Quality control analyst jobs in Corpus Christi, TX

You will support the production and testing of various reagents for qPCR and sample preparation applications including master mixes, nucleic acid purification, and internal positive controls for use in various workflows such as veterinary diagnostics, USDA-certified, and custom products. Our team is dynamic and fast-paced, relying on collaboration, multitasking, and communication within the team and the larger organization. Responsibilities: •Formulate buffers and other reagents for biotech applications in a clean manufacturing environment. •Isolate and dilute nucleic acids using pipetting and spectrophotometric techniques. •Perform quality control testing on buffers and nucleic acids, including pH, conductivity, agarose gels, and nucleic acid purification using magnetic beads and quantification by qPCR. •Troubleshoot manufacturing and quality control activities and record results in technical reports. •Revise and edit existing manufacturing protocols;participate in the development of manufacturing protocols for new products. •Participate in Practical Process Improvement projects. •Run manufacturing metrics for process control and productivity savings. •Prioritize and schedule work to ensure on-time delivery. •Handle inventory accurately and effectively. •Collaborate with peers from various groups. •Train co-workers on instrumentation and manufacturing processes. •Adhere to ISO guidelines, USDA regulations, and quality policy. Requirements: •Bachelor's degree (B.S.) in Biochemistry or related field, or equivalent experience. •0-2 years of related undergraduate and post-undergraduate experience preferred. •Demonstrated ability in operating, troubleshooting, and maintaining complex laboratory equipment. •Detailed understanding of chemical interaction necessary for PCR systems. •Familiarity with troubleshooting techniques and statistical quality control. Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

PenFed is hiring a (Hybrid) Sr Analyst, Real Estate QC Underwriting at our Omaha, Nebraksa; San Antonio, Texas; Eugene, Oregon or Tysons, Virginia location. The primary purpose of this job is to perform quality control reviews for first trust conventional, VA, FHA and equity real estate loans. This role will evaluate the integrity and quality of the credit, compliance, and collateral aspects of the mortgage loan origination process through pre-funding and post-funding loan reviews designed to verify the accuracy and integrity of the information and loan documentation used to support the lending decision for conventional, VA, FHA, and Equity Line of Credit loans. It will validate adherence to PenFed's policies and procedures and secondary marketing investor guidelines. This role requires expertise in evaluating property valuations, including all types of appraisals, AVMs and property condition inspections, with knowledge of Interagency guidelines and Appraisal Independence Requirements. Responsibilities Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. This is not intended to be an all-inclusive list of job duties, and the position will perform other duties as assigned. + Conduct reviews of first trust conventional, VA, FHA and equity mortgage loans to ensure that loans were properly underwritten, and that sound judgment was used in the underwriting process. Complete a thorough analysis of loan files to determine member credit worthiness and collateral values were adequate. Review legal and compliance documentation as applicable. + Conduct reviews of mortgage loans to evaluate the accuracy and integrity of the information and loan documentation used to support the lending decision. + Conduct reviews of mortgage loans to ensure compliance with PenFed's policy and procedures, investor, agency, and secondary market requirements. + Analyze and determine accurate defect ratings based on investor's loan eligibility requirements. Evaluate the entire credit package and collateral for residential mortgage loans and ultimately ensure an investment quality loan product. + Follow up on previous deficiencies and examine samples of corrected files. + Ability to work collaboratively with Mortgage Operations, providing clarification of review results as needed. + Understand and interpret all credit underwriting documentation required to be reverified in each loan file and conduct further research as necessary. + Perform peer reviews and provide guidance to junior analysts as needed. + Assist with process testing as assigned and participate in special projects. + Maintain a working knowledge of internal policies, procedure, external regulations, secondary market underwriting guidelines, investor, and private mortgage insurance guidelines. + Maintain current knowledge of Fannie Mae, Veterans Administration (VA), Freddie Mac, FHA and external investors. Qualifications Equivalent combination of education and experience is considered. + Bachelor's degree in business, accounting, finance, or another related field required. + Minimum of three (3) years progressive experience in real estate lending with underwriting experience required, preferably in a bank or credit union environment. + Advanced knowledge of real estate loans (origination, processing, closing, funding) required. Broad knowledge of consumer real estate lending, including first trust mortgage loans, home equity loans and lines of credit. + Knowledge of lending compliance regulations and system definitions. + Active or recent VA SAR and/or FHA DE underwriting authority preferred. + Proficiency with Encompass is highly desirable. Supervisory Responsibility This position will not supervise employees. Licenses and Certifications There are no additional certifications required. Work Environment While performing the duties of this job, the employee is regularly exposed to an indoor office setting with moderate noise. *Most roles require working in an office setting with moderate noise and the ability to lift 25 pounds.* Travel The ability to travel to various worksites and be on-call may be required. About Us Established in 1935, PenFed today is one of the country's strongest and most stable financial institutions with over 2.9 million members and over $31 billion in assets. We serve members in all 50 states and the District of Columbia, as well as in Guam and Puerto Rico. We are federally insured by NCUA and we are an Equal Housing Lender. We are available to members worldwide, via the web, seven days a week, twenty-four hours a day. We provide our employees with a lucrative benefits package including robust medical, dental and vision plan options, plenty of paid time off, 401k with employer match, on-site fitness facilities at our larger locations, and more. Equal Employment OpportunityPenFed management will maintain and observe personnel policies which will not discriminate or permit harassment or retaliation against a person because of race, color, creed, age, sex, gender, gender identity, gender expression, religion, national origin, ancestry, marital status, military or veteran status or obligation, the presence of a physical and/or mental disability or medical condition, genetic information, sexual orientation, and all statuses protected by applicable state or local law in all recruiting, hiring, training, compensation, overtime, position classifications, work assignments, facilities, promotions, transfers, employee treatment, and in all other terms and conditions of employment. PenFed will also prohibit retaliation against individuals for raising a complaint of discrimination or harassment or participating in an investigation of same. PenFed will also reasonably accommodate qualified individuals with a disability so that they can apply for a job or perform the essential functions of a job unless doing so causes a direct threat to these individuals or others in the workplace and the threat cannot be eliminated by reasonable accommodation or if the accommodation creates an undue hardship to PenFed. Contact human resources (HR) with any questions or requests for accommodation at ************. #LI-Hybrid

