Chemist Jobs in Jesup, GA

Performs routine patient assessments, scores sleep records, documents other test results, and collects and transmits biological specimens for analysis. Entity MUSC Community Physicians (MCP) Worker Type Employee Worker Sub-Type PRN Cost Center CC005005 MCP - Beaufort MUSC Sleep Medicine Pay Rate Type Hourly Pay Grade Health-27 Scheduled Weekly Hours 40 Work Shift Under the direction of a physician, administers various sleep studies in order to diagnose the type and extent of sleep disorders. Performs routine patient assessments, scores sleep records, documents other test results, and collects and transmits biological specimens for analysis. Additional Job Description Education: Bachelors Degree or equivalent Work Experience: 4-6 years If you like working with energetic enthusiastic individuals, you will enjoy your career with us! The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need. Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: ***************************************

Associate Scientist II Kelly Services has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a multiple direct hire opportunities to work as an Associate Scientist II located near the Ft. Lauderdale/Miami, FL area. Shift: Monday-Friday, 2nd shift, 4pm-12am Function: Chemistry, Manufacturing, and Control (CMC) Relocation offered Salary: Associate Scientist II : $65,000-85,000 plus 10% target bonus Job Summary: We are seeking a highly motivated Scientist (multiple levels) to join our Analytical Sciences team. The successful candidate will be responsible for conducting laboratory activities related to the development, optimization, transfer, and validation of analytical methods for drug products. The role involves using a variety of analytical techniques, such as liquid chromatography (LC), spectroscopy, and aerosol performance techniques for orally inhaled and nasal drug products (OINDP). The Scientist will also be responsible for conducting physico-chemical characterization studies, performing data analysis, and drafting scientific documents to meet global regulatory standards, including those from the US FDA and EMA. Key Responsibilities: Independently conduct standard and advanced laboratory activities, including liquid chromatography (LC), spectroscopy, and aerosol performance characterization studies for OINDPs. Perform physico-chemical and aerosol analytical characterization of OINDPs, including the evaluation and selection of raw materials such as APIs, excipients, and packaging materials. Develop, verify, optimize, transfer, and validate analytical methods in accordance with cGMPs, EH&S guidelines, and other regulatory requirements. Conduct in-depth data analysis using advanced statistical tools and techniques, identifying trends and making data-driven recommendations. Draft protocols, reports, SOPs, and regulatory submission documents regularly. Present data analysis and recommendations to senior management and communicate findings effectively with team members and external stakeholders. Troubleshoot technical issues and implement solutions in a timely manner. Ensure compliance with safety rules and corporate guidelines in all lab activities. Qualifications: Associate Scientist II: BSc in Chemistry, Pharmacy, or related fields with at least 3 years of experience in Pharmaceutical R&D, or MSc in Chemistry, Pharmacy, or related fields with 1-2 years of experience in Pharmaceutical R&D. Extensive knowledge and hands-on experience with chromatography (HPLC, GC), spectroscopy (UV, FTIR), and other analytical techniques. Must have at least 3 years of experience in method development and validation using HPLC and Empower software for pharmaceutical products Proven experience in analytical method development, verification, and validation. Strong technical writing skills with the ability to draft high-quality documents, including protocols, reports, and regulatory submission sections. Experience with orally inhaled and nasal drug products (DPI, MDI, or nasal drug products) is a plus. Familiarity with USP methodologies, ICH guidelines, FDA, and cGMP regulations. Strong English language communication skills, both written and oral. This position offers competitive salary and benefits, and the opportunity to contribute to cutting-edge pharmaceutical research and development.

