Research scientist jobs in San Juan, PR

Company: Popular Workplace Type: Hybrid Customer Researcher Job Title: Customer Researcher General Description This role will leverage human-centered design approaches to perform customer research and bring insights to the design teams to deliver solutions that exceed our customers' needs and desires. As a Customer Researcher you will apply divergent human-centered design techniques that support cross-functional teams to develop innovative design concepts for products and services. You will guide and support teams to conduct qualitative research and bring the findings to life by turning them into insights, journey maps and personas. Essential Duties and Responsibilities You will support the design and execution of ethnographic research and user testing by: * Identifying customer profiles relevant to the work * Identifying the methods for gathering qualitative feedback * Coordinating and preparing for interviews/shadows/ immersions * Building rapport/trust with customers * Take notes in a way that helps synthesis * Listen to understand / Pick up on what is not being said * Support synthesis of interviews/ shadows with their own insights * Perform customer interviews and observations * Collaborate with Marketing on the coordination and alignment of quantitative research You will conduct quantitative customer research by: * Supporting the creation and execution of customer surveys in collaboration with Marketing * Interpreting customer data from different sources and understanding customer pain points You will apply divergent human-centered design techniques that support cross-functional teams to develop innovative design concepts for products and services, as demonstrated by: * Being the "voice of the customer" and ensure the customer perspective is a guiding principle throughout the progress of ideation, as a participant or lead * Support design and facilitation of hands-on work sessions (including but not limited to strategic alignment, problem framing, solution ideation, synthesis, prototyping, and testing) * Provide teams with exemplars (e.g., benchmarking, mystery shopping) * Contribute to articulating features in customer language, along with set of assumptions being tested * Defining test plans (Who to interview, How many, interview guides, note capture templates) * Plan and conduct interviews for additional concept feedback * Synthesize feedback from interviews and articulate impact on design * Bring to life the user experience associated with priority concepts by creating suitable scenario/storyline * Support the translation of insights to concepts and features in collaboration with business, technology, and other relevant stakeholders. * Provide creative direction for sketches and prototyping Minimum Requirements * Bachelor's Degree in either Design, Business, Engineering or related field. * Relevant experience in coaching teams on human-centered design/design thinking topics, conducting qualitative research, synthesis and facilitating workshops in a corporate setting. * Fluent in Spanish and English Important: The candidate must provide evidence of academic preparation or courses related to the job posting, if necessary. Our hybrid work model benefit applies to certain positions and is subject to changes based on the organizational needs. Applicants must be authorized to work for any employer in the United States. This position is not open to applicants who need visa sponsorship or transfer of visa sponsorship at this time. ABOUT US Popular is Puerto Rico's leading financial institution and have been evolving since it was founded over a century ago. From a small bank it has developed into a large corporation that offer a wide variety of services and financial solutions to our customers, with presence in the United States, the Caribbean and Latin America. As employees, we are dedicated to making our customers dreams come true by offering financial solutions in each stage of their life. Our extensive trajectory demonstrates the resiliency and determination of our employees to innovate, reach for the right solutions and strongly support the communities we serve; therefore, we value their diverse skills, experiences and backgrounds. We reaffirm our commitment to always offer essential financial services and solutions for our customers and communities, including during emergency situations and/or natural disasters. Popular's employees are considered essential workers, whose role is critical in the continuity of these important services even under such circumstances. By applying to this position, you acknowledge that Popular may require your services during and immediately after any such events. If you have a disability or need more information about requesting an accommodation, please contact us at ***************************. This email inbox is monitored for such types of requests only. All information you provide will be kept confidential and will be used only to the extent required to provide needed exemptions or reasonable accommodations. Any other correspondence will not receive a response. Are you ready for a rewarding career? Popular is an Equal Opportunity Employer, including Disability/Vets Learn more about us at *************** and keep updated with our latest job postings at ********************* Connect with us! LinkedIn | Facebook | Twitter | Instagram If you are a California resident, please click here to learn more about your privacy rights.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Job Overview Provides technical support to achieve the reliable and compliant manufacture of bulk drug substance to predetermined global quality standards via a detailed set of manufacturing instructions and procedures. The candidate will serve as an expert of Contamination Control Strategy. The candidate will be responsible for: * Definition and implementation of the routine environment monitoring plan and ensure that such plan is aligned with the Contamination Control Strategy (CCS)and thus the process remains in control and capable. * Provide technical support to operational staff in terms of Environmental Monitoring (EM), Sanitization, CCS and Cleaning programs. * Primary responsible for proactively detecting any CCS related data variability and identifying/implementing actions as response to it. * Contributing to the improvement agenda. * Performing periodic evaluations for Environmental Monitoring and generating reports to analyze system performance. * Technical documentation of the CCS program in official sources such as: Process Flow Diagrams (PFDs), Quality Risk Assessments, manufacturing instructions, SOP's and technical reports. * Participate in the design and execution of Process, Cleaning, Bioburden Control Strategies and Validation exercises as needed. Ensure CCS process is maintained through the support and oversight of floor operations, Manufacturing Campaign Reviews, Ongoing Process Verification (OPV) and Annual Product Reviews (APR). * Carry out investigations, identify CAPA plans and present them to deviation board as applicable. * Own change controls implementation, which is expected to be completed in an effective and timely manner. * Maintain an effective collaboration with secondary loop personnel, TS/MS laboratory, other functions, and other Lilly manufacturing sites to identify best practices for replication. * Ensure data integrity and verification procedures are followed. Provide technical support on cleaning processes for new product introduction. Basic Requirements * Bachelor's degree in scientific disciplines such as Molecular Biology or Microbiology with 3 to 5 years of experience in pharmaceutical manufacturing and/or in a CCS program is required. * Master or PhD degree in scientific disciplines such as Molecular Biology or Microbiology with 1-3 years of experience in pharmaceutical manufacturing and/or in a CCS program. * Candidate should demonstrate a strong scientific and technical knowledge in microbiology, and statistical data analysis, technical writing. * Knowledge of cGMPs. * Strong technical writing and presentation skills. * Proficiency in process data analysis using statistical tools. * Excellent interpersonal skills that foster engagement and teamwork in a cross-functional environment. * Fully bilingual (English and Spanish). * Team-oriented with strong collaboration skills. * Ability to influence and exercise sound judgment. * Demonstrated leadership capabilities. * Excellent oral and written communication skills. * Ability to manage multiple assignments in a dynamic environment. * Availability to support 24/7 operations. * Relevant industrial experience in Chemical Engineering, development or Quality in Pharmaceutical or Protein Manufacturing Operations is desirable. Important Notice: In order to maintain the excellent reputation of our company, the quality of our products, and the safety of our working environment, the company will take all reasonable measures to ensure that drug abuse by employees or other persons does not jeopardize the safety of our operations or the quality of our products or adversely affect in any way the company or its employees. The company recognizes that drug use both on and off the job can be detrimental to the company and its efforts to provide a drug-free workplace. Even if prescribed under a state medical marijuana law, marijuana remains illegal under federal law. Marijuana is considered unauthorized by Lilly. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $52,500 - $154,000 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

