Chemist jobs in Mesa, AZ

FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, AZ facility for an Associate Research Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The Associate Research Chemist will be responsible for design, develop and commercialization of new semiconductor etchants, post etch selective cleaners and strippers for advanced technology. 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 applied research & development and commercialization of new post etch cleaners and selective etchants for advanced IC technologies. Responsibilities include designing, lab testing and managing new chemical products under rigorous business and customer timelines. Specific activities include: Investigate and develop new chemical formulations for cleaning integrated circuit wafers with awareness of the status of the intellectual property field. Perform wet bench formulation and testing of new chemicals to meet customer requirements. Manage existing product testing and qualification using customer wafers. Support thin film surface analysis using tools including Ellipsometer, 4-Point probe, XRR, XPS, TOF-SIMS, SEM. Assist with IP searches and initial patent drafts. Assist in pilot line builds of successful beaker formulations. Generating and communicating product data and technical reports internally and to customers Write and present internal presentation updating technical and business groups on project status. REQUIREMENTS PhD in Chemistry with 1 to 5 years of experience in formulation. Prior industrial research experience in product development in semiconductor technology is highly prefered. Experience in developing and applying inorganic or organic solution chemistry to meeting customer requirements. Must be comfortable working safely with hazardous chemicals. Understanding Si wafer device processing in wet processing tool operation and process implementation. Experience with thin film surface analysis tools such as Ellipsometer, 4-Point probe, XRR, XPS, TOF_SIMS, SEM Must have a strong comprehension of surface cleaning methods and chemicals. Must be proficient in design of experiments, technical writing, literature search processes and methods and Intellectual property processes and methods. Must be a team player and collaborator. Must be able to communicate and work effectively with peers and customers. Organizational skills and prior project management experience desired. This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner. 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 Description Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset - Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Ensures incoming biological samples are processed and triaged maintaining chain of custody. Performs and interprets a variety of specialized tests and strains, detection, and identification of pathogenic microorganisms. Prepares written and oral reports, answers questions, troubleshoot and makes recommendations to the supervisor for inclusion in comprehensive reports on test findings. Maintains and operates equipment including performing calibrations, adjustments, and to operate equipment and instruments properly and in a safe manner. Participates in cross training related to bioterrorism and other public health emergencies. Additionally, will be responsible for maintaining knowledge and skills related to position and program and to carry out all procedures in accordance with proper handling and storage of various biological materials. Must be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. Kindly be aware that drug screening is a mandatory condition of employment for this position. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable. This position supports a federal contract which requires that all employees and job applicants hold a valid US Green Card or US Citizenship at the time of application. #LI-OnSite A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status. Verification of education may be requested before or during the hiring process.

The Receiving Chemist I is responsible for Lab Pack Coding/Processing, Drum Receiving/Coding, and the Shipping of waste materials. This position verifies counts and container sizes for incoming loads, conducts initial sampling to confirm acceptance, applies barcodes for material tracking, and ensures all activities comply with facility permits, RCRA, DOT, and EPA regulatory requirements. Day Shift Pay - $19.00 to $22.00 hr Qualifications Education & Experience Required: 2 years of college or specialized training in Chemistry, Environmental Science, or related field. Experience: 0-3 years (alternative combinations of education/experience considered). Knowledge, Skills & Abilities Ability to work effectively in a team and adapt to changing business needs. Strong understanding of math, chemistry, and chemical testing. Strong communication and organizational skills. Proficiency with Windows-based applications. Experience in Receiving, Shipping, or Lab Pack operations preferred. Understanding and tested knowledge in at least two of the following: Lab Pack Coding/Processing Drum Receiving/Coding Shipping of Waste Materials EEO Statement Clean Harbors is an Equal Opportunity Employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We are committed to fostering an inclusive and diverse workplace. #LI-TA1 Responsibilities Regulatory & Compliance Ensure compliance with 49 CFR, 40 CFR, facility permits, and all applicable environmental and safety regulations. Properly manage all waste generated from analytical procedures. Lab Pack Coding & Processing Receive and code all lab pack containers according to disposal requirements. Perform consolidation or repack processes and complete associated paperwork. Manage cylinder activity, reactive materials, and lab pack bulking as needed. Operate lab pack systems using Clean Harbors proprietary software. Drum Receiving & Coding Operations Sample incoming drums and perform basic chemical analysis per established procedures. Calibrate and use laboratory instrumentation for required testing. Complete QA/QC documentation, drum sampling forms, and analysis paperwork. Investigate missing/extra drums and non-conforming shipments. Apply barcodes, assign routing, and weigh drums when needed. Move drums from staging to appropriate storage areas. Shipping & Outbound Materials Manage all outbound drum and bulk shipments. Ensure least-cost routing using proper profiles and shipping paperwork. Prepare, stage, and label shipments according to DOT and facility guidelines. Coordinate with National Logistics for scheduling and compliance. Sampling & Material Verification Open and sample all plant-received materials following WAP and CHES guidelines. Record results and collect lab-analysis samples as required. Verify inbound material counts against shipping documentation. General Duties Maintain safe working conditions and comply with OSHA, Health & Safety, and company protocols. Train and mentor Receiving Technicians and Chemist I employees. Manage supplies within assigned areas. Other duties as assigned.

FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, AZ facility for an Associate Research Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role The Associate Research Chemist will be responsible for design, develop and commercialization of new semiconductor etchants, post etch selective cleaners and strippers for advanced technology. 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 applied research & development and commercialization of new post etch cleaners and selective etchants for advanced IC technologies. Responsibilities include designing, lab testing and managing new chemical products under rigorous business and customer timelines. Specific activities include: Investigate and develop new chemical formulations for cleaning integrated circuit wafers with awareness of the status of the intellectual property field. Perform wet bench formulation and testing of new chemicals to meet customer requirements. Manage existing product testing and qualification using customer wafers. Support thin film surface analysis using tools including Ellipsometer, 4-Point probe, XRR, XPS, TOF-SIMS, SEM. Assist with IP searches and initial patent drafts. Assist in pilot line builds of successful beaker formulations. Generating and communicating product data and technical reports internally and to customers Write and present internal presentation updating technical and business groups on project status. REQUIREMENTS PhD in Chemistry with 1 to 5 years of experience in formulation. Prior industrial research experience in product development in semiconductor technology is highly prefered. Experience in developing and applying inorganic or organic solution chemistry to meeting customer requirements. Must be comfortable working safely with hazardous chemicals. Understanding Si wafer device processing in wet processing tool operation and process implementation. Experience with thin film surface analysis tools such as Ellipsometer, 4-Point probe, XRR, XPS, TOF_SIMS, SEM Must have a strong comprehension of surface cleaning methods and chemicals. Must be proficient in design of experiments, technical writing, literature search processes and methods and Intellectual property processes and methods. Must be a team player and collaborator. Must be able to communicate and work effectively with peers and customers. Organizational skills and prior project management experience desired. This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner. 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 (********************************).

Who We Are FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, Arizona facility for a QC Chemist! The Role The QC Chemist serves as a Quality Control Specialist responsible for analyzing semiconductor materials in support of product qualification and to support all Quality Control laboratory processes. 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 analyzing raw materials, intermediates, and final products following company processes and procedures. * Investigating non-compliance test results to assure the substance meets internal and external specifications. * Review analytical long-term stability charts to assure laboratory equipment meet fit-for-use criteria. * Perform troubleshooting repairs and maintenance activities. * Reviewing and updating laboratory documents consistent with Good Laboratory Practices. REQUIREMENTS * BA/BS in Chemistry or related degree such as Biochemistry, Biology, Physics or Mathematics. * 0 -1 Years of experience in a production lab environment. * Instrumentation experience preferred with tools such as ICP/MS, GC/MS, UV-Vis, GC/FID/TCD, IC, HPLC, GFAA, ICP/OES, or liquid particle counters. * Experience using Good Lab Practices. * Statistical based software experience preferred. * Candidate must be able to multi-task and handle change in priorities. * Good communication skills within different functional groups. * Must be able to work first or second shift. This includes weekends and holidays as required. * This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner. 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 (********************************).

About Medivant Healthcare Medivant Healthcare is a U.S.-based pharmaceutical manufacturer dedicated to producing high-quality sterile injectable medications for hospitals, clinics, and healthcare facilities nationwide. With FDA-inspected facilities in Chandler and Deer Valley, Arizona, Medivant is committed to compliance, innovation, and excellence in pharmaceutical manufacturing. Position Summary The Analytical Chemist supports the Quality Control laboratory through analytical testing, HPLC method development, data interpretation, and compliance with regulatory standards. This role requires strong technical expertise in HPLC, excellent attention to detail, and the ability to troubleshoot analytical and instrumentation issues. The position ensures accurate testing and documentation to uphold product quality, safety, and regulatory expectations. Key Responsibilities • Perform quantitative and qualitative analyses using HPLC and other analytical techniques for raw materials, in-process, and finished products. • Develop, optimize, and validate analytical methods in accordance with GMP and ICH guidelines. • Interpret analytical results and prepare accurate, detailed analytical reports. • Troubleshoot analytical methods, HPLC systems, and related laboratory equipment to ensure uninterrupted operations. • Ensure full compliance with GMP, GLP, ICH, USP, and internal SOP requirements. • Collaborate with R&D, Production, and QA to support investigations and continuous improvement activities. • Perform routine calibration, qualification, and maintenance of HPLC systems and other analytical instruments. • Maintain accurate and complete laboratory records in compliance with regulatory expectations. • Stay updated on current analytical techniques, regulatory guidelines, and laboratory best practices. QualificationsRequired: • Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field. • 1-3 years of hands-on laboratory experience including HPLC, pH, conductivity, TOC, UV, analytical balance operation, sample preparation, and dilution techniques. • Proficiency in HPLC method development, validation, troubleshooting, and system suitability testing. • Experience working with UV, DAD, RID, or similar chromatographic detectors. • Familiarity with analytical software such as Empower, OpenLab, or equivalent systems. • Strong knowledge of GMP, GLP, ICH, and USP guidelines. • Strong analytical thinking, documentation accuracy, and problem-solving skills. • Effective written and verbal communication skills. Preferred: • Experience with additional analytical instruments (GC, UV-Vis, FTIR, titrations, spectroscopy). • Experience working in sterile injectable or regulated pharmaceutical manufacturing environments. Work Environment & Physical Requirements • Full-time onsite position in QC laboratories at Chandler and Deer Valley facilities. • Ability to stand for extended periods and perform repetitive laboratory procedures.

