Quality control inspector jobs in Caguas, PR

In a world of possibilities, pursue one with endless opportunities. Imagine Next! At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what's possible. **Job Description:** Parsons is looking for an amazingly talented **QC Inspector** to join our team! **This job is not remote but located in Puerto Rico!** **What You'll Be Doing:** + Performing inspections and surveillances based on training and project requirements. + Interacting with project team members and management to support quality initiatives. + Implementing and documenting inspection, examination, and testing procedures. + Planning and setting up evaluations and tests, including equipment preparation. + Assessing and reporting the validity of inspection and testing results. + Reviewing training programs for inspection personnel and evaluating their effectiveness. + Conducting and documenting inspections of subcontractor work. + Overseeing subcontractor inspections and auditing quality records. + Performing First-Article and In-Process Inspections, including source inspections as needed. + Ensuring compliance with Health, Safety, and Environmental (HSE) requirements. + Supporting the development and implementation of a Quality Control Inspectors certification program. + Communicating inspection results clearly and concisely. + Understanding and applying contract and subcontractor requirements. **What Required Skills You'll Bring:** + Experience in quality control inspection within a project or functional environment. + Knowledge of inspection, examination, and testing procedures. + Ability to document and communicate inspection results effectively. + Familiarity with subcontractor oversight and quality record auditing. + Understanding of HSE compliance related to inspection activities. **What Desired Skills You'll Bring:** + Experience with First-Article and In-Process Inspections. + Prior involvement in inspector certification programs. + Ability to evaluate training programs for inspection personnel. + Strong cross-functional collaboration and communication skills. **Security Clearance Requirement:** None This position is part of our Corporate team. For over 80 years, Parsons Corporation, has shaped the future of the defense, intelligence, and critical infrastructure markets. Our employees work in a close-knit team environment to find new, innovative ways to deliver smart solutions that are used and valued by customers around the world. By combining unique technologies with deep domain expertise across cybersecurity, missile defense, space, connected infrastructure, transportation, smart cities, and more, we're providing tomorrow's solutions today. Salary Range: $29.95 - $52.40 We value our employees and want our employees to take care of their overall wellbeing, which is why we offer best-in-class benefits such as medical, dental, vision, paid time off, Employee Stock Ownership Plan (ESOP), 401(k), life insurance, flexible work schedules, and holidays to fit your busy lifestyle! This position will be posted for a minimum of 3 days and will continue to be posted for an average of 30 days until a qualified applicant is selected or the position has been cancelled. Parsons is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status. We truly invest and care about our employee's wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest-APPLY TODAY! Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to *********************************************** . About Us Parsons is a digitally enabled solutions provider focused on the defense, security, and infrastructure markets. With nearly 75 years of experience, Parsons is uniquely qualified to deliver cyber/converged security, technology-based intellectual property, and other innovative services to federal, regional, and local government agencies, as well as to private industrial customers worldwide. Parsons is an equal opportunity, drug-free employer committed to diversity in the workplace. Minority/Female/Disabled/Protected Veteran/LGBTQ+. For more about Parsons, visit parsons.com and follow us on Facebook, Twitter, LinkedIn, and YouTube.

