Quality assurance chemist entry level jobs - 24 jobs

**Allied Mineral Products** is a leading manufacturer of monolithic refractories worldwide. We are seeking a **QA Tech, predictions** in our Columbus, Ohio location. the tech, under the direction of the Quality Supervisor and Quality Manager, predict formulas using current inventory to exceed customer's expectations while safely utilizing all applicable SOP's and following all company policies. **Duties and Responsibilities** + Effectively train and coach team members in all applicable SOP's and ensure that these SOP's are rigorously followed. + Mentor new employees. + Be a positive role model to all employees. + Predict all formulas using current lots of raw materials for manufacturing. + Print and verify correctness of all batch sheets for operations to use in production. + Apply re-blend, when possible, to all batches. + Work with batching to use up WIP, partial bulk bags, and Dead Stock raw materials. + Recommend measures to improve inspection and production methods, equipment performance, and quality of product. + Suggests changes in working conditions and use of equipment to increase efficiency of production. + Analyze and resolve work problems or assists workers in solving work problems. + Initiate or suggest plans to motivate workers to achieve work goals. + Maintain quality records (i.e. batch sheets and prediction and bulk batch print outs). + Work to eliminate all waste. + Help implement World Class Manufacturing and Quality initiatives. + Perform work of others as directed. This job description illustrates the types of duties performed in this job. It is not intended to be an exhaustive listing of each essential function of the job. Employees in this job may be required to perform other duties as assigned by supervisors although not specifically listed herein and those duties may be essential to the job. Because job content may change from time to time, the Company reserves the right to add and/or delete tasks from this job at any time. **Qualifications** + Must be physically and mentally fit for duty. + Must be at least 18 years old. + Dependable and able to maintain the attendance required to perform the job. + Must have work and educational experience to satisfy job competencies. Able to participate in external training. + Must be able to compute basic math functions: Calculate % of additives needed, Calculate % moisture present in sample, add, subtract, multiply and divide. Mut be able to operate using units of American money and weight measurement, volume, and distance. Must be familiar with metric units as well. + Ability to read, write, comprehend, and fully understand: SOPs, SDSs, labeling, safety and health regulations, and procedures within the job, this job group and the plant. + Ability to operate computerized equipment, read scales, recognize product problems, malfunctions, and patterns out of specification. + Thorough knowledge of Microsoft Office is essential, particularly Excel graphing and charting. + Good human relation skills and a practical approach to problem solving are necessary. + Ability to maintain close attention to detail and accuracy. **Working Environment** + The job is in a dusty and dirty environment. + Working in a hot and/or cold environment. + Shift varies from early morning start, evenings and weekends. + Required to wear respirator, safety glasses, hearing protection, and safety shoes. **Physical Requirements** + Work requires sitting, standing, and/or walking for long periods of time. + Must be able to qualify for and wear a respirator **Allied Mineral Products offers competitive wages, health, dental, STD, LTD, ESOP retirement plan and profit sharing. Passing a drug screen is required prior to starting work should an offer be made.** **Allied Mineral Products Holding, Inc. is an Equal Opportunity Employer/Veterans/Disabled.**

Cardinal Staffing Services, is immediately hiring for Quality Lab Technician in Defiance, OH. As a Quality Lab Technician for Cardinal Staffing, you will work in a fast-paced production and testing environment and be involved in key quality operations including: Quality inspections & dimensional measurement Product testing and sample evaluations Packaging validation (ISTA 6) Documentation, reporting, and data entry Cardinal Staffing Services is invested in their team members! All temporary employees are offered competitive compensation ($21/hr) as well as a benefits package including health insurance (medical, dental, and vision). Generous referral bonuses are available upon hire. Current Available Shifts: 1st Shift: 6:00 AM - 6:00 PM 3rd Shift: 6:00 PM - 6:00 AM Weekend overtime is twice a month. Responsibilities of the Quality Lab Technicians: Perform dimensional inspections using precision tools including gages, scanners, optical systems, and CMM-based equipment. Conduct product and packaging testing including ISTA 6 protocols; set up and operate vibration, drop, and compression equipment. Read and interpret engineering drawings, GD&T, specifications, and work instructions. Document quality findings, prepare reports, and maintain accurate testing records. Support production by identifying quality issues, assisting with containment decisions, and conducting preliminary investigations. Record and analyze test data; support continuous improvement activities. Maintain a clean and safe work environment and report any unsafe conditions. Required Qualifications of the Quality Lab Technicians: Experience with quality inspection, metrology tools, or laboratory/packaging testing. Ability to read and interpret engineering drawings and GD&T. High attention to detail and strong documentation accuracy. Analytical problem-solving skills and strong communication abilities. Proficiency with Excel or similar data-tracking tools. Ability to work independently and follow detailed procedures. Ability to work overtime as needed. Training/Experience in ISTA 6 Packaging Testing & Validation Preferred Qualifications: Experience in plastics, molding, packaging, or manufacturing environments. Familiarity with ISO 9001, GMP, or other quality systems. Experience supporting audits and corrective actions. Training or coursework in metrology, GD&T, SPC, or data analysis. About Cardinal StaffingAt Cardinal Staffing, a Surestaff Company, we are dedicated to helping individuals unlock their career potential through meaningful job opportunities. As a leading staffing agency in the light industrial and manufacturing space, we pride ourselves on connecting talent with top employers across the Midwest.We understand that finding the right job is about more than just a paycheck - it's about finding the opportunity that fits your skills, goals, and lifestyle. Here are the benefits you'll enjoy when you partner with us: Access to a wide range of job opportunities Competitive pay Health and Wellness Programs (including EAP) Medical benefits including medical, vision, dental, and prescriptions Electronic weekly pay Employee Advocacy & Personalized Job Support Notice Regarding the Use of Artificial Intelligence in Employment Decisions In accordance with state mandates, we are providing this notice to inform all applicants and employees that artificial intelligence (AI) tools may be used at various stages of our employment processes. This may include recruitment, screening, hiring, promotion, or other employment?related evaluations. AI tools may assist in reviewing application materials, assessing qualifications, or supporting decision?making. These tools do not replace human judgment; rather, they are used to support consistent and efficient evaluation. Our commitment to speed-to-hire means we work efficiently to get you placed in the right role, fast. If you're ready to take control of your career, explore exciting opportunities, and gain experience that lasts, then Surestaff is the place for you. Let's get started today! #IND1

