Chemist Jobs in Louisiana

PURPOSE: The Chemist is responsible for performing testing utilizing laboratory equipment/instrumentation and communicating results to support the continuous operations of the Princeton refinery. The Chemist maintains laboratory equipment and verifies instrument performance to ensure data being reported is accurate and reliable. The Chemist writes SOPs and mentors/trains hourly lab techs as needed. KEY OBJECTIVES AND RESPONSIBILITIES: * Maintain knowledge of laboratory procedures and testing requirements * Conduct and analyze specific tests on process streams and finished products * Perform instrument performance verification at specified intervals to ensure data integrity * Leads and supports the development and improvement of lab test methods and procedures * Ensure all lab equipment is maintained and operational for use * Works with service vendors to get instrumentation repaired as needed * Works with lab supply vendors to keep the laboratory stocked with essential supplies * Works with Lab Management and operations to ensure product quality issues are addressed as needed * Capable of recording data as needed both manually and in electronic databases * Employs creativity and problem solving skills to support operations * Ensures data integrity and cleanliness of the laboratory * Work in a safe and timely manner to ensure accurate completion of all duties * Other duties as assigned REQUIRED EDUCATION/EXPERIENCES: * Bachelor's Degree from a four-year College or University * Solid understanding of analytical chemistry * Proficiency with and maintains current knowledge of ASTM petroleum test methods * Ability to lift and transfer contents of five-gallon (~forty pound) sample cans * Ability to occasionally travel * Good working knowledge of lab methods and procedures * Proficient in Microsoft Office Package, including word processing, spreadsheets, database, presentation software, email and scheduling * Experience and understanding of standardized and non-standardized test methods PREFERRED EDUCATION/EXPERIENCES: * Bachelor's degree in Chemistry * 3 or more years of petroleum or chemical related experience and/or training * Knowledge of lab methods and procedures in the petroleum industry COMPETENCIES: * Maintain confidentiality of intellectual property and data * Strong safety focus * Self-starter and quick learner * Strong organizational skills, including the ability to work effectively with personnel at all levels * Team player * Effectively communicates at all levels of the organization * Demonstrate decision making and analytical skills * Results-driven, action-oriented, and delivers on commitments * Effective time management with the ability to manage multiple tasks and responsibilities· * Strong organization, interpersonal and communication skills with the ability to effectively communicate with all levels, both internally and externally * Demonstration of Calumet Values - Safety, Environment & Social Responsibility, Teamwork, Ownership, Passion for Customers, and Excellence Other details * Job Family R&D / Laboratory * Pay Type Salary Apply Now

Principal Scientist Food Manufacturing - Midwest Location Salary Up To $125,000 + Benefits + Bonus & Paid Relocation to the Midwest Ready to work for a leader in the food manufacturing industry? Our client has a great opportunity for a Principal Scientist who has experience in co-drying and dry blending combinations of dairy, dairy flavors, seasonings, flavors, colors and other ingredients (seasoning and flavor development and agglomeration and instantization of powders). This person must have a proven track record in new product development directly or under their leadership. If you have a proven career advancement in dairy flavors, natural, process and cheese sauces and products, this is the position for you. MUST HAVE THIS EXPERIENCE TO APPLY. Minimum requirements for this Principal Scientist position: • Bachelor's degree in food science, microbiology, biology, chemistry, chemical engineering or related field required • Graduate degree in Food Science, microbiology, biology, chemistry, chemical engineering, or related field required (work experience may be substituted for the required graduate education on a year-for-year basis) • At least 5 years' experience working in R&D, product development, or innovation at food or ingredient company preferred • Proven successful track record in new product development with multiple examples of commercialized products/solutions directly or under your leadership • MUST HAVE THIS EXPERIENCE TO BE CONSIDERED. TO APPLY: Email your resume OR jeannie ATaustinallenDOTcom in MS Word or PDF (please remove the capital letters and replace with proper symbols). * All Interview, relocation, & fee expenses paid by hiring companies. Hiring companies offer excellent compensation packages, benefits, and, where available, generous relocation assistance or packages. Areas of Specialization... * Engineering * Six Sigma Black Belts * Accounting * Distribution * Human Resources * Materials / Purchasing * Quality Engineers & Managers * Manufacturing Management

LLC River Birch LLC is a leader in environmental solutions, specializing in waste management, recycling, and sustainable disposal methods. Our Injection Well Facility plays a critical role in managing and disposing of non-hazardous liquid industrial waste in compliance with regulatory standards. We also work closely with clients to recover valuable chemicals from waste streams for use in oil production Job Summary River Birch LLC is seeking a Chemist to support operations at our Injection Well Facility, focusing on the classification and analysis of non-hazardous waste streams, ensuring compliance with regulatory and operational standards. Additionally, this role will involve identifying, managing, and optimizing chemical components within client waste streams for enhanced oil production applications. Key Responsibilities Conduct chemical analysis and classification of non-hazardous waste materials to determine suitability for injection well disposal. Identify, extract, and optimize chemical components from client waste streams that can be repurposed for oil production. Review and interpret TCLP, SDS, and other chemical data to confirm compliance with EPA, state, and local regulations. Assist in preparing and reviewing waste profiles, including the RBL IW Generator Waste Profile forms. Perform laboratory testing, including pH, specific gravity, viscosity, and compatibility assessments to ensure proper waste handling and chemical reuse potential. Collaborate with operations and oil industry partners to develop chemical solutions that enhance oil recovery and production efficiency. Maintain accurate records, documentation, and compliance reports. Stay up-to-date with industry regulations, best practices, and advancements in oil recovery chemicals and non-hazardous waste management. The hiring department will conduct interviews of qualified individuals prior to requesting a criminal background check, and no job application submitted prior to such interview shall inquire into an applicant's criminal history. If this position is subject to a background check for any convictions related to its responsibilities and requirements, employment will be contingent upon successful completion of a background investigation including criminal history. Criminal history will not automatically disqualify a candidate.

