Quality Control Analyst jobs at Alaant Workforce Solutions

A well respected and leading specialty chemical company that supports a variety of industries is seeking a Chemist to join their team in Ohio. This role will be focused on QC testing of raw materials, in-process samples, and finished goods within a GXP environment. Day Shift and Night Shift available Schedule is 3 days per week (12hr shifts) and 1 day every other weekend. Pay: $28.00/hr Responsibilities Conduct analytical testing (HPLC and GC) per SOPs using instrumentation and wet chemistry methods. Provide in-process testing support and ensure clear shift handoffs. Calibrate and maintain lab equipment. Lead OOS investigations and monitor CAPA effectiveness. Assist with method optimization, troubleshooting, and equipment upkeep. Maintain and update product specifications in internal systems. Qualifications Bachelor's in Chemistry or related field and 2+ years industry lab experience. Proficient with GC, GC-MS, HPLC, LC, titrations, spectroscopy, physical testing, and related techniques Comfortable with working a 12hr schedule This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you

We are seeking QC Chemist, to Conduct QC testing on raw materials, in-process samples, and finished products to deliver accurate, timely results aligned with ISO and cGXP requirements. Support method development, data review, and QA/regulatory needs. Location: Montgomery County, OH Hours: Day Shift 4AM-4PM or Overnight Shift 4PM-4AM (rotating 3 days per week, 1 day every other weekend) Pay: Quality Control Chemist: $28-30 hour Quality Control Lab Tech: $23-26 hour Contract to Hire Responsibilities Perform routine calibrations and maintain equipment readiness. Run analytical tests per SOPs using a variety of instruments and wet chemistry techniques. Support production with in-process testing and ensure smooth shift handoffs. Lead OOS investigations and track CAPA effectiveness. Assist with method improvements, troubleshooting, and equipment maintenance. Maintain and update product specifications across internal systems. Qualifications Chemist: Bachelor's degree in Chemistry or related field with 2+ years of lab experience. Lab Tech: HS diploma with 2+ years of lab experience. Knowledge of GLP, ISO 9001, and preferred experience with cGMP/GDP and FSSC 22000/ISO 22002. Hands-on experience with GC, GC-MS, HPLC, LC, titrations, spectroscopy, physical testing, and related techniques. Strong documentation, communication, and problem-solving skills. Ability to work rotating shifts and overtime as needed; organoleptic testing ability required. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

We're growing and looking for a detail-driven, process-minded Business Analyst to join our Business Operations team. This role is critical to enhancing the quality and consistency of our work through rigorous review programs and operational controls. You'll be a key player in driving continuous improvement, ensuring compliance, and elevating our service delivery. The Gig: * Lead and manage quality assurance initiatives across Business Operations. * Design, test, and refine frameworks for quality review and control programs. * Conduct complex recurring quality audits and controls. * Gather and analyze functional and data requirements to support quality initiatives. * Facilitate discovery sessions and document findings with internal stakeholders. * Collaborate across departments to ensure alignment and timely execution. * Identify gaps and escalate deficiencies in quality programs and propose updates and strategies for mitigation. * Drive process standardization and improvement efforts through creative problem solving and efficiency tool implementation (ie. VBA, SQL, etc) * Own the end-to-end lifecycle of assigned work, from intake to resolution. * Support data analysis and research efforts across departments related to quality and control initiatives. * Maintain confidentiality and uphold company standards. * Other duties as assigned. What you need to make the cut: * Bachelor's degree in Business Systems, Finance, Accounting, or related field (preferred). * 2+ years of operations experience in benefits administration operations, HRIS, payroll, or insurance required. * Proven expertise in internal audit methodologies and operational control design. * Lean Six Sigma or similar methodology experience a plus. * Strong background in process review and risk identification. * Advanced proficiency in Microsoft Excel (pivot tables, lookups, nested functions, advanced functions). * Exceptional time management and organizational skills with the ability to manage conflicting priorities. * Strong critical thinking and problem-solving abilities. * Excellent communication and stakeholder engagement skills. * Project management experience is a plus. The pay range for this position is 45K to 71K per year (pay to be determined by the applicant's education, experience, knowledge, skills, abilities, balanced against internal equity and competitive market based geographic ranges). This role is eligible to participate in the annual bonus incentive plan.

