Chemist Jobs in Doral, FL

At Aldevron, we shape the future of medicine by advancing science in meaningful ways. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. We believe people are our most valuable asset. Whether this is your first step on a rewarding career path or are a seasoned professional ready to take your career to the next level, we hire the best from all backgrounds and experiences. Aldevron is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This is a third shift position with the hours being 8pm-6:30am Monday-Thursday. This position is part of the Quality and Regulatory Affairs department located in Fargo, ND, and will be onsite working a third-shift position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Team and report to the QC Supervisor. The QC Analyst I activities include but are not limited to developing and implementing testing, sampling, and inspection procedures on raw materials, equipment, in-process materials, and/or finished products to ensure that product specifications and company and regulatory requirements are met. In this role, you will have the opportunity to: Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Accurately generate and record raw data and analyze, as well as calculate, interpret, and trend the results while adhering to GMP Standards. Document and compare testing results against control/specification limits. The essential requirements of the job include: Experience working in a laboratory environment is preferred, not required. Bachelor's degree in a science related field is required. Knowledge of basic laboratory practices, including an in-depth knowledge of biological processes. It would be a plus if you also possess previous experience in: Working in a GMP or Clinical Laboratory Environment . Biotech-related Quality Control Laboratory. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to use hands, stand, sit, and bend. Ability to lift minimum of 50lbs. #LI-GC1 #LI-Onsite Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Title: Analytical Scientist About the Company Are you passionate about groundbreaking science and innovative healthcare solutions? We are a rapidly growing, well-funded biotech company with a hybrid platform that combines both innovative and specialty products. Our mission is to revolutionize the biotech industry by developing cutting-edge therapies and specialty products that address unmet medical needs. Job Description As an Analytical Scientist, you will play a crucial role in our research and development efforts. You will be responsible for developing and validating analytical methods from scratch, ensuring compliance with Good Manufacturing Practices (GMP), and utilizing advanced analytical techniques to support our projects. Key Responsibilities Develop and validate analytical methods independently. Perform routine and non-routine analysis using techniques such as High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV-Visible Spectroscopy (UV-Vis). Ensure all work complies with GMP regulations and standards. Troubleshoot and optimize analytical methods and instrumentation. Document and report analytical data accurately and promptly. Collaborate with cross-functional teams to support product development and quality control. Maintain and calibrate analytical instruments and equipment. Qualifications Bachelor's, Master's, or Ph.D. in Chemistry, Analytical Chemistry, or a related field with minimum 2 years GMP industry experience. Proven experience in developing analytical methods from scratch. Strong knowledge of GMP regulations and practices. Proficiency in using HPLC, MS, and UV-Vis techniques. Excellent problem-solving skills and attention to detail. Strong communication and teamwork abilities. Ability to work independently and manage multiple projects simultaneously. Benefits Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and inclusive enviornment

Barentz is a leading global life science and specialty performance ingredients distributor. We source branded specialty ingredients from leading manufacturers worldwide and our ingredient experts provide value-added technical support which includes pre-mixing, blending, ingredient formulation, and ingredient testing from our state-of-the-art, customized formulation centers and application laboratories. Established in 1953, Barentz has operations in more than 70 countries with a strong presence in Europe and North America and a rapidly growing network in Latin America and Asia-Pacific. With a turnover of $2.5 billion, the company employs over 2,600 people worldwide and serves more than 25,000 customers. For more information, visit: **************** About this role What will you do? The Lab Chemist is responsible for overall quality control of toll manufactured materials, testing, data management, sample oversight and guidance in a laboratory/office setting. Critical results Perform preventative and corrective maintenance on instrumentation as needed. • Responsible for updating QC documentation, recording analysis and calibration results. • General lab duties including clean-up, maintenance of equipment, track and order chemicals and disposables used in the lab. • Data processing and documentation using common software tools such as Excel, PowerPoint as well as internal systems • Support and lead by example Barentz's culture, values and fundamentals. • Participate in ongoing personal development opportunities including, but not limited to, formal as well as informal training. Responsibilities • Responsible for ensuring quality control measures are in place, understood and followed at all times. • Responsible for approving, generating and maintaining Certificates of Analysis and USMCA Certificates. • Data management - responsible for acquiring, validating, and maintaining data for the lab. • Provide sample department oversight and guidance as necessary. • Perform biological testing (counts for wet and dry biological products). • Set up and troubleshoot laboratory equipment and instrumentation required for tests, research, or process control. • Ensure safety procedures and housekeeping are maintained to protect yourself, co-workers, and the environment. • Perform, interpret, and record quality About You Education / Experience • University or College degree, preferably in Chemistry, Biology, Engineering, Etc., or equivalent combination of education and experience required. • Minimum 1 year of previous experience in a laboratory setting. Skills • Demonstrated organizational, complex problem-solving, and analytical skills. • Must be self-motivated, high energy, and engaging level of enthusiasm and positive outlook. • Effective written and verbal communication skills, and ability to adapt communication style to the audience as needed. • Software knowledge of Microsoft Office including Outlook, Word, Excel and Power Point. • Act legally and ethically in all professional relationships in adherence with Barentz' culture, values and fundamentals. • Fluent in English, a second language would be considered an asset Why Barentz? Barentz is a fast-growing organization with an open culture and short lines of communication. We offer you the freedom and opportunity to operate independently within the set objectives and frameworks. Barentz is looking for employees who are creative, independent, and energetic and like to take on challenges. You like to work in a dynamic and rapidly changing environment, which requires a high degree of flexibility. • Competitive benefits package • 401K with matching • An inspiring multinational company in a fast-growing and innovative business Interested? Looking for an exciting position? Then join us. We're investing in our future, starting by adding talented people (like you) to our rapidly expanding team. Please apply using our apply button below.