**Who Are We?** Taking care of our customers, our communities and each other. That's the Travelers Promise. By honoring this commitment, we have maintained our reputation as one of the best property casualty insurers in the industry for over 160 years. Join us to discover a culture that is rooted in innovation and thrives on collaboration. Imagine loving what you do and where you do it. **Job Category** Product **Compensation Overview** The annual base salary range provided for this position is a nationwide market range and represents a broad range of salaries for this role across the country. The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. As part of our comprehensive compensation and benefits program, employees are also eligible for performance-based cash incentive awards. **Salary Range** $79,400.00 - $130,900.00 **Target Openings** 1 **What Is the Opportunity?** Product Development teams play a critical role in the achievement of Travelers financial objectives (growth, profit & retention) for one or more insurance products through the development, implementation and monitoring of product strategies and corresponding actions. As a Sr Analyst, Product Development, you will assist and implement analysis and evaluation of existing market and new product opportunities that deliver product development and product enhancements to the marketplace. In this role you will implement existing and new product solutions including monitoring and evaluating product performance and action plans. **What Will You Do?** + Execute and enhance existing product strategies and actions by collaborating and communicating with business unit stakeholders and management to achieve financial objectives. + Conduct high level market, competitor, and consumer research analysis to identify and recommend new products, markets and services or enhance existing ones. + Identify potential opportunities through root cause analysis and propose solutions. + Understand and assist with developing and implementing system and process solutions that align with the product's strategy. + Execute product enhancement work including launch and rollout plans related to established product strategies and action plans. Ensure strategies and plans address compliance needs and regulatory requirements. + Perform analysis by accessing and utilizing data to update recommendations on new or existing products. When appropriate, partner with data analytic teams to build support for recommendations. + Develop communication, training, and marketing materials in support of new or enhanced products and initiatives and may deliver training to stakeholders when appropriate. + Support the post implementation monitoring and measurement mechanisms for product strategies and initiatives in support of outlined success criteria. + Perform other duties as assigned. **What Will Our Ideal Candidate Have?** + Bachelor's Degree. + Three years of product development experience preferably in the financial services industry. + General knowledge of underwriting, coverage, rules, compliance/regulatory environment, and insurance financials. + Ability to think strategically and use judgment to resolve issues as they arise. + Strong data analysis skills with the ability to interpret trends and provide insights and recommendations to business partners. + Excellent communication skills with the ability to consult and present information effectively. + Experience working on cross-functional teams. + Have strong innovation skills including thinking critically about multiple perspectives and approaches to solving problems. + Demonstrated ability to interact and across levels and organizations, including consensus and team building. **What is a Must Have?** + Bachelor's Degree or equivalent combination of education and experience. + Two years of relevant experience with understanding and knowledge of insurance products. **What Is in It for You?** + **Health Insurance** : Employees and their eligible family members - including spouses, domestic partners, and children - are eligible for coverage from the first day of employment. + **Retirement:** Travelers matches your 401(k) contributions dollar-for-dollar up to your first 5% of eligible pay, subject to an annual maximum. If you have student loan debt, you can enroll in the Paying it Forward Savings Program. When you make a payment toward your student loan, Travelers will make an annual contribution into your 401(k) account. You are also eligible for a Pension Plan that is 100% funded by Travelers. + **Paid Time Off:** Start your career at Travelers with a minimum of 20 days Paid Time Off annually, plus nine paid company Holidays. + **Wellness Program:** The Travelers wellness program is comprised of tools, discounts and resources that empower you to achieve your wellness goals and caregiving needs. In addition, our mental health program provides access to free professional counseling services, health coaching and other resources to support your daily life needs. + **Volunteer Encouragement:** We have a deep commitment to the communities we serve and encourage our employees to get involved. Travelers has a Matching Gift and Volunteer Rewards program that enables you to give back to the charity of your choice. **Employment Practices** Travelers is an equal opportunity employer. We value the unique abilities and talents each individual brings to our organization and recognize that we benefit in numerous ways from our differences. In accordance with local law, candidates seeking employment in Colorado are not required to disclose dates of attendance at or graduation from educational institutions. If you are a candidate and have specific questions regarding the physical requirements of this role, please send us an email (*******************) so we may assist you. Travelers reserves the right to fill this position at a level above or below the level included in this posting. To learn more about our comprehensive benefit programs please visit ******************************************************** .

The Chemist will plan, manages and supervises the activities of a company facility laboratory and performs standard organoleptic, physical, and chemical testing in an accurate and timely fashion using within GLP's/cGMP's guidelines. Job Responsibilities: This position is responsible for ensuring customer expectations are met or exceeded in areas pertaining to the quality, testing, and timeliness of work. He or she ensures sample turnaround times and testing accuracy are met, closely monitors and guides lab analysts and technicians to prepare media and samples for analysis, perform physical stability, organoleptic, and analytical testing on a wide variety of raw material, premix samples follow company's standard operation procedures. Support facility production operation effectively. Support company overall quality and food safety compliance. Duties and Day-to-Day Responsibilities, but not limited to the development and monitoring of following areas: Monitor receiving and recording of samples upon arrival into the laboratory. Lead lab staff performing sample preparation including weighing of samples, selection of glassware, and performance of necessary analysis. Inspection of instrumentation to be used. Troubleshooting of instrumentation and calibration when required. Lead and monitor lab staff perform quantitative and qualitative chemical analyses using the following laboratory equipment: HPLC, ICP/AA, FTIR, GC, titrator, pH, Bulk Densities, Colorimeter. Accurately document observations made during the performance of an analytical method to determine if the analytical system is in control. Responsible for analysis and recording/plotting of Quality Control samples and data. Maintain laboratory equipment including scheduling routine calibration and maintenance and arranging for service repairs as needed, order and maintain supplies of chemicals, reagents, solutions, and standards. Make and record scientific observations accurately, prepare and present scientific records and reports. Test new and improved laboratory methods and procedures. Prepares laboratory notes, charts and graphs and writes up results of examinations. Keep accurate daily records, documentation and record keeping. Conduct investigations and problem solving on testing issues. Provide instruction and training in theory, technical skills, safety protocols, and the application of laboratory test protocols to lab staff. Evaluate quality control and quality assurance statistics and modifies procedures and methods as needed. Develop and perform installation, operational, and performance qualification on new laboratory equipment in accordance with GLP's/cGMP's observe safety precautions and practices Participate in and may provide continuing education and professional development for laboratory personnel. Plan workload distribution and makes schedules. Supervise purchase of supplies and maintains equipment inventory. Develops a budget for the laboratory and maintains control of lab costs. Able to thrive in a fast paced environment. Ability to multi-task and prioritize actions and workload resulting in maintaining sample turnaround times is required. Able to make decisions and lead with minimal supervision/direction. Maintain a clean work area. Communicate effectively with other functional areas in the facility. Responsible for overall GLP compliance Responsible for final review and reporting testing data and final COA approval. Support and coordinate inter-facility QC activities with other company facilities. Minimum Training, Education and Experience Requirements: Bachelor's degree in chemistry (analytical chemistry is ideal), microbiology, food science, biology or health science; or 3 to 5 year work related experience and/or training; 2 to 5 year experience in a dietary supplement, food, or chemical related laboratory. Experience with USP, FCC, and AOAC testing methodologies. Experience with lab instrumentation such as HPLC, ICP, GC, FTIR, etc. Additional experience in microbiological and contaminant testing is desired. Considerable knowledge of the basic principles and laboratory applications of chemistry and microbiology. Knowledge of current laboratory facilities, methods, equipment, reagents. Understand GLP. Skillful in performing standardized chemical and microbiological examinations. Strong leadership. Strong time management skill. Customer service oriented. Knowledge of use of computers for laboratories. English Language Proficiency Key Metrics: This position is held accountable but not limited to the following metrics as they relate to the operational area assigned. Attendance Customer Complaints Resamples Reworks Maintaining required in house 3-day turnaround time on testing (In house only) Reduction in laboratory related testing errors. Perform other duties as required and directed. Behavior Competencies: To perform the job successfully, the individual must demonstrate the following competencies: Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Ability to present and interpret data for management and staff. Communication Skills - Possesses excellent written and oral communication skills; Speaks clearly and persuasively in positive or negative situations; Listens and gets clarification; Demonstrates group presentation skills; Participates in meetings; Writes clearly and informatively; Assure spelling and grammar are correct; Presents numerical data effectively; Able to read and interpret written information. Teamwork - Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Contributes to building a positive team spirit; Puts success of team above own interests; Able to build morale and group commitments to goals and objectives; Supports everyone's efforts to succeed. Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently; Plans for additional resources; Sets goals and objectives; Able to manage multiple projects and initiatives on tight deadlines and delegate accordingly. Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Treats others with respect and consideration regardless of their status or position; Accepts responsibility for own actions; Follows through on commitments. Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality. Safety and Security - Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly. Adaptability - Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events; Travel to other Wright Group facilities as needed Dependability - Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan. May be required to work in other departments. Performs other duties as required and directed. The Company may, from time to time, change the nature of the employee's job responsibilities. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job: Laboratory environment Standing for long periods of time. Exposure to chemical odors may be encountered. Personal protection equipment is available for use. Handling of hazardous chemicals including caustics, acids and flammable hydrocarbons. Gloves, aprons, glasses and other P.P.E. are available and required when handling certain chemical. (overtime and weekends may be required at peak business hours.