First Quality was founded in 1989 and, in nearly three decades, has grown to be a global privately held company with over 4,000 employees. Its corporate offices are located in Great Neck, New York, with manufacturing facilities and offices in Pennsylvania, South Carolina, Georgia, and Canada. First Quality is a diversified family of companies manufacturing consumer products ranging from Absorbent Hygiene (adult incontinence, feminine care, and baby care), Tissue (bath and towel), and Industrial (print and packaging materials), serving institutional and retail markets throughout the world. First Quality focuses on private label and branded product lines. Our core business philosophy is built on a proud culture driven by safety and quality, respect, humility, integrity, customer focus, and teamwork. With leading edge manufacturing technologies and processes and visionary leadership, First Quality is positioned to continue significant growth in the coming years. We are seeking an experienced Product Development Raw Material Scientist for our First Quality Baby Products facility located in Macon, GA. This position will be responsible for the development and innovation of current and new products that meet and exceed customer/consumer needs while still meeting required cost targets. This position reports directly to the Product Development Leader and plays a crucial role in driving innovation and ensuring the successful launch of high-quality products. Primary responsibilities include: Leads the development of new products from concept through commercialization. Benchmarks competitive products, creates initial specification, produces concept samples, scales up process, confirms process capabilities, and finalizes specifications as needed to ensure successful commercial production. Works in close collaboration with Sales/Marketing, Engineering, and Operations in order to identify opportunities for new products and improvements to current products. Researches and maintains up-to-date information on competitive products and relevant research and patent literature. Works closely with suppliers' technical staff on development efforts. Works with Process Engineers and Quality Assurance to optimize the technical and economic performance of existing products. Maintains extensive contacts with material suppliers to allow development of new materials and optimizes the performance of current raw materials. Responsible for coordinating, analyzing, & documenting Product Development trials while interacting with Process Engineering, Operations and Quality Assurance. Organizes trials from the planning stages, monitoring runs and post-trial requirements. Ability to leverage Design of Experiments; Test products to assess product performance and attributes, New raw materials to evaluate their properties and determine their impact on finished goods, and Competitive products (benchmarking). Maintains a historical database, and provide summaries as needed. Responsible for interpreting data for such purposes as quality control, process control, cost savings, and/or product development. Assists in Consumer Usage Testing through product preparation and record keeping as well as data compilation and basic analysis. Maintains excellent data collection and research records. Devises/revises procedures, work instructions, and specifications (raw material, in-process, and finished goods). Ensures that all pertinent FQ GMP and Design Control requirements are met and maintain the necessary records. Prepares product samples for Sales, independent lab assessments, and product safety evaluations. Establishes effective working relationships with other departments (Engineering, Quality, Production Planning, & Production) to achieve product improvement, new product development, cost saving, and/or quality initiatives. Provides recommendations for improvements to our products, testing methods, processes, and potential cost savings. Assists the Product Development Leader with other responsibilities, as requested. The ideal candidate should possess the following: Four-year technical degree (e.g. Materials Science, Chemical Engineering, Mechanical Engineering) or equivalent; additional business studies preferred. Two + years Product Development experience in the Consumer Products or Medical /Healthcare industries, or equivalent combination of education and experience. Ability to define problems, collect data, establish facts, and draw valid conclusions. Excellent project management skills, with the ability to prioritize tasks, meet deadlines, and manage multiple projects simultaneously. Strong analytical skills and attention to detail; strong written and oral communication skills. Self-motivated and proactive attitude, with a passion for innovation and continuous improvement. Proficiency with computer applications, including Microsoft Office. Knowledge of statistical applications preferred. Knowledge of GMP, FDA, ISO 13485, and other applicable quality standards and regulations is preferred. Excellent compensation and benefits, which are effective the first day of employment! First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.

PRIMARY PURPOSE: The Quality Assurance Chemist has the responsibility of performing analysis on raw materials, products at any of the various stages of production, and finished goods, including toll produced materials.Has the authority, within guidelines, to approve and release, or quarantine raw materials and/or finished goods. REQUIRED SKILLS, KNOWLEDGE & EXPERIENCES: Minimum of 2 years post secondary education (BS degree in Science a plus). Preferred 2 years' experience in an industrial type environment, quality assurance experience preferred. Strong familiarity with PC's and Windows software. Capable of making decisions and working unsupervised (safely and effectively). Familiarity with Statistical Quality Control (SQC). Familiarity with Six Sigma principles. Strong GC/HPLC experience. Competent on or able to learn SAP system for QA transactions KEY RESPONSIBILITIES: QA Inspection, reporting, approval/release, record keeping for raw materials, in process and finished goods testing. Detailed administrative record keeping and filing of all QA activities as required, including generation of COA's and data entry into the Laboratory Information Management system (LIMS). Determine and calculate batch adjustments as necessary, mathematical and bench blends. Prepare and standardize reagents, maintain stock of supplies and chemicals, write up requisitions. Maintain lab instruments, equipment and apparatus in good condition. Calibrate as directed and keep records. SAP entry of analytical values; SAP transaction as required by QA; nonconformance tracking in SAP and Access. Participate in customer complaint and process incident investigations. Participate in Plant Safety Program effort, specifically completing safety training modules, and completing observations and incident reports. Responsible for Assembly Area I duties (roll call) during evacuations and drills. Participate in ISO 9001 Quality System improvement process. Contact and communicate with raw material suppliers, customers, Solvay customer satisfaction representatives, as necessary. Identify your internal and external customer and develop skills for working effectively. Train new chemists and technicians as necessary. Good housekeeping discipline. Collect, segregate and empty hazardous lab waste. Display commitment to continuous improvement in quality including ISO 9001 and EFFCI. HSE Responsibilities: Always approach your job with the principle that all incidents are preventable. To that end you need to keep the following aspects in mind: Always perform your job in a sound HS&E manner to protect yourself and those around you. Risk assessment is a mind set, where you are always assessing hazards and thinking about means to avoid those hazards. Take a proactive approach to maintain excellence in all your assignments. Be aware of your state of mind (rushing, frustration, fatigue & complacency) that leads to distractions from the task on hand. Those distractions lead to errors resulting in unwanted incidents. Use all the available tools for your benefits: HS&E training, Risk Assessment, Incident Reporting, checklists, and Manufacturing Excellence tools. Job completion means Good Housekeeping, filling necessary reports, and watching for your safety and those around you. Your Personal Protective Equipment is the most important tool you have as a professional chemical industry worker. Maintain and clean it properly. Participation leads to ownership. Get involved as often as you can. Physical Demand Requirements: The QA Chemist must be physically able to perform work such as operating lab testing equipment, moving waste drums, and other tasks typical of a QA Chemist. He/she must have the mental dexterity necessary to accomplish a multitude of tasks safely and effectively. The QA Chemist must be able to recognize unusual conditions, reason out the cause, and use good judgment in being able to deal with them safely.