Arvida Labs is seeking an analytical technician to join our team and support our in-house hemp cannabinoid testing efforts in our processing facility located in Fort Lauderdale, FL . The successful candidate will be responsible for carrying out chemical analysis using an HPLC & GC. The technician will be responsible for maintaining and calibrating the equipment, as well as preparing samples and analyzing data. The technician will also be responsible for ensuring that all lab procedures are followed according to established protocols and safety guidelines, and will play a key role in helping to ensure the quality and safety of our hemp products. The technician will be responsible for managing the Certificate of Analysis (COA) process and ensure that all products comply with the FDA and 2018 Farm Bill regulations. This role involves managing COA databases, coordinating product sampling and testing, and monitoring regulatory compliance for Alpha Brands LLC and Arvida Labs products in our processing facility located in Fort Lauderdale, FL Responsibilities: Conduct cannabinoid analysis using Shimadzu LC-2030, Agilent 1200 HPLC, Agilent GC Daily operation and maintenance of LC and/or GC systems Generate quality system-compliant data Work with team members to execute analysis conforming to SOPs and to maintain good record keeping practices Identify instrument problems and perform routine troubleshooting Participate in and promote continuous improvement efforts within the laboratory Prepare samples for analysis Analyze data and report results Follow established lab procedures and safety guidelines Requirements: 1 or more years experience in an analytical laboratory preferred Experience with the operation and maintenance of chromatographic instrumentation preferred Experience operating analytical instrumentation, specifically Shimadzu LC-2030, Agilent 1200, and Agilent GC Strong problem-solving and analytical skills Ability to maintain and troubleshoot analytical equipment Laboratory experience performing method development, qualification, and validation activities Ability to work independently and as part of a team Attention to detail and strong organizational skills Motivated self starter Preferred Qualifications: Bachelor's degree in chemistry or related field Experience working in a cGMP environment Familiarity with regulatory guidelines for the hemp industry Strong verbal and written communication skills Benefits: Arvida Labs offers a competitive and comprehensive benefits package including health and paid time off Job Type: Full-time Pay: Starting at $20+ per hour Benefits: 401(k) 401(k) matching Dental insurance Flexible spending account Life insurance Paid time off Vision insurance Schedule: 8 hour shift Work Location: In person

The Amazon Web Services Professional Services (ProServe) team is seeking a skilled Delivery Consultant to join our team at Amazon Web Services (AWS). In this role, you'll work closely with customers to design, implement, and manage AWS solutions that meet their technical requirements and business objectives. You'll be a key player in driving customer success through their cloud journey, providing technical expertise and best practices throughout the project lifecycle. Possessing a deep understanding of AWS products and services, as a Delivery Consultant you will be proficient in architecting complex, scalable, and secure solutions tailored to meet the specific needs of each customer. You'll work closely with stakeholders to gather requirements, assess current infrastructure, and propose effective migration strategies to AWS. As trusted advisors to our customers, providing guidance on industry trends, emerging technologies, and innovative solutions, you will be responsible for leading the implementation process, ensuring adherence to best practices, optimizing performance, and managing risks throughout the project. The AWS Professional Services organization is a global team of experts that help customers realize their desired business outcomes when using the AWS Cloud. We work together with customer teams and the AWS Partner Network (APN) to execute enterprise cloud computing initiatives. Our team provides assistance through a collection of offerings which help customers achieve specific outcomes related to enterprise cloud adoption. We also deliver focused guidance through our global specialty practices, which cover a variety of solutions, technologies, and industries. Key job responsibilities As an experienced technology professional, you will be responsible for: - Designing, implementing, and building complex, scalable, and secure GenAI and ML applications and models built on AWS tailored to customer needs - Providing technical guidance and implementation support throughout project delivery, with a focus on using AWS AI/ML services - Collaborating with customer stakeholders to gather requirements and propose effective model training, building, and deployment strategies - Acting as a trusted advisor to customers on industry trends and emerging technologies - Sharing knowledge within the organization through mentoring, training, and creating reusable artifacts About the team About AWS: Diverse Experiences: AWS values diverse experiences. Even if you do not meet all of the preferred qualifications and skills listed in the job below, we encourage candidates to apply. If your career is just starting, hasn't followed a traditional path, or includes alternative experiences, don't let it stop you from applying. Why AWS? Amazon Web Services (AWS) is the world's most comprehensive and broadly adopted cloud platform. We pioneered cloud computing and never stopped innovating - that's why customers from the most successful startups to Global 500 companies trust our robust suite of products and services to power their businesses. Inclusive Team Culture - Here at AWS, it's in our nature to learn and be curious. Our employee-led affinity groups foster a culture of inclusion that empower us to be proud of our differences. Ongoing events and learning experiences, including our Conversations on Race and Ethnicity (CORE) and AmazeCon (diversity) conferences, inspire us to never stop embracing our uniqueness. Mentorship & Career Growth - We're continuously raising our performance bar as we strive to become Earth's Best Employer. That's why you'll find endless knowledge-sharing, mentorship and other career-advancing resources here to help you develop into a better-rounded professional. Work/Life Balance - We value work-life harmony. Achieving success at work should never come at the expense of sacrifices at home, which is why we strive for flexibility as part of our working culture. When we feel supported in the workplace and at home, there's nothing we can't achieve in the cloud. Basic Qualifications - Experience developing software code in one or more programming languages (java, python, etc.) - Bachelor of Science degree in Computer Science, or related technical, math, or scientific field (or equivalent experience) - 3+ years of cloud architecture and implementation - 2+ years of experience hosting and deploying GenAI/ML solutions (e.g., for training, fine tuning, and inferences) Preferred Qualifications - AWS Experience preferred, with a proficiency in a wide range of AWS services (e.g. SageMaker, Bedrock, EMR, S3, OpenSearch Service, Step Functions, Lambda, and EC2) - AWS Professional level certifications (e.g., Solutions Architect Professional, DevOps Engineer Professional) preferred - Experience with automation and scripting (e.g., Terraform, Python) - Knowledge of security and compliance standards (e.g., HIPAA, GDPR) - Strong communication skills with the ability to explain technical concepts to both technical and non-technical audiences - Masters or PhD degree in computer science, or related technical, math, or scientific field - Hands on experience with deep learning (e.g., CNN, RNN, LSTM, Transformer), machine learning, CV, GNN, or distributed training Amazon is committed to a diverse and inclusive workplace. Amazon is an equal opportunity employer and does not discriminate on the basis of race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. Los Angeles County applicants: Job duties for this position include: work safely and cooperatively with other employees, supervisors, and staff; adhere to standards of excellence despite stressful conditions; communicate effectively and respectfully with employees, supervisors, and staff to ensure exceptional customer service; and follow all federal, state, and local laws and Company policies. Criminal history may have a direct, adverse, and negative relationship with some of the material job duties of this position. These include the duties and responsibilities listed above, as well as the abilities to adhere to company policies, exercise sound judgment, effectively manage stress and work safely and respectfully with others, exhibit trustworthiness and professionalism, and safeguard business operations and the Company's reputation. Pursuant to the Los Angeles County Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit ********************************************************* for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $118,200/year in our lowest geographic market up to $204,300/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit ******************************************************* . This position will remain posted until filled. Applicants should apply via our internal or external career site.

