Chemist jobs in Pompano Beach, FL

Full-time Description The R&D and Laboratory Support Technician will support the Research & Development team in the preparation, testing, and documentation of lab batches and experimental formulations. This role will maintain meticulous documentation, and support a variety of formulation and packaging development processes. The position is essential to the success of new product development and product improvements by ensuring consistent execution of lab procedures, accurate data recording, and support during scale-up initiatives. Primary / Key Essential Functions and Responsibilities Assist in preparing and modifying lab batches according to standard procedures or under chemist direction. Maintain accurate lab logs, batch sheets, formulation files, and experimental records. Conduct basic physical and chemical tests on raw materials, prototypes, and finished products (e.g., pH, viscosity, stability). Input test results, formulation data, and sample information into the tracking system/database. Support formulation scale-up trials in collaboration with compounding and manufacturing teams. Assemble and label packaging components for testing or presentation purposes. Assist in managing packaging specifications and updating technical documentation. Assist in creating, revising, and transferring specifications for formulas and packaging. Maintain up-to-date libraries of raw materials, samples, formulas, and packaging components. Participate in calibration of lab equipment and ensure instruments are in good working order Maintain lab cleanliness and organization. Support regulatory, compliance and qualify initiatives by ensuring documentation accuracy. Adhere to lab safety protocols, Good Laboratory Practices (GLP), and standard operating (SOP) procedures. Other duties as assigned Requirements Education and/or Experience and Qualifications Minimum Education: Associate or Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science or other related scientific field. Minimum Experience: Prior laboratory experience preferred; experience in cosmetics or consumer products a plus. Knowledge, Skills and Abilities Strong Computer literacy, and data entry accuracy. Demonstrated ability to work methodically, organize information, and troubleshoot in a lab environment. High attention to detail , ability to follow instructions and work within SOPs and GMP guidelines. Critical thinking and adaptability to evolving processes or systems. Excellent organization and documentation habits. Strong verbal and written communication skills; strong interpersonal collaboration across departments (Spanish is a plus) Proficiency in Google Workspace (Sheets, Docs, Drive) and Microsoft Office (Outlook, Word, Excel, and PowerPoint). Ability to work independently and as part of a collaborative team. Ability to manage multiple tasks under deadlines in a fast-paced environment. A collaborative, team-oriented mindset with a proactive and flexible work ethic. Management / Supervisory Authority N/A Physical Requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is occasionally required to stand; reach with hands and arms; walk. The employee must frequently sit; use hands to finger, handle, or feel objects, tools or controls; talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee is exposed to inside weather conditions, moderate noise, and vibrations. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. External and internal applicants, as well as position incumbents who become disabled, must be able to perform the essential job functions either unaided or with assistance of a reasonable accommodation as determined on a case by case basis.

Job DescriptionDescription: Under limited supervision, oversee execution of and review data analysis for Client product tech transfers and assay verifications for the Protein Characterization team. Provide analytical support testing, as needed, to Upstream Processing, Downstream Processing and Bioconjugation groups. On occasion, collaborate with Quality Control in performing method transfers as well as with troubleshooting existing qualified/validated assays. Support PD'in evaluating product stability and monitoring degradation pathways. Generate Experimental Plans'imd Project Summary reports as needed. Serve as in-lab leader and help direct day-to-day test planning activities. Requirements: • Perform Protein Characterization, Routine Testing or In-Process Support testing as required including ELISA, SOS PAGE, IEF, HPLC, Western Blot, BCA, Capillary Electrophoresis, cell-based assays, spectrophotometric, spectrotluorometric and other pertinent biological and biochemical assays as they pertain to GLP and GMP standards in support of tech transfer and process development activities. • Evaluate emerging techniques in protein characterization for the production of biotherapeutics and develop assay as required. • Assist PC teammates in troubleshooting assay optimization difficulties. • Direct day-to-day PC-related laboratory activities and ensure that experimental plans are being followed. • Be responsible for data review and data collaboration for assay projects. • Work collaboratively and communicate data with depa11ment head as well as other involved parties. • Communicate directly with Scientist II counterparts for various Clients during the project on boarding and initiation stage. • Act as SME for commonly performed analytical methods. • Create and/or Review of technical reports such as SOPs, experimental plans, interim project status reports and summary reports. • Be prepared to optimize and troublesh"ot new assays using sound scientific judgement with approval of department head. • Assist in onboarding and document creation for new instrumentation in the PD Lab. • Perform PD Lab inventory checks. Create and manage Purchase Order requests for new projects. • Record laboratory activities and results in appropriate notebooks. • Assist Quality Control group in troubleshooting assays, where appropriate. • Effectively interact and assist other groups within the Development groups (Cell Culture, Protein Purification, and Bio-Conjugation) and the Quality/Regulatory and Manufacturing groups on assay, and process related matters. • Must be able to manage multiple projects. • Demonstrate high attention to detail and proven track record of organizational excellence. • Demonstrate strong problem-solving skills. • Strong oral and written communication skills. • Train on and become familiarized with all pertinent analytical techniques. Education and Experience: • BS or MSc in Biological or Biochemical sciences, and 5+ years relevant laboratory experience in antibody/protein characterization or quality control - particularly in the areas of immunology, molecular and cell biology, and protein chemistry. • 2+ years' experience in Technical Writing. • Previous CRO/CDMO experience is a plus. • Leadership skills