At Kelly Science, Engineering, Technology & Telecom (SETT), we're passionate about helping you find a job that works for you. How about this one? We're seeking a **Process Development Scientist** to work with one of our top global biopharmaceutical clients in the Juncos PR area. With us, it's all about finding the job that's just right. **Requirements:** + Doctorate or master's degree and 2 years of Scientific experience or bachelor's degree and 4 years of Scientific experience. + Advanced scientific analysis, laboratory work skills, and troubleshooting skills. + Must be well organized, have multi-task project experience, and be able to communicate and work well with other departments. + Strong technical writing skills, negotiation, and conflict resolution. + Computer literacy Windows environment: Word, Excel, PowerPoint. + Strong knowledge of cGMP. + Fully bilingual English/Spanish. + Administrative Shift. **What happens next:** Once you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry-even if this position doesn't work out, you're still in our network. That means all our recruiters will have access to your profile, expanding your opportunities even more. Helping you discover what's next in your career is what we're all about, so let's get to work. Apply to be a **PD Scientist** today! **Kelly PR Offers!** Exposure to a variety of career opportunities because of our expansive network of client companies Career guides, information, and tools to help you successfully position yourself throughout every stage of your career Access to more than 3,000 online training courses through our Kelly Learning Center Bi-weekly pay Among other benefits! **Apply Today!** 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.

Department Operations Employment Type Full Time Location FDI Clinical Research - San Juan Workplace type Onsite Reporting To Michelle Echeandia Key Responsibilities Skills, Knowledge and Expertise Benefits About Alcanza Clinical Research Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all. We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these new therapies, and the entire medical community. Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life. Alcanza is a culturally competent organization. We treat each other with dignity, creating an environment where all individuals feel welcome, heard, and respected for their unique perspectives and aspirations. We put considerable effort into finding exceptional employees who mirror the values most important to us: Inclusive, Impactful, Compassionate, and Determined. Alcanza Clinical Research is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company.