We are seeking a dedicated and detail-oriented Associate Scientist to perform routine tests of finished products, stability samples, raw materials, and CV samples in a regulated laboratory environment. The ideal candidate will have experience with assays, chromatographic purity, content uniformity, particle size distribution, water determination, and other tests in compliance with in-house monographs and USP standards. Responsibilities * Perform routine tests of finished products, stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using various techniques, and water determination by KF. * Evaluate test results and decide on the acceptability of the samples based on the test results. * Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. * Maintain the laboratories with good housekeeping practices and in compliance with cGMP. * Ensure notebooks are reviewed promptly in accordance with SOPs. * Analyze and interpret results in both written and oral formats. * Assist in the training of new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. * Strong chemistry experience. * Experience in a regulated laboratory environment. * Familiarity with FDA and GMP standards. * Ability to maintain accurate lab notebooks and documentation. * Experience in analyzing and interpreting test results. * Knowledge of instrumentation software used in laboratories. Additional Skills & Qualifications * Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis OR Master's degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. * Ability to deal with problems involving several concrete variables in standardized situations. * Ability to carry out necessary computations and to draw and interpret graphs. Work Environment This role is based in a lab environment regulated by FDA and GMP standards. The laboratory is equipped with advanced analytical instrumentation and follows strict compliance with safety guidelines and good housekeeping practices. Pay and Benefits The pay range for this position is $28.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Pembroke Pines,FL. Application Deadline This position is anticipated to close on Apr 4, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Piper Companies is currently seeking an experienced Chemist to support a highly reputable Pharmaceutical company in Miami, FL. Responsibilities for the Chemist * Conduct analytical testing along with perform qualitative and qualitative chemical and physical testing * Operates laboratory equipment which includes balances, pH meters, HPLC, GC, UV, IR, Dissolution equipment * Draft proper laboratory records in accordance with cGMP and company SOPs and policies * Ensure materials meet compliance standards and specifications Qualifications for the Chemist * 1-5 years of experience in a regulated/cGMP environment * Previous experiences performing HPLC, GC, UV, IR is preferred * Current knowledge of SCM concept and principles * Bachelor's degree in related field Compensation for the Chemist * Salary Range: $50,000 - $75,000 * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays This job opens for applications on 3/24/2025. Applications for this job will be accepted for at least 30 days from the posting date." Keywords: Chemistry, Chemist, HPLC, GC, Gas Chromatography, Mass Spectrometry, Karl Fischer, cGMP, GMP, GLP, LIMS, Laboratory Technician, Quality Control, Pharmaceutical, SCM, pH, Dissolution, Disintegration, Compendial, #LI-JM1 #LI-ONSITE

Job Details Level: Experienced Position Type: Full Time Education Level: 4 Year Degree Salary Range: Undisclosed Travel Percentage: None Job Shift: Day Job Category: Pharmaceutical Description ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist II in Boca Raton, FL! The Chemist II will perform quality control testing of raw materials, in-process goods, and final products with minimal supervision. Uses knowledge of corporate policies to resolve routine problems. Qualifications * Perform quality control testing for raw materials, in-process and final product sample testing according to approved Standard Operating Procedures. * Complete testing documentation and data entry as required for procedures and tests performed. * Apply knowledge of analyzes issues and uses judgment to make decisions. * Utilize cGMP practices in documentation and execution of job functions. * Perform instrument calibration or qualification according to written procedures. * Write and revise SOPs and/or Validation Protocols. * Perform testing as needed to generate data for Validation and Special Projects. * Fulfill requests from management for assistance in other matters as needed. * Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines. * Review documentation on trained tasks as assigned by manager. Education Requirements: B.S. in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Experience Requirements: At least three years of experience in a laboratory setting. Work in a regulated environment (FDA, EPA, etc). is preferred, but not required. In addition to competitive compensation, we offer a comprehensive benefits package including: * 401K plan with employer match and immediate vesting * Medical, Vision, Life and Dental Insurance * Pet Insurance * Company paid STD and LTD * Company Paid Holidays * 3 Weeks' Paid Time Off (within the first year) * Tuition Assistance (after the first year) * Easily accessible to Tri-Rail * Company paid shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

