Quality control analyst jobs in Brandon, FL - 75 jobs

Full-time Description QUALITY CONTROL COORDINATOR Lakeland, FL Hiring now! Weekly pay! The Quality Control Coordinator is a professional responsible for ensuring that a company's products or services meet established quality standards. Essential Job Functions: Includes, but is not limited to, the job specifications contained herein. Additional duties or job functions may be required as deemed necessary by management personnel to contribute to the team effort by accomplishing related results as needed. Maintain accurate inventory records, oversee stock levels, and coordinate timely restocking Manage the entire process of receiving and shipping goods, including verifying incoming shipments and preparing outgoing orders Organize and maintain a clean, safe and efficient warehouse environment Stand and walk for extended periods of time Complete daily paperwork as required by supervisor Perform all other duties as assigned What's In It for You? Competitive pay and growth Full comprehensive benefits package including medical, dental, and vision insurance. Vacation and PTO (paid time off) 401(k) plan + Company match Performance bonus Overtime Paid Holidays Requirements · Strong organizational and time management skills · Extreme attention to detail · Excellent communication skills · Physical stamina and the ability to operate warehouse equipment like forklifts · Punctuality · Multitasking

We are looking for a Quality Control Inspector to join our team! Are you ready for an amazing, thrilling, fast paced career in hospitality? Are you looking to enhance your talents and grow in the industry? We have open opportunities to provide you with an amazing future as a part of our team. Position Summary: We are seeking a detail-oriented and proactive Quality Control Inspector to ensure the highest standards of cleanliness, presentation, and functionality in guest rooms across our hospitality properties. This role is critical in maintaining our commitment to exceptional guest experiences by conducting thorough inspections and collaborating with housekeeping, maintenance, and front office teams. Key Responsibilities: Conduct daily inspections of guest units to verify cleanliness, maintenance, and overall presentation meet company standards. Use checklists and digital tools to document inspection results and track recurring issues. Identify and report deficiencies in housekeeping, maintenance, or room setup. Provide immediate feedback to housekeeping staff when standards are not met. Collaborate with the housekeeping supervisor and maintenance team to resolve issues promptly. Ensure compliance with health and safety regulations and brand standards. Monitor inventory of room supplies and amenities, reporting shortages or inconsistencies. Assist in training new housekeeping staff on quality expectations and procedures. Participate in periodic audits and contribute to continuous improvement initiatives. Qualifications: High school diploma or equivalent; hospitality certification is a plus. Minimum 1 year of experience in housekeeping, hospitality operations, or quality control. Strong attention to detail and organizational skills. Ability to work independently and manage time effectively. Excellent communication and interpersonal skills. Familiarity with inspection software or mobile apps is a plus. Ability to stand, walk, and bend for extended periods; lift up to 25 lbs. Work Schedule: Full-time position with flexible hours, including weekends and holidays as needed. NDM Hospitality is an equal opportunity employer, and all qualified applicants will receive consideration for employment 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.