About Us Signature Sauces is a family-owned manufacturing facility that packages various types of sauces for surrounding restaurants and grocery stores. Our facility is ever growing and we need friendly and reliable people to join us on our journey. No experience is necessary as we are willing to train on any position. If you're still wondering why you should join our team, here's a quick list of reasons: On the job training - no manufacturing experience required. Access to our comprehensive benefits package on day 1. Our pay is competitive; overtime is paid at time and a half. Benefits: 401(k) matching Dental insurance Disability insurance Employee discount at our sister company Stancato's Italian Restaurant Health insurance Health Savings Account Company Paid Life Insurance 5 Days Paid Time Off 2 Paid Sick Days Paid Holidays Paid Down Maintenance Days Retirement plan Vision insurance Free Catered Lunch Every Shift Company Provided Lockers & Lock Free Laundered Uniforms Performs a variety of duties relating to Quality Assurance in a facility specializing in sauces, dressings, marinades, and other fluid goods that is not only 3rd party inspected but USDA compliant. DUTIES AND RESPONSIBILITIES include the following: Day to day supervision of QA team (4-5 direct reports) Knowledge of food ingredient functionality Ability to read and analyze formulas Ability to write product specs and procedures Ability to collect and analyze data Must be able to use lab analytically equipment Knowledge and understanding of GMP's, SSOP's, food safety rules and regulations Knowledge of USDA and FDA regulations Complies with all company policies and procedures Must have excellent communication skills Understand and adhere to government regulations and documentation requirements Taking retains; of finished and raw product Oversees production QA checks and audits all data of daily production Handling all USDA paperwork Assurance of safe and sanitary practices upheld throughout the plant according to company policies and product specific events/tasks. Responsible for managing the Document Management Program Product testing against spec sheets Microbiological testing Master Sanitation Schedule Ensures Allergen Management Program is being followed Understands and can learn to write HACCP plans Ensures company Quality Management system is in place and up to date EDUCATION and/or EXPERIENCE Two to four years related experience and/or training; or equivalent combination of education and experience. This position requires a well organized individual that is self motivated and takes charge, is dependable and responsible, enjoys new opportunities and challenges, enjoys working with and developing people, deals with criticism calmly and effectively, is careful about detail and is thorough in completing tasks as assigned and on time, is flexible and open to change LANGUAGE SKILLS Able to read, analyze, and interpret ingredient specifications and recipes, general business periodicals, and or governmental regulations. Able to write and develop specific, accurate, and scalable recipes and procedure manuals. Able to effectively present information and respond to questions from customers, staff and owners. MATHEMATICAL SKILLS Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of weights and measures. Ability to apply concepts such as ratios, and proportions for ingredient and nutritional information. PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to reach with hands and arms; and talk or hear. The employee is required to regularly stand, stoop, kneel and walk. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus. WORK ENVIRONMENT The noise level in the office environment is usually quiet. Exposure to outdoor elements is possible on a daily basis. Must be responsible for dressing accordingly and being prepared for any type of weather.

Required Qualifications: * Valid Driver's license * Strong customer service skills * College degree in Chemistry or Natural Science , obtain a CDL Class B with hazmat and tanker endorsement within 6 months of employment * Perform physical functions per job requirements * Successfully complete a background check, drug test, and physical, by position * Per OSHA's Respiratory Protection Standard, 29 CFR 1910.34, employees in positions requiring respirators are required to meet facial hair standards. Preferred Qualifications: * Previous experience in Environmental Services (i.e. remediation, abatement, emergency spill response, etc.) Our Environmental Field Chemist is an entry level position into an exciting and rewarding career at Clean Harbors. Transitioning Military, this is a great opportunity to leverage your skills, experience, and training as you return to civilian life. This position is an entry level management position. From this role, there are approximately 15 other roles one can be promoted into within Clean Harbors. A significant number of our middle and senior management staff all started in this role, from less than 5 years ago to 30 plus years ago. Many others who have started in this role have significant positions within our customers as Environmental Health and Safety staff members at significant universities, pharmaceutical manufacturers as well as other customers. We will accelerate your training, so you learn the skills and knowledge to succeed in this position and start your career. You can work in any of our 200+ branch locations and can transfer internally. After successfully learning this position in approximately 18 to 36 months, then you will have the opportunity to move into a Salary Management position. Clean Harbors Technical Services * Waste Disposal - Comprehensive disposal of hazardous and non-hazardous waste at Company-owned facilities * Recycling Services - Extensive recycling, reuse and reclamation options for materials such as solvents, chemicals, oil and electrical equipment * Chemical Packing - Safe, efficient handling and disposal of the widest range of chemicals, including reactives and compressed gases * Household Hazardous Waste (HHW) Services - HHW collection programs of all types and sizes, facilitated by Clean Harbors expert personnel Clean Harbors is an equal opportunity employer. Clean Harbors is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, contact ******************** or **************. Clean Harbors is a Military & Veteran friendly company. Clean Harbors is committed to complying with applicable pay transparency laws and ensuring fair and equitable compensation. The posted salary range reflects the minimum and maximum target for this role. Final compensation may vary based on factors such as location, experience, skills, and business needs. In addition to the base salary, some roles may be eligible for bonus or incentive compensation and a comprehensive benefits package. #CH Key Responsibilities: * Ensure that Health and Safety is the number one priority by complying with all safe work practices, policies, and processes and always acting in a safe manner * Prepare computer generated packing lists, labels, manifest, and land disposal restriction notifications * Perform inspections of staging, accumulating and storage areas to ensure proper housekeeping procedures and compliance * Inspect storage area and drums for leaks or spills * Inspect drums for compliance with labeling regulations * Collects, segregates, and properly packages waste chemicals for disposal to maximize efficiency and maintain compliance * Executes Jobs at Clean Harbors customer locations including fortune 500 companies * Responsible for final preparation and approval of all projects before shipment in accordance with OSHA, EPA, DOT and company policies * Conducts projects/jobs according to site specific Federal, State, and local regulations and health and safety plans * Understand customer specific disposal restrictions/special packaging requirements * Sample and profile of new waste streams or any waste needing analytical testing * Ensures drum count is correct and that drum conditions are shippable in accordance our company's policies and procedure * Follow all local, state (provincial) and federal compliance regulations and rules * Safely operate vehicles in accordance with U.S. DOT, local, state (provincial) and federal requirements * Safely observe all corporate operating guidelines and procedures * Observe all company environmental health and safety operating guidelines * Perform other duties as assigned