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

Our client is seeking a Senior Formulation Chemist to help drive innovation and lead product development at a fast-growing cosmetic manufacturer. This role is pivotal in shaping formulation strategy, overseeing regulatory compounding, and mentoring junior chemists in a high-performing lab environment. You will play a key role in creating clean, high-quality cosmetics and skincare products using natural, ethically sourced ingredients. Key Skills: Strong hands-on experience in formulation development for cosmetics and skincare Proven ability to lead lab operations and manage multiple product development projects Expertise in raw material evaluation, ingredient functionality, and cost-effective formulation Familiarity with regulatory compounding practices and product safety standards Skilled in cross-functional collaboration with R&D, marketing, and regulatory teams Qualifications: 5+ years of experience in cosmetic product formulation or R&D In-depth knowledge of color cosmetics, skin care formulation, and texture development Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science, or related field (Master's preferred) This is a high-impact opportunity to influence product innovation and lead formulation efforts at a company known for its dedication to clean beauty and ethical production practices. For immediate consideration, apply today or contact Scot Widjaja at **************.

Do you dream of crafting groundbreaking culinary creations? Are you passionate about experimenting with flavors, textures, and techniques that push the boundaries of food science? If you're eager to be at the forefront of food innovation, Stampede Culinary Partners has the perfect opportunity for you! We're seeking a full-time Research Development Technician to join our cutting-edge team, where your creativity meets science to shape the next generation of food products. If you thrive in a fast-paced environment and love the challenge of bringing ideas to life-keep reading! WHY WE'RE A GREAT PLACE TO WORK Stampede Culinary Partners is an innovative protein solutions company that focuses on custom protein development and processing. Our customers include leading restaurants, top retailers, leading food service distributors, home delivery customers, and other emerging segments. The ability to satisfy our mission depends largely on our greatest asset, our employees! Our company culture is built on the expertise and experience of all our employees and driven by the 5 pillars that we hold ourselves to daily: perform passionately, challenge directly and respectfully, commit to teamwork, and embrace innovation. OUR GENEROUS BENEFITS Competitive salary Health, dental, and vision HSA/FSA STD/LTD Life and AD&D Accident insurance Pet insurance 401K with employer match Group hospital indemnity Floating holiday Pension plan after 1 year Mental health support program Employee discounts on meat and veggies Event BBQs and recognition programs On-site parking and bus route access TAKE A GLIMPSE INTO YOUR DAY As our Research Development Technician, your day will be a dynamic blend of creativity, science, and problem-solving. You'll conduct hands-on research and development, crafting new and improved food products both in a test kitchen and in a production setting. You'll work side-by-side with Production and Quality Assurance teams, ensuring smooth new product rollouts while enhancing flavor, texture, color, and nutritional value. You'll dive into competitive product analysis, refining formulas and optimizing processing, packaging, and distribution methods. Whether you're assisting in food safety regulations, collaborating with our Vice President of Technical Innovation and Culinary Development, or providing support to sales and marketing, every task you tackle will shape the future of food innovation. KEY QUALIFICATIONS AND SKILLS Experience as a research coordinator Proficiency with computers, including internet software, inventory software, manufacturing software, order processing systems, spreadsheets, and MS Word Excellent communication and customer service skills BECOME OUR RESEARCH DEVELOPMENT TECHNICIAN! At Stampede Culinary Partners, you'll be part of a team that doesn't just create food-we reinvent it. If you're ready to bring your research skills, technical expertise, and passion for food science to an industry-leading company, apply today with our initial 3-minute, mobile-friendly application! v

