Research and development technician jobs in Bayamn, PR

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

We are seeking a detail-oriented and reliable **Data Collector** to gather information from supermarkets and retail stores in the south area of Puerto Rico, mainly Ponce, Juana Díaz and Yauco, among others. This role requires conducting visits **incognito** , similar to a mystery shopper, to observe and collect data on product availability, pricing, displays, and customer service without revealing your identity. **Responsibilities:** + Visit assigned stores according to schedule and collect required data discreetly. + Observe and document details such as product placement, inventory levels, pricing accuracy, and overall store conditions. + Take notes as needed while maintaining a low profile. + Submit accurate and timely reports using provided tools or software. + Communicate any challenges or irregularities to the supervisor. **Requirements:** + Available to work in the south of Puerto Rico. + High school diploma completed. + Valid Puerto Rico driver's license. + Own reliable transportation in good condition. + Available to work part-time between 15-25 hours per week with a flexible schedule. + Must be proficient 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

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. In the IPM Research Associate 2 role, you will spend a large amount of your time in the field working with auto-propelled sprayers and backpacks, performing applications and assisting in diagnosing, identifying, and controlling weeds, diseases, pest problems, and other issues that may jeopardize the viability of the crops. Accountabilities: Conduct or supervise pesticide spraying events according to the plan established by the IPM Research Associate 3. Ensure that spraying equipment is in optimal operating condition. Inform the supervisor, Farming System Manager, or shop personnel of any failures. Participate in regular maintenance of sprayers, including backpacks. This could include fluid checks, filter replacements, hose replacements, refueling, nozzle body replacements, and cleaning of the equipment. Be accountable for technical aspects of the sprayer, such as calibrations, to perform effective pest control. Train new hires to operate and maintain the sprayer equipment and its components. Collaborate with the farming team in other tasks or cross-training activities, such as land preparation, planting, and irrigation when necessary. Guarantee proper mixing and application of pesticides on fields. Ensure compliance with all EPA, USDA, and local regulations, as well as all site HSE and quality protocols. Be able to assist in crops and site activities according to company needs. Qualifications Required: B.S. in Agriculture or related field. Understanding of all relevant agronomic/cultural practices in a tropical environment (IPM, pesticide applications). Knowledge of seed crop research, production, and quality assurance practices. Knowledge and experience in corn and soybean seed production. Knowledge of and ability to use computer software for data management, e.g., Microsoft Word, Excel, GIS mapping software, and other relevant software required to operate efficiently. Proficient in English: written and spoken. Desired: 3+ years of experience in agronomy roles and preferably in IPM (Integrated Pest Management). Ability to communicate and influence key stakeholders through challenges and opportunities; ability to facilitate solutions. Analytical skills; ability to demonstrate critical thinking across complex situations. Results-oriented with demonstrated ability to manage multiple projects/priorities simultaneously. 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: 2A #LI-ONSITE

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: Quality Control Scientist III Qualifications: Bachelor's Degree in Science. Minimum of 8 years of experience in direct pharmaceutical quality control areas and regulatory operations. 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 as well as understanding of how they are applied to regulatory compliance. Strong knowledge (according to related area). Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays. Responsibilities: Evaluate compendial changes from the different pharmacopeias. Generate trend reports of investigations based on the company's procedures. Evaluate global documents against site-specific procedures and update the site procedure accordingly. Draft technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports, based on corporate policies, SOPs, compendial guidelines, ICH, DEA, and FDA regulatory guidance. Generate required change requests for analytical documents and route documents for review and approval. Conduct laboratory event/out-of-specification/out-of-trend investigations and close them on time.