Requirements Primary Responsibilities: Provides regulatory expertise Provide regulatory support across the LTF enterprise including development of technical data for labels (i.e. Nutrition Facts Panel, Ingredient Declaration, Standards of Identity) Nutrient Content Claims, PDCAAS, and Structure/Function Claims), for other packaging(cases, displays, pallets), for export to Canada and Mexico, and for entering/maintaining Regulatory information in LTF and customer data bases. Help develop and maintain regulatory technical systems (i.e. Oracle, PLM, TG) to support LTF Regulatory activities, which includes helping develop Regulatory policies and procedures to be in compliance with evolving state and federal regulations (i.e. National Bioengineered Food Disclosure, Nutritional Label Reform (NLR), emerging novel claims, packaging legislation). Coordinate and execute timely Regulatory approvals for labels and promotional materials with Marketing, Product Development, Legal and Creative Services. Provide Regulatory response to inquiries by customers relating to labeling and/or allowed use of ingredients in LTF products. Development and approval of labels for export. Provide regulatory guidance and approval in managing label changes relative to formula updates under training/guidance from supervisor to maximize regulatory compliance, while also minimizing labeling scrap and production complexity. Delivers new or renovated products OTIF Formulates new products, line extensions and renovations according to Customer/Product Brief requirements Manages prioritization of projects and communicates status updates Plans, leads preparation, and executes plant trials collaborating with all x-functional groups Prepares and performs product cuttings/sensory tests Maintains concise recipe record of project work and outcomes Interprets consumer research to support formulation efforts Maintains clear project communication and timelines Communicates cross-functionally required information for successful product launch Sources raw materials and ingredients as required to support formulation activities Researches and procures raw materials for new product development efforts · Achieves cost reduction by finding new sources for key raw materials · Partners with purchasing team to source ingredients that drive process improvement · Leverages knowledge of supplier and vendor base to identify new sources Evaluates the specification sheets from supplier to determine viability of raw materials 4 - Performs other duties as assigned · Schedules meetings, coordinates calendars, tracks budget expenditures, generates and distributes reports while providing administrative support Assists the R&D department in continuous improvement efforts and follow up on corrective action implementation Assist in sample shipping Keeps R&D Director informed about problems and opportunities for improvement · Provides weekly reports of project status · Background Requirements BS in Food Science, Nutrition, Culinology or related discipline is required. 5+ years of food labeling experience or other related fields such as regulatory compliance, or product development. At least a minimum of 2 years of recent US (FDA and/or USDA) Food regulatory labeling experience. Labeling experience in processed foods sold to consumers at retail preferred. Well versed in FDA and USDA labeling regulations. Possesses good project management skills Must have a solid understanding of food manufacturing, product development, food safety principles, guidelines and objectives. Able to quickly learn and deftly use technical formulation, data base, and routing systems (Oracle, PLM, TG). Intermediate user of Genesis software and PLM for nutritional calculations, ingredient declarations, claim management, etc. Solid understanding of international (Mexican, Canadian) labeling laws, label layout requirements, and international regulatory experts for consultation is helpful. Able to execute complex calculations by interpreting multiple regulations, and or federal guidance documents, for substantiating dip/bake/salad/snack serving equivalencies and product claims Must have practical understanding and the ability to apply key food science concepts such as, functions of microbiology inhibitors and inherent ingredient functions. Must have the practical understanding and the ability to apply basic culinary techniques, baking, reading and following recipes, stove top cooking and cold salad/dip preparation. Must have the ability to work autonomously and to hold others accountable, as required. · Must have strong analytical skills. Must be able to interpret and provide recommendations or feedback on products and revisions. Must have good communications skills, with the ability to be effective in both verbal and written communication. Must have great attention to detail, be able to work effortlessly in a team environment and apply good judgment. Must be completely familiar with GMPs, hazards, safety principles and constraints. Strong computer skills are required, including the Microsoft office platform, ERP systems. Spanish language fluency is desirable. Physical Requirements Frequently requires standing, lifting, walking, reaching, stooping, bending, smelling, listening, speaking, and seeing to perform the essential job duties. Work conditions vary, working time will vary based upon work / project needs, and flexibility is critical. Temperatures range from 5 to 90 F degrees in processing departments. Exposure to potentially dangerous machinery and equipment are present in the plant. Potential electrical, mechanical, and chemical, hazards are also present. The noise level is high and constant. Floors are damp and slick. Must be able to bend, stoop, pull and lift up to 50 lbs. to stand for long periods of time Close visual acuity to view a computer terminal, analyze reports, manage data and detail Taste a wide variety of foods This description is not intended to be a complete list of duties or tasks, but instead is to provide a guideline of fundamental responsibilities, tasks and duties. La Terra Fina reserves the right to make edits and changes to this role description as business needs require and new tasks and duties may be periodically added or revised. This a hybrid job-3-4 days in our Union City office Salary Description $104,000.00 to $126,000.00

