Industrial Engineer Jobs in Bayamn, PR

Country: United States of America Hybrid Looking for an exciting opportunity to learn more about the Aerospace industry while finishing your degree? Consider joining us here at Collins Aerospace, where we're working side-by-side with customers on exciting industry possibilities. With a comprehensive portfolio, extensive capabilities and broad expertise, we're crafting intelligent solutions to meet the demands of a rapidly evolving global market - all representing the best in innovation and technology for the industries we serve across commercial, business, space, and military and defense aviation. Partner with our dedicated people leaders to experience meaningful work aligned with your university curriculum, powerful exposure to leadership at all levels, tailored career growth and more! At Collins, we're redefining aerospace and we're just getting started. Come soar with us. This is a seven-month CO-OP beginning June 2025 (Summer/Fall Session) and the work will be completed at our Aguadilla, Puerto Rico site. Candidate must be residing in Puerto Rico at the time of starting employment. What You Will Do Gains knowledge of analyzes, research, designs, and develops materials and their related fabrication and application processes to develop and optimize materials for use in engineering design of and/or application in structures, systems and subsystems Performs material analyses that include, but are not limited to, systems and subsystems, and definition and requirement specifications Applies principles of chemistry, physics, and material behavior to develop metallic, non-metallic and composite material and processing specifications and processes. Add to the department and team by suggesting continuous improvements/optimization value adds. Observe processes, conduct research, and find ways to increase efficiency Qualifications You Must Have Requires a High School Diploma or equivalent and student must be pursuing a Bachelor's in Chemistry or Mechanical or advanced degree in an applicable discipline. U.S. citizenship is required, as only U.S. citizens are authorized to access the information under this program/contract Qualifications We Prefer Experience working Manufacturing process, materials, regulations is a plus. Pro-efficient in Siemens NX, Visio, Solidworks, Python is a plus. Experience interacting with Mechanical/Electrical Computer Aided Design Resources (MCAD and ECAD) is a value. Experience working with Teamcenter and/or SAP is a plus. Knowledge and Experience working Geometric Dimensioning and Tolerancing (GD&T). We value the knowledge in different analysis like fungus, fluids, structures, etc. Programming knowledge on Python, or MATLAB is a value Knowledge in metals, structures, polymers and composites and regulations is a big value. Learn More & Apply Now! Diversity drives innovation; inclusion drives success. We believe a multitude of approaches and ideas enable us to deliver the best results for our workforce, workplace, and customers. We are committed to fostering a culture where all employees can share their passions and ideas so we can tackle the toughest challenges in our industry and pave new paths to limitless possibility. *Please ensure the role type (defined below) is appropriate for your needs before applying to this role. Hybrid: Employees who are working in Hybrid roles will work regularly both onsite and offsite. Ratio of time working onsite will be determined in partnership with your leader. At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. Apply now and be part of the team that's redefining aerospace, every day. RTX is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class. Privacy Policy and Terms: Click on this link to read the Policy and Terms

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: * Industrial Engineer for Quality Engineering / Quality Manufacturing in Medical Devices Qualifications: * Bachelor's Degree in Science or Engineering, preferable in Industrial Engineering (BSIE) * Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. * Experience in direct process / manufacturing areas. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Knowledge in Statistics * Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. * Technical Writing skills and investigations processes. * Available to work extended hours, possibility of weekends and holidays.

Carolina, PR We are seeking a driven and experienced Chemical or Industrial Engineer with a strong background in the pharmaceutical industry and hands-on experience in laboratory projects. The ideal candidate will bring a blend of technical expertise, problem-solving skills, and executional focus to deliver successful outcomes in a dynamic laboratory environment. **Key Responsibilities:** * Lead and execute laboratory projects within a pharmaceutical environment, ensuring compliance with industry standards and best practices. * Collaborate with cross-functional teams to design, implement, and improve laboratory processes. * Conduct risk assessments, troubleshoot issues, and optimize laboratory performance and efficiency. * Maintain a high level of quality control and regulatory compliance in all project activities. **Qualifications:** * Bachelor's degree in Chemical Engineering or Industrial Engineering. * 5-6 years of relevant experience in the pharmaceutical sector, with a focus on laboratory projects. * Demonstrated knowledge and hands-on experience in executing lab projects and optimizing lab workflows. * Strong problem-solving skills and attention to detail. * Self-motivated, with a high level of drive and a proactive approach to project challenges. **Skills and Competencies:** * In-depth knowledge of pharmaceutical regulations and laboratory standards. * Excellent organizational and time-management skills. * Ability to work independently and as part of a collaborative team. * Effective communication skills for cross-functional coordination. We are an Equal Employment Opportunity Employer.

