Quality control technician jobs in Rochester, NY - 135 jobs

SummaryThe Quality Specialist supports the inspection, testing, and verification of products and processes to ensure they meet established quality standards. Perform measurements using precision tools, document inspection results, assist in root cause analysis, and help resolve nonconformities. The role often involves working closely with Manufacturing and Engineering teams, following quality procedures, and supporting continuous improvement to maintain compliance with customer and regulatory requirements.Job Description Duties and Responsibilities: Capable of performing inspections on incoming parts and raw materials, utilizing appropriate tools such as variable gauges, hand tools, and vision systems. Conduct inspections throughout the assembly process-from raw materials to finished goods-to ensure compliance with specifications. Perform visual inspections of completed products, scan barcodes to record serial numbers, and process move transactions in SAP. Partner with operations to evaluate and address quality events including, non-conformances, product dispositions, root cause investigations and implement appropriate CAPA based on risk-level. Perform final product audit Perform process audit to ensure all procedures are compliant with ISO 9001 Create change order requests for manufacturing floor; act as a back-up for change order processing, as needed. Plant supplier quality performance - meet with purchasing to manage any minor quality issues on the manufacturing floor. Analyze and monitor quality metrics; creating charts and graphs and develop action plans to address unfavorable trends. Promote continuous improvement by enhancing systems or processes through change. Participate in Kanban/Kaizen events. Update existing work process instruction per ECO change process or marked-up request by operators on MFG floor. Submit updated WPI's using Support Central. Change requests, for approval. After approval, Document Control Clerk will upload approved new WPI's in Support Central for MFG use. Assembly prep, as needed Requirements: High School Diploma/GED required; Associates' degree preferred 3-5 years of inspection experience or Quality Control/Assurance Thorough understanding of ISO 9001 Prior IPG-A-610 experience Familiar with failure analysis and supplier quality component analysis Ability to interpret drawings, schematics and board layout Other: Must be able to visually observe details at close range. Must be able to operate hand tools and computers. Must be able to remain in a stationary position 50% of a work shift. Must be able to move about inside the manufacturing area to access equipment, files, etc. Must be able to lift up to 35 lbs. Additional Information GE Vernova offers a great work environment, professional development, challenging careers, and competitive compensation. GE Vernova 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. GE Vernova will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: No For candidates applying to a U.S. based position only:*The Company pays a geographic differential of 110%, 120% or 130% of salary in certain areas.This posting is expected to remain open for at least seven days after it was posted on November 10, 2025.Available benefits include medical, dental, vision, and prescription drug coverage; access to Health Coach from GE Vernova, a 24/7 nurse-based resource; and access to the Employee Assistance Program, providing 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Vernova Retirement Savings Plan, a tax-advantaged 401(k) savings opportunity with company matching contributions and company retirement contributions, as well as access to Fidelity resources and financial planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability benefits, life insurance and 12 paid holidays. New hires also two weeks of annual vacation (which may be pro-rated based on start date).GE Vernova Inc. or its affiliates (collectively or individually, “GE Vernova”) sponsor certain employee benefit plans or programs GE Vernova reserves the right to terminate, amend, suspend, replace, or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a GE Vernova welfare benefit plan or program. This document does not create a contract of employment with any individual.