Responsibilities The technologist assumes the responsibility and accountability, under the direction of a cardiologist, or electro physiologist, or radiologist for providing safe and competent care, both technically and clinically in the diagnosis, treatment and intervention of cardiac and vascular disease in accordance with Manatee Memorial Hospital policies, procedures and philosophy. The technologist also provides professional leadership and support to all healthcare team members. Demonstrates Service Excellence at all times. Other duties as assigned. About Manatee Memorial Hospital (MMH): Manatee Memorial Hospital in Bradenton, Florida, has served the citizens of Manatee, Sarasota and surrounding counties for 70 years. Part of the Manatee Healthcare System, the hospital has earned The Joint Commission's Gold Seal of Approval. The 295-bed hospital with over 550 physicians, residents and allied health professionals, offers advanced healthcare services in a caring and compassionate environment. Services include cardiac care and cardiovascular medicine, emergency care for all ages, surgery services - including robotic-assisted surgery with the da Vinci Surgical System, a weight-loss program, orthopedic services, outpatient and inpatient radiology and rehabilitation, respiratory care, sleep, oncology, wound care and women's and children's services. Manatee Memorial Hospital offers a Level II Neonatal Intensive Care Unit for babies with special needs. MMH offers comprehensive benefits such as: Challenging and rewarding work environment Competitive Compensation Excellent Medical, Dental, Vision, and Prescription Drug Plan Generous Paid Time Off 401(K) with company match and discounted stock plan About Universal Health Services One of the nation's largest and most respected providers of hospital and healthcare services, Universal Health Services, Inc. (UHS) has built an impressive record of achievement and performance. Growing steadily since its inception into an esteemed Fortune 500 corporation, annual revenues were $14.3 billion in 2023. During the year, UHS was again recognized as one of the World's Most Admired Companies by Fortune; and listed in Forbes ranking of America's Largest Public Companies. Headquartered in King of Prussia, PA, UHS has approximately 96,700 employees and continues to grow through its subsidiaries. Operating acute care hospitals, behavioral health facilities, outpatient facilities and ambulatory care access points, an insurance offering, a physician network and various related services located all over the U.S. States, Washington, D.C., Puerto Rico and the United Kingdom. *********** Qualifications RTR, RCVT, RCVIT, RRT, CCPT, CVT, RCIS, RCES, or PMD, current licensee required, AAS in ICT or 10 years cardiac cath experience. Previous Cardiac Cath, Electrophysiology, Structural Heart, or Invasive Vascular Lab experience preferred. BLS required (or obtained within 90 days of employment) Associates in Applied Science in Invasive Cardiovascular Technology preferred ACLS certification (or obtained within 90 days of employment) EEO Statement All UHS subsidiaries are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and teammates. UHS subsidiaries are equal opportunity employers and as such, openly support and fully commit to recruitment, selection, placement, promotion and compensation of individuals without regard to race, color, religion, age, sex (including pregnancy, gender identity, and sexual orientation), genetic information, national origin, disability status, protected veteran status or any other characteristic protected by federal, state or local laws. We believe that diversity and inclusion among our teammates is critical to our success. Notice At UHS and all our subsidiaries, our Human Resources departments and recruiters are here to help prospective candidates by matching skillset and experience with the best possible career path at UHS and our subsidiaries. We take pride in creating a highly efficient and best in class candidate experience. During the recruitment process, no recruiter or employee will request financial or personal information (Social Security Number, credit card or bank information, etc.) from you via email. The recruiters will not email you from a public webmail client like Hotmail, Gmail, Yahoo Mail, etc. If you are suspicious of a job posting or job-related email mentioning UHS or its subsidiaries, let us know by contacting us at: ************************* or **************.

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

Duration: 12 Months Contract Provide technical assistance to laboratory scientists for the precise execution of experiments and research studies. Operate laboratory tools and equipment, process data for experiments, collect samples for studies, record observations, analyze experimental results, help manage inventories and stock supplies, and create study reports for further examination by team/management Research Technician key duties: Support the development, validation and execution of analytical assays based on a variety of biological techniques including but not limited to DNA/RNA isolation, PCR, qPCR, ELISA, Flow cytometry, Western blots Processing of biological matrices including but not limited to: plasma, serum, tissue, PBMC isolation Support the establishment, characterization, maintenance, banking, expansion and freezing of cell lines Assist in the printing of compounds using specialized dispensing equipment Transportation of samples between sites as needed. Coordinate and organize shipment of reagents/samples within the US and outside the US as needed Support of animal experiments by provision of the conceptual test article and subsequent analysis of animal samples resulting from animal experiments Documentation and execution of experiments is in compliance with internal procedures and guidance Ensure lab space and equipment is functional and well maintained Prepare reports on laboratory activities as required by management Inventory and consumables are managed in an efficient and cost-effective way Adherence to all applicable Legal, Environmental, Health and Safety regulations for handling and disposing of reagents/samples Keep abreast of new developments in the field of research and incorporate them into the lab's operations as appropriate Skills: Ability to execute experiments with precision, analyze data and maintain accurate records Ability to work independently while also being effective in a multi-disciplinary environment Excellent organizational and interpersonal skills Education: Minimum of a Bachelor's degree in Life Sciences (biology, microbiology, genetics, immunology etc). Master's Degree preferred. 3 years hands-on experience in a research laboratory, conducting hands-on cell culture, biological assays including but not limited to DNA/RNA isolation, PCR, qPCR, ELISA. Flow cytometry and cell sorting experience is a plus About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions 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, disability, or status as a protected veteran. Recruiter Details: Name: Swati Email: *********************************** Internal Id: 25-35535