Working Title: CHEMIST III - 42001526 Pay Plan: Career Service 42001526 Salary: $56,500.08 - $62,150.14 Total Compensation Estimator Tool CHEMIST III FLORIDA DEPARTMENT OF AGRICULTURE AND CONSUMER SERVICES DIVISION OF CONSUMER SERVICES BUREAU OF STANDARDS * OPEN COMPETIVE OPPORTUNITY * CONTACT: Matthew Christianson ************** MINIMUM REQUIREMENTS: A bachelor's degree from an accredited college or university with a major course of study in chemistry or biochemistry and two (2) years of professional chemical or biochemical experience; or A master's degree from an accredited college or university with a major course of study in chemistry or biochemistry and one (1) year of professional experience as described above; or A doctorate from an accredited college or university with a major course of study in chemistry or biochemistry. Certain positions within this class require individuals to meet specific federal or state regulations as identified by the employing agency. EDUCATIONAL NOTE: Graduates utilizing education attained in the United States to meet the minimum requirements of a position will not be appointed until verification of the applicable degree has been obtained. Foreign trained graduates utilizing a degree attained outside of the United States to meet the minimum requirements of a position must be prepared to provide a copy of a credential evaluation conducted by an Approved Credential Evaluation Agency. A list of approved agencies can be viewed at "Approved Credential Evaluation Agencies, Florida Department of Education." Approved Credential Evaluation Agencies (fldoe.org) * ATTENTION CANDIDATES* To be considered for a position with the Florida Department of Agriculture and Consumer Services: * All fields in the Candidate Profile must be completed (an attached resume is not a substitution for the information required on the candidate profile). * Work history, duties and responsibilities, hours worked, supervisor, and formal education fields, etc. must be filled out to determine qualifications for this position. * Responses to Qualifying Questions must be verifiable in the Candidate Profile. The Florida Department of Agriculture and Consumer Services values and supports employment of individuals with disabilities. Qualified individuals with disabilities are encouraged to apply. NOTES: Successful applicant must pass a background screening, including fingerprinting, as a condition of employment. JOB DUTIES: Analyze petroleum, antifreeze, and brake fluid products to verify compliance with the latest ASTM and/or State of Florida specifications using the appropriate methods and Standard Operating Procedures. Utilize the bureau's Laboratory Information Management System (LIMS) to aide in the collection, analysis, review and authorization of analytical results, quality control system and other associated laboratory information. Maintain, calibrate and operate analytical instrumentation with minimal supervision by senior chemists and/or laboratory manager, to facilitate accurate and timely sample analyses. Maintain inventory of supplies and parts required to ensure accurate and timely analyses of samples via assigned instrumentation. Under direction of laboratory manager, monitor the daily laboratory functions in assigned area and provide feedback to the laboratory manager to aide in efficient and accurate operation of the laboratory. This includes monitoring analyses, data recording, and reporting for all types of fuel samples and ensuring that all samples are properly analyzed according to the appropriate ASTM and/or screening methods. Reports substandard products in a timely manner to the laboratory manager. Be familiar with Florida law as it relates to fuel testing and specifications. Monitor the workflow of the laboratory and assist the manager with prioritizing the daily sample work load. Be thoroughly familiar with the latest test methods, procedures, equipment changes, and fuel specifications in order to act as an in-laboratory contact and technical resource for other Chemists and Technicians. Recommend and oversee maintenance, calibration, and repair of equipment. Assist in the training of any present or new employees. Maintain a safe, organized and clean environment throughout the areas of responsibility. Participate in and assist the Laboratory Manager in the monitoring and verfication of the locations implementation of the bureau's Quality Control Program. This includes proper and successful analyses of proficiency samples in addition to routine quality control procedures as dictated by the bureau's quality control plan. Assist other laboratories and management on needed specifications, ordering and set up of equipment. This will include writing of specifications and research to determine the maximum efficiency and requirements to perform a given task and to meet appropriate ASTM methods. Assist supervisor as requested to conduct daily work and fill in as the person-in-charge in their absence. This will require being familiar with the over all operation of the laboratory and coordinating laboratory operations with the Laboratory Administrator or designate in the absence of the laboratory manager. Perform other duties such as, but not limited to, administrative paperwork, shipping/receiving, sample custody and other non-technical duties as required by management. The Benefits of Working for the State of Florida Working for the State of Florida is more than a paycheck. The State's total compensation package for employees features a highly competitive set of employee benefits including: * Annual and Sick Leave benefits; * Nine paid holidays and one Personal holiday each year; * State Group Insurance coverage options, including health, life, dental, vision and other supplemental insurance options; * Retirement plan options, including employer contributions (For more information, please visit *************** * Flexible Spending Accounts; * Tuition waivers; * And more! For a complete list of benefits, visit ***************************** For an estimate of the total compensation package for this position, please visit the "Total Compensation Estimator Tool" located above under the "Posting Closing Date." SPECIAL NOTES: The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (***************. Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. VETERANS' PREFERENCE. Pursuant to Chapter 295, Florida Statutes, candidates eligible for Veterans' Preference will receive preference in employment for Career Service vacancies and are encouraged to apply. Certain service members may be eligible to receive waivers for postsecondary educational requirements. Candidates claiming Veterans' Preference must attach supporting documentation with each submission that includes character of service (for example, DD Form 214 Member Copy #4) along with any other documentation as required by Rule 55A-7, Florida Administrative Code. Veterans' Preference documentation requirements are available by clicking here. All documentation is due by the close of the vacancy announcement. Location: POMPANO BEACH, FL, US, 33069 POMPANO BEACH, FL, US, 33060 POMPANO BEACH, FL, US, 33068 POMPANO BEACH, FL, US, 33064 POMPANO BEACH, FL, US, 33062 POMPANO BEACH, FL, US, 33073

