Chemist jobs in Venice, FL - 639 jobs

Why Mayo Clinic Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans - to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. Benefits Highlights Medical: Multiple plan options. Dental: Delta Dental or reimbursement account for flexible coverage. Vision: Affordable plan with national network. Pre-Tax Savings: HSA and FSAs for eligible expenses. Retirement: Competitive retirement package to secure your future. Responsibilities Integral team member for cardiac device therapy and electrophysiology (EP) procedures in a subspecialty referral center of excellence. Training is provided so that the applicant develops into an EP lab specialist for invasive heart rhythm care. Three EP labs focus on high level complex care; fellow and resident training; while utilizing all technologies including 3D electroanatomical mapping, to intracardiac arrhythmia analysis, transvenous and subcutaneous pacing, intracardiac echo and ablation with radiofrequency and cryotherapy. Applicants will develop support expertise in all avenues of this specialist lab in a mentored, guided program where education is prioritized. The team members are responsible for all aspects of intra-operative patient care and teamwork, communication and flexibility is prized. 2-3 years of experience preferred. Qualifications • Graduate from an accredited cardiovascular program or radiology program with cardiac experience. • Cath lab or EP lab experience is preferred but not required for those with cardiac education background. • Experience: Two years in either Cath or EP is preferred, but not required. • Qualities: Organized, efficient, team-based attitude, excellent interpersonal skills, and ability to demonstrate effective communication. • Requirements: Ability to work varied hours and shifts. • License or Certification: ACLS & BLS. CVT or RTR. Must obtain RCIS within six months of hire. RCES is required after 2 years of EP experience. Exemption Status Nonexempt Compensation Detail Education, experience and tenure may be considered along with internal equity when job offers are extended. Benefits Eligible Yes Schedule Full Time Hours/Pay Period 80 Schedule Details Monday-Friday; 6:45am-5:15pm with scheduled late shifts depending on unit needs. Weekend Schedule N/A International Assignment No Site Description Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is. Equal Opportunity All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the "EOE is the Law". Mayo Clinic participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. Recruiter Jorida Musta

Aegis Medical Group is a comprehensive healthcare network dedicated to providing respectful, efficient, and patient-centered care. With a team comprising experts in primary care, internal medicine, cardiology, endocrinology, pain management, among other specialties, we offer a wide range of medical services. Our network also includes preferred providers for home health care, skilled nursing, assisted living facilities, and outpatient therapies. We continue to expand our offerings, providing patients with seamless transitions between services. At Aegis Medical Group, we aim to be the trusted home for all your medical needs. Role Description This is a full-time on-site role for a Sleep Lab Technician, located in Summerfield, FL. The Sleep Lab Technician will be responsible for operating specialized equipment to monitor patients during sleep studies, ensuring the accurate collection of data. Key tasks include preparing patients for polysomnography, performing diagnostic and therapeutic sleep studies, maintaining equipment, and adhering to quality control standards. The role also involves collaborating with healthcare professionals to analyze results and assist in patient care. Qualifications Proficiency with laboratory equipment and tools relevant to sleep study operations Strong quality control and analytical skills for accurately interpreting study results Comprehensive knowledge of laboratory skills and experience as a laboratory technician Excellent attention to detail and ability to maintain accurate reporting and documentation Effective communication skills and ability to empathize with patients Certification in polysomnography or relevant experience in sleep studies preferred RST certification required

HealthTrust Workforce Solutions Local is seeking a per diem / prn Cath Lab Technologist for a per diem / prn job in West Bradenton, Florida. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: Ongoing Employment Type: Per Diem Posted rates reflects the maximum rate, including night and weekend shift differentials Entrust Your Career to HealthTrust! At HealthTrust, we believe that healthcare is not defined by the four walls in which it is practiced; it's defined by its people. We pride ourselves on crafting opportunities that expand skill sets, broaden career horizons, provide economic stability, and cultivate personal growth. HealthTrust Offers: Getting to know HCA facilities within 50mi of home zip code Self scheduling through our Mobile GO HWS App Minimum of just three shifts a month, however, you can work more! 401K Matching Weekly pay every Friday Not required to work weekends Not Required to work holidays To get started, you will need: RN's a minimum of 1 year in specialty Allied 6 months of experience An adventurous spirit and fierce dedication Degree in corresponding specialty as required Appropriate certifications for the specific position HealthTrust Benefits: Opportunities for a lifetime: When you become a part of the HCA family, you will have exclusive access to more opportunities than any other healthcare system in the nation. At HWS, we help open the door to a lifetime of lasting career opportunities. A culture of care: Our clinicians have made HWS an industry leader for over 25 years. We are passionate about our mission that, above all else, we are committed to the care and improvement of human life. Career Development: As a wholly owned subsidiary of HCA Healthcare, HWS is a preferred partner to thousands of top-performing hospitals. We provide our healthcare professionals with first-priority access to more than 200,000 jobs nationwide. We are uniquely positioned to offer you exclusive and direct access to HCA Healthcare's vast network of facilities. Let us open the door to nationwide opportunities that fit your lifestyle! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Job Requirements Certifications ACLS (Required) BLS (Required) HealthTrust Workforce Solutions Per Diem Job ID #407855. Posted job title: Per Diem Cath Lab Tech - General - Cath Lab Tech