We supply industrial hardware and components to customers across multiple industries in North and South America. The company underwent massive growth over the past few years, and we are happy to be adding to our team, therefore, we are looking for a Quality Control Specialist to join us. This would be a mid-level position in a fast-paced environment with a culture that is conducive to teamwork, professional development, and a chance to be an integral part of our global team. Quality engineer ensures consistent quality of production and received material by utilizing good automated manufacturing practice (GAMP) systems, validating processes, and efficiently communicating information about parts' defects to affected parties. Skills/Qualifications required: 2-4 years of experience in quality assurance with industrial hardware Reading and interpreting engineering drawings Have experience in using basic measuring equipment - measuring tape, calipers, & height gage Experience in quality processes & tools (FAI, PPAP, CAR & gage calibration) Experience in process Improvement and analyzing Information Good verbal and written communication Experience in using ISO standards (ideally ISO 9001) Knowledge of REACH & RoHS Attention to detail, thoroughness, and dealing with complexity Timely relay of information Able to use Microsoft Excel & Word QA tasks: Achieving quality assurance operational objectives by contributing information and analysis to strategic plans and reviews Assisting in developing & implementing action plans Enforcing quality and customer-service standards Identifying and resolving problems within the inspection function Assisting in determining system improvements and implementing change. Performing routine inspections and quality tests. Identifying and resolving workflow and shipment issues. Conducting First Article Inspections (FAIs) and Production Part Approval Process (PPAP) evaluations for customers on new components Investigating root cause issues & assisting in developing & implementing corrective actions pertaining to customer complaints Validating quality processes by monitoring products to specifications and quality attributes Maintaining and improving product quality by participating in product, company, system, compliance, and surveillance audits. Preparing quality documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes and re-validations.

Your Job Georgia-Pacific Cellulose LLC has an opportunity for a talented person to enhance operations at its cellulose facility in Brunswick, Georgia. The Lab Technician performs environmental and process lab tests using various chemicals and equipment. The ability to carefully grasp and adhere to lab procedures while maintaining a high level of attention to detail in all aspects of the work is paramount to be successful in the role. Tasks include collecting samples for testing throughout mill; sample collection will include carrying loads of up to 50 pounds, navigating stairs and ladders, as well as executing tasks like bending, reaching, and operating valves. Shift: 7am to 3:30pm - Monday - Friday -includes one weekend a month, some holidays, and overtime as needed. GP Cellulose is a leading producer of high-quality fluff pulps, meeting the needs of the personal hygiene industry and disposable absorbent products manufacturers around the globe. We create real, long-term value in our business by anticipating our customers' needs and working with them closely to help them achieve their business goals. For more information about GP Cellulose, please visit *************************** What You Will Do Follow procedures while working in a mill environment to draw samples Perform laboratory tests from samples in the field in order to produce reliable and precise data Collect samples for analysis from industrial equipment Perform calculations and enter test results into spreadsheets/databases and verify results Report laboratory results to team members and the wider team when appropriate Microsoft Office usage daily Understand and apply site's safe work practices including but not limited to Lock, Tag, Verify and Permitting requirements Utilize mechanical aptitude to troubleshoot, adjust and repair routine equipment issues Lift and carry up to 50 pounds Climb stairs and/or ladders to reach sample locations throughout the mill while being exposed to noise levels > 85 dB; and in hot, humid environment (>100°F, >80% RH) Who You Are (Basic Qualifications) Associate degree or higher within a Science related program (Biology, Chemistry, Environmental Science or similar) OR Three (3) years testing responsibilities in a laboratory environment Chemistry analysis experience What Will Put You Ahead Bachelor's degree in Chemistry or Biology Five (5) or more years of experience in laboratory environment Experience with testing in an industrial facility such as an integrated pulp manufacturing facility Experience with wastewater treatment testing Wastewater and/or potable water laboratory technician certification At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy. Hiring Philosophy All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds. We are Military Ready and Second Chance employers. Learn more about our hiring philosophy here. Who We Are At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company. Our Benefits Our goal is for each employee, and their families, to live fulfilling and healthy lives. We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing on overall wellbeing so you can focus on what matters most. Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance. Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region. If you have questions on what benefits apply to you, please speak to your recruiter. Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results. Equal Opportunities Equal Opportunity Employer, including disability and protected veteran status. Except where prohibited by state law, some offers of employment are conditioned upon successfully passing a drug test. This employer uses E-Verify. Please click here for additional information. (For Illinois E-Verify information click here, aquí, or tu).