Within Accenture's Utilities (Energy Retail and Customer Experience) Practice, We use our deep industry expertise in digital customer engagement and operations, connected energy services and customer platforms to help retail energy and utility providers with cost effectiveness, revenue assurance/extension and customer satisfaction and loyalty. In Strategy & Consulting we work with C-suite executives, leaders and boards of the world's leading organizations, helping them reinvent every part of their enterprise to drive greater growth, enhance competitiveness, implement operational improvements, reduce cost, deliver sustainable 360° stakeholder value, and set a new performance frontier for themselves and the industry in which they operate. Our deep industry and functional expertise is supported by proprietary assets and solutions that help organizations transform faster and become more resilient. Underpinned by technology, data, analytics, AI, change management, talent and sustainability capabilities, our Strategy & Consulting services help architect and accelerate all aspects of an organization's total enterprise reinvention. Benefits of Working at Accenture: + Impactful Projects with Leading Clients: Opportunity to partner with top-tier clients in the CNR Industry on transformative projects. + Collaborative Work Culture: Join a dynamic and collaborative environment that values professional growth and development. + Competitive Compensation and Benefits: Enjoy a rewarding compensation package, including extensive benefits. Key Responsibilities: + Lead strategic consulting engagements in energy retail and customer service, focusing on digital transformation, customer experience enhancement, and operational efficiencies. + Serve as a primary client contact for senior executives, building trusted advisory relationships and ensuring alignment with client business objectives. + Develop and execute strategies to improve client business performance, drive revenue growth, and support customer-centric transformation initiatives. + Manage project teams, guiding junior members and ensuring project delivery meets quality, timeline, and budgetary expectations. + Lead business development activities by identifying new opportunities, crafting proposals, and representing Accenture's Utilities practice in sales pursuits. + Actively contribute to thought leadership, staying current on industry trends, regulatory changes, and technological advancements in the energy retail sector. + Drive team development and growth by mentoring team members and fostering a collaborative, high-performance work Note: We are open to hiring in most major cities in the US that are near to an Accenture corporate office. Here's what you need: + Minimum of 3 years of experience in the Utility Industry, Customer Service project delivery / Customer Transformation project delivery + Minimum of 2 years of functional experience with either an SAP or Oracle platform. + Expertise in Meter to Cash operations, functions, and technologies. + Expertise in major Customer Transformation and technology implementations (e.g., CIS replacements) + Bachelor's degree or equivalent work experience. + Ability to travel as needed. Bonus Points If: + You have at least 2 years of experience in an advisory or consulting role Professional Skill Requirements: + You improvise and adapt to lead clients and teams through change and ambiguity + You've gained the trust of your clients and partnered with them to: design business process, lead design thinking workshops, develop business case, deliver agile projects, develop new operating model, manage talent and change, co-create intellectual property Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. (************************************************************ Role Location Annual Salary Range California $63,800 to $205,800 Cleveland $59,100 to $164,600 Colorado $63,800 to $177,800 District of Columbia $68,000 to $189,300 Illinois $59,100 to $177,800 Maryland $63,800 to $177,800 Massachusetts $63,800 to $189,300 Minnesota $63,800 to $177,800 New York/New Jersey $59,100 to $205,800 Washington $68,000 to $189,300 #LI-NA #LI-MP Requesting an Accommodation Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired. 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For details, view a copy of the Accenture Equal Opportunity Statement (******************************************************************************************************************************************** Accenture is an EEO and Affirmative Action Employer of Veterans/Individuals with Disabilities. Accenture is committed to providing veteran employment opportunities to our service men and women. Other Employment Statements Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States. Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration. Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process. Further, at Accenture a criminal conviction history is not an absolute bar to employment. 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Job Title: Senior Formulating Chemist Company: Cosmetic Solutions Innovation Labs Employment Type: Full-Time Experience Level: Senior (7+ Years) Cosmetic Solutions Innovation Labs is a cutting-edge, full-scale cosmetics and OTC manufacturing company specializing in advanced formulation, clean beauty, and custom turnkey product development. We bring innovation, science, and speed to market for some of the most forward-thinking skincare and beauty brands in the industry. We are seeking a highly technical, experienced, and innovative Senior Cosmetic Chemist to join our R&D team. This is a high-impact role focused on leading new product development, troubleshooting complex formulations, and working closely with manufacturing to scale concepts into commercial success. Responsibilities will include, but are not limited to: Lead end-to-end development of skincare, OTC, and cosmetic formulations-from concept through scale-up. Design, test, and optimize formulations for performance, safety, sensory profile, and stability. Troubleshoot formulation issues, both in the lab and during manufacturing, applying deep technical knowledge to solve challenges efficiently. Collaborate with manufacturing teams during pilot batches and scale-up to ensure product consistency and process viability. Conduct raw material research and apply advanced formulation principles to support innovation goals. Maintain accurate and detailed documentation of all formulation processes, including batch records, lab notebooks, and experimental notes. Apply and enforce Good Laboratory Practices (GLP) in daily lab activities. Work cross-functionally with regulatory, marketing, and quality teams to align technical objectives with business needs. Utilize Coptis software for formulation tracking and documentation (proficiency is a plus). Ensure compliance with FDA, OTC, EU, and international cosmetic regulations. Qualifications: Bachelor's or Master's in Chemistry, Cosmetic Science, Chemical Engineering, or a related field. 7+ years of hands-on formulation experience in cosmetics, personal care, or OTC products. In-depth knowledge of emulsion systems, surfactants, active ingredients, thickeners, and preservative systems. Strong ability to troubleshoot, adjust, and optimize formulas under varying lab and production conditions. Experience with manufacturing scale-up and pilot batches in a GMP environment. Proficient in Microsoft Word and Excel; Experience with Coptis software a plus. Excellent communication and documentation skills. Detail-oriented with strong organizational abilities. Passion for innovation and staying current with industry trends and raw material technologies. What we Offer: The opportunity to work with a leading innovator in cosmetic and OTC manufacturing. Competitive salary and comprehensive benefits package. A collaborative, fast-paced environment that fosters creativity and innovation. Access to modern lab facilities, technologies, and ingredients. The chance to directly influence the success of top-tier beauty and wellness brands. Cosmetic Solutions LLC is committed to equal employment opportunities for all employees and applicants for employment without regard to age, color, disability status, gender, national origin, race, religion, sexual orientation or veteran status, or any other legally protected status. Ready to help us formulate the future of beauty? Please submit your resume.