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About BioLife Plasma Services Every day at BioLife, we feel good knowing that what we do helps improve the lives of patients with rare diseases. While you focus on our donors, we'll support you. We offer a purpose you can believe in, a team you can count on, opportunities for career growth, and a comprehensive benefits program, all in a fast-paced, friendly environment. " Position will be based out of our brand new plasma donation facility in the Rochester, NY opening October 2025! BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. OBJECTIVES/PURPOSE Monitors designated systems and activities, according to tasks trained and assigned, to ensure that source plasma manufacturing is performed consistently according to current Good Manufacturing Practices (cGMP), the Shire Quality System, and other applicable regulations for a plasma center. Is able to perform all technical tasks required within the work areas and will work in these areas as a Lead Technician (or Center Supervisor by exception) when not acting as the Quality Lead Technician. All below listed responsibilities must be completed in compliance with federal, state, local and company-specific regulations related to quality of product, employee and donor safety, and to the proper performance of day-to-day activities. Employees must also maintain complete and accurate records, in accordance with cGMP. ACCOUNTABILITIES Performs duties associated with Quality (including but not limited to): (50%) Reviews operational records in association with tasks trained and assigned to ensure they are complete, accurate and compliant with cGMP requirements. Tracks deviations in operating procedures and policies through established mechanisms. Reports error, deficiencies, discrepancies and observations to center management and Quality Management Representative (QMR). Conducts monthly quality assurance audits for critical control points and key elements for the systems related to donor suitability, source plasma collection, sample collection, plasma storage, product release, quality assurance, and employee training program. Ensures SOP's are current and that staff perform routine tasks according to SOP through direct observation. In the absence of a QMR, works in collaboration with the management team to prepare for and host (if needed) internal auditors and external inspectors. Assists center management teams to ensure timely closure of observations. Maintain qualifications and perform all duties (core and elective) for Medical History, Phlebotomy, and Sample Processing areas. Train new and existing staff on donor center procedures through demonstration, instruction, observation, and feedback. (30%) Provide leadership and training assistance in support of center management and supervisory team, including oversight of operational flow. (10%) Maintain certification and perform all required duties of Lead Technician. (10%) DIMENSIONS AND ASPECTS Technical/Functional (Line) Expertise A minimum of one year of relevant work experience, preferably in a regulated industry, or an equivalent combination of education and experience. Certification in all three primary operational areas of the plasma center (Medical Historian, Phlebotomy, and Processing Technician). Completion of all training through Lead Technician. Demonstrated understanding of quality assurance in an FDA-regulated environment. Effective communication, organizational, and technical/problem-solving skills. Supports the center management team in identifying operational opportunities for continuous improvement, initiating changes to center processes as needed, through use of company approved procedures (including but not limited to 5S, Value Stream Mapping and Kaizen). Maintain general cleanliness of work area and assist other work areas as needed to ensure a clean and professional environment. Ability to read and follow Standard Operating Procedures (SOPs) and to maintain complete and accurate records. Leadership Integrity Fairness Honesty Perseverance Putting the patient at the center Building trust with society Reinforcing our reputation Developing the business Decision-making and Autonomy Refers to Center Manager for guidance on complex, medium-impact or above decisions (internal) Refers to management team for escalated donor/employee concerns (internal) Interaction Responsible for providing exceptional customer service to donors (external) and fellow employees (internal) Attend staff meetings and other team meetings as required. Good verbal communication and customer service skills. Ability to multi-task and work as a team player. Innovation Coordinates will all other center roles to effectively problem solve, ensure safety of staff and donors, and provide an exceptional customer experience. Complexity Production environment requiring the ability to walk and stand for the entire work shift. Requires frequent leaning, bending, stooping, crouching, and reaching above the shoulders and below the knee. Requires frequent lifting up to 26 lbs. and occasional lifting of materials 32 lbs. - 50 lbs. Must have fine motor coordination, depth perception, and ability to hear equipment sounds from a distance. Due to potential exposure to blood borne pathogens (risk level 1), 90% of work tasks require pro-longed glove wear EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: Essential: High School Diploma or equivalent required Desired: Associate or Bachelor's degree preferred ADDITIONAL INFORMATION FLSA Classification (US) - Non-Exempt Other duties and responsibilities as assigned. BioLife Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - NY - Rochester U.S. Hourly Wage Range: $21.00 - $28.88 The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations USA - NY - Rochester Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt No

General Job Description: In this position, the Quality Technician performs dimensional and/or functional inspection on purchased materials and manufactured parts. Uses technical expertise and inspection instrumentation to verify conformance of materials/parts to prints, process sheets and specifications. Minimum Qualifications: Know & understand the use of all inspection equipment including (but not limited to): Micrometers Calipers Dial Indicators Height Gages Optical Comparators Gage Pins and Gage Blocks Sine Blocks and Setups Surface Finish Testers CMM Thread Gages Understand basic Geometric Tolerance. Able to read and understand drawings Knowledgeable about current quality system standards such as ISO-9002 and/or TS16949 Ability to multitask in response to numerous demands; time management skills Computer literate: Excel, Word, etc. Attention to detail Desired Skills: Experience with inspection and measuring equipment calibration Previous auditing experience and skills Experience writing procedures and work instructions PPAP documentation experience

The Quality Control Technician is responsible for inspecting and testing products to ensure they meet quality standards and specifications throughout the manufacturing process. This role involves conducting tests, recording results, and collaborating with production teams to implement corrective actions when necessary. The ideal candidate will have strong attention to detail, a solid understanding of quality control principles, and the ability to work in a fast-paced manufacturing environment. Key Responsibilities: Inspection and Testing: Conduct inspections and tests on raw materials, in-process components, and finished products to ensure compliance with quality standards. Utilize precision measuring instruments (e.g., calipers, micrometers, gauges) and testing equipment to evaluate product specifications and performance. Identify and document defects or deviations from specifications and communicate findings to the quality control supervisor and relevant departments. Documentation and Reporting: Maintain accurate records of inspection results, test data, and quality control activities. Prepare reports summarizing findings, trends, and recommendations for improvement. Assist in the development and maintenance of quality control procedures and protocols. Collaboration and Communication: Work closely with production teams to ensure adherence to quality standards and implement corrective actions when necessary. Participate in team meetings to discuss quality issues, performance metrics, and continuous improvement initiatives. Train production personnel on quality control standards and best practices as needed. Continuous Improvement: Assist in root cause analysis and problem-solving efforts to identify and address quality issues. Collaborate on quality improvement projects to enhance product quality and reduce defects. Stay updated on industry trends and advancements in quality control methodologies. Compliance and Safety: Follow all safety protocols and guidelines while performing inspections and tests. Ensure compliance with industry standards, regulations, and company policies related to quality control. Qualifications: Education: High school diploma or equivalent required. Technical or vocational training in quality control, manufacturing, or a related field is preferred. Experience: 1-3 years of experience in quality control or assurance, preferably in a manufacturing environment. Familiarity with quality control tools and methodologies, such as Six Sigma or ISO standards, is a plus. Skills: Strong attention to detail and analytical skills. Excellent problem-solving abilities and critical thinking. Good communication and interpersonal skills for collaboration with team members. Proficient in using measuring instruments and quality control software. Physical Requirements: Ability to stand for long periods and perform repetitive tasks. Ability to lift and carry materials weighing up to 50lbs. Good manual dexterity and hand-eye coordination. Preferred Qualifications: Experience with inspection and testing equipment specific to the industry. Knowledge of statistical process control (SPC) and quality assurance techniques. Salary: $22-$24/hour Benefits: Health, dental, and vision insurance 401(k) with company match Paid time off and holidays Opportunities for career advancement and training