At PNNL, our core capabilities are divided among major departments that we refer to as Directorates within the Lab, focused on a specific area of scientific research or other function, with its own leadership team and dedicated budget. Our Science & Technology directorates include National Security, Earth and Biological Sciences, Physical and Computational Sciences, and Energy and Environment. In addition, we have an Environmental Molecular Sciences Laboratory, a Department of Energy, Office of Science user facility housed on the PNNL campus. The Energy and Environment Directorate delivers science and technology solutions for the nation's biggest energy and environmental challenges. Our more than 1,700 staff support the Department of Energy (DOE), delivering on key DOE mission areas including: modernizing our nation's power grid to maintain a reliable, affordable, secure, and resilient electricity delivery infrastructure; research, development, validation, and effective utilization of renewable energy and efficiency technologies that improve the affordability, reliability, resiliency, and security of the American energy system; and resolving complex issues in nuclear science, energy, and environmental management. The Earth Systems Science Division, part of the Energy and Environment Directorate, provides leadership and solutions that advance Earth system opportunities for energy systems and national security. We are a multidisciplinary division connected by a shared commitment to innovate and collaborate towards solving complex problems in the dynamic Earth system. **Responsibilities** PNNL's Environmental Subsurface Science Group is seeking a mid-level scientist or engineer with broad experience in geophysics, reservoir modeling, geologic carbon storage, geothermal energy production, and environmental remediation. The position requires the ability to lead and support the development of simulation capabilities and the application of advanced simulation tools to diverse problems. The candidate will lead and work collaboratively with teams in multiple disciplines, including geophysics, geochemistry, and environmental engineering. The Team studies the geosphere, hydrosphere, biosphere, atmosphere, and/or interactions of these systems with human activities. It uses scientific principles, instrument measurements, computer models, data analysis, and knowledge of policy and regulatory drivers to study the environment and/or develop solutions to environmental problems. Leverages knowledge and tools from fields such as ecology, biology, physics, chemistry, geochemistry, soil science, geology, hydrology, atmospheric science, economics, and/or integrated assessment. Studies the geosphere, hydrosphere, biosphere, atmosphere, and/or interactions of these systems with human activities. Uses scientific principles, instrument measurements, computer models, data analysis, and knowledge of policy and regulatory drivers to study the environment and/or develop solutions to environmental problems. Leverages knowledge and tools from fields such as ecology, biology, physics, chemistry, geochemistry, soil science, geology, hydrology, atmospheric science, economics, and/or integrated assessment. **Qualifications** Minimum Qualifications: + BS/BA and 9+ years of relevant experience -OR- + MS/MA and 7+ years of relevant experience -OR- + PhD with 5+ year of relevant experience Preferred Qualifications: + Experience leading technical teams. + Experience modeling carbon sequestration, enhanced geothermal systems, gas hydrates, and contaminant fate andtransport. + Experience working with reactive transport software. + Experience developing simulation software for high performance computers. + Proficiency with Python. + Experience with analysis and visualization tools (e.g., Matplotlib, Paraview). + Experience with open source software development, distributed version control, and continuous integration. + Candidates should have a demonstrated commitment to data quality and accuracy, strong written and oralcommunication skills as evidenced by scientific publications and conference presentations, and be able to workindependently and in a team setting. + Candidates should have experience with business development, such as proposal development and clientengagement. + Candidates should have experience mentoring students, interns, or junior staff. + Candidates should have experience leading small project tasks. **Hazardous Working Conditions/Environment** Not Applicable **Additional Information** This position requires the ability to obtain and maintain a federal security clearance. A security clearance background investigation includes review of your employment, education, financial, and criminal history, as well as interviews with you and your personal references, neighbors, and co-workers to determine trustworthiness, reliability, and loyalty to the United States. The investigation also examines your foreign connections, drug and alcohol use, foreign influence, and overall conduct. Requirements: + U.S. Citizenship + Background Investigation: Applicants selected will be subject to a Federal background investigation and must meet eligibility requirements for access to classified matter in accordance with 10 CFR 710, Appendix B. + Drug Testing: All Security Clearance positions are Testing Designated Positions, which means that the applicant selected for hire is subject to pre-employment drug testing, and post-employment random drug testing. In addition, applicants must be able to demonstrate non-use of illegal drugs, including marijuana, for the 12 consecutive months preceding completion of the requisite Questionnaire for National Security Positions (QNSP). Note: Applicants will be considered ineligible for security clearance processing by the U.S. Department of Energy if non-use of illegal drugs, including marijuana, for 12 months cannot be demonstrated. **Testing Designated Position** This position is a Testing Designated Position (TDP). The candidate selected for this position will be subject to pre-employment and random drug testing for illegal drugs, including marijuana, consistent with the Controlled Substances Act and the PNNL Workplace Substance Abuse Program. **About PNNL** Pacific Northwest National Laboratory (PNNL) is a world-class research institution powered by a highly educated, diverse workforce committed to the values of Integrity, Creativity, Collaboration, Impact, and Courage. Every year, scores of dynamic, driven people come to PNNL to work with renowned researchers on meaningful science, innovations and outcomes for the U.S. Department of Energy and other sponsors; here is your chance to be one of them! At PNNL, you will find an exciting research environment and excellent benefits including health insurance, and flexible work schedules. PNNL is located in eastern Washington State-the dry side of Washington known for its stellar outdoor recreation and affordable cost of living. The Lab's campus is only a 45-minute flight (or ~3 hour drive) from Seattle or Portland, and is serviced by the convenient PSC airport, connected to 8 major hubs. **Commitment to Excellence and Equal Employment Opportunity** Our laboratory is committed to fostering a work environment where all individuals are treated with fairness and respect while solving critical challenges in fundamental sciences, national security, and energy resiliency. We are an Equal Employment Opportunity employer. Pacific Northwest National Laboratory (PNNL) is an Equal Opportunity Employer. PNNL considers all applicants for employment without regard to race, religion, color, sex, national origin, age, disability, genetic information (including family medical history), protected veteran status, and any other status or characteristic protected by federal, state, and/or local laws. We are committed to providing reasonable accommodations for individuals with disabilities and disabled veterans in our job application procedures and in employment. If you need assistance or an accommodation due to a disability, contact us at **************** . **Drug Free Workplace** PNNL is committed to a drug-free workplace supported by Workplace Substance Abuse Program (WSAP) and complies with federal laws prohibiting the possession and use of illegal drugs. If you are offered employment at PNNL, you must pass a drug test prior to commencing employment. PNNL complies with federal law regarding illegal drug use. Under federal law, marijuana remains an illegal drug. If you test positive for any illegal controlled substance, including marijuana, your offer of employment will be withdrawn. **Security, Credentialing, and Eligibility Requirements** As a national laboratory, PNNL is responsible for adhering to the Homeland Security Presidential Directive 12 (HSPD-12) and Department of Energy (DOE) Order 473.1A, which require new employees to obtain and maintain a HSPD-12 Personal Identify Verification (PIV) Credential. To obtain this credential, new employees must successfully complete the applicable tier of federal background investigation post hire and receive a favorable federal adjudication. The tier of federal background investigation will be determined by job duties and national security or public trust responsibilities associated with the job. All tiers of investigation include a declaration of illegal drug activities, including use, supply, possession, or manufacture within the last 1 to 7 years (depending on the applicable tier of investigation). Illegal drug activities include marijuana and cannabis derivatives, which are still considered illegal under federal law, regardless of state laws. For foreign national candidates: If you have not resided in the U.S. for three consecutive years, you are not eligible for the PIV credential and instead will need to obtain a favorable Local Site Specific Only (LSSO) Federal risk determination to maintain employment. Once you meet the three-year residency requirement thereafter, you will be required to obtain a PIV credential to maintain employment. The tier of federal background investigation required to obtain the PIV credential will be determined by job duties at the time you become eligible for the PIV credential. **Mandatory Requirements** Please be aware that the Department of Energy (DOE) prohibits DOE employees and contractors from having any affiliation with the foreign government of a country DOE has identified as a "country of risk" without explicit approval by DOE and Battelle. If you are offered a position at PNNL and currently have any affiliation with the government of one of these countries, you will be required to disclose this information and recuse yourself of that affiliation or receive approval from DOE and Battelle prior to your first day of employment. **Rockstar Rewards** Employees and their families are offered medical insurance, dental insurance, vision insurance, robust telehealth care options, several mental health benefits, free wellness coaching, health savings account, flexible spending accounts, basic life insurance, disability insurance*, employee assistance program, business travel insurance, tuition assistance, relocation, backup childcare, legal benefits, supplemental parental bonding leave, surrogacy and adoption assistance, and fertility support. Employees are automatically enrolled in our company-funded pension plan* and may enroll in our 401 (k) savings plan with company match*. Employees may accrue up to 120 vacation hours per year and may receive ten paid holidays per year. * Research Associates excluded. **All benefits are dependent upon eligibility. Click Here For Rockstar Rewards (****************************************** **Notice to Applicants** PNNL lists the full pay range for the position in the job posting. Starting pay is calculated from the minimum of the pay range and actual placement in the range is determined based on an individual's relevant job-related skills, qualifications, and experience. This approach is applicable to all positions, with the exception of positions governed by collective bargaining agreements and certain limited-term positions which have specific pay rules. As part of our commitment to fair compensation practices, we do not ask for or consider current or past salaries in making compensation offers at hire. Instead, our compensation offers are determined by the specific requirements of the position, prevailing market trends, applicable collective bargaining agreements, pay equity for the position type, and individual qualifications and skills relevant to the performance of the position. **Minimum Salary** USD $173,400.00/Yr. **Maximum Salary** USD $274,100.00/Yr.