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 Hussman Institute has an exciting opportunity for an Associate Scientist (AS) position. The incumbent will work on the statistical genetic aspects of Alzheimer's Disease (AD), as part of several multidisciplinary national and international consortiums. This position will work on research directed towards identifying genes and the mechanisms that they influence to increase the risk of or prevent the onset of AD. This position will also include admixture analysis of several population data sets. As a certified bioinformatician, the AS will also be involved in the functional genomic analysis. The AS primary responsibilities will include data interpretation, manuscript preparation, training of post (pre) doctoral students and master's level analysts and reporting of results to an international AD community. 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 * Ph.D., M.D. or other doctoral level degree required * Minimum 5 years of relevant experience Department Specific Functions Lead and perform complex analyses of genome-wide association and high throughput sequencing data with particular focus on identification of risk and protective loci relevant to Alzheimer Disease and related dementias. Design and implement robust statistical frameworks for integrative genomic analyses, including the identification of gene:gene and gene:environment interactions in multi-ancestry populations Conduct functional bioinformatics and statistical analyses for interpretation of AD-associated loci and genes using computational pipelines developed in R, Python, or other appropriate computing language Publish original research articles both independently and in conjunction with the principal investigators Collaborate closely with principal investigators to shape experimental design and analytical strategies, ensuring reproducibility and high statistical rigor; suggest changes to current protocols that would enhance ability to complete project aims more readily Maintain active engagement with the scientific literature to integrate emerging techniques in statistical genetics and computational biology into ongoing projects Supervise, train and instruct fellows, students, and staff in computational genomics, emphasizing best practices in statistical modeling, reproducible research, and open-source software development. Seek independent funding from federal agencies and foundations for original research efforts with the appropriate guidance from institute leadership Participate and contribute to grant applications in large international consortia research collaborations as MPI or Co-Investigator to advance the understanding of complex disease with focus on Alzheimer Disease and related dementias Adhere to University and unit-level policies and procedures and safeguards University assets. #LI-GD1 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

Belzona Global, an established leader in industrial protective coatings and repair composites, has gained incomparable success by acknowledging the need to provide not only technologically advanced products, but also to present uncompromising service to our customers - offering one solution to their maintenance challenges. With a reputation for products and services of the highest quality, it is essential that our people can represent the company's values. An exciting new opportunity has arisen for a Project Manager to join our Miami based team. Primarily a lab-based role, the successful candidate will have responsibility for the development of new polymeric solutions for arduous industrial environments. This will involve the design and lab-scale manufacture of coatings and repair composites, and subsequent testing to validate product performance. The ideal candidate will have a PhD or Master Degree in Chemistry/Polymer Chemistry and possess a good knowledge of formulating industrial coatings, composites or adhesives. Alternatively, a Bachelors degree in Chemistry/Polymer Chemistry would also be acceptable if the candidate can demonstrate expert formulating knowledge. The ideal candidate must be able to show a proven track record of innovation; have excellent hands-on laboratory skills; good communication and interpersonal skills; have a keen eye for detail; and be able to show a good understanding of the different polymer technologies used within the industrial coatings and repair industry. The candidate should also be available for occasional overseas travel in order to support Belzona's global partners. Successful candidates will need to have the following qualifications and experience: Essential · Masters or PhD in Chemistry preferred (Polymer Chemistry or Materials Science qualifications will also be considered) · Knowledge of formulating industrial coatings, adhesives or fiber-reinforced composites · Knowledge and/or experience of cold-curing thermoset polymers (e.g. epoxies, polyurethanes, etc.) · Knowledge and/or experience of the test methods used to assess performance of coating, adhesive and/or composite systems · Track record of innovative thinking and generation of new ideas · Knowledge and experience of laboratory safety protocols · Knowledge of the key formulation elements of cold-curing thermoset polymer systems · Knowledge of the test methods commonly used to categorize the performance of coatings, adhesives or composites · Excellent practical hands-on laboratory skills, whether formulating, manufacturing, applying or testing polymer materials Desirable · Knowledge of international chemical supply regulations (e.g. REACH, chemical inventories, hazchem transport rules, etc) · Knowledge of substrate surface preparation standards and coating/composite application techniques used in the industrial sector Candidates will also need to display the following skills & abilities: · Excellent practical laboratory skills · Excellent organizational abilities including prioritization and management of multiple projects for the timely delivery of objectives · Confident communicator with ability to foster strong working relationships between the R&D, Technical Service and Production departments · High level of IT literacy and competence with MS Windows/Office packages · Excellent basic maths · High standard of written English (in a scientific style) Finally, the successful candidates will display the following personal attributes: · Proactive and independent worker · Flexible attitude to work · Excellent attention to detail and problem solving · Safety conscious If you enjoy working in a challenging and rewarding environment, then this may be the opportunity for you. If you are a pro-active, confident team player who believes their skills and experience can make a real impact on our business we look forward to hearing from you and invite you to apply by clicking on the "Apply Now" link below.