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. If you would like to be considered for employment opportunities with Accenture and have accommodation needs such as for a disability or religious observance, please call us toll free at **************** or send us an email or speak with your recruiter. Equal Employment Opportunity Statement We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. 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. The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Additionally, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the Company's legal duty to furnish information. California requires additional notifications for applicants and employees. 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Job Requisition Name Quality Analytical Chemist Job Requisition No VN8368 USA - Sarasota Worker Basis Full Time Worker Type Employee Applications Close Date Mar 31, 2026 Purpose As a Quality Control Analytical Chemist, you will be responsible for performing analytical testing of incoming materials, in-process samples, and finished materials within a regulated medical device manufacturing environment. You will ensure that materials meet defined specifications and regulatory requirements through accurate chemical analysis, thorough documentation, and close collaboration with internal and external stakeholders. * Perform analytical testing of incoming, in-process, and finished materials using techniques such as HPLC, GC, FTIR, UV-Vis, pH, titration, and conductivity * Inspect materials visually and dimensionally and approve or reject them based on specifications and test results * Accurately document analytical results and quality data in quality systems and databases * Prepare and maintain Certificates of Analysis, Nonconformance Reports, and related quality documentation * Ensure compliance with GMP, ISO 13485, and FDA regulatory requirements * Support internal and external audits by providing analytical data and documentation * Collaborate with internal teams and suppliers on quality issues, root cause analysis, CAPA, and continuous improvement * Associate or Bachelor's degree in Chemistry, Chemical Engineering, or a related field * Minimum 3 years of experience in analytical testing or quality inspection within a regulated industry * Proficiency in analytical techniques and laboratory instruments such as HPLC, GC, FTIR, UV-Vis spectroscopy, pH measurement, titration, and conductivity testing * Strong understanding of GMP, ISO 13485, and FDA regulatory requirements * Ability to interpret technical drawings, specifications, and tolerances * High attention to detail with strong documentation and communication skills Preferred Skills * Knowledge of statistical process control (SPC) * Familiarity with risk management and validation protocols BVI is refocusing the future of vision. As one of the fastest-growing, diversified surgical ophthalmic businesses in the world, our purpose-built portfolio of trusted brands includes: Beaver (Knives and Blades), Visitec (Cannulas), Malosa (Single-Use Instruments), Vitreq (Vitreoretinal Surgical Products) and PhysIOL (Premium IOLs), and spans more than 90 countries. We've set our sights on touching the lives of millions of patients affected by conditions such as cataracts, refractive error, glaucoma, retinal disease, and dry eye. Unburdened by legacy or bureaucracy, we have developed our strategy around a simple concept - taking pride in delivering innovative solutions for our physicians and patients, based on their needs. We trust and empower our associates to make decisions and solve problems because collaboration drives us. Valuing agility, simplicity, and transparency, we stay committed to listening to our customers, delivering for our patients, and keeping the future in focus. Learn more at ******************

It is the primary responsibility of the Analytical Chemist to maintain the instrumentation and analytical methods in the Analytical Sciences laboratory in a state of readiness for the analysis of essential oils and isolates for agricultural residues and other trace contaminants. DUTIES & RESPONSIBILITIES: Preparation, dilution and extraction, where appropriate, of samples for trace analysis Calibration of analytical balances and pipettes Instrument preparation including creation of sequences (GLC, GC-MS, GC-MSMS, GC-XSD and UHPLC) Data analysis, interpretation and reporting of trace analytical results (GLC, GC-MS, GC-MSMS, GC-XSD and UHPLC) Maintenance of the analytical calibration and verification spreadsheets (GC; GC-MS; GC-MSMS, GC-XSD and UHPLC) Advanced instrument maintenance & troubleshooting (GC; GC-MS; GC-MSMS, GC-XSD and UHPLC) Maintenance of the equipment down time log Method development and maintenance of advanced quantitative methods Preparation and appropriate storage of calibration standards for trace analysis Assist and contribute to Global Technical projects Maintain the supply of gas to the instrumentation by changing gas cylinders when required Monitor and log the ordering, receipt and return of gas cylinders on site including maintenance of the gas usage log Perform classical and/or instrumental analysis on any QC samples as and when requested by the Global Analytical Innovation Manager or the Quality Control Manager. Raise purchase orders where appropriate to replenish consumables and reagents. Report and address any deficiencies in equipment or analytical practices to Global Analytical Innovation Manager Undergo training in areas specific to Treatt PLC business Statistical data evaluation of new and existing analytical methods Write Quality Policies, Procedures and Operating Instructions. Ensure that the working area in the laboratory is maintained in a clean and orderly condition and that any hazard or potential hazard is reported to the Line Manager or H&S Officer Act in the best interest of Treatt PLC at all times Employees have a legal duty to take reasonable care of their own health and safety and that of others who may be affected by what they do at work. EDUCAION & TRAINING: Bachelor of Science Degree with Science Major or Master of Science Degree KNOWLEDGE & EXPERIENCE: Strong analytical skills with a minimum of 3 years' laboratory experience. Significant experience in working with GC-FID, HPLC, GC/MS Some experience in working with GC/MSMS and LC/MSMS preferred Knowledge of analytical disciplines, methods, developments and troubleshooting. Significant experience in data collection, extraction and analysis with strong analytical, problem-solving and research skills. Passionate about keeping up to date with relevant scientific and technological developments. The capability to organize and prioritize with a strong eye for detail. Excellent interpersonal and relationship skills with the ability to support teams and colleagues. Intermediate classical analytical skills. Exposure to hazardous Chemical WORKING CONDITIONS: Exposure to hazardous Chemical Open Office - typical spacious room, desks close together Shop floor, including some time inside and outside production

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.