Company TSMC Arizona Corporation Career Area Manufacturing (fabs) Posted Nov 16, 2023 At TSMC, We Develop the Technologies that Shape the Future and Change the World! Technology is our cornerstone, and Innovation is our passion. At TSMC, we bring together the most creative minds in science and technology to provide the best foundry services possible, and drive innovation in fields that revolutionize our world and daily lives including high performance computing, mobile, automotive electronics, and the Internet of Things (IoT). If you want to challenge yourself and unleash innovation with brilliant colleagues located around the world, come join us! Responsibilities * Perform routine sampling and analysis for Fab process chemical, Fab process water, and clean room environment for a semiconductor company. * Spend significant time in a clean room environment. * Work with industrial chemicals, specifically concentrated acids and bases. * Collect and organize data, and report to internal/external customers. * Assist engineers with analytical method development. * Record and identify contamination levels. * Manage equipment-related maintenance and chemicals. * Maintain laboratory housekeeping (5S) environment and protocols. * Support Fab manufacturing operations and be part of our teams' on-call schedule. Requirements * Associate's degree at a Science/Engineering/Technology school or equivalent experience is required. * 6-12+ months of experience working in a chemical lab is highly preferred. * Basic PC skills (Microsoft Windows and Microsoft Office) are required. * Be a good analytical thinker and exhibit problem-solving abilities. * Must be a team player and have a positive attitude and strong work ethic. * Be a logical thinker and attentive to numbers accuracy. * Follow the standard operating procedures for chemical handling. * Be able to work night and weekend shifts when assigned, and work overtime if needed (there will be a cap on overall work hours). * Basic to intermediate knowledge of instrumental analysis techniques. * New hire will be required to attend a 3-6-month overseas training at TSMC in Taiwan. * *

Benefits: 401(k) 401(k) matching Competitive salary Dental insurance Health insurance Training & development Vision insurance Primarily responsible for routine production and quality control testing of clinical Positron Emission Tomography (P.E.T.) radiopharmaceuticals and to assist Radiochemists with synthesis, analytical and other research and development activities. ESSENTIAL FUNCTIONS Responsibilities include but are not limited to: Responsible for assisting chemists in research and development activities. Responsible for the production and quality control testing of routinely produced PET radiopharmaceuticals. Responsible for general upkeep of equipment used in manufacturing and QC procedures (synthesis modules, HLPCs, gas chromatograph, strip scanner, MCA). Responsible for ordering, receiving, and testing of chemicals, equipment, and supplies needed for production and distribution of PET radiopharmaceuticals. Assists with operation of cyclotron and maintenance of chemistry modules. Assists administrative personnel in maintaining shipping paperwork, tracking of deliveries, and preparing for future deliveries. Follows and upholds: Standard Operating Procedures (SOP) cGMP (Current Good Manufacturing Procedures) Radiation safety guidelines Pharmacy rules and regulations Company policies and procedures Rules and regulations of other applicable governing organizations (DOT, NRC, DEQ) Utilizes aseptic technique to ensure sterilization of final product and continued sterility testing. Responsible for organization and general housekeeping of laboratory. MINIMUM QUALIFICATIONS AND EDUCATION REQUIREMENTS Bachelor of Science Degree in Chemistry is required. Minimum of one year of experience working in research or production laboratory environment. Experience with cGMP, radiation safety principles, or aseptic technique a plus. Work Schedule: Monday - Friday 2 am - 10 am REQUIRED KNOWLEDGE SKILLS AND ABILITIES Must have hands-on experience with chemistry/laboratory equipment, techniques and processes, including familiarity with operating HPLC, gas chromatography and thin layer chromatography. Work Schedule: Monday - Friday 2AM - 10AM Compensation: $45,000.00 per year We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Details: Stefanini Group is hiring! Stefanini is looking for a Chemistry Lab Technician in Geismar, LA 70734 For quick Apply, please reach out to Rogelio Agas, call ************/ email: ************************** Job Title: Chemistry Lab Technician Location: 8404 River Road, Geismar, LA 70734 Shift Timings: This position will work rotating, 12-hour shifts: (5am-5pm) and (5pm-5am) Every other weekend off. One week: 3 days/36 hours, Sunday, Wednesday, Thursday. Following Week: 4 days/48 hours, Monday, Tuesday, Friday, Saturday. Qualifications: This position will work rotating, 12-hour shifts: (5am-5pm) and (5pm-5am) Every other weekend off. One week: 3 days/36 hours, Sunday, Wednesday, Thursday. Following Week: 4 days/48 hours, Monday, Tuesday, Friday, Saturday. Minimum 2-year Associate's degree in Chemistry or 2-year technical degree in analytical testing in Chemistry or related field is preferred, OR at least 2 years recent experience working in a chemical manufacturing laboratory environment. Basic understanding of general chemistry. Basic understanding of theory, operation, calibration, maintenance and troubleshooting of laboratory instrumentation such as gas chromatographs, viscometers, spectrophotometers, pH meters, titrators, etc. Basic understanding of the techniques of quality assurance and quality control- Basic understanding of math and statistics- Basic understanding of ISO/RCMS quality system requirements Basic computer skills using software packages such as Microsoft Office, Power BI, SAP, Lotus Notes, etc. Skill and Education Requirements: Perform all tests on applicable products Analyze and record the test results. Effectively communicate with operations Interpret and follow documented procedures and STI's. Effectively communicate results to the appropriate personnel. Participate in safe work practices. Perform equipment control plan to verify conformance. Maintain a clean working environment. Perform effectively in a team-based environment. Perform all required health and safety inspections at prescribed frequencies. Computer literate; scientific minded and detail oriented. Must be willing to work nights, weekends, and occasional overtime. High School diploma required. Desired Skills: Previous quality control experience including preferred 2 years chemistry related, environment preferred. Physical Requirements: occasional lifting, bending and twisting of various range and motion requiring physical exertion when handling materials, drums or equipment. Ability to lift 30-50 pounds. Ability to stand and walk in work environment majority of time. Occasional use of stairs required. Occasional use of respiratory protection. Details: Responsibilities: This position is responsible for quality assurance testing of in-process samples, raw materials, intermediates, and finished goods within the scope of the Company Quality Policy. Using appropriate software to evaluate data based on internal and external specifications, support the continuous improvement of lab and plant processes through QA/QC activities and meet and/or exceed customer expectations. The selected candidate must have the ability to work as part of a team, understand chemical and instrument measurement processes, be self-motivated, and willing to develop technical knowledge and understanding of the chemical and measurement processes involved in their respective units. Perform analysis of raw materials, intermediates, and finished goods, in a timely manner, to verify conformance to or prescribe appropriate adjustment to product so they meet specifications that have been agreed upon by Company and their customers or suppliers. Associate must be willing to work in a team-oriented atmosphere. This includes learning all tasks and equipment associated with product testing, helping coordinate the flow of work within the team and with other departments, and helping team associates to meet changing work demands (i.e. go where the work is). Analyze raw materials, intermediate products, finished products and other chemical samples and evaluate suitability according to established specifications to ensure quality and availability of final product- Analyze samples, provide quality data and become an active member along with the Lab Supervisor and Production personnel to provide innovative ideas to improve lab and plant processes and demonstrate continuous improvement Know, understand and use software tools such as Lotus Notes, LabWare, SAP, Microsoft Office Programs, etc. which enhance quality reporting Ensure the suitability of laboratory equipment through proper operation, maintenance, calibration, verification and good quality control and assessment activities. Generate quality data and significant statistical data to support plant personnel in their efforts to enhance process control, meet customer requirements and continuously improve our product quality characteristics. Listed salary ranges may vary based on experience, qualifications, and local market. Also, some positions may include bonuses or other incentives. Stefanini takes pride in hiring top talent and developing relationships with our future employees. Our talent acquisition teams will never make an offer of employment without having a phone conversation with you. Those face-to-face conversations will involve a description of the job for which you have applied. We also speak with you about the process including interviews and job offers. About Stefanini Group The Stefanini Group is a global provider of offshore, onshore and near shore outsourcing, IT digital consulting, systems integration, application, and strategic staffing services to Fortune 1000 enterprises around the world. Our presence is in countries like the Americas, Europe, Africa, and Asia, and more than 400 clients across a broad spectrum of markets, including financial services, manufacturing, telecommunications, chemical services, technology, public sector, and utilities. Stefanini is a CMM level 5, IT consulting company with a global presence. We are CMM Level 5 company. #LI-ROGH #LI-ONSITE

