Chemist Jobs in Tamarac, FL

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.

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

Job Title: Associate Scientist Type: Contract Shifts: 1st Shift 9:00am to 6:00pm or 2nd Shift: 3:00 pm to 11:00 pm Pay Rate: $26/h to $30/h DOE and shift. Join our team as an Associate Scientist Analytical in Coral Springs, FL, where you'll conduct fundamental laboratory activities following Standard Operating Procedures (SOPs). You'll ensure that quality standards are upheld and document activities in accordance with cGMP regulations. This role offers the chance to contribute to pharmaceutical product development while adhering to stringent regulatory standards. Essential Duties and Responsibilities: Perform fundamental laboratory activities, including the analysis of raw materials, in-process materials, and finished pharmaceutical products to ensure quality, safety, purity, strength, and identity using appropriate methods. Adhere to cGMP, EH&S, and other relevant guidelines set by regulatory bodies such as the FDA. Operate laboratory equipment, prepare reagents, solvents, and solutions for analytical and formulation activities. Maintain precise electronic and paper-based records of all testing conducted and review analytical data. Process analytical data using lab equipment such as HPLC/UPLC, input data into spreadsheets, and perform routine calculations. Provide support for the production of Dry Powder Inhaler and Metered Dose Inhaler drug products. Participate in project team activities, contribute to meeting project timelines, and actively contribute to achieving team objectives. Cultivate effective relationships with team members and adhere to SOPs, corporate safety protocols, and policies. Education & Experience: Bachelor's degree preferably in chemistry, pharmacy, or related fields. Analytical Experience (Industrial or academic) Familiarity with analytical methodology, laboratory practices, wet-chemistry, and laboratory equipment such as HPLC/UPLC, UV-Vis, GC, IR, etc. Proficiency in computer applications Strong written and verbal communication skills in English. ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees. At ttg, “We believe in making a difference One Person at a Time,” ttg OPT IND2

Essential Duties and Responsibilities NOTE: This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US without visa sponsorship or visa transfer. Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in the training of other scientists. Perform other tasks as assigned. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate safety rules and procedures Comply with all Corporate guidelines and policies Qualification Requirements Must be eligible to work in the United States without any visa sponsorship or visa transfer requirements. Not open to H1B holders. Must be willing to work 2nd shift. Must be able to work On-site in Weston, FL. (West of Ft. Lauderdale) Must have at least 2-3 years of experience of pharmaceutical industry R&D experience Must have strong HPLC and Empower experience. BSc in Chemistry, Pharmacy or related fields with 3-6 years of experience MSc in Chemistry, Pharmacy or related fields with 2+ years of experience in Pharmaceutical R&D Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment. Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting. Specific experience with analytical and/or process equipment used in laboratories such as HPLC, IR/FTIR, UV-Vis AA, powder blender etc. Knowledge and understanding of the FDA cGMP requirements as it applies to the Pharmaceutical industry. Effective English written and oral communication skills. Ability to write short technical documents such as memos, laboratory investigations, protocols and reports.

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 based solution (AWS or equivalent), system, network and operating system experience - 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.

Actalent is Hiring a Team of Associate Scientists!!Job Description 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 (%20actalentaccommodation@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 3/31/2025. 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 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, Bioanalytics in Boca Raton, FL! The Chemist II, Bioanalytics will perform quality control testing of raw materials, in-process, and final products with minimal supervision, with a concentration in immunoassays. Uses knowledge of corporate policies to resolve routine problems and ensure compliance with procedures. Qualifications ESSENTIALS OF THE JOB: * Perform quality control testing for raw materials, in-process, and final product samples, according to approved Standard Operating Procedures (SOPs) and cGMP guidelines * Complete testing documentation and data entry as required for procedures and tests performed * Apply knowledge of analyzing issues and uses judgment to make decisions * Knowledge of immunoassays, specifically plate-based assays and ELISAs * 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 participate in validation protocol execution, as needed * Perform testing, as needed, to generate data for qualification/validation and special projects * Fulfill requests from management for assistance in other matters, as needed * Accountable for following SOPs and adhering to cGMP guidelines * Review documentation on trained tasks as assigned by QC management * Use technical and scientific knowledge to recommend solutions to problems as directed by QC management * Mentor junior analysts and provide training as requested on QC assays Education Requirements: Bachelor's degree in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Experience Requirements: At least three years of experience performing chemical/biochemical testing or developing immunoassays. Work in a regulated environment (FDA, EPA, etc.) is highly 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 * 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.