Working Title: OPS QUALITY CONTROL ANALYST (STAFF ASSISTANT)- 65650024 Pay Plan: Temp 65650024 Salary: $15.00-$17.00 HOURLY Total Compensation Estimator Tool DEPARTMENT OF ELDER AFFAIRS LONG-TERM CARE OMBUDSMAN PROGRAM * OPEN COMPETITIVE* POSITION OVERVIEW AND RESPONSIBILITIES: The ombudsman is a designated representative of the Office of State Long-Term Care Ombudsman as authorized by federal and state law. The ombudsman serves under the direction of the District Ombudsman Manager. PAY: Salary will be commensurate with experience and qualifications, ranging from $15.00 to $17.00, hourly. DUTIES AND RESPONSIBILITIES: * Answers the phone and maintains phone log for all incoming calls; checks and responds to voice mail. * Enters complaint, case, and assessment information in web-based documentation system; enters updates as received. * Tracks incoming reports and information such as Adult Protective Services reports, nursing home discharge and transfers, facility contact information, etc.; updates appropriate log or tracking tool. * Following certification as ombudsman, travels to facilities and conducts assessments as needed. * Following certification as ombudsman, travels to facilities and investigates and resolves long-term care facility residents' complaints as needed. Identifies significant individual and systemic problems affecting residents. problems and brings them to the attention of the District Ombudsman Manager (DOM); obtains access to long-term care facilities and to residents' records; and protects the confidentiality of residents' records, complainants' identities, and ombudsman files. Conducts interviews, reviews documents, and writes report of findings. * Assists in preparing, processing and maintaining volunteer paperwork including applications, travel, activity reports, and continuing education training hours. * Processes miscellaneous incoming mail, emails, and faxes; respond as appropriate; general office filing. * Assists the District Ombudsman Manager (DOM) with preparing and arranging monthly ombudsman district council meetings. * Tracks inventory of office items such as forms, brochures, promotional items, office supplies, and electronic equipment; prepares orders as needed; coordinate distribution of items to volunteers. * Coordinates and implements the volunteer ombudsman approval process in HQ ensuring that all paperwork is completed, and potential volunteers are notified in a timely manner. * Serves as primary office contact in the absence of the DOM. * Maintains the program's emergency contact list and district office contact list. * Performs other duties as assigned * Travel is required. * Attendance is an essential function of this job. KNOWLEDGE, SKILLS, AND ABILITIES: * Possess good organizational skills. * Ability to handle telephone calls in a courteous and effective manner. * Ability to communicate effectively both orally and in writing. * Ability to operate general office equipment. * Ability to conduct assessments and fact-finding interviews. * Ability to investigate, analyze and resolve complaints. * Ability to write reports. * Ability to deal effectively with people. * Ability to perform basic arithmetic calculations. * Knowledge of basic investigative techniques. * Knowledge of the rules governing Ombudsman investigations and assessments. * Ability to collect and analyze evidence. * Ability to use deductive reasoning. * Ability to analyze information and determine its validity. * Ability to write accurate investigative reports. * Ability to make independent decisions. * Ability to conduct thorough investigations. * Ability to maintain strict confidentiality. * Ability to establish and maintain effective working relationships with others. * Apply the policies, procedures, and programs governing the agency. * Ability to communicate with others to obtain and verify information. * Ability to analyze and interpret written, numerical, and verbal data from various sources. * Ability to type and prepare reports and memoranda accurately and timely. * Ability to plan and organize to ensure work is completed in accordance with applicable laws, regulations, rules and policies. * Ability to read, understand, and apply regulations, and policy directives. * Ability to fulfill all ombudsman program certification and continuing education training requirements. * Proficiency in Microsoft Office Suite and Windows. REQUIREMENTS: * If selected for employment applicant will be required to become a certified Ombudsman upon time frame set by employer. * Travel is required. Operates own private motor vehicle for routine travel within the assigned office's planning and service area. All applicable State and local driving laws and insurance regulations must be strictly adhered to in the operation of the private vehicle while performing State business. You must possess a valid Florida driver's license. THE BENEFITS OF WORKING FOR THE STATE OF FLORIDA: Working for the State of Florida is more than a paycheck. The State's total compensation package for employees features a highly competitive employee benefits including: * Participation in state group insurance (must meet eligibility requirements*). For more details consult with People First at ************ or go to: ************************************************************************************ * Participation in the Florida Deferred Compensation Plan (457b). (For additional details and online enrollment visit MyFloridaDeferredComp.com) * State of Florida 401(a) FICA Alternative Plan (tax deferred Retirement Savings Plan). (For more information, please click Social Security Alternative Plan (aigrs.com) and read OPS Social Security Alternative Plan) * Flexible Spending Accounts * Seasonal and part-time OPS employees (less than 30 hours average per week) refer to the links above for detailed eligibility requirements. OUR ORGANIZATION AND MISSION: The Department is dedicated to promoting the well-being, safety, and independence of Florida's seniors, their families, and caregivers. Its vision is for all Floridians to live well and age well. SPECIAL NOTE: Candidate Profile (application) must be complete in its entirety. * Include supervisor names and phone numbers of all periods of employment. * Account for and explain any gaps in employment so that the hiring process is not delayed. Gaps of employment for 3 months or more MUST be addressed on application. * Experience, education, training, knowledge, skills, and/or abilities as well as responses to pre-qualifying questions must be verifiable to meet the minimum qualifications. * It is unacceptable to use the statement "See Resume" in place of entering work history. * Periods of employment should be entered with the most recent/current listed first. * If you are a retiree of the Florida Retirement System (FRS), please contact the FRS to determine if your current benefits may be affected if you are reemployed with the State of Florida in an FRS-covered position. Your current retirement benefits may be canceled, suspended, or deemed invalid depending upon the date of your retirement. * If claiming Veteran's Preference, candidates MUST attach supporting documentation (DD214). * If claiming Right to First Interview, candidates MUST attach a copy of your official layoff letter when applying. * All documentation is due by the close of the vacancy announcement. If you experience problems applying online, please call the People First Service Center at **************. BACKGROUND CHECKS: Successful completion of a Level 2 Criminal History Background Check is required for all applicants selected for this position. APPLICANT INFORMATION: Applicants should apply on-line via the People First Website ********************************* by 11:59 p.m. (EST) on the closing date of the position vacancy advertisement but are strongly encouraged to apply by 6:00 p.m. on the closing date to avoid any system down times or any other complications that may arise. If you have problems applying on-line, call the People First Service Center at 1-************. Paper applications will not be accepted by the agency. The Department of Elder Affairs is an "older worker-friendly" employer and also lists vacancies on the Silver Edition website, found at ******************************** that connects persons age 50 and older with other businesses/volunteer organizations/employers who specify they are "older worker-friendly." The Department of Elder Affairs is an E-Verify employer and will provide the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS), with information from each New Employee's I-9 Form to confirm work eligibility. The State of Florida is an Equal Opportunity Employer/Affirmative Action Employer, and does not tolerate discrimination or violence in the workplace. Candidates requiring a reasonable accommodation, as defined by the Americans with Disabilities Act, must notify the agency hiring authority and/or People First Service Center (***************. Notification to the hiring authority must be made in advance to allow sufficient time to provide the accommodation. The State of Florida supports a Drug-Free workplace. All employees are subject to reasonable suspicion drug testing in accordance with Section 112.0455, F.S., Drug-Free Workplace Act. Location:

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

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

Job DescriptionBenefits: Bonus based on performance Competitive salary Opportunity for advancement We are seeking a detail-oriented and dependable Field Quality Control Inspector to join our team. This role involves walking residential construction sites to ensure all work meets established quality standards and complies with client and regulatory requirements. The ideal candidate will have hands-on experience in construction inspections and a strong understanding of residential building practices. Key Responsibilities: Conduct daily field inspections at residential job sites to verify that work meets quality, safety, and compliance standards Inspect construction activities such as trenching, conduit installation, grounding, structural mounting, and equipment placement Ensure contractors adhere to approved specifications, codes, and client requirements Document inspection findings using detailed field notes, reports, and photo documentation Identify deficiencies or deviations and communicate corrective actions to the appropriate team Coordinate with project managers, subcontractors, and utility representatives to resolve issues in the field Ensure proper use and handling of materials and equipment on-site Maintain organized and up-to-date records of all inspections and communications Travel between job sites as required Qualifications: Previous experience in field inspection, construction, or utility-related work (OSP/telecom/electrical a plus) Strong understanding of residential construction processes and safety standards Ability to read and interpret construction drawings, site plans, and specifications Comfortable working outdoors and walking sites daily in various weather conditions Excellent communication and reporting skills Detail-oriented with a proactive approach to identifying and resolving issues Valid drivers license and reliable transportation Job Type: Full-time, Permanent (1099 Sub-Contractor) Pay: $21$25 per hour (based on experience) Expected Hours: 40 per week Schedule: 8-hour shift Day shift Monday to Friday Work Location: Field-based (on the road; residential job sites)