Dubose National Energy Fasteners & Machined Parts has a unique opportunity for a Nuclear Quality Assurance Manager for their Cleveland, OH location. About Dubose National Energy: DuBose National Energy (DNES) is a major, strategic supplier of metal and metal products to the international nuclear and domestic military industries, including utilities, component manufacturers, contractors, & shipyards. You will find our products in most every nuclear power plant in the United States and many plants abroad. DNES is part of the largest steel distributor group in North America, Reliance, Inc., a Fortune 500 Company. Click on the "Watch DuBose Precision in Action" video to learn more - Watch DuBose Precision in Action ******************************************* Benefits are excellent and include: * Competitive Pay * 401(k) * 401(k) Matching * Dental Insurance * Employee Assistance Program * Flexible Spending Account * Health Insurance * Health Savings Account * Company Paid Life Insurance * Paid Time Off * Vision Insurance #IND Function in the Job Light work - Exerting up to 20 pounds of force frequently, and/or a negligible amount of force constantly to move objects. If the use of arm and/or leg control requires exertion of forces greater than that of sedentary work and if the worker sits most of the time, the job is considered light work. Job Function Responsibilities (including but not limited to): * Assist with Customer Audits of DNE F&MP and performance of Supplier Audits. * Provide technical information needed by employees and secondary processors. * Perform Quality system training of employees and maintenance of qualification records. * Perform Research and development of new item commercial grade dedication plans. * Determine testing and inspection requirements for: * Commercial Grade Dedication * Upgrade/Utilization of Unqualified source material * Military and Commercial requirements imposed by customer orders * Perform customer order reviews by evaluating Quality requirements of orders based on review of: * Material Specifications & Standards * ASME Code * Customer Specifications and Purchase Order requirements * Engineering Drawings * Ensure required Quality tests and inspections have been carried out. * Evaluate results of Quality tests and inspections. * Prepare and Issue Customer Certifications. * Review, evaluate and approve Vendor & Material certifications. * Review and approve internal quality documentation. * Be available outside of typical business hours for assisting with processing of emergency customer orders. Required Skills Nuclear manufacturing company has an opportunity for a Quality Assurance Manager. Candidate must be detail oriented and able to manage multiple ongoing items at one time. Position reports to the Director of Quality. This position will provide day-to-day oversite of personnel within the QA department, while constantly observing for process improvement opportunities. Successful candidate will assist the QA Staff with order review and certification processing in addition to management responsibilities. The candidate should have an intimate knowledge of fasteners & machined parts. Must have a strong ability to withstand high stress situations without losing composure or focus. Required: * Intimate knowledge of: * 10CFR50 Appendix B * 10CFR Part 21 * NQA-1 * ASME Section III (Subsection NCA) * Fasteners & Machined parts * Familiarization with: * Regulatory Guide 1.28 * NEI 14-05 * EPRI 5652 * ASME Section II * ASME Section III: NX-2000, and NX-4000 * GD&T and print reading. * Associates or Bachelors Degree. * Three years minimum in Managerial Quality Assurance. * Audit experience and qualification as an NQA-1 Lead Auditor. * Proficiency with Adobe PDF, Microsoft Word, Excel, and Outlook. Preferred experience: * Engineering Degree and equivalent work experience. * Experience with military specifications. * Experience in military supply (e.g. EB2678 and MIL-I-45208), and/or steel applications such as supply of raw steel, piping, and/or fasteners. Physical Requirements Stand or Sit(Stationary position), Walk(Move, Traverse), Use hand/fingers to handle or feel (Operate, Activate, Use, Prepare, Inspect, Place, Detect, Position), Climb (stairs/ladders) or balance (Ascend/Descend, Work atop, Traverse), Stoop, kneel, crouch, or Crawl(Position self(to), Move), Talk/hear(Communicate, Detect, Converse with, Discern, Convey, Express oneself, Exchange information), See (Detect, Determine, Perceive, Identify, Recognize, Judge, Observe, Inspect, Estimate, Assess), Pushing or Pulling, Reaching, Repetitive Motion

About Us Signature Sauces is a family-owned manufacturing facility that packages various types of sauces for surrounding restaurants and grocery stores. Our facility is ever growing and we need friendly and reliable people to join us on our journey. No experience is necessary as we are willing to train on any position. If you're still wondering why you should join our team, here's a quick list of reasons: On the job training - no manufacturing experience required. Access to our comprehensive benefits package on day 1. Our pay is competitive; overtime is paid at time and a half. Benefits: 401(k) matching Dental insurance Disability insurance Employee discount at our sister company Stancato's Italian Restaurant Health insurance Health Savings Account Company Paid Life Insurance 5 Days Paid Time Off 2 Paid Sick Days Paid Holidays Paid Down Maintenance Days Retirement plan Vision insurance Free Catered Lunch Every Shift Company Provided Lockers & Lock Free Laundered Uniforms Performs a variety of duties relating to Quality Assurance in a facility specializing in sauces, dressings, marinades, and other fluid goods that is not only 3rd party inspected but USDA compliant. DUTIES AND RESPONSIBILITIES include the following: Day to day supervision of QA team (4-5 direct reports) Knowledge of food ingredient functionality Ability to read and analyze formulas Ability to write product specs and procedures Ability to collect and analyze data Must be able to use lab analytically equipment Knowledge and understanding of GMP's, SSOP's, food safety rules and regulations Knowledge of USDA and FDA regulations Complies with all company policies and procedures Must have excellent communication skills Understand and adhere to government regulations and documentation requirements Taking retains; of finished and raw product Oversees production QA checks and audits all data of daily production Handling all USDA paperwork Assurance of safe and sanitary practices upheld throughout the plant according to company policies and product specific events/tasks. Responsible for managing the Document Management Program Product testing against spec sheets Microbiological testing Master Sanitation Schedule Ensures Allergen Management Program is being followed Understands and can learn to write HACCP plans Ensures company Quality Management system is in place and up to date EDUCATION and/or EXPERIENCE Two to four years related experience and/or training; or equivalent combination of education and experience. This position requires a well organized individual that is self motivated and takes charge, is dependable and responsible, enjoys new opportunities and challenges, enjoys working with and developing people, deals with criticism calmly and effectively, is careful about detail and is thorough in completing tasks as assigned and on time, is flexible and open to change LANGUAGE SKILLS Able to read, analyze, and interpret ingredient specifications and recipes, general business periodicals, and or governmental regulations. Able to write and develop specific, accurate, and scalable recipes and procedure manuals. Able to effectively present information and respond to questions from customers, staff and owners. MATHEMATICAL SKILLS Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of weights and measures. Ability to apply concepts such as ratios, and proportions for ingredient and nutritional information. PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to reach with hands and arms; and talk or hear. The employee is required to regularly stand, stoop, kneel and walk. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus. WORK ENVIRONMENT The noise level in the office environment is usually quiet. Exposure to outdoor elements is possible on a daily basis. Must be responsible for dressing accordingly and being prepared for any type of weather.