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Protomer is a recently -acquired, wholly owned subsidiary of Eli Lilly and Co. based in Pasadena, CA. The team operates as a group within Lilly Research Laboratories (LRL). LRL is focused on the discovery and development of new therapeutics for the treatment of a plethora of diseases. The scientists in LRL work cross-functionally between therapeutic target area disciplines, including Diabetes, Heart Failure, Renal, Neuroscience, ASCVD, Incretins and Insulins. The team at Protomer is working on responsive biotherapeutics that can be controlled using small molecule modulators. Protomer team is based in Pasadena and the research labs are located in Pasadena. We are currently expanding the team to advance several programs, including glucose sensing insulins (GSIs), and are looking for a research associate with experience in biochemistry, synthesis, bioconjugations, and purification/characterization of therapeutic compounds of interest. The ideal candidate will have a bachelor's or master's degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a great teammate in a fast-paced research setting. The applicant will be responsible for assisting Protomer's senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively engage and present in team meetings and is expected to contribute to the team's progress and success. Responsibilities: * Work closely with senior scientist to accomplish team objectives and research milestones * Purify and characterize compounds using HPLC, FPLC, and various biochemical methods * Introduce and maintain innovative technologies with respect to peptide therapeutics, including developing and implementing assays and maintaining critical instruments. * Perform data analysis. Critically evaluate data and results and troubleshoot experiments. * Demonstrable ability to function independently, work within a team-oriented lab environment, and work within cross-functional project teams. * Maintain accurate record keeping, perform independent data analysis, and report data in written and oral formats and retain excellent electronic lab notes. * Perform work in compliance with Lilly Research Policies. Basic Qualifications: Undergraduate degree in chemistry, biochemistry, chemical engineering with working knowledge of standard biochemistry or chemistry lab techniques. Additional Skills/Preferences: * Academic or industry research experience * Proven ability to work in a flexible, team-oriented environment. * Experience with standard biochemistry techniques. * Strong communication skills and experience presenting data in a team environment. * Strong relationship-building and interaction skills with peers and management. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $69,000 - $179,300 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

**Have you ever thought about being part of a company that reimagines chemistry every day to build a better world?** That's the purpose of Indorama Ventures, and we want you with us on this journey! We are looking for innovative, collaborative professionals who are ready to embrace the challenge of working in a company that is constantly expanding internationally. We value flexibility, partnership, and believe that the impact of our actions goes far beyond the chemical industry. Here, diversity matters. Our work environment is inclusive, diverse, and guided by respect, ethics, and equal opportunities for all. **What we're looking for:** Indorama Ventures- Indovinya is currently looking for a dynamic individual to work as a Research Chemist I located at our The Woodlands, Texas facility. In this role, you will be responsible to work with Research Scientists to evaluate existing and new chemistries, processes, or applications related to Indorama products. This position is focused on the laboratory working on directed experiments in a safe manner. The lab work may include glassware reactors, Parr reactor reactions, etc. Also, the work could include application specific testing for areas such as agricultural, oilfield, paints/coatings, personal care, etc. **What will be expected from you?** + Maintain an awareness of the literature and other sources of information to remain current with developments in the area of functional products of interest to the Corporation. + Work to complete projects in the US project pipeline. + Set up and execute laboratory to meet both internal and external customer expectations. + Set up and execute laboratory work to as outlined by R&D scientist. + Analyzing samples by analytical methods or applications testing. + Keep neat and orderly notebooks containing a record of all work performed. Maintain other records as necessary to support patent applications for innovative products. + Maintain orderly laboratory space. + Follow all safety and training requirements. + Manage and optimize all process under your responsibility taking into consideration Quality, Legality and Food Safety (if applicable) and client needs on Indorama's products and services. + Guarantee all documentation under your responsibility updated and available for consulting. + Support R&D Lab Manager with properly managing the lab resources + Interact with TS&D team to improve the lab, lab methods, etc. + Work in cross functional /cross discipline teams as needed **What are we looking for in the ideal candidate?** + BS in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering required. + BS in other science field plus 2+ years in Research laboratory work + Associates Degree with 5+ years in Research laboratory work + 0-3 years' experience (more 3 years' experience preferred) in: + R&D laboratory preferred. + Surfactants knowledge in laboratory or application use strongly preferred. + Use and knowledge of Parr Reactors preferred. + Computer literacy w/ databases, word processing, spreadsheets + Excellent organizational and communications skills + Demonstrated presentation skills preferred. + Experience in chromatography, spectroscopy, wet analysis, or other analytical techniques preferred. + Formulation experience in Agricultural, Home Care, or Coatings preferred. + English with Bilingual Portuguese or Spanish strongly preferred. **What do we offer?** A competitive compensation package, including: - Health insurance - WellHub / TotalPass - Life insurance - And other exclusive benefits The division you'll be joining is a global leader in the chemical industry. We offer a broad portfolio of solutions and high delivery standards to markets such as Crop Solutions, Home and Personal Care, Coatings, Energy & Resources, and Performance Products. **Here, you can make a difference.** **Join us!** We're Indovinya, a top producer of chemical intermediates and surfactants. Our extensive portfolio is designed to meet our customers' most diverse needs. As producers of solutions used for crops, oil and gas, coatings, home and personal care, and other applications, we are present in the daily lives of millions worldwide. Through our increasingly sustainable chemistry, designed to meet the needs of each of our customers carefully, we want to transform our operations and products into something increasingly relevant for the planet. We are part of Indorama Ventures Public Company Limited, one of the world's leading petrochemical producers, and are present globally with manufacturing in Europe, Africa, Americas, and Asia-Pacific. With 18 plants, seven R&D centers, and an experienced management team, we have a strong track record of environmental stewardship. Our expertise lies in innovative, eco-friendly chemistry. Today, Indovinya emerges as a more robust and strategic company dedicated to driving new business opportunities while prioritizing the well-being of countless individuals as employees, customers, suppliers and mainly the communities close to our operations worldwide.