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: * The C&Q Lead Inspection Lines oversees and coordinates all Commissioning and Qualification activities for visual inspection systems used in sterile drug product operations, including both manual and automated inspection technologies. This role ensures equipment, control systems, and supporting utilities are qualified in compliance with regulatory standards (FDA, EMA, Annex 1) and ready for GMP use at site start-up. Key Responsibilities Project Leadership & Planning * Lead end-to-end C&Q scope for automated and semi-automated inspection lines, including: * Vision systems for vial, syringe, and cartridge inspection * Conveyance and reject mechanisms * Integration with MES / SCADA / Serialization systems * Container closure integrity test (CCIT) systems * Develop and maintain the Inspection C&Q Master Plan, aligning with the overall site Validation Master Plan. * Coordinate activities across Engineering, QA Validation, Automation, and Manufacturing Operations. * Establish and monitor C&Q milestones for inspection systems to meet project timelines and regulatory readiness. Commissioning & Qualification Execution * Oversee preparation, review, and approval of URS, FAT/SAT, IOQ protocols, and summary reports. * Ensure equipment and vision systems meet GAMP 5, 21 CFR Part 11, and data integrity standards. * Manage vendor FAT/SAT and site integration testing; ensure punch-list closure. * Supervise execution of C&Q protocols in accordance with ASTM E2500 and ISPE Baseline guides. * Maintain traceability between design requirements and executed testing. Technical Oversight * Serve as Subject Matter Expert (SME) for vision inspection and serialization systems. * Review and approve: * Vision and camera configuration documentation * Control system design (PLC, HMI, SCADA, MES interfaces) * CCIT and reject logic configuration * Troubleshoot technical issues and support automation integration with packaging and filling operations. Compliance & Documentation * Ensure C&Q documentation aligns with GMP, GDP, and corporate validation standards. * Support Quality Assurance during audits and regulatory inspections. * Ensure all deviations, CAPAs, and change controls related to C&Q are properly documented and closed. * Maintain digital records in the validation platform (e.g., Kneat or ValGenesis). Collaboration & Leadership * Work closely with Process Engineering, Packaging, and QA Validation to ensure seamless qualification and handover. * Mentor junior C&Q engineers assigned to inspection or packaging areas. * Participate in daily coordination and readiness meetings to track progress and resolve issues proactively. Qualifications Education * Bachelors degree in Engineering (Mechanical, Electrical, Automation, or related field). Experience * 8+ years of experience in Commissioning & Qualification for pharmaceutical or biotech facilities. * 3+ years specific to automated visual inspection or packaging systems. * Experience in aseptic operations and data integrity requirements (GAMP 5, 21 CFR Part 11). * Strong understanding of Annex 1 and ISPE GPG: Visual Inspection of Parenterals. Technical Competencies * Knowledge of camera systems, vision software, reject mechanisms, serialization, and MES connectivity. * Proficient in using electronic validation tools such as Kneat or ValGenesis. * Skilled in reviewing FAT/SAT documents, IOQ protocols, and risk assessments. Preferred * Previous experience qualifying inspection lines from Syntegon, Antares, Brevetti, or Seidenader. * Knowledge of CCIT methods (vacuum decay, laser headspace, or HVLD). * Experience in greenfield or expansion projects for aseptic/sterile operations.

Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. FUNCTIONS: Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot for assays as necessary Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, Lead audit teams May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, Independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. REQUIREMENTS: EDUCATION High school/GED + 10 years of directly related experience. Associates + 8 years of directly related experience Bachelors + 4 years of directly related experience Masters + 2 years of directly related experience Preferable Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management and Quality processes. Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering PREFERRED QUALIFICATIONS Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses. Strong knowledge in Microsoft Excel as a Tool for Data Analysis. Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable). Strong knowledge and experience with quality process management. Basic Knowledge on equipment preventive maintenance and troubleshooting. Agile on prioritization of critical tasks. Ability to develop inspection or qualification protocols in a short timeframe period. Strong negotiation skills COMPETENCIES/ SKILLS: Understand, support and demonstrate the AMGEN values. Excellent communication skills, facilitation and presentation skills. Excellent technical writing skills. Strong computer operation skills including work processing, presentation, database and spreadsheet application skills. Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion. Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities. Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution. Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility. Knowledge of pharmaceutical processes. Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products. Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products. Extensive knowledge and application of GMPs/CFRs. Ability to evaluate compliance issues. Skill in evaluating and documenting according to Company and various guidelines. Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. Advanced scientific data analysis and interpretation skills. Advanced skills in solving complex problems. Advanced data trending and evaluation. Strong skill in working independently and to effectively interact with various levels. Ability to interact with regulatory agencies both orally and in writing. Initiate, coordinate and lead cross functional teams. Excellent skill in leading, motivating, influencing, and negotiating. WORK METHODOLOGY: Full on site job in Juncos, PR Full time job Expected project duration: 7 months for the first contract Administrative shift from Monday to Friday Professional services contract with potential extension based on performance and budget Expected hiring date: January 2026