Discover Your Next Big Opportunity: See Why Quality Vision International Is the Place to Be! Schedule: Monday - Friday, 7:30am -4:00pm Compensation: $22.00-$28.00 based on experience The Mechanical Quality Inspector is responsible for interpreting blueprints form GD&T to guide their inspection of all materials mechanical in nature. This is a critical function as the first check point for supplier quality. Additionally, the Inspection department provides inspection services for the floor when there are questionable issues. The Mechanical Quality Control Inspector works with a high level of independence and contributes to inspections of incoming material that is mechanical in nature, received from both external and internal suppliers, formally rejected by assemblers, or returned from the field. Role and Responsibilities: · Reads blueprints to inspects incoming mechanical materials thoroughly. · Utilizes quality control processes, sampling systems, and procedures to ensure part conformance to specifications. · Ensures QVI incoming quality control product specifications and standards are achieved and maintained. · Maintains detailed and accurate record keeping practices. · Accepts or rejects parts that are purchased externally or manufactured within the corporation. · Works independently and provides guidance and mentorship as needed to Level I inspectors · Utilize CMMs, vision systems, calipers, micrometers, plug/thread gages, etc., as well as GD&T · Other related duties or tasks assigned by management. Those who have worked as a mechanical quality inspector, machinist, or in a role that involves mechanical design may do well in this role! Candidates who have quality experience with plate inspection and GD&T could be a fit for this role as well. Requirements · High School Diploma required. Associate's or bachelor's degree in a manufacturing or quality-related field preferred. · At least 2 years experience in a quality control environment specific to manufacturing and/or mechanical · At least 2 years experience in a machinist role preferred (helpful in this role along with the knowledge of GD&T!) · Working knowledge with machining practices and sheet metal components. · Ability to read mechanical drawings, sometimes often of a complex nature. · Advanced knowledge of part requirements with very close tolerances - Typical +/-.005mm (+/- .0002 inch.) and proficiency of both metric and English systems · Experience with Enterprise Resource Planning (ERP) systems preferred. · Familiarity with QVI/OGP products preferred. · Good written and verbal communication skills as well as effective interaction with team members and with other departments. · Commitment to being a team player with a flexible, positive, adaptive approach to resolving problems or changes. · Working understanding in computer software products such as: Microsoft Excel and Word. · Proficiency in the use of a CMM, Vision systems, calipers, micrometers, plug/thread gages, etc. · Working knowledge with machining practices and sheet metal components. · Working knowledge of GD&T. · Basic understanding of machining practices preferred. Physical and/or Environmental Requirements: · Ability to walk, stand, or sit for extended periods of time. · Ability to independently and safely move materials utilizing a pallet jack, work cart, etc. Visual acuity and manual hand dexterity are needed to operate said tools. · Ability to lift material up to 50 pounds as needed. · Ability to manually handle and transfer material parts to and from inspection operations. What We Offer Paid Time Off · 10 paid holidays each year · Over 3 weeks of PTO (vacation/sick/personal) to start, with additional time after 5 and 10 years Health & Financial Benefits · Health coverage where QVI pays 97-100% of premiums on our most affordable HDHP - free single coverage for employees! · Employer-paid Short-Term & Long-Term Disability Insurance · Employer-paid Life Insurance · QVI 401k Retirement Savings Plan: Up to 5% gross wages · Tuition Reimbursement: up to $7,000 annually · College Scholarship Programs for employee dependents · Annual discretionary bonuses (for non-commission roles) · $1,500 Employee Referral Bonus Wellness & Extras · Employee Assistance Program (EAP) & Wellness perks: on-site nurse, biometric screenings, chronic condition support, and cash incentives for healthy living programs and challenges · Free on-site electric vehicle charging stations and cash reimbursement toward the purchase of qualified EVs Quality Vision International Inc. 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. Salary Description $22.00-$28.00 based on experience

Insero Talent Solutions is recruiting a Mechanical Quality Test Technician for a manufacturing company in Rochester, NY. We are seeking a detail-oriented and technically skilled mechanical lab technician to support our engineering and testing teams. The role involves setting up and conducting mechanical tests, recording and analyzing data, maintaining lab equipment, and ensuring a safe and organized laboratory environment. Key Responsibilities: Prepare, set up, and operate laboratory equipment for mechanical testing (e.g., tensile, compression, fatigue, vibration, hardness tests). Assist engineers and researchers with prototype testing and validation. Collect and document test data accurately and assist in preparing technical reports. Perform routine maintenance and calibration of lab instruments and machinery. Ensure all lab activities comply with company safety protocols and industry standards. Support failure analysis and troubleshooting of mechanical components. Assist in fabricating test fixtures and mechanical assemblies. Maintain inventory of tools, parts, and consumables used in the lab. Collaborate with cross-functional teams including design, quality, and manufacturing. Qualifications: Education: Diploma or Associate Degree in Mechanical Engineering Technology, Mechanical Engineering, or related field. Experience: 1-3 years in a lab or mechanical testing environment preferred (entry-level candidates may be considered). Skills: Strong understanding of mechanical systems and testing principles. Hands-on experience with lab instruments and mechanical tools. Ability to read and interpret mechanical drawings and technical documents. Proficiency in data collection and basic analysis (Excel, LabView, etc.). Knowledge of safety practices in a lab environment. Preferred Qualifications: Experience with CNC machines, 3D printing, or other prototyping equipment. Familiarity with materials testing standards (ASTM, ISO, etc.). Basic knowledge of CAD software (e.g., SolidWorks, AutoCAD).