Title: Quality Control Inspector Duration: 6 months (Possible extension) 1 PM TO 9 PM PAY RATE: $22/hR. Qualifications: 1 PM TO 9 PM Plans and directs activities concerned with development, application, and maintenance of quality standards for industrial processes, materials, and products. Tests and inspects products at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Must have Basic Computer Proficiency to include fundamental tasks such as email, word processing software, creating and maintaining spreadsheets in MS Excel and navigating Operating systems. EDUCATION and/or EXPERIENCE: Associate degree in an aviation related field preferred At least 1-year relevant aviation work experience Minimum of 2 years'experience in basic dimensional/visual inspection required on aviation related equipment (airframe, powerplant, and or avionic) Certify visual acuity to NAS-410 Airframe and Powerplant FAA certifications preferred Responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Provide quality control final inspection support, and shipping / receiving inspection support. Accurately interpret engineering drawings, customer specifications, company specifications, sampling procedures, designs, forms, and instructions for recording, evaluating, and reporting quality and reliability data. Utilize precision tools and equipment with accuracy for testing and measurement of products. Recommend modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability.

Are you looking to join Florida's fastest growing mechanical contracting team? B&I Contractors, Inc., a proud four-time winner of the Great Place to Work certification, is seeking an experienced and dedicated Commercial HVAC Piping Quality Control to join our dynamic and expanding team. Why Choose B&I Contractors, Inc.? * Industry Leader: As Florida's fastest growing mechanical contractor, we specialize in large-scale commercial projects. * Continuous Development: Benefit from our NCCER-certified in-house and online training that equips you with the skills needed to advance in your career. * Comprehensive Benefits: Enjoy employer-paid health insurance, accrued vacation, and sick time, along with a wellness reimbursement program to support your overall well-being. * Retirement Benefits: We are a 100% employee-owned company with an ESOP. You can also participate in our 401(k) plan with company match and explore post-tax Roth IRA options to secure your financial future. * Established Legacy: Join a team of over 1000 employees contributing to our success since 1960, with a proven track record of excellence in mechanical contracting. General Description: The Commercial Pipefitter Quality Assurance (QA) Representative is responsible for implementing and maintaining the quality management system for commercial piping projects. This role ensures that all quality standards and procedures are met and maintained on-site, with a focus on mechanical piping systems as well as air side equipment. The QA Representative coordinates with project stakeholders to guarantee compliance with quality objectives and industry standards such as ASME, ASTM, and local code requirements. Essential Functions: * Control and distribute all quality documentation for assigned piping projects. * Monitor and oversee all quality-related activities on the project, with a focus on plumbing and mechanical piping standards. * Attend client quality management meetings and represent the project's QA interests. * Prepare and maintain project-specific quality system documentation, including inspection and test plans (ITPs). * Oversee the disposition and resolution of nonconformance reports (NCRs) or rolling completion lists (RCL's). * Recommend and implement quality improvements based on field observations and audit findings in accordance with contract documents, plans, specs, and equipment manufacturers' recommendations. * Coordinate QA/QC activities with the Project Manager and Site Superintendent. * Maintain quality-related communication with customer representatives and inspectors. * Monitor and report statistical data related to quality performance and outcomes. * Address and resolve customer complaints related to piping quality and installation. * Archive all project documentation upon project completion in accordance with company procedures (ACC). * Perform light administrative duties to support the Project Superintendent. * Perform hands-on piping-related tasks at project sites as needed to verify installation quality and assist with inspections. Competencies: * Strong collaboration and communication skills. * Excellent organizational and problem-solving abilities. * Effective time management and task prioritization. * Proficiency in interpreting construction drawings and piping specifications. * Ability to review and understand submittals for piping materials, valves, and equipment. * Experience with Procore, ACC or similar construction management software. * Proficiency in using iPads or tablets for field reporting and documentation. * Ethical conduct and attention to detail. * Computer literacy and familiarity with QA/QC reporting tools. Physical Demands: This position requires the ability to lift and carry materials weighing up to 50 pounds on a frequent basis. The employee must be able to perform tasks involving physical labor, including lifting, pushing, pulling, and carrying materials, tools, or equipment. Manual material handling must be performed in accordance with OSHA safety standards and company policies to minimize risk of injury. Esta posición requiere la capacidad de levantar y transportar materiales de hasta 50 libras de manera frecuente. El empleado debe poder realizar tareas que involucren trabajo físico, incluyendo levantar, empujar, jalar y transportar materiales, herramientas o equipo. El manejo manual de materiales debe realizarse de acuerdo con los estándares de seguridad de OSHA y las políticas de la compañía para minimizar el riesgo de lesiones. Required Education and Experience: * 8+ years of field experience in commercial piping systems. * Proficiency in reading and interpreting blueprints, drawings, and piping specifications. * Strong problem-solving skills, especially with layout and installation concepts. * Proficiency in basic math and ability to perform relevant calculations. #bandi1