Job Description Title: Process Development Technician Employment Type: [Contract/Full-time/Onsite] Our client is seeking a Process Development Technician to support the development, optimization, and transfer of capable manufacturing processes into production. The ideal candidate will work closely with engineers, scientists, and cross-functional teams to test, document, and implement process improvements while maintaining and qualifying automated manufacturing equipment. This position requires technical proficiency, independence, and hands-on experience with automation and process development tools. Key Responsibilities Execute functional deliverables associated with Process Development and Technology Development projects. Assess process capabilities, identify opportunities for improvement, and implement innovative solutions for complex manufacturing processes. Collaborate with engineers and internal/external vendors to maintain, troubleshoot, calibrate, and qualify manufacturing equipment. Support prototype and material testing activities with minimal supervision. Collect, organize, and document testing data; prepare detailed reports to communicate results effectively. Apply technical knowledge to assist in the design and development of processes, procedures, tooling, and automation systems. Contribute technical expertise as part of a multidisciplinary project team. Work collaboratively with R&D, Process Development, Quality, Production, Regulatory, Equipment Engineering, Supply Chain, and Marketing functions to ensure project success. Identify technical issues and propose practical, effective solutions within area of responsibility. Research, evaluate, and support the implementation of new technologies within the functional area; stay informed of industry advancements and potential applications. Demonstrate familiarity with manufacturing technologies such as Laser Welding, Stringing, Staking, Heat Bonding, Injection Molding, Vision Systems, and automated equipment (PLC, servos, pneumatics, sensors, etc.). Collaborate effectively with engineers, scientists, and production personnel to achieve process development objectives. Provide training to others on new product processes, procedures, and equipment operation. Required Qualifications Associate degree or equivalent combination of education and relevant work experience. 1-2 years of related experience in process development, manufacturing, or engineering support. Proven experience collaborating effectively with manufacturing and process development engineers. Basic understanding of documentation requirements within regulated environments. Strong work ethic, positive attitude, and eagerness to learn new skills. Preferred Qualifications Experience in a manufacturing or regulated industry environment. Prior exposure to the medical device or life sciences industry. Strong technical writing and documentation skills. Ability to read and interpret electrical schematics and technical drawings. Interaction and Communication Demonstrate professionalism and sensitivity when exchanging ideas and technical information. Communicate complex concepts clearly, concisely, and logically to both technical and non-technical stakeholders. Quality System Responsibilities Maintain a strong commitment to patient safety and product quality through compliance with the Quality Policy and established procedures. Ensure adequate resources (personnel, tools, and equipment) are maintained to support Quality System compliance. Promote and uphold a work environment that fosters continuous quality improvement and adherence to regulatory standards. Join Our Client's Team This is an excellent opportunity to apply your technical expertise and contribute to innovative process solutions that improve product quality and manufacturing efficiency. If you are a motivated professional seeking growth in process development, apply through the job link provided with your updated resume for immediate consideration.

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.

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

For Scientist Services in the Process Development: Oral & Parenteral Mfg area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience in a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: Administrative, and according to business needs. Experience in: Design, and characterization of inspection/packaging process, process optimization strategies and/or troubleshooting. Implementation of system, equipment or process modifications, experiments, process and/or capital projects. Process Validation. Inspection Systems, Visual Inspection, and Machine Vision. Deep Learning, Statistical Analysis. Process Characterization. The Personality Part: Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work. Picture as well an environment of healthy competition, teamwork, being ethical and of using the scientific method in all ways possible. If you like how this sounds, then this might be the job for you. Bring it on! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) 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. WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?

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.

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

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.

Invent, implement and deploy state-of-the-art machine learning and/or specific domain industry algorithms and systems. Build AI Agents on top of the latest reasoning LLMs (both frontier and open source) and analyze agent trajectories. 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 etc. 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** Identify data science use cases and design scalable solutions that can be built as a feature of the product/service. Contributes to writing production model code. Work with Software Engineering teams to deploy them in production. Set up environment needed to run experiments for all projects. Set up distributed environments. Design and implement algorithms, train models, and deploy both to production to validate premises and achieve goals. Design and execute offline/online experiments and model performance testing. Work with large, complex data sets. Solve difficult, non-routine analysis problems, applying advanced analytical methods as needed. Address business/customer problems and questions using statistical and machine learning techniques to achieve business goals and KPI's. Come up with innovative solutions to address tradeoffs or challenges faced by team. Stay up-to date with research and trends regarding latest algorithms in ML or other industry/domain space. Perform research in emerging areas, which may include efficient neural network development including quantization, pruning, compression and neural architecture search, as well as novel differentiable compute primitives. 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: $97,500 to $199,500 per annum. May be eligible for bonus and equity. Oracle maintains broad salary ranges for its roles in order to account for variations in knowledge, skills, experience, market conditions and locations, as well as reflect Oracle's differing products, industries and lines of business. Candidates are typically placed into the range based on the preceding factors as well as internal peer equity. Oracle US offers a comprehensive benefits package which includes the following: 1. Medical, dental, and vision insurance, including expert medical opinion 2. Short term disability and long term disability 3. Life insurance and AD&D 4. Supplemental life insurance (Employee/Spouse/Child) 5. Health care and dependent care Flexible Spending Accounts 6. Pre-tax commuter and parking benefits 7. 401(k) Savings and Investment Plan with company match 8. Paid time off: Flexible Vacation is provided to all eligible employees assigned to a salaried (non-overtime eligible) position. Accrued Vacation is provided to all other employees eligible for vacation benefits. For employees working at least 35 hours per week, the vacation accrual rate is 13 days annually for the first three years of employment and 18 days annually for subsequent years of employment. Vacation accrual is prorated for employees working between 20 and 34 hours per week. Employees working fewer than 20 hours per week are not eligible for vacation. 9. 11 paid holidays 10. Paid sick leave: 72 hours of paid sick leave upon date of hire. Refreshes each calendar year. Unused balance will carry over each year up to a maximum cap of 112 hours. 11. Paid parental leave 12. Adoption assistance 13. Employee Stock Purchase Plan 14. Financial planning and group legal 15. Voluntary benefits including auto, homeowner and pet insurance The role will generally accept applications for at least three calendar days from the posting date or as long as the job remains posted. Career Level - IC3 **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.