Syngenta Seeds is one of the world's largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs. Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions. Syngenta Seeds is headquartered in the United States. Job Description At Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, Syngenta's R&D team is seeking a Research Associate 2 in Salinas, Puerto Rico. This role will support continuous nursery operations for corn and soybean by developing integrated pest management strategies, overseeing pesticide selection and application, maintaining records, and ensuring compliance with company, local, and federal regulations. Responsible for executing and managing diverse operational tasks in agricultural research, with a focus on operations, yield trials, nursery operations, and/or agronomy in seed production across multiple crops. Performs role responsibilities with weekly supervision. Accountabilities: Execute daily operational activities within functional areas such as operations, trialing, agronomy, or nursery operations. Perform data collection and reporting, inventory management, field activities, accurate data and/or observations from trials and nursery plots, plant care, machine operation and/or maintenance, and perform standard processes and protocols. Update records and documentation and present performance metrics to management. Implement compliance in areas that may include industry regulations, internal policies, HSE, EPA and WPS, equipment handling, quality standards, and best practices in agricultural research and operations. Train and mentor junior team members and seasonal staff in operational and/or agronomic processes, equipment handling, required protocols and/or data collection. Collaborate with cross-functional teams to streamline processes, improve communication, and ensure project success. Identify and implement process improvements and optimization strategies to enhance efficiency and productivity. May monitor and maintain greenhouse environments, including plant care, pest management, and equipment operation. Qualifications Required: Associate's degree in Agriculture, Operations Management, or related field or 2+ years of relevant experience. Valid driver's license and ability to travel to off-site facilities/ field locations as required. Ability to effectively work in outdoor field environment, greenhouse or controlled laboratory environments Ability to lift 50 pounds Ability to perform manual labor tasks, such as bending, lifting, and standing for extended periods Ability to obtain necessary license or certification Ability to work flexibly, including weekends or different shifts when required Desired: Demonstrated experience in agricultural operations, process improvement, and data collection. Strong understanding of agriculture, agronomy practices, and field trial operations. Excellent organizational skills with the ability to manage multiple projects simultaneously. Strong written and verbal communication skills, including the ability to train and lead others. Experience operating, maintaining, and performing minor repairs on field and plot equipment. Proficiency in data analysis and interpretation of research results. Familiarity with greenhouse or indoor growing systems (preferred). Problem-solving skills and ability to identify root causes and apply corrective actions. Additional Information What We Offer: A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs. Full Benefit Package (Medical, Dental & Vision) that starts your first day. 401k plan with company match, Profit Sharing & Retirement Savings Contribution. Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits. Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: ******************************************* Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. WL: 2B #LI-ONSITE

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 consultant will develop and execute Environmental Qualification, Airflow Visualization Study (AVS) and Aseptic Process Simulation (APS) deliverables for operational readiness projects. Responsibilities: * Responsible for the Activities before Environmental monitoring performance qualification (EMPQ) execution * Responsible for the EMPQ execution & post approval * Responsible for the Air Visualization Studies * Responsible for the Aseptic Process Simulation Media Fill (MF) * Participate in project meetings, as applicable * Generate Validation Plan establishing lean strategies, as required. * Develop and execute EM PQ, AVS and APS protocols for applicable systems * Develop EM PQ, AVS and APS reports for applicable systems * Evaluate, coordinate, and execute the required efforts (resources, plant support, equipment, materials, etc.) to support projects deliverables. * Comply with projects schedule and escalate any roadblock or issues immediately including proposed mitigation plan. * Provide support during documentation transfer to DMS or Quality. Shift: (1st, 2nd, and 3rd Shift) Location: Juncos, PR Education: Bachelor's degree in Engineering or a Scientific field. Preferred Qualifications: * 5+ years of experience in a regulated industry. * Experience with Environmental monitoring performance qualification (EMPQ) execution * Preferred experience with Aseptic Process Simulation Media Fill (MF) * Strong knowledge of cGMP/FDA regulations * Strong communication skills (oral and written) * Ability to organize and manage multiple tasks in a fast-paced environment * Attention to detail * Demonstrated problem solving and analytical skills 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

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 consultant will develop and execute Environmental Qualification, Airflow Visualization Study (AVS) and Aseptic Process Simulation (APS) deliverables for operational readiness projects. Responsibilities: * Responsible for the Activities before Environmental monitoring performance qualification (EMPQ) execution * Responsible for the EMPQ execution & post approval * Responsible for the Air Visualization Studies * Responsible for the Aseptic Process Simulation Media Fill (MF) * Participate in project meetings, as applicable * Generate Validation Plan establishing lean strategies, as required. * Develop and execute EM PQ, AVS and APS protocols for applicable systems * Develop EM PQ, AVS and APS reports for applicable systems * Evaluate, coordinate, and execute the required efforts (resources, plant support, equipment, materials, etc.) to support projects deliverables. * Comply with projects schedule and escalate any roadblock or issues immediately including proposed mitigation plan. * Provide support during documentation transfer to DMS or Quality. Shift: (1st, 2nd, and 3rd Shift) Location: Juncos, PR Education: Bachelor's degree in Engineering or a Scientific field. Preferred Qualifications: * 5+ years of experience in a regulated industry. * Experience with Environmental monitoring performance qualification (EMPQ) execution * Preferred experience with Aseptic Process Simulation Media Fill (MF) * Strong knowledge of cGMP/FDA regulations * Strong communication skills (oral and written) * Ability to organize and manage multiple tasks in a fast-paced environment * Attention to detail * Demonstrated problem solving and analytical skills 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