Job Details ADMA Biologics FL - Boca Raton, FL Full Time 4 Year DegreeDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist I, Bioanalytics in Boca Raton, Florida! The Chemist I, Bioanalytics performs quality control testing of raw materials, in-process, and final products; following general instructions on routine work and detailed instructions on new assignments. Qualifications Perform quality control chemistry and/or Immunoassays for raw materials, in-process, and final products according to approved Standard Operating Procedures (SOP's). Perform instrument calibration or qualification according to written procedures. Perform testing as needed to generate data for method validations and other special projects, following general instructions on routine work and detailed instructions on new assignments. Fulfill requests from management for assistance in other matters as needed. Accountable for following Standard Operating Procedures (SOP's) and adhering to cGMP guidelines. Utilize cGMP practices in documentation and execution of job functions. Review documentation on trained tasks as assigned by manager. Education Requirements: B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline is required. Experience Requirements: This position requires experience in a laboratory setting. Work experience in a regulated environment (FDA, EPA, etc.) is preferred. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting Medical, Vision, Life and Dental Insurance Pet Insurance Company paid STD and LTD Company Paid Holidays 3 Weeks' Paid Time Off (within the first year) Tuition Assistance (after the first year) Easily accessible to Tri-Rail Free shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

JOB QUALIFICATIONS: BS or MS in Chemistry with a minimum of 5+ years of pharmaceutical experience or equivalent combination of education and experience with testing Finished Products and Raw Materials Strong technical skills in HPLC, and GC required, including theoretical understanding of technique Demonstrated use of the analytical techniques in support of product development activities Comprehensive knowledge of current Good Manufacturing Practices (cGMP), FDA Guidance, and ICH Guidelines Familiar with requirements of various pharmacopeias (USP, EP, JP) and basic regulatory requirements and applies knowledge appropriately to activities Ability to successfully direct or manage various analytical projects and to contribute / facilitate team investigations Demonstrated ability to work well in a fast-paced setting. Demonstrate ability to take concepts and produce laboratory results Self-starter with a strong work ethic. Must be able to operate with minimal supervision Demonstrated ability to train and/or mentor new employees Excellent written and verbal communication skills. Problem solving skills POSITION RESPONSIBILITIES: Creates and executes new methods or procedures through appropriate research, development and validation stages Creates and executes project protocols and reports to support new product research and development as assigned by management Performs testing on raw material, in-process, & finished good samples when applicable Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Supports pilot scale manufacturing to scale up of new manufacturing processes Responsible for analytical method validation/verification/transfer from R&D or client site to QC when assigned Interface with contract labs regarding QC sample handling and reporting Evaluate and interpret the test results and other related technical documentation Document writing includes, but not limited to, preparation and review of SOPs, STMs, failure investigation and process deviation report, stability study protocol/report, method transfer protocol/report, method validation/verification protocol/report, instrument qualification protocol/report and analytical technical transfer protocol/report when assigned Other duties may be assigned as deemed appropriate by management PHYSICAL REQUIREMENTS: Employees are required to wear eye protection and lab coats while in the lab area Work safely and follow all OSHA regulations and company safety policies and procedures Ability to frequently lift and/or move up to 25 lb Ability to occasionally lift and/or move up to 35 lb Ability to regularly stand, sit and walk to perform task

Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that impacts MISSION! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset - Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Ensures incoming biological samples are processed and triaged maintaining chain of custody. Performs and interprets a variety of specialized tests and strains, detection, and identification of pathogenic microorganisms. Prepares written and oral reports, answers questions, troubleshoot and makes recommendations to the supervisor for inclusion in comprehensive reports on test findings. Maintains and operates equipment including performing calibrations, adjustments, and to operate equipment and instruments properly and in a safe manner. Participates in cross training related to bioterrorism and other public health emergencies. Additionally, will be responsible for maintaining knowledge and skills related to position and program and to carry out all procedures in accordance with proper handling and storage of various biological materials. Must be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. Kindly be aware that drug screening is a mandatory condition of employment for this position. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable. This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application. #LI-OnSite A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status.

**Associate Scientist II** Kelly Science & Clinical is seeking an **Associate Scientist II** for a direct-hire position at a growing client in the Miami/Fort Lauderdale, FL area. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. **Salary/Pay Rate/Compensation:** $65,000-$85,000/year **Overview:** This client is an industry-leading pharmaceutical company offering room for growth within the organization, a full relocation package, and 10% bonus potential. **Schedule:** Monday-Friday 4pm-12am **Responsibilities:** + Conduct laboratory activities with limited supervision, including analyzing raw materials, in-process materials, and finished pharmaceutical products for quality, safety, purity, strength, and identity, following applicable methods and relevant guidelines (cGMP, EH&S, FDA, and other governing bodies). + Independently set up and operate lab equipment, prepare reagents, solvents, and solutions for analytical and formulation activities. + Maintain accurate records in lab notebooks for all testing performed. + Process analytical data using lab equipment such as HPLC/UPLC and enter data into spreadsheets; conduct routine calculations. + Support the manufacture of inhalation drug products and prepare samples for blend uniformity. + Perform equipment qualification and calibrations as directed. + Execute approved method transfer protocols. + Assist in training other scientists and team members. + Participate in project activities, support project timelines, and proactively contribute to meeting team objectives. + Communicate effectively with team members and maintain effective relationships. + Conduct lab work in accordance with SOPs and STPs and follow corporate safety rules and procedures. + Comply with all corporate guidelines and policies. **Qualifications:** + **BSc in Chemistry, Pharmacy, or related fields** with at least **3+ years** of experience in Pharmaceutical R&D, or **MSc in Chemistry, Pharmacy, or related fields** with **1+ years** of experience in Pharmaceutical R&D. + **Minimum 2 years** industry experience with **HPLC method development and Empower software.** + Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment. + Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting, including experience with analytical and/or process equipment such as HPLC, IR/FTIR, UV-Vis, AA, powder blenders, etc. + Knowledge and understanding of FDA cGMP requirements as it applies to the pharmaceutical industry. **What happens next:** Once you apply, you'll proceed to 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 our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. 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.