Since 1998, Businessolver has delivered market-changing benefits technology and services supported by an intrinsic responsiveness to client needs. The company creates client programs that maximize benefits program investment, minimize risk exposure, and engage employees with easy-to-use solutions and communication tools to assist them in making wise and cost-efficient benefits selections. Founded by HR professionals, Businessolver's unwavering service-oriented culture and secure SaaS platform provide measurable success in its mission to provide complete client delight. We're growing and looking for a detail-driven, process-minded Business Analyst to join our Business Operations team. This role is critical to enhancing the quality and consistency of our work through rigorous review programs and operational controls. You'll be a key player in driving continuous improvement, ensuring compliance, and elevating our service delivery. The Gig: Lead and manage quality assurance initiatives across Business Operations. Design, test, and refine frameworks for quality review and control programs. Conduct complex recurring quality audits and controls. Gather and analyze functional and data requirements to support quality initiatives. Facilitate discovery sessions and document findings with internal stakeholders. Collaborate across departments to ensure alignment and timely execution. Identify gaps and escalate deficiencies in quality programs and propose updates and strategies for mitigation. Drive process standardization and improvement efforts through creative problem solving and efficiency tool implementation (ie. VBA, SQL, etc) Own the end-to-end lifecycle of assigned work, from intake to resolution. Support data analysis and research efforts across departments related to quality and control initiatives. Maintain confidentiality and uphold company standards. Other duties as assigned. What you need to make the cut: Bachelor's degree in Business Systems, Finance, Accounting, or related field (preferred). 2+ years of operations experience in benefits administration operations, HRIS, payroll, or insurance required. Proven expertise in internal audit methodologies and operational control design. Lean Six Sigma or similar methodology experience a plus. Strong background in process review and risk identification. Advanced proficiency in Microsoft Excel (pivot tables, lookups, nested functions, advanced functions). Exceptional time management and organizational skills with the ability to manage conflicting priorities. Strong critical thinking and problem-solving abilities. Excellent communication and stakeholder engagement skills. Project management experience is a plus. The pay range for this position is 45K to 71K per year (pay to be determined by the applicant's education, experience, knowledge, skills, abilities, balanced against internal equity and competitive market based geographic ranges). This role is eligible to participate in the annual bonus incentive plan. Other Compensation: If this position is full-time or part-time benefit eligible, you will receive a comprehensive benefits package which can be viewed here: ************************************************************************************ Dear Applicant. At Businessolver, we take our responsibility to protect our clients, employees, and company seriously and that begins with the hiring process. Our approach is thoughtful and thorough. We've built a multi-layered screening process designed to identify top talent and ensure the integrity of every hire. This includes quickly filtering out individuals who may attempt to misrepresent themselves or act in bad faith. We also partner with trusted, best-in-class providers to conduct background checks, verify identities, and confirm references. These steps aren't just about compliance, they're about ensuring fairness, safety, and trust for everyone involved. Put simply: we will always confirm that you are who you say you are. It's just one of the many ways we uphold the standards that matter most, to you, to us, and to the people we serve. With heart, The Businessolver Recruiting Team Businessolver is committed to maintaining an environment that protects client data. We train our employees to maintain leading class security practices and expect all employees to adhere to policy, procedures and controls. (Applicable to all roles at an AVP, DIR, VP, Head Of or SVP and above level): Serve as a security contact for the business unit. Responsible for driving adoption and compliance with information security and privacy practices. Serve as a liaison with the information security team on security and privacy matters. Equal Opportunity at Businessolver: Businessolver is an Affirmative Action and Equal Opportunity Employer and is proud to offer equal employment opportunity to everyone regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, veteran status, and more. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. #LI-Remote