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. In the IPM Research Associate 2 role, you will spend a large amount of your time in the field working with auto-propelled sprayers and backpacks, performing applications and assisting in diagnosing, identifying, and controlling weeds, diseases, pest problems, and other issues that may jeopardize the viability of the crops. Accountabilities: * Conduct or supervise pesticide spraying events according to the plan established by the IPM Research Associate 3. * Ensure that spraying equipment is in optimal operating condition. Inform the supervisor, Farming System Manager, or shop personnel of any failures. * Participate in regular maintenance of sprayers, including backpacks. This could include fluid checks, filter replacements, hose replacements, refueling, nozzle body replacements, and cleaning of the equipment. * Be accountable for technical aspects of the sprayer, such as calibrations, to perform effective pest control. * Train new hires to operate and maintain the sprayer equipment and its components. * Collaborate with the farming team in other tasks or cross-training activities, such as land preparation, planting, and irrigation when necessary. * Guarantee proper mixing and application of pesticides on fields. * Ensure compliance with all EPA, USDA, and local regulations, as well as all site HSE and quality protocols. * Be able to assist in crops and site activities according to company needs.

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.

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: Master's + 2 years of Scientific experience. Bachelor's + 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 7 months (1st Contract) Administrative Shift (weekends and overtime may also be required). Professional Service Contract

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

**Kelly Science & Clinical** is seeking **_Stability Chemist_** for a **contract** position at client in **Naguabo, Puerto Rico.** **Salary: $16.00 per/hour** **Schedule:** 1st shift & 2 nd shift, overtime hours and weekends may be required as necessary _In this role you'll be responsible for Performs chemical and physical analysis to stability products and is involved in the development and validation of analytical procedures following R&D guidelines_ **Responsibilities:** + Perform analytical testing on stability products and samples from other plants. + Assure that test activities are performed in accordance with written procedures + Prepares reports of analytical results. + Maintain informed the progress of test schedules. + Inform the Lab. Manager of supplies needs, standards, and instrument change parts. + Discuss with Lab. Manager of any failure in the analysis results + Manage and handling of hazardous waste in the generation area and coordinate the proper manage to the hazardous waste shed. + Records all analytical result in the analysis forms and laboratory notebooks following specifications, SOP'S and CGMP Guidelines. + Prepares all test solutions to be used in the laboratory, following appropriate specification or analitical procedures. + Maintains Laboratory area in an orderly and clean manner, always following the Current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (cGLP + Performs other specific stability work as assigned by the Lab Manager or designee. + Notifies Lab Manager when errors, incongruities or out specification conditions are observed on documentation and in the analytical data. **Qualifications:** + Bachelor's Degree in Chemistry and at least two years of experience in an analytical laboratory, or equivalent combination of education and experience. + Laboratory equipment: HPLC, GC, UV/VIS, pH meters, IR, RI,Karl Fisher Titrators, analytical balances, scientific calculators and others. + Spanish/English communication skills, both written and verbal. **For this position Kelly** ** ** **Science PR Offers!** + Exposure to a variety of career opportunities as a result of our expansive network of client companies + Career guides, information and tools to help you successfully position yourself throughout every stage of your career + Access to more than 3,000 online training courses through our Kelly Learning Center + Weekly pay + **Sick, Vacations &** **H** **olidays paid *** + **Christmas bonus*** + **_*_** **_Must comply with minimum established requirements to qualify._** **Apply to be a Stability** **_Chemist_** **today! ** **Recruiter: Lilly Abouomar** **\#SETTPuertoRico** As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

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** Drives and plans implementation of company policy for achieving business goals. Defines the bar for science practices, and helps teams achieve those goals. Identifies and mitigates risks across full set of systems, particularly at the intersection of business and engineering. Innovate AI and ML powered solutions (rich APIs, ML models and end to end services) with strategic ISVs and customers. Develop deep product intuition to influence future product roadmaps and drive decision making. Clearly articulate technical work to audiences of all levels and across multiple functional areas in both internal and external settings. Engage in forward looking research both internal and with academic institutions globally. Hires and mentors across the org. Perform an active role in team planning, review and retrospective events. Ensures experiments are ready for hand-off to Software Developers ship into production. 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: $139,400 to $291,800 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 - IC5 **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.