Job Description Job Summary Product Development Scientist- Dietary Supplements, Confectionery Nutraceuticals Gummi World is a fast-growing nutraceutical manufacturer based in Chandler, Arizona. We strive to deliver the highest quality vitamin supplement products to our clients and maintain long-standing relationships with them. We think of each client as our partner, and we do everything we can to help them grow their businesses. When we provide you with the highest level of quality and consistency for your products, it allows you to always provide your customers with the brand they have learned to trust. Gummi World is seeking an accomplished, talented, and dynamic insights-driven leader to be a founding member of our Business Development/ Research & Development team. Confectionary experience is required for this role, preferably in starch & starchless gummy formulation, capsules and powders are a plus. The Product Development Scientist will work with the product development team on strategic initiatives to expand the Gummi World supplement product line. This role is responsible for developing products that are delicious, and consistently manufactured while ensuring all safety and quality requirements are met. The Product Development Scientist will have KPI's in all stages of the process for specified projects spanning, innovation, flavor, collaborating with clients and manufacturers, cost optimization, and commercialization. Responsibilities Develop concepts for the Innovation process Collaborate with the Regulatory Team on formulations and claim substantiation. Maintain branded ingredient and raw material database Research potential ingredients based on physical properties such as solubility for particular form factors. Follow up with R&D and Business Development teams on samples, prototypes, and test batches. Help with the development of different pack-out options for existing products. Lead product tastings, evaluations, etc., and analyze/record results in a statistical/analytical manner. Scope secondary contract manufacturers to match existing formulations Support Quality in new product specifications, change controls and label initiation forms. Contribute to innovation, troubleshooting, and brainstorming ideas in a team environment for future platform growth in key consumer needed state areas. Understand customer needs, business needs, and strategy by attending and participating in cross-functional team meetings. Forge relationships with key suppliers, and purchasing team to keep abreast of upcoming trends, to solicit and secure opportunities for new food ideas, technologies, ingredients, and packaging materials. Maintain professional and technical knowledge by attending regulatory training, educational workshops, reviewing professional publications, establishing personal networks, and participate in professional societies. Support company growth initiatives Requirements Bachelor's Degree (BA/BS) from a 4-year accredited college or university in Food Science, Biology, Engineering, Chemistry or Equivalent BS degree, with 5+ years of experience in R&D, Product Development, Manufacturing and/or Quality Assurance in food and/or supplement industry is preferred. Must have advanced knowledge in more than one of the aforementioned formats (Confectionary, starch & starchless gummies, formulations, Capsules, powders etc.) is required as well as having a proven track record developing clean (i.e. short ingredient list) and delicious food that meet specific requirements on a large scale. Must have strong interpersonal and presentation skills, ability to work in a team environment as well as independently, and have the ability to manage numerous projects simultaneously in a high-paced environment while staying in control under pressure. Must have excellent analytical, written, and organizational skills with the ability to manage complex technical information and have an industry-leading understanding of ingredient functionality, product evaluation, health and nutrition, food manufacturing processes, microbiology, quality assurance principles, and market research practices. Preferred candidates must have demonstrated technical sales experience with a wide range of clients. Powered by JazzHR 7LXwKufrN0

At American Express, our culture is built on a 175-year history of innovation, shared values and Leadership Behaviors, and an unwavering commitment to back our customers, communities, and colleagues. As part of Team Amex, you'll experience this powerful backing with comprehensive support for your holistic well-being and many opportunities to learn new skills, develop as a leader, and grow your career. Here, your voice and ideas matter, your work makes an impact, and together, you will help us define the future of American Express. Seeking an Associate - Technology Risk & Control within our Global Infrastructure - Distributed Infrastructure & Data Services organization. You will focus on Compliance, Risk and Audit priorities assisting with activities designed to support internal audit and regulatory requests, control testing, standard and procedure documentation, issue reporting and risk mitigation priorities. This role works closely with technology infrastructure partners, risk oversight partners and other stakeholder groups to ensure alignment, understanding and communications on IT controls, compliance and information security risk management. Works individually and with teams on both structured and unstructured assignments. **Responsibilities:** + Conducts assessments to identify potential risk within the organization's technology environments, ensuring that all critical areas are evaluated for security weaknesses. + Monitors technology environments to detect and respond to emerging threats in real-time, minimizing any potential security incidents + Maintains a balanced approach towards risk management practices, ensuring alignment with the organization's risk appetite and adhering to compliance requirements and industry best practices + Develops and maintains comprehensive risk management documentation by standardizing, documenting, and consistently applying all risk management activities across the organization, under the guidance of peers and leaders + Prepares reports and documentation to support risk management activities and compliance efforts, for internal stakeholders and leaders + Conducts risk assessments to determine the residual risk within the organization's technology environments, ensuring all areas are evaluated for non-compliance + Supports the identification and evaluation of controls and adherence to controls + Collaborates and co-creates effectively with teams in infrastructure to align technology initiatives with business objectives **Qualifications:** + Work experience in information risk, technology, compliance, audit or similar functions in a large technology organization + Having a Compliance Mindset and understanding a Culture of Compliance + Experience gathering/synthesizing requirements and performing data analysis + Ability to translate complex information into easily understandable terms + Aptitude to forge strong working relationships with internal and external partners + Prior experience supporting internal, external audit and regulatory requests a plus + Ability to work independently and collaboratively as a member of a team + Bachelor's degree in Computer Science, Information Systems, Cybersecurity or other related fields preferred + Certifications are a plus but not required **Qualifications** Salary Range: $78,000.00 to $124,750.00 annually bonus benefits The above represents the expected salary range for this job requisition. Ultimately, in determining your pay, we'll consider your location, experience, and other job-related factors. We back you with benefits that support your holistic well-being so you can be and deliver your best. This means caring for you and your loved ones' physical, financial, and mental health, as well as providing the flexibility you need to thrive personally and professionally: + Competitive base salaries + Bonus incentives + 6% Company Match on retirement savings plan + Free financial coaching and financial well-being support + Comprehensive medical, dental, vision, life insurance, and disability benefits + Flexible working model with hybrid, onsite or virtual arrangements depending on role and business need + 20 weeks paid parental leave for all parents, regardless of gender, offered for pregnancy, adoption or surrogacy + Free access to global on-site wellness centers staffed with nurses and doctors (depending on location) + Free and confidential counseling support through our Healthy Minds program + Career development and training opportunities For a full list of Team Amex benefits, visit our Colleague Benefits Site . American Express is an equal opportunity employer and makes employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability status, age, or any other status protected by law. American Express will consider for employment all qualified applicants, including those with arrest or conviction records, in accordance with the requirements of applicable state and local laws, including, but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For positions covered by federal and/or state banking regulations, American Express will comply with such regulations as it relates to the consideration of applicants with criminal convictions. We back our colleagues with the support they need to thrive, professionally and personally. That's why we have Amex Flex, our enterprise working model that provides greater flexibility to colleagues while ensuring we preserve the important aspects of our unique in-person culture. Depending on role and business needs, colleagues will either work onsite, in a hybrid model (combination of in-office and virtual days) or fully virtually. US Job Seekers - Click to view the " Know Your Rights " poster. If the link does not work, you may access the poster by copying and pasting the following URL in a new browser window: *************************** Employment eligibility to work with American Express in the U.S. is required as the company will not pursue visa sponsorship for these positions. **Job:** Technologies **Primary Location:** US-Arizona-Phoenix **Schedule** Full-time **Req ID:** 25020863