Yorktown Systems Group, Inc. is seeking a qualified Quality Control Lead to provide professional services and mission support to the U.S. Army Joint Readiness Training Center (JRTC) located at Fort Polk, Louisiana. Mission Support services for the JRTC, one of the US Army's Combat Training Centers, entails providing realistic, graduate-level collective training experience at the Brigade Combat Team (BCT) level with the primary objective of training light infantry, airborne, air assault, rangers and other special operations units. Historically, the JRTC has hosted rotational exercises for US Army motorized and mechanized formations, as well as select units from the US Marine Corp, US Navy or US Air Force. The JRTC typically hosts ten standard rotational exercises each Fiscal Year (FY). Typical standard rotational exercises are designed based on a 14-calendar day training period with 18 calendar days of Live Fires typically starting prior to Force on Force (FOF) and running concurrently during the fourteen (14) training days. The standard training exercise is scripted and typically based on any combination of offense, defense, and stability operations. Standard rotations take place in a generic region with scenarios and Opposing Forces (OPFOR) threats based on the Decisive Action Training Environment (DATE). Rotational Training Unit (RTU) missions conducted during standard rotations are generally in direct alignment to the RTU's standard Mission Essential Task List (METL) and training objectives. Specific duties may include, but are not limited to: Shall implement an effective, economical QC Program. Shall develop and implement procedures to identify, prevent and ensure nonrecurrence of defective services. Shall provide continuous quality improvement and measures of customer satisfaction. Shall develop and maintain SOPs for each functional area covered under this contract. Requirements Required Qualifications: Must be a US Citizen. Must possess, at a minimum, military or civilian supervisory experience commensurate with management of all aspects of QC IAW PWS requirements. An individual with Six Sigma experience or a certificate in quality control is desired. Clearance: Requires SECRET Security Clearance Location: FT Polk, LA Travel: Some travel may be required

**Physical Location:** **_Multiple Locations- Must be willing to relocate in the immediate future and eventually travel up to 50% as needed._** **Pay Rate** : $65,100 - $86,800 Multiple factors, including Individual experience, skills and abilities will determine where an employee is ultimately placed in the pay range. Variable pay may provide additional opportunities for financial awards. This job is eligible to participate in IP's annual incentive plan. **Category/Shift** : Salaried Full-Time **The Job You Will Perform:** - Work under the daily guidance of the site controller as part of a division-wide finance development program, gaining exposure to all aspects of the Container business through formal training, cross-site job rotations, special projects, and mentorship from NAC Finance leadership. - Generally, serve as one of two exempt financial professionals at the manufacturing site, typically working alongside a team that includes non-exempt staff-offering valuable leadership and managerial development opportunities as you progress. - While building the skills necessary for future leadership roles within the Finance organization, provide support to the plant controller, plant general manager, region controller, and NAC division staff. - Key responsibilities include ensuring strong internal controls to protect company assets, preparing financial statements in accordance with professional and corporate standards, delivering timely and actionable financial analysis, identifying and proposing solutions to business challenges, and mentoring and developing accounting staff. **The Skills You Will Bring:** - Bachelor's degree in Accounting, Finance, or Business Administration, with at least 12 credit hours in Accounting - Minimum of 2 years' experience in an Accounting or Finance role; experience in a converting facility is a plus - Geographic flexibility and willingness to travel up to 50% during the training period - Strong initiative and self-motivation, with excellent written, verbal, and active listening skills - Proven ability to collaborate effectively and contribute to team success - Comfortable working in a manufacturing environment - Strong knowledge of general and cost accounting, including month-end close processes and financial statement preparation - Experience with developing, maintaining, and assessing internal controls - Strong analytical and financial skills, including budgeting, forecasting, KPI tracking, working capital management, and supporting special projects - Familiarity with financial and operational information systems, preferably SAP, including system oversight and management - Understanding of sales, marketing, and distribution processes - Knowledge of quality improvement and manufacturing processes, including root cause analysis and implementation of corrective actions **The Benefits You Will Enjoy:** International Paper offers a benefits package that includes health, welfare and retirement plans including Medical, Dental, Life insurance, Flexible Spending Accounts, Short-term and Long-term Disability, 401(k), Company-funded retirement contributions, Paid Time Off, Education & Development (including Tuition Reimbursement), Student Loan Repayment Assistance, and Voluntary Benefits including insurance for home, auto, vision and pets. **The Impact You Will Make:** We continue to build a better future for people, the planet, and our company! IP has been a good steward of sustainable practices across communities around the world for more than 120 years. Join our team and you'll see why our team members say they're **Proud to be IP** . **The Culture You Will Experience:** International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. We have team members all around the world with diverse backgrounds, experiences, and perspectives. These are our strengths. We are committed to creating a culture where all individuals are respected, valued, engaged and have an opportunity to do their best work every day. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly inclusive and diverse culture. **The Company You Will Join:** International Paper (NYSE: IP) is the global leader in sustainable packaging solutions. With company headquarters in Memphis, Tennessee, USA, and EMEA (Europe, Middle East and Africa) headquarters in London, UK, we employ more than 65,000 team members and serve customers around the world with operations in more than 30 countries. Together with our customers, we make the world safer and more productive, one sustainable packaging solution at a time. Net sales for 2024 were $18.6 billion. In 2025, International Paper acquired DS Smith creating an industry leader focused on the attractive and growing North American and EMEA regions. Additional information can be found by visiting internationalpaper.com Share this job: Location: STATE WIDE, FL, US, #STATE WIDE, UT, US, #STATE WIDE, KY, US, #STATE WIDE, MI, US, #STATE WIDE, WA, US, #STATE WIDE, OR, US, #STATE WIDE, NH, US, #STATE WIDE, MA, US, #STATE WIDE, SC, US, #STATE WIDE, IL, US, #STATE WIDE, CT, US, #STATE WIDE, IA, US, #STATE WIDE, LA, US, #STATE WIDE, NC, US, #STATE WIDE, WI, US, #STATE WIDE, GA, US, #STATE WIDE, MN, US, #STATE WIDE, VA, US, #STATE WIDE, MD, US, #STATE WIDE, TN, US, #STATE WIDE, OK, US, #STATE WIDE, AR, US, #STATE WIDE, SD, US, #STATE WIDE, CA, US, #STATE WIDE, NJ, US, #STATE WIDE, AZ, US, #STATE WIDE, NE, US, #STATE WIDE, OH, US, #STATE WIDE, ME, US, #STATE WIDE, RI, US, #STATE WIDE, AL, US, #STATE WIDE, NM, US, #STATE WIDE, NY, US, #STATE WIDE, KS, US, #STATE WIDE, NV, US, #STATE WIDE, PA, US, #STATE WIDE, CO, US, #STATE WIDE, MO, US, #STATE WIDE, IN, US, #STATE WIDE, MS, US, #STATEWIDE, VT, US, #STATE WIDE, TX, US, # Category: Finance Date: Apr 2, 2025 If you are not finding suitable opportunities, please click below to join our talent community!