**At Kelly** ** ** **Science, we're passionate about helping you find a job that works for you. How about this one?** We're seeking **Specialist QC** to work for one of our top **Biotechnology Industry client at Juncos, PR** . **Salary: $38.00 p/h** **Requirements:** + PHD or MS degree and 2 years of directly related experience OR BS degree and 4 years of directly related experience OR AD degree and 8 years of directly related experience. Preferable scientific background in Science or Engineering Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering + Scientific Data Analysis + Strong Technical Writing (English and Spanish) mainly focuses + Strong knowledge in Microsoft Excel as a Tool for Data Analysis + Knowledge in Computer System and Method Validation (Experience preferable) + Strong knowledge and experience with quality process management + Ability to develop inspection or qualification protocols in a short timeframe period. The **Specialist QC** will be responsible for: + Providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. + Resolve technical issues and troubleshoot for assays as necessary + Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. + Manage existing and/or develop and implement new programs, processes and methodologies. + Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. + Approve lab investigations, Lead audit teams **Kelly** ** ** **Science 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** + **Biweekly pay ( W2)** + **Sick, Vacations & Holidays paid*** + **Christmas bonus*** + * Must comply with minimum established requirements to qualify. **APPLY TODAY!** 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 is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. 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For Quality Control in the Technical Resources area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience in a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: Administrative, and according to business needs. Experience in: Scientific Data Analysis and Technical Writing. Computer System and Method Validation. Quality process management and equipment preventive maintenance and troubleshooting. Develop inspection or qualification protocols in a short timeframe period. The Personality Part: Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work. Picture as well an environment of healthy competition, teamwork, being ethical and of using the scientific method in all ways possible. If you like how this sounds, then this might be the job for you. Bring it on! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Responsible for providing technical guidance. Provide reports, data analysis and ensure flow of communication between technical groups. Resolve technical issues and troubleshoot for assays as necessary. Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, Lead audit teams May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, Independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. 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?

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

Job Description The position focuses on complex technical issues, multi-department and/or multi-site initiatives, and coordination with external resources when needed. Responsibilities include advanced troubleshooting, method support, documentation oversight, compliance, and cross-functional leadership. Key Responsibilities Provide technical guidance and ensure effective communication between scientific and technical groups. Analyze data, generate reports, and follow up on technical issues to ensure timely resolution. Troubleshoot assay and testing challenges as necessary. Ensure laboratory compliance by implementing and maintaining GMP, GLP, and safety procedures. Manage, develop, and implement programs, processes, and methodologies that support laboratory operations. Develop, revise, and audit complex controlled documents with multi-department or multi-site impact. Approve laboratory investigations and lead internal audit teams. Serve as a subject matter expert (SME) and support the development of technical training. Perform routine work within area of responsibility as required. Represent the department on cross-functional teams and independently manage multi-site action items. Interact with regulatory agencies as needed, including preparing written responses. Support issue resolution with external partners and resources. Lead or assist with special projects assigned by leadership. May supervise or mentor employees to meet technical and operational requirements. Core Competencies & Skills Excellent communication, facilitation, and presentation skills. Strong technical writing abilities. Advanced computer proficiency (word processing, presentations, databases, spreadsheets). Strong project management and organizational abilities; able to manage complex tasks independently. Ability to manage multiple priorities and shift focus as needed. Extensive experience in quality analytical labs, validation, manufacturing, QA, process development, or distribution. Deep understanding of assay development, validation, and laboratory testing. Knowledge of pharmaceutical and biological product testing processes. Strong understanding of U.S. regulations, GMPs, CFRs, and basic international regulatory practices. Ability to evaluate and document compliance-related issues. Skilled in interpreting scientific data and solving complex technical problems. Proficient in trending, analyzing, and evaluating data. Strong ability to work independently and collaborate across organizational levels. Capable of interacting with regulatory agencies both orally and in writing. Ability to lead, motivate, influence, negotiate, and drive cross-functional teams. Requirements Required Education & Experience Doctorate, OR Master's degree + 2 years of directly related experience, OR Bachelor's degree + 4 years of directly related experience, OR Associate degree + 8 years of directly related experience, OR High school diploma/GED + 10 years of directly related experience. Preferred Qualifications Strong scientific data analysis expertise. Advanced technical writing skills in English and Spanish. High proficiency with Microsoft Excel for data analysis. Excellent communication and project management skills. Knowledge of Computer System Validation (CSV) and Method Validation. Experience with quality process management. Basic understanding of equipment preventive maintenance and troubleshooting. Ability to prioritize critical tasks with agility. Experience developing inspection or qualification protocols on short timelines. Strong negotiation and influencing skills. Benefits Administrative Shift 6-months contract