Job Description Position Overview Engineered Bonding Solutions, LLC seeks an experienced Chemist to lead product development, formulation, and materials testing. This salaried role involves creating and modifying adhesives, performing rigorous testing (including Instron or comparable equipment such as the Frank Bacon SSTM-20kN), and preparing technical reports. The Chemist will collaborate closely with sales, customers, and manufacturing to support commercialization, quality, and process improvements. Key Responsibilities Develop and modify adhesive formulations for targeted applications and markets. Conduct product testing and evaluation, including specimen preparation per ASTM standards. Operate and interpret data from mechanical testing equipment (Instron, Frank Bacon SSTM-20kN). Prepare clear, concise technical reports and visual presentations. Partner with sales and customers to provide input, technical service, and field support. Implement cost savings through formula optimization, raw material selection, and process improvements. Manage product scale-up from lab to full production. Oversee technical aspects of manufacturing and provide production support as needed. Perform quality control testing on products and incoming raw materials. Maintain ISO-compliant documentation and support internal/external audits. Ensure lab notebooks meet legal and intellectual property requirements. Promote safe laboratory practices and maintain organized, clean work areas. Qualifications Bachelor's degree or higher in Chemistry. Minimum 10 years' experience in adhesives development, technical service, or manufacturing. Strong knowledge of polymers (unsaturated polyesters, urethanes, epoxies) and reactive monomers. Experience with raw material analysis and mechanical testing of composites. Proficiency with ASTM testing methods for adhesives and composites (ASTM D1002, D5868, D638, etc.). Skilled in writing technical reports and documenting product testing. Familiarity with Quality Assurance, ISO procedures, and Good Manufacturing Practices. Physical Requirements Ability to perform light labor in varied indoor/outdoor conditions (including heat and humidity). Comfortable working around fumes, airborne particles, vibration, and noise with proper PPE. Ability to lift, push, or pull up to 25 lbs. and stand for extended periods. Strong vision requirements including color, depth perception, and focus adjustment. E04JI800t97s407tqe8

1. Conduct sample processing and perform established complex analytical procedures, adhering to QA/QC protocols, methods, and instrumentation, under the supervision of a professional staff member. 2. Spend at least 50% of time performing work requiring scientific or specialized Analytical studies; supporting other NCASI programs for about 50+ % of time and no more than 20% of work week devoted to activities that are not a part of professional work. 3. Ability to manage multiple tasks concurrently while maintaining exceptional organizational skills. 4. Consistently exercise discretion and judgment with respect to scientific or specialized work. 5. Potential for effective self-direction and independent action in providing technical support. 6. Advise local managers and professional staff on technical support matters in your area of expertise. 7. Ensure the preparedness of the local site to perform laboratory work in program areas, such as the flawless operation of all analytical instrumentation on-site, operation of a computer-based model, or performance of certain field studies. 8. Read, understand, absorb, process, and communicate complex information. Respond to internal technical queries in a competent and timely manner. Work at the office location or during special projects from a field location for extended periods. 9. Must be able to get to and work from the Newberry Office & Laboratories and field locations as required. Skills Chemistry, Hplc, Analytical chemistry, Laboratory, Quality control, Wet chemistry, Chemical, Gas chromatography, Chromatography, Icp, Gcms, Qc Top Skills Details Chemistry,Hplc,Analytical chemistry,Laboratory,Quality control,Wet chemistry,Chemical,Gas chromatography,Chromatography Additional Skills & Qualifications BS in Chemistry or related discipline 3+ years of Chemistry lab experience Proficiency in Gas Chromatography: Sample Prep, Instrumentation Maintenance, GC Analysis/operation Experience Level Entry Level Job Type & Location This is a Contract to Hire position based out of Newberry, FL. Pay and Benefits The pay range for this position is $26.00 - $38.00/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 Newberry,FL. Application Deadline This position is anticipated to close on Dec 31, 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Tampa is seeking a QC Chemist to join the Quality Control team. The incubment will be Conduct analysis of raw materials, In process items and finished products Key Accountabilities Analysis of dry product stability and finished product samples according to the assigned specifications, analytical methodology and protocols in a GMP laboratory setting with emphasis on attention to detail and accuracy of execution. Documentation of results in accordance with cGMP Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Reports lab testing data and completes documentation accurately and in accordance with laboratory procedures and regulatory requirements Reviews results for conformance to standards Perform analytical testing of pharmaceutical products following analytical methodology Read and interpret analytical methodology and the USP Supports method development and validation of new methods Performs investigations and completes CAPA in response to deviations. Develops and executes validation protocols for test methods and equipment qualification as requested. Meet fundamental cGMP requirements relating to conduct and work practices to ensure the SISPQ (Safety, Identity, Strength, Purity, and Quality) of the all products manufactured/tested at Lonza Tampa. Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible Stop work where deemed necessary to maintain safety Key Requirement Associate's Degree in Science, preferably chemistry Minimum of 3 years experience in a GMP pharma environment Actively participates in customer and regulatory audits Demonstrated experience with peer review work and data of other analysts to ensure compliance with method and regulatory requirements Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