Have you ever thought about being part of a company that reimagines chemistry every day to build a better world? That's the purpose of Indorama Ventures, and we want you with us on this journey! We are looking for innovative, collaborative professionals who are ready to embrace the challenge of working in a company that is constantly expanding internationally. We value flexibility, partnership, and believe that the impact of our actions goes far beyond the chemical industry. Here, diversity matters. Our work environment is inclusive, diverse, and guided by respect, ethics, and equal opportunities for all. What we're looking for: Indorama Ventures- Indovinya is currently looking for a dynamic individual to work as a Research Chemist I located at our The Woodlands, Texas facility. In this role, you will be responsible to work with Research Scientists to evaluate existing and new chemistries, processes, or applications related to Indorama products. This position is focused on the laboratory working on directed experiments in a safe manner. The lab work may include glassware reactors, Parr reactor reactions, etc. Also, the work could include application specific testing for areas such as agricultural, oilfield, paints/coatings, personal care, etc. What will be expected from you? Maintain an awareness of the literature and other sources of information to remain current with developments in the area of functional products of interest to the Corporation. Work to complete projects in the US project pipeline. Set up and execute laboratory to meet both internal and external customer expectations. Set up and execute laboratory work to as outlined by R&D scientist. Analyzing samples by analytical methods or applications testing. Keep neat and orderly notebooks containing a record of all work performed. Maintain other records as necessary to support patent applications for innovative products. Maintain orderly laboratory space. Follow all safety and training requirements. Manage and optimize all process under your responsibility taking into consideration Quality, Legality and Food Safety (if applicable) and client needs on Indorama's products and services. Guarantee all documentation under your responsibility updated and available for consulting. Support R&D Lab Manager with properly managing the lab resources Interact with TS&D team to improve the lab, lab methods, etc. Work in cross functional /cross discipline teams as needed What are we looking for in the ideal candidate? BS in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering required. BS in other science field plus 2+ years in Research laboratory work Associates Degree with 5+ years in Research laboratory work 0-3 years' experience (more 3 years' experience preferred) in: R&D laboratory preferred. Surfactants knowledge in laboratory or application use strongly preferred. Use and knowledge of Parr Reactors preferred. Computer literacy w/ databases, word processing, spreadsheets Excellent organizational and communications skills Demonstrated presentation skills preferred. Experience in chromatography, spectroscopy, wet analysis, or other analytical techniques preferred. Formulation experience in Agricultural, Home Care, or Coatings preferred. English with Bilingual Portuguese or Spanish strongly preferred. What do we offer? A competitive compensation package, including: • Health insurance • WellHub / TotalPass • Life insurance • And other exclusive benefits The division you'll be joining is a global leader in the chemical industry. We offer a broad portfolio of solutions and high delivery standards to markets such as Crop Solutions, Home and Personal Care, Coatings, Energy & Resources, and Performance Products. Here, you can make a difference. Join us!

We have an exciting opportunity at our Carrollton, Texas facility for a QC Chemist. This position serves as a Quality Control Chemist and maintains quality standards by performing analytical testing on incoming and finished products for composition and impurities, as well as recording quality results. In addition, this role will accommodate preparations for new formulations (Gauge studies, method development, instrument installation, etc). Company Overview FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry-where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more. We're a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you've got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what's possible-for the world and your future. We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island-each offering unique local experiences, from vibrant cultural scenes to historic charm. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Key responsibilities for this role include: * Responsible for testing and approving raw materials, intermediates, and final products following company processes and procedures via use of lab equipment (eg: GC, Karl Fischer titration, ICP-MS, NVR). * Complete and issue Certificates of Analysis (COA). * Investigate out of specification and out of control results. * Review process control charts and take action as required. * Develop, review, and update laboratory documents and procedures. * Respond to deviations by assessing the impact on product safety and quality. * Instrument validation, troubleshooting, repair, and maintenance. * Laboratory upkeep and cleaning, waste disposal, and gas maintenance. * Maintain safe and healthy work environment by following standards and procedures. * Comply with legal regulations REQUIREMENTS * Requires a Master's degree or BA/BS Chemistry degree and minimum of 1-2 years of experience in the semiconductor or related field or in a production laboratory environment. * Instrumentation and analytical skills experience preferred - wet chemistry techniques, UV-Vis, GC/FID/TCD, IC, HPLC, GFAA, ICP/OES, ICP/MS, FTIR, GC/MS, and liquid particle counters. Additional mass spectroscopy experience a plus. * Ability to multi-task and handle change in priorities. * Strong organization skills, good attention to detail, and the ability to function effectively as part of a cross functional team. * Strong verbal and written communication skills. * Must have excellent computer skills (Word, PowerPoint, Excel and statistical software tools). * Strong troubleshooting skills * Must be able to work 2nd shift. 12:00PM - 9:00PM / Monday thru Friday ADDITIONAL REQUIREMENTS We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication. * Resilience - Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively. * Communication - Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships. * Reasoning & Decision Making - Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions. * Comprehension - Capability to understand and complete tasks as assigned and solve problems effectively. * Organizational Skills - Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).