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

The Quality Assurance (QA) Microbiologist plays a pivotal role in upholding our product quality standards by actively supporting the Quality Management System. This position primarily focuses on investigating the growth, potential sources, and specific attributes of microscopic organisms within Treatt products. The QA Microbiologist collaborates closely with the Quality Assurance Supervisor and cross-functional teams to ensure product safety and quality compliance. The duties and tasks of the Quality Assurance (QA) Microbiologist involve the following: Oversee and maintain the Retain Program to ensure proper storage and organization of retained samples for future reference. Manage and maintain the ATP Program, including the weekly calibration of ATP equipment, to ensure accurate and consistent results. Send monthly trending report to QA Supervisor. Manage and maintain the Environmental Program, which includes monitoring and maintaining cleanliness and hygiene within the production environment. Send monthly trending report to QA Supervisor. Administer and maintain weekly water analysis to verify the quality and safety of water sources. Send monthly trending report to QA Supervisor. Manage and maintain the Temperature Monitoring Program, ensuring temperature controls are in place and documented as per quality standards. Review and report on area cleaning logs weekly. Assist in conducting daily walkthroughs and reporting findings. Manage and maintain the Glass and Knife Programs Assist in investigating and consulting microbiological complaints and CAPAs to resolve quality issues effectively. Provide necessary training to operators on plant hygiene as needed to uphold cleanliness and microbiological safety standards. Conduct validation studies related to environmental and equipment testing, ensuring the reliability of our quality control processes. Actively contribute as a member of the internal audit team, ensuring timely completion of internal audits and adherence to compliance standards. Participate as a key member of the HACCP team, supporting the implementation and maintenance of food safety protocols. Support the QA Supervisor in the implementation of corrective action plans pertaining to microbiological concerns identified during audits. Assist in investigating Soleris anomalies as requested by the QA Supervisor or QC Manager to maintain product quality and safety. Analyze and interpret microbiological data as requested by the QA Supervisor or QC Manager to identify trends and areas for improvement. Provide consultation on laboratory equipment upgrades, as requested by the QC Manager, to enhance testing and analysis capabilities. Collaborate with the Innovation team to assess potential microbiological contamination risks in new product developments and offer guidance on risk mitigation strategies. Assist with microbiological training as needed for new laboratory hires or during method/equipment changes as requested by QC Manager. Undertake any other tasks that align with the overall job description and contribute to the quality and safety of our products. EDUCATION: Bachelor's or MS degree in Microbiology or Food Science, or related, from an accredited college or university. Previous experience of working in a microbiological laboratory and knowledge of quality assurance, preferred. A track record of successful teamwork in a manufacturing environment. Knowledge of HACCP, GMP, food safety, and related food safety regulations and processes is preferred. KNOWLEDGE AND EXPERIENCE: A minimum of 2-4 years of relevant work experience, with an understanding of food safety and regulations. Proficiency in Microsoft Office is required. Familiarity with ERP systems like SAP or JD Edwards is preferred.