We are currently accepting applications for future Quality Control Chemists. WHY CORERX CoreRx, a dynamic pharmaceutical technology company that empowers its employees with responsibility and offers a supportive and highly progressive work environment. At CoreRx you will find a challenging career path directed towards growth and opportunity. We employ talented, motivated people - team players who are innovative thinkers. We offer our employees a comprehensive, competitive program of benefits and a corporate culture based on core values that include innovation, a results-oriented focus and ethical behavior. If we do not have any positions that fit your needs at this time; We invite you to join our talent network and stay informed about future opportunities by submitting your resume. Thank you for choosing CoreRx as your employer of choice. DESCRIPTION The Analytical Chemist II is an integral part of the team, contributing to our success by performing raw materials and clinical and commercial pharmaceutical products testing according to compendial method and/or methods provided by analytical development team or clients. ESSENTIAL DUTIES AND RESPONSIBILITIES Performs relevant QC testing, such as HPLC, GC, Dissolution, Malvern and wet chemistry testing as required in compliance with cGMP requirements, compendia standards, and internal procedures 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, and stability products in an FDA regulated lab environment Perform analysis with a practical understanding of the test procedure and instrument operation Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results Conducts laboratory investigation under the supervision of laboratory manager. Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, documentation Maintain required level of training needed to perform a GMP task Notify manager immediately of nonconforming data or unexpected occurrences Organize work schedule to complete assigned tasks efficiently and on schedule Work under direction provided by manager Conscientious with safety procedures and knowledgeable of hazardous waste procedures Performs other related duties as assigned by management EXPERIENCE AND EDUCATION REQUIREMENTS Experience in UPLC/HPLC GMP operations Knowledge with analytical equipment and Part 11 compliant software, such as Chemstation™, Chromeleon™, EMPOWER™, and Laboratory Information Management System. Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment Proficient in Microsoft Office Suite or similar software Minimum of 2 years experience preferred in an FDA-regulated pharmaceutical environment Experience in other highly regulated laboratory settings will be considered BS/BA in life science or chemistry required Equivalent experience may substitute for stated requirements PHYSICAL DEMANDS Regularly required to stand. Frequently required to sit, walk, talk, hear, handle or feel tools or controls Occasionally required to reach with hands and arms, stoop, crouch, climb or balance, kneel Vision suitable for performing detailed inspections May be required to move items weighing up to 25 lb Ability to communicate clearly in both written and verbal form We are an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all applicable Federal and State laws, regulations, and executive orders regarding nondiscrimination and affirmative action with our hiring activities. We do not discriminate based on race, color, religion, ethnic or national origin, gender, genetic information, age, disability, sexual orientation, gender identity, gender expression, and veteran's status. Notification to Agencies: Please note that CoreRx Inc. does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, CoreRx Inc. will not consider or approve payment regarding recruiter fees or referral compensation.

Job Description and Objectives The Analytical Chemist job duties consist of the technical aspects of the department in support of directions from the QC Analytical Lab Supervisor and the Quality Operations Manager. He/She is responsible for ensuring regulatory compliance to FDA Guidelines (DSHEA), customer requirements, and departmental function. The primary responsibility is to develop and validate analytical methods for various dietary finished product matrixes and train analysts and chemists. He/She will support analytical testing of incoming raw materials, in-process samples, stability, and finished goods within the QC Laboratory. Essential Job Functions Coordinate the testing of raw materials and finished goods with outside labs when required, and allocate results of said testing to the necessary persons. Develop and perform analytical methods based on adaptations of USP, AOAC, NSF, or other industrial resources. Write SOPs and methods to meet cGMP's and GLP. Validate and qualify laboratory methods including writing of protocols and reports. Train chemists and analysts on laboratory methods & procedures when requested. Assist and supervise incoming raw materials and finished product analytical analysis. Perform daily testing of incoming samples using wet chemical and instrumental techniques, as needed. Maintain and record analytical data within prescribed notebooks. Compile analytical testing data and issue testing justification documentation. Compile lab results and issue completed worksheets for final review. Prepare various laboratory reagents as required for daily operations. Order and stock all lab supplies required for operation while keeping cost down through effective sourcing and purchasing. Ensure accuracy and completeness of all QC logbooks and binders. Provide peer review of other chemists' work as needed. Ensure that the QC lab is kept in good repair. Communicate issues and non-conformances to the QC Analytical Lab Supervisor and Quality Operations Manager immediately. Conduct Lab Investigations for all unexpected results. Knowledge, Skills, and Abilities Required Must be Proficient in PC functions, (WORD, EXCEL, ACCESS, POWERPOINT, etc.) and Empower software. Must be well organized and detail oriented. Demonstrate good verbal and written communication skills. Be familiar with and demonstrate excellent advanced laboratory problem solving skills. Must be experienced in advanced laboratory testing methods. Must be knowledgeable in HPLC configuration including column designs, flow rates, reagent variabilities, wavelengths, and detectors. Must be knowledgeable in solubility factors, oil products, water-based products, and oil/water emulsions and the impacts to testing formulations of these designs. Must demonstrate Good Laboratory Practice in completing daily work assignments. Competent in performing mathematical and scientific calculations as they relate to job function. Communication and management skills. Ability to manage, carry out, and prioritize analytical functions. Ability to see areas that need improvement and to address them. Supervisory Responsibility Responsible for ensuring all requirements for Analytical functions are met. Responsible for providing an evaluation of the technical performance of analytical chemists as requested. Working Conditions Working functions are generally limited to the QC lab with some facility work at times. Minimum Qualifications BS Degree in chemistry, analytical chemistry, instrumental analysis, physical chemistry (or extensive analytical laboratory experience in lieu of degree) . 10 years previous laboratory experience. Driven, intelligent, and motivated to succeed and improve. Extensive Analytical (HPLC) analysis experience Excellent people skills, and ability to function under pressure. Success Factors Driven and motivated. Technical leadership. Intelligent and displays aptitude. Problem solving skills. Detail oriented. Self-motivated team player. Well organized. Willingness to cooperate and work with other departments. Benefits Retirement plan 401(k) - 401(k) matching Dental, Vision, Health, Short/long term disability and Life insurance Paid time off Holiday