We seek an experienced Quality Specialist to work directly with our customer sites and installation teams to ensure quality standards are adhered to in all aspects of installations while acting as a catalyst for continuous improvement in our products and systems. This role will interface with install partners, equipment suppliers, sub-tiers, engineering, program team, and sourcing to drive high levels of quality and field reliability in critical sub-systems and components. This position will require both a collaborative nature and ability to influence across organizational lanes, partners, suppliers, and customers. Responsibilities and Duties: + Become familiar with the project technical requirements such as the specifications, installation SOP's, SOW Terms & Conditions and applicable standards. + Execute the Site Installation Quality checklist, ensuring that all in scope work is performed per pre-defined standards and deficiencies are reported to and resolved with the relevant Installation Contractors. + Provide Quality leadership at customer installation sites, focusing on identification and timely resolution of issues via structured quality methods. + Provide surveillance of installation partners to ensure that all installation processes are complied with and critical to quality parameters adhered to. + Communicate issues across our operations team and drive closed loop problem resolution. + Provide weekly Quality Status reporting outlining accomplishments, 2 week look ahead plan and any blockers + Inspire others to share acquired knowledge and can take a supportive role during technical discussions. + Hold quality kickoff meeting with contractors. + Notify project management team of any issues found in the field or instances where contractors not following the quality plan. + Attend morning job huddle meetings and be aware of all work being performed that day by various installation contractors. + Verify calibrated tools are in valid working condition. + Work with construction on closing installation deficiencies and NCR's. + Mentor & coach site personnel to efficiently execute quality SOPs to identify and resolve issues. Job Type & Location This is a Contract position based out of Grove City, OH. Pay and Benefits The pay range for this position is $20.00 - $27.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Grove City,OH. Application Deadline This position is anticipated to close on Dec 15, 2025. h4>About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

IRI believes in commitment, Integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description BS or higher in science related discipline, chemistry is preferred Minimum 3 years of experience in a pharmaceutical environment Performs analyses, inspection, and tests of products, raw materials, in-process materials, packaging materials, and quantitative assays on samples, to ensure quality standards and compliance with company standards, customer and regulatory requirements, and tolerance specifications for the chemical or physical property. Performs a variety of qualitative tests or qualitative assays on samples using techniques that vary from standard analytical equipment to highly modern and automated instrumentation, aides in maintenance and certification of test instruments and apparatus to ensure compliance. Performs required inspections, checks, analysis and documentation of studies. Prepares and monitors quality statistics and reports. Perform qualitative and quantitative analyses using analytical instrumentation such as HPLC; GC, UV/Vis, KF and FTIR. Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data Basic knowledge and understanding of USP, cGMP, and FDA regulations Requires knowledge and experience in own discipline; still acquiring higher level knowledge and skills Solves a range of straightforward problems Analyzes possible solutions using standard procedures Receives a moderate level of guidance and direction Additional Information Regards, Indu Clinical Recruiter 732-844-8725 indu @irionline.com

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Position: Quality Control Analyst Location: Cincinnati Ohio 45213 Duration: 4+ months (Possibility of extension) Job Responsibilities: BS or higher in science related discipline, chemistry is preferred Minimum 1 year of related experience in FDA regulated environment Perform routine chemical testing of raw materials and packaging components in accordance with USP or in-house methodology Perform qualitative and quantitative analyses using analytical instrumentation Utilize electronic laboratory information systems such as LIMS for processing analytical data Analyze data against approved specifications, notifying management of any OOS and aberrant results Perform peer review of laboratory testing, as required Create and maintain lab record documentation according to GMPs Must be able to stand on feet for extended periods of time throughout the work day Must have the ability to lift up to 20 lbs. on an occasional basis in order to perform job Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus Thank you for your time and consideration. I look forward to hearing from you! Kind Regards Ruchi Kumari Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I (DIRECT BOARD) # 732-844-8716 (F) 732-549-5549 LinkedIn: https://www.linkedin.com/in/ruchi-kumari Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Major Responsibilities : Responsible for implementing and maintaining the effectiveness of the quality system. · Weighs ingredients, prepares batches, and supports production at the product research center · Submits samples for analysis and consolidates/tabulates results · Organizes non-routine testing, completes these tests and summarizes results B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3 years technical work experience, preferably in developing food/nutritional products The candidate should also demonstrate the ability to handle multiple priorities as well as a good work ethic Qualifications B.S. in Food Science and Technology, Chemistry or Sciences preferred. 0 - 3 years technical work experience, preferably in developing food/nutritional products Additional Information Thanks & Regards ________________________________________________________________________ ___ Riya Seth | Team Recruitment | Mindlance, Inc. | W: ************

DUTIES & RESPONSIBILITIES Collecting, receiving, labeling, and/or analyzing samples using the appropriate testing equipment, in accordance with Smithers CTS OH procedures and state guidelines Performing analytical testing with SME supervision using instrumentation and procedures including, but not limited to, HPLC, LCMS/MS, ICP-MS, GC-MS, microbiological testing, wet chemistry techniques and extractions, and minor lab equipment Recording all experimental data and test results accurately in lab notebooks and LIMS systems Organizing and storing all chemical substances, fluids, and compressed gases according to safety instructions Ensuring that safety guidelines are followed within the laboratory Maintaining daily logs and equipment record books Cleaning, sterilizing, maintaining, and calibrating laboratory equipment Performing inventory checks and reporting counts to Lab Manager/Lab Director as assigned Performing sample intake duties as assigned Performing other minor duties as assigned by management, such as sample disposal and lab/facility cleaning #Cannabistestingjobs #LI-LO1