About Us Signature Sauces is a family-owned manufacturing facility that packages various types of sauces for surrounding restaurants and grocery stores. Our facility is ever growing and we need friendly and reliable people to join us on our journey. No experience is necessary as we are willing to train on any position. If you're still wondering why you should join our team, here's a quick list of reasons: On the job training - no manufacturing experience required. Access to our comprehensive benefits package on day 1. Our pay is competitive; overtime is paid at time and a half. Benefits: 401(k) matching Dental insurance Disability insurance Employee discount at our sister company Stancato's Italian Restaurant Health insurance Health Savings Account Company Paid Life Insurance 5 Days Paid Time Off 2 Paid Sick Days Paid Holidays Paid Down Maintenance Days Retirement plan Vision insurance Free Catered Lunch Every Shift Company Provided Lockers & Lock Free Laundered Uniforms Performs a variety of duties relating to Quality Assurance in a facility specializing in sauces, dressings, marinades, and other fluid goods that is not only 3rd party inspected but USDA compliant. DUTIES AND RESPONSIBILITIES include the following: Day to day supervision of QA team (4-5 direct reports) Knowledge of food ingredient functionality Ability to read and analyze formulas Ability to write product specs and procedures Ability to collect and analyze data Must be able to use lab analytically equipment Knowledge and understanding of GMP's, SSOP's, food safety rules and regulations Knowledge of USDA and FDA regulations Complies with all company policies and procedures Must have excellent communication skills Understand and adhere to government regulations and documentation requirements Taking retains; of finished and raw product Oversees production QA checks and audits all data of daily production Handling all USDA paperwork Assurance of safe and sanitary practices upheld throughout the plant according to company policies and product specific events/tasks. Responsible for managing the Document Management Program Product testing against spec sheets Microbiological testing Master Sanitation Schedule Ensures Allergen Management Program is being followed Understands and can learn to write HACCP plans Ensures company Quality Management system is in place and up to date EDUCATION and/or EXPERIENCE Two to four years related experience and/or training; or equivalent combination of education and experience. This position requires a well organized individual that is self motivated and takes charge, is dependable and responsible, enjoys new opportunities and challenges, enjoys working with and developing people, deals with criticism calmly and effectively, is careful about detail and is thorough in completing tasks as assigned and on time, is flexible and open to change LANGUAGE SKILLS Able to read, analyze, and interpret ingredient specifications and recipes, general business periodicals, and or governmental regulations. Able to write and develop specific, accurate, and scalable recipes and procedure manuals. Able to effectively present information and respond to questions from customers, staff and owners. MATHEMATICAL SKILLS Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of weights and measures. Ability to apply concepts such as ratios, and proportions for ingredient and nutritional information. PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to reach with hands and arms; and talk or hear. The employee is required to regularly stand, stoop, kneel and walk. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus. WORK ENVIRONMENT The noise level in the office environment is usually quiet. Exposure to outdoor elements is possible on a daily basis. Must be responsible for dressing accordingly and being prepared for any type of weather.

Job Title: Manager, Quality Assurance Job Type: Full-Time About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them. Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Quality Assurance Manager to join our team. In this role, you will be responsible for the staffing, organization, operation, budget, and maintenance of all activities related to QA monitoring of production activities, assuring that products are manufactured in compliance with cGMP guidelines, USP and FDA, EU requirements. In addition, you will be responsible to direct batch record review, control and release, handle investigation process (CAPA) assuring that any discrepancies are investigated thoroughly and in a timely manner. Key Responsibilities: Regular and predictable onsite attendance and punctuality. Directs the batch record review process. Makes final accept/reject disposition on product lots. Assures batch is manufactured in compliance with NDA/ANDA/EU, cGMP and Validation parameters. Ensures that records are reviewed and released in a timely manner. Coordinates communication for status of lots and status of and resolves issues related to accept/reject disposition of batches. Places lots on HOLD if Quality issues are detected and notifies senior management. Coordinates destruction of rejected finished goods and assures destruction occurs in a timely manner. Expedites and prioritizes product releases by coordinating the Review, testing, and releases with site management to meet customer service requirements. Conducts routine investigation and departmental meetings to facilitate the performance of release function. Manages personnel for in-process filling and inspection/packaging monitoring Provide QA oversight of Operation for the entire Manufacturing process, supporting Clean room technicians and production technicians as needed to identify and address product quality compliance issues as they arise. Provide training and assistance to all Clean room and operation personnel for NCR, CAPA and Change Control. Provides QA review and approval of manufacturing investigations assuring timely review, follow-up, tracking and trending of MIRs. Perform Root Cause analysis and assure corrective action (CAPA) implementation associated with manufacturing investigations. Provide guidance to the investigation scientists on reporting and metrics required for different levels within organization. Performs QA review and approval of LIR's (Laboratory Investigation Reports). Reviews and approves SOPs, Job-Aids, Specifications, FMEA documents, Change Controls and Validation documents (Protocols, GTR's, Commissioning Documents, FAT's), engineering documents. Establish a qualification and Requalification program for Clean Room Certification and Recertification, for ISO 5 and 7 environments. Develop and implement Quality Systems Improvements through participation in cross functional teams. Performs and/or assures cGMP and technical training for and certification of staff. Assists the QA management in developing on department budget. Attends interdepartmental meetings representing Quality Assurance and makes sound quality decisions. Manages attendance records for all direct reports. Qualifications: We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: Minimum: Bachelor's degree in Pharmacy, Biology, Chemistry or a related field Preferred are beneficial [List the required qualifications such as education, skills, and experience] Preferred Qualifications: Additional college courses in Microbiology, cGMPs, Statistics or Quality Management Skills: Must have history of strong documentation skills and attention to detail Familiarity with cGMPs and CFR for US and EU Excellent organizational skills and ability to multi-task and perform work in a timely manner Demonstrates ability to lead a department, projects and meetings effectively Ability to work in a team environment with good communication skills and ability to communicate effectively with peers, and senior management General computer skills and ability to prepare presentations and address large groups Demonstrated attention to details and accuracy The incumbent must possess the strong knowledge of quality assurance systems. Dealing with FDA, third party during inspection is a must Compensation: Base Salary: $92,850 to $158,450 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process. What We Offer*: Annual performance bonus, commission, and share potential Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries 3 personal days (prorated based on hire date) 11 company paid holidays Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits Employee discount program Wellbeing rewards program Safety and Quality is a top organizational priority Career advancement and growth opportunities Tuition reimbursement Paid maternity and parental leave *Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