The Quality Associate plays a vital role within the Quality Assurance Department, contributing to the consistent delivery of high-quality products and processes. This multifaceted position encompasses a wide range of responsibilities, including inspection and testing activities, internal audits, documentation control, and cross-functional collaboration to ensure compliance with established quality standards. The ideal candidate will possess a keen eye for detail, exceptional organizational abilities, and a proactive mindset geared toward continuous improvement. Success in this role requires the ability to work effectively in a fast-paced, team-oriented environment, applying analytical thinking and problem-solving skills to uphold and advance quality excellence across the organization. Qualifications QUALIFICATIONS Associate's Degree or Technical Certificate required 2-3 years of experience in Quality Assurance or Quality Engineering within electronics manufacturing. Familiarity with electronic/electrical components and inspection tools (e.g., calipers, multimeters, AOI). Understanding of environmental regulations (RoHS, REACH, Prop 65). Experience with ISO 9001 or similar quality systems. KNOWLEDGE, SKILLS, AND ABILITIES Strong work ethic and professional relationship-building skills. Self-motivated and capable of working independently after training. Flexible and willing to cross-train across QA functions. Analytical mindset with a focus on process improvement. Ability to interpret technical documentation and visual aids. Competent in computer navigation and data entry. Team-oriented with a track record of success in fast-paced environments. Able to perform job functions without posing a safety risk to others. Experience with IPC-A-610 and J-STD-001 Standards. Experience with SAP or similar ERP systems. Skilled in maintaining accurate inspection records. Proficient in Microsoft Office; experience with Access, SPC, or quality software is a plus. Strong communication skills and ability to work in cross-functional teams. Proficient in reading technical drawings and specifications (GD&T). ABOUT US DITEK, a leader in surge protection solutions, is proud to have been voted one of Tampa Bay's Top Workplaces for 16 years in a row. We are dedicated to fostering a positive and dynamic work environment where employees can thrive and contribute to our ongoing success. Join us and be part of a team that values innovation, excellence, and employee satisfaction. DITEK is a drug-free workplace and participates in E-Verify. DITEK provides equal employment opportunities (EE0) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics.

The Lab Technician is responsible for testing raw materials to ensure they are of standard quality for Metromont. RESPONSIBILITIES Collect and remove all mold test specimens from previous day. Remove cylinders that needed to be broken down for curing tanks. Perform aggregates (rock/sand) radiations which includes put test sample in oven and dry, run through splitter, weigh, put in shaker, weigh each breakdown, and enter data in system. Make 12x12 color samples as needed. Break tank specimens after drying, record beaks in system. Assist in testing wet concrete (air, slump, temperature, and unit weight). Make test specimens cylinders as needed. Actively participate in companies “6S”, “Lean” and Safety Programs. Inspect beds before and after pours. Must adhere to all Metromont and OSHA safety rules and regulations. Housekeeping as necessary to maintain work area, tools, and equipment in a clean and orderly manner. SCOPE OF AUTHORITY This position has no supervisory responsibilities Reports to the QC Manager Works independently with little supervision CHARACTERISTICS (Knowledge, Skills, and Abilities) Advanced reading, writing, and math skills Able to read a tape measure to 1/16 Basic knowledge of blueprint plans and reading Precise with measurements Accurate with data recording Attention to detail and accuracy Computer literate Knowledge of Microsoft Office products including Word, Excel, and Outlook Able to adapt to changes in work schedules, tasks, or processes Values and demonstrates safe working behaviors EDUCATION AND TECHNOLOGY High school diploma or GED equivalent preferred WORK ENVIRONMENT / SCHEDULE Monday-Friday Outdoor/unsheltered Work area is not climate controlled and may be exposed to changing weather and temperature conditions Schedule varies with workload and location Unscheduled overtime may be required depending on production needs PERSONAL PROTECTION EQUIPMENT (PPE) Safety glasses High-visibility vest Hard hat Steel-toed shoes Hearing protection Gloves (various types) PHYSICAL REQUIREMENTS This position requires standing for long periods of time, frequent lifting (up to 50 pounds) and bending, repetitive motion with medium force, and an ability to climb up to 15 feet above the ground using stairs. Disclaimer: This job description is not intended to be all-inclusive. Other duties as assigned may be required. All associates are expected to conduct themselves in a manner that is consistent with Metromont's core values and to actively participate in all company safety, training, and observation programs.