The Quality Control Inspector checks products in the warehouse to make sure they meet quality standards. This includes inspecting items for damage, verifying labels, and reporting any issues to supervisors. Key Duties: Inspect incoming and outgoing products for defects or damage Ensure items are labeled and packaged correctly Record inspection results and report any issues Follow warehouse safety and quality procedures Work closely with warehouse staff to maintain quality standards

Job Description Chemical Analyst / Lab Technician - 3rd Shift ???? Entry Level | ???? Thursday-Sunday, 8:00pm-6:00am (4×10-hour nights) We're looking for a detail-oriented Chemical Analyst/Lab Technician to join our team. You'll perform a mix of classical wet chemistry (titrations, gravimetric analysis, pH measurements) and modern instrumental techniques (GC, FTIR, ICP) to support quality control, product development, and process optimization. What You'll Do: Test raw materials, in-process samples, and finished products Perform classical analyses: • Acid/base & redox titrations (Acid Value, Iodine Value) • Gravimetric analyses (density, filterable impurities) • pH & moisture determination Operate, calibrate, and maintain lab instruments: GC, FTIR, ICP-OES, Karl Fischer titrators Interpret results and keep accurate, detailed records (SOP & GLP compliance) Assist in method development, validation, and troubleshooting Follow all lab safety protocols and PPE requirements Contribute to continuous improvement initiatives What We're Looking For: ✅ Bachelor's degree in Chemistry (preferred), Biology, Chemical Engineering, or related field ✅ Solid foundation in classical chemistry techniques & analytical instrumentation ✅ Knowledge of Good Laboratory Practices (GLP) ✅ Strong organizational & problem-solving skills ✅ Ability to work independently and in a team environment Work Environment: Laboratory-based with routine chemical and instrumentation use PPE required

IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • Perform a variety of analytical laboratory testing of raw material, processed material and finished products and assure compliance with applicable laws, rules and regulations • Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. Set up instruments and conduct sample tests • Utilize a variety of methods to assure compliance to established standards and testing controls; • Interpret test results and prepare and submit reports related to test results • Perform, interpret, evaluate and record standard process control laboratory tests on ; • Perform calculations as needed and record results; • Notify appropriate personnel of abnormal or critical results and significant changes in lab results • Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; • Assure an adequate supply of test materials to perform daily testing; • Perform preventive maintenance on equipment. • Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality Qualifications • 2 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques • Perform a variety of laboratory testing. Perform mathematical calculations applicable to chemistry testing. • Work cooperatively with others. Must be able to read, write, speak and understand fluent English • Strong understanding of GMP concepts and requirements. • Able to demonstrate accuracy and thoroughness while completing work in a timely manner • Follows instructions, policies, and procedures. • Bachelors of Science degree in chemistry or closely related field. Additional Information Regards Ricky 732-49-1925

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. • Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. • Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. • Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. • Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality. Qualifications: • 2 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques. • Perform a variety of laboratory testing. • Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others. • Must be able to read, write, speak and understand fluent English. Strong understanding of GMP concepts and requirements. • Able to demonstrate accuracy and thoroughness while completing work in a timely manner. • Follows instructions, policies, and procedures. Non-Essential Skills - Operate, maintain and repair equipment required to perform related duties. Qualifications Education Requirements: Bachelor's of Science degree in chemistry or closely related field. Physical Demands: While performing the duties of this job, the employee is frequently required to stand and use hands to finger, handle, or feel. The employee is occasionally required to walk; sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. The employee is occasionally exposed to moving mechanical parts or airborne particles. The noise level in the work environment is usually moderate. These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of this job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of this job. Additional Information Best Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. • Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. • Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. • Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. • Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality. Qualifications: • 2 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques. • Perform a variety of laboratory testing. • Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others. • Must be able to read, write, speak and understand fluent English. Strong understanding of GMP concepts and requirements. • Able to demonstrate accuracy and thoroughness while completing work in a timely manner. • Follows instructions, policies, and procedures. Non-Essential Skills - Operate, maintain and repair equipment required to perform related duties. Qualifications Education Requirements: Bachelor's of Science degree in chemistry or closely related field. Physical Demands: While performing the duties of this job, the employee is frequently required to stand and use hands to finger, handle, or feel. The employee is occasionally required to walk; sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. The employee is occasionally exposed to moving mechanical parts or airborne particles. The noise level in the work environment is usually moderate. These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of this job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of this job. Additional Information Best Regards, Anuj Mehta ************