SitusAMC is where the best and most passionate people come to transform our client's businesses and their own careers. Whether you're a real estate veteran, a passionate technologist, or looking to get your start, join us as we work together to realize opportunities for everyone, we proudly serve. At SitusAMC, we are looking to match your unique experience with one of our amazing careers, so that we can help you realize your potential and career growth within the Real Estate Industry. If you are someone who can be yourself, advocate for others, stay nimble, dream big, own every outcome, and think global but act local - come join our team! This role will assist in running engagements or multiple engagements on a day-to-day basis. This role will assist in being the Subject Matter Expert and assist in reviewing residential loan scenarios and loan level questions needed by the Analyst and Senior Analyst before presenting such information to the manager. Included in this responsibility will be interfacing directly with Analysts and Senior Analysts on an as needed basis to assist in answering questions before escalating to the manager. This role should work with the manager to understand the timing of the engagement, ensure that required servicing data is available or, if such data is not available, that the manager is aware of the status to ensure that all necessary information has been acquired so the review to begin. If problems are identified, this role should notify the manager to remedy any issues. This role will assist in reviewing and implementing all investor and regulatory guidelines communicated and determine which communications impact the department and make any necessary revisions to scripts as needed. Essential Job Functions: + Review client responses/rebuttals and provide SitusAMC feedback as needed + Attend client calls as needed/required + Review all investor and regulatory communications and complete Compliance Committee change summary forms for management review + Add all relevant regulatory communications to the compliance tracker once change summary forms are approved + Implement any/all investor and regulatory changes by updating scripts as needed + Provide assistance and answer questions for analysts; escalate as needed + Host monthly meetings for Analysts and Senior Analysts to field any questions and discuss any regulatory updates and/or audit issues as a team + Assist with any special projects as needed, including any assigned reviews for specific clients + Assist in creating new exceptions in Clarity and periodically review exceptions to ensure they are updated with current information in a uniform manner and are active on appropriate scripts + As regulatory guidelines change, review and update the client document request lists to ensure prudent and up-to-date requests for loan audits are made + Assist and discuss any issues, questions, etc. + Other activities as may be assigned by your manager Qualifications/ Requirements: + College degree preferred or combination of education and experience + Experienced professional with 5+ years of industry and/or relevant experience, typically at a Senior Analyst or Analyst level role or external equivalent + Over five years in the mortgage industry preferred + Demonstrated ability to work with team members and clients + Strong excel skills + Team oriented + Ability to multitask + Excellent PC skills and possess high level of proficiency in Microsoft products + Strong communication (written and oral) skills + Strong analytical ability, good judgement, strategic and multidimensional thinker + Detail oriented and organized + Demonstrate professional behavior and teamwork, dependable and adhere to company policies and procedures. \#LI-Remote Note: This job description is not intended to be all inclusive or exclusive. At any time, employees may perform other related duties as required to meet the ongoing needs of the organization and participate in additional trainings. SitusAMC does not accept unsolicited resumes from staffing agencies, search firms or any third parties. Any unsolicited resume submitted to SitusAMC in any manner will be considered SitusAMC property, and SitusAMC will not pay a fee for any placement resulting from the receipt of an unsolicited resume. The annual full time base salary range for this role is $56,000.00 - $85,000.00 Specific compensation is determined through interviews and a review of relevant education, experience, training, skills, geographic location and alignment with market data. Additionally, certain positions may be eligible to receive a discretionary bonus as determined by bonus program guidelines, position eligibility and SitusAMC Senior Management approval. SitusAMC offers PTO and paid holidays, the terms of which are set forth in the program policies. All full time employees also are eligible to participate in various benefit plans, including medical, dental, vision, life, disability insurance and 401K; in each case in accordance with the terms of the applicable plans. Pay Transparency Nondiscrimination Provision (****************************************************************************************************** SitusAMC is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Know Your Rights, Workplace Discrimination is Illegal (*********************************************************************************************** SitusAMC does not accept unsolicited resumes from staffing agencies, search firms or any third parties. Any unsolicited resume submitted to SitusAMC in any manner will be considered SitusAMC property, and SitusAMC will not pay a fee for any placement resulting from the receipt of an unsolicited resume.

divspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanh2spanspanspanbJob Title/b/span/span/span/h2/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span Associate Scientistspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanspanh2br/spanspanspanb Location(s)/b/span/span/span/h2/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span/span Lafayettep/ppbspan About Us/span/b/pp/ppspan Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world's greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we're able to push boundaries in pursuit of better human health. /spanspan /span/pp/pp Find your future at Revvity /pp/ppb This is a 2nd shift position- 4-day work week- Monday-Thursday 12pm-10:30pmMT. /b/pp/ppb Job Summary/b/pp Horizon Discovery, a division of Revvity, is an award-winning biotech company headquartered in Cambridge, UK with a global presence across the US, Europe and APAC regions. Using our proprietary gene-editing platform and deep scientific expertise, we design and engineer a diverse portfolio of inspired cell solutions to pharmaceutical, biotech, CRO, diagnostic, clinical laboratory and academic areas across the globe. /pp/pp Revvity has a rewarding and exciting opportunity for an Associate Scientist for our Synthetic Manufacturing laboratory. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. This includes quality and quantity determination, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry. /pp/ppb Key Responsibilities /b/pulli Manufacture oligonucleotides for our customers while adhering to established Standard Operating Procedures (SOPs). /lili Utilize a Manufacturing Execution System to manage data related to customer orders and inventory. /lili Operate liquid handling robotics and automated sample management equipment. /lili Conduct quality control testing to ensure order quantity specs using Spectrophotometry. /lili Accurately and efficiently complete final packaging of customer samples, maintain stocks of catalog product, and create larger library collections. /lili Prioritize workload to meet customer needs and new product launches. /lili Accurately and effectively complete basic equipment tasks including, but not limited to, reagent filling, liquid-handling robot setup, operation, and cleanup, and handling of customer samples for final packaging. /lili Cross-train to ensure the capability to complete the primary tasks in each Manufacturing laboratory, including, but not limited to, Oligonucleotide Synthesis, Quality Control, and Post Synthetic Process. ulli Process and purify customer samples using HPLC and Gel Electrophoresis. /lili Conduct quality control testing using HPLC, LCMS and UV-VIS spectroscopy. /li/ul/lili Collect requested data and communicate to the Manager. /lili Ensure process compliance by regularly monitoring, reviewing, and updating SOPs and documentation as needed. /lili Maintain proper lab maintenance per SOPs and 5S standards. /lili Comply with all EHamp;S regulations and policies. /lili Fulfill other trainings, tasks and responsibilities as assigned and/or required. /lili Must be willing to work in a lab with hazardous chemicals. /li/ulp/ppi Nothing in this job description restricts management's right to assign or reassign duties and responsibilities of this job at any time. /i/pp/ppb Basic Qualifications:/b/pulli Bachelor's Degree in Life or Natural Sciences/lili0-3 years of laboratory experience/li/ulp/ppb Preferred Qualifications:/b/pulli Familiarity with laboratory standard concepts, practices, and procedures/lili Ability to learn, troubleshoot, and operate specialized laboratory equipment, computers, and instrumentation software/lili Advanced analytical skills using Microsoft Excel, with proficient data entry and typing skills/lili Professional and clear communication skills, both written and verbal, teamwork is essential/lili Excellent interpersonal skills with the talent for teamwork/lili Exceptional attention to detail and accuracy. /li/ulp/ppb Physical Requirements amp; Expectations:/b/pulli Ability to regularly move items weighing 30-60 pounds, with or without accommodation/li/ulp/ppb Compensation Range:/b/pp/pp The base salary range for this full-time position is $53,500-62,500. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. /pp/pp Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered. /pp/ppbu What do we offer?/u/b/pp We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits:/pullip Medical, Dental, and Vision Insurance Options/p/lilip Life and Disability Insurance /p/lilip Paid Time-Off/p/lilip Parental Benefits/p/lilipspan Compassionate Care Leave/span/p/lilip 401k with Company Match/p/lilip Employee Stock Purchase Plan/p/li/ulp/pp Learn more about Revvity's benefits by visiting our a href="************** safelinks. protection. outlook. com/?url=http%3A%2F%2Frevvity. bswift. com%2Famp;data=05%7C02%7CAssil. Farhat%40revvity. com%7C48096b64594e4f908e8a08dd5286bd3b%7C66a92d0f8ca8403c84e65503c5643994%7C0%7C0%7C**********50808743%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7Camp;sdata=LpNrWwHdACTfzESzvRXS%2FuiE7Zv071C2LXBuMpx1XRA%3Damp;reserved=0" target="_blank"uBswift/u/a page. span Log-In instructions are provided towards the bottom of the Bswift page. /span/pp/ppi*For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information. /i/pp/ppspan Revvity is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to any characteristic or status protected by applicable federal, state, and/or local laws. If you are an applicant with a disability that requires reasonable accommodation to complete any part of the application process or are limited in the ability-or unable to use-the online application system and need an alternative method for applying, you may contact /spanspana href="mailto:OpenJobs@revvity. com" target="_blank"span OpenJobs@revvity. com/span/a/spanspan. /span/p/div

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description This role is not available for immediate hire. Chemical Laboratory Technician responsibilities include, but are not limited to, the following Responsible for processing of incoming food and feed samples for analytical testing in compliance with all applicable standard operating procedures and quality systems as well as care and maintenance of equipment associated with this testing. Qualifications The ideal candidate would possess : Strong computer, scientific and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team Self-motivated, adaptable, high ownership of assigned tasks and results oriented Ability to work with minimal supervision in a fast paced environment Ability to learn new analytical laboratory techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions and comply with company policies Basic Minimum Qualifications : Bachelor's degree in a scientific field. BS in Chemistry preferred. Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is Full-Time, First Shift, with additional hours as needed. Candidates currently living in a commutable distance to New Orleans, LA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description This role is not available for immediate hire. Chemical Laboratory Technician responsibilities include, but are not limited to, the following * Responsible for processing of incoming food and feed samples for analytical testing in compliance with all applicable standard operating procedures and quality systems as well as care and maintenance of equipment associated with this testing. Qualifications The ideal candidate would possess : * Strong computer, scientific and organizational skills * Excellent communication (oral and written) and attention to detail * Ability to work independently and as part of a team * Self-motivated, adaptable, high ownership of assigned tasks and results oriented * Ability to work with minimal supervision in a fast paced environment * Ability to learn new analytical laboratory techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions and comply with company policies Basic Minimum Qualifications : * Bachelor's degree in a scientific field. BS in Chemistry preferred. * Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is Full-Time, First Shift, with additional hours as needed. Candidates currently living in a commutable distance to New Orleans, LA are encouraged to apply. * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Flow Cytometry Laboratory Specialty Analyst Department: 9010|NIRC Administration Responsibilities: The New Iberia Research Center (NIRC) provides essential resources for the conduct of both basic and applied research using non-human primates to address human health and societal challenges. The Center also serves the broader biomedical community by enabling external investigators to conduct all or part of their research at NIRC. Position Summary: The Flow Cytometry Laboratory Specialty Analyst is responsible for developing and executing specialized flow cytometry procedures, including the generation of standard operating procedures (SOPs) and validation of relevant methods and instrumentation. This role supports pharmacodynamics and efficacy testing of novel preclinical therapeutics, particularly those involving non-human primate samples. The position requires expertise in flow cytometry, data analysis, and the coordination of laboratory activities. Key Responsibilities: * Develop and perform specialty procedures in flow cytometry, ensuring high-quality data generation and adherence to SOPs. * Validate and optimize flow cytometry instrumentation, including the BD FACSAria Fusion and Miltenyi MACsQuant16, for pharmacodynamics and efficacy testing. * Provide technical and scientific support for biomarker combination studies, data analysis using FlowJo, and analysis of large datasets through tSNE or equivalent methodologies. * Interpret and present complex flow cytometry data to support research objectives. * Maintain flow cytometers and related equipment to ensure optimal performance. * Order and manage laboratory supplies specific to cytometry needs. * Train new personnel in flow cytometry procedures and proper use of laboratory equipment. * Collaborate with research teams on the isolation of cells from blood, bone marrow, and other tissues, as well as assist in dose formulation procedures. Qualifications: Required Qualifications: * Bachelor of Science degree * Expertise in multi-parametric flow cytometry/sorting Preferred Qualifications: * Prior experience in preparing preclinical trial dosing formulations, cell separation techniques and ELISPOT assays * Strong computer skills are a must, as are skills in managing, planning, and organizing multiple activities. * A motivated self-starter capable of meeting established deadlines. * Demonstrate the ability to communicate effectively with all staff members and visitors of the UL Lafayette NIRC. Job Ad# (req3998)

