Support Other duties may be assigned. * Requirements 2 to 8 years of experience in Manufacturing processes, builds and Layout change. Experience in Process Validation Lifecycle (from Installation qualification, TMV, process characterization, operational qualification to performance qualification, PFMEA). Basic knowledge of drawings interpretation. Bilingual(Manage a Conversation in English). Bachelor Degree in Engineering completed. Willing to work 100% On-Site in Villalba and work 2nd shift or weekends when necessary). (2 year contract opportunity)

For engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering & two (2) years of relevant experience within the Medical Devices or Pharmaceutical industry. Bilingual (Spanish & English). Shift: 1st and 2nd according to business needs. Experience in: Drawings interpretation. Manufacturing processes, products, and builds knowledge. Process Validation Lifecycle (IQ, TMV, OQ, PQ, PFMEA, Process Characterization). SOP Development. The Personality Part: 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? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Designs and plans layouts for activities such as machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling. Adapts machine or equipment design to factory and production conditions. Designs the 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. 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 for problems. Complies with company programs, procedures, and applicable quality system regulations and standards. Leverages technical expertise and knowledge of standard engineering approaches, design concepts, and specification requirements. 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?

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

Job Description Under general supervision, the Engineer Specialist will play a key role in characterizing process optimization strategies and troubleshooting operational issues in the manufacturing, pilot plant, or capital projects environments. This position will involve applying basic engineering principles to system modifications, experiments, and/or capital projects. The engineer will collaborate with cross-functional teams to support operational excellence and ensure regulatory compliance in a GMP-regulated environment. Responsibilities Troubleshoot and resolve a variety of technical problems of moderate complexity within manufacturing and production systems. Serve as a technical expert to equipment and systems, actively supporting daily operations and resolving complex issues as required. Routinely audit operational performance, ensuring compliance with regulatory standards and identifying areas for system improvement. Work closely with manufacturing, maintenance, research, process development, utilities, facilities, quality assurance, and validation teams to recommend and implement system modifications. Analyze equipment-related problems, understand the variables that impact processes, and propose solutions to resolve issues effectively. Work under the direct supervision of project managers to complete design, engineering, and construction projects within specified schedules and budget constraints. Collaborate with consultants, architects, and engineering firms on the development of design documents and equipment specifications. Obtain, review, and critique quotes for equipment modifications or installations, ensuring feasibility and cost-effectiveness. Generate project cost estimates and schedules, providing detailed and accurate documentation to support project execution. Ensure compliance with GMP, GLP, and other regulatory requirements in all engineering processes and activities. Provide support for validation activities, including writing validation protocols and assisting in validation execution. Contribute to equipment startup and troubleshooting, particularly in relation to control systems, failure modes, and operational performance. Skills & Competencies Excellent problem-solving and technical skills Strong written and verbal communication skills, including technical report writing Ability to create and deliver basic technical presentations Proficiency in using technology and computer systems to enhance engineering practices Demonstrated ability to self-learn and adapt to new technologies or processes Strong organizational skills and the ability to manage multiple tasks efficiently Requirements Qualifications Bachelor’s or Master’s degree in Engineering (Chemical, Mechanical, Electrical, or a related field) Minimum of 2 years of engineering experience in a pharmaceutical or biotech manufacturing environment Preferred Qualifications Experience working in GMP-regulated environments (manufacturing operations, engineering operations) Familiarity with validation processes and documentation in highly regulated environments Ability to operate specialized laboratory and manufacturing equipment as required Strong understanding of control systems (input, output, control) and their impact on manufacturing processes Experience in troubleshooting equipment such as valves, pumps, and utilities systems Familiarity with drug substance/API operations Experience in equipment startup, troubleshooting, and PLC systems Proven ability to apply engineering principles to resolve technical problems and optimize manufacturing processes Benefits 1 year contract with possible extension 12 hours shifts, 48 hours a week