All the benefits and perks you need for you and your family: Benefits from Day One Paid Days Off from Day One Career Development $15,000 Sign-on Bonus for eligible applicants $3,000 Relocation Bonus for eligible applicants Our promise to you: Joining AdventHealth is about being part of something bigger. It's about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better. Schedule: Full Time Days Shift : 4 10-hour shifts, plus call Location: 7727 LAKE UNDERHILL ROAD ORLANDO 32822 The community you'll be caring for: AdventHealth East Orlando AdventHealth East Orlando, a 265-bed community hospital, has been serving East Orlando residents since 1941 as an innovative local leader that fills a vital need in a fast-growing area A recent 200,000 square-foot expansion project upgraded the hospital to 265 beds, with a spacious patient tower and 80 new private rooms designed to enhance the holistic care experience Annual number of emergency cases: 89,018 The role you'll contribute: The Cardiovascular Invasive Laboratory Specialist III (CILS III) performs a wide range of technical skills, which are utilized during a variety of Interventional Cardiovascular, Non-ablation Electrophysiology or Interventional Radiology procedures to provide an efficient, comfortable, and safe examination of all patients. The CILS III is proficient in all aspects of angiography, preparation, assessment, documentation and monitoring consistent with the policies, procedures and processes of the Cardiovascular Services department and Hospital Administration. Adheres to the guidelines and standards of professional practice associations. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all. The value you'll bring to the team: Follows CDC isolation guidelines, appropriately uses PPE, and performs hand hygiene according to accepted standards of care. Identifies and prepares patient using aseptic technique as dictated by procedure ordered. Exhibits awareness of hazards which may endanger patients. Ensures adherence to regulatory standards and enforces safety regulations. Annually meets all required department specific competencies Verifies orders and facilitates implementation, communicating with physician as needed. Performs treatments and administers medications according to policy and training. Functions appropriately in clinical emergencies. Evaluates effectiveness of interventions and medications. Performs within the bounds of the applicable scope of practice for Cardiovascular Invasive Lab Technologists. Facilitates timely patient throughput Produce an accurately written, promptly completed medical record for each patient based on the scope and complexity of the intervention procedure and patient clinical conditions. Maintains authenticity and security of the record, and follows prescribed process for amending documents Performs effectively in all three procedural roles (circulate, monitor, scrub) required in a therapeutic cardiac laboratory team based on the Society of Invasive Cardiovascular Professionals Scope of Practice. Takes call as rotated/assigned and responds (in hospital) per policy. Proficiently performs coronary diagnostic and interventional procedures, non-ablation electrophysiology interventional procedures, and peripheral diagnostic and interventional procedures. The expertise and experiences you'll need to succeed: Minimum qualifications : Associate degree OR Bachelors in Cardiovascular Technology, Emergency Medical Services, Nursing, Radiologic Technology or Respiratory Therapy Basic Life Support (BLS) Advanced Cardiovascular Life Support (ACLS) Must possess and maintain one of the following: Current valid State of Florida or multi state license as a Registered Nurse (RN) Radiologic Technologist [R.T.(R)] Respiratory Therapist (RRT) Registered Cardiovascular Invasive Specialist (RCIS) Registered Cardiovascular Electrophysiology Specialist (RCES) Nationally Registered Paramedic (NREMT-P) Preferred qualifications: Cardiovascular Lab experience Interventional Radiology Lab experience Peripheral Lab experience Electrophysiology Lab experience This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location. Category: Cath Lab/Special Procedures Organization: AdventHealth East Orlando Schedule: Full-time Shift: 1 - Day Req ID: 24039740 We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.

We are hiring for our client in the biotechnology industry. 12 months contract In this role, you will have the opportunity to: • Assisting engineers with daily testing tasks and documenting test results to assist with Distribution Test Reports. • Coordinate incoming and outgoing shipments of products and be responsible for the Lab Housekeeping and organization of supplies and materials. • Define packaging materials, with a focus on waste reduction. The essential requirements of the job include: • Education: Higher Education or College coursework in Packaging, or Material Sciences, or like programs. Preferred experience in related FDA regulated field. • Attention to Detail • Experience in technical writing; ISO and GMP as required. It would be a plus if you also possess previous experience in: • Experience or knowledge with Packaging Standards such as ASTM D series and/or ISTA. • CAD Software experience, or similar • Packing or Warehouse experience

$26.88/hr + benefits on W2 Onsite in Miami, FL. 12+ month contract with likely extension/conversion. If you thrive in a multi-faceted role and want to work to build a world-class Package Engineering organization with us-read on. In this role, you will have the opportunity to: Assisting engineers with daily testing tasks and documenting test results to assist with Distribution Test Reports. Coordinate incoming and outgoing shipments of products and be responsible for the Lab Housekeeping and organization of supplies and materials. You will Execute packing instructions. Conduct test sequences. Download and manage data files. Provide input to the other engineers. Assist engineers with daily testing tasks and documenting test results to assist with Distribution Test Reports. Manage the Lab schedules and participate in weekly status report out of all projects coming in and out of the Labs. Assist engineers with coordinating incoming and outgoing shipments of products. Lab Housekeeping and organization of supplies and materials. Attention to detail is critical to this position. Qualifications: Ability to lift 50lbs. You are detail oriented. Follow processes and procedures. Timely Nice to have: College education in Packaging, or Material Sciences, or like programs. Experience or knowledge with Packaging Standards such as ASTM D series and/or ISTA. Other Engineering course work, such as Mechanical or Electrical. Packing or Warehouse experience. CAD or drafting and design experience. Interested? Apply today!