We are looking for full-time Entry Level Assurance Associates in our Abilene, Texas office. Who We Are Eide Bailly is a Top 25 CPA and business advisory firm with over 50 offices in the U.S. and India. Since 1917, we've built our firm around one thing: people. We believe meaningful work starts with meaningful relationships - with our clients, our communities, and each other. That's why we focus on creating an environment where you feel supported, connected, and empowered to grow. You'll be part of a team that values authenticity, fosters trust, and provides you with the tools to thrive. Why You'll Love Working Here * You'll belong. We foster an inclusive, supportive environment where people look out for each other. You're a valued part of the team from day one. * You'll grow. You'll get hands-on experience with a variety of clients and industries or projects, all while working directly with experienced professionals who want you to succeed. * You'll be supported. Whether it's your Eide Guide, Career Advisor, or a co-worker you meet at lunch, you'll always have someone available to answer questions and help you navigate your career. * You'll have balance. Meaningful work is only one part of a meaningful life. We offer flexibility and benefits designed to support your well-being - inside and outside of work. * You'll have fun. Yes, we're accountants and business advisors - but we also like to celebrate, connect, and have a good time. Office events, volunteer opportunities, and casual team activities are all part of the experience. Typical Day in the Life A typical day in the life of an Assurance Associate with Eide Bailly might include the following: * Attend a client engagement meeting to determine timelines and goals of an audit. * Research business trends within an industry to professionally represent a company and apply this knowledge to the client's solutions, potentially developing new or additional business for the Firm. * Prepare accounting-related reports through a paperless environment. * Provide financial analysis upon completion of fieldwork in an effort to improve client internal controls and accounting procedures. * Attend a technical training on Knowledge Coach (auditing software). Who You Are * You are inquisitive and enjoy learning about various client business processes and traveling to different locations to help clients (20-40 percent travel is required in the role). * You like the challenge of in-charging engagements and providing constructive feedback to other team members. * You are a multi-tasking master, and there has never been a deadline you could not meet. * You have knowledge of and exposure to a variety of industries. * You hold yourself to the highest professional standards and maintain strict client confidentiality. * In addition to all of this, you have a Bachelor's degree in Accounting and are working towards obtaining your CPA license Must be authorized to work in the United States now or in the future without visa sponsorship. Eide Bailly LLP offers a competitive salary and a comprehensive benefits package. Eide Bailly LLP is proud to be an affirmative action/equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, or any other status protected under local, state or federal laws. What to Expect Next We'll be in touch! If you look like the right fit for our position, one of our recruiters will be reaching out to schedule a phone interview with you to learn more about your career interests and goals. In the meantime, we encourage you to check us out on Facebook, Twitter, Instagram, LinkedIn or our About Us page. #LI-MP1

PRIMARY DUTIES AND RESPONSIBILITIES: * Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products. * Utilize analytical laboratory instrumentation with supervision. * Comply with cGMP regulations and follow all standard operating procedures. * Peer review data generated by other technicians. * Maintain and troubleshoot laboratory equipment and analytical instrumentation within level of experience. ASSOCIATED DUTIES AND RESPONSIBILITIES: * Perform and/or assist with equipment calibrations and qualifications. * Other related duties as required. REQUIRED SKILLS, ABILITIES, AND QUALIFICATIONS: * Bachelors degree in chemistry or related discipline. * 2-5 years' experience in a chemistry laboratory. * 2- 5 years' experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus. * Ability to follow standard operating procedures. * Strong communication skills, both written and verbal. * Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision. * Strong attention to detail. * Desire and ability to work in a positive team environment. At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

We have an exciting opportunity at our Carrollton, Texas facility for a QC Chemist. This position serves as a Quality Control Chemist and maintains quality standards by performing analytical testing on incoming and finished products for composition and impurities, as well as recording quality results. In addition, this role will accommodate preparations for new formulations (Gauge studies, method development, instrument installation, etc). Company Overview FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry-where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more. We're a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you've got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what's possible-for the world and your future. We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island-each offering unique local experiences, from vibrant cultural scenes to historic charm. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Key responsibilities for this role include: Responsible for testing and approving raw materials, intermediates, and final products following company processes and procedures via use of lab equipment (eg: GC, Karl Fischer titration, ICP-MS, NVR). Complete and issue Certificates of Analysis (COA). Investigate out of specification and out of control results. Review process control charts and take action as required. Develop, review, and update laboratory documents and procedures. Respond to deviations by assessing the impact on product safety and quality. Instrument validation, troubleshooting, repair, and maintenance. Laboratory upkeep and cleaning, waste disposal, and gas maintenance. Maintain safe and healthy work environment by following standards and procedures. Comply with legal regulations REQUIREMENTS Requires a Master's degree or BA/BS Chemistry degree and minimum of 1-2 years of experience in the semiconductor or related field or in a production laboratory environment. Instrumentation and analytical skills experience preferred - wet chemistry techniques, UV-Vis, GC/FID/TCD, IC, HPLC, GFAA, ICP/OES, ICP/MS, FTIR, GC/MS, and liquid particle counters. Additional mass spectroscopy experience a plus. Ability to multi-task and handle change in priorities. Strong organization skills, good attention to detail, and the ability to function effectively as part of a cross functional team. Strong verbal and written communication skills. Must have excellent computer skills (Word, PowerPoint, Excel and statistical software tools). Strong troubleshooting skills Must be able to work 2nd shift. 12:00PM - 9:00PM / Monday thru Friday ADDITIONAL REQUIREMENTS We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication. Resilience - Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively. Communication - Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships. Reasoning & Decision Making - Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions. Comprehension - Capability to understand and complete tasks as assigned and solve problems effectively. Organizational Skills - Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).