Job Description Dyson Corporation headquartered in Painesville, OH is seeking a quality control professional for reviewing and testing materials, components, and finished products to ensure they meet specifications and quality standards using various tools like calipers, gauges, and micrometers. The quality department performs inspections on materials and products, monitoring production processes, documenting issues and corrective actions, ensuring compliance with standards, and collaborating with various teams to resolve problems. PRINCIPAL DUTIES AND RESPONSIBILITIES: Inspect in-process and finished products using micrometers, calipers, gauges, and other precision tools. Review and maintain quality records for accuracy and completeness. Interpret blueprints and work orders to verify product specifications. Document nonconforming materials and support corrective actions. Collaborate with production and engineering teams to resolve quality issues. Maintain a clean and organized work area. Meet production goals and perform additional duties as assigned. REQUIREMENTS: High School Diploma or GED required. 1-3 years of quality control experience in a manufacturing setting. Proficient in using inspection tools: micrometers, calipers, thread & pin gauges, surface plates, and height gauges. Ability to read and interpret technical documents and blueprints. Strong communication skills and a team-oriented mindset. PHYSICAL REQUIREMENTS: Ability to work on the shop floor for extended periods. Must be able to lift up to 50 lbs. Strong visual acuity is essential. Dyson Corporation is a leading manufacturer of large diameter fasteners and forgings, proudly headquartered in Painesville, Ohio. With over 130 years of industry expertise, we are committed to precision, quality, and innovation. Join a team where craftsmanship meets opportunity. What We Offer Career Growth: Opportunities to advance within the Quality, Production, or Engineering departments. Training & Development: On-the-job training and mentorship to support your professional growth. Team Culture: Work with experienced professionals in a collaborative and supportive environment. Stability: Be part of a company with a long-standing reputation for excellence. Dyson Corporation offers a competitive pay range and industry leading benefits while also being committed to working with and providing reasonable accommodation to individuals with disabilities. Dyson Corporation is an equal opportunity employer - M/F/Veteran/Disability. We are a drug-free workplace and conduct pre-employment screening as a condition of employment.

Job Description Quality Control Associate The role is open to cover for a long term leave of absence. If the person does not return, there is potential for extension/ possible temp to perm. Must Have Chemistry Background - will be working in a chemistry lab Open to recent grads - up to 5 years experience Hours: 8am-5pm (site has flexibly and different shifts. the preference is an early shift. earliest start time 6:30am/9:30) Self-Motivator, willingness to ask questions and question is something is wrong. ideal candidate has 2 or 3: FT-IR, UV, Moisture content via Karl Fischer, and other wet chemistry analysis - pH and limit testing on bench. Compendial Testing - nice to have Lab is full service - 70-75% in lab 2 interview rounds: 1st virtual, 2nd on-site Your Role: The Quality Control department carries out release testing for raw materials, manufactured good, purchased materials for repackaging, and packaged good for sale. The department is made of an analytical Chemistry lab and Microbiology lab. In this position, analytical chemistry testing will be performed against a multitude of analytical specifications that would show the material either meets or does not meet requirements, which can include wet chemistry testing and/or instrumental analysis. Who You Are: Essential Job Functions and Responsibilities: An individual that is detailed oriented, has good communication skills, and is organized. Included in communication skills is the ability to ask questions and report findings/issues to senior analysts, team leads, supervision, or management when necessary. Within this role, being able to read and execute a variety of test methods put in place by the site, compendia, or customers is essential for success. Work closely with department supervisor and Team Leads to ensure that departmental tasks are completed on time. Follow all safety requirements and refer to MSDS for PPE and other safety guidance. Practice proper laboratory safety and waste disposal. Perform testing per documented procedure. Able to recognize out-of-spec (OOS) results and initiate OOS investigation. Pays attention to detail and brings issues to Team Lead(s) or Supervisors attention. Has the ability to take on smaller projects/reoccurring tasks with minimal oversight. Demonstrate Good Documentation Practices (GDP) and Data Integrity Principles. Knowledge of the chemistry and instrumentation for the following analysis: FT-IR, pH, Moisture content via Karl Fischer, and other wet chemistry analysis. Preferred Experience: Executing laboratory investigations Compendial testing: USP, EP, JP Ability to demonstrate critical thinking skills. Solution focused when faced with any problems or setbacks. Required Education, Qualifications, Experience: Bachelors degree in Chemistry or Life Science field with a minimum 2 years laboratory experience (academic or industry). -OR- Associate degree in Chemistry or other Life Science field with a minimum of 3 years experience outside of academic laboratories. Travel Requirements: N/A. Employment Testing Requirements: Pre/Annual-employment screening/medical monitoring. Pass background check, drug/alcohol screen. Physically/medically cleared to wear a respirator. Physical Requirements: The ability to stand for long periods of time. The ability to lift 25 lbs.