This is an engineering/ technical focused position acting as the primary point of contact for rack-level hardware as it moves from NPI to mass production and through to end of life. The successful applicant will be familiar with L6 through L11 manufacturing processes and have knowledge and experience in + hardware products including GPU, CPU, memory, storage, NICs, rack power systems, and network switches. + product firmware/software that includes Linux, baseboard controllers and storage firmware. + General test system software/systems that cover test control, diagnostics, and data collection. Provide engineering technical support to manufacturing teams for a specific product or group of products after transfer from design to high volume production. Interface with design, process, test and reliability engineering teams to solve problems. You will work in a fast-paced, demanding, and dynamic environment as part of a core team responsible for rapidly deploying leading edge technology to our customers. Translate specifications into clearly defined test requirements. Work closely with test engineering teams to validate test plans. Implement tests at various manufacturing sites. Detect, debug and troubleshoot issues (hardware, firmware, test) as they arise in the manufacturing process. Demonstrate comprehensive knowledge of BOM structure. Manage all ECO cut-in/phase-in processes for the smooth integration of product changes. Proactively identify and report on quality trends and issues. Be able to speak truth to power by taking a position and backing it up with facts and observations gleaned from experience. Leading contributor individually and as a team member, providing direction and mentoring to others. Work is non-routine and very complex, involving the application of advanced technical/business skills in area of specialization. 8 years relevant work experience. BS/BA preferred. Career Level - IC4 **Responsibilities** We are seeking a talented hardware systems integration engineer who can strengthen our capabilities and enable the transition of technology from a development environment to production manufacturing. The Oracle Product Engineer (PE) is a position within the Supply Chain Operations organization and is an important part of hardware manufacturing. PEs require a mix of hardware, firmware, software, and networking skills coupled with excellent technical management skills. The PE will lead the technical activities of Oracle hardware products from prototype builds through end of life. The PE is responsible for engaging with the development engineering team and transforming general specifications into specific requirements for manufacturing. Disclaimer: **Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.** **Range and benefit information provided in this posting are specific to the stated locations only** US: Hiring Range: from $87,000 to $178,200 per annum. May be eligible for bonus and equity. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. **About Us** As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's problems. True innovation starts with diverse perspectives and various abilities and backgrounds. When everyone's voice is heard, we're inspired to go beyond what's been done before. It's why we're committed to expanding our inclusive workforce that promotes diverse insights and perspectives. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity. Oracle careers open the door to global opportunities where work-life balance flourishes. We offer a highly competitive suite of employee benefits designed on the principles of parity and consistency. We put our people first with flexible medical, life insurance and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by calling ***************, option one. **Disclaimer:** Oracle is an Equal Employment Opportunity Employer*. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law. *** Which includes being a United States Affirmative Action Employer**

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.

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the LifeThe 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 This position will be for a specific project and will last until the completion of the related activities. 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. Required Knowledge and Experience: Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience. 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. Engineering Degree Required Nice to have Experience in equipment IQ Experience in OQ (Operational Qualification) and PQ (Performance Qualification) and/or process validation Process Validation Lifecylce ( from process characterization, operational qualification to performance qualification) Preferred experience in DOE (with minitab) Other skills: Computer and software validation CSV SOP Development Change control of Medical Devices Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 90,000+ passionate people. We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

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. JOB DESCRIPTION For the job assignment, the resource must have knowledge in Process Validation, Equipment IQ and Computer software validation. Knowledgeable on statistical techniques. In addition, the resource needs to be schedule-oriented to meet projects objectives and assignments without impacting deadlines. Also, it is very important for the resource to have good communication skills (written and oral) in English and Spanish to have successful and productive meetings within a cross functional team. DIFFERENTIATING FACTORS: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / cross functional assignments. Delivers and/or manages tasks assigned and works with other stakeholders to achieve desired results. Contacts others to share information, status, needs and issues to meet objectives, inform, gain input, and support decision making. What are the top 3 things you are looking for in a candidate's experience: + Process Validation, Equipment IQ and Computer software validation knowledge + Technical writing knowledge and Communication skills + Investigation and root cause analysis skills Education Required: Bachelor's degree required in Engineering Years' Experience Required: Minimum of 2 years of relevant experience 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. Powered by JazzHR

For Engineer services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering and three (3) years of exposure within the Pharmaceutical & Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Problem Solver, and Good Communication Skills. Shift: 1st Shift. Experience in: Quality, Root Cause Analysis, and Process Control. Validation Activities. Equipment, and Process Ownership. Excel, and Minitab. Technical Expertise ( Cost, Compliance, and Troubleshooting). 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, processing, machining, and material. Design arrangements of machines within plant facilities to ensure the most efficient and productive layout. Designs sequence of operations and specifies procedures for fabricating 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. 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. Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / cross functional assignments. 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?