Job DescriptionSalary: Quality Control Chemist About Rowe Casa: From the beginning, Rowe Casa Organics has been on mission to provide safe, natural, and non-toxic products that you can trust. In 2017, sisters Jill and Alicia embarked on a mission seeking greater health and wellness for their families. Frustrated by the lack of transparency and truly safe, effective options, Jill Rowe took matters into her own hands by making our very first product, Elderberry Immune Support. Today, Rowe Casa Organics produces over 300 products to help people thrive in their health, wellness, and lifestyle. From wellness necessities and household essentials to the finest of self-care, each product that we offer is crafted with the utmost quality, care, and love. About the Position: The Quality Control Chemist will be part of the Quality Department reporting to the QC Manager or designee. This position will be responsible of the analytical laboratory for testing samples of RCO products across all manufacturing facilities and logistics. Duties/Responsibilities: Perform laboratory analysis on all materials and samples. Perform tests on component samples, identify any contamination, conduct an analysis and initiate corrective measures. Perform tests on all incoming ingredients and document all records. Develop and prepare research papers and documents for all protocols. Perform audits on various environmental programs and perform reviews. Develop various testing processes for all raw materials and equipment. Monitor all finished products. Investigate all issues and prevent any GMP problems on samples. Maintain accurate records and perform tests on all activities conducted in the laboratory. Develop and document various analytical laboratory processes and prepare final reports. Any other duties and responsibilities required by Quality Management. Required Skills/Abilities: Bachelors degree (or equivalent) in chemistry, biochemistry, or another relevant field. Ability to plan and execute experimental protocols. Knowledge of laboratory tests, IR, UV, HPLC, etc. Proficient in methods and practices of microbiological analysis. Ability to prepare research papers and technical reports (is a plus). Analytical thinker with strong conceptual and research skills. Previous experience in a cGMP facility is a plus. Excellent laboratory skills. Ability to compile information Ability to work under pressure Excellent organizational skills and attention to detail Positive attitude Ability to adapt Physical Requirements: Prolonged periods sitting at a desk and working on a computer Must be able to lift up to 50 pounds at times Rowe Casa Organics is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, disability, or any other legally protected status.

Lab Analyst I - Early Phase Clinical Research- ICON San Antonio- Full Time/Permanent ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Lab Analyst I to join our diverse and dynamic team. As a Lab Analyst I at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. **Title** : Lab Analyst I **Location:** On-Site San Antonio TX USA **Job Type:** Full Time-Permanent **Shift/Schedule** : M-F 11 AM-7 PM **What You Will Be Doing:** + Under general supervision, Performs and reports routine and special laboratory tests on clinical trial specimens to aid in subject safety and in accordance to protocol requirements. + Detect abnormalities as indicated in protocol. + Performs specimen processing and testing independently to include waived and moderate complexity testing. Analyzes test results and assumes accountability for accuracy. + Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary and knows when to notify lab management. + Understands, performs, and practices quality control management to include running controls, evaluating data, documentation of data, and taking corrective action as required. Communicates any relevant QC information to Supervisor or Manager. + Must cross-train to other laboratory sections as needed. + Calculates, enters, and/or verifies results of laboratory procedures. + Utilizes the Laboratory Information System and eSource system. + Provides notification and documentation of critical laboratory values obtained to Principal Investigator. + Participates in the evaluation, development, and implementation of new or updated testing procedures and protocols. + Demonstrates competence to perform laboratory testing. + Demonstrates adherence to ICON Own It Values based on Integrity, Inclusion, Agility, Collaboration. + Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. + Performs other duties as assigned. **Your Profile:** + Associate or bachelor's degree in medical laboratory science. + MT/MLT/ASCP required (Clinical Lab Scientist license) + Minimum 2 years in a laboratory environment, preferably in a clinical pathology laboratory or related industry. + Proficient in laboratory techniques + Good communication skills and the ability to work effectively in a team environment. **What ICON can offer you:** Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: + Various annual leave entitlements + A range of health insurance offerings to suit you and your family's needs. + Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. + Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. + Life assurance + Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site (************************************* to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (****************************************************** Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here (****************************************************** to apply