and Objectives The Analytical Chemist job duties consist of the technical aspects of the department in support of directions from the QC Analytical Lab Supervisor and the Quality Operations Manager. He/She is responsible for ensuring regulatory compliance to FDA Guidelines (DSHEA), customer requirements, and departmental function. The primary responsibility is to develop and validate analytical methods for various dietary finished product matrixes and train analysts and chemists. He/She will support analytical testing of incoming raw materials, in-process samples, stability, and finished goods within the QC Laboratory. Essential Job Functions * Coordinate the testing of raw materials and finished goods with outside labs when required, and allocate results of said testing to the necessary persons. * Develop and perform analytical methods based on adaptations of USP, AOAC, NSF, or other industrial resources. * Write SOPs and methods to meet cGMP's and GLP. * Validate and qualify laboratory methods including writing of protocols and reports. * Train chemists and analysts on laboratory methods & procedures when requested. * Assist and supervise incoming raw materials and finished product analytical analysis. * Perform daily testing of incoming samples using wet chemical and instrumental techniques, as needed. * Maintain and record analytical data within prescribed notebooks. * Compile analytical testing data and issue testing justification documentation. * Compile lab results and issue completed worksheets for final review. * Prepare various laboratory reagents as required for daily operations. * Order and stock all lab supplies required for operation while keeping cost down through effective sourcing and purchasing. * Ensure accuracy and completeness of all QC logbooks and binders. * Provide peer review of other chemists' work as needed. * Ensure that the QC lab is kept in good repair. * Communicate issues and non-conformances to the QC Analytical Lab Supervisor and Quality Operations Manager immediately. * Conduct Lab Investigations for all unexpected results. Knowledge, Skills, and Abilities Required * Must be Proficient in PC functions, (WORD, EXCEL, ACCESS, POWERPOINT, etc.) and Empower software. * Must be well organized and detail oriented. * Demonstrate good verbal and written communication skills. * Be familiar with and demonstrate excellent advanced laboratory problem solving skills. * Must be experienced in advanced laboratory testing methods. * Must be knowledgeable in HPLC configuration including column designs, flow rates, reagent variabilities, wavelengths, and detectors. * Must be knowledgeable in solubility factors, oil products, water-based products, and oil/water emulsions and the impacts to testing formulations of these designs. * Must demonstrate Good Laboratory Practice in completing daily work assignments. * Competent in performing mathematical and scientific calculations as they relate to job function. Communication and management skills. * Ability to manage, carry out, and prioritize analytical functions. * Ability to see areas that need improvement and to address them. Supervisory Responsibility * Responsible for ensuring all requirements for Analytical functions are met. * Responsible for providing an evaluation of the technical performance of analytical chemists as requested. Working Conditions * Working functions are generally limited to the QC lab with some facility work at times. Minimum Qualifications * BS Degree in chemistry, analytical chemistry, instrumental analysis, physical chemistry (or extensive analytical laboratory experience in lieu of degree) . * 10 years previous laboratory experience. * Driven, intelligent, and motivated to succeed and improve. * Extensive Analytical (HPLC) analysis experience * Excellent people skills, and ability to function under pressure. Success Factors * Driven and motivated. * Technical leadership. * Intelligent and displays aptitude. * Problem solving skills. * Detail oriented. * Self-motivated team player. * Well organized. * Willingness to cooperate and work with other departments. Benefits * Retirement plan 401(k) - 401(k) matching * Dental, Vision, Health, Short/long term disability and Life insurance * Paid time off * Holiday