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: + Collaborate and communicate with other functions to develop reports and give suggestions and ideas. + Ensure Process instructions are accurate, effective and support compliance with applicable regulations + Provide technical expertise to define and implement ideas strategies while optimizing cost, compliance, and effectiveness. + Ability to understand finance term and perform calculations of scrap, burden, etc. + Validation activities + Equipment and or process Ownership + Collaborate with operators and identify ideas, perform troubleshooting of defects and find root cause + Provides technical and sustaining engineering support in a manufacturing area; therefore, investigation and root cause analysis skills are required to solve problems or improve effectiveness of job area (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). + Knowledgeable on statistical techniques. In addition, the resource needs to be schedule oriented in order to meet projects objectives and assignments without impacting deadlines and it is really important for the resource to have good writing skills and communication skills in English and Spanish to have successful and productive meetings within a cross functional team. Qualifications: + Bachelor degree in Engineering + 3 to 5 years of relevant experience. + Quality / Process Control / Assurance of Medical Devices (*********************************************************************** + Extensive knowledge in Excel and Minitab. + Ability to understand finance terms and able to analyze finance data and information. + Equipment and Process performance metrics (ex. Yield, Downtime, OEE, etc.) + Change control assessment and requirements + Validation, Equipment IQ and Computer software validation knowledge + Availability for 1st shift 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. Powered by JazzHR

TransPerfect Is More Than Just a Job… Our greatest asset is our people, and nothing is more important to us than ensuring that everyone knows that. Each of our 100+ offices has its own individual identity, and each also has its own unique rewards. Who We Are: DataForce by TransPerfect is part of the TransPerfect family of companies, the world's largest provider of language and technology solutions for global business, with offices in more than 100 cities worldwide. DataForce offers high-quality data for Human-Machine Interaction to some of the most prestigious technology companies in the world. Our department focuses on gathering, enriching and processing data for Machine Learning in different AI domains. We are seeking an AI Production Engineer to join our team. AI Production Engineers are technically skilled individuals with a desire to troubleshoot and create solutions for technical production issues within DataForce data services projects including: script development for data manipulation and defining strategies for project executions. The successful candidate is a team player who thrives in a fast-paced work environment, working alongside our Solutions Engineers and Technology Project Managers to develop creative solutions for handling complicated workflows ad project executions. S/he is self-motivated to learn and become an expert in data services and our company's technology products. What You Will Be Doing: Role Responsibilities Provide daily, project-based technical support to production and sales departments Facilitate company-wide technology rollouts Assist project managers and external contributors in troubleshooting issues related to the project processes Implement automation for asset pre- and post-processing to enhance efficiency Develop scripts and/or macros in various programming languages to automate repetitive tasks performed by project managers, optimizing workflow Generate various file types as per project requirements, including re-coding and script writing as necessary, ensuring compliance with client specifications and data integrity Validate new features in our DataForce technology products Work closely with Software Product Managers to report and test fixes for bugs found by product users Perform other special projects or duties when required Automate asset pre- and post-processing tasks through scripting and macro writing in various programming languages Who We Are Looking For: Role Requirements - Knowledge, Skills and Abilities Business English language proficiency Scripting knowledge in Python, Java or VB High level of proficiency in Microsoft Office (Word, Excel, PowerPoint), Adobe software High level of proficiency in Windows platform Strong analytical, problem-solving and reasoning skills Ability to identify problems, propose solutions, and make effective decisions Exceptional communication skills with the ability to communicate important project updates both verbally and in writing Adaptability to new challenges and continuous learning High-level scripting and programming abilities Capability to visualize and present different types of data Role Requirements - Education and/or Experience Minimum Bachelor's degree or its equivalent Experience with REST APIs Experience meeting project deliverable dates on tight schedules and within a defined scope Experience with Mac and Windows platforms (no certifications needed) Experience with API/commands of storage cloud services (like AWS S3, Google Cloud, MS Azure, FTP, Box, etc.) Experience working in a multinational/multicultural virtual working environment Experience working in a cross-functional/matrix organization Preferred Role Requirements 1 - 2 years of experience in a similar role Proficiency in Linux systems Knowledge of JSON and XML are highly desired Experience creating schemas in JSON Knowledge of regular expressions within programming tasks Experience as Project Lead on a notable and/or innovative Industry specific development Where Your Career Is Going: At TransPerfect, there are a lot of growth opportunities. All departments offer career growth and development that can combine your skills, interest and experience. We encourage our employees to have a continuous dialogue with management about growth opportuinties throughout your tenure with the company. End your job search and find your career at TransPerfect #careers NOTjobs. Why TransPerfect: For more than 25 years, we have honed a culture where all kinds of ideas are shared and new ventures are not only welcomed, but also encouraged. In this fast-paced environment, employees are intellectually stimulated so they can grow alongside the organization. From Intern to President, we believe that every single employee should have a voice and contribute to the amazing services we offer our clients. We also offer a comprehensive benefits package including medical, dental, and vision insurance, 401k matching, membership to child-care providers, and other TransPerks. You even get your birthday off because let's face it, we're stoked that you were born. TransPerfect provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law For more information on the TransPerfect Family of Companies, please visit our website at *********************