Salary: $18 - $25 Depending on Experience Freedom Metal Finishing Inc. is seeking an entry level Quality Assurance Inspector to visually and mechanically inspect parts to ensure they meet customer related quality and Aerospace industry specifications. Essential Functions: Perform visual and mechanical inspections using measurement and test equipment such as: X-ray, Eddy-current, micrometers, calipers, pin gauges, bore gages etc. Calibrate inspection equipment and assist in maintaining calibration database. Stage, inspect, and document monthly periodic testing. Monitor and verify quality. Recommend improvements. Improve quality practices. Qualifications: Ability to be trained to be able to read and interpret work orders, customer po's, blueprints, and specifications. Maintain a safe work environment and good housekeeping practices. Skills and Abilities: Able to setup necessary quality tools as it relates to this position. Must be able to perform all physical requirements as it relates to this position as outline in the Functional job description. Knowledge of basic safety awareness in the workplace. Able to lift and transport up to 35 pounds. Required experience: None Required Recommended Experience: -Previous QC and QA experience in the aerospace industry. -Manufacturing experience in the use of quality measurement tools (calipers, micrometers, bore gauges). -Ability to read and interpret blueprints, layouts, inspection plans, engineering drawings and specifications. -Ability to communicate effectively. -Proficient with Microsoft Office.

• Perform detailed visual and paperwork inspection for compliance to quality requirements and specifications. • Primary interface with Customers and DCMA to resolve concerns relating to production hardware or requirements, ensure product meets company/customer requirements. • perform process and product audits • Ensure product meets and is documented in the configuration management systems. • Participate in RCCA (Root Cause Corrective Action) with cross functional groups Qualifications • Must be a United States Citizen. • High School Diploma or Equivalent is required. • Min 2 years inspection or related manufacturing experience • Must be familiar with fine pitch leads, component identification, soldering, bonding and conformal coating applications. • Previous experience in the manufacture of aerospace electronics highly preferred. • Must be familiar with ISO9001, AS9100, requirements. • Must be able to organize, prioritize and multitask. • Must be a motivated individual with a bias for action. • Must have basis computer skills and be familiar with Microsoft Excel, Word • Energetic team player that interfaces well at all levels of an organization. • Excellent communication skills both oral and written. • Ability to visually inspect using a microscope • Ability to interpret drawing requirements, perform work to inspection instructions Additional Information Shifts: Monday - Friday, 7:00am to 3:30pm Pay: 13/hr 6+ Month Contract *****This is an opportunity for contract to hire based on individual work performance and attendence***** **Looking for candidates with good work history, good attendance record, a positive attitude, and willingness to learn. Must be able to pass a background check and drug screen.

• Perform detailed visual and paperwork inspection for compliance to quality requirements and specifications. • Primary interface with Customers and DCMA to resolve concerns relating to production hardware or requirements, ensure product meets company/customer requirements. • perform process and product audits • Ensure product meets and is documented in the configuration management systems. • Participate in RCCA (Root Cause Corrective Action) with cross functional groups Qualifications • Must be a United States Citizen. • High School Diploma or Equivalent is required. • Min 2 years inspection or related manufacturing experience • Must be familiar with fine pitch leads, component identification, soldering, bonding and conformal coating applications. • Previous experience in the manufacture of aerospace electronics highly preferred. • Must be familiar with ISO9001, AS9100, requirements. • Must be able to organize, prioritize and multitask. • Must be a motivated individual with a bias for action. • Must have basis computer skills and be familiar with Microsoft Excel, Word • Energetic team player that interfaces well at all levels of an organization. • Excellent communication skills both oral and written. • Ability to visually inspect using a microscope • Ability to interpret drawing requirements, perform work to inspection instructions Additional Information Shifts: Monday - Friday, 7:00am to 3:30pm Pay: 13/hr 6+ Month Contract *****This is an opportunity for contract to hire based on individual work performance and attendence***** **Looking for candidates with good work history, good attendance record, a positive attitude, and willingness to learn. Must be able to pass a background check and drug screen.