Job Title: QC Chemist Ready to make an impact? Join Lonza Tampa as a QC Chemist and help ensure the quality and safety of life-changing medicines. In this role, you'll work in a cutting-edge GMP laboratory, collaborating with passionate professionals to deliver products that improve lives worldwide. What you will get * An agile career and dynamic working culture. * An inclusive and ethical workplace. * Compensation programs that recognize high performance. * Medical, dental, and vision insurance. * Our full list of global benefits can be found here: *************************************** What you will do * Perform analytical testing of raw materials, in-process items, and finished products in a GMP laboratory setting. * Document results accurately in compliance with cGMP and regulatory standards. * Review data for conformance to specifications and report findings promptly. * Support method development, validation, and equipment qualification activities. * Investigate deviations and implement corrective and preventive actions (CAPA). * Ensure adherence to FDA, EPA, and OSHA regulations while maintaining safety and sustainability standards. * Contribute to maintaining product Safety, Identity, Strength, Purity, and Quality (SISPQ). What we are looking for * Associate's Degree in Science, preferably Chemistry required. * Minimum of 3 years' experience in a GMP pharmaceutical environment required. * Proficient in HPLC techniques, including hands-on experience with Empower software required. * Familiarity with Solutia systems or similar platforms required. * Strong knowledge of analytical methodologies and USP standards. * Ability to review peer data for compliance with regulatory requirements. * Experience supporting audits and regulatory inspections. * Detail-oriented with strong documentation and problem-solving skills. * Commitment to safety and quality in all work practices. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now

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.

Disclaimer: Please note, if you are selected to have an interview with Thermacell, you will receive an email from our applicant tracking system Paylocity (**********************************) or an email from a Thermacell.net domain. Be aware of phishing emails/text messages. Thermacell will never text or Skype you about your candidacy or personal confidential information. If you are unsure, please contact **********************. THE COMPANY Thermacell Repellents, Inc. (TRI) is a privately held company with a mission to liberate people who love the outdoors from the harmful effects of insects . Founded in 1999 and based outside of Boston in Bedford, Massachusetts, Thermacell makes the world's leading spatial mosquito repellent and targeted tick control solutions. Dedicated to delivering the best consumer experience, we have an ever-expanding product line for both adventure and home use. We aim to change the way people repel insects, and through disruptive innovation, strong distribution across multiple retail channels, and a global footprint, our base of users is growing rapidly. TRI currently employs 125+ full time employees at our 4 locations: Bedford Massachusetts (Corporate HQ), Buford Georgia (Manufacturing & Distribution), Hampton, FL (Science & Research Center). POSITION PURPOSE: Thermacell is seeking a highly motivated Chemist - Formulations as part of the Science and Research team to take an active role in developing and refining new and existing product chemistries and performing necessary regulatory and analytical testing. This new position will work at the Thermacell testing facility in Hampton, Florida under the daily supervision of and reporting to the Science Manager. STATUS: Exempt WORKING HOURS: Typically, between 8 - 4 pm M-F (Weekend and evening availability as needed) WORK LOCATION: Hampton, FL (~20 miles from Gainesville, FL and ~70 miles from Jacksonville, FL) Please note: Immigration Sponsorship is not available for this role. What Success Looks Like: A successful employee assimilates to our company culture quickly, takes pride in ownership, and demonstrates expertise across all areas of responsibility. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES: In this role, you'll get to: • Develop new formulas that meet performance targets and create new product concepts using innovative formulation ideas. • Conduct Good Laboratory Practice (GLP) and non-GLP laboratory studies to accurately document the quality, safety, and characterization of chemical compounds and formulations. • Utilize contract labs as needed to develop primary and supporting data requiring specialized equipment or to meet project timelines. • Collaborate with cross-functional teams, including product development, engineering, manufacturing, marketing, and regulatory affairs to ensure that new and existing products meet company specifications. • Assist with logistics needed to support chemistry laboratory and quality assurance requirements. • Maintain an orderly laboratory space and ensure compliance with laboratory, facility, and organizational safety programs. • Mentor and guide junior team members. • Assist in other duties as assigned to support the laboratory and global business. THE IDEAL CANDIDATE PROFILE We are looking for a candidate who: · Lives our core values of Drive, Ownership, Integrity, Teamwork and Evolution · Authentic and personable, humble, smart · Relentless work ethic juiced by results, not titles or activities · Externally competitive, internally collaborative · Highly resourceful. Hands-on and practical · Chooses curiosity and a commitment to learning over being right · Radically candid - always with positive intention · Motivated by challenge, resilient in the face of setbacks or adversity · Able to critically think and navigate within a variety of ambiguous situations · Even keeled energy, brings calm to chaos, low drama · Make impeccable agreements, deliver end to end results with excellence · Makes high quality data-based decisions with autonomy · Unquenchable thirst for learning and self-improvement · Effective communicator meeting people where they are · Manages multiple, complex, and competing priorities · Can anticipate data needs to support existing products and new product applications. · Maintains and delivers timely, accurate reports to support the global business. · Shows STRONG attention to detail and accuracy. · Is a highly resourceful problem solver that is not discouraged by creative troubleshooting. · Has proven ability to handle confidential information with discretion and maturity. · Believes safety is paramount. COMPENSATION Compensation for this position will include a competitive base salary and an Annual Target Bonus program-details proved separately. Benefits for this position will consist of vacation benefits at a competitive level & 10 paid company holidays. Additionally, a company shut-down period is offered for one week between Christmas and New Year's Day. We are proud to offer a competitive & valuable benefits package that enables you to protect your health, your family, and your way of life. It includes best-in-class medical & dental insurance where Thermacell pays for 82.5% of the premiums; Thermacell also pays for the first half of your medical deductible through our Health Reimbursement Account. Long & Short-term Disability & Group Term Life insurance (one-time base salary plus bonus up to max) is also available at no cost to you. Forty hours of sick time is also available on your first day of employment. Additionally, you will have access to a variety of additional benefits such as vision, supplemental life, critical illness, Medical FSA (Flexible Spending Account), Dependent Care FSA, accident, SecureSave savings account, EAP (Employee Assistance Program), product benefit, wellness benefit, and pet insurance for your furry family members! You can find all the details and additional discounts in our benefits guide. You may start contributing to our 401k after completing 30 days of service (enrolling on the first of the following month). You will be eligible for the employer match up to 4% (base salary + overtime wages - subject to the IRS (Internal Revenue Service) legal limit) after completing one year of service. WHY WORK HERE? We are proud of our company culture - it's the fuel behind our dynamic and buzzing community! Our people are authentic, competitive and compassionate. It's truly a unique formula for success. We believe in the virtuous cycle of thriving employees fueling a thriving business. We believe in growing great leaders and helping people to unleash their full human potential. We believe in creating a frictionless organization where clarity and empowerment to do the work that matters as fast as possible. We believe in making impeccable agreements and relentlessly tracking exceptional results and celebrating achievements together! We believe in creating inspiring impact everywhere we can in support of our mission where everyone can be a force multiplier. OUR CORE VALUES: Drive - An optimistic can-do spirit, a passion to delight our consumer, a belief in the importance of determination and the freedom to make a difference. Ownership - We are empowered to take accountability for our contributions and desire to do the highest quality work with responsible urgency to drive business results. Integrity - We will always do the right thing guided by truth and sincerity. We exercise constructive candor and have the willingness to challenge and be challenged in all interactions. Teamwork - The belief that we is greater than me, and with collective brainpower we are better together. We are a community of compassionate support and collective success. We win as one and play hard in celebration together. Evolution - We are committed to continuous improvement, always learning, growing, and adapting to constant change. We seek progress over perfection. OUR COMMITMENT: Thermacell is committed to preserving a culture of diversity, inclusion, and belonging. The collective sum of our individual differences, knowledge, life experiences, and unique talents represents a significant part of our culture and is the foundation for our accomplishments and impact. We strive to create a supportive community where we all can show up as our authentic selves and are confident and comfortable to be genuine with our teammates in our day-to-day work environment. We are proud to be an equal-opportunity employer. We do not discriminate on the basis of race, color, religion, citizenship, national origin, sex (including pregnancy), sexual orientation, gender identity or expression, age, physical or mental disability, veteran status, marital status, genetic information, or any other characteristic protected by state, federal or local law. OUR AWARDS: Popular Mechanics - Grand Award Winner - Recreation - Best of What's New 2018 New York Times Wirecutter - The Best Mosquito Control Gear for Your Patio or Yard Outside Magazine - Best Car Camping Gear 2018 Backpacker Magazine - Best Backpacking Accessory 2019 Field & Stream “Best of the Best” Award - Good Housekeeping Research Institute #1 Tabletop Mosquito Repellent - LIV Smart Mosquito Repellent System - CES TWICE Awards 2022-2021 - Canadian Tire Digital Excellence Award - CES New Tech Award - IDEA Good Design Award - Good Housekeeping Home Products Award - This Old House Editor's Choice - Time Magazine Best Inventions 2022, Outside Gear Guide Editor's Choice 2022, NYT Wirecutter pick for “The Best Mosquito Control Gear for your Patio or Yard” 2023, CNN Underscored Editor's Pick 2024 Requirements Bachelor's degree in chemistry is required Master's is preferred Minimum 2-5 years of professional industry experience in formulation and/or analytical chemistry - experience in pesticide/bioactive product formulation preferred. Proven ability to develop analytical and formulation methods and to write protocols, repots and SOPs Familiarity with global regulatory standards; Good Laboratory Practice (GLP) experience is preferred. Familiarity and proficiency with wet chemistry techniques and analytical laboratory equipment (e.g. GC-MS, GC-FID, HPLC, etc.). Ability to plan, organize, and troubleshoot multiple projects on concurrent timelines and adapt to shifting priorities. Ability to stand for extended periods of time (4 or more hours) and conduct repetitive laboratory tasks. Comfortable using Microsoft Office 365 and other software. Salary Description $75,000-$85,000