Up to $10,000 Sign-on Bonus Based on Eligibility Cath Lab Tech Full Time Days Performs direct and indirect functions in the Cardiac Cath Lab. Assists all Physicians/staff with clinical and technical aspects of cardiovascular care performs miscellaneous duties as assigned. Scrubs monitors and circulates in all invasive procedures in the Cath lab and IVR. (Invasive/surgical and interventional procedures) inventory control. Able to function on all cardiac alerts and STEMI cases. Responsibilities Assesses physical, psychosocial, and growth and development needs of the patient, completes pre, intra and post procedure assessment, informs nurse/MD of any changes in patients condition. Develops a plan of care for procedure being performed, plan of care is individualized to include specific patient problems, needs and scheduled procedure. Provides teaching and guidance to patient and/or family as well as staff members. Able to execute x-ray for desired views- abdominal aorta gram, runoff, division, storing and printing images, sets priorities for care of patients based on patient's needs and resources available, identifies and performs appropriately in emergency patient care solutions. Knowledge of set up and monitoring of IABP, assists with set-up, insertion and care of temporary and permanent pacemakers. THE CATH LAB TECH FULL TIME DAYS CANDIDATE WILL POSSESS THE FOLLOWING EDUCATION, LICENSE/CERTIFICATIONS, AND EXPERIENCE. Education: Required: Associate Degree in Radiology or equivalent, Basic EKG course. Preferred: Bachelor in Radiology or equivalent. Experience: Required: 6 months in Cath Lab/Cardiac Intervention Lab. Preferred: 1 year experience providing cardiac cath, radiology care Required Certifications/Registrations/Licenses: Required: BLS . ACLS within 6 months of hire. Preferred: RCIS certification ********** Employment practices will not be influenced or affected by an applicants or employees race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. By applying, you consent to your information being transmitted by snagajob to the Employer, as data controller, through the Employers data processor SonicJobs. See SonicJobs Terms & Conditions at ********************************************* and Privacy Policy at ******************************************* and SonicJobs Privacy Policy at ******************************************* and Terms of Use at *********************************************