**At Kelly** ** ** **Science, Engineering, Technology & Telecom (SETT), we're passionate about helping you find a job that works for you. How about this one?** We're seeking a **Process Development Associate Scientist** to work with one of out top biotechnology industry client at the East area of **PR.** With us, it's all about finding the job that's just right. **Administrative shift** **Responsibilities:** + To perform experiments, organize data and analyze results under minimal supervision. + Plans, conducts or monitors experiments, records and organizes data, analyses results. + Generates robust and reliable data and/or ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. + Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision. + Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data. + Effectively transfers experimental methods from literature to the lab and makes modifications as necessary. **Requirements:** + Master's degree AND 2 years of Scientific experience OR Bachelor's degree AND 4 years of Scientific experience + Fully bilingual (English/Spanish) **What happens next** Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry-even if this position doesn't work out, you're still in our network. That means all our recruiters will have access to your profile, expanding your opportunities even more. Helping you discover what's next in your career is what we're all about, so let's get to work. Apply to be a Process Development Associate Scientist today! **Kelly PR Offers!** + Exposure to a variety of career opportunities as a result of our expansive network of client companies + Career guides, information and tools to help you successfully position yourself throughout every stage of your career + Access to more than 3,000 online training courses through our Kelly Learning Center + Bi -weekly pay + Among other benefits! ** Apply Today! (************************************* **\#SETTPuertoRico** As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly ? As a worker today, it's up to you to take charge of your career and look for opportunities to learn, grow, and achieve your potential. Helping you find what's next is what we're all about. We know what's going on in the evolving world of work-just ask the 440,000 people we employ each year. Connecting with us means getting the support, guidance, and opportunities needed to take your career where you may have never imagined. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

At Trane Technologies (*********************************** and through our businesses including Trane (*********************** and Thermo King (**************************** , we create innovative climate solutions for buildings, homes, and transportation that challenge what's possible for a sustainable world. We're a team that dares to look at the world's challenges and see impactful possibilities. We believe in a better future when we uplift others and enable our people to thrive at work and at home. We boldly go. **What's in it for you:** Are you ready to make a difference? Heating, ventilating and cooling commercial buildings consumes a large portion of the world's energy today and, as the world economy grows, it will make an ever-increasing impact on the environment, human health and safety and the global economy. At Trane, we strive to produce the very best HVAC systems to help building owners provide optimum human comfort and safety while using less energy. In so doing, we partner with our customers to build a sustainable future! As a **Senior Engineer -** **Manufacturing Engineer** you will create Plans, directs, and coordinates manufacturing processes and/or projects in site facilities to optimize manufacturing of units and the required components. Collaborate closely with cross-functional teams to design, build, test, and deploy projects while adhering to best practices and maintaining high-quality standards. Lead plant Process Failure Mode and Effects Analysis (PFMEA) to evaluate and identify potential failures related to operational processes. **Thrive at work and at home:** + You will have the opportunity to participate in the **Company's private medical and life insurance program** prior to meeting eligibility requirements, following the policies, terms, and conditions set by the Company. The coverage and conditions for employees and their family members may vary based on the location. + You will also have access to the all-inclusive **Wellbeing Program** , which provides resources to support the emotional, legal, and financial well-being of you and your family. + The Company offers continuous **learning opportunities** through its continuing education programs. + Additionally, you will be granted one full day (8 hours) of paid time off per calendar year to volunteer with non-profit charitable organizations through the **Employee Volunteerism program.** + In cases of unforeseen personal hardship, the Trane Technologies **Helping Hands Fund** is available to provide support to employees facing financial challenges. **Where is the work: Arecibo, Puerto Rico** **What you will do:** + Owns all plant manufacturing instructions and analyzing routine process steps to reduce potential risks of quality defects during assembly processes. + Identify the cause of failure, testing and improve manufacturing processes to avoid the repetition of similar incidents. + Keep updated all documentation related to manufacturing process (JBS, Control Plans and Process Failure Mode and Effects Analysis) during new layout or lean events. + Coordinate and follow up all necessary activities to revise and approve all documentations protocols on time. + Work together with the Training Manager to ensure that employees affected during any plant changes will be trainee with the last revision updated related to the new initiative + Create detailed technical specifications, documentation, and standard operating procedures for manufacturing instructions and systems. + Perform system integration, configuration, testing, and deployment of quality control level improvements to improve warranty customers claims + Collaborate with cross-functional teams, including software developers, quality assurance, and operations teams, to reduce workmanship errors by integrate engineering solutions and methods to reduce the opportunities to create defects during the assembly processes. + Oversees the operations and maintenance of machinery/software in manufacturing. + Conducts / leads or participates in Process Mapping, FMEA and Problem-Solving initiatives to promote and ensure that Thermo King processes are continuously improving and operating in a waste elimination mode. + Implements processes in accordance to Lean / DFT principles and serves as facilitator for other employees including supervision, management and hourly to work within lean principles. + Lead assigned team in developing new strategies for optimal processes and addressing issues and concerns to improve quality issues. Identify areas necessary to change or improve technology on the current manufacturing processes. Prepares and implements detailed plans to ensure that new technology and product transfers and new product introductions are implemented within the required timeframe and cost. + Facilitates / leads implementation of processes required to achieve elements of the facility Strategic Plan and Scorecard objectives including elements such as Five S, ISO, Ergonomics program and Operational Excellence Plan. Create metrics or methods to measure project execution and adherence to budget and productivity. + Analyzes and plans work force utilization, space requirements, and workflow, and designs layout of equipment and workspace for maximum efficiency. + Define project plans and delivery commitments aligned with the operations plan using UTM and Windchill as the official business platforms for work. Confers with planning and design staff concerning product design and required tooling to ensure efficient production methods. + Confers with vendors to determine tools, product and services specifications and arranges for purchase of equipment, materials, or parts, and evaluates products according to specifications and quality standards. + Estimates production times, staffing requirements, and related costs to provide information for management decisions. Oversees development of new projects and their financial execution + Confers with management, engineering, and other staff regarding manufacturing capabilities, production schedules, and other considerations to facilitate production processes. + Manage the administration of the Capital Funding and Productivity Project Deck assisting projects leaders in the business case completion. Monitors, measures, and reports plant productivity projects. Coordinates implementation of Projects included in the facility annual Capital Plan and ensures timely implementation of it as per schedule. + Identifies needs and proposes elements to be included in the annual Capital Plan. + Trains other employees in Lean and other processes such as ISO procedures, PFMEA, Process Mapping and use of appropriate manufacturing methods. + Performs other duties and projects as assigned. + Maintain the work area clean and organized. + Support lean initiatives (5s, RIE's, SQDIP, MDI, 9 step). + Comply with company policies and procedures, including EHS and ISO requirements. **What you will bring:** + Bachelor's degree in Engineering (BSIS, BSME, BSEE) + Minimum 5 years' experience in engineering. + Proficient in Project Management + Ability to read, analyze, and interpret technical procedures. Problem solving and analytical skills + Excellent presentation and communications skills. + Teamwork and customer service oriented. + Good interpersonal skills. + Bilingual (English and Spanish) + Computer knowledge (MS office, etc.) + Knowledgeable of ISO + Knowledge of Lean / DFT theory and implementation + EIT and active member of CIAPR **Equal Employment Opportunity:** We offer competitive compensation and comprehensive benefits and programs. We are an equal opportunity employer; all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, pregnancy, age, marital status, disability, status as a protected veteran, or any legally protected status.