We are seeking a detail-oriented and safety-conscious Chemical Technician to support our manufacturing operations in the medical device industry. This role involves hands-on work with raw chemicals in a lab setting and with specialized equipment to ensure the safe and efficient processing of production parts. The ideal candidate will have strong communication skills, a commitment to quality, and a proactive approach to continuous improvement. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements minimum of an associates degree or equivalent hands on experience 2 years of experience in a lab setting experience working with regulated SOPs and documentation great teamwork and communication

Job Details Division: Nucor Rebar Fabrication Southeast Other Available Locations: N/A Welcome to Nucor, where our unique culture sets us apart. Joining Nucor means becoming part of North America's largest steel and steel products manufacturer, offering unmatched career opportunities and stability. We are known for our innovative sustainability practices and are the continent's largest recycler. Our vibrant culture, built on personal connections and teamwork, empowers every team member with the freedom to innovate and contribute to our collective success. Experience a workplace where safety, efficiency, and meaningful personal connections define every day, enriching both our teammates and the communities we serve. Nucor supports its teammates with top-tier benefits like Medical, Dental, Vision, and Disability Insurance, 401K and Roth accounts, Profit sharing, Pay-for-performance bonuses, Paid parental leave, Tuition reimbursement, Stock program, Scholarships and more. Basic Job Functions: Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times. Nucor Rebar Fabrication is looking for an experienced Quality Control Coordinator to support our Weekend Shift (Friday-Sunday), 9:00AM to 9:30PM. Nucor - North America's largest steel and steel products producer * Forge deep bonds with teammates, celebrate wins together, and put safety first * Shape your own future with the freedom to activate your ideas that propel us forward * Get the foundation you need to create a stable and lifelong career * All Nucor Teammates have the opportunity to receive full benefits package including: Medical/Dental/Vision insurance; Long-Term Disability; Life Insurance; Vacation Days; Holiday Pay; 401K with company match; Nucor Profit Share Program; Nucor stock purchase program; College Tuition Reimbursement program for you and your spouse, and a College Tuition Scholarship Program for children of employees Basic Job Functions The Quality Coordinator's responsibilities include but are not limited to: * Must adhere to Nucor Rebar Fabrication's safety programs and standards * Demonstrate conduct consistent with Nucor Rebar Fabrication's vision and values * Continued education and knowledge of all rebar standards and expectations * A strict adherence to all NRF Milton quality procedures * Thorough inspection of fabricated product * A complete understanding of daily customer shipment schedules, shop work order organization * Strict inspections of all customer shipments against production tags to ensure all product is loaded * Yard truck operation; aiding loading and unloading team; heavy equipment operation when necessary * Any other tasks assigned Minimum Qualifications: * Legally authorized to work in the United States without company sponsorship now or in the future. * High school diploma, GED or state/local equivalent * Willingness to work unplanned, unscheduled overtime, weekends, holidays, and rotating shift * Willingness to work in extreme situations including: hot, cold, and rainy weather, dusty conditions, and a fast-paced, high-pressure environment * Fundamental computer skills including basic experience using the Microsoft Office Suite of products * Demonstrated ability to communicate effectively with all levels of teammates, 3rd party vendors, and others in a professional and respectful manner Preferred Qualifications: Demonstrated commitment to quality of product Previous experience operating heavy equipment and lull or yard trucks A track record of being a positive, problem-solving leader who continuously looks for improvement Organized, goal oriented, and results driven Energetic with enthusiasm that is motivating to others Nucor is an Equal Opportunity Employer and a drug-free workplace

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

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