Job Details Experienced ADMA Biologics FL - Boca Raton, FL Full Time 4 Year Degree None PharmaceuticalDescription 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, Bioanalytics in Boca Raton, FL! The Chemist II, Bioanalytics will perform quality control testing of raw materials, in-process, and final products with minimal supervision, with a concentration in immunoassays. Uses knowledge of corporate policies to resolve routine problems and ensure compliance with procedures. Qualifications ESSENTIALS OF THE JOB: Perform quality control testing for raw materials, in-process, and final product samples, according to approved Standard Operating Procedures (SOPs) and cGMP guidelines Complete testing documentation and data entry as required for procedures and tests performed Apply knowledge of analyzing issues and uses judgment to make decisions Knowledge of immunoassays, specifically plate-based assays and ELISAs 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 participate in validation protocol execution, as needed Perform testing, as needed, to generate data for qualification/validation and special projects Fulfill requests from management for assistance in other matters, as needed Accountable for following SOPs and adhering to cGMP guidelines Review documentation on trained tasks as assigned by QC management Use technical and scientific knowledge to recommend solutions to problems as directed by QC management Mentor junior analysts and provide training as requested on QC assays Education Requirements: Bachelor's degree in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Experience Requirements: At least three years of experience performing chemical/biochemical testing or developing immunoassays. Work in a regulated environment (FDA, EPA, etc.) is highly 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 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.

**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.

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.

JOB QUALIFICATIONS: BS or MS in Chemistry or equivalent combination of education and experience 1-3 years of industry experience Demonstrated use of the analytical techniques in support of product development activities Understanding of the fundamentals of analytical chemistry and instrumentation Knowledge of current Good Manufacturing Practices (cGMP) Demonstrated ability to work well in a fast-paced setting with excellent organizational skills Excellent written and verbal communication skills, problem solving skills and basic computer skills POSITION RESPONSIBILITIES: Performs testing on raw material, in-process & finished product samples Executes method transfer, verification and validation protocols Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Evaluate and interpret the test results and other related technical documentation Writes methods and reports Performs routine lab maintenance including equipment calibration, glassware cleaning, chemical and supplies inventory management (includes ordering, cleaning and organization) 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 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 tasks

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

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, Essential Duties and 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 control data. Record corrective actions where appropriate. 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 Datacor/Chempax and eChempax. 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. Perform other duties as requested. Qualifications 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. 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.

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

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 has an exciting opportunity for a Full Time Associate Scientist - (Med Onc-Dr. Hosein) to work at the UHealth Medical Campus in Miami, FL. CORE JOB SUMMARY The Associate Scientist, SOM 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. CORE JOB FUNCTIONS Contributes to basic and applied research activities including authorship of scientific publications, technical and agency reports, and patent preparations. Publishes in refereed journals in collaboration with department leadership or independently. Supervises research employees and non-exempt staff. Writes extramural proposals with approval of senior managing staff. Creates and conducts experiments and analyzes results. Works with other researchers to use and develop end products. Provides ready access to all experimental data for the faculty researchers, supervisors, and other relevant staff. Requests or acquires equipment and supplies for assigned project(s). Applies for grants to continue research and prepares materials for submission to granting agencies and foundations. 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: Ph.D., M.D. or other doctoral level degree required Experience: Minimum 5 years of relevant experience required Knowledge, Skills and Attitudes: Skill in collecting, organizing, and analyzing data. Ability to recognize, analyze, and solve a variety of problems. Ability to exercise sound judgment in making critical decisions. 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.

Analyzes Products and Materials and the composition of their ingredients. Includes the following. Other duties may be assigned. Following approved procedures and under general direction: Develops formulas, processes, and methods for solution of technical problems. - Provides input to the development of procedures. - Follows established procedures and documents all findings and results timely, concisely, clearly and accurately. - Analyzes compounds to determine chemical and physical properties. - Conducts research on manufactured products to develop and improve products. - Conducts research into composition, structure, properties, relationships, and reactions of matter. - Prepares standards and specifications for processes, facilities, products, and tests. - Measures products for compliance to standards and specifications and reports same. - Contributes to a continuous improvement process to lower product costing and/or add product value. - Follow Prime Enterprises, Inc. SOPs, STPs and cGMP. - Keeps records updated, distributed, and filed. Job Performance Standards: Neither suffers nor contributes to any injury or accident. Maintains an exemplary attendance and punctuality performance record. Adheres to all Prime Personnel Policies as established by the company. Performs all tasks and assignments in a safe and timely manner. Strives toward continuous self-improvement in personal productivity. Skills: requires a combination of technical skills, analytical capabilities, and attention to detail. Candidate should have a solid working knowledge of laboratory instrumentation such as FTIR, HPLC. Candidate must have a demonstrated proficiency in laboratory instrument troubleshooting and knowledge of statistical techniques. Education: Minimum of a BS in Chemistry, Chemical Engineering or Biochemistry. Degrees in other scientific disciplines will be considered.