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 consultant will develop and execute Environmental Qualification, Airflow Visualization Study (AVS) and Aseptic Process Simulation (APS) deliverables for operational readiness projects. Responsibilities: Responsible for the Activities before Environmental monitoring performance qualification (EMPQ) execution Responsible for the EMPQ execution & post approval Responsible for the Air Visualization Studies Responsible for the Aseptic Process Simulation Media Fill (MF) Participate in project meetings, as applicable Generate Validation Plan establishing lean strategies, as required. Develop and execute EM PQ, AVS and APS protocols for applicable systems Develop EM PQ, AVS and APS reports for applicable systems Evaluate, coordinate, and execute the required efforts (resources, plant support, equipment, materials, etc.) to support projects deliverables. Comply with projects schedule and escalate any roadblock or issues immediately including proposed mitigation plan. Provide support during documentation transfer to DMS or Quality. Shift: (1st, 2nd, and 3rd Shift) Location: Juncos, PR Education: Bachelor's degree in Engineering or a Scientific field. Preferred Qualifications: 5+ years of experience in a regulated industry. Experience with Environmental monitoring performance qualification (EMPQ) execution Preferred experience with Aseptic Process Simulation Media Fill (MF) Strong knowledge of cGMP/FDA regulations Strong communication skills (oral and written) Ability to organize and manage multiple tasks in a fast-paced environment Attention to detail Demonstrated problem solving and analytical skills 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

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 Process Development Scientist provide direct support to the requirement, design, and characterization of inspection/packaging process, process optimization strategies and/or troubleshooting of operational issues in the operations. Apply advanced and diverse engineering principles to the design and implementation of system, equipment or process modifications, experiments, process and/or capital projects. Develop, organize, analyze and present interpretation of results for operational issues or engineering projects. 1. Provide advanced technical support in automatic packaging equipment and processes. Strong Knowledge on Vision system technologies. Inspection/packaging Concepts Knowledge Strong Knowledge with local process flow, layouts and general packaging SOP's to be able to define details of serialization solution. 2. Support troubleshooting, investigations, root cause analysis related to the packaging area and inspection process. 3. Identify and implement initiatives in the inspection/packaging processes in order to reduce manufacturing operational costs while maintaining product quality 4. Development and Execution of Processes Characterization Establish Testing Strategies Design / Development of Characterization Protocols Technical Reports Development Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies. Risk assessments and QRAES knowledge, to support risk assessments activities. 5. Project execution activities coordination (Material requests, Trainings, Production Windows, Work Orders generation) Qualifications Technical Documentation abilities Oral and written - Documentation software (MS word, Excel, Power point, PDF, Visio, MS project) - Project management basic concepts (timeline follow up, schedule reviews, predecessor) - Flexibility in working time based on project needs, including 1st, 2nd and 3th shifts and extended hours up to 12 hrs. - People skills for OEM's and interdisciplinary share. - Self driven and schedule oriented Education: -Doctorate or Master's + 2 years of Scientific experience or Bachelor's + 4 years of Scientific experience. Additional Information All your information will be kept confidential according to EEO guidelines.

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: Qualification / Computer System Validation (CSV) Scientist Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. Experience in direct process / manufacturing areas. Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Strong knowledge in cGxP and regulatory guidance. SDLC documents (i.e. URS, FDS, VP, DQ, TMX, Risk Assessment), Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test (SAT).and IOPQ Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.

Looking for a role that lets you hit the road, explore different stores, and work on a flexible schedule? We're hiring a detail-driven **Data Collector** to visit supermarkets and retail stores across the south of Puerto Rico-mainly Ponce, Juana Díaz, Yauco, and surrounding areas. This position involves discreet store visits, similar to a mystery shopper, to observe and gather key information on product availability, pricing, displays, and customer service. **What You'll Do** + Visit assigned stores and collect information with professionalism and discretion. + Observe and document product placement, inventory levels, pricing accuracy, and overall store conditions. + Take notes as needed while staying low-profile. + Submit accurate, timely reports through our tools or software. + Communicate any challenges or unusual findings to your supervisor. **Requirements:** + Availability to work in the south region of Puerto Rico. + High school diploma completed. + A valid Puerto Rico driver's license. + Reliable, well-maintained transportation. + Flexibility to work **15-25 hours per week** with a schedule that adapts to your availability. + Comfort communicating in conversational English. **Pay Details:** $14.00 per hour Benefit offerings available for our associates include short-term disability and additional voluntary benefits including medical, dental, vision, life insurance, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave and Vacation Leave or any other paid leave required by Federal, State, or local law where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ********************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance

Inteldot has over 14 years of experience in the life sciences industry, with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico. Job Description: To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor. Administrative shift Requirements: Provide direct support to the requirement, design, and characterization of inspection/packaging process, process optimization strategies and/or troubleshooting of operational issues in the operations. Apply advanced and diverse engineering principles to the design and implementation of system, equipment or process modifications, experiments, process and/or capital projects. Develop, organize, analyze and present interpretation of results for operational issues or engineering projects. Provide advanced technical support to the automatic packaging equipment and processes: Strong Knowledge on Vision system technologies Inspection/packaging Concepts Knowledge Strong Knowledge with local process flow, layouts and general packaging SOP's to be able to define details of serialization solution. Support troubleshooting, investigations, root cause analysis related to the packaging area and inspection process. Identify and implement initiatives in the inspection/packaging processes to reduce manufacturing operational costs while maintaining product quality Development and Execution of Processes Characterization: Establish Testing Strategies Design / Development of Characterization Protocols Technical Reports Development Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies. Risk assessments and QRAES knowledge, to support risk assessments activities. Project execution activities coordination (Material requests, Trainings, Production Windows, Work Orders generation). General skills: Technical Documentation abilities verbal and written Documentation software (MS word, Excel, Power point, PDF, Visio, MS project) Project management basic concepts (timeline follow up, schedule reviews, predecessor). Flexibility in working time based on project needs, including 1st, 2nd and 3rd shifts and extended hours up to 12 hrs. General Functions: Conceives and designs, executes or evaluates, and interprets experimental strategies. Provides input to new processes to generate robust and reliable data. Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Designs, monitors or conducts experimental strategies with general guidance from supervisor. Provides data analysis and interpretation and assesses impact of the data on the project. Monitors field of expertise, including literature and technology development, and communicates relevant observations. Develops and implements new and novel protocols to address specific issues. Assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies. Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents. Education: Master's degree and 2 years of Scientific experience or bachelor's degree and 4 years of Scientific experience.

To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor. Functions: Conceives and designs, executes or evaluates, and interprets experimental strategies. Provides input to new processes to generate robust and reliable data. Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Designs, monitors or conducts experimental strategies with general guidance from supervisor. Provides data analysis and interpretation, and assesses impact of the data on the project. Keeps current in field of scientific expertise and areas relevant to their function. Monitors field of expertise, including literature and technology development, and communicates relevant observations. May introduce advanced scientific methods. Develops and implements new and novel protocols to address specific issues. May represent the department on project teams under supervision of a senior scientific staff member. May initiate productive collaborations within and outside of the department or company. Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies. Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents. Participates in external scientific community. May assume lead role in department-wide support efforts such as safety, recruiting and committees. May develop supervisory and mentoring skills. Develops and follows timelines for completing project team work. Education: Masters + 2 years of Scientific experience. Bachelors + 4 years of Scientific experience. Preferred Qualifications: Provide direct support to the requirement, design, and characterization of inspection/packaging process, process optimization strategies and/or troubleshooting of operational issues in the operations. Apply advanced and diverse engineering principles to the design and implementation of system, equipment or process modifications, experiments, process and/or capital projects. Develop, organize, analyze and present interpretation of results for operational issues or engineering projects. Requirements: 1. Provide advanced technical support to AML-1 automatic packaging equipment and processes Strong Knowledge on Vision system technologies Inspection/packaging Concepts Knowledge Strong Knowledge with local process flow, layouts and general packaging SOP's to be able to define details of serialization solution. 2. Support troubleshooting, investigations, root cause analysis related to the packaging area and inspection process. 3. Identify and implement initiatives in the inspection/packaging processes in order to reduce manufacturing operational costs while maintaining product quality 4. Development and Execution of Processes Characterization Establish Testing Strategies Design / Development of Characterization Protocols Technical Reports Development Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies. Risk assessments and QRAES knowledge, to support risk assessments activities. 5. Project execution activities coordination (Material requests, Trainings, Production Windows, Work Orders generation) 6. General skills: Technical Documentation abilities Oral and written. Documentation software (MS word, Excel, Power point, PDF, Visio, MS project). Project management basic concepts (timeline follow up, schedule reviews, predecessor). Flexibility in working time based on project needs, including 1st, 2nd and 3th shifts and extended. hours up to 12 hrs. People skills for OEM's and interdisciplinary share. Self driven and schedule oriented. Skills: Advanced scientific analysis and troubleshooting skills. Advanced laboratory work skills. Ability to motivate and/or supervise the activities of others. Must be well organized, have multi-task project experience, and be able to communicate and work well with other departments. Must have demonstrated skills and competencies in the following areas: Verbal communication, Written communication including technical writing skills, negotiation and conflict resolution. Analytical problem solving Project management. Ability to be flexible and manage change. Computer literacy (Windows environment: Word, Excel, Power Point). Skills requiring the application of scientific theory. Creative skills in the design and performance of scientific experiments and interpretation of results. Strong knowledge of cGMP Fully bilingual (English/Spanish). Work Methodology: 100% On-site 6 months (1st Contract) Administrative Shift (weekends and overtime may also be required). Professional Service Contract

Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build prototypes and explore conceptually new solutions. Work collaboratively with science, engineering, and product teams to identify customer needs in order to create and implement solutions, promote innovation and drive model implementations. Applies data science capabilities and research findings to create and implement solutions to scale. Responsible for developing new intelligence around core products and services through applied research on behalf of our customers. Develops models, prototypes, and experiments that pave the way for innovative products and services. Build cloud services that work out of the box for enterprises, e.g. decision support, anomaly detection, forecasting and recommendations), natural language processing (NLP), Natural Language Understanding (NLU),Time Series, Automatic Speech Recognition (ASR), Machine Learning (ML), and Computer Vision (CV). Design and run experiments, research new algorithms, and find new ways of optimizing risk, profitability, and customer experience. Conversant on ethical problems in consideration of sciences. **Responsibilities** Leading contributor providing guidance and mentorship to define, design and deliver product quality improvements from ideation stage to shipping to the customer. Write high quality code to power experiments and build models. Contributes to writing production model code. Work closely with product management and engineering to deliver products which solves the needs of our customers by building relevant, innovative results which strategically differentiates Oracle in the market. Set up environment needed to run experiments for all projects. Set up distributed environments. Engage with customers and help solve complex problems with the customer/partner. Directly impact our customers via innovation in products and services that make use of ML/AI technology. Clearly articulate technical work to audiences of all levels and across multiple functional areas. Keep track of the progress and ensure the team is following the best practices. Works on training data collection, feature engineering, model training, offline and online experimentation. Drives independent research and development. Advance the state-of-the-art machine learning and algorithms for real-world large-scale applications. Ensure solutions are designed with fairness and explainability in mind. May perform other duties as assigned. Disclaimer: **Certain US customer or client-facing roles may be required to comply with applicable requirements, such as immunization and occupational health mandates.** **Range and benefit information provided in this posting are specific to the stated locations only** US: Hiring Range in USD from: $120,100 to $251,600 per annum. May be eligible for bonus, equity, and compensation deferral. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. Career Level - IC4 **About Us** As a world leader in cloud solutions, Oracle uses tomorrow's technology to tackle today's challenges. We've partnered with industry-leaders in almost every sector-and continue to thrive after 40+ years of change by operating with integrity. We know that true innovation starts when everyone is empowered to contribute. That's why we're committed to growing an inclusive workforce that promotes opportunities for all. Oracle careers open the door to global opportunities where work-life balance flourishes. We offer competitive benefits based on parity and consistency and support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs. We're committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_************* or by calling *************** in the United States. Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans' status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.