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: Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot for assays as necessary. Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, lead audit teams. May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, may supervise employees as necessary to meet technical requirements. Qualifications: Bachelor's degree in preferably with Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management and Quality processes. +4 years of directly related experience. (Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering). Knowledge of pharmaceutical processes. Extensive knowledge and application of GMPs/CFRs. Knowledge in Scientific Data Analysis. Strong Technical Writing (English and Spanish) mainly focuses. Strong knowledge in Microsoft Excel as a Tool for Data Analysis. Good Communication skills Project Management skills Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experience with quality process management. Basic Knowledge on equipment preventive maintenance and troubleshooting. Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. Agile on prioritization of critical tasks. Ability to develop inspection or qualification protocols in a short timeframe period. Strong negotiation skills Administrative 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.

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

Description/Responsibilities: The Quality Assurance Inspector l is responsible to provide general quality assurance support in the areas of inspection manufacturing and assembly. Performs mechanical, electrical and visual inspection of manufactured product and/or processes per documentation (drawings, specifications and procedures) and industry standards. Freedom to act, under supervision, in semi-structured assignments that requires adherence to defined procedures and/or specific, detailed instructions with limited originality, Solves problems of limited scope and com complexity. Demonstrates Viant values. Position Authority: This position has the authority to accept or reject materials, subassemblies, assemblies and processes that affect the quality and safety of products. This includes the authority to stop production if necessary to assure that nonconforming products are not released for distribution. Essential Functions: Follows all Good Manufacturing Practices and SOP's as defined by Viant's policies, practices and procedures to ensure that FDA regulations, GMP, ISO13485, and Viant quality standards are met. Checks material disposition and identification in order to meet GMP regulations. Inspect and document in-bound raw materials for conformance. Collects samples at scheduled intervals from each machine. Perform in process dimensional and visual inspection to assure compliance with customer specification giving appropriate disposition according to Viant's procedures. Responsible for documentation of (in-process) sampling plan, disposition and inspection results Perform basic ERP transactions. Work on validation projects as needed. Manage retains of production and validation projects. Audits assigned areas. Verifies that the process inspections and areas in charge are in conformance with Viant's procedures. Perform SPC/SQC as a preventive tool using suitable software to assure and maintain compliance with customer requirements and Viant's procedures. Maintain documentation filling update. Accurately record information consistent with the department format. Support the calibration of gaging and equipment Train operators in products quality requirements. Report any defect found to Manufacturing and/or Quality Supervisor. Provide feedback to employees on defects found for ensure quality of our product. Place non-conforming product on hold and create non-conforming records Conduct quality inspection on rework product Follow all departmental procedures with respect to routine daily assignments. All workstation areas will be maintained in a neat and orderly manner. Ensures efficient material flow, storage of inspected parts, and accurate inventory transactions are maintained with the ERP system. Skills: Proficient in knowledge of a variety of testing equipment (pin gauges, snap gauges, micrometer, caliper, etc.). Ability to interpret component specifications, drawings and quality procedures. Proficient technical writing skills and use of documentation programs (e.g., Office Windows, Excel, Access, PowerPoint, etc.) Performs basic arithmetic calculations: add, multiply, subtract, and divide in all units of measure using whole numbers, common fractions and decimals. Requires the ability to adjust a microscope e lens to bring an object into sharp focus. Physical Requirements: Light physical activity performing non-strenuous, day-to-day activities of a primarily productive nature. Moderate lifting (20 lbs.), carrying (10 lbs.), bending, and prolonged sitting. Manual dexterity sufficient to reach/handle items, work with fingers, and perceive attributes of objects and material. Intensive handwork. Requires the ability to identify and distinguish colors and shapes. Well-lighted, air-conditioned, indoor production setting with adequate ventilation. Equipment Used: Mechanical and electrical teste equipment, calipers, gauges, and standard office computer. Utilize tools, gauges and other inspection equipment to obtain product specification data. Qualifications: Associates degree or equivalent in work experience. Bachelor Degree in Natural Sciences preferable. English understanding, quality oriented and statistical knowledge. 3 months to 1 year of recent experience in medical device industry, with experience of different medical products with as molding operator.