**Department:** Field - LL **Location:** Arecibo, 013 ***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: * **Manufacturing Engineer I** **Responsibilities:** * Develops, evaluates, and improves manufacturing methods. * Conducts / leads or participates in Process Mapping, FMEA, and Problem-Solving initiatives to promote and ensure that plant processes are continuously improving and operating in a waste elimination mode. * Implements processes in accordance to Lean / DFT principles and serves as facilitator for other employees including supervision, management and hourlies, to work within lean principles. * Prepares and implements detailed plans to ensure that new technology and product transfers and new product introductions are implemented within required timeframe and cost. * Facilitates / leads implementation of processes required to achieve elements of the facility Strategic Plan and Scorecard objectives including elements such as Five S, ISO, Ergonomics program and Operational Excellence Plan. * Analyzes and plans work force utilization, space requirements, and workflow, and designs layout of equipment and workspace for maximum efficiency. * Confers with planning and design staff concerning product design and required tooling to ensure efficient production methods. * Applies statistical methods to estimate future manufacturing requirements and potential. * Confers with vendors to determine tools, product and services specifications and arranges for purchase of equipment, materials, or parts, and evaluates products according to specifications and quality standards. * Estimates production times, staffing requirements, and related costs to provide information for management decisions. * Confers with management, engineering, and other staff regarding manufacturing capabilities, production schedules, and other considerations to facilitate production processes. * Identifies needs and proposes elements to be included in the annual Capital Plan. * Coordinates implementation of projects included in the facility annual Capital Plan and ensures timely implementation of it as per schedule. * Trains other employees in Lean and other processes such as ISO procedures, PFMEA, Process Mapping and use of appropriate manufacturing methods. * Performs other duties and projects as assigned. * Maintain the work area clean and organized. * Support lean initiatives (5s, RIE's, SQDIP, MDI, 9 step). * Comply with company policies and procedures, including EHS and ISO requirements. **Qualifications** * **Bachelor's degree in Engineering (BSIE, BSME, BSEE)** * **Minimum 3 years' experience in manufacturing industry.** * Ability to read, analyze, and interpret technical procedures. * Problem solving skills. * Excellent presentation and communications skills (English/ Spanish). * Team work oriented. * Computer knowledge (MS Office, project planning, etc.) * Knowledgeable of ISO. * Knowledge of Lean / DFT theory and implementation. * **EIT and active member of CIAPR, preferred.** * Bilingual (English/Spanish).