Job DescriptionSalary: DB Environmental (DBE) is accepting resumes for an Associate Scientist to join their team, in their West Palm Beach, FL office, and provide field project management of research and monitoring projects in Florida's freshwater ecosystems. DBE is a small business that provides applied research, management guidance, field monitoring, and analytical laboratory services in wetland and aquatic ecosystems throughout Florida. Areas of expertise include nutrient and metals biogeochemical cycling; design and implementation of in situ and ex situ experiments; remote marsh sampling and instrumentation; high-quality routine and on-demand sample collection services. DBEs scientists have published more than 20 peer-reviewed journal articles. Position Summary This position will perform, organize and/or assist with all aspects of project lifecycles: conception, design, field sample collection, coordination with field support staff and analytical laboratory, data quality review, data analysis, reporting, and client communications. This highly collaborative position requires close communication with DBE Principal Scientists, field and laboratory support staff, and clients. This position requires expertise in field sampling, laboratory techniques, data analysis and reporting, and ecological knowledge, with an emphasis on the unique biogeochemistry of South Florida wetland environments. Required Skills, Knowledge, and Experience Bachelors degree in Environmental Science, Biology, Ecology, or related field required; Masters degree preferred. A Masters degree may substitute for one (1) year of required experience. Minimum of 2 years of experience working in South Florida wetlands (1 year with Masters). Experience in related ecosystems may be substituted, including coastal/estuarine seagrass, mangrove forests, or lakes and streams. Demonstrated knowledge of biogeochemistry in South Florida freshwater wetland environments. Proven ability to analyze data, present findings, and write technical reports. Proficiency with Microsoft Excel, Word, and PowerPoint. Familiarity with FDEP SOPs for field sampling, including quality control samples. Ability to perform essential field processes: collect samples of soils, plants, and water in order to conduct qualitative and quantitative analyses. Strong organizational, time management, and communication skills. Preferred Skills, Knowledge, and Experience Proficiency with R, Python, Tableau, or other statistical and data visualization packages strongly preferred, including software for ecological applications. Experience managing interdisciplinary projects integrating field, lab, and data analysis components. Experience with analytical chemistry: laboratory analysis of water, plant, and soil matrices for nutrient and/or metals; data analysis of laboratory results. Ability to identify Florida native wetland plants (emergent and submerged). Experience with scientific proposal development and reporting. Physical Requirements and Working Environment This position requires the ability to swim and the ability to lift a minimum of 50 lbs. This position often requires work in adverse field and weather conditions. Compensation and Benefits Compensation for the position is based on individual experience and qualifications. DBE offers competitive pay, paid vacation and holidays, health/dental insurance, life insurance, and retirement benefits. Work Authorization Applicants must be currently authorized to work in the United States on a full-time basis. DBE is unable to sponsor or take over sponsorship of employment visas at this time. DBE is an equal opportunity employer. Submission Please submit your resume and cover letter by November 21, 2025. We would like to thank all applicants for their interest. However, only those selected for an interview will be contacted.

Join MAPEI Corporation, a global leader in the manufacturing of construction chemicals and building materials, including adhesives, sealants, and specialty products used in flooring, tile, and concrete restoration. We are currently seeking a Lab Tech to join our R&D team. In this role, you will prepare samples, operate lab equipment to test and blend MAPEI products, and ensure adherence to safety protocols. You'll work closely with chemists and supervisors to perform tests and document results, supporting MAPEI's commitment to quality and innovation Key Responsibilities: * Organize and execute test procedures as requested, including accurate reporting of collected data. * Prepare laboratory equipment, materials, and mixtures in alignment with test requirements. * Follow established lab procedures and best practices to ensure quality and safety. * Support general lab operations and assist with additional tasks as assigned. * Run errands for materials and supplies to support ongoing lab activities. * Adhere to safety regulations and maintain a clean, organized workspace. * Perform additional duties as required. What's in it for you: * Highly competitive base pay * FREE MEDICAL INSURANCE for our employees or the option of a highly competitive medical plan with minimal monthly employee contributions. * 17 Days of paid, sick and vacation time annually (days are prorated in year one). * 401K retirement with up to 6% matching program. * Excellent dental, vision programs, flex spending accounts, employer paid life insurance and free tele-med physician services. * Various other company employee-centric perks initiatives; tuition reimbursement programs, discounted home/auto insurance programs, supplemental life insurance, and more. Qualifications: * High school diploma or equivalent (GED); a Bachelor's degree in Chemistry is preferred but not required. * Some related experience preferred, ideally in chemicals or construction products (e.g., grouts, mortars, adhesives). * Familiarity with lab equipment, including strength testing and blending tools. * Proficiency in Microsoft Word, Excel, and Outlook. * Ability to lift up to 50 pounds. Equal Opportunity Employer - Minority/Female/Disability/Veteran (M/F/D/V) MAPEI1

Job DescriptionDescription: Job purpose The Quality Control Analyst is responsible for performing and managing results of quality control testing for human tissue donors, recovered tissues, and final processed grafts. The QCA communicates directly with outside laboratories to obtain records and internally with Operations and Quality Assurance to ensure appropriate samples are available for testing and results are properly communicated. The QCA performs multiple tests on tissue samples including but not limited to sterility, bioburden, endotoxin, residual moisture, cell count and analytical testing. Must perform all functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Duties and responsibilities Quality Control Testing and Results Perform Quality Control (QC) testing of tissue samples to include, but not limited to, residual moisture, sterility, endotoxin, bioburden, cell characterization, flow cytometry, microorganism identification, and gram staining. Perform QC release testing of microbiology media, materials, and reagents. Support environmental monitoring (EM) of the facility by performing routine testing and processing samples. Perform inspection of incoming materials and reagents, microbiology media, and in-process and final product. Review and manage test results reported by third parties to ensure proper disposition of tissues and grafts. Maintain proper documentation of tests performed in-house and test results reported by third parties. Preparation of blood specimens, tissue samples, and media samples for shipment to outside testing facilities. Assist Manager in maintaining the laboratory stock of media and reagents and ordering laboratory supplies. Support and execute qualification / validation protocols of QC testing methods. General Responsibilities Maintain knowledge of appropriate federal and state regulatory and statutory requirements as well as accrediting body requirements. Responsible for reporting all variances, errors, and deviations to QA management. Participate in the investigation complaints and deviations including the formulation and implementation of corrective actions. Participate in audits and inspections, as needed. Support accreditation and licensing activities. Perform other duties as assigned by the QC Manager and/or Director of Quality Assurance. Requirements: Qualifications Education/Experience: Bachelor in Science degree preferred or Associate in Science with two years of experience. An equivalent combination of education and experience in a regulated environment (e.g., Biologics, Pharmaceutical, etc.) will be considered. Laboratory Skills: Aseptic techniques, bioburden, sterility, endotoxin, growth promotion, flow cytometry, gram staining. Other Skills: Excellent interpersonal, verbal, and written communication skills required. Must demonstrate excellent organizational and record keeping skills. Must be detail oriented with the ability to multi-task in a high-pressure environment. Must gain knowledge of all regulations, laws, and/or standards that govern the tissue banking industry within the first year of employment. Computer and Equipment: Proficient in Microsoft Office. Working knowledge of Vitek 2, Spectrophotometer, Cell Analyzers, Autosampler, MAGPIX preferred. Working conditions Primarily, a fast pace, lab-oriented work environment. Evening and weekend work may be required. Physical requirements While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds. Direct Reports No direct reports.