Job Details Miramar, FL $75,000.00 - $85,000.00 Salary/year AnyDescription About Us: Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide. Job Summary: Laboratory position which involves development and validation of analytical methodology in support to the research projects involving testing of pharmaceutical components and/or drug products. This position also involves designing and completion experiments and providing scientifically sound recommendations based on the data obtained. Key Responsibilities: Developing new analytical methods using innovative solutions for actives, excipients, drug release, residual solvents and to support product development. Validating analytical methodologies following ICH guidance Executing complex experiments in support to R&D for development and validation of process under minimum supervision. Ability to identify creative and innovative solutions of non routine analytical tasks Improves analytical applications by implementing new analytical techniques Clearly interpret problems, make scientific judgment based on outcome of the obtained data and take appropriate actions to resolve the issues. Writing/reviewing protocols, reports, SOP's, specifications & test procedures. Compiling necessary documentation to support regulatory submissions such as Abbreviated New Drug Applications (ANDAs) or New Drug Applications (NDA), as required. Adhering to laboratory SOP guidelines, GMP requirements and safety rules. Maintaining analytical instrumentation through the proper performance and/or maintenance as required. Train junior scientists and QC chemists as necessary. Demonstration ability of problem solving and offer necessary recommendations. Works as a member of a team to achieve all outcomes Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements. Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion All other relevant duties as assigned Qualifications Education Bachelor's degree (B.S.) in chemistry or related field Master's degree (M.S.) or Ph.D. Experience At least five (5) years experience in pharmaceutical laboratory (B.S) At least two (2) years laboratory experience (M.S.) Knowledge, Skills and Abilities Proficiency in using analytical equipments such as UV/Visible and Infrared spectrophotometers, automatic titrators, pH potentiometers, dissolution apparatus, HPLC, GC, GC/MS, LC/MS/MS and other techniques as needed. Strong verbal and written communication skills, interpretation of experimental results, technical protocols and reports writing. Broad knowledge of methods development in support Active Pharmaceutical Ingredients, Intermediates, excipients and drug products. Ability to clearly indentify problems and take appropriate actions based on available information Organization skills and ability to plan and prioritize work to meet deadlines. Proficiency in the use of computer hardware, software and databases such as Word processing software, MS office, TrackWise, Empower, or other applicable to analytical instrumentation software. Demonstrate accuracy and thoroughness of work and adhere to high quality standards related to cGMPs. Benefits: Aveva Drug Delivery Systems and DifGen Pharmaceuticals provides a comprehensive benefits plan Medical/Dental/Vision Insurance Paid Time Off 401k with employer match Paid Holidays and Floating Holiday Equal Opportunity Employer

tdp The Sun Orchard Innovation team plays a critical role in driving company growth by developing and optimizing products and processes that deliver customer and consumer satisfaction while maximizing profitability./p pThe Product Scientist position will lead and support projects focused on the development and commercialization of new products and processes, and the enhancing of existing product and process efficiencies. The position will also collaborate with cross-functional team members and external partners to deliver high-quality, safe, and cost-effective products that deliver against customer and consumer needs. The position will involve working in laboratory, test kitchen and food manufacturing environments./p pLOCATION: Boca Raton, FL/p ul li Engage directly in product formulations and calculations, laboratory bench experiments and prototype development, sensory evaluations, process integration, shelf-life validations, and technical specifications development, through collaboration with a cross-functional team, from concept through commercialization and launch./li li Manages multiple projects involving product and process development and optimization, including manufacturing trials and scale-up./li li Represent the Innovation department in teams formed across company functions, including but not limited to Food Safety amp; Quality Assurance, Operations, Procurement, Finance and Sales./li li Evaluate ingredients and suppliers for suitability in new product applications, or as potential substitutes for existing products./li li Develop product prototypes that meet organoleptic, nutritional and cost targets./li li Conduct shelf-life studies to determine the stability and performance of finished products and raw ingredients through analytical and sensory testing./li li Conduct and participate in sensory tests and tastings, supports external consumer testing, and manages 3rd party laboratory testing./li li Ensure compliance of ingredients and products with applicable regulatory nutritional and labeling requirements./li li Partner with the Sales, Procurement, Operations and Finance teams to assess and determine the financial viability of assigned initiatives./li li Support the scale-up and optimization of new and existing products by creating production formulations, blending instructions, and process guidelines in collaboration./li li Develop recipes and product applications for food shows, sales, and media content./li li Write detailed amp; accurate reports of analyses, experiments, shelf-life studies, specifications, and standard operating procedures./li li Effectively communicates activity and project updates./li li Serve as a subject matter expert for internal and customer presentations and at industry events./li li Provide training to team members to develop product and applications expertise./li li Demonstrates adaptability and resourcefulness in responding to changing priorities./li li Excellent written, verbal, listening and presentation skills/li li Ability to effectively communicate and engage with fellow scientists, cross-functionally with Sales, Procurement, Operations, Finance and other associates, and externally with customers and suppliers./li li Self-starter, collaborative, with strong problem-solving and project management skills, with an ability to thrive in a fast-paced, dynamic environment./li li Domestic and international travel as required for project management and support./li li Other duties as assigned./li /ul p /p /td

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet. The University of Miami/UHealth Department of SCCC - Human Genetics has an exciting opportunity for a Full Time Associate Scientist to work at the UHealth Medical Campus in Miami, FL CORE JOB SUMMARY The Associate Scientist supports the University's research goals and objectives by performing laboratory experiments in his/her areas of interest, expertise, or assignment. Moreover, the incumbent performs various analytical procedures involving method development and application development and synthesis. This position will report to Dr. Reinberg's lab. CORE JOB FUNCTIONS 1. Contributes to basic and applied research activities including authorship of scientific publications, technical and agency reports, and patent preparations. 2. Publishes in refereed journals in collaboration with department leadership or independently. 3. Supervises research employees and non-exempt staff. 4. Writes extramural proposals with approval of senior managing staff. 5. Creates and conducts experiments and analyzes results. 6. Works with other researchers to use and develop end products. 7. Provides ready access to all experimental data for the faculty researchers, supervisors, and other relevant staff. 8. Requests or acquires equipment and supplies for assigned project(s). 9. Applies for grants to continue research and prepares materials for submission to granting agencies and foundations. 10. Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. CORE QUALIFICATIONS Education: Doctorate degree - Philosophy (PhD) required Experience: Minimum 5 years of relevant experience required Certification and Licensing: Refer to department description for applicable certification requirements Knowledge, Skills and Abilities: Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands. Teamwork: Ability to work collaboratively with others and contribute to a team environment. Technical Proficiency: Skilled in using office software, technology, and relevant computer applications. Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders. #LI-YC1 The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for. The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information. Job Status: Full time Employee Type: Staff Pay Grade: A11