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide. Currently, one of our clients in the East Region is looking to hire a Manufacturing Engineer I. * Bachelor degree in Engineering, with at least 1 - 3 of relevant experience. * Previous experience in the medical device industry. * Validation/ Qualification Knowledge. * Technical writing knowledge * Fully bilingual - Spanish & English This position does not offer visa sponsorship. Applicants must be fluent in both Spanish and English

* Posted 2 months ago * $85000 per year USD / Year * Posted 2 months ago * $85000 per year USD / Year **Job title:** 2025 Graduate - Cyber Engineer - Capabilities Development **Company:** **Job description**: **Description** If so, we want you to join our team at APL's Capabilities Development Group (QCC)! We work as a multi-disciplinary team of systems, cybersecurity, and software engineers, who enable mission resilience by developing novel tools. We leverage the latest threat intelligence along with cutting-edge cybersecurity trends, techniques and technologies to achieve an operational advantage for our sponsors. As a member of our team you will… * Be mentored by top experts to learn the art and science of developing cyber capabilities * Work with sponsors and end users in defense or intelligence organizations to understand their operational needs and identify requirements * Build mission-aligned capabilities * Develop novel approaches to solving cybersecurity challenges in operational environments * Explore promising new research areas and seek ways to apply ideas to today's problems * Share approaches and methods with others team members, APL management, and government decision makers Qualifications You meet our minimum qualifications for the job if you… * Are graduating with a Bachelor's or Master's degree in Computer Science, Computer Engineering, Mathematics or a Cybersecurity-related field * Have experience in one or more programming languages * Have experience developing concepts, systems, or analytics, with an understanding of systems engineering or operational planning * Have strong analytical and problem-solving skills, excellent interpersonal and communication skills, good organizational skills, and the ability to work in teams * Are able to obtain an Interim Secret level security clearance by your start date and can ultimately obtain a Secret Clearance. If selected, you will be subjected to a government security investigation, and you should meet the eligibility requirements for access to classified information up to the Secret level. Eligibility requirements include US citizenship. You'll go above and beyond our minimum requirements if you… * Have experience developing software using Java/Kotlin, Python, C#, JavaScript/TypeScript, C/C++, or equivalent * Can apply software development skills to different domains and subject matters (e.g. biotechnology, cybersecurity, etc.) * Have knowledge of geospatial information systems, deep learning, and computer vision * Have experience in DevSecOps, and/or network security and systems integration * Have experience with Department of Defense and/or Intelligence Community cyber operations/mission forces * Have experience in conducting research, development, and testing of cyber capabilities * Have experience in the development of related documents that define processes, solutions, requirements, and specifications for government agencies (military, federal departments/agencies, state, and local) and public organizations to collaborate and achieve greater cybersecurity * Hold an active Secret or Top Secret security clearance and can ultimately obtain TS/SCI level clearance. At APL, we celebrate our differences and encourage creativity and bold, new ideas. Our employees enjoy generous benefits, including a robust education assistance program, unparalleled retirement contributions, and a healthy work/life balance. APL's campus is located in the Baltimore-Washington metro area. Learn more about our career opportunities at *********************** APL is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, creed, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, physical or mental disability, genetic information, veteran status, occupation, marital or familial status, political opinion, personal appearance, or any other characteristic protected by applicable law. APL is committed to promoting an innovative environment that embraces diversity, encourages creativity, and supports inclusion of new ideas. In doing so, we are committed to providing reasonable accommodation to individuals of all abilities, including those with disabilities. If you require a reasonable accommodation to participate in any part of the hiring process, please contact . Only by ensuring that everyone's voice is heard are we empowered to be bold, do great things, and make the world a better place. The referenced pay range is based on JHU APL's good faith belief at the time of posting. Actual compensation may vary based on factors such as geographic location, work experience, market conditions, education/training and skill level with consideration for internal parity. For part-time salaried employees, annual salary will be prorated based on the number of hours worked. APL may offer bonuses or other forms of compensation per internal policy and/or contractual designation. Additional compensation may be provided in the form of a sign-on bonus, relocation benefits, locality allowance or discretionary payments for exceptional performance. APL provides eligible staff with a comprehensive benefits package including retirement plans, paid time off, medical, dental, vision, life insurance, short-term disability, long-term disability, flexible spending accounts, part-time study and training and development. Applications are accepted on a rolling basis. Minimum Rate $85,000 Annually Maximum Rate $150,000 Annually **Expected salary**: $85000 per year **Location**: Ponce, PR **Job posting date**: Thu, 03 Oct 2024 22:54:05 GMT ** To apply for the job** ** To apply for the job** **Contact us**