Insight Global is seeking an experienced Senior Laboratory Systems Analyst to lead the implementation, Epic integration, and long-term sustainment of the Haemonetics SafeTrace TX Blood Bank application. This role is ideal for someone with a strong background in laboratory or Blood Bank information systems and hands-on experience configuring, fixing, and building backend solutions. The ideal candidate will have: - Experience with SafeTrace TX and Epic Beaker. - Familiarity with HL7 interfaces and middleware solutions like Data Innovations. - A solid understanding of Blood Bank workflows and regulatory compliance. - Previous experience as a Medical Technologist who now works on the technical side of Blood Bank systems. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements - Bachelor's degree in Computer Science, MIS, Information Sciences, or related discipline OR equivalent work experience. - 3-5 years of experience supporting or implementing laboratory or Blood Bank information systems in a hospital setting. - Familiarity with HL7 interfaces, data integration, and middleware solutions such as Data Innovations. - Understanding of Blood Bank workflows, including product management, crossmatching, transfusion documentation, and regulatory compliance. - Strong analytical, troubleshooting, and problem-solving skills. - Excellent communication and collaboration abilities to work with cross-functional clinical and IT teams. - Ability to manage multiple priorities in a fast-paced environment. - Local to South Florida Tri-County area (Miami-Dade, Broward, Palm Beach) or willing to relocate. Relocation will be compensated for. - Experience with Haemonetics SafeTrace TX (highly preferred). - Knowledge of Epic Beaker or prior Epic implementation experience. - Certification as an MT/MLS (ASCP) or equivalent. - Prior experience as a Medical Technologist who transitioned into backend system configuration, troubleshooting, and build.

