Laboratory assistant jobs in Arecibo, PR

**LAB-Field Science Intern** **Job Description:** Corteva Agriscience is seeking a Field Research Intern to participate in a 3-month internship designed to give broad-based exposure to the day-to-day activities of a breeding program in the Salinas, Puerto Rico, research center. You will participate in all aspects of the research center's activities. **Responsibilities:** + Work in field activities, agronomy activities, seed production, harvesting, analyzing samples, and data collection of traits important to plant breeding and other research programs. + Perform laboratory activities, such as tissue culture, media preparation, and seed screening. + Collect high-quality data on specific traits of economic importance. + Assist Corteva employees located in Salinas, Puerto Rico. + Manage your own research presentation with the expectation of a verbal final report. + Gain excellent experience that can be applied to full-time positions in the industry or in preparation for additional graduate-level training in the plant sciences. **Qualifications:** + Priority will be given to students who are at least current sophomores at an accredited university. + Interns can be undergraduate or graduate students. + Knowledge and experience in Agronomy, Plant Physiology, Plant Pathology, Genetics, Biology, Biotechnology, or related fields. + Preference will be given to students with a minimum GPA of 3.0. + Must be enrolled at an accredited university at the time of the internship. + Must be able to relocate to the geography of the R&D center for the duration of the internship. + Creative thinking and the ability to work independently and in a team environment. **Benefits:** + Gain practical experience in a dynamic and innovative environment. + Work with a diverse and talented team of professionals. + Enjoy the rich culture and beautiful landscapes of Puerto Rico. + Opportunity to contribute to cutting-edge projects and research. + Develop professional skills and build a network in the agricultural research field. Corteva Agriscience is an equal opportunity employer. We are committed to boldly embracing the power of inclusion, diversity, and equity to enrich the lives of our employees and strengthen the performance of our company, while advancing equity in agriculture. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. Discrimination, harassment and retaliation are inconsistent with our values and will not be tolerated. If you require a reasonable accommodation to search or apply for a position, please visit:Accessibility Page for Contact Information For US Applicants: See the 'Equal Employment Opportunity is the Law' poster. To all recruitment agencies: Corteva does not accept unsolicited third party resumes and is not responsible for any fees related to unsolicited resumes.

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 V&EG's Bio Pharma Fair is the exclusive online job fair organized by Validation & Engineering Group, entirely dedicated to professionals in the medical, biomedical, healthcare, pharmaceutical and biotechnological sectors with at least one of these experiences: * Commissioning, qualification, validation * CSV life cycle experience * Automation * QA/QC * Project Management * Facilities/Maintenance Engineering * EHS Qualifications V&EG's Bio Pharma Fair is addressed to young professionals with a biomedical, biotechnological, pharmaceutical, medical and healthcare, medical and biomedical engineering or Science background coming from Puerto Rico and United States . Minimum of three (3) years of experience in the mentioned sectors. Additional Information Positions available for Puerto Rico and The United States. Only candidates that meet the minimum requirements will be considered. Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer.

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: Process Development Technician Purpose Statement: Supports development of capable processes and ensures efficient and effective transfer of products into production. Contributes with Process Development engineers, scientists, and/or teams in the development and analysis of processes and equipment. This position requires high independence and knowledge on automated manufacturing equipment. Key Responsibilities: Executes functional deliverables associated with Process Development and Technology Development projects. Assesses process capabilities, innovates, and implements process improvements on complex processes. Work with engineers and internal/external vendors to maintain/fix/calibrate/qualify manufacturing equipment. Support testing or manufacture of prototypes/materials with minimal engineering guidance. Organize and document testing data and prepare reports/documentation to communicate results. Applies technical knowledge to support, design, and the development of processes, procedures, tooling and automation. Typically makes important technical contributions as part of an extended team. Work cooperatively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain and Marketing to ensure project success. Identifies problems and proposes solutions to technical challenges. Independently solves basic issues within functional area. Supports, researches, and evaluates new technologies within functional area. Remains knowledgeable of available technologies within functional area. May identify new applications for established technologies. Familiarity with a variety of technologies and equipment used in the industry to carry out manufacturing processes, such as Laser Welding, Stringing, Staking, Heat Bonding, Injection Molding, Vision Systems, general experience with automated equipment (PLC/Servos/Pneumatics/ Sensors), etc. Ability to collaborate with other engineers, scientists, and production personnel to achieve manufacturing process development objectives and solve problems effectively. Train others on new product processes and procedures. Required Qualifications: Associate's degree or equivalent combination of education/work experience 1-2 years of related experience Proven record of working closely and successfully with manufacturing and process development engineers Basic understanding of medical device documentation requirements Great attitude and strong desire to learn new skills Preferred Qualifications: Manufacturing background Medical Device industry experience Good technical writing skills Ability to read electrical prints and schematics