Brief description Plan, write, implement, and review the Computer Systems Validation documentation. Make sure that all computer-based systems are operating as intended (with documents to prove it) and meet regulatory requirements. Determines systems software requirements. Work across a variety of software lifecycle activities as determined by project needs. Generate and execute qualification protocols and reports. Organize and maintain project status progress detail. Work with process owners to address process changes to existing work instructions and/or standard operating procedures. What are the top 3 things you are looking for in a candidates experience: Process and Computerized Systems Validation Experience in FDA regulated industries Excellent verbal and written communication skills (English and Spanish). Education Required: Bachelor's degree in Engineering or related field. Years' Experience Required: 1-3 years JOB DESCRIPTION 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. TECHNICAL SPECIALIST CAREER STREAM: 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. DIFFERENTIATING FACTORS 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. Leadership and Talent Management: N / A - job at this level is focused on self-development. Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education. Requires a Bachelor's Degree in Engineering , 1-3 years of experience required. *Weil Group is proud to be an Equal Employment Opportunity Employer.*

This position is responsible for exercises on validations of new and existing products, including equipment as needed. Assists in activities related to product design, development, qualification and production. Exhibits knowledge of operations in the assigned work area. Projects a positive example for others to follow in the workplace. Freedom to act, under close supervision, in semi-structured assignments that generally require adherence to defined procedures and specific, detailed instructions with limited originality. Solves problems of moderate scope and complexity. Demonstrates Viant Values. Essential Job Functions: * Develops protocols based on external and internal requirements. * Executes protocols and perform reports. Follows up for approval and closure up to mfg implementation. * Applies basic technical skills, standard methodologies, or processes to perform routine activities. * Assists Manufacturing staff in monitoring daily validations and/or product manufacturing as assinged. * Performs testing per engineering protocols, recording equipment used, and results achieved in verification test reports. * Collaborates with manufacturing and engineering to develop molding or assembly manufacturing instructions. * Creates manufacturing aids and procedures as assigned. * Collaborates with management and engineering to brainstorm on process issues and provide suggestions for process improvements. * Provides technical assistance to production by answering questions when needed. * Interfaces with production teams to improve manufacturing processes. * Performs research for new product components, tools, and equipment, as required. * Assists Quality Assurance with incident/problem investigations and reviews. * Assists with and participates in technical engineering projects * Participates effectively in cross-organization projects and team tasks. * Identifies areas for process improvement and makes recommendations to management. * Uses standard operating procedures to solve routine problems. * Able to participate in and support training * Able to execute engineering study with provided instructions/protocol * Other duties as assigned or requested Knowledge and Education: High school diploma or equivalent. 2-year associate degree in engineering technology or related technical field preferred. 1 to 3 years of experience in a related field. Job Experience: * Working knowledge of quality system requirements. * Advanced knowledge - MS office. Basic - Minitab Experience working in a production facility or cleanroom a plus. * Knowledge and experience with manufacturing related equipment. * Thorough understanding of product manufacturing and validation requirements. Skills and Competencies: * Detail-oriented and able to exercise sound judgment in problem-solving. * Ability to develop technical solutions to address problems while minimizing cost and impact on the schedule. * Reads and comprehends simple specifications, plans, and shop drawings. * Ability to communicate problems to effect corrective action. * Maintains a positive attitude with respect to changes in processes and methods. * Maintains high standards of quality. * Possesses written and oral communications skills sufficient to speak clearly and distinctly, write reports, and read work-related instructions, rules, and procedures. * Ability to add, subtract, multiply, and divide into all units of measure, using whole numbers, common fractions, and decimals * Ability to handle multiple tasks simultaneously. * Exchange complex technical information and ideas concisely and logically. * Accountable for own contribution. Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn. Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Other details * Pay Type Hourly Apply Now * Vega Baja, 00693, Puerto Rico

Job Title: Manufacturing Engineer Department: Engineering Reports To: Sr. Engineering Manager Be part of something altogether life-changing! 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. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Manufacturing Engineer 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 engineering services to production, test and packaging machinery. Also, assist in the design and implementation plans for cost reduction, quality improvements, process support and verification. This position is part of the Manufacturing Operations located in Cytiva Fajardo Puerto Rico and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: * Assist in the design, development, and optimization of manufacturing processes to improve efficiency and product quality. * Support multiple projects simultaneously, ensuring timely completion and adherence to project goals. * Collaborate with cross-functional teams to resolve technical issues and improve manufacturing operations. * Ensure compliance with OSHA, FDA, ISO, and GMP regulations relative to manufacturing operations. * Prepare and maintain documentation related to manufacturing processes, including standard operating procedures (SOPs) and work instructions. Who you are: * Bachelor's Degree in Industrial, Mechanical or Electrical Engineering. * Cero (0) to two (2) years in the manufacturing environment, preferably Medical Device or Pharmaceutical industries. * Good oral and written communication skills (English and Spanish). * Computer Literate (Microsoft Office, Project Management, Statistics) * Knowledge in Statistical Process Control (SPC). Travel, Motor Vehicle Record & Physical/Environment Requirements: * Ability to travel - N/A * Must have a valid driver's license with an acceptable driving record - N/A * 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. 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.