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: Humacao , PR Education: BS in Engineering Preferred Qualifications: * Validations * Change Management * Statistical Analysis * Years' Experience Required: 2 years relevant experience minimum 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 decisionmaking. * 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. 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

div class="col col-xs-7 description" id="job-description" pQUALITY 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 amp; USA./pp Responsibilities:/pulli Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling./lili Designs arrangement of machines within plant facilities to ensure most efficient and productive layout./lili Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance./lili Adapts machine or equipment design to factory and production conditions./lili May incorporate inspection and test requirements into the production plan./lili 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./lili Develops manufacturing processes that are applicable to statistical process control and may develop those techniques./lili Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques./lili Ensures processes and procedures are in compliance with regulations./li/ulp Qualifications:/pulli Bachelor's degree in engineering/lili Two (2) or (8) eight years of relevant experience/lili Validations/lili Change Management/lili Statistical Analysis/lili Availability for 1st shift/lili Need availability during weekends/li/ulpspan style="font-size:10px"em 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./em/span/p /div

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Engineering Tech for Cytiva is responsible of providing support to manufacturing and packaging operations to assure continuous efficiency. Ensures overall process performance to design capability. Provide effective technical services to production, test and packaging machinery. Also, assist engineering in the design and implementation plans for cost reduction, quality improvements, process support and verification. This position reports to the Sr. Engineering Team Manager and is part of the Manufacturing Operations located in Cytiva Fajardo Puerto Rico and will be on-site. What you will do: * Perform and overview all line equipment set up to optimize product process yields and minimize scrap. Assist in equipment operation when required. * Support multiple projects simultaneously, ensuring timely completion and adherence to project goals. * Assists production to obtain line output requirements by providing technical and troubleshooting support to equipment and filters performance issues. Who you are: * Vocational degree in electronics, mechanics or graduate technical school. Associate degree in Engineering Technology preferably. * Four (4) to six (6) years in the manufacturing environment, preferably Medical Device or Pharmaceutical industries. * Good Troubleshooting Skills. Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role * Ability to travel - Not Applicable * Must have a valid driver's license with an acceptable driving record - Not Applicable * Ability to lift, move or carry equipment up to 25lb, any other physical requirements It would be a plus if you also possess previous experience in: * Excellent skills in problem solving and critical thinking techniques. * Develop solutions to routine technical problem of limited scope. Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Develop Validations Documents (Master Validation Plans/Reports, Test Method Validations, IQ, OQ and/or PQ, CSV related documents), Execute Validations in assigned Manufacturing Areas, and generate Reports. Document and execute IQ for label printing, Implement Manufacturing processes changes through CCB. Able to implement EU MDR requirements (such as PIC card implementation, Manufacturing/PFMEA, FAI, manuals and new pins implementation / FW Configuration changes and other required activity per EU MDR requirements). Develop and/or revise PPM or DOTM as required. Support during submission documents review as applicable. Responsibilities may include the following and other duties may be assigned. 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. 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 . 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 decisionmaking. 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. Requires a University Degree and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience. 1. Some experience in process validation , test method validation, CSV, handling of manufacturing process changes implementation (at packaging and/or manufacturing process flow). 2. Responsible, able to learn fast and adapts to continues changes in project schedule priorities as required. Able to coordinate and manage activities with multiple functions, able to apply problem solving techniques (critical thinking skills) to move roadblock without impact project schedule activities 3. Teamwork oriented, good communication skills, results oriented Education Required: Bachelor degree in engineering Years' Experience Required: Minimum of two years preferred with some experience, intermediate position. Willing to evaluate good potential candidates at entry level

For engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering & two (2) years of relevant experience within the Medical Devices or Pharmaceutical industry. Bilingual (Spanish & English). Shift: 1st and 2nd according to business needs. Experience in: Drawings interpretation. Manufacturing processes, products, and builds knowledge. Process Validation Lifecycle (IQ, TMV, OQ, PQ, PFMEA, Process Characterization). SOP Development. The Personality Part: 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? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Designs and plans layouts for activities such as machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling. Adapts machine or equipment design to factory and production conditions. Designs the 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. 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 for problems. Complies with company programs, procedures, and applicable quality system regulations and standards. Leverages technical expertise and knowledge of standard engineering approaches, design concepts, and specification requirements. 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?