Full-time Description Primary responsibility is the daily execution of all Quality Assurance processes. This includes all product testing, field testing, and data tracking. This team member must have a drive for continuous improvement in all processes, critical thinking skills, and the desire to lead by example. Responsibilities: Perform daily laboratory analyses capturing data points necessary to track the health of fermentation. Daily analyses include, but not limited to: Daily Brix, pH, Titratable Acidity, temperature, Free Sulfur Analysis, and Dissolved Oxygen Content Assist/lead with data collection, data entry, and reporting of compiled data Perform laboratory analyses to effectively monitor fermentation health Be responsible for the cleaning and calibration of all laboratory equipment/machines Ensure that all team members uphold Blake's Quality Standards Perform routine checks on packaging line throughout the day to ensure equipment and product is being held up to industry standards Perform Incoming ingredient and material inspections for compliance with food safety programs Willing to assist in any other tasks or duties as requested by the manager Education, Skills & Knowledge: High school diploma or general education degree (GED) required Preference of 1-2 years of experience working in a lab Well-developed tasting skills Understanding of Food and Beverage Industry Computer proficient in Excel and Word Good organizational, planning, and presentation skills Clear commitment to high quality and attention to details Able to work independently with minimum supervision. Must have the ability to be on your feet for an entire shift. Strong attention to detail Knowledge of GFCO and GMPs preferred On-site training available and Course training available periodically Working Conditions: The work for this position will be in a climate-controlled, smoke-free environment. The noise level in the work environment is usually moderate with some periods being loud. Work will be performed as per the schedule you create for the team. Some weekend work required as needed. Must be able to work safely in both hot and cold environments Requirements Additional Duties: This job description in no way states or implies that these are the only duties to be performed. You will be expected to follow any other job-related instructions and to perform other job-related duties as requested by your supervisor. Salary Description $19-$21/hr

Description: Primary responsibility is the daily execution of all Quality Assurance processes. This includes all product testing, field testing, and data tracking. This team member must have a drive for continuous improvement in all processes, critical thinking skills, and the desire to lead by example. Responsibilities: Perform daily laboratory analyses capturing data points necessary to track the health of fermentation. Daily analyses include, but not limited to: Daily Brix, pH, Titratable Acidity, temperature, Free Sulfur Analysis, and Dissolved Oxygen Content Assist/lead with data collection, data entry, and reporting of compiled data Perform laboratory analyses to effectively monitor fermentation health Be responsible for the cleaning and calibration of all laboratory equipment/machines Ensure that all team members uphold Blake's Quality Standards Perform routine checks on packaging line throughout the day to ensure equipment and product is being held up to industry standards Perform Incoming ingredient and material inspections for compliance with food safety programs Willing to assist in any other tasks or duties as requested by the manager Education, Skills & Knowledge: High school diploma or general education degree (GED) required Preference of 1-2 years of experience working in a lab Well-developed tasting skills Understanding of Food and Beverage Industry Computer proficient in Excel and Word Good organizational, planning, and presentation skills Clear commitment to high quality and attention to details Able to work independently with minimum supervision. Must have the ability to be on your feet for an entire shift. Strong attention to detail Knowledge of GFCO and GMPs preferred On-site training available and Course training available periodically Working Conditions: The work for this position will be in a climate-controlled, smoke-free environment. The noise level in the work environment is usually moderate with some periods being loud. Work will be performed as per the schedule you create for the team. Some weekend work required as needed. Must be able to work safely in both hot and cold environments Requirements: Additional Duties: This job description in no way states or implies that these are the only duties to be performed. You will be expected to follow any other job-related instructions and to perform other job-related duties as requested by your supervisor.