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. Responsibilities: ● Work within a cutting-edge genomics workflow to provide quality control support in a high-volume clinical molecular laboratory. ● Test and document new lots of reagents for clinical lab team processing and label reagents approved for use. ● Maintain reagent qualification records and manage quality control of reagent inventory. ● Document all results and findings in order to satisfy CLIA/CAP/NYS-DOH/ISO compliance. ● Collect and help analyze metrics. ● Investigate reagent related issues and help facilitate and implement corrective and preventative actions. ● Interact with lab management and personnel to provide training, troubleshoot issues, and prioritize QC tasks. ● Report significant findings/deviations and system deficiencies to lab management, as appropriate. ● Update SOPs and records within the document control system, including creation/ revision/ review of internal SOPs and other quality documentation. ● Complete Performance Qualifications (PQs) and support the Lab QC team with equipment and documentation tasks as needed. ● Monitor and respond to laboratory temperature excursions. Qualifications: ● Highly organized and systematic, superb attention to detail and ability to complete tasks with a high degree of accuracy. ● Proven ability to learn new skills quickly and adapt to new processes smoothly. ● BS in medical technology, clinical laboratory science, chemical, physical or biological science. Prefer 1 year previous experience in a molecular lab or with laboratory liquid handlers. ● Moderate experience with Microsoft Excel and/ or Google Sheets. ● Previous experience in a clinical lab regulated by CAP/ CLIA/ NYS/ ISO is highly desirable. ● Good time management skills. ● Excellent communication skills. We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Pay: $20/hour Schedule: Monday-Saturday | 8:00 AM - 5:00 PM or 3:00 PM - 11:00 PM About the Role We are seeking an experienced Quality Control and Inventory Associate to join our team. In this role, you'll ensure that all produce meet our rigorous quality standards through hands-on inspection, data tracking, and consistent communication with management. This position is ideal for individuals who are detail-oriented, data-driven, and passionate about maintaining top-tier produce quality from field to shelf. Overview of Responsibilities Conduct visual inspections of produce (melons, asparagus, and other fruits), packing facilities, and before transport, assessing size, shape, color, texture, and overall appearance. Collect and record data from quality assessments, noting any defects or irregularities. Sample and prepare produce for laboratory testing to evaluate sugar content, firmness, and shelf-life. Document quality control findings and produce detailed reports outlining deviations from standards. Communicate findings and recommendations to management to address quality trends or concerns. Support inventory tracking and control, ensuring consistent and organized documentation of product flow. Requirements 3+ years of Quality Assurance or Quality Control experience in produce Proven ability to: Measure and assess shape, size, color, texture, and appearance of produce Collect randomized product samples for lab testing Record and analyze quality metrics such as sugar content, firmness, and shelf life Create detailed quality reports documenting discrepancies from established standards Differentiate between premium and standard fruit Ability to lift up to 50 lbs Comfortable working in refrigerated facilities (35 degrees F or less) Preferred Qualifications Previous warehouse, produce supervisory, or management experience

Performs professional, technical laboratory functions with versatile capabilities throughout the laboratory. Serves as a technical resource in the laboratory providing scientific expertise and problem-solving skills. Responsibilities The Analytical QC Analyst II is an integral part of the team, contributing to our success by performing raw materials and commercial pharmaceutical products testing according to compendial methods and/or internal standards test procedures (STPs). Conducts Analytical testing of Raw Materials, Intermediate Products and Finished products as per written procedures and protocols to support material/product release, stability studies, method transfers, method verifications and investigations. Troubleshoot, operate, and train for testing associated with general analytical instruments for testing of raw material, in process and finished products using instruments such as HPLC, GC, Dissolution, UV, IR, automatic titrator, and viscometer. Ensures testing is properly conducted and documented for all performed activities with emphasis on data integrity. Prepare test solutions, volumetric solutions, and samples used in analysis. Performs assigned physical tests, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, components, and stability products in an FDA regulated lab environment. Notifies supervisor immediately regarding testing abnormalities, OOS/OOT results, and deviations from established testing procedures. Serves as a lead investigator in conducting and documenting the investigation. Functions as a subject matter expert within the analytical laboratory and always provides support. Performs training and provides technical support to junior analysts as required. Works under minimal supervision and is expected to independently carry-out non-routine assignments. Actively completes assigned training activities and documents training within assigned time frames and before performing any activity associated with the training topic. Maintains proper documentation of laboratory data (which requires adequate proficiency in written and computational skills). Reviews analytical testing records/logbooks for compliance with cGMPs, compendial requirements, and Noven procedures/protocols. Reviews and/or writes technical reports, procedures, and protocols. Draws conclusions from data and communicates those conclusions is writing. May Schedule laboratory testing and associated activities to minimize operational disruptions to departments. May manage inter-departmental projects to ensure timely completion of objectives. Completes any other duties assigned by QC management as required. Qualifications Competencies: Education / Experience: Minimum of four years of experience with a bachelor's degree in chemistry or related scientific field required. Alternately, three to six years of experience with a master's degree in chemistry or related scientific field. Alternately, zero to three years of experience with a PhD in chemistry or related scientific field -Required. Broad knowledge of scientific principles, methods, chromatographic analysis, analytical methods (i.e. HPLC, GC, Dissolution) and a good understanding of separation theories -Required. Candidate must have broad knowledge in all types of compendia testing (USP, EP, JP, BP) and wet chemistry techniques-Required. Good written English and verbal communication skills-Required. Must be highly organized and able to work under pressure. Must have strong interpersonal and leadership skills. Must be computer literate with knowledge in all Microsoft business applications. Strong background in scientific software such as Waters Corp. Empower and LIMS is a plus. Judgment / Decision Making: Duties are performed under general direction toward broad assignments with periodic reviews. Duties are performed within framework of departmental or functional guidelines, requiring interpretation and original thinking. Work Environment: A laboratory environment with exposure to chemicals, caustics, fumes, heat and electrical current. Physical Demands: Visual acuity and manual dexterity required to operate computer, analytical instrumentation, sample preparation and proofread documents. Majority of time spent sitting and walking. Often required to lift objects weighing up to 20 pounds.

