Quality control technician jobs in Bayamn, PR - 33 jobs

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

Job Description QA/QC Site Inspector- Construction Reports to: Site Manager 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

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

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

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.

Join our team as an Agronomy IPM Controlled Environments (greenhouses) Intern and take part in a 3-month internship designed to provide broad exposure to the day-to-day operations of a breeding program at our research center in Salinas, Puerto Rico. Gain hands-on experience on crop production in controlled environments, focused on better practices for a sustainable strategy using Integrated Pest Management principles. The intern will help scout for pests and diseases, collect data, and support biological control and cultural management strategies to maintain optimal plant health. Work alongside experienced agronomists and agricultural professionals and contribute to the successful implementation of technology and solutions to support agricultural challenges. Responsibilities: * Conduct weekly scouting and identification of pests, beneficial insects, and disease symptoms. * Record pest population data and report findings to the IPM Supervisor. * Assist in releasing beneficial insects and applying approved biocontrol products. * Assist in the process of agrochemicals spraying for structure sanitation, pest and weed control. * Installation, management and data collection of different insect traps used in the greenhouses. * Assist in the process of manual removal and mechanical control of pests. * Support trials for evaluating pest management products and strategies. * Participate in team meetings and contribute to continuous improvement initiatives. * Support irrigation and plant nutrition activities. * Assist in the process of pot filling and plants transplant. * Participate in manual pollination and harvest activities. * Support greenhouse sanitation activities before, during and after greenhouse use. * Prepare and present your findings, culminating in a verbal final report. Qualifications: * Current sophomore or higher pursuing a bachelor's degree in Agronomy, Entomology, Horticulture, Phytopathology or Crop Protection at an accredited university. * Minimum GPA of 3.0. * Basic understanding of crop production principles, entomology and phytopathology. * Must be enrolled at an accredited university during the internship period. * Willing to relocate to Salinas, Puerto Rico. * Ability to work in greenhouse environments and in varied weather conditions. * Basic computer skills and mobile devices management. * Strong attention to detail and data accuracy. * Interest in sustainable and biological pest control. * Good communication and teamwork skills. * Creative, team-oriented, and passionate about sustainable agriculture. Benefits: * Gain hands-on- experience in IPM principles and biological control in greenhouse systems. * Opportunity to contribute to ongoing pest management innovations. * Exposure to commercial crop management and data collections methods. * Work with a diverse and collaborative team of professionals. * Enjoy the rich culture and beautiful landscapes of Puerto Rico during your internship.

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: Quality Lead is responsible for overseeing all aspects of product quality within the injection molding operations. Develop, implement, and maintain quality systems (ISO 9001, or customer-specific standards). Establish and monitor quality control plans, inspection procedures, and testing protocols. Lead root cause analysis and corrective/preventive actions (CAPA) for nonconformities. Ensures compliance with customer specifications, industry standards, and regulatory requirements while driving continuous improvement initiatives. Establish and inspect quality control processes and audits. Perform inspection of parts and interpret engineering drawings/blueprints. Ensure inspections and documentation comply with GMP and quality standards. Support quality activities during the assigned shift and provide guidance as needed. Qualifications: Bachelor's degree in quality management, or a related field. (Preferred but no required) 3 to 5 years of experience in quality assurance within injection molding or plastics manufacturing. Strong knowledge of ISO standards, Validations, PPAP, FMEA, SPC, and GD&T. Experience with metrology equipment and statistical analysis tools Proficient in the use of measurement tools and verification of their calibration. Strong documentation skills. Leadership abilities. Quality-driven and detail-oriented mindset. Proven knowledge in the use of micrometers, calipers, optical comparators, and basic measuring equipment. Bilingual (English/Spanish) preferred. 1st shift but candidate must be available to work 2nd or 3rd shift if needed. 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.

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

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us Program dates: June 1, 2026 - August 7, 2026. The hourly compensation for this assignment is $15/hr. Please note that the final individual compensation and any applicable benefits will be determined by your employer of record (and not BMS). Factors influencing this decision may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location of the job. Compensation details are subject to change. This is a temporary, time-bound position intended for the duration of the internship or co-op program. Employment in this role does not imply or guarantee ongoing or permanent employment with BMS. Position Summary Selected employee will be responsible for QC Laboratories Equipment calibration and maintenance Program Optimization. This role requires collaboration with multiple functional areas. The incumbent must comply with all Security Guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices required by the Job Function. Key Responsibilities 1) List all QC equipment. 2) Evaluate current equipment Job Plans. 3) Challenge current Job Plans against vendor recommendations and historical performance. 4) Propose and implement identified changes for the improvement of the Equipment calibration and maintenance Program. Qualifications & Experience * Applicants must attend an accredited university in Puerto Rico or reside in Puerto Rico. * Seniors graduating in Spring or Summer 2026 are eligible to apply only if they will be continuing their education for the following semester (Fall 2026). * Minimum 2 years of subgraduate studies in Science disciplines such as Biology, Chemistry, Microbiology or Engineering. * Good knowledge of Personal Computers and computer applications such as Microsoft Office. * Excellent communications skills (Oral and Written) in English and Spanish. * Strong interpersonal and teamwork skills; ability to develop and maintain effective professional relations with colleagues at all levels across the organization; ability to integrate actions toward objectives. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit ************************************* Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: * Health Coverage: Medical, pharmacy, dental, and vision care. * Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). * Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work-life benefits include: Paid Time Off * US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) * Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. * Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **************************. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: ********************************************* Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at ***************************************** Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ********************. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1598115 :

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

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

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

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

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

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

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

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

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

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: QC Chemist Scientist The position will support the organization with initial compliance and ongoing preparation, testing, monitoring and reviewing of conformance to established quality control process and standards for manufacturing and production. Perform evaluation of internal controls, and review of documentation related to compliance with external and internal safety, quality, and regulatory standards. Conducts moderately complex chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods. Perform analyses in a chemistry environment within defined procedures and practices. Prepare documentation of the testing/analysis and obtained results. Document, calculate, verify, approves and/or report results of the analysis in accordance with prescribed lab procedures and systems. Support and/or coordinate sample analysis and maintain a schedule plan to ensure goals and objectives are met within the prescribed time frame. Qualifications: Bachelor's degree in Chemistry, Biology, Life Sciences or other related field. Minimum of 5 years position related experience. Excellent interpersonal oral and written communication skills. Proficiency in the English language. Available to work on different shifts. Licensed preferred. Experience with quality system, stability specific laboratory systems and laboratory chromatographic data acquisition systems. Experience with Microsoft Word and Excel.