**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. **Security Clearance:** None/Not Required Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace technology. Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market. We are looking for a detail-oriented Quality Inspector to ensure our products meet stringent design and contractual requirements. The role involves conducting thorough inspections of parts, assemblies, raw materials, tooling, and instruments at various stages of the manufacturing process. Using basic inspection methods and tools, you will validate compliance with drawings, specifications, and contract requirements. Join our team and play a critical role in maintaining our high standards of quality and excellence. **What You Will Do** + Possess the ability to inspect parts, understand all assembly aspects of electronic components and sub assemblies (such as PCBs) by following specification on drawings, bills of material, wiring diagrams, process sheet drawings and/or verbal instructions. + Use various measuring devices including torque screwdrivers, calipers or custom gauges. + Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action. + Protect product during handling and storage in the performance of work. + Assist with distribution and control of process documentation and quality records. + Comply with and reinforce the requirements of Standard Operating Procedures, ISO 9000, Quality System Regulations and other customer standards. + Performs job duties with little or no supervision or assistance. + Follow established documentation for product manufacturing. + Document all work performed on inspection reports, work orders and receiving/shipping documents. + Maintain the segregation of conforming non-conforming product. + Perform in-process inspection of all parts and/or assemblies in accordance with the requirements stated in the work order or as otherwise stated on drawings or work instructions. + Perform other duties as assigned. **Qualifications You Must Have** + Typically requires HS diploma (or equivalent, e.g. G.E.D. in the US) or vocational/technical education in related discipline with a minimum of 1 year of relevant experience + Demonstrated professional or educational experience communicating in English (verbal and written). + U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract **What We Offer** Some of our competitive benefits package includes: + Medical, dental, and vision insurance + Three weeks of vacation for newly hired employees + Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option + Participation in the Employee Scholar Program (ESP) + Life insurance and disability coverage + Employee Assistance Plan, including up to 8 free counseling sessions + And more! **Learn More & Apply Now!** The next chapter of our future as an aerospace company is here, and we are excited about what this means for our employees and customers! Get onboard the Collins Aerospace Operations team and play a part in managing our innovative products from inception to delivery. The Operations team continues to grow and aims to strengthen the connection of Manufacturing Operations, Supply Chain and Environment, Health & Safety (EH&S) across Collins Aerospace. In this dynamic environment, you will have the opportunity to network across our businesses and functions, all while improving the productivity, quality and efficiency of our operations worldwide. **WE ARE REDEFINING AEROSPACE.** * Please consider the following role type definitions as you apply for this role. + **Onsite:** Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. 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 Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act._ **Privacy Policy and Terms:** Click on this link (******************************************************** to read the Policy and Terms Raytheon Technologies 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.