Elmira Stamping & Manufacturing is currently seeking a skilled Quality Technician to join our quality control team. As a Quality Technician, you will be integral to maintaining and improving our high standards by ensuring that products meet specific standards of quality and safety. This position is based in our Rochester, NY location. About Us: Elmira Stamping & Manufacturing has specialized in medium- to high-volume contract metal stamping, progressive die stamping, and CNC machining since 1970. Elmira Stamping & Manufacturing specializes in both deep-draw and progressive die stamping. We are equipped with man servo, high-speed, mechanical, and hydraulic stamping presses ranging from 30 to 400 tons. Our machines are optimized for automation with in-die contact and non-contact sensors. We are also experts in secondary put-and-take operations for parts that cannot be completed in a progressive die. Additionally, we have multiple 5-axis Emmegi XT extrusion milling centers with a bed capacity of 30 feet, plus turrets, lasers, and more. The foundation for everything we do and make at Elmira Stamping is an unwavering commitment to quality and customer satisfaction. Position Overview Responsibilities May Include: Inspection & Approval: Inspect first and final parts and materials, accepting or rejecting them based on specifications. Documentation: Record inspection results and test data accurately; document rework including issue identification, cause analysis, and corrective actions. Communication: Discuss inspection outcomes with production teams and collaborate with the Quality Manager on daily tasks. Quality Assurance: Assist in achieving QA compliance and targets; develop and maintain quality procedures and controls. Supplier & Product Assessment: Evaluate product specifications and customer requirements, including those of suppliers. Training & Reporting: Identify quality-related training needs and assist with technical and management system reports. Data Monitoring: Gather and analyze performance data, producing relevant statistical reports. Blueprint Reading: Interpret blueprints, technical documents, and manuals to ensure product quality. Operational Oversight: Monitor production operations, recommend adjustments, and use tools such as rulers, calipers, gauges, or micrometers for measurement. Qualifications: Attention to Detail: Keen eye for detail and accuracy. Technical Skills: Basic math and computer skills, ability to use specialized testing tools and machinery. Physical Requirements: Ability to stand for extended periods and read technical documents and blueprints. Quality Standards: Ensure all products and parts meet stringent quality standards. Shift Hours: Monday-Thursday 6:00am-3:30pm, Friday 6:00am-10:00am. Total Compensation Package: Wage This role is based in the State of New York which requires the disclosure of salary ranges. The expected salary range for this position is $18.00 - $22.00 per hour. Elmira Stamping & Manufacturing provides salary ranges as a good faith estimate of what the company reasonably expects to pay for the position at the time of posting. Compensation offered to a selected candidate may vary based on factors such as (but not limited to) a candidate's job-related qualifications, skills, competencies, experience, and geographic location. The expected salary range for this position is subject to change and may be modified in the future. Benefits - We recognize the value of a comprehensive benefits package and work vigorously to ensure our package meets the needs of our employees and their families. Eligible employees can elect and participate in variety of benefits including: Paid Holidays Paid Vacation / Sick Time 401 (k) Retirement Plan with Company Match Medical, Dental & Vision Insurance Employee Assistance Program (EAP) Health Savings Account (HSA) Company Paid Life Insurance Voluntary Insurance Benefits including Disability Insurance, Accident Insurance, Cancer Insurance, Critical Illness Insurance, Hospital Indemnity Insurance and Life Insurance Elmira Stamping & Manufacturing is an Equal Opportunity Employer. We provide 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.

Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients' lives to as many people as possible. With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees. Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 300 employees. Your role Reporting to the Quality Assurance Manager, JOB SUMMARY: As Quality Technician, you will help ensure and assist with site-specific quality compliance according to Standard Operating Procedures (SOPs) & specifications, quality review of batch records and other documents, label control, and assist with release activities and product inspections on the production lines. The on-the-floor quality team is responsible for making sure the process and documentation records are compliant with patient safety in mind. Attention to detail is a must to be successful in this role. We are currently seeking 2 Quality Technicians, one C-shift and one D - shift. C - Shift Hours: Sunday-Thursday, 11:00pm-7:30am, 15% shift differential D - Shift Hours: Friday, Saturday, Sunday 11:00am - 11:00pm, 20% shift differential ESSENTIAL FUNCTIONS / RESPONSIBILITIES: Quality Technicians work with production operators completing inspections on the lines and completing batch record review. Includes verifying appropriate cleanings and line clearance have been performed, verifying differential pressures are within the limits, verifying labels and other quality checks in real time during production runs. Additionally, you will help lead investigations when deviations occur and support routine media fills on the BFS lines. Quality Technicians will also be completing routine inspections of the production areas and be part of the internal audit team. Your profile QUALIFICATIONS/EXPERIENCE: * High School Diploma/GED required. Bachelor's degree in Chemistry, Biology, Pharmacy or related field, preferred. * Must have 2-5 years working in an FDA regulated pharmaceutical or medical device manufacturing environment. PHYSICAL REQUIREMENTS/ENVIRONMENT: Standing 40% of the time. Walking 40% of the time. Sitting 20% of the time. Able to exert up to 10 pounds of force occasionally to lift, carry, push, pull or otherwise move objects. Must be able to work safely with materials and equipment; works with chemicals, tools, and equipment. May work in an environment with variable but moderately high noise levels (hearing protection recommended). Must wear safety glasses, safety shoes, gloves, and other protective items as required. Must wear appropriate garments and coverings per cGMP (uniforms, hair/beard nets, etc.). Visual acuity necessary to perform activities such as: label inspection, component inspection, and ability to complete detailed review of documents. The ability to write and communicate information via handwriting, telephone and computer keyboard. SCOPE OF DECISION MAKING: Decisions require basic/routine analytical judgment. Plan and perform diversified duties requiring knowledge of a particular field and the use of a wide range of procedures. Involves the exercise of judgment in the analysis of facts or conditions regarding individual problems or transactions to determine what action should be taken within the guidelines or standard practice. LEVEL OF SUPERVISION PROVIDED: Individual contributor, not responsible for the work others. INTERNAL / EXTERNAL CONTACTS: Regular inside and outside: Requires contacts to carry out company policy and programs. Improper handling will have considerable effect on operating results. Must often deal with persons of substantially higher rank on matters requiring explanation, persuasion and obtaining approvals. Compensation range 25.00 - 32.00 USD * The referenced compensation range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations. More Than Just a Paycheck At Unither, we don't just offer competitive hourly wages-we also pay 100% of your medical premiums. That means no paycheck deductions for your healthcare, which can be worth an extra $1 to $3.50 an hour in your pocket compared to jobs where you pay part of the premium. Learn more about us: We are a dynamic company driven by a spirit of victory and are therefore pursuing strong growth while maintaining a close relationship with our customers and employees. Our culture is based on 5 values: Respect, Responsibility, Trust, Courage and Innovation. We are committed to bringing these values to life with our employees by granting them a high degree of autonomy in the exercise of their profession and by encouraging their initiatives. We are committed to providing them with working conditions and atmosphere that is conducive to their development and the expression of their potential. We propose you to integrate a site that values the meaning of work and that entrusts our employees with a high level of responsibility. Join us and make a difference! Unither is an Equal Opportunity Employer. We are committed to providing reasonable accommodations for qualified individuals with disabilities and to ensuring equal employment opportunity for all applicants.