LAB-Field Science Intern Job Description: Corteva Agriscience is seeking a Field Research Intern to participate in a 3-month internship designed to give broad-based exposure to the day-to-day activities of a breeding program in the Salinas, Puerto Rico, research center. You will participate in all aspects of the research center's activities. Responsibilities: Work in field activities, agronomy activities, seed production, harvesting, analyzing samples, and data collection of traits important to plant breeding and other research programs. Perform laboratory activities, such as tissue culture, media preparation, and seed screening. Collect high-quality data on specific traits of economic importance. Assist Corteva employees located in Salinas, Puerto Rico. Manage your own research presentation with the expectation of a verbal final report. Gain excellent experience that can be applied to full-time positions in the industry or in preparation for additional graduate-level training in the plant sciences. Qualifications: Priority will be given to students who are at least current sophomores at an accredited university. Interns can be undergraduate or graduate students. Knowledge and experience in Agronomy, Plant Physiology, Plant Pathology, Genetics, Biology, Biotechnology, or related fields. Preference will be given to students with a minimum GPA of 3.0. Must be enrolled at an accredited university at the time of the internship. Must be able to relocate to the geography of the R&D center for the duration of the internship. Creative thinking and the ability to work independently and in a team environment. Benefits: Gain practical experience in a dynamic and innovative environment. Work with a diverse and talented team of professionals. Enjoy the rich culture and beautiful landscapes of Puerto Rico. Opportunity to contribute to cutting-edge projects and research. Develop professional skills and build a network in the agricultural research field.

At **Kelly Science, Engineering, Technology & Telecom (SETT** **)** , we're passionate about helping you find a job that works for you. How about this one? We're seeking an **Laboratory Technician** to work with one of our top global biopharmaceutical clients in the **Barceloneta PR** area. With us, it's all about finding the job that's just right Perform laboratory analytical tests on raw materials and finished products following the established parameters (company policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory workflow. Follow Good Manufacturing Practices), safety rules, and Good Laboratory Practices (GLP). **Responsibilities:** * Responsible for performing laboratory analytical tests on the raw materials and finished products following the established parameters (Customer policies, FDA, cGMP) and applicable regulations without impact to the manufacturing cycle or the laboratory workflow. * Document The results of the test and analysis performed accurately. * Perform preventive maintenance and standardize the laboratory equipment. * Participate in the implementation of special projects and test method transfers. * Assure that all samples are collected, tested, and authorized as per the schedule and following applicable procedures. **Qualifications** * Associate or Bachelor degree in Science required, with a major in **Chemistry** * A minimum of two years of experience in the pharmaceutical industry or equivalent in an analytical laboratory.. * Availability to work the third shift, ALL Shifts weekends, and holidays according to business needs. 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.

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 The CSV Specialist - Laboratory to lead and execute computer systems validation activities associated with the decommissioning of laboratory equipment, instruments, and systems. This role ensures compliance with regulatory requirements and internal standards during retirement, archival, and documentation of assets and data within a GMP-regulated environment. Responsibilities Decommissioning Execution Generate and manage Change Controls related to laboratory decommissioning. Prepare and execute CSV Decommissioning Packages for equipment, instruments, and computerized systems. Coordinate final calibration and cleaning documentation for decommissioned assets. Manage CMMS retirement/inactivation documentation and update/deactivate assets in Maximo (equipment, instruments, computer systems). Review and archive preventive maintenance job plans, calibration records, and spare parts inventories. Collect and archive equipment/instrumentation manuals and technical documentation. Prepare and submit Finance Decommissioning documentation. Data Integrity & System Controls Perform system periodic assessment verification, audit trail reviews, and user access evaluations. Coordinate backup and archival of electronic data in compliance with data integrity standards. Review and update or retire SOPs, forms, and validation documents. Evaluate open records including Data Integrity Assessments, investigations, CAPAs, Infinity records, change controls, and change actions. Verify and remove hardware components as part of system retirement. Compliance & Documentation Coordinate closure of EHS-related change actions. Update and archive technical drawings associated with decommissioned assets. Compile and deliver turnover packages for final QA review. Ensure proper closure of change controls and documentation handoff. Qualifications Bachelor's degree in Science or related field. Minimum 3 years of experience in CSV, QA, or laboratory systems within a regulated environment. Strong understanding of GMP, data integrity principles, and system lifecycle management. Experience with CMMS systems (e.g., Maximo), calibration documentation, and electronic data archival. Fluent in English and Spanish (spoken and written). Additional Information All your information will be kept confidential according to EEO guidelines.