Job Description 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: The C&Q Lead - Inspection Lines oversees and coordinates all Commissioning and Qualification activities for visual inspection systems used in sterile drug product operations, including both manual and automated inspection technologies. This role ensures equipment, control systems, and supporting utilities are qualified in compliance with regulatory standards (FDA, EMA, Annex 1) and ready for GMP use at site start-up. Key Responsibilities Project Leadership & Planning Lead end-to-end C&Q scope for automated and semi-automated inspection lines, including: Vision systems for vial, syringe, and cartridge inspection Conveyance and reject mechanisms Integration with MES / SCADA / Serialization systems Container closure integrity test (CCIT) systems Develop and maintain the Inspection C&Q Master Plan, aligning with the overall site Validation Master Plan. Coordinate activities across Engineering, QA Validation, Automation, and Manufacturing Operations. Establish and monitor C&Q milestones for inspection systems to meet project timelines and regulatory readiness. Commissioning & Qualification Execution Oversee preparation, review, and approval of URS, FAT/SAT, IOQ protocols, and summary reports. Ensure equipment and vision systems meet GAMP 5, 21 CFR Part 11, and data integrity standards. Manage vendor FAT/SAT and site integration testing; ensure punch-list closure. Supervise execution of C&Q protocols in accordance with ASTM E2500 and ISPE Baseline guides. Maintain traceability between design requirements and executed testing. Technical Oversight Serve as Subject Matter Expert (SME) for vision inspection and serialization systems. Review and approve: Vision and camera configuration documentation Control system design (PLC, HMI, SCADA, MES interfaces) CCIT and reject logic configuration Troubleshoot technical issues and support automation integration with packaging and filling operations. Compliance & Documentation Ensure C&Q documentation aligns with GMP, GDP, and corporate validation standards. Support Quality Assurance during audits and regulatory inspections. Ensure all deviations, CAPAs, and change controls related to C&Q are properly documented and closed. Maintain digital records in the validation platform (e.g., Kneat or ValGenesis). Collaboration & Leadership Work closely with Process Engineering, Packaging, and QA Validation to ensure seamless qualification and handover. Mentor junior C&Q engineers assigned to inspection or packaging areas. Participate in daily coordination and readiness meetings to track progress and resolve issues proactively. QualificationsEducation Bachelor's degree in Engineering (Mechanical, Electrical, Automation, or related field). Experience 8+ years of experience in Commissioning & Qualification for pharmaceutical or biotech facilities. 3+ years specific to automated visual inspection or packaging systems. Experience in aseptic operations and data integrity requirements (GAMP 5, 21 CFR Part 11). Strong understanding of Annex 1 and ISPE GPG: Visual Inspection of Parenterals. Technical Competencies Knowledge of camera systems, vision software, reject mechanisms, serialization, and MES connectivity. Proficient in using electronic validation tools such as Kneat or ValGenesis. Skilled in reviewing FAT/SAT documents, IOQ protocols, and risk assessments. Preferred Previous experience qualifying inspection lines from Syntegon, Antares, Brevetti, or Seidenader. Knowledge of CCIT methods (vacuum decay, laser headspace, or HVLD). Experience in greenfield or expansion projects for aseptic/sterile operations.

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. JOB SUMMARY Verify the quality of the products against the customer specifications. Develops and maintains all Lot History Records. Controls and issues all related Quality documentation. Maintains documents and records within GMP regulation guidelines. KEY RESPONSIBILITIES Performs and documents inspection as the result of product quality plan, including cosmetic, dimensional and functional inspection. Determines product / process acceptability based on sampling results. Identifies and segregate of non-conforming product to avoid mixes and errors. Responsible to control and release Product