Job DescriptionDescription: Please apply on our website *************** could also be a split shift @ 10am - 6:30pm for the right candidate This opening is for an experienced QA professional. Please have experience working in quality control in a manufacturing environment. Position Summary Performs basic receiving, first-piece, in-process and final inspection in accordance with applicable quality system procedures and work instructions. Evaluates materials, components and/or assemblies for conformance to specification requirements or established workmanship standards. Applies basic statistical techniques, including statistical process control and sampling plans, to assess the stability of various processes or reduce collected raw data. May train new or lower grade level employees in department protocol. Requirements: Essential Duties and Responsibilities Perform receiving inspection of incoming supplies requiring quality assurance evaluation prior to dispatch using the appropriate sampling plan. Perform first-piece inspection of machined product and conduct in-process audits of work-in-progress in accordance with documented procedures under supervision. Perform final inspection and test of deliverable product in accordance with documented procedures prior to release for shipment or storage. Complete all required inspection and test records appropriate to the particular task and results of the inspection. Understand and apply basic geometric dimensioning and tolerancing symbology. Employ basic statistical tools to interpret data. Understand Vantage operation for time and data reporting. Perform other duties assigned by supervisor. Supervisory Responsibilities This position has no supervisory responsibilities. The Inspector II is required to interact effectively in cross-functional teams dedicated to the resolution of issues in a timely manner. Education, Training and/or Experience Associate's degree (AA) or equivalent from a two-year college or technical school; or one to three years related experience and/or training; or equivalent combination of education and experience. Benefits: Competitive Pay Medical effective on start date Dental Life Insurance (plus additional supplemental coverage) 401(k) program Short & Long Term Disability Profit Sharing Program Vacation Program Educational Financial Assistance Flexible Spending Accounts Health Savings Accounts And others! PGM is an EOE Employer

Founded in 1968, our company has become a niche player in the manufacturing industry as we continue to create high quality, graphite-based components for the aerospace industry. We are happy to say that we will be expanding into new facilities! With the expansion comes growth, and we are in need of a valuable member of our Quality team to ensure our highest standards ar met! What we offer: We offer one of the best work environments in Rochester along with all the benefits you will need for personal stability. This includes healthcare, dental, vision, PTO, 401k, and supplemental insurances. Moreover, we have an outstanding breakroom and onsite gym! Shift: B (3pm to 11:30pm) Pay: $25-28/hour. There is also a 10% differential for B shiftt. Scope of The Role: This is a higher-level QC position that involves the use and programming of CMM equipment using PC-DMIS. Other functions include: The use of standard measuring equipment i.e. micrometers, verniers, etc. Reading of blueprints Use of comparators Utilizing Microsoft Office suite Tool calibration Experience with SPC, ISO9002, and other quality standards/techniques Review proposals and institute quality plans for WIP jobs Help reduce scrap through accurate First-Off inspections Interface with customers for inspection techniques, quality issues, and reporting Oversee all operations when AFM is absent Your Abilities and Background: High School diploma or equivalent Minimum four years experience in QC work Must have knowledge of CMM operation and programming in PC-DMIS Thank you so much for taking the time to consider working with us. We hope to speak with you soon!

SUMMARY: The Quality Control Inspector position conducts inspection of materials used for the manufacturing of products. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. ESSENTIAL FUNCTIONS: · Inspect products using gauges, tools and scales prior to the manufacturing of product. · Spreadsheets for data collection. · Reconcile final inspection documentation for manufacturing and shipment of product. · Interact with Plant Manager as needed. · Test incoming raw materials. · Ensure that all quality control procedures and policies for Lakelands, NPCA and NYSDOT are being implemented to produce a quality product. · Make sure Inspection Summary Report is being updated in real time, completed, accurate and turned into Plant Manager at the end of each day. · Immediately report and communicate any and all problems and/or issues. · All other duties as assigned. Requirements COMPETENCIES: · Technical Capacity. · Safety Principles. · Organizational Skills. · Problem Solving/Analytical. · Time Management. · Initiative. KNOWLEDGE/SKILLS/EDUCATION: · Up to 3 years of experience in quality control function in manufacturing environment. · High School Diploma or GED required. MINIMUM EXPERIENCE: · Some industry experience required. · ACI certification is preferred. (will train) · NPCA Certification is preferred. (will train) SUPERVISORY FUNCTIONS AND SKILLS: This position has no supervisory responsibilities. WORKING CONDITIONS: · While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles, moving mechanical parts and vibration. · The noise level in the work environment can be loud. · The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. · The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. · Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. OTHER: Project a positive and professional image of the company and of management to employees at all levels. This position may be required to follow other job-related instructions and to perform other job-related duties as requested or assigned, subject to all applicable state and federal laws. Duties, responsibilities and activities may change at any time with or without notice.