Candidate will be working on the introduction of a new product that may include: Process Development and documentation Equipment validation SOP Development Line layout and infrastructure and development MES (Manufacturing Execution System) Special Build Documentation and Line Support *Other duties may be assigned. * Requirements Minimum 3 years of experience working in the regulated industry. Experience in SOP, Equipment IQ, OQ, PQ and Process Validation Life Cycle. Experience in DOE with Minitab (Preferred). Computer Software Validation, SOP Development, Change Control of Medical Devices and MES system Knowledge. Bachelor Degree in Engineering Completed. Bilingual. Administrative Shift, Willing to OT or Weekend when necessary.

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's degree in engineering Two (2) or (8) eight years of relevant experience Validations Change Management Statistical Analysis Availability for 1st shift Need availability during weekends 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.

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 Tech Engineering Job Description: The Specialist Tech Engineering 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. Ensure 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. Ensure the maintenance team training program, standard operating procedures and equipment/system operational standards are consistent throughout the team. Coordinate 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. Provide technical support for 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. Support the maintenance team when responding to high purity water systems and environmental monitoring alert/action notifications. Support the investigation on all alert/action notifications. Support 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. Assist plant engineering in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs. Evaluate sanitization and maintenance procedure s. Propose changes to the Department Manager. Propose modifications for process, utility and clean room systems to the Plant Engineering Group. EDUCATION: Masters degree & 3 years of Engineering experience OR Bachelors degree & 5 years of Engineering experience Must have above average skills in the following areas: * Leadership and teambuilding * Verbal communication * Written Communication/Technical Writing * Organization, Facilitation, dealing with and managing change.

Designs and plans layout for activities such as machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling. Adapts machine or equipment design to factory and production conditions. 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. 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. Complies with company programs, procedures and applicable quality system regulations and standards. Leverages technical expertise and knowledge of Company's standard engineering approaches, design concepts and specification requirements to best utilize equipment and manufacturing techniques. The candidate will be working on the introduction on a new product that may include: Process Development and documentation Equipment validation SOP Development Line layout and infrastructure and development MES (Manufacturing Execution System) Special Build Documentation and Line Support *Other duties may be assigned* Requirements Minimum 2 to 7 years of experience in Equipment IQ, OQ, PQ and/or process validation. Experience in Process Validation Lifecycle (Process Characterization, Operational Qualification to Performance qualification). Experience in DOE (Minitab)preferred. Knowledge in Investigation, Root cause analysis, Technical writing knowledge and Computer software validation. Ability to use statistical techniques to analyze data. Good documentation skills. Bilingual (Spanish & English). Bachelor Degree in Engineering Completed. Willing to work weekend and overtime when needed.

div class="col-12 col-md-8"div class="sc-ca SCKo fLrkuv"divp Responsibilities may include the following and other duties may be assigned. br/ Designs and plans layout for activities such as machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling. br/ br/ Adapts machine or equipment design to factory and production conditions. br/ Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. br/ br/ Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. br/ br/ May incorporate inspection and test requirements into the production plan. br/ 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. br/ Complies with company programs, procedures and applicable quality system regulations and standards. br/ br/ Leverages technical expertise and knowledge of Medtronic's standard engineering approaches, design concepts and specification requirements to best utilize equipment and manufacturing techniques. br/ br/ SPECIALIST CAREER STREAMbr/ br/ 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. br/ /p pDIFFERENTIATING FACTORS br/ br/ Autonomy: Established and productive individual contributor. br/ Works independently with general supervision on larger, moderately complex projects / assignments. br/ Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments. br/ Contributes to the completion of project milestones. br/ May have some involvement in cross functional assignments. br/ 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. br/ Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area. br/ br/ Communication and Influencebr/ br/ Communicates primarily and frequently with internal contacts. br/ External interactions are less complex or problem solving in nature. br/ Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making. br/ br/ Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream. br/ Required Knowledge and Experience: Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience. br/ Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A) and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience. /p/div/div/div

For Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's degree in Engineering & two (2) year of relevant experience within the Medical Devices or Pharmaceutical industry. Bilingual (Spanish & English). Skills: Proactive and task oriented. Shift: 1st and according to business needs. Experience in: Statistical Analysis Validations Change Management 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 take on this new challenge? 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, processing, and material handling. Designs the 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. 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. 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 comply with regulations. 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?