Job Description We are adding to our Pharmaceutical Quality Control Chemistry Staff. We are currently seeking entry level individuals to: Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP's and author Change Controls. Other general lab related duties as necessary. We are seeking individuals with: Bachelor's degree in Chemistry, Biochemistry, Biology, or related field One to two years' experience with hands on testing such as pH, titrations, determination of physical appearance, UV, IR and other wet chemistry tests. Instrumentation work with KF, HPLC, and GC, including instrumentation software a plus. Hands-on analytical chemistry experience Prior success working with regulatory, USP, GLP, GDP, and cGMP requirements. Ability to use Microsoft Suite of tools. Pharmaceutical experience a plus.

We are adding to our Pharmaceutical Quality Control Chemistry Staff. We are currently seeking entry level individuals to: * Perform analytical testing of raw material, in-process product, final product release and stability testing. * Clear documentation of test activities in approved worksheets and laboratory notebooks. * Execute mathematical calculations as outlined in test methods. * Assess data to determine if the material tested meets specifications. * Peer review of quality control data. * Participate in investigational testing and assist with root cause analysis. * Create and review SOPs and author Change Controls. * Other general lab related duties as necessary. We are seeking individuals with: * Bachelor's degree in Chemistry, Biochemistry, Biology, or related field * One to two years' experience with hands on testing such as pH, titrations, determination of physical appearance, UV, IR and other wet chemistry tests. Instrumentation work with KF, HPLC, and GC, including instrumentation software a plus. * Hands-on analytical chemistry experience * Prior success working with regulatory, USP, GLP, GDP, and cGMP requirements. * Ability to use Microsoft Suite of tools. * Pharmaceutical experience a plus.

Lingo Staffing is Now Hiring for a Quality Control Inspector in Hartville, OH Hours: 1st Shift: 7:30am- 4pm ($15) 2nd Shift: 3:30pm-12:00am ($16/hr) Days: Monday-Friday Pay: $15/hr (1st shift) • $16/hr (2nd shift) Short Description: We are seeking reliable and detail-oriented Quality Control Inspectors for a fast-paced plastics manufacturing environment in Hartville, OH. QC Inspectors are responsible for performing first-piece inspections, monitoring in-process quality, completing documentation, auditing packaging, identifying defects, and ensuring all production meets LMT's established quality standards. Candidates must be comfortable working independently, communicating across shifts, and maintaining accuracy throughout the shift. Requirements: Minimum 1 year experience in manufacturing or similar environment (plastics preferred) High school diploma or GED Ability to inspect parts visually and identify defects (splay, burns, shorts, contamination, flash, etc.) Ability to complete inspection paperwork, production sheets, and documentation accurately Able to use scales, gauges, check fixtures, and basic testing tools Ability to read, compare, and verify first-piece samples Strong attention to detail and accuracy Ability to follow written and verbal instructions Good communication skills; able to communicate across shifts Must be dependable and able to work with minimal supervision Must be willing to comply with a national background check ? Physical Requirements: This position requires the ability to walk extended distances (approximately 2.5+ miles per day) and remain on your feet for the entire shift. Employees must be able to bend, twist, stand, stoop, and lift as part of daily duties, with or without reasonable accommodation. We Are Seeking Candidates Who Have Held the Job Titles of: Quality Inspector, Quality Assurance Technician, Manufacturing Inspector, Production Inspector, or Assembly Quality Checker #INDAKR