Pay: $16.00/hour (Full-Time, Non-Exempt) Let's Be Blunt Cannabis isn't just an industry - it's a movement. At Mint Cannabis, innovation and precision drive everything we do - especially in our production labs. We're looking for a Formulation Technician to join our team and help create high-quality cannabis products by carefully blending distillates, terpenes, and other components. This hands-on role is perfect for someone who's detail-oriented, science-minded, and passionate about product consistency and safety. You'll work alongside our production and extraction teams to ensure every batch meets Mint's high standards for quality and compliance. Ready to mix things up and make an impact? 🌱 Let's make it happen. What You'll Do Accurately measure, mix, and blend cannabis distillates and terpenes according to established formulations and SOPs Operate and maintain laboratory equipment and mixing tools in a clean, safe, and compliant manner Assist in the preparation of raw materials and finished products for packaging and testing Follow safety and sanitation procedures to maintain a compliant work environment Conduct visual inspections and quality checks during formulation to ensure consistency and accuracy Collaborate with production leads and management to troubleshoot and optimize processes Maintain organization and cleanliness of the formulation lab and storage areas Support inventory tracking of ingredients, materials, and finished batches What You'll Bring 1+ year of experience in a production, laboratory, or food/pharmaceutical manufacturing environment (cannabis experience a plus) Strong attention to detail and ability to follow precise measurements and procedures Familiarity with basic lab or production equipment and safety protocols Strong organizational and record-keeping skills Ability to work efficiently in a fast-paced, high-volume environment Team player with good communication and collaboration skills Must be at least 21 years of age Must be able to obtain and maintain a Facility Agent Card in accordance with Florida state regulations Why You'll Love Mint Cannabis A work culture that's welcoming, passionate, and built on good vibes Opportunities for growth as we expand into new markets Employee discounts on Mint products and merch Health, dental, and vision benefits (for eligible roles) Paid time off to recharge and take care of you A chance to be part of something ama Zing 🌱 A Few Things You'll Need Ability to stand, bend, and perform repetitive tasks for extended periods Ability to lift up to 30 lbs Comfortable working around strong odors and raw cannabis materials Manual dexterity and visual acuity for precision measuring and mixing PPE required based on task or department policy About Mint Cannabis At Mint Cannabis, we're passionate about creating a premium cannabis experience - for everyone! Headquartered in Arizona, we're a national, multi-state operator proudly serving both medical patients and recreational customers. From state-of-the-art production facilities to dispensaries that redefine the retail experience, Mint is raising the bar in every market we enter. Our flagship location in Arizona - one of the largest dispensaries in the country - features a 24/7 storefront, the nation's first cannabis kitchen offering delicious infused foods, and a drive-thru for ultimate convenience. We're proud to offer a carefully curated menu of premium flower, concentrates, edibles, and more, designed to elevate the experience for seasoned consumers and newcomers alike. Named “Most Innovative Medical Cannabis Dispensary” by the International Commercial Cannabis Awards, Mint Cannabis continues to grow rapidly across Arizona, Michigan, Missouri, and beyond. Our team - from budtenders to leadership - is driven by passion, education, and a commitment to helping every guest feel welcome, informed, and supported. At Mint Cannabis, we're not just changing the cannabis industry - we're growing a community. Equal Opportunity Employer Statement Mint Cannabis is proud to be an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Verdant Specialty Solutions is a dynamic, innovation-driven specialty chemicals company with a global footprint. Born from the McIntyre Group of the 1970s and relaunched in 2021, Verdant combines the agility of a small business with the safety, reliability, and scale of a larger organization, offering personal attention backed by industry-leading manufacturing and technical capabilities. With over 375 product offerings, nine strategic sites across the U.S. and Europe, and a steadfast commitment to sustainability, compliance, and customer-centric solutions, Verdant brings functional chemistry to life safely, reliably, and responsively. Are you a hands-on chemist who loves ensuring quality, safety, and operational excellence? Verdant Specialty Solutions, a global specialty chemical company serving world-leading consumer, industrial, and energy brands, is looking for a Quality Control Chemist to join our University Park team. Why this role is exciting: * Play a key role in a fast-growing, start-up-like environment with global impact * Work with cutting-edge specialty surfactant chemistries for top-tier clients * Contribute directly to safety, quality, and operational excellence across multiple sites * Opportunities to grow professionally in a collaborative, innovative culture What you will do: * Perform in-process, final product, and raw material analyses * Certify products for shipment and maintain accurate lab records * Collaborate with operators, engineers, and QC colleagues to optimize processes * Participate in process improvements, investigations, and quality initiatives * Maintain compliance with ISO 9001, EFfCI, GMP, RSPO, and HSSE standards * Operate lab systems (SAP) to track data, generate certificates, and manage inventories