As the North American headquarters for G-TEKT Corporation, Jefferson Industries actively participates in the Global Automotive Industry. As part of our involvement, Jefferson Industries Corporation offers design and development for press dies and other tools necessary to produce automotive products. We embrace programs for product development including product design review and Advanced Product Quality Planning. Our facilities support high quality product manufacturing, and we provide a timely and flexible approach to meeting the needs of our customers. We are actively seeking Quality Assurance Metrology Coordinator to join our Quality Assurance Department on 1st Shift (core schedule, Monday through Friday 7:30 am to 4:00 pm or 6:00 am to 2:30 pm). Position Description Note - The following is not intended to be all-inclusive. Business conditions change and develop, as well as the individual develops requiring flexibility, straight forward communication, and forward thinking to prepare and adapt to change. The individual is expected to grow within these guidelines focusing on excellence within the role. You work in a friendly and courteous manner providing an accurate flow of communication. (both internal and external). This will prepare the individual for potential future positions as the business needs require and the individual demonstrates their contribution and potential. Your position is responsible for providing professional and dependable service and to develop our Team's capability to deliver JIC's key objectives to all our customers and suppliers. You will have a complete understanding of all customer/supplier requirements. Your understanding of JIC's Management Policy “To become the best supplier” through our philosophy and guiding principles “Safety, Morale, Quality, Cost & Delivery” is imperative. This role will be measured against specific targets as noted in the departmental business plan. SUMMARY: THE QUALITY ASSURANCE METROLOGY COORDINATOR IS RESPONSIBLE FOR THE COORDINATION OF ACTIVITIES FROM THE TIME OF INITIAL PRODUCT DESIGNS THROUGH THE DESIGNATED MODEL BUILD OUT. DUTIES ARE BASED ON ENSURING ON-TIME DELIVERY OF QUALITY EQUIPMENT AND ACHIEVEMENT OF NEW MODEL EVENT AND MASS PRODUCTION ACCURACY GOALS SET BY THE CUSTOMER. ASSOCIATE IS RESPONSIBLE FOR THE MANAGEMENT OF THESE ACTIVITIES AS IT RELATES TO MEETING COMPANY GOALS BY PERFORMING THE FOLLOWING DUTIES PERSONALLY OR THROUGH DEPARTMENTAL MANAGEMENT TEAM. Position Responsibilities Include: SAFETY Ensures each member of assigned team supports safety program by promoting safety and enforcing safety policies. Ensures safety of all measurement systems and inspection fixtures meet JIC safety standards. QUALITY ASSURANCE Ensures measurement systems, programs, and fixtures are in place prior to the start of new model trial events in order to meet quality expectations. Communicates with other departments to assure smooth operation. Participates in customer new model drawing reviews and suggests design countermeasures to improve quality and productivity. Coordinates New Model Quality activities to meet customer requirements including: Reviews, develops and approves part quality requirements in the early design stage. Facilitates inspection fixture development and manufacturing including preparation of quality plan, development of concepts, procurement, calibration, and buy-off. Develops Level 1 deliverable Inspection Data Sheets. Supports quality activities before, during, and after trial events Evaluates part quality at events and customer build meetings; provides input and implements countermeasures for tool and equipment Support scanning activities and dimensional accuracy improvements throughout the model life of all parts (stamping, welding COST Supports department budgets and costs. Utilizes best practices when integrating New Model equipment and process improvements. Minimizes the cost to fabricate, purchase and maintain equipment. Promotes efficient use of time during new model trial events and any quality activities. DELIVERY Maintains software licensing and calibration on all equipment. Ensure customer data requirements are met prior to part shipment. MANAGEMENT Helps to develop current best practices for measurement systems. Researches new technologies and strategies that can be utilized to improve products and processes. Supports the department business plan. Demonstrates ability to work independently with little or no supervision. Accepts job assignments and changes in a positive manner, takes responsibility for own and team's performance and job assignments. Seeks out new assignments and finds better ways to complete tasks. Makes sound and prompt decisions. Other duties may be assigned. Compensation: Weekly Pay Holiday Pay Shutdown Pay Summer - around July 4th holiday Winter - around Christmas/New Year's holiday Bi-annual TEAM Achievement Bonus Annual Profit Share Bonus Benefits: Paid vacation Three (3) medical options to allow you the flexibility to choose what level of coverage best fits you and your family's needs Flexible Spending Accounts (medical and dependent care) Free Dental & Vision (must be enrolled in medical benefit) Voluntary Supplemental Life Insurance Hospital Indemnity Group Accident Critical Illness Company-paid Short-term Disability Long-term Disability Basic Life & AD&D Employee coverage - 2 times annual base earnings Spouse - flat $10,000 Child - flat up to $5,000 401k Retirement Traditional Contribution ROTH Contribution Company Match 401k Retirement Profit Share Funded 100% by Company based on a percentage of eligible earnings each quarter Eligible regardless of participation in 401K Retirement Referral Bonus Tuition Reimbursement Safety Equipment Reimbursement (safety boots & prescription safety glasses) Company-paid uniforms, including laundering Tickets@Work - web-based discount program (hotels, car rental, tickets, etc.) Qualifications Essential Skills and Competencies: Able to collaborate cross functionally with all company divisions, and all levels of associates Clear and concise communication skills (verbal and written) Ability to present ideas with evidence Able to quickly identify defects and solve problems with equipment and process to prevent quality, delivery or safety concerns Ability to do root cause analysis on complex issues Must be detail oriented Able to plan and meet short and long-term deadlines Maintain an acceptable attendance record Advanced Experience with Microsoft Office (Excel, PowerPoint, Word) - able to create, read and understand and analyze intricate formulas, and create charts and graphs Strong organizational skills Exceptional time-management skills Experience with a Romer Arm or other scanning technology, preferred Advanced experience with Polyworks software, preferred Experience with Catia or CAD, preferred Qualifications: Technical School Certification and/or Associate's Degree, preferred 1 -3 years previous experience in leadership role Must successfully pass pre-employment drug screen and physical JIC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Union Supply Group Union Supply Group Since its founding in 1991, Union Supply Group has grown into the most innovative and price sensitive supplier of commissary goods and services. Union Supply provides food, apparel, footwear, electronics, and personal-care products to State, Federal and County correctional institutions nationwide. Work with a team culture of respect, career growth, job security and competitive compensation! We strive for a positive environment where everyone can grow and learn at every step of their journey. With Union Supply Group you will know you will be entrusted with making a great impact on the organization. Quality Control Inspector The Quality Control is responsible for ensuring any warehouse inventory, entering and leaving the building, is accurately accounted for and documented via the appropriate Warehouse Management System (WMS) processes. Report any discrepancies to the DC Manager and Inventory Specialist with specifics and documentation for justification. Adhering to prescribed USG standards, policies, and procedures within the company and when performing any inventory control functions within the WMS. ESSENTIAL DUTIES AND RESPONSIBILITIES Ability and knowledge to accurately perform all inventory control operations as required; physically and via the warehouse management system Bill Of Materials Procedure - WMS Maintain Master Planning Menu - Planned Orders: to ensure adequate levels of inventory are available, via inter-company and outside vendor, to cover preset min/max assessments Create BOM journals, and record the change of bulk product to finished item number Remove Expired/Quarantined product from available-to-sell inventory Perform Cycle Count Adjustments as needed and record in the WMS Create Counting Journals for verification of proposed product quantities as needed Create Movement Journals for removing, adding and re-location of product product location set-up and movements Poor rotation, damaged product, improper stacking, wrong product in position, etc. Cycle Count all warehouse product as prescribed by company policy and frequency benchmarks Perform Bin Audits and document discrepancies Maintain Liquidation process as necessary, per prescribed company policy Responsible for any product Returns Inspection and evaluation, processing for return to stock, destroying of unusable inventory, etc., per prescribed company policy Investigate, document and take corrective action on Departmental Lead, Picker or Replenishment Personnel reported product discrepancies Damaged, expired or short dated product, spoilage, etc. Ensure your lift equipment, RF Guns, radios, knives and tools are returned to the their proper charging and/or storage locations at end-of-business each day Ability to operate forklift and other necessary equipment required in performing daily inventory functions Work with Warehouse Supervisor to improve labor efficiencies of the inventory control operations Provide Warehouse Supervisor with suggestions/proposals for cost effective operation enhancements Maintain monthly reports of inventory control statistics Complete miscellaneous duties, tasks, and projects as assigned by the Distribution Center Manager or Corporate - Inventory Specialist. We offer: Career advancement. We continuously strive to upskill our employees and offer internal employees the opportunity to thrive and grow within the company. Training & New skills. You'll learn. The opportunities are limitless. You will be given the opportunity to learn beyond your expertise and cross train to allow you to expand your knowledge base. Team environment. At Union Supply Group, we are a Team. It isn't uncommon to work on small or large teams where everyone supports each other. Benefits Continued: Competitive wage Team environment Good Work-Life Balance Healthcare (medical, dental, vision) 401(k) savings plan Paid Time Off (PTO) Holiday pay opportunities Birthday PTO On-the-job training and skills development Employee Assistance Program Qualifications JOB QUALIFICATIONS Ability to understand basic math. Inventory control and replenishment. Ability to read, understand orders, and write legibly. Be able to lift 30+lbs Equal Employment Opportunity Policy Union Supply Group provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. E-Verify This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9.