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential. Summary The Technician, Laboratory Minerals under general supervision performs laboratory tests to determine chemical and physical characteristics or composition of solid, liquid, or gaseous materials for such purposes as quality control, process control, or product development by performing the following duties. •Performs laboratory testing, following relevant company's Standard Operating Procedures (SOP's) and methods. • Prepares a representative subsample from client sample that meets specific requirements using defined methods (Dry, Crush, Pulverize, Pressure Filter, Mix, Riffle Split, etc.). • Weighs and tests samples on relevant equipment. • Weighs and digest samples for analysis using relevant equipment. • Accurately completes and maintains all laboratory reports. • Receives, sorts and logs client samples into the data base, and prepares samples' labels. • Archives, returns, or disposes of client samples as per established procedure. • Prepares monthly composites. • Performs daily, weekly, and monthly Quality Assurance/Quality Control checks on equipment. • Demonstrates good and safe work habits and enforces a clean working environment. • Performs general upkeep and housekeeping of the laboratory. • Ensures all equipment and containers are organized and cleaned before and after use • Ensures all personal protective equipment (PPE) relevant for tasks is worn at all times. • Ensures compliance with all required local and federal safety processes and procedures. • May also have preparation or field responsibilities, as required by business needs. • May assist Junior Technicians as required. • Adheres to internal standards, policies and procedures. • Performs other duties as assigned. Qualifications EDUCATION AND EXPERIENCE • High School diploma or equivalent Required • 3+ years working in Industrial Laboratory or Field Services setting Required • Water Laboratory only: Where required by the state law, Post-secondary (Associate or Bachelor's) degree in science, or minimum 1-year supervised water testing experience Required • Associate degree in or including some Science Preferred • 5+ years working in industrial/lab/field setting with experience following strict safety standards Preferred LICENSES / CERTIFICATIONS • A valid and current Driver's license may be required if the role requires driving a company vehicle. Required • May be required to obtain 24-hour surface Mine Safety and Health Administration (MSHA) certificate, training is available through SGS. Required KNOWLEDGE / SKILLS / ABILITIES • Language Skills: Intermediate English Required • Advanced level Preferred • Mathematical Skills: Basic level Required • Intermediate level Preferred • Reasoning Skills/Abilities: Intermediate level required, uses logical and practical approach to solve problems Required • Ability to effectively communicate (in writing or verbally), presenting information individually or in small group situations to internal or external customers Required TRAVEL • No travel required. EQUIPMENT • This job operates in a laboratory environment. This role routinely uses standard office equipment such as computers, printers, and phones. • This role routinely uses sample prep equipment that may include Jaw Crusher, Bowl & Disc Pulverizing Mills, Pressure Filters, Riffle Splitters, Compressed Air. • This role routinely uses laboratory equipment/instruments that may include Bottle-top Dispensers, Eppendorf Pipettes, Balances, Muffle Furnace, Sulfur Analyzer, Compressed gases, and ICP-OES as needed. PHYSICAL DEMANDS OF THE JOB Physical/Sensory Demands Frequency Requirements: Frequency Weight lbs/kg • Stand Constantly • Move or traverse Constantly • Sit Occasionally • Use hands Constantly • Reach with hands and arms Frequently • Climb or balance Occasionally • Stoop, kneel, crouch or crawl Occasionally • Talk/hear Frequently • Taste/Smell None • Lift/carry/push or pull Frequently 50 lbs WORK CONDITIONS / EXPOSURE TO ENVIRONMENTAL CONDITIONS Location of the Job: Kershaw, SC WORK SCHEDULE • Day Shift; will require incumbent to have flexible schedule • Position requires occasional overtime. Environmental Conditions Requirements: • Wet or humid (non-weather) conditions: Occasionally • Work near moving mechanical pats: Frequently • Work in high, precarious places: Occasionally • Fumes or airborne particles: Frequently • Toxic or caustic chemicals: Occasionally • Outdoor weather conditions: Occasionally • Extreme cold (non-weather): None • Extreme heat (non-weather): None • Risk of electrical shock: Occasionally • Work with explosives: None • Risk of radiation: None • Vibration: Frequently • Ability to follow directions ensuring the end results are accurate and completed with the required timeframe Required • Ability to deal with problems involving a few concrete variables in standardized situations Required • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals Required • Ability to work independently and under moderate supervision Required • Team player attitude, customer care focus Required COMPUTER SKILLS • MS Office (Word, Excel) - Intermediate user proficiency Preferred Noise Level: Moderate noise (examples: business office with computers and printers, light traffic) Other Physical/Work Environmental Exposures: None Vision Requirement: • Close vision (clear vision at 20 inches/50 centimeters or less) • Distance vision (clear vision at 20 feet/6 meters or more) • Peripheral vision (ability to observe an area that can be seen up and down or to the left and right while eyes are fixed on a given point) • Depth perception (three-dimension vision, ability to judge distance and three-dimensional relationships) • Ability to adjust focus (ability to adjust the eye to bring an object into sharp focus) • Ability to see color Auditory Requirements: • Provide with specific auditory requirements: Must be able to hear equipment operating, alarms sounding, traffic, telephones Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

We are seeking a detail-oriented Laboratory Technician to join our team. In this role, you will be responsible for operating and maintaining extraction equipment, ensuring efficient and safe processing of plant material to produce high-quality products. You will follow strict safety protocols, adhere to standard operating procedures, and assist in refining extraction techniques to optimize yield and purity. The ideal candidate will have experience working in a laboratory or production setting, with a strong understanding of extraction processes, chemistry, and equipment maintenance. Attention to detail, adherence to regulatory compliance, and the ability to work both independently and as part of a team are essential for success in this role. Key Responsibilities: Operate extraction and refinement equipment efficiently and safely. Follow standard operating procedures (SOPs) to ensure consistency and quality. Monitor and adjust processing parameters for optimal results. Conduct routine maintenance and troubleshooting of extraction equipment. Maintain accurate records of extraction processes, yields, and quality control results. Adhere to safety and compliance regulations to ensure a clean and secure work environment. Assist in developing and refining extraction techniques to improve efficiency. Qualifications: Previous experience in extraction, laboratory work, chemistry, or related fields preferred. Familiarity with extraction technologies, solvent recovery, and purification methods. Strong attention to detail and ability to follow protocols. Ability to work in a fast-paced environment while maintaining accuracy. Knowledge of safety protocols and regulatory compliance.

Field Lab Tech Duration: 6-12 months to start Pay Rate: Around $22/hr This role provides field and plant metallurgical support to mining operations through sampling and testing of phosphate rock prospect core samples and plant samples. These samples are used by mine planning, engineering and operations management to evaluate mining plans, operating conditions and ore reserves. Are you our next Met Lab Tech? This role provides field and plant metallurgical support to mining operations through sampling and testing of phosphate rock prospect core samples and plant samples. These samples are used by mine planning, engineering and operations management to evaluate mining plans, operating conditions and ore reserves. What will you do? Miscellaneous job-related duties. Perform routine preventative maintenance on lab equipment. Conduct plant tests and sampling related to processes within minerals operations. Operate and maintain various laboratory equipment (core washer, flotation machines etc.). Perform processing and testing procedures on matrix prospect core samples. What do you need for this role? High School/GED required. 1+ years of Laboratory experience required.