in Quality Hold. Responsible for the reconciliation of labels and release of product in quality hold once the report these issues. Responsible for the verbal and written report to the supervisor for each defect found in a product. Performs startup and process as required following Jabil documented procedures. Authorizes to reject lots, accept conforming materials and to identify or segregate nonconforming materials and fill reports. Verify the correct identification for the resin used, mold preventive maintenance status, operator inspection documentation and cleaning conditions in the assembly operation. Verify the correctness and neatness of documents and forms being to record inspections performed using Good Documentation Practices. Responsible to communicate with the next shift Technician, regarding any important issue that occurred in the station, with the product, quality, etc. Maintains retains samples and logs. Observes all company rules, regulations, and procedures such as safety and housekeeping (6's). Expedites records and reports to customers. Maintains all product Lot History Records Maintains working area clean, organized, and safe. Verify the accuracy of all records and reports. Assures compliance to good documentation practices on history file (GMP). Conduct audit of material at staging areas, process and / or parameters attributes if it is necessary or requested. Complies with Good Manufacturing Practices. Notifies shift supervisor of non-conforming conditions for corrective action Complies with all Manufacturing Procedures and Instruction applicable. Follow rules that apply to clean room. Responsible for the verbal and written report to the supervisor for each defect found in a product. Responsible that his/her payroll clock punches are registered before entering or leaving, following, and accepting company payroll policies Responsible of performing as per Job Description's SOP's and work instructions. Attends all requested training or company meetings. May participate in internal committees as Safety, improvement events, etc. as required. Performs other responsibilities as assigned. JOB SPECIFICATIONS Education and Experience: Associate Degree in Science related field preferred or minimum two year of College School or two years' experience in related Quality area. One-year experience will be validated as one year of college education, if incumbent have basic knowledge of computer use and statistics. Knowledge and skills: Able to communicate clearly with others Able to follow directions or make requirements clear Works with minimum supervision Keeps concentration on task on hand Accepts changes in priority with good attitude Basic Mathematic knowledge Basic Statistical knowledge Legible handwriting Computer skills (Power point, Excel, Word, Etc.) GMP and GDP knowledge Interpersonal relations Must read and understand English Team Player Abilities to manage and implement change Knowledge of office equipment Knowledge of dimensional equipment (Calipers, Indicator, OGP, CMM, Micrometer, etc.) Basic knowledge of drawing reading or interpretation BE AWARE OF FRAUD: When applying for a job at Jabil you will be contacted via correspondence through our official job portal with a jabil.com e-mail address; direct phone call from a member of the Jabil team; or direct e-mail with a jabil.com e-mail address. Jabil does not request payments for interviews or at any other point during the hiring process. Jabil will not ask for your personal identifying information such as a social security number, birth certificate, financial institution, driver's license number or passport information over the phone or via e-mail. If you believe you are a victim of identity theft, contact the Federal Bureau of Investigations internet crime hotline (************* the Federal Trade Commission identity theft hotline (********************** and/or your local police department. Any scam job listings should be reported to whatever website it was posted in. Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law. Accessibility Accommodation If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to Always_******************** or calling ************ with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.#whereyoubelong#AWorldofPossibilities#EarlyCareer