EverStaff, a specialized recruiting firm, is actively searching for a potential candidate for a Direct Hire position with one of our top clients. This position entail direct employment with the client that offers exceptional work culture, benefits, PTO, and growth potential. Title: Quality ManagerPay Rate: $70,000/yr. - $80,000/yr.Shift: 1st JOB SUMMARY Responsible for quality inspection procedures and testing for raw materials and finished products. Conduct daily monitoring and enforcing Good Manufacturing Practices in Production and Warehousing. Verify compliance of all applicable regulatory standards, including but not limited to FDA, ODA, HACCP and FSMA standards. PRIMARY RESPONSIBILITIES Design and implement quality inspection procedures for raw materials and finished products. Daily monitoring of all quality test results for raw materials and finished products. Establish corrective and preventive actions when needed. Supervise and guide the work of the laboratory technician Define and implement Good Manufacturing Practices in Production and Warehousing. Conduct daily monitoring and enforcing of GMPs. Review and validate certificate of analysis (COA) for all incoming materials and perform quality tests as needed. Verify compliance of all applicable regulatory standards, including but not limited to FDA, ODA, HACCP and FSMA standards. Perform and review all applicable environmental and sanitation testing Keep records of quality reports, statistical reviews, and relevant documentation KNOWLEDGE AND SKILL REQUIREMENTS FSQA Certification Thorough knowledge of methodologies of quality assurance and standards BSc/BA in relevant field Excellent numerical skills and understanding of data analysis/statistical methods Good knowledge of MS Office and databases Great attention to detail and a result driven approach Excellent organizational and leadership abilities KEY COMPETENCIES Critical thinking and problem-solving skills Excellent fault-finding skills Excellent planning, organizational and time management skills Willingly provides assistance/support to others If you feel you have the above qualifications, please apply for immediate consideration. All qualified applicants will receive consideration for employment without regard to race, color, religion, ethnicity, national origin, sex, gender identity, sexual orientation, disability status, protected veteran status or any other protected status under the law. EverStaff is an equal opportunity employer (M/F/D/V/SO/GI)

System One is seeking a NDE Quality Oversight professional for a long-term contract to hire, full time opportunity, onsite in Orville, Ohio. The ideal candidate will have a strong background in nuclear quality assurance, NDE, and fabrication operations, with a deep understanding of NQA-1 and ASME standards. This role will focus on ensuring quality through oversight, auditing, and compliance within a nuclear fabrication environment. Responsibilities: + Provide quality assurance oversight of NDE (Non-Destructive Testing) and fabrication operations. + Ensure compliance with NQA-1, ASME, and other nuclear quality standards. + Conduct audits to maintain quality program integrity. + Review and approve procedures, ensuring alignment with applicable standards. + Generate and review final quality packages for completeness and accuracy. + Collaborate with teams to identify and resolve quality issues. Qualifications: + Required Experience: + Hands-on expertise in nuclear quality programs, including NQA-1 and ASME standards. + Proficiency in NDE techniques and fabrication processes. + Experience in auditing, procedure review, and final package generation. + Must be local to Orrville, OH or willing to commute (no per diem provided). + Strong communication and organizational skills. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #161-Managed Staffing Charlotte System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Who We Are Founded in 1971, Clifton Steel Company (the Company) is a nationally recognized leader in the manufacturing of military armor plate and commercial specialty steel products. Clifton has served the armor plate market for over forty years and is the premier industry supplier of many of its commercial products. The Company is a specialist in abrasion and impact resistant steel fabrication, particularly for quenched and tempered alloy and manganese steel. As a result of investments in production capabilities, access to critical materials and strong customer relationships, Clifton has established a defensible and sustainable market position. What You Will Do/Need (Job Summary) Quality Assurance Technician is responsible for the verification and validation of Clifton Steel's production processes through inspection and containment of nonconforming product. This position will adhere to all requirements of the ISO 9001 Standard and any regulatory/statutory requirements. As part of the Quality Department, this position will be responsible for providing feedback on nonconformances of product and processes, supplier and vendor receiving inspections, verifying/creating material certifications and inspection reports, and providing support to all other functions. Responsibilities (Essential Duties and Responsibilities) Conduct inspections (including receiving, first article, in-process, and customer-specific requirements) and identify nonconformances to perform DMR processing of nonconforming materials Verify and validate materials and products to all documentation and testing requirements, including but not limited to: mill certs, heat treat certs, COCs, coil chemistries, cert verification and correction, 3 rd party material reports, industry-specific reports, industry-specific specifications, ASTM specifications, internal communications, etc. Uphold and fulfill requirements of the Work Instructions and Procedures within the QMS (with the occasional creation of these documents being required) and have a firm understanding of the ISO 9001 standard and its application Document, generate, and effectively communicate SPNRs for supplier material nonconformances, received goods nonconformances, specification nonconformances, etc. Must be able to read engineering drawings, translate requirements, adhere to specifications, and identify opportunities for and submit Engineering Change Requests for drawings and/or part descriptions requiring revision Must be able to read and accurately use multiple gages including calipers, micrometers, taper gages, tape measures, radius gages, angle gages, Brinell hardness testers, etc. while maintaining internal gaging validation records against NIST standards Maintain physical and electronic storage of data and applicable supporting documents, regarding Quality requirements Create, verify, and/or properly store material certifications from vendors and internal heat treat operations Conduct manufacturing process walk-through audits, communicate findings/nonconformances, and follow-up on implementation and effectiveness of corrections. Above all this position will be responsible for performing to expectations of the directives and goals set by the Quality department or executive management staff within Clifton Steel. The requirements of the position, listed above, are not intended to be an all-inclusive list. The position must be able to work in a dynamic environment with multiple inputs from several sources, while maintaining a commitment to the QMS. The individual may periodically be asked to perform additional tasks beyond the responsibilities listed. Minimum Qualifications (Knowledge, Skills, and Abilities Required) High School Diploma or GED equivalent What Will Make You Special (Preferred Knowledge, Skills, and Abilities) Drive for continual process improvement in all endeavors of Clifton Steel Co. Proficient verbal and written communication skills within Clifton Steel Co. and externally Ability to learn quickly and apply lessons learned to everyday situations Characteristics of the Position (Competencies) Adhere to and encourage others to uphold Clifton Corporate Behaviors, all company rules, regulations, and policies and enforce them throughout the facility in everyday activities Detail-oriented approach with understanding of instructions in a variety of forms including written, oral, or scheduled tasks Ability to recognize opportunities for improvement and propose/implement effective solutions to problems Carry oneself with competence and excellence in work presentation and preservation; while fulfilling daily activities in a professional, respectable manner with consideration towards other roles and individuals within the organization Must be able to read engineering drawings and apply the appropriate measuring technique(s) for validation Ability to work alone, or in a group, to complete tasks in a thorough, timely manner Proficiency in Microsoft Office package (Word, Excel, PowerPoint), company ERP system, and general organization of public shared drive through Windows explorer Perform the duties of the position with the intention of strengthening the department's standing, while establishing practices and systems to be utilized for the foreseeable future Physical Demands and Work Environment While performing the duties of the position, the employee will be required to: Stand, walk, sit, twist the body, reach with hands/arms, climb stairs, balance, stoop, kneel, and/or crouch/crawl Use hands repeatedly to handle, move, and/or lift objects up to 50lbs Communicate, talk, and hear in an environment with reasonable manufacturing noise levels Routinely requires use of standard office equipment such as computers, phones, scanners, etc While performing the duties of the position, the work environment: May be exposed to uncontrolled climate on the production floor or shipping areas Is frequently changing between an office setting and production environment Is exposed to dirt, dust, and debris caused by the manufacturing processes within the facility The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position Position Type and Expected Hours of Work This is a full-time position that will operate during first shift production. As the responsibilities of the position or demands of the company evolve, the hours may vary to accommodate off-shift needs. Expected hours are 8:00am to 5:00pm, but may be adjusted to accommodate the needs of the department, the individual, or Clifton Steel Co. These hours include up to an hour lunch break, per the demand and availability of the individual. Travel This position requires no planned travel Clifton Steel Company is an EEO Employer - M/F/Disability/Protected Veteran Status View all jobs at this company