Why Us? At Par Health, we believe great healthcare is built on getting the essentials right. We're looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose-prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn't just our tagline, it's the higher standard we live by every day. Summary The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. May participate in investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. Job Description Scope of Authority - span of control (work unit, site, department, division, etc.), monetary value of budget/spend authority ( capital, operating, etc.), P&L responsibility, etc. Typically supports one Par business, at a single site Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time Accountability Responsibilities % of Time Analysis & Testing * Conducts routine laboratory analyses: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. * Uses laboratory software for analyses 65% Lab Equipment * Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping * Cleans lab working surfaces and disposes of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals * Under close supervision, learns to troubleshoot basic instrument problems 20% Investigations * With guidance, participates in OOS/OOT/NOE and other investigations * Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor * May assist in drafting, editing, and reviewing SOPs and laboratory investigations 10% Training * Maintains assigned training records current and in-compliance * May assist in the training of less senior laboratory staff 5% Compliance * Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting * Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs * Follows internal processes related to controlled substances continuous Safety * Follows EH&S procedures to ensure a safe work environment * Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS continuous Total 100% Qualifications Education & Experience Minimal acceptable level of education, work experience and certifications required for the job * Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required. * Some pharmaceutical laboratory experience preferred. Knowledge Proficiency in a body of information required for the job e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. * Proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. * Basic knowledge of wet chemistry techniques * Knowledge of applicable safety and standards guidelines: SOP, cGMP, GLP, DEA regulations and/or MSDS * Competency in Microsoft Office Suite Skills & Abilities Often referred to as "competencies", leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc. * Ability to display and analyze data in a logical manner * Good verbal and written communication skills as well as good computer skills * Attention to details and accurate record keeping * Establish and maintain cooperative working relationships with others * Solid organizational skills * Ability to take initiative, set priorities and follow through on assignments Physical Requirements Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc. * Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals * Must occasionally lift and/or move up to 15-25 lbs. * Ability to wear personal protective equipment, including respirators, gloves, etc. * Specific visions abilities are required by this job include close vision and color vision * Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. EEO Statement: We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. 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.

Requirements QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Position requires a high degree of self-motivation and good organizational skills. Two to four months of training are required to properly prepare a person for this position. EDUCATION and/or EXPERIENCE: Associate degree (A. A.) or equivalent from two-year college or technical school; or six months to one year related experience and/or training; or equivalent combination of education and experience. LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. MATHEMATICAL SKILLS Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. REASONING ABILITY Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally required to walk, sit, and talk or hear. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics 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. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts and fumes or airborne particles. The noise level in the work environment is usually moderate. American Packaging Corporation is committed to equal opportunity for all, without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. American Packaging Corporation will make reasonable accommodations for known physical or mental limitations of otherwise qualified employees and applicants with disabilities unless the accommodation would impose an undue hardship on the operation of our business. EOE/AA Disability/Veteran. If you are interested in applying for an employment opportunity and need special assistance or an accommodation to apply for a posted position, please contact our Human Resources department at: ***************************************.

Looking for a fresh start? A company help grow your skillset and advance your career? Apply Today! We are happy to speak with you about your experience and how you may be a fit within our teams. Lots of exciting things are happening at KDP and we'd love for you to be a part of it! Want to see more? Click the link to visit our website to view some awesome, short clips and information to show you what we're all about KDP Company Overview. You may also view all of our current openings on our Careers Page: KDP Careers - Williamson, NY About the facility: The Williamson, NY operation is a roughly 1 million sq ft production facility with 217 acres of land. The site is the Home of the Brand Motts that has been delighting our consumers for more than 140 years. We produce a wide variety of products with diverse packaging capabilities going from Apple sauce, to juices and concentrates . Alongside production, the site includes a raw apple operation that is key for the success of the site. This facility is a Unionized location. We are adding to our facility and have lots opportunity to grow and learn our industry! Production Technician II - Williamson, NY The Production Technician is responsible for the complete operation and changeover of assigned machines within PhD and all other associated work. This includes safely maintaining, repairing, replacing and assisting in modifying all processing, packaging, and facility equipment in accordance with on-line quality and Best Practice procedures. Shift / Schedule: This is a union facility so flexibility to work any day or any night shift pattern is required. Positions are mainly 12 hour positions, with few 8 hour shifts available but not guaranteed; based on seniority. 6:00pm - 6:00am 2:00pm - 10:30pm 10:00pm - 6:30am Position Responsibilities Operate machine in accordance with on-line quality and Best Practice procedures Handle empty cases Perform Best Practice quality checks Watch for defective materials Clean and sanitize equipment and facility Perform preventative maintenance Complete mechanical repairs Assist mechanics during repairs Perform quality inspections and associated paperwork Make data driven process adjustments Troubleshoot potential problems Train other operators Perform all work in accordance with established safety procedures Wear all required safety gear and follow all GMP rules and regulations Total Rewards: Pay starting at $26.33 per hour plus a $0.60 shift differential Where Applicable: Benefits eligible day one!! Benefits, subject to eligibility, and collective bargaining agreements (where applicable): Medical, Dental, Vision, Disability, Paid Time Off (including vacation and sick time), 401k with company match, Tuition Reimbursement, and Mileage Reimbursement Requirements: Ability to lift up to 35 pounds and 50 pounds occasionally. Ability to bend, stretch and stand during entire shift. Ability to frequently kneel, squat, climb stairs/ladders, bend, stoop, twist, and reach overhead with repetitive motions. Ability to work in a variety of temperature and humidity conditions. Company Overview: Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partner brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work. Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law. A.I. Disclosure: KDP uses artificial intelligence to assist with initial resume screening and candidate matching. This technology helps us efficiently identify candidates whose qualifications align with our open roles. If you prefer not to have your application processed using artificial intelligence, you may opt out by emailing your resume and qualifications directly to **************** in lieu of clicking Apply. Please include the job title and location or Job ID # in the email subject line.