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 Process Development Sr. Associate Scientist with experience in Pharmaceutical, Biotechnology or Medical devices industries to optimizes, and scales up laboratory processes to ensure efficient production of biologics and therapeutic products. RESPONSIBILITIES: Conduct research into the structures and properties of materials, such as metals, polymers, and ceramics to obtain information that could be used to develop new products or enhance existing ones. Determine ways to strengthen or combine materials or develop new materials with new or specific properties for use in a variety of products and applications. Develop testing methods to evaluate the effects of various conditions on containers materials Plan laboratory experiments to confirm feasibility of processes and techniques used in the production of materials having special characteristics. Perform experiments, records, organize data and analyze results under minimal supervision. Generates robust and reliable data in compliance with the respective protocols, methods or SOPs. Identify container components defects and provide solutions related to possible technical problems of moderate scope and complexity. Perform Container Defects, Primary Packaging and Glass/Polymer Forensics Evaluations Study the nature, structure and physical properties of glass and polymer containers and their responses to applied forces. Test material samples for tolerance under tension, compression and shear, to determine the cause of failures. Test individual parts and products to ensure that manufacturer and governmental quality and safety standards are met. Evaluate and interpret results using imaging acquisition equipment's. Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision. Operate specialized laboratory equipment and computers as appropriate. Perform assignments that have clear and specific objectives and require investigation of limited number of variables. Initiate and complete laboratory routine technical tasks. Complete complex or novel assignments requiring development of new and/or improved scientific/engineering techniques and procedures. Monitor and maintain inventory of supplies and sample inventory. Coordinate and review work with peers on an ongoing basis. Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations. Must be independent, self-motivated, organized, able to multi-task in laboratory environments, and skilled in communication, facilitation, and collaboration. Individual must be a team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making. Apply knowledge of scientific/engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields. Generates robust and reliable data in compliance with the respective protocols or SOPs. Support commissioning and qualification activities. Share knowledge to develop the teammates in expertise discipline. TASKS: Monitors field of expertise, including literature and technology development, and communicates relevant observations. Understands and interprets primary components specifications and methods. Demonstrates knowledge regarding metal, glass and polymer formation process and primary container components defects and classifications. Perform Primary Packaging Evaluations and Glass/Polymers Forensic Analysis. Introduce advanced scientific methods. Develops and implements news and novel protocols to address specific issues. Represent the department on project teams under supervision. Initiates productive collaborations within and outside of the Process Development Department and Network. Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies. Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents. Participates with the external scientific community. Assumes lead role in department-wide support efforts such as safety, OE and other committees. Develops and follows timelines for completing project teamwork. Qualifications Educational background in Engineering and/or Sciences. Knowledge in Material Sciences (glass/polymers). Knowledge of the practical application of engineering, sciences, and technology. This includes applying principles, techniques, procedures, and equipment to the design and production of various goods and services. Knowledge of arithmetic, algebra, geometry, calculus, statistics, and their applications. Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations that they undergo. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods. Knowledge and prediction of physical principles, laws, interrelationships, and applications to understanding fluid, material, and atmospheric dynamics, and mechanical, electrical, atomic and sub- atomic structures and processes. Understanding of equipment commissioning and qualification, validation and documentation processes in a highly regulated environment. Familiarity with Biopharmaceutical Environment. Knowledge in Primary Packaging Components (vials, syringes, cartridges, etc.) Knowledge in Secondary Packaging Components (labels, dispensing cartons, blisters, etc.). Knowledge in Glass/Polymer Forensics. Bilingual (Spanish/English). Computer literacy. Additional Information All your information will be kept confidential according to EEO guidelines.

At Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, Syngenta's R&D team is seeking a Research Associate 2 in Salinas, Puerto Rico. This role will support continuous nursery operations for corn and soybean by developing integrated pest management strategies, overseeing pesticide selection and application, maintaining records, and ensuring compliance with company, local, and federal regulations. Responsible for executing and managing diverse operational tasks in agricultural research, with a focus on operations, yield trials, nursery operations, and/or agronomy in seed production across multiple crops. Performs role responsibilities with weekly supervision. Accountabilities: * Execute daily operational activities within functional areas such as operations, trialing, agronomy, or nursery operations. * Perform data collection and reporting, inventory management, field activities, accurate data and/or observations from trials and nursery plots, plant care, machine operation and/or maintenance, and perform standard processes and protocols. Update records and documentation and present performance metrics to management. * Implement compliance in areas that may include industry regulations, internal policies, HSE, EPA and WPS, equipment handling, quality standards, and best practices in agricultural research and operations. * Train and mentor junior team members and seasonal staff in operational and/or agronomic processes, equipment handling, required protocols and/or data collection. * Collaborate with cross-functional teams to streamline processes, improve communication, and ensure project success. * Identify and implement process improvements and optimization strategies to enhance efficiency and productivity. * May monitor and maintain greenhouse environments, including plant care, pest management, and equipment operation.