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Job Summary The Analyst, QC Aseptic Control is responsible for reviewing sampling and laboratory data and autonomously performing tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Grade A aseptic environment and in a laboratory setting, and includes the maintaining of gowning qualification. This is a Monday - Friday Day shift position. Position Responsibilities: Supports coordination of workflow for Environmental Monitoring team. Verifies QC data, while monitoring for trends and abnormalities. Trained and able to perform all Environmental Monitoring technician responsibilities (including maintaining aseptic qualification) when needed. Review completed production documentation (for example: logbooks) for quality, completeness, and cGMP (Good Manufacturing Practices) compliance. Troubleshoots methods and processes. Train others on systems, software, equipment, machines, procedures, and/or processes. Answer compliance and process questions from others. Communicate policies and procedures to employees. Fill in for Analyst II/Team Lead when absent. Gather, organize, and communicate operational information to others. Lead and coordinate investigations and studies with little supervision. Lead process improvement activities and teams to meet strategic goals. Other duties that support Environmental Monitoring, Operations, or Laboratory processes may be assigned. Minimum Qualifications: General experience in a pharmaceutical production or quality control environment (GMP/GDP) Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language. Good attention to detail is required. Must be capable of keeping accurate records and performing mathematical calculations Preferred Qualifications: Bachelor's degree, scientific discipline Significant experience in a sterile or cGXP environment Lab experience Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $24.00 - $34.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

* Branch Details We are currently hiring Quality Inspector to join our Akron team! Open interviews 9am-1pm | Partners Personnel 286 E Exchange St Akron OH | (330)991-5010 * Sorting and counting product * Visual inspection * Verifying quality assurance * Documenting * Support production Plastics experience is a plus! Pay: $16-17 Based on experience Employee Perks: * Weekly Pay * Benefits Day One * Referral Bonus * Busline Accessible * Opportunity for advancement * Paid training Apply today, start tomorrow! #AkronBranchCA Akron OH 3183

???????Quality Control Inspector duties and responsibilities A Quality Control Inspector performs assessment, documentation and organization tasks to support the efficiency and effectiveness of their organization's supply chain. Their duties and responsibilities include: Inspecting output samples using industry-appropriate methods, such as comparing to standards, measuring dimensions and examining functionality Checking that the assembly or production line adheres to standards and procedures and complying with legal requirements Reviewing blueprints and specifications to compare to produced goods Recording inspection results by completing reports, summarizing re-works and wastes and inputting data into quality database Training the production team on quality control measures to improve product excellence Proposing improvements to the production process Monitoring the use of equipment to ensure it is safe and discard any that do not meet requirements Updating job knowledge by engaging in educational opportunities and regular training Keeping measurement equipment operating accurately by following calibration requirements and calling for repairs

Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? * Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. * Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. * Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, or Not at All. * Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Field Chemist - Traveling Responsible for sorting, and transporting hazardous and non-hazardous materials and waste. Will ensure compatibility and safety processes at all time for each job and lab pack services provided to customers. Heavy travel for extended periods of time will be required as this position will fill in at outside locations as necessary. Essential Functions & Requirements: * Ensures Health & Safety is the number one goal by following policies, processes, and acting in a safe manner at all times. * Assist in the segregation of chemicals by hazard class; packing compatible materials in appropriate containers and preparing for transportation; completing necessary paperwork per job. * Determines and loads supplies needed for job completion and travels to various industry, laboratory, and school sites to perform lab pack services. * Assists in characterizing materials at field project sites. * Follows proper placarding and load segregation requirements when transporting hazardous materials. * Develop good client relations by effectively communicating with Customers. * Directs Field Technicians/Drivers assisting with waste collection. * Introductory knowledge of high hazard materials management /assessment and cylinder handling. Education: * Four-year college degree (Science or environmental majors preferred) or 2+years related experience required. Experience: * Prior lab packing or environmental waste experience preferred. Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. 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 protected veteran or status as a qualified individual with a disability. A post-offer drug screen will be required.