General Job Description: In this position, the Quality Technician performs dimensional and/or functional inspection on purchased materials and manufactured parts. Uses technical expertise and inspection instrumentation to verify conformance of materials/parts to prints, process sheets and specifications. Minimum Qualifications: Know & understand the use of all inspection equipment including (but not limited to): Micrometers Calipers Dial Indicators Height Gages Optical Comparators Gage Pins and Gage Blocks Sine Blocks and Setups Surface Finish Testers CMM Thread Gages Understand basic Geometric Tolerance. Able to read and understand drawings Knowledgeable about current quality system standards such as ISO-9002 and/or TS16949 Ability to multitask in response to numerous demands; time management skills Computer literate: Excel, Word, etc. Attention to detail Desired Skills: Experience with inspection and measuring equipment calibration Previous auditing experience and skills Experience writing procedures and work instructions PPAP documentation experience

Job Description Insero Talent Solutions is recruiting a Mechanical Quality Test Technician for a manufacturing company in Rochester, NY. We are seeking a detail-oriented and technically skilled mechanical lab technician to support our engineering and testing teams. The role involves setting up and conducting mechanical tests, recording and analyzing data, maintaining lab equipment, and ensuring a safe and organized laboratory environment. Key Responsibilities: Prepare, set up, and operate laboratory equipment for mechanical testing (e.g., tensile, compression, fatigue, vibration, hardness tests). Assist engineers and researchers with prototype testing and validation. Collect and document test data accurately and assist in preparing technical reports. Perform routine maintenance and calibration of lab instruments and machinery. Ensure all lab activities comply with company safety protocols and industry standards. Support failure analysis and troubleshooting of mechanical components. Assist in fabricating test fixtures and mechanical assemblies. Maintain inventory of tools, parts, and consumables used in the lab. Collaborate with cross-functional teams including design, quality, and manufacturing. Qualifications: Education: Diploma or Associate Degree in Mechanical Engineering Technology, Mechanical Engineering, or related field. Experience: 1-3 years in a lab or mechanical testing environment preferred (entry-level candidates may be considered). Skills: Strong understanding of mechanical systems and testing principles. Hands-on experience with lab instruments and mechanical tools. Ability to read and interpret mechanical drawings and technical documents. Proficiency in data collection and basic analysis (Excel, LabView, etc.). Knowledge of safety practices in a lab environment. Preferred Qualifications: Experience with CNC machines, 3D printing, or other prototyping equipment. Familiarity with materials testing standards (ASTM, ISO, etc.). Basic knowledge of CAD software (e.g., SolidWorks, AutoCAD).

At American Packaging Corporation (APC), you'll find the packaging career you've been looking for. With competitive salaries, excellent benefits, 401(k) plans and tuition reimbursement programs, we nurture our employees while advancing and promoting diversity and inclusion. As the leading flexible packaging converter in North America for over a century, APC's longstanding success is fueled from the inside out. We're constantly seeking to improve our internal operations and were named a “Best of the Best” in the Best workplaces in the America's awards for 12 years in a row. It's how and why we engage the best and brightest talent to continue propelling our shared success into the future. LOCATION: Chili, NY HOURS: DAYS 7am - 7pm on a 2-2-3 schedule SUMMARY: Tests and inspects products at various stages of production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. This position can present the motivated employee with several career options as the company grows and he/she gains expertise and knowledge. ESSENTIAL DUTIES AND RESPONSIBILITIES: Performs visual inspections and physical tests utilizing equipment in Lab. Products are tested for a variety of qualities such as dimensions, performance or chemical characteristics. Records and evaluates test data and writes reports. Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability. Enters data into computer for analysis. Prepares certificates of analysis on finished product for our customers. Able to use and read measuring instruments as well as operating instructions and procedure manuals. Trial reports, inspection and tracking. Assist QA and Technical departments in their duties. Must take responsibility for work assigned. Effective communication skills, both verbal and written. Support and follow all plant Safety Rules, GMPs, and other procedural training requirements. Requirements QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Position requires a high degree of self-motivation and good organizational skills. Two to four months of training are required to properly prepare a person for this position. EDUCATION and/or EXPERIENCE: Associate degree (A. A.) or equivalent from two-year college or technical school; or six months to one year related experience and/or training; or equivalent combination of education and experience. LANGUAGE SKILLS Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. MATHEMATICAL SKILLS Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Ability to apply concepts of basic algebra and geometry. REASONING ABILITY Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally required to walk, sit, and talk or hear. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics 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. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts and fumes or airborne particles. The noise level in the work environment is usually moderate. American Packaging Corporation is committed to equal opportunity for all, without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. American Packaging Corporation will make reasonable accommodations for known physical or mental limitations of otherwise qualified employees and applicants with disabilities unless the accommodation would impose an undue hardship on the operation of our business. EOE/AA Disability/Veteran. If you are interested in applying for an employment opportunity and need special assistance or an accommodation to apply for a posted position, please contact our Human Resources department at: ***************************************.