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: To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor. Responsibilities: Conceives and designs, executes or evaluates, and interprets experimental strategies. Provides input to new processes to generate robust and reliable data. Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Designs, monitors or conducts experimental strategies with general guidance from supervisor. Provides data analysis and interpretation, and assesses impact of the data on the project. Keeps current in field of scientific expertise and areas relevant to their function. Monitors field of expertise, including literature and technology development, and communicates relevant observations. May introduce advanced scientific methods. Develops and implements new and novel protocols to address specific issues. May represent the department on project teams under supervision of a senior scientific staff member. May initiate productive collaborations within and outside of the department or company. Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies. Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents. Participates in external scientific community. May assume lead role in department-wide support efforts such as safety, recruiting and committees. May develop supervisory and mentoring skills. Develops and follows timelines for completing project team work. Shift: Administrative. Flexibility in working time based on project needs, including 1st, 2nd and 3th shifts and extended hours up to 12 hrs. Location: Juncos, PR Education: Doctorate OR Masters + 2 years of Scientific experience OR Bachelors + 4 years of Scientific experience. Preferred Qualifications: Provide advanced technical support to automatic packaging equipment and processes Strong Knowledge on Vision system technologies Inspection/packaging Concepts Knowledge Strong Knowledge with local process flow, layouts and general packaging SOP's to be able to define details of serialization solution. Support troubleshooting, investigations, root cause analysis related to the packaging area and inspection process. Identify and implement initiatives in the inspection/packaging processes in order to reduce manufacturing operational costs while maintaining product quality Development and Execution of Processes Characterization Establish Testing Strategies Design / Development of Characterization Protocols Technical Reports Development Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies. Risk assessments and QRAES knowledge, to support risk assessments activities. Project execution activities coordination (Material requests, Trainings, Production Windows, Work Orders generation) General skills: Technical Documentation abilities Oral and written Documentation software (MS word, Excel, Power point, PDF, Visio, MS project) Project management basic concepts (timeline follow up, schedule reviews, predecessor) Flexibility in working time based on project needs, including 1st, 2nd and 3th shifts and extended hours up to 12 hrs. People skills for OEM's and interdisciplinary share. Self driven and schedule oriented Skills: Advanced scientific analysis and troubleshooting skills. Advanced laboratory work skills. Ability to motivate and/or supervise the activities of others. Must be well organized, have multi-task project experience, and be able to communicate and work well with other departments. Must have demonstrated skills and competencies in the following areas: Verbal communication, Written communication including technical writing skills, negotiation and conflict resolution. Analytical problem solving Project management. Ability to be flexible and manage change. Computer literacy (Windows environment: Word, Excel, Power Point). Skills requiring the application of scientific theory. Creative skills in the design and performance of scientific experiments and interpretation of results. Strong knowledge of cGMPs. Fully bilingual (English/Spanish). 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: To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor. Responsibilities: * Conceives and designs, executes or evaluates, and interprets experimental strategies. * Provides input to new processes to generate robust and reliable data. Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. * Designs, monitors or conducts experimental strategies with general guidance from supervisor. * Provides data analysis and interpretation, and assesses impact of the data on the project. * Keeps current in field of scientific expertise and areas relevant to their function. * Monitors field of expertise, including literature and technology development, and communicates relevant observations. * May introduce advanced scientific methods. Develops and implements new and novel protocols to address specific issues. * May represent the department on project teams under supervision of a senior scientific staff member. * May initiate productive collaborations within and outside of the department or company. * Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies. Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents. Participates in external scientific community. * May assume lead role in department-wide support efforts such as safety, recruiting and committees. * May develop supervisory and mentoring skills. Develops and follows timelines for completing project team work. Shift: Administrative. Flexibility in working time based on project needs, including 1st, 2nd and 3th shifts and extended hours up to 12 hrs. Location: Juncos, PR Education: Doctorate OR Masters + 2 years of Scientific experience OR Bachelors + 4 years of Scientific experience. Preferred Qualifications: * Provide advanced technical support to automatic packaging equipment and processes * Strong Knowledge on Vision system technologies * Inspection/packaging Concepts Knowledge * Strong Knowledge with local process flow, layouts and general packaging SOP's to be able to define details of serialization solution. * Support troubleshooting, investigations, root cause analysis related to the packaging area and inspection process. * Identify and implement initiatives in the inspection/packaging processes in order to reduce manufacturing operational costs while maintaining product quality * Development and Execution of Processes Characterization * Establish Testing Strategies * Design / Development of Characterization Protocols * Technical Reports Development * Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies. * Risk assessments and QRAES knowledge, to support risk assessments activities. * Project execution activities coordination (Material requests, Trainings, Production Windows, Work Orders generation) * General skills: * Technical Documentation abilities Oral and written * Documentation software (MS word, Excel, Power point, PDF, Visio, MS project) * Project management basic concepts (timeline follow up, schedule reviews, predecessor) * Flexibility in working time based on project needs, including 1st, 2nd and 3th shifts and extended hours up to 12 hrs. * People skills for OEM's and interdisciplinary share. * Self driven and schedule oriented Skills: * Advanced scientific analysis and troubleshooting skills. * Advanced laboratory work skills. * Ability to motivate and/or supervise the activities of others. * Must be well organized, have multi-task project experience, and be able to communicate and work well with other departments. * Must have demonstrated skills and competencies in the following areas: Verbal communication, Written communication including technical writing skills, negotiation and conflict resolution. * Analytical problem solving Project management. * Ability to be flexible and manage change. * Computer literacy (Windows environment: Word, Excel, Power Point). * Skills requiring the application of scientific theory. * Creative skills in the design and performance of scientific experiments and interpretation of results. * Strong knowledge of cGMPs. * Fully bilingual (English/Spanish). 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