Brief Description The Quality Control Inspector is responsible for ensuring compliance with quality standards in the reception, processing, and packaging of meat and marinated products. They will conduct inspections at each stage of production, supervise staff to ensure adherence to procedures, and record results to maintain product traceability. Attention to detail, effective communication skills, and leadership ability are required. Responsibilities Supervision and Quality Control Supervise production staff, ensuring compliance with quality and hygiene procedures. Train employees in good manufacturing practices, food safety, and quality standards. Ensure food safety and sanitation regulations are followed at all stages of meat and marination processing. Monitor the proper handling, storage, and temperature of meat and marinated products. Inspection of Raw Materials and Final Product Verify that meat and marination ingredients meet quality specifications before use in production. Inspect meat cuts for defects, cross-contamination, or irregularities in weight and presentation. Approve or reject in-process and finished products based on established standards. Coordinate with the production team to correct any deviations in real-time. Safety and Hygiene Ensure staff use appropriate protective equipment (gowns, gloves, hairnets, etc.). Supervise the cleaning and sanitization of work areas and equipment before, during, and after production. Guarantee compliance with food safety regulations and USDA guidelines. Documentation and Reporting Record inspection results in quality control logs. Report any non-compliance or findings to supervisors and management for corrective action. Keep sanitation and temperature monitoring records up to date. Record and analyze daily production. Conduct inventories and report shortages as necessary. Equipment Operation and Maintenance Supervise the safe handling of knives, meat saws, and processing machinery. Report equipment malfunctions or maintenance needs for production and/or refrigeration equipment. Other Duties Assist in internal and external quality and food safety audits. Collaborate with other departments to improve efficiency and compliance with standards. Perform other tasks as needed. Physical Requirements Ability to move, lift, and carry products exceeding 50 pounds, with or without assistance. Willingness to work in environments with variable temperatures, including refrigerated and frozen areas, as well as high-temperature production zones. Ability to stand for extended periods, perform repetitive movements such as bending, lifting, and handling heavy products. Possible use of stairs and platforms to access higher storage and production levels.

Join Our Team as a Quality Control Inspector We are excited to announce a fantastic career opportunity for a skilled Quality Control Inspector to join our dynamic team at a well-established oil and gas company in the region. The selected candidate will have a key role in upholding and improving quality standards within the organization, particularly focusing on the oil and gas sector. Key Responsibilities: Conduct detailed quality control assessments on a range of products, materials, and equipment Ensure strict compliance with industry regulations and established standards Promptly identify and rectify any deviations or faults in the quality control process Prepare comprehensive quality control reports for documentation and analysis Collaborate closely with production and engineering teams to address quality-related issues effectively If you are passionate about maintaining exceptional quality standards and are prepared to excel in the role of a Quality Control Inspector, we look forward to receiving your application.

ABOUT YOU Are you passionate and ready to join an inclusive work environment, committed to leading new ideas and pathways, and to delivering value? If the answer is, “Yes!” then we have an exciting career opportunity for you as a Reporting QC Associate. Who are we? We are Montrose, a global environmental services provider offering environmental planning and permitting, measurement and analytical services, and environmental resiliency and sustainability solutions. Our qualified engineers, scientists, technicians, associates, and policy experts are proud of our collective expertise and the collaborative nature of our approach to helping clients. We strive to optimize environmental resiliency in a way that effectively complements our clients' decision-making and operations and efficiently fulfills their project requirements. We have over 135 global locations across the United States, Canada, Europe and Australia and 3000+ employees - all ready to provide solutions for environmental needs. WHAT WE CAN OFFER YOU As a key member of our Montrose team, you can expect: Mentorship and professional development resources to advance your career Direct exposure to our industry's leading experts who are solving the world's toughest environmental challenges An entrepreneurial environment where you can learn, thrive and collaborate with talented colleagues Opportunities to engage and contribute in our Diversity, Fairness and Inclusion and Women Empowering Leadership employee resource groups Competitive compensation package: annual salary ranging from $20.00/hr. to 25.00/hr., commensurate with accomplishments, performance, credentials and geography Competitive medical, dental, and vision insurance coverage 401k with a competitive 4% employer match Progressive vacation policies, company holidays and paid parental leave benefits to ensure work/life balance A financial assistance program that supports peers in need, known as the Montrose Foundation Access to attractive student loan rates to optimize your student loan payoff plans A DAY IN THE LIFE This role supports the Montrose's Stack Testing Services (“Stack) division. As a key member of the reporting team, this role will be responsible for a full range of activities including: Compiles, analyzes, and reports field data collected from test projects under the supervision of Reporting QC Specialists and Managers. This position works with Project Managers, Field Technicians and other reporting staff to ensure data quality, accuracy, and timely delivery of test reports and other documents. Write and assemble documents such as test protocols or test reports using templates, following style guides and SOPs. Perform review of draft documents for details like grammar and spelling Communicate regularly with field and reporting staff to ensure test reports are completed in a timely manner Perform all duties with integrity, safety and a professional mentality Understand roles and responsibilities within the Quality Management System and third-party accreditation standards Communicate all program deficiencies and improvements Report all non-conforming work Promote a positive and inclusive work/team environment Demonstrate discretion, confidentiality and good judgement when dealing with sensitive company, personnel and client information Participate in training for career development, safety and maintaining required certifications YOUR EXPERTISE AND SKILLS To perform this job successfully, individuals must be able to perform each duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Bachelor degree in science/engineering or related field preferred High School diploma is acceptable where writing/math/other skills can be demonstrated Technical writing experience beneficial Familiarity with EPA test methods, permits, and regulatory requirements beneficial Field testing experience is beneficial Intermediate user of cloud-based platforms (ex. Google Workspace), Microsoft Office Suite products (Excel & Word), and PDF editing software The above statements are intended to describe the general nature of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties and skills required of employees so classified. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact ************ or ************************ for assistance. MAKE THE MOVE TO ACCELERATE YOUR CAREER We are going to be blunt - the way we work may not suit everyone. We are a fast-paced, dynamic and high-growth company. You are your own boss, but you will get tons of guidance and plenty of support from talented, super-smart colleagues and its service providers. Therefore, if freedom, autonomy, and head-scratching professional challenges attract you, we could be the perfect match made in heaven. Want to know more about us? Visit montrose-env.com and have fun! Montrose is an Equal Opportunity Employer. Montrose is committed to recruiting and hiring qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status. Montrose is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. #LI-MEG #LI-KJ1