Temp To Hire Quality Control: $14hourly Schedule: Monday thru Friday ( Some Saturday's ) 7:00am to 5:30 pm ( willing to work over time ) Bilingual ( English/Spanish ) Basic Computer use RF scanner use NO forklift required. Employee will be checking orders picked by order pullers to ensure the right quantity and quality of the product is correct before shipping to customers. Requires a detail oriented person.

SUMMARY/OBJECTIVE We are looking for an experienced and detail-oriented Quality Control (QC) Specialist. The ideal candidate will be responsible for ensuring that all products meet the required quality standards throughout every stage of the production process - from raw material inspection to final product verification. ESSENTIAL FUNCTIONS Perform in-line and final quality checks to ensure compliance with technical and quality specifications. Collaborate with production, procurement, and development teams to identify and resolve quality-related issues. Prepare and maintain up-to-date quality control reports and documentation. Identify recurring issues and propose improvements to production processes. Ensure compliance with company standards, customer requirements, and industry regulations. Participate in quality audits and support supplier and subcontractor assessments. Train internal staff and production partners, when needed, on quality standards and control procedures. QUALIFICATIONS 1 year of experience in quality control within luxury manufacturing environments. Solid knowledge of inspection techniques, production processes, and common quality issues. Proven experience working with suppliers and manufacturing sites, both domestically and internationally. Strong attention to detail, analytical skills, and problem-solving abilities. Ability to work independently and manage multiple tasks in a dynamic environment. Proficiency in Microsoft Office (Excel, Word). Experience with AQL QC reporting is a plus. Willingness to travel regularly for inspections and visits to production sites. Good command of written and spoken English. BENEFITS 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance ADDITIONAL INFORMATION Chrome Hearts provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. **Security Clearance:** None/Not Required Pratt & Whitney is working to once again transform the future of flight-designing, building and servicing engines unlike any the world has ever seen. And because transformation begins from within, we're seeking the people to drive it. So, calling all curious. Come ready to explore and you'll find a place where your talent takes flight-beyond the borders of title, a country or your comfort zone. Bring your passion and commitment and we'll welcome you into a tightknit team that takes our mission personally. Channel your drive to make a difference into shaping an organization and an industry that's evolving fast to the future. At Pratt & Whitney, the difference you make is on display every day. Just look up. Are you ready to go beyond? **What You Will Do:** + Demonstrate a high level of customer focus, business judgment and teamwork. + Communicate with various levels of management to identify Military Engines quality risks and mitigation plans. + Work in collaboration with the Military Engines Program Quality F135 focused sustainment teams for best practice sharing, read-across activities and continuous improvement. + Collect and analyze process data to minimize workflow disruptions and eliminate non-conformances/escapes. + Collaborate with Engineering when approving First Article Inspections (FAI). + Lead quality system, process, and product audits. + Assist in the development of the annual audit schedule and support 3rd party audits as required. + Raise notifications of non-conformance, quarantines non-conforming product and, when approved to do so, provides disposition. + Manages supplier quality issues through monitoring / escalation processes, escape management, processing of supplier submission of non-conforming material and supporting internal MRB processes. + Facilitate investigations to determine root cause and corrective actions while preventing future recurrence. + Achieving Competitive Excellence; Lead process improvement initiatives to increase organizational efficiency and effectiveness. + Generate and modify applicable quality-controlled documentation to ensure processes and requirements are clearly defined. + Customer satisfaction; Identify and assist all stakeholders with product deficiencies and resolution. **Qualifications You Must Have:** + Requires a University Degree or equivalent experience and minimum 5 years prior relevant experience, or An Advanced expected Degree in a related field and minimum 3 years experience. **Qualifications We Prefer:** + Experience with demonstrated ability to work with skilled workforces. AS9100/9110 experience preferred Strong written and verbal communication skills. + Ability to interface with internal and external customers. + ACE-DIVE - minimum ACE associate is a plus (or Engineering ACE B) Adaptability. + Engineering/Technical Skills. + Jet Engine Manufacturing/Assembly/Overhaul experience. + Regulatory for requirements and System Procedures Skills. + MS Office proficiency: Excel and PowerPoint required. + The ability to read and comprehend work instructions, quality manuals, and other detailed instructions. **Learn More and Apply:** What is my role type? In addition to transforming the future of flight, we are also transforming how and where we work. We've introduced role types to help you understand how you will operate in our blended work environment. **This role is:** Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance workers, as they are essential to the development of our engines. Candidates will learn more about role type and current site status throughout the recruiting process. For onsite and hybrid roles, commuting to and from the assigned site is the employee's personal responsibility. **_As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote._** The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. _RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act._ **Privacy Policy and Terms:** Click on this link (******************************************************** to read the Policy and Terms Raytheon Technologies 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, disability or veteran status, age or any other federally protected class.