Lab Analyst I - Early Phase Clinical Research- ICON San Antonio- Full Time/Permanent ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Lab Analyst I to join our diverse and dynamic team. As a Lab Analyst I at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. Title: Lab Analyst I Location: On-Site San Antonio TX USA Job Type: Full Time-Permanent Shift/Schedule: M-F 11 AM-7 PM What You Will Be Doing: Under general supervision, Performs and reports routine and special laboratory tests on clinical trial specimens to aid in subject safety and in accordance to protocol requirements. Detect abnormalities as indicated in protocol. Performs specimen processing and testing independently to include waived and moderate complexity testing. Analyzes test results and assumes accountability for accuracy. Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary and knows when to notify lab management. Understands, performs, and practices quality control management to include running controls, evaluating data, documentation of data, and taking corrective action as required. Communicates any relevant QC information to Supervisor or Manager. Must cross-train to other laboratory sections as needed. Calculates, enters, and/or verifies results of laboratory procedures. Utilizes the Laboratory Information System and eSource system. Provides notification and documentation of critical laboratory values obtained to Principal Investigator. Participates in the evaluation, development, and implementation of new or updated testing procedures and protocols. Demonstrates competence to perform laboratory testing. Demonstrates adherence to ICON Own It Values based on Integrity, Inclusion, Agility, Collaboration. Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. Performs other duties as assigned. Your Profile: Associate or bachelor's degree in medical laboratory science. MT/MLT/ASCP required (Clinical Lab Scientist license) Minimum 2 years in a laboratory environment, preferably in a clinical pathology laboratory or related industry. Proficient in laboratory techniques Good communication skills and the ability to work effectively in a team environment. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Lab Analyst I - Early Phase Clinical Research- ICON San Antonio- Full Time/Permanent ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Lab Analyst I to join our diverse and dynamic team. As a Lab Analyst I at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. Title: Lab Analyst I Location: On-Site San Antonio TX USA Job Type: Full Time-Permanent Shift/Schedule: M-F 11 AM-7 PM What You Will Be Doing: Under general supervision, Performs and reports routine and special laboratory tests on clinical trial specimens to aid in subject safety and in accordance to protocol requirements. Detect abnormalities as indicated in protocol. Performs specimen processing and testing independently to include waived and moderate complexity testing. Analyzes test results and assumes accountability for accuracy. Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary and knows when to notify lab management. Understands, performs, and practices quality control management to include running controls, evaluating data, documentation of data, and taking corrective action as required. Communicates any relevant QC information to Supervisor or Manager. Must cross-train to other laboratory sections as needed. Calculates, enters, and/or verifies results of laboratory procedures. Utilizes the Laboratory Information System and eSource system. Provides notification and documentation of critical laboratory values obtained to Principal Investigator. Participates in the evaluation, development, and implementation of new or updated testing procedures and protocols. Demonstrates competence to perform laboratory testing. Demonstrates adherence to ICON Own It Values based on Integrity, Inclusion, Agility, Collaboration. Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. Performs other duties as assigned. Your Profile: Associate or bachelor's degree in medical laboratory science. MT/MLT/ASCP required (Clinical Lab Scientist license) Minimum 2 years in a laboratory environment, preferably in a clinical pathology laboratory or related industry. Proficient in laboratory techniques Good communication skills and the ability to work effectively in a team environment. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Lab Analyst I - Early Phase Clinical Research- ICON San Antonio- Full Time/Permanent ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Lab Analyst I to join our diverse and dynamic team. As a Lab Analyst I at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. Title: Lab Analyst I Location: On-Site San Antonio TX USA Job Type: Full Time-Permanent Shift/Schedule: M-F 11 AM-7 PM What You Will Be Doing: * Under general supervision, Performs and reports routine and special laboratory tests on clinical trial specimens to aid in subject safety and in accordance to protocol requirements. * Detect abnormalities as indicated in protocol. * Performs specimen processing and testing independently to include waived and moderate complexity testing. Analyzes test results and assumes accountability for accuracy. * Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary and knows when to notify lab management. * Understands, performs, and practices quality control management to include running controls, evaluating data, documentation of data, and taking corrective action as required. Communicates any relevant QC information to Supervisor or Manager. * Must cross-train to other laboratory sections as needed. * Calculates, enters, and/or verifies results of laboratory procedures. * Utilizes the Laboratory Information System and eSource system. * Provides notification and documentation of critical laboratory values obtained to Principal Investigator. * Participates in the evaluation, development, and implementation of new or updated testing procedures and protocols. * Demonstrates competence to perform laboratory testing. * Demonstrates adherence to ICON Own It Values based on Integrity, Inclusion, Agility, Collaboration. * Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. * Performs other duties as assigned. Your Profile: * Associate or bachelor's degree in medical laboratory science. * MT/MLT/ASCP required (Clinical Lab Scientist license) * Minimum 2 years in a laboratory environment, preferably in a clinical pathology laboratory or related industry. * Proficient in laboratory techniques * Good communication skills and the ability to work effectively in a team environment. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Laboratory Technician (Analytical Chemistry) Revised January 2024 Supervisor's Title: Laboratory Shift Manager Reports to: Laboratory Shift Manager Department : Quality Assurance Exempt Status: Non-Exempt - Hourly Work Schedule: Shift Work Job Summary This position performs and documents routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods, and/or basic laboratory techniques, functions, and equipment. The position conducts specific procedures and tests within the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience. Essential Functions Responsibilities include but are not limited to Registers and prepares samples for general analytical testing through data entry, weighing, and physical preparation. Preps and performs routine to more complex analyses per PPLLQA methods. Reads and records results of analyses, making sure to keep identification numbers matched with correct samples. Operates basic laboratory equipment such as balances, pH meter, etc. Prepares (and assures accuracy of) standards, reagents, etc. needed for analyses. Functions as primary data generator, records and calculates data. Performs routine lab and department maintenance to keep area clean and orderly. Conducts preliminary interpretations of data or observations. Carries out assignments in a timely, diligent, and safe manner and performs work in accordance with PPLLQA SOPs. Perform other duties appropriate to the position as requested. Promotes and adheres to all policies and procedures relating to Good Manufacturing's Practices (GMP's), food safety, and regulatory compliance. Complies with all applicable food safety regulations and mandates (Safe Quality Foods, Food and Drug Administration, Pasteurized Milk Ordinance). Complies with all company food safety policies and procedures (including Good Manufacturing Practices). Responsible for providing food safety and quality feedback to the appropriate manager. Perform other duties as assigned. Qualifications High School diploma or equivalent required. Undergraduate degree in closely related science preferred (i.e. Microbiology, Chemistry, Biology, et al.) Basic computer skills (Microsoft Office Applications: Outlook, Word, Excel, etc.) Professionalism Ability to perform trained tasks at an above base level efficiency pace. Contributes to a team environment and builds effective relationships. Speaks up and gives productive feedback. Moderate learning agility with ability to pick up new skills in a timely manner. Can execute non routine tasks with little supervision. Emerging level initiative, results focus, and follow through. Strong organizational skills and attention to detail. Excellent written and verbal communication. Excellent analytical and problem-solving skills. Punctual and regular attendance is required. English skills must be proficient to understand, read, write, and speak. Complies with all safety policies, practices, and procedures. Reports all unsafe activity to manager and/or Human Resources. Physical Requirements and Environmental Conditions Physical Requirements: Physical effort is regularly required. May be trained and required to operate a forklift. Ascending or descending ramps, stairs, ladders, and/or scaffolding. Frequently involves crouching, stooping, kneeling, and/or climbing or balancing. Frequently involves lifting more than 50lbs. Typical Environmental Conditions: Works in food processing manufacturing facility with moderate noise. May be exposed to moderate to high noise levels (i/e., production equipment, forklifts, heavy traffic). May be exposed to humidity, intense heat and cold, outdoor weather conditions, fumes, and toxic chemicals. May work in areas with mechanical moving parts, above ground with risk of failing, or areas with risk of electrical shock. May be exposed to ingredients that may cause allergic reactions and may be exposed to various allergen ingredients.