Sr. Mortgage Post Closing QC Analyst Agility 360 is searching for experienced Sr. Post Closing QC Analyst for a permanent position with our established Banking client in the Phoenix, AZ. The Sr. Post Closing QC Analyst is responsible for coordinating the operational aspects for an assigned pipeline of mortgage whole loan transactions, which will often be the larger and more complex transactions. Interacting with 3rd party diligence firms, and work closely with counterparties to clear conditions on loans for purchase or sale. Review collateral, trailing docs and custodian reports as needed. Direct servicing transfers and MERS updates. Act as subject matter expert for assignment of mortgages outside of MERS. Utilize strong spreadsheet skills to streamline the operations of the mortgage purchase team. Job Responsibilities: Interact with counterparties in the operational aspects of mortgage loans purchases and sales, which will often be the larger and more complex transaction. Interact with 3rd party Due Diligence vendors that review mortgage loans for the bank. Utilize knowledge of underwriting to help resolve conditions. Previous experience as an underwriter will be favorably considered. Work closely with customers to clear conditions needed to purchase loans. Work closely with investors to clear conditions on loan sales by the bank. Review collateral, trailing documents, and reporting from document custodians. Coordinate servicing transfers. Act as a primary MERS system user and subject matter expert for AOMs outside of MERS. Manage assigned loan pipeline to ensure deadlines are met. Serve as customer liaison to ensure customer expectations are met, service standards are adhered to, and issues are elevated and resolved in a timely manner. Utilize strong excel/spreadsheet skills to streamline operations. Experience: 3+ years of experience in mortgage operations (processing, underwriting, closing, post-closing, or mortgage whole loan trading operations). Past experience with mortgage loans that have small defects (Scratch & Dent) will be favorably considered. Ideal candidate has experience in the operational aspects of mortgage whole loan transactions. Knowledge of credit, compliance, and collateral conditions that are commonly found on TPR securitization reports is a plus. Proficiency in: MERS, servicing transfer coordination, document custodian report review, collateral review and collateral tracking. Attention to detail. Strong oral, written, and interpersonal communication skills. Strong spreadsheet skills College degree preferred, but not required. Self-starter, self-reliant, dependable, ability to work within and meet specific time constraints. Ability to take ownership of items and see them thru to completion. Comfortable in a fast-paced work environment. Strong problem-solving skills. Job Details: Permanent role with an established Bank/Lender Location: Phoenix, AZ Pay range: Based on experience Benefits: Medical and Dental insurance, Paid Time Off, A Great 401k matching program, Tuition Assistance Program, Employee Volunteer Program, and a Wellness Program. In addition, you'll have the opportunity to bolster your business knowledge, learning the ins and outs of how successful companies operate and manage their finances, giving you invaluable hands-on experience to help grow your career! Employment is contingent on passing a background check and drug screening

Job Description The Medical Data Entry/Quality Control Assistant will serve as a key point of contact between operations and the laboratory team. Work is highly self-directed, and role may include additional responsibilities such as client communications, internal training and problem solving related to special accounts and compliance. This individual will have completed the necessary training in ordering tests, pre-analytical processing for shipping specimens, and advanced data-entry knowledge. Must have high attention to detail. Duties and Responsibilities: Maintain Patient Service Center (PSC) Laboratory Info. Systems Database to ensure proper specimen processing. Understands available resources to fill in for any function within the Data Entry & Quality Control department as necessary Identifies problems and in some cases, may resolve issues with specimen types such as missing information etc. Understands complex relationship between test(s) ordered and specimen received Completes all required documentation, legibly and within the assigned time frame Track quality control metrics and work with leadership team to ensure accurate data entry and high quality sample processing for staff Ensure specimen collections and data entry performed by client and lab staff are informed in a timely manner of any issues that impact patient results Keeping leadership informed in a timely manner of any inconsistencies or problems between the lab or staff that could impact or are not consistent with quality standards Meets standards for production and accuracy within 3 months Validates and verifies orders for other employees and may provide on-going training Performs other duties as assigned Position Type/Hours of Work: This is a full-time position with hours of Tuesday-Saturday 6am to 2:30pm. Saturday hours may vary depending on business and coverage needs, but the Saturday shift is required. Pay range is $18-$20/hour, depending on education and experience. Physical Requirements Must be able to lift up to 25 pounds Prolonged periods sitting at a desk and working on a computer screen Must be able to perform repetitive tasks with both hands constantly throughout the day. Daily tasks involve walking, standing, reaching, lifting, and bending Education: Bachelor's Degree or equivalent experience is preferred Work Experience: Medical background preferred which includes medical terminology applicable to a clinical laboratory Previous experience in a production environment preferred PC skills in MS office/Google applications Other: Communicates effectively with all levels of internal and external staff Maintains composure while working under pressure Demonstrates strong interpersonal skills that fosters a positive attitude at all times Demonstrates flexibility and is able to adapt to changes in work assignments