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success. At Integer, our values are embedded in everything we do. Customer We focus on our customers' success Innovation We create better solutions Collaboration We create success together Inclusion We always interact with others respectfully Candor We are open and honest with one another Integrity We do the right things and do things right Who are we? Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEM's (original equipment manufacturers) to enhance the lives of patients worldwide and a provider of high-end niche batteries for specialized applications in the energy, military, and environmental markets. We are guided by our six Values, including focus on Customers, Innovation, Collaboration, Inclusion, Candor, and Integrity. Working at Integer means you are part of a team passionately pursuing excellence in all that we do and always reaching for the next great achievement. What you'll do in this role: The primary purpose of this position is to perform work which involves general engineering methods and tools; but you may also utilize more advanced technologies and engineering concepts while you are developing in your role as an engineer in the medical device industry. In this role, you will ensure that Integer's internal and external customer expectations are met or exceeded with occasional direction, instruction and guidance from more experienced engineers and managers in your organization. You adhere to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. You will generally work independently with occasional guidance from supervisors or mentors to evaluate, select and apply standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications to existing specifications, procedures, and work instructions. You will review procedures and plans prior to implementation as well as evaluate existing products, processes and materials for failure analysis and potential improvements. You will participate in projects that require you to investigate, develop, document and implement new product and process technologies of moderate complexity and scope. While often you may be responding to situations presented to you by others, you will also be able to demonstrate proactive insight into technical challenges and mitigates potential issues or incorporates improvements. You will plan, schedule and execute the engineering work in a part of a major project; or you may lead a smaller scope project. You will perform work on technical projects where you will follow Integer's standard quality management and production system methodologies to investigate opportunities for product and process improvements. You will apply standard data analysis practices and techniques to establish root cause for product and process failures or to support the justification for improvements to products and processes. You will be required to observe products and processes to recognize discrepancies in results and follow operations throughout a series of detailed steps or processes to establish root cause of the discrepancies. You are expected to collaborate with others in the exchange of information, ask questions and regularly check for understanding in support of your development as an engineer. You embed Quality within the Engineering discipline - “I own Quality.” You are a standard bearer for Quality in everything we do at Integer, by assuring adherence to our Quality Management System (QMS), facilitating and/or contributing to corrective and preventive actions, and contributing to the successful attainment of our quality KPI's and journey to 5 Sigma. You may perform other duties as needed and as directed by your line of supervision. Provide support of Integer's Manufacturing Excellence and Market Focused Innovation Strategies You champion the development of and deployment of the systems and tools to drive innovation and continuous improvement. You embrace the Manufacturing Excellence culture based on the Integer Production System and its five focus areas: Strategy Alignment through Site Hoshin Plans, the regular cadence of Sales, Inventory, and Operations' Planning (SiOP) meetings, and regular updates to the value stream maps. Leadership of Sustained Change by ensuring production monitoring & improvement activities and deployment of Leader Standard Work. Standardization through workplace organization & visual controls (5S), Manufacturing Standard Work, and robust training & certification programs. Associate Engagement promoted through the adoption of standardized problem solving. methodologies, behavior-based safety programs, and improvement idea and suggestion systems. Systems & Process Optimization through adoption of principles of built in quality, optimized scheduling & material system designs, work cell design, and total productive maintenance. How you will be measured: The specific measures listed below may be subject to change and are not intended to be an all-inclusive list Safety is our highest priority; you will be an active supporter of the Integer Environmental Health & Safety programs. Quality - Achievement of site Quality KPI's You will have defined Goals and Objectives specifying key projects and expected milestones to achieve. Given your capabilities and experience, you will identify ways to shorten the project durations and make changes to current processes and procedures that enable greater efficiencies. Innovation and ideation are critical aspects of your role and you will be expected to generate continuous improvement suggestions and support the implementation of them. What sets you apart: You earned, as a minimum, a bachelor's degree in an engineering or related technical field; and have at least three years of relevant experience. While you will have occasional support and guidance from more experienced engineers, supervisors or managers, you will demonstrate the ability to work independently as well as collaboratively with other associates and cross functional teams. You demonstrate a solid technical aptitude with the ability to be an effective contributor to a team or produce results of a technical nature as an individual. You have a functional understanding of the Integer Quality Management Systems and are able to complete required Quality System documentation tasks with little or no direction from others. You demonstrate competency in both written and oral communications. You maintain a calm demeanor that transcends the high energy, constantly changing production environment. You possess a positive, can-do attitude with an underlying belief that failure is not an option. U.S. Applicants: EOE/AA Disability/Veteran