Benefits: 401(k) Competitive salary Health insurance Paid time off As a Team member of the Food Microbiology Department, you will use your organization, communication and aseptic skills to help prepare media, assist in the routine laboratory workflow. You will be responsible for: Calculate, weigh, dilute, composite media and samples as needed. Media preparation, dispensing, autoclaving as per SOP, creating Lot numbers and documenting in the LIMS Performing QC on prepared media Store and distribute media to the lab Demonstrate technical skill with balances, pH meters, pipetting devices Aseptically pour plates, label and store as needed Receiving & scanning samples in the lab. Sample sorting and scanning in the LIMS system Sample preparation for analysis Cleaning and washing glassware as per SOP Cleaning and disinfection of instruments, microscopes, laboratory work area on a routine basis Batch samples in the LIMS, Transcribe data and Data entry. Attention to detail. Disposing spent bio-hazard samples Inventory control and ordering supplies. Stocks supply of consumables Prepare kit orders, receive samples and ensure accurate and timely documentation (Log in) in LIMS. Cleaning coolers, organizing storage area, restocking consumables. Maintain and document temperature records of equipment. Filing, storing, scanning of documents Participate in HACCP training and sampling Assist with Sample pick up from client locations. Follows biosafety, aseptic techniques as per needed. Follows policies and procedures and conducts all operations in a safe and compliant manner. Must be able to lift and move up to 50lb. Must be 23 y and above, with a valid driver's license. Willingness to learn, multitask, cross train and work as a Team. Flexibility with working hours needed depending on client requirement. CHARACTERISTICS The Laboratory technician must have good personal habits, work well with others, be technically conscientious, be able to stay on task and complete work on schedule, be able to work independently as well as on a team, and promote the principles and professionalism of the company. EDUCATION High school diploma or equivalent EXPERIENCE 1-2 years of laboratory experience in a microbiology lab or related field will be an advantage. COMPUTER AND SOFTWARE SKILLS Must be computer literate and experienced in using Microsoft Office Suite (Word, Excel). Proficient in the Windows environment and use of Internet E-mail. OTHER SKILLS Must be organized Must have good written and oral communication skill (English) and Spanish Must manage multiple projects with minimal supervision. Must manage multiple projects with minimal supervision Must be able to work flexible hours as required WORKING CONDITIONS Work will occur in an office environment and may have client site visits. The employee may be required to stand, walk or move to various locations around the office and visiting facilities outside the office environment. At the office, this role routinely uses standard office equipment such as computers, phones, photocopiers, etc. WORK AUTHORIZATION This position requires proof of United States citizenship or authorization to work in the United States. UNPLANNED ACTIVITIES This position requires flexibility and adaptability. There will be tasks assigned that are outside of this from time to time. DRUG TESTING POLICY Selected candidates will be required to take a Drug Test prior to start working with the company. The company will pay for the drug test cost. If tested positive, Company will not submit a job offer to selected candidate. Please note that this job description is not designed to be an exhaustive listing of all the activities, duties or responsibilities that are required for employment.

As a member of the ShipBob Team, you will... Grow with an Ownership Mindset: We champion continuous learning and proactive innovation. Team members are encouraged to identify challenges and take ownership of initiatives that drive merchant, company and personal growth. By tackling complex problems and exploring creative solutions, you won't just follow a playbook, you'll be actively building the future of ShipBob. Collaborate with Peers and Leaders Alike: ShipBob values collaboration and support, where team members and leaders alike are committed to helping each other succeed. We all set high standards and understand the importance of transparency at all levels. We've created an environment where trust, open communication, and mutual respect motivate our teams to reach new heights. Experience a High-Performance Culture and Clear Purpose: Our commitment to delivering results creates a goal-driven, high-performance culture where everyone is empowered to contribute to our mission with a clear understanding of their direct impact and accountability. We measure success in tangible ways, allowing each team member to see the positive outcomes of their work and celebrate shared victories. Location: Fort Worth, TX Schedule: Sunday-Wednesday 7am- 5:30pm Compensation: $18.00/hr Role Description: This is an incredibly important position that helps to monitor inventory activities of all clients at each fulfillment center while allowing all existing operations team members to remain focused on their day-to-day responsibilities. As ShipBob continues to grow, it is imperative to provide a great experience in serving our clients' needs while maintaining sustainable growth and scalability from an operations perspective. This role reports to the Area Manager, Supply Chain ICQA. The backup for this role is the Area Manager, Supply Chain ICQA. What you'll do: Investigate inventory discrepancies reported by the Operations team. Perform physical inventory cycle counts and reconcile inventory variances. Communicate updates and relay important operational information about clients directly to ICQA Lead. Resolve merchant facing requests around inventory related issues. Comprehension of cycle counts and inventory control processes according to written SOP's. Ensure inventory variances are researched and resolved in a timely manner, allowing fulfillment of outbound orders. Ensure timely communications to MC team for any orders not able to be fulfilled due inventory discrepancies. This role includes responsibility for ensuring products are handled, stored, and distributed in a manner that maintains their safety, quality, and legality. Team members are expected to follow all standard operating procedures, report any concerns related to product condition or integrity, support traceability through accurate record-keeping, and contribute to a culture of continuous improvement and product safety awareness. Additional duties and responsibilities as necessary. What you'll bring to the table: Demonstrates the ability to quickly adapt to changing conditions and solve problems in a timely fashion. Ability to determine inventory discrepancies, perform physical inventory cycle counts, and reconcile inventory variances. Possesses effective written and verbal communication skills; displays reading comprehension skills. Displays the ability to multitask and handle multiple issues at the same time without stress. Displays attention to details. Ability to lift up to 50 lbs without any health limitations. Able to stand and walk continuously during and up to an 8-10hr shift. Able to bend, stoop, reach above, and push/pull frequently. May be required to flex into other departments as needed. Perks and Benefits: Medical, Dental, Vision & Basic Life Insurance 401K Match Weekly paycheck with paid overtime eligibility Pay Progression Program Paid Time Off & Sick Time Off Comprehensive Benefits Package >>> ******************************** See Our High-Performing Culture >>> Check us out on Instagram (@lifeatshipbob) #LI-DNI We recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and excellence; therefore, we encourage people from all backgrounds to apply to our positions. About You: The work we do at ShipBob is both challenging and rigorous, which means our environment isn't the right fit for everyone, and that's okay. We welcome energetic high performers who thrive in a dynamic, collaborative, results-driven environment. We value individuals who embrace accountability and humility, push boundaries, and are motivated by challenging work. Every team member, no matter their role or tenure, is expected to roll up their sleeves and tackle the complex problems we face in today's global supply chain. Learn more about our core values and how we perform at a high level in our day-to-day work on our Culture page (********************************culture/). About Us: ShipBob is a leading global supply chain and fulfillment technology platform designed for SMB and Mid-Market ecommerce merchants to provide them access to best-in-class capabilities and to deliver a delightful shopper experience. Merchants can outsource their entire fulfillment operations, utilize ShipBob's proprietary warehouse management system for in-house fulfillment, or take advantage of a hybrid solution across ShipBob's dozens of fulfillment center network in the United States, Canada, United Kingdom, Europe, and Australia. ShipBob is backed by leading investors like Menlo Ventures, Bain Capital Ventures, Hyde Park Venture Partners, and SoftBank Vision Fund 2, and is one of the fastest-growing tech companies headquartered in Chicago. ShipBob provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. There is no deadline to apply for this position, as ShipBob accepts applications on an ongoing basis.

Full-time Description At SPL, we turn science into impact. We're searching for a driven Laboratory Analyst (Organics) to join our team in Kilgore, TX. In this role, you'll be trained by industry experts, work with advanced laboratory technology, and deliver the accurate data our clients rely on for compliance and decision-making. Every analysis you perform helps ensure cleaner water, safer communities, and a healthier world. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! Why You'll Love This Role Perform on the front line of environmental analysis by generating analytical data to support environmental compliance and decision-making; Grow hands-on skills in analytical instrumentation, Laboratory Information Management Systems (LIMS), and advanced testing methods; Gain exposure to real-world applications in environmental science, regulatory compliance, and client services; Join a team where your contributions directly support public safety, regulatory standards, and cleaner environments. What You'll Do Perform sample preparation and analytical testing in accordance with approved methods and established protocols to ensure accuracy, timeliness, and regulatory compliance; Enter and manage data in the Laboratory Information Management System (LIMS) or other designated systems; Develop and maintain proficiency with a broad range of analytical equipment, laboratory software platforms, and technology relative to assigned analyses; Review and interpret results to ensure accuracy and completeness; Document all work clearly, maintaining traceable laboratory records; Perform routine equipment checks, troubleshooting, calibrations, and preventative maintenance; Adhere to quality systems, SOPs, and continuous improvement initiatives; Follow and promote Good Laboratory Practices (GLP) and all health, safety, and environmental standards; Assist with general laboratory housekeeping, glassware cleaning, inventory, and supply management; Participate in cross-training to support workload balance and operational needs; Perform other duties as assigned. Requirements What Makes You a Great Fit High School Diploma or equivalent; Associate's or Bachelor's Degree in Science or related area strongly preferred; Equivalent experience may be considered in lieu of degree; Previous hands-on experience in a professional or academic lab setting strongly preferred; Ability to manage and process high volumes of samples efficiently; Hard working, tenacious, and committed to delivering high-quality, defensible data; Strong problem identification and problem-solving skills; Strong accountability, attention to detail, and ability to work independently and as part of a team; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 9 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a standard Monday through Friday schedule; Flexibility to work outside of normal hours to support business needs and deadlines; Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.

Ideal Candidate Profile Do you fit this profile? Wants to start a CAREER / not just another "job" Wants to make a difference High Moral Standards & Values Positive Helpful Team Player Professional Wants to be the best of the best Is Ready Envirocheck is a growing company and has exciting opportunities for “A” players on our team. Job Summary Analysis of environmental samples consists of asbestos fibers, fungal spores, bacteria, and lead (Pb). Applicable equipment includes: A variety of microscopes, including Compound, Stereo, PLM (Polarized Light), and PCM (Phase Contrast). Flame Atomic Absorption Spectrometer IDEXX Colisure, Colilert, and Enterolert Microbiological media Requirements Bachelor's Degree in Biology, Microbiology, Geology, or related science is required Preferred Experience (not required, will train) Asbestos Analysis by PLM Fiber Analysis by PCM NIOSH 7400 Mold Spore Analysis ISO 17025 Microscopes Knowledge of construction (building) materials is a plus Benefits Health Insurance 401K with matching Paid sick / Vacation & Personal Time Paid Company Holidays