*REQUIRED: PLEASE ATTACH A RESUME Under general supervision, to inspect produce upon arrival at the Distribution Center and existing produce for quality; accepts or rejects produce that does not meet quality and other standards. Employees in this job classification provide quality control support to management, vendors, stores and the Distribution Center. This job classification requires knowledge of the products, procurement practices and methods and the ability to select and provide produce to customers that meet the company's budgetary and quality requirements EDUCATION AND EXPERIENCE: High school diploma or G.E.D and a minimum of three or more (3+) years' experience in a retail produce department. REQUIRED KNOWLEDGE: Knowledge of local, state and federal laws and regulations, such as FDA and Health. SKILLS/ABILITIES: Ability to work independently. Able to communicate effectively, both verbally and in writing. Able to maintain effective working relationships. Ability to be flexible in changing work priorities. Ability to handle multiple tasks simultaneously within established timelines. Ability to generate work in an accurate and timely manner. Ability to communicate effectively both verbally and in writing; maintain effective working relationships. Good customer service skills. WORK ENVIRONMENT Worked is performed in a distribution center environment with refrigeration temperatures ranging from 34-52 degrees Fahrenheit. Work around pallet jacks and forklifts. PHYSICAL DEMANDS - Employees may occasionally experience the following physical demands for extended periods of time: Standing Sitting Walking throughout the facilities Viewing Computer Monitor Keyboarding Essential Job Functions and Basic Duties POSITION PURPOSE Under general supervision, to inspect produce upon arrival at the Distribution Center and existing produce for quality; accepts or rejects produce that does not meet quality and other standards. Employees in this job classification provide quality control support to management, vendors, stores and the Distribution Center. This job classification requires knowledge of the products, procurement practices and methods and the ability to select and provide produce to customers that meet the company's budgetary and quality requirements. ESSENTIAL JOB FUNCTIONS AND BASIC DUTIES 1. *Performs a physical inspection of all produce received at the Distribution Center prior to product acceptance. Inspects for company standards in quality, size and condition. 2. *Approves produce delivery when standards are met. Rejects produce when standards are not met and informs appropriate staff and vendor. Obtains buyer approval in some situations. 3. *Performs a physical inspection and monitors warehoused produce for quality, shelf life and possible rotation problems. Notifies appropriate staff and vendors for resolution. 4. *Trains new employees in the Distribution Center on produce acceptance standards prior to receiving products from vendors and others. 5. *Coordinates orders with the produce buying team. MINIMUM QUALIFICATIONS EDUCATION AND EXPERIENCE: • High school diploma or G.E.D and a minimum of three or more (3+) years' experience in a retail produce department. REQUIRED KNOWLEDGE: • Knowledge of local, state and federal laws and regulations, such as FDA and Health. SKILLS/ABILITIES: • Ability to work independently. • Able to communicate effectively, both verbally and in writing. • Able to maintain effective working relationships. • Ability to be flexible in changing work priorities. • Ability to handle multiple tasks simultaneously within established timelines. • Ability to generate work in an accurate and timely manner. • Ability to communicate effectively both verbally and in writing; maintain effective working relationships. • Good customer service skills. 1/1/23 Quality Control Produce *Performs a physical inspection of all produce received at the Distribution Center prior to product acceptance. Inspects for company standards in quality, size and condition. *Approves produce delivery when standards are met. Rejects produce when standards are not met and informs appropriate staff and vendor. Obtains buyer approval in some situations. *Performs a physical inspection and monitors warehoused produce for quality, shelf life and possible rotation problems. Notifies appropriate staff and vendors for resolution. *Trains new employees in the Distribution Center on produce acceptance standards prior to receiving products from vendors and others. *Coordinates orders with the produce buying team CERTIFICS REQ None PHYSICAL DEMANDS - Employees may occasionally experience the following physical demands for extended periods of time: • Standing • Sitting • Walking throughout the facilities • Viewing computer monitor • Keyboarding WORK ENVIRONMENT Worked is performed in a distribution center environment with refrigeration temperatures ranging from 34-52 degrees Fahrenheit. Work around pallet jacks and forklifts.

WGNSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a WGNSTAR career today! Schedule: Compressed Work Week Pay Rate: $24+ DOE Location: Chandler, AZ Position Type: Full Time Benefits: This position is eligible for WGNSTAR's full benefits package, including Medical, Dental, Vision, and 401(k). Additional benefits are listed at the end of this posting. Principal Duties and Responsibilities: * Work on systems and maintain supply of chemicals and gases to a semiconductor manufacturing environment that makes the chips used in electronic devices such as Smart Phones, LEDs, and Flat Screen TV's. * Operate assigned chemical and/or gas distribution systems. * Perform the handling and change-out of gas, chemical, and slurry containers. * Troubleshooting and preventative/repair maintenance on gas and chemical equipment. * Operate a computer to support job functions. Requirements: * Must be comfortable with physical activity, including walking up to 5 miles per day and occasionally climbing ladders with fall protection. * Ability to work with chemicals, including using a Supplied Contained Breathing Air Respirator for short periods of time. * Ability to lift up to 40 pounds and perform tasks requiring bending, overhead reaching, and basic physical agility. * High attention to detail with a strong focus on safety procedures. Preferences: * Previous experience in a technical or maintenance role, ideally in a manufacturing or semiconductor environment. * Familiarity with chemical or gas handling and distribution systems. * Strong computer skills for system operation and troubleshooting. Physical Effort/Activities: May be required to walk up to 5+ miles per day, be on feet for 8-10 hours at a time, and occasionally climb ladders while utilizing fall protection. The ability to bend, twist, push/pull, crouch, kneel in confined spaces, and lift up to 40 pounds is required. Some tasks may require wearing a Supplied Contained Breathing Air Respirator for short periods (10-15 minutes) while working with chemicals. PPE made available includes safety glasses, hard hat, ear plugs, chemical aprons, gloves, and more. Additional Benefits: Paid Vacation, Select Holidays, Overtime Opportunities, On-site Facilities & Career Development Opportunities. This is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. But this job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position. The people who thrive most on our teams are those individuals who perform well in a team environment, enjoy interacting and engaging with several different stakeholders, adapt quickly to changing environments, and leverage their skills, quality, and knowledge to drive themselves and their teams towards continuous improvement and success. #LP Apply for this job

It's fun to work in a company where people truly BELIEVE in what they're doing! We're committed to bringing passion and customer focus to the business. This position will be responsible for the daily quality control of production of critical, time-sensitive mail pieces with a focused emphasis on the timely and accurate execution of contractual agreements with our clients. This generally includes helping to develop, document and implement QC processes in all Covius production facilities and interfacing with other Covius corporate teams regarding production changes. Essential Functions Develops a working knowledge of client templates and related processes. Performs a daily sampling of printed materials throughout the day, reviewing for print quality, overlay issues and template completeness. Provides additional checks for go-live of critical client production changes. Creates tickets on quality concerns discovered in the QC process. Performs ongoing reviews of log sheets for identification of miss-configured production processes. Trains and complies with all relevant Covius Standard Operating Procedures. Performs QC processes on production materials and production processes. Performs QC reviews of inbound processes. Problem-solves issues as they arise. Regular and predictable onsite attendance is required. Ability to work overtime and weekends if needed. Perform other related duties as assigned. Education High School Diploma or equivalent. Experience 1-2 years previous experience in a high-volume mail production facility preferred 1 year previous experience on each of the stages of the lifecycle of mail preferred Compensation and Benefits Covius offers an extensive benefits package for all employees, including medical, dental, vision and 401(k)! Compensation: $18.46-$23.08/hr Application Guidelines: For best consideration, please submit your resume and application materials as soon as possible. Review of applications will begin immediately. Essential Knowledge, Skills & Abilities Excellent verbal and written communication skills. Excellent interpersonal and customer service skills. Advanced knowledge of Microsoft Office Suite, including Word, Excel, and PowerPoint. Ability to prioritize multiple objectives to meet client deadlines and department goals. Strong analytical and problem-solving skills. Ability to work in a fast-paced, metrics driven environment. Commitment and ability to cultivate a diverse and inclusive work environment. Working Conditions Work is performed in a climate controlled indoor warehouse setting. The noise level in the work environment is usually moderate to high, depending upon production machinery operations. Physical Demands While performing the duties of this job, the employee is frequently required to communicate. The employee occasionally is required to remain stationary. The employee is frequently required to move about the office, operate a computer and other office machinery, such as calculator, copy machine, and computer printer; frequently position self to maintain files; frequently moves boxes weighing up to 50 lbs. The employee is frequently required to operate heavy machinery and/or power tools. Close and distance observation required with ability to observe objects at close range in presence of glare or bright lighting (e.g., computer screen). Must possess the ability to communicate information and ideas so others will understand and have the ability to interact with external and internal stakeholders. Covius is committed to equal opportunity in all employment practices to all qualified applicants and employees without regard to race, color, religion, gender, gender identity, age, national origin, pregnancy, disability, genetics, marital status, military or veteran status or any other protected category as established by local, state, and federal law. This policy applies to all aspects of the employment relationship including recruitment and hiring, placement, promotion, transfer, compensation, disciplinary action, layoff, leaves of absence, training, and termination. All such employment decisions will be made without unlawful discrimination based on any prohibited basis. The essential functions, working conditions and physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. Please note that all s are not intended to be all-inclusive. This job description is not designed to cover all activities, duties or responsibilities that are required of the employee for this job. Employees may be required to perform other duties at any time with or without notice to meet the ongoing needs of the organization. If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!