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Pratt & Whitney is working to once again transform the future of flight-designing, building and servicing engines unlike any the world has ever seen. And because transformation begins from within, we're seeking the people to drive it. So, calling all curious. Come ready to explore and you'll find a place where your talent takes flight-beyond the borders of title, a country or your comfort zone. Bring your passion and commitment and we'll welcome you into a tightknit team that takes our mission personally. Channel your drive to make a difference into shaping an organization and an industry that's evolving fast to the future. At Pratt & Whitney, the difference you make is on display every day. Just look up. Are you ready to go beyond? What You Will Do: Demonstrate a high level of customer focus, business judgment and teamwork. Communicate with various levels of management to identify Military Engines quality risks and mitigation plans. Work in collaboration with the Military Engines Program Quality F135 focused sustainment teams for best practice sharing, read-across activities and continuous improvement. Collect and analyze process data to minimize workflow disruptions and eliminate non-conformances/escapes. Collaborate with Engineering when approving First Article Inspections (FAI). Lead quality system, process, and product audits. Assist in the development of the annual audit schedule and support 3rd party audits as required. Raise notifications of non-conformance, quarantines non-conforming product and, when approved to do so, provides disposition. Manages supplier quality issues through monitoring / escalation processes, escape management, processing of supplier submission of non-conforming material and supporting internal MRB processes. Facilitate investigations to determine root cause and corrective actions while preventing future recurrence. Achieving Competitive Excellence; Lead process improvement initiatives to increase organizational efficiency and effectiveness. Generate and modify applicable quality-controlled documentation to ensure processes and requirements are clearly defined. Customer satisfaction; Identify and assist all stakeholders with product deficiencies and resolution. Qualifications You Must Have: Requires a University Degree or equivalent experience and minimum 5 years prior relevant experience, or An Advanced expected Degree in a related field and minimum 3 years experience. Qualifications We Prefer: Experience with demonstrated ability to work with skilled workforces. AS9100/9110 experience preferred Strong written and verbal communication skills. Ability to interface with internal and external customers. ACE-DIVE - minimum ACE associate is a plus (or Engineering ACE B) Adaptability. Engineering/Technical Skills. Jet Engine Manufacturing/Assembly/Overhaul experience. Regulatory for requirements and System Procedures Skills. MS Office proficiency: Excel and PowerPoint required. The ability to read and comprehend work instructions, quality manuals, and other detailed instructions. Learn More and Apply: What is my role type? In addition to transforming the future of flight, we are also transforming how and where we work. We've introduced role types to help you understand how you will operate in our blended work environment. This role is: Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance workers, as they are essential to the development of our engines. Candidates will learn more about role type and current site status throughout the recruiting process. For onsite and hybrid roles, commuting to and from the assigned site is the employee's personal responsibility. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

R&D Lab Technician Boca Raton, FL Beauty innovation starts here. An exciting opportunity has opened up to join our R&D team as Lab Technician and join the world's leading partner for Turnkey Performance Product Solutions, Custom Formulation and Contract Manufacturing. Our team of expert chemists operates a state-of-the-art, in-house laboratory full-time to maximize research and development efficiency, streamline manufacturing processes, and significantly reduce time-to-shelf. We are looking for talent that is passionate about problem-solving, can use data to support conclusions and claims, and has a deep drive to ensure cosmetic products are held to the highest standards in quality and safety. Job Title: Lab Technician The Lab Technician works within the Cosmetic Solutions Innovation Lab and supports innovation activities, including raw material and finished product testing, laboratory scale batching, support research and development and Quality Control. The ideal candidate must be able to show a proven track record of accuracy, have excellent hands-on laboratory skills, good communication and interpersonal skills, and have a keen eye for detail. They will be self-motivated, solution-focused, highly detail-oriented, organized, and able to work autonomously. Responsibilities include, but are not limited to: Perform laboratory tests such as pH, viscosity, melting point, specific gravity, titrations, and other analyses as assigned. Weigh, measure, and mix raw materials while adhering to safety, SOPs, and GMP requirements. Prepare laboratory-scale batches according to established formulas and written instructions. Document results accurately, maintain complete laboratory records, and adhere to regulatory and quality guidelines. Assist chemists with preparing documents, filling and labeling samples, and general project support. Assist with scale-up testing and support production transfer when needed. Participate in the formulation and preparation of prototype cosmetic products, including emulsions, gels, serums, cleansers, and color cosmetics. Maintain a clean, organized, and safe laboratory environment, including cleaning, trash removal, and glassware washing. Follow all Company SOPs, safety procedures, and GMP standards. Conduct product stability testing and record observations throughout study timelines Experience: 1. Working knowledge of basic laboratory equipment and analytical skills such as pipetting, precision weighing, dilutions. 2. Product batching and compounding experience a Plus. 3. Computer skills: Proficient with Microsoft Outlook, Word and Excel. EDUCATION: BS/BA in Chemistry or related Science fields preferred. Benefits: Comprehensive Employer Contributed Medical plans offered for you and your family (including PPO) Dental and Vision Insurance for you and your family Employer Paid Life Insurance, including additional Voluntary Life and AD&D Flexible Spending Account and Dependent Care FSA Employee Assistance Program Annual Bonus Program Competitive PTO offered 401(k) Retirement Plans with up to 4% match Who we are: Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven, innovative personal care products. With a focus on, face, body, hair, OTC, and professional use formulations, we create some of the most cost effective, high quality and powerful products on the market. Cosmetic Solutions LLC. is committed to equal employment opportunity for all employees and applicants for employment without regard to age, color, creed, disability status, gender, national origin, race, religion, sexual orientation or veteran status, or any other legally protected status.