Description As the Product Development Category Analyst, you are accountable for the analytics for the category performance, campaigns, planograms & market analysis. In addition to analytics, the role also is responsible to project manage the successful flow of new product development through the stage gate Product Development process. Reporting to the Head Non-Core Product Development, the Product Development Category Analyst is a key member of the Product Development team and is responsible for supporting continuous improvement in a fast-paced and demanding production & innovation environment. The scope of category analytics covers the Wild Fork business units in both the US & Canadian markets. Additionally, you will maintain positive relationships with Production Operations, Logistics, Supply Chain & Marketing as well as your vendor community and other internal and external contacts. You have a customer-centric approach and are comfortable flexing between regulatory execution and innovation/ product development. This is an in-office role, Monday - Friday, based in Doral, FL. Principal Responsibilities: Provide daily, week end & period end data analytics for all Categories for our store locations & website Provide weekly data analytics for Campaign performance Provide periodic data analytics for planogram and merchandising performance Monthly review of market and competitive conditions with view of competitive advantages and gaps Project manage the movement of new product through the Product Development stage-gate process Support the team in process building and continuous process improvement Work closely with the store operations team for weekly store visits to ensure successful execution of planogram & merchandising changes for new product introductions & campaigns Knowledge, Skills and Experience: 3 years experience in analytics in Food Service or Retail sector (Food retail preferred) Deep understanding of trends in retail & food service environments Prior Food Service or Retail experience an asset Prior start up experience an asset, in Tech or Food-Tech environments Passion for Food & obsession for quality Strong command of various analytical tools in MS Office (Excel/ Smart Sheets as example) Support in Process & Continuous Improvement through the Product Development Function Establishes trust and inspires others Demonstrated effectiveness navigating cross divisional boundaries Command of negotiation and relationship building skills Makes effective organization and people decisions in a manner consistent with Wild Fork Foods values and ethics. Champions the organization and advocates solutions in the overall Company's best interest. Uses business knowledge, innovative thinking, and sound judgment in the solution of problems or the pursuit of business opportunities. Consolidates information from various sources including feedback from others to reach sound decisions. Considers the ultimate impact of decisions and actions on internal and external customers. Lean Six Sigma training or black belt certification is an asset Exceptional written, verbal communication & systems skills (including MS Office) EOE, including disability/vets.

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet. The University of Miami/UHealth Department of SCCC - Human Genetics has an exciting opportunity for a Full Time Associate Scientist to work at the UHealth Medical Campus in Miami, FL CORE JOB SUMMARY The Associate Scientist supports the University's research goals and objectives by performing laboratory experiments in his/her areas of interest, expertise, or assignment. Moreover, the incumbent performs various analytical procedures involving method development and application development and synthesis. This position will report to Dr. Reinberg's lab. CORE JOB FUNCTIONS 1. Contributes to basic and applied research activities including authorship of scientific publications, technical and agency reports, and patent preparations. 2. Publishes in refereed journals in collaboration with department leadership or independently. 3. Supervises research employees and non-exempt staff. 4. Writes extramural proposals with approval of senior managing staff. 5. Creates and conducts experiments and analyzes results. 6. Works with other researchers to use and develop end products. 7. Provides ready access to all experimental data for the faculty researchers, supervisors, and other relevant staff. 8. Requests or acquires equipment and supplies for assigned project(s). 9. Applies for grants to continue research and prepares materials for submission to granting agencies and foundations. 10. Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. CORE QUALIFICATIONS Education: Doctorate degree - Philosophy (PhD) required Experience: Minimum 5 years of relevant experience required Certification and Licensing: Refer to department description for applicable certification requirements Knowledge, Skills and Abilities: * Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands. * Teamwork: Ability to work collaboratively with others and contribute to a team environment. * Technical Proficiency: Skilled in using office software, technology, and relevant computer applications. * Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders. #LI-YC1 The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for. The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information. Job Status: Full time Employee Type: Staff Pay Grade: A11