Join the dynamic team at JX Nippon Mining & Metals USA, Inc., a leader in the semiconductor industry, as a Quality Control Associate. This role offers a unique opportunity to uphold the impeccable quality of our products, materials, and equipment, playing a vital part in our commitment to excellence. In this role, you will: Conduct inspections and tests on a range of items, from raw materials to finished products, ensuring adherence to our high-quality standards. Compute and measure various dimensions of workpieces, ensuring precision in every detail. Test units for mechanical functioning and fit of moving parts, ensuring seamless operation. Work in a clean room environment, adhering to stringent quality control measures. Inspect and verify the accuracy of gauges and measuring instruments, maintaining our commitment to precision. Examine defective parts, providing valuable insights for improvements and modifications. Write detailed reports on inspection and testing results, contributing to our continuous improvement efforts. Perform minor equipment preventative maintenance, ensuring the longevity of our tools and machinery. Maintain a clean and organized work area, promoting a productive work environment. Qualifications: A minimum of one year of experience in a quality control or related role. Proven ability to compute and measure various dimensions of workpieces. Experience in writing detailed reports on inspection and testing results. Familiarity with minor equipment preventative maintenance. An equivalent combination of practical experience and education will be considered. Physical Requirements: This role involves frequent standing, walking, sitting, and use of hands. You may need to lift and/or move up to 20 pounds. Close vision and the ability to adjust focus are required. Work Environment: Our work environment involves exposure to moving mechanical parts and a moderate noise level. Benefits We offer a comprehensive benefits package that includes: 401k with company matching Medical, dental, and vision insurance Tuition reimbursement Training and development opportunities Vacation time Short and long-term disability coverage Basic life and AD&D insurance Supplemental life and AD&D insurance At JX Nippon Mining & Metals USA, Inc., we believe in fostering an inclusive and supportive environment for all our employees. We invite you to join our team and contribute to our shared success. Let's shape the future of the semiconductor industry together! Background & Drug Screen Disclaimer At JX Advanced Metals USA, we conduct background checks and drug screenings for all potential employees to ensure a safe and productive work environment. Background Checks: We verify employment history, education, and criminal records. Information is used only for employment purposes and kept confidential. Drug Screenings: Pre-employment tests for substances, including THC products. Positive results may lead to the job offer being withdrawn. By applying, you agree to these checks and screenings to help us maintain a secure workplace.

Bad Dragon is a modern production, design, and fulfillment facility in Phoenix, AZ, specializing in adult product manufacturing and retail sales. We strive to foster a fun, unique, and creative work environment and pride ourselves on the supportive atmosphere we have worked hard to promote. Job Brief We are seeking an experienced quality control technician who will be responsible for the implementation of Bad Dragon's quality assurance processes. The individual will perform quality checks and product processing on various products to ensure that they conform to the standards and specifications set by the company. This is a full-time, on-site position in Phoenix, AZ, with an expected hourly workload of 40 hours per week. The shift will be Monday through Friday from 7:00 am to 3:30 pm or Tuesday through Friday from 2:00 pm to 12:30 am. The company's needs will determine shifts. Job Duties Visual and physical inspection of manufactured products to ensure compliance with standards such as color, texture, and product attributes Physical processing of product, such as removal of excess material, cleaning and photographing the product, and processing and packaging the finished item Maintain records of testing results required by the company. Report findings and results of products that did not meet the required specifications to leadership. Requirements High School Diploma or Equivalent Minimum 1 year of work experience in Quality, Production or related technical field Intermediate computer skills (Microsoft Office and Google Suite preferred) Strong organization and time management Ability to follow established guidelines, focusing on detail, in order to complete tasks attentively and accurately. Excellent written and verbal communication skills to convey information and report findings Ability to occasionally lift, carry or move objects weighing more than 25 pounds. Benefits We offer competitive salaries and excellent benefits for candidates who qualify. We offer company-provided health, vision, and dental insurance coverage to associates and their dependents. Relocation assistance for out-of-state candidates (we are based in Phoenix, AZ). Fixed schedules with generous company holidays, a break room pantry with drinks and food, an employee discount of 30% off retail prices, quarterly store credit, and potential bonuses. Compensation Starting pay is $20 an hour but is negotiable based on experience and level of education and is competitive for the greater Phoenix area. Equal Opportunity We are an equal-opportunity employer and value diversity at our company. We are firmly committed to providing equal employment opportunities for all employees and all applicants. For us, this is the only acceptable way to do business.

We are looking to fill a **Scientist 3 - Analytical Chemist** position working as **a full-time employee of Parexel FSP on long-term assignment** onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer any sponsorship.** **Responsibilities** + General understanding of analytical method development and method validation + Hands-on experience with chromatographic analysis using various ultra-high-performance liquid chromatography (UPLC), high-performance liquid chromatography (HPLC), and gas chromatography (GC) techniques + General knowledge of separations science + Experience with Empower chromatographic software and with analysis of drug formulations + Hand-on experience with Fourier transform infrared (FTIR) spectroscopic analysis and ultraviolet-visible (UV-VIS) spectroscopic analysis + Skilled on method and instrument troubleshooting, specifically for HPLC and GC methods and systems **Required Skills** + Strong computer, scientific, and organizational skills + Excellent organization to multi-task and manage multiple ongoing projects in parallel including routine testing (for example, assay and impurity testing) and data processing and interpretation + Excellent communication (oral and written) and attention to detail + Proficient in written and spoken English, is required **Desired Skills and Experience** + Empower software + Analysis of drug products + Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude **Qualifications** + BS degree and 3-5 years of relevant experience, or + MS degree with at least 1-2 years relevant experience **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset - Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Ensures incoming biological samples are processed and triaged maintaining chain of custody. Performs and interprets a variety of specialized tests and strains, detection, and identification of pathogenic microorganisms. Prepares written and oral reports, answers questions, troubleshoot and makes recommendations to the supervisor for inclusion in comprehensive reports on test findings. Maintains and operates equipment including performing calibrations, adjustments, and to operate equipment and instruments properly and in a safe manner. Participates in cross training related to bioterrorism and other public health emergencies. Additionally, will be responsible for maintaining knowledge and skills related to position and program and to carry out all procedures in accordance with proper handling and storage of various biological materials. Must be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. Kindly be aware that drug screening is a mandatory condition of employment for this position. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable. This position supports a federal contract which requires that all employees and job applicants hold a valid US Green Card or US Citizenship at the time of application. #LI-OnSite A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status. Verification of education may be requested before or during the hiring process.