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

**At Kelly** ** ** **Science, we're passionate about helping you find a job that works for you. How about this one?** We're seeking **QA Laboratory Technician ** to work with one of out top medical device and pharmaceutical industry clients at **San Lorenzo, PR.** **Salary: 1st shift $14 hr** **2nd shift 14.30 hr** **3rd shift 14.50 hr** **Requirements:** + Bachelor Degree In Natural Science and 6 months to 1 + year of experience at Quality related position at regulated industry + Experience with GMP's , SOP's and Documentation (GDP's) + Knowledge of QSR's and ISO Standards. + Computer system knowledge required + Intermediate English communication skills. Spanish is required. + Available any shift, 3rd shift required The **QA Lab Technician** will be responsible to perform inspection according to the specifications following QSR's and written procedures. Notify any non-conformance related to the QA inspection and test methodologies.Inspects tests and/or evaluates the precision and accuracy of products, production equipment, and/or testing equipment. Performs all Finished Goods inspections / testing according to the specifications. **For this position Kelly** ** ** **Science 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 + Weekly pay + **Sick, Vacations &** **H** **olidays paid *** + **Christmas bonus*** + **_*_** **_Must comply with minimum established requirements to qualify._** ** Apply to be a QA Lab Technician today! ** **Recruiter: Lilly Abouomar** **\#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 Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace technology. Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market. We are looking for a detail-oriented Quality Inspector to ensure our products meet stringent design and contractual requirements. The role involves conducting thorough inspections of parts, assemblies, raw materials, tooling, and instruments at various stages of the manufacturing process. Using basic inspection methods and tools, you will validate compliance with drawings, specifications, and contract requirements. Join our team and play a critical role in maintaining our high standards of quality and excellence. What You Will Do * Possess the ability to inspect parts, understand all assembly aspects of electronic components and sub assemblies (such as PCBs) by following specification on drawings, bills of material, wiring diagrams, process sheet drawings and/or verbal instructions. * Use various measuring devices including torque screwdrivers, calipers or custom gauges. * Control non-conforming product in accordance with documented procedures and verify timely corrective and preventative action. * Protect product during handling and storage in the performance of work. * Assist with distribution and control of process documentation and quality records. * Comply with and reinforce the requirements of Standard Operating Procedures, ISO 9000, Quality System Regulations and other customer standards. * Performs job duties with little or no supervision or assistance. * Follow established documentation for product manufacturing. * Document all work performed on inspection reports, work orders and receiving/shipping documents. * Maintain the segregation of conforming non-conforming product. * Perform in-process inspection of all parts and/or assemblies in accordance with the requirements stated in the work order or as otherwise stated on drawings or work instructions. * Perform other duties as assigned. Qualifications You Must Have * Typically requires HS diploma (or equivalent, e.g. G.E.D. in the US) or vocational/technical education in related discipline with a minimum of 1 year of relevant experience * Demonstrated professional or educational experience communicating in English (verbal and written). * U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract What We Offer Some of our competitive benefits package includes: * Medical, dental, and vision insurance * Three weeks of vacation for newly hired employees * Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option * Participation in the Employee Scholar Program (ESP) * Life insurance and disability coverage * Employee Assistance Plan, including up to 8 free counseling sessions * And more! Learn More & Apply Now! The next chapter of our future as an aerospace company is here, and we are excited about what this means for our employees and customers! Get onboard the Collins Aerospace Operations team and play a part in managing our innovative products from inception to delivery. The Operations team continues to grow and aims to strengthen the connection of Manufacturing Operations, Supply Chain and Environment, Health & Safety (EH&S) across Collins Aerospace. In this dynamic environment, you will have the opportunity to network across our businesses and functions, all while improving the productivity, quality and efficiency of our operations worldwide. WE ARE REDEFINING AEROSPACE. * Please consider the following role type definitions as you apply for this role. * Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. 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 Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services. Job Description Document Control / Data Management Will verify Commissioning, Qualification and Validation Documents as needed. Will Generate data management metrics. Will work with Excel and pivot tables. Administrative and Non Standard Shift. Qualifications Bachelor Degree in Science or Engineering. Not less than 5 years of experience in Pharmaceutical Industry QA experience as CQV reviewer preferred. Excel / pivot tables advanced knowledge is a must. Highly organized. Additional Information More Positions available for Puerto Rico and USA. Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace technology. Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market. We are looking for a detail-oriented Quality Inspector to ensure our products meet stringent design and contractual requirements. The role involves conducting thorough inspections of parts, assemblies, raw materials, tooling, and instruments at various stages of the manufacturing process. Using basic inspection methods and tools, you will validate compliance with drawings, specifications, and contract requirements. Join our team and play a critical role in maintaining our high standards of quality and excellence. What You Will Do * Inspects a variety of electronic units using measuring/inspection instruments (e.g. micrometers, gauges and calipers) with proper inspection techniques. * Reads, interprets and utilizes Quality policies, procedures, blueprints and other documentation. * In-process inspection & 1st article approval of manufactured, assembled, and tested hardware and components. * Operates computer systems to perform inspection tasks (e.g. Via Search, JD Edwards, One World, Engineering Information System, labor charging). * Verifies all work order documentation for accuracy and completeness. * Administers visual and physical inspections of units and subassemblies. * Completes unit shakedowns (when required) to check for foreign objects, rattles and loose internal hardware. * Responsible for First Article Inspections and completes related documentation. * Performs administrative tasks associated with files management. Qualifications You Must Have * Typically requires HS diploma (or equivalent, e.g. G.E.D. in the US) or vocational/technical education in related discipline with a minimum of 1 year of relevant experience * Demonstrated professional or educational experience communicating in English (verbal and written). * U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract What We Offer Some of our competitive benefits package includes: * Medical, dental, and vision insurance * Three weeks of vacation for newly hired employees * Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option * Participation in the Employee Scholar Program (ESP) * Life insurance and disability coverage * Employee Assistance Plan, including up to 8 free counseling sessions * And more! Learn More & Apply Now! The next chapter of our future as an aerospace company is here, and we are excited about what this means for our employees and customers! Get onboard the Collins Aerospace Operations team and play a part in managing our innovative products from inception to delivery. The Operations team continues to grow and aims to strengthen the connection of Manufacturing Operations, Supply Chain and Environment, Health & Safety (EH&S) across Collins Aerospace. In this dynamic environment, you will have the opportunity to network across our businesses and functions, all while improving the productivity, quality and efficiency of our operations worldwide. WE ARE REDEFINING AEROSPACE. * Please consider the following role type definitions as you apply for this role. * Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. 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 Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

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