Full-time, Holland, OH. Onsite first 60 days and then move to hybrid rotation. Midwest Tape | Hoopla For over 30 years, Midwest Tape has served libraries and their patrons with unparalleled access to the best content available in the media world. Our digital offering, hoopla Digital, combines the media and library expertise of Midwest Tape with the latest in web and mobile technology, delivering an all-in-one experience to the library world. As hoopla continues to grow on a global scale, we are expanding our team. At Midwest Tape, we know our people are the reason for our success. We value our employees and believe in empowering them to help them thrive. We offer competitive pay and benefits, a healthy work/life balance, and appreciation for a job well done. Position Summary: Conduct manual or automated Quality Assurance evaluation of all hoopla digital products. Identify, analyze, and document problems with content playback as discovered within QA process as well as those reported by patrons or customers. Primary Duties and Responsibilities: To perform this position successfully, an individual must fulfill the knowledge, skill, and/or ability requirements listed below: Conduct QA evaluation of digital content on test programs, websites, and mobile devices for hoopla products that include: Audiobooks eBooks Comics Music Video Review applicable reports and administrative tools for the following and work to correct deficiencies found: Missing digital media assets, artwork, or metadata Lendability and playability of content Create and maintain databases of known problems. Work cooperatively with others in the organization in problem identification and resolution Troubleshoot content that has failed evaluation or that has been reported through patron errors. Skills: Excellent focus and strong attention to detail Self-directed with the ability to work with minimal supervision and meet goals Effective communication skills, both oral and written, including the ability to communicate technical issues Experience of working both independently and in a team-oriented, collaborative environment. Excellent computer skills, including but not limited to: Media Playback and Testing programs. Preferred Education Requirements: Associates or Bachelor's Degree in related field. Preferred Experience: 0-2 years of experience quality assurance or relevant experience. Working knowledge of digital media entertainment services Familiarity with mobile devices such as Apple's iPad/iPhone and Android smart phones/tablets. General knowledge of digital compression formats/techniques Physical Requirements/Work Environment: The work environment characteristics and physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Ability to regularly sit for extended periods of time. Perform repetitive motion-type tasks Must be physically present for meetings, presentations, and training. Ability to work on site in a collaborative team environment. Employee may be exposed to graphic content in the course and scope of this position, including but not limited to, explicit language, graphic descriptions or depictions of violence and graphic descriptions or depictions of sex or sexual acts. The company does not intend for any such exposure to employee and has implemented automated quality control systems to try to identify and remove explicit content prior to employee's review. However, the system is not infallible. Report such content for identification and determination of removal. By agreeing to continue to be employed in this role, employee acknowledges that company is not responsible for such content or employee's response to the content. Benefits: Medical, dental, & vision insurance 401k + match Profit sharing Paid vacation and personal time Flex time 10 paid holidays Company performance bonus Holiday bonus Paid time to volunteer Training & career development opportunities All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. We are currently unable to sponsor employment visas. All candidates must have authorization to work in the U.S. without current or future sponsorship.

At Universal Pure, we're dedicated to giving people everywhere safe, fresh, and delicious food to eat and drink. We provide high-pressure processing (HPP), value-added services and cold storage for our partners in the food industry. We are focused on safety and driven by service. Join the Food Manufacturing Industry in a Quality Assurance role! Benefits offered at Universal Pure: Employer-sponsored medical, dental, vision, and EAP 401(k) with company match! Paid vacation and holidays that start accruing your first week! Multiple medical plans (PPO and HDHP) Voluntary disability plans, accident insurance, critical illness, hospital indemnity, AD&D, and Life insurance A culture of people development and internal career growth A culture of caring, collaboration, and respect Position Purpose: The FSQA technician provides guidance and leadership to production personnel regarding food safety measures and practices. Ensures all customer concerns and or complaints are handled with extreme professionalism and care. Applies available tools and resources for reaching desired outcome with food specifications and production. Major tasks, responsibilities, and key accountabilities: Provide daily monitoring of facility and personnel to ensure compliance with the food safety system of the facility; perform formal audit on GMPs Ensure training of facility personnel on GMPs, risk preventive controls, hazard analysis, pre-requisite programs, and other applicable food safety system elements as required Responsible for pre-operational inspections Collect and analyze product samples as required, as well as document information derived from analysis Safely keep records of all facility analytical results; immediately report results discovered to be out of specification to the QA supervisor Provide documented reports of analytical results to the QA supervisor, also responsible for tracking and reporting data trends Inspecting raw materials coming in; assisting in investigating non-conformance and complaint about product; and provide leadership for the facility team in performing self-audits Aid in hosting visitors to the facility, including regulatory agency representatives and customer representatives, function as main host for the facility's third-party auditors Ensure product is processed to company HACCP/HARPC programs Inform Quality Assurance Management of any food safety concerns Implementing and manage food safety corrective actions Provide assistance to local and corporate management in carrying out changes to the food safety system of the facility; give assistance in creating, reviewing, authenticating, and maintaining food safety system documents, including standard operating procedures (SOPs) and programs working in collaboration with the quality assurance team; provide assistance in maintaining document registers and documentation Possess innovative, resourceful, and proactive disposition, committed to ensuring continuous improvement of capacity and delivering quality service Ability to prioritize and perform position responsibilities accurately and to deadline Follow health, safety, and cleanliness standards Handle any other duties as assigned by QA supervisor and QA manager Job requirements Additional Responsibilities: Excellent attendance and punctuality for an hourly role Utilize soft skills to maintain good relationship with customers and production personnel Preferred Qualifications: Prior quality assurance experience preferred Food manufacturing experience Knowledge and understanding of applicable FDA regulations and GMPs preferred Experience performing administrative work including completing and reconciling paperwork preferred Qualifications: High School Diploma/GED required Computer skills including basic Microsoft Excel required Ability to think analytically and problem solve. Ability to stay organized and multitask. Ability to perform basic mental math. Ability to effectively work with others and as part of a team. Ability to communicate effectively in English language Ability to balance productivity, quality, and safety Ability to work in a fast-paced environment Working Conditions This is largely a static role with standing, however, the ability to perform repetitive bending and standing up is also required. This would require the ability to lift 10-35 lbs. repetitively and up to 45 lbs. occasionally. Must also be able to push/pull up to 250 lbs on rollers occasionally. This role operates in a wet and cold/refrigerated environment (around 35 degrees F) located within a manufacturing, warehousing, and production type facility. Must be able to withstand cold temperatures for duration of shift. Hourly Employees: Universal Pure facilities may process, pack, and store products containing allergenic food ingredients as referenced by FDA, team members who may come in direct contact, must be able to work with these ingredients. All done! Your application has been successfully submitted! Other jobs