The Analytical Chemist will be responsible for providing leadership in analytical development, validation, API, and Drug Product Stability testing as well as writing CMC sections of applicable regulatory and ANDA submissions. Incumbents will have the responsibility for research experiments and data integrity, as assigned by management. Incumbents will also be responsible for design and implementation of experiments based on an overall description of the intended outcome. Will serve a primary role in method development and method validation Conduct literature search and make recommendations for robust analytical methods for product and analytical method development Screen various methods to implement validate-able analytical methods for new products Conduct analytical method validation in accordance with ICH Guidelines Write protocols and reports for method development and validations that are ready for submission to regulatory authorities. Provide analytical testing and support for all current (parenteral) dosage forms. Help develop test specifications for new products Routine testing for release of various materials. Ensure data integrity, conduct data collection and interpretation, and ensure proper documentation of experimental data. Maintain laboratory notebooks. Complete assignments requiring an expert knowledge level of techniques' and practices related to the analytical area. Expertise in GMP laboratory requirements and compliance in accordance with relevant regulations Manage site inventory. Order laboratory supplies and equipment. Maintain the laboratories and perform other job-related duties as assigned. Accumulate knowledge and skills to support development and management of research protocols in support of multiple drug discovery efforts. Achieve business goals, share learning's, knowledge, and skills and promote cross-functional, teamwork. Use knowledge and experiences to interpret and properly document experimental data. Other work as assigned based on the project and company needs. Qualifications: Education: BS/MS or PhD in Chemistry or related science and minimum of 5 years of related experience. Prior experience in working with analytical instrumentation such as HPLC, GC, UV/VIS, in a cGMP environment. Knowledge of ICH and FDA guidelines Prior chromatographic data acquisition and LIMS System experience A high degree of computer proficiency and the ability/interest to learn new software programs is required. Excellent skills in collecting data and accurately maintaining laboratory notebooks required. Expert level of technical skills. Flexibility and the ability to work in a fast-paced, team-oriented environment.

WGNSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a WGNSTAR career today! Schedule: Compressed Work Week Pay Rate: $24+ DOE Location: Chandler, AZ Position Type: Full Time Benefits: This position is eligible for WGNSTAR's full benefits package, including Medical, Dental, Vision, and 401(k). Additional benefits are listed at the end of this posting. Principal Duties and Responsibilities: Work on systems and maintain supply of chemicals and gases to a semiconductor manufacturing environment that makes the chips used in electronic devices such as Smart Phones, LEDs, and Flat Screen TV's. Operate assigned chemical and/or gas distribution systems. Perform the handling and change-out of gas, chemical, and slurry containers. Troubleshooting and preventative/repair maintenance on gas and chemical equipment. Operate a computer to support job functions. Requirements: Must be comfortable with physical activity, including walking up to 5 miles per day and occasionally climbing ladders with fall protection. Ability to work with chemicals, including using a Supplied Contained Breathing Air Respirator for short periods of time. Ability to lift up to 40 pounds and perform tasks requiring bending, overhead reaching, and basic physical agility. High attention to detail with a strong focus on safety procedures. Preferences: Previous experience in a technical or maintenance role, ideally in a manufacturing or semiconductor environment. Familiarity with chemical or gas handling and distribution systems. Strong computer skills for system operation and troubleshooting. Physical Effort/Activities: May be required to walk up to 5+ miles per day, be on feet for 8-10 hours at a time, and occasionally climb ladders while utilizing fall protection. The ability to bend, twist, push/pull, crouch, kneel in confined spaces, and lift up to 40 pounds is required. Some tasks may require wearing a Supplied Contained Breathing Air Respirator for short periods (10-15 minutes) while working with chemicals. PPE made available includes safety glasses, hard hat, ear plugs, chemical aprons, gloves, and more. Additional Benefits: Paid Vacation, Select Holidays, Overtime Opportunities, On-site Facilities & Career Development Opportunities. This is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. But this job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position. The people who thrive most on our teams are those individuals who perform well in a team environment, enjoy interacting and engaging with several different stakeholders, adapt quickly to changing environments, and leverage their skills, quality, and knowledge to drive themselves and their teams towards continuous improvement and success. #LP This position is not eligible for visa sponsorship. All applicants must be legally authorized to work in the United States without the need for current or future sponsorship (e.g., H-1B, O-1, etc). Additionally, WGNSTAR does not participate in the STEM OPT extension program for this role. Equal opportunities and Social Governance WGNSTAR is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable. WGNSTAR places an immense emphasis on equal employment, encourages diversity in the workplace, and applies an open-door policy for inclusion of all employees. Our diversity program encourages people from any gender, background, ethnicity, culture, education, and experience to join the company and more importantly build a career through employee development. Through our Global wellness programs, WGNSTAR ensures our employees and families have access to a full range of wellness services through our Employee Assistance Program (EAP). In the communities that surround our business operations, we support individual and group sponsorships for local sports and those that are vulnerable in society. Powered by JazzHR py7ujtRHxf