Visa is a world leader in payments and technology, with over 259 billion payments transactions flowing safely between consumers, merchants, financial institutions, and government entities in more than 200 countries and territories each year. Our mission is to connect the world through the most innovative, convenient, reliable, and secure payments network, enabling individuals, businesses, and economies to thrive while driven by a common purpose - to uplift everyone, everywhere by being the best way to pay and be paid. Make an impact with a purpose-driven industry leader. Join us today and experience Life at Visa. Job Description Visa Consulting and Analytics, VCA, is the externally facing strategy consulting group of Visa. We draw on our expertise in strategy consulting, data analytics, and pragmatic industry experience to develop fact-based recommendations to improve client performance. Our clients span the continuum of companies that participate in the payment card industry, to include financial institutions, merchants, fintechs, acquirers, and payment processors. As the Director, VCA, Tech Advisory Practice, you will be the General Manager responsible for growing a critical pillar focused on Technology Strategy and Implementation. Technology Strategy enable clients to assess their current technical architecture, envision their future state, and clarify the roadmap to long term success. Technology Implementation services build on the success of Technology Strategy engagements, equipping clients with the dev teams needed to bring their vision to life. You will be ultimately responsible for achieving quarterly and annual revenue targets. You will ideate, develop, price, sell, and oversee the delivery of technology strategy and technology implementation services. You are a natural in front of clients, including SVP plus leadership stakeholders, and can use that skill set to tailor new and existing services to meet their needs. You are excited by the prospect of measuring your success through attainment of revenue growth targets. You are sufficiently expert conversant in technical architecture, ideally within the context of banking and payments, to scope development efforts effectively with dev resources. The successful candidate will be a seasoned consultant, entrepreneur, and general manager specialist who can partner across Visa client types. The role will identify common client needs, develop offerings that leverage Visa extensive capabilities, subject matter expertise, and third-party partners, price the solution appropriately, pitch the client, close the sale, and oversee delivery. The role will collaborate with a host of internal and external partners to develop, sell, and deliver solutions. This person will articulate the value proposition to clients, customize the offerings as needed to address client feedback, and ultimately close the sale. The team member will be able to flex across various client stakeholders, to include those in digital, data sciences, marketing, CRM, payments, and fraud and risk. For clarity, this leader will not be involved in the day to day of tech dev with clients. Rather, this leader will engage at more of an executive steering committee level to ensure that delivery teams are scoped appropriately and are delivering against client goals and objectives, making any necessary course corrections. This is a hybrid position. Expectation of days in office will be confirmed by your hiring manager. Qualifications Basic Qualification -10 or more years of work experience with a Bachelor's Degree or at least 8 years of work experience with an Advanced Degree (e.g. Masters/ MBA/JD/MD) or at least 3 years of work experience with a PhD -Educational background in Computer Science or Engineering. An MBA is a plus. Preferred Qualification -12 or more years of work experience with a Bachelor's Degree or 8-10 years of experience with an Advanced Degree (e.g. Masters, MBA, JD, MD) or 6+ years of work experience with a PhD -Consultative Selling involves uncovering client needs, challenges, and opportunities with respect to managed services. -Presenting solutions to clients that address their needs, quantifying the value and differentiation of the solution for clients, and identifying the client decision making stakeholders and processes are key aspects. -Offering Development requires identifying white space challenges and opportunities across client sets. -It involves developing bespoke and scalable products leveraging Visa assets and, as needed, third party partner assets. -Additionally, identifying third party partners who can complement and supplement solution sets, defining the value proposition, and developing sales collateral, including sales presentations and tear sheets, are crucial. -Developing a product pricing strategy and ensuring product profitability are also essential. -Solution Delivery demands strong project and program management skills and demonstrated experience in delivering flawlessly. -Customer Centricity emphasizes a strong executive presence, the ability to speak to technical and non technical aspects of solutions, and comfort in working across the spectrum of Visa clients, from institutional banking relationships to fintech startups. -Industry Knowledge involves maintaining a deep understanding of the competitive environment for Visa solutions and leveraging that understanding to shape solutions that differentiate Visa. -Communications require demonstrating executive presence in leading conversations with clients, communicating across functional stakeholders of varying levels and technical expertise, and incentivizing cross functional teamwork by aligning cross functional incentives. Strong diplomacy skills and fostering goodwill between different groups are necessary, along with coaching teams. -People Leadership is demonstrated by the ability to structure a team and lead high-performers to even higher performance levels. General Accountabilities -Perform technical product management functions including creating functional specifications, managing roadmaps, handling issue and risk management, and defining success criteria for pilots. Collaborate extensively with internal VISA groups and external partners to ensure requirements are clearly understood. -Interface with various technology teams and business stakeholders to identify requirements, convert them into functional specifications, prioritize tasks, and drive execution. -Act as the customer advocate within the engineering team, demonstrating a deep passion for satisfying customer needs and influencing design and priorities appropriately. -Define milestones for each group to ensure delivery dates are met without causing delays for planned pilots. -Represent the product team in engineering meetings, ensuring there are no roadblocks and eliminating any external dependencies. -Partner with Product Management and Business Teams to define the product pipeline and different phases of the pilot. -Own the roadmap in collaboration with the product and engineering teams. -Work closely with engineers and contribute to the development of design artifacts and Quality Assurance test plans. -Plan and conduct User Acceptance Testing with key stakeholders, organize bug bashes, and hackathons. -Develop clear and concise product documentation to outline pilot requirements and technical architecture. -Provide weekly updates and highlight any technical issues to executive management. -Manage multiple projects simultaneously and ensure on time, high quality delivery. -Preferred 10 or more years of relevant experience in technical product or program management. -Excellent analytical and problem solving abilities, ability to use hard data and metrics to support assumptions and evaluate outcomes. -Reputation as a collaborative thought partner and business leader, with the ability to organize and motivate work across multiple team boundaries. -Ability to fully understand technical architecture, APIs, and overall system design. -Management skills with demonstrated ability to facilitate product planning, development, and user acceptance testing efforts. -Excellent communication and presentation skills at all organizational levels. -Experience working with agile lifecycle and tracking and process management tools such as Rally and JIRA. Additional Information Work Hours: Varies upon the needs of the department. Travel Requirements: This position requires travel 5-10% of the time. Mental/Physical Requirements: This position will be performed in an office setting. The position will require the incumbent to sit and stand at a desk, communicate in person and by telephone, frequently operate standard office equipment, such as telephones and computers. Visa is an EEO Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status. Visa will also consider for employment qualified applicants with criminal histories in a manner consistent with EEOC guidelines and applicable local law. Visa will consider for employment qualified applicants with criminal histories in a manner consistent with applicable local law, including the requirements of Article 49 of the San Francisco Police Code. U.S. APPLICANTS ONLY: The estimated salary range for a new hire into this position is $143,700 to per $208,600 year, which may include potential sales incentive payments (if applicable). Salary may vary depending on job-related factors which may include knowledge, skills, experience, and location. In addition, this position may be eligible for bonus and equity. Visa has a comprehensive benefits package for which this position may be eligible that includes Medical, Dental, Vision, 401 (k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness Program.