Under limited supervision, oversee execution of and review data analysis for Client product tech transfers and assay verifications for the Protein Characterization team. Provide analytical support testing, as needed, to Upstream Processing, Downstream Processing and Bioconjugation groups. On occasion, collaborate with Quality Control in performing method transfers as well as with troubleshooting existing qualified/validated assays. Support PD'in evaluating product stability and monitoring degradation pathways. Generate Experimental Plans'imd Project Summary reports as needed. Serve as in-lab leader and help direct day-to-day test planning activities. Requirements • Perform Protein Characterization, Routine Testing or In-Process Support testing as required including ELISA, SOS PAGE, IEF, HPLC, Western Blot, BCA, Capillary Electrophoresis, cell-based assays, spectrophotometric, spectrotluorometric and other pertinent biological and biochemical assays as they pertain to GLP and GMP standards in support of tech transfer and process development activities. • Evaluate emerging techniques in protein characterization for the production of biotherapeutics and develop assay as required. • Assist PC teammates in troubleshooting assay optimization difficulties. • Direct day-to-day PC-related laboratory activities and ensure that experimental plans are being followed. • Be responsible for data review and data collaboration for assay projects. • Work collaboratively and communicate data with depa11ment head as well as other involved parties. • Communicate directly with Scientist II counterparts for various Clients during the project on boarding and initiation stage. • Act as SME for commonly performed analytical methods. • Create and/or Review of technical reports such as SOPs, experimental plans, interim project status reports and summary reports. • Be prepared to optimize and troublesh"ot new assays using sound scientific judgement with approval of department head. • Assist in onboarding and document creation for new instrumentation in the PD Lab. • Perform PD Lab inventory checks. Create and manage Purchase Order requests for new projects. • Record laboratory activities and results in appropriate notebooks. • Assist Quality Control group in troubleshooting assays, where appropriate. • Effectively interact and assist other groups within the Development groups (Cell Culture, Protein Purification, and Bio-Conjugation) and the Quality/Regulatory and Manufacturing groups on assay, and process related matters. • Must be able to manage multiple projects. • Demonstrate high attention to detail and proven track record of organizational excellence. • Demonstrate strong problem-solving skills. • Strong oral and written communication skills. • Train on and become familiarized with all pertinent analytical techniques. Education and Experience: • BS or MSc in Biological or Biochemical sciences, and 5+ years relevant laboratory experience in antibody/protein characterization or quality control - particularly in the areas of immunology, molecular and cell biology, and protein chemistry. • 2+ years' experience in Technical Writing. • Previous CRO/CDMO experience is a plus. • Leadership skills

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Pratt & Whitney is working to once again transform the future of flight-designing, building and servicing engines unlike any the world has ever seen. And because transformation begins from within, we're seeking the people to drive it. So, calling all curious. Come ready to explore and you'll find a place where your talent takes flight-beyond the borders of title, a country or your comfort zone. Bring your passion and commitment and we'll welcome you into a tightknit team that takes our mission personally. Channel your drive to make a difference into shaping an organization and an industry that's evolving fast to the future. At Pratt & Whitney, the difference you make is on display every day. Just look up. Are you ready to go beyond? What You Will Do: * Demonstrate a high level of customer focus, business judgment and teamwork. * Communicate with various levels of management to identify Military Engines quality risks and mitigation plans. * Work in collaboration with the Military Engines Program Quality F135 focused sustainment teams for best practice sharing, read-across activities and continuous improvement. * Collect and analyze process data to minimize workflow disruptions and eliminate non-conformances/escapes. * Collaborate with Engineering when approving First Article Inspections (FAI). * Lead quality system, process, and product audits. * Assist in the development of the annual audit schedule and support 3rd party audits as required. * Raise notifications of non-conformance, quarantines non-conforming product and, when approved to do so, provides disposition. * Manages supplier quality issues through monitoring / escalation processes, escape management, processing of supplier submission of non-conforming material and supporting internal MRB processes. * Facilitate investigations to determine root cause and corrective actions while preventing future recurrence. * Achieving Competitive Excellence; Lead process improvement initiatives to increase organizational efficiency and effectiveness. * Generate and modify applicable quality-controlled documentation to ensure processes and requirements are clearly defined. * Customer satisfaction; Identify and assist all stakeholders with product deficiencies and resolution. Qualifications You Must Have: * Requires a University Degree or equivalent experience and minimum 5 years prior relevant experience, or An Advanced expected Degree in a related field and minimum 3 years experience. Qualifications We Prefer: * Experience with demonstrated ability to work with skilled workforces. AS9100/9110 experience preferred Strong written and verbal communication skills. * Ability to interface with internal and external customers. * ACE-DIVE - minimum ACE associate is a plus (or Engineering ACE B) Adaptability. * Engineering/Technical Skills. * Jet Engine Manufacturing/Assembly/Overhaul experience. * Regulatory for requirements and System Procedures Skills. * MS Office proficiency: Excel and PowerPoint required. * The ability to read and comprehend work instructions, quality manuals, and other detailed instructions. Learn More and Apply: What is my role type? In addition to transforming the future of flight, we are also transforming how and where we work. We've introduced role types to help you understand how you will operate in our blended work environment. This role is: Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance workers, as they are essential to the development of our engines. Candidates will learn more about role type and current site status throughout the recruiting process. For onsite and hybrid roles, commuting to and from the assigned site is the employee's personal responsibility. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms