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Job Description Company Summary: Radienz Living is a leading North American manufacturer of home and personal care products, such as unit dose, facial wipes, and baby wipes. With manufacturing plants and warehouses in North America, the company provides customers with private label solutions and contract manufacturing services for products found in retail and institutional markets. Radienz Living is passionate about providing its customers with exceptional manufacturing capabilities through its commitment to agility in innovation, trust and reliability, and sustainable creation that support a cleaner way of living. Throughout the years, the company has built robust quality systems, multiple GMP certifications, and in-house FDA/EPA microbiology, quality control, chemistry, and R&D labs. Background: Under the direction of the Supervisor/Plant Manager, the Production Inspector is responsible for ensuring products are being produced in a manner that meets all cGMP and Product Specification criteria. This position will support production as their primary responsibility but will assist the Quality dept., when necessary (i.e., absent personnel). Primary Responsibilities: Production: • Constructs, packages, tapes, labels, products compliant with written procedures., • Inspects packages for defects. Works as a team to help co-workers when necessary., • Strong attention to detail with the ability to identify packaging defects or discrepancies., • Contributes to a continuous improvement in culture., • Collaborate with team members to meet production goals while adhering to safety guidelines., • Attends company scheduled meetings when applicable (i.e., safety meetings, production meetings, department meetings.), • Inform direct supervision of any problems or complications that may arise, • Maintains a clean and orderly environment free of hazards. Quality • Conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks., • Consistently reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices, company SOP’s and cGMP’s., • Discusses errors and reviews production logbooks for accuracy and compliance., • Collects data and supports release of batch records., • Conduct regular quality line audits of in-process and finished goods against pre-defined characteristics to validate that all process and product requirements have been satisfied., • Document audit results on the appropriate QA paperwork making notes about out-of-spec conditions found or other observations of interest., • Perform Leak test on in-process material to ensure that product meets intended performance requirements., • Perform Lot Code validations., • Monitor the performance of metal detection equipment, as applicable., • Investigate production-related QA problems and make recommendations., • Visual verification of raw material and packaging material to validate material is in spec to artwork and functionality requirements and is used for its intended purpose on the correct product., • Execute the plant non-conforming materials procedure when out-of-specification conditions are observed. Qualifications: • High school degree or GED, preferred., • Must be able to keep up with the line speed of machinery., • Must be able to communicate, respond to verbal and written instructions in English., • Flexibility in work schedules to support production schedule, based on volume needs, which could require weekends, and/or working overtime during high demand., • Prior working knowledge in a CPG, manufacturing, packaging, or pharmaceutical industry, preferred., • Understand, follow, and ensure compliance with Good Manufacturing Practices (cGMP) and adherence to defined procedures, company policies, safety rules and SOPs., • Ability to work in various weather/temperature conditions to include heat, humidity and cold., • Understanding basic measurement concepts, such as length, width, height, weight., • Ability to effectively troubleshoot problems and recognize when to escalate issues to manager., • Support departmental and organizational goals and objectives., • The manager may require an employee to perform 'other duties as assigned' on a temporary and infrequent basis., • Must work well with others. Shift 1st Schedule: Monday-Friday 5:00pm-1:30am Join our team as a Production Inspector and contribute to our commitment to delivering high-quality products while ensuring customer satisfaction through efficient packaging processes! Shift 1st Schedule: Monday-Friday 5:00pm-1:30am

Job Description ELECTRONIC QUALITY INSPECTOR-AEROSPACE JOB DESCRIPTION • Perform in-process inspections during various stages of production to ensure compliance with quality standards and engineering drawings., • Complete final QA audits of finished products prior to release, • Accurately enter inspection results and perform transactions in internal ERP tracking systems., • Use precision hand tools such as micrometers, calipers, and height gauges to measure and inspect parts., • Strong verbal and written communication skills., • Knowledge of JSTD-001 and IPC-610 required, • Ability to read, and understand engineering drawings and related technical documents, • Knowledge of ISO-9000 and AS9100

Job Description Company Summary: Radienz Living is a leading North American manufacturer of home and personal care products, such as unit dose, disinfectant wipes, all-purpose cleaners, facial wipes, and baby wipes. With manufacturing plants and warehouses in North America, the company provides customers with private label solutions and contract manufacturing services for products found in retail and institutional markets. Radienz Living is passionate about providing its customers with exceptional manufacturing capabilities through its commitment to agility in innovation, trust and reliability, and sustainable creation that support a cleaner way of living. Throughout the years, the company has built robust quality systems, multiple GMP certifications, and in-house FDA/EPA microbiology, quality control, chemistry, and R&D labs. Background: Under the direction of the Supervisor/Plant Manager, the Production Inspector is responsible for ensuring products are being produced in a manner that meets all cGMP and Product Specification criteria. This position will support production as their primary responsibility but will assist the Quality dept., when necessary (i.e., absent personnel). Primary Responsibilities Production: • Constructs, packages, tapes, labels, products compliant with written procedures., • Inspects packages for defects. Works as a team to help co-workers when necessary., • Strong attention to detail with the ability to identify packaging defects or discrepancies., • Contributes to a continuous improvement in culture., • Collaborate with team members to meet production goals while adhering to safety guidelines., • Attends company scheduled meetings when applicable (i.e., safety meetings, production meetings, department meetings.), • Inform direct supervision of any problems or complications that may arise, • Maintains a clean and orderly environment free of hazards. Quality • Conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks., • Consistently reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices, company SOP’s and cGMP’s., • Discusses errors and reviews production logbooks for accuracy and compliance., • Collects data and supports release of batch records., • Conduct regular quality line audits of in-process and finished goods against pre-defined characteristics to validate that all process and product requirements have been satisfied., • Document audit results on the appropriate QA paperwork making notes about out-of-spec conditions found or other observations of interest., • Perform Leak test on in-process material to ensure that product meets intended performance requirements., • Perform Lot Code validations., • Monitor the performance of metal detection equipment, as applicable., • Investigate production-related QA problems and make recommendations., • Visual verification of raw material and packaging material to validate material is in spec to artwork and functionality requirements and is used for its intended purpose on the correct product., • Execute the plant non-conforming materials procedure when out-of-specification conditions are observed. Qualifications: • High school degree or GED, preferred., • Must be able to keep up with the line speed of machinery., • Must be able to communicate, respond to verbal and written instructions in English., • Flexibility in work schedules to support production schedule, based on volume needs, which could require weekends, and/or working overtime during high demand., • Prior working knowledge in a CPG, manufacturing, packaging, or pharmaceutical industry, preferred., • Understand, follow, and ensure compliance with Good Manufacturing Practices (cGMP) and adherence to defined procedures, company policies, safety rules and SOPs., • Ability to work in various weather/temperature conditions to include heat, humidity and cold., • Understanding basic measurement concepts, such as length, width, height, weight., • Ability to effectively troubleshoot problems and recognize when to escalate issues to manager., • Support departmental and organizational goals and objectives., • The manager may require an employee to perform 'other duties as assigned' on a temporary and infrequent basis., • Must work well with others. Join our team as a Production Inspector and contribute to our commitment to delivering high-quality products while ensuring customer satisfaction through efficient packaging processes! Monday-Friday 5:pm-1:30am 40 Hrs.

Job Description Who Are We? FDH Aero is a trusted global supply chain solutions partner for aerospace and defense companies, helping to shape the industry by simplifying the supply chain. With over 60 years serving as a leading independent industry partner, FDH specializes in hardware, electrical, consumables and expendables, licensed products, and value-added services for global OEM and aftermarket customers. FDH is headquartered in Commerce, California, and has operations across the Americas, EMEA and APAC. FDH Aero – named a Best Places to Work in Aviation in 2024 – has locations in 14 countries across the globe, with more than 1,500 best-in-industry employees and over 650,000 square feet of inventory space. FDH is headquartered in Commerce, California, and has operations across the Americas, EMEA and APAC. FDH Aero – named a Best Places to Work in Aviation in 2024 – has locations in 14 countries across the globe, with more than 1,500 best-in-industry employees and over 650,000 square feet of inventory space. Why Work Here? At FDH Aero, we understand that the strength of our brand comes from our people. We invest in driven, diverse and experienced professionals who are naturally curious, courageous and motivated towards action. We value tempering confidence with humility, and a mission that always starts with service-first. Our values guide everything we do: We Are Service First - We act with agility and intelligence to solve our partner’s most pressing needs. We safeguard our trusted relationships by communicating with clarity and unmatched follow through. We Are Respectful - We behave with dignity, fairness, and acceptance. We thrive by prioritizing empathy, humility, and connection to our collective community. We are Amplifiers - We invest in driven, diverse and experienced professionals, businesses and partners. We fuel the entrepreneurial spirit by providing autonomy, authority and a clear mission. We Are Open-Minded - We communicate with intention, curiosity, and diversity of thought. By actively contributing with courage and candor, we challenge the status quo and innovate together. We Are Accountable - We own responsibility for our outcomes. We set expectations, embrace critique, and empower every employee to take immediate actions on challenges they encounter. We Value Our People - That’s why we offer competitive benefits, including medical, dental, vision, Flexible Spending Accounts (FSA), 401k matching, and wellness programs. We invest in training, mentorship, and career development to empower our employees to reach their full potential. Our commitment to culture and excellence has earned us recognition as one of Aviation Business News' Best Places to Work in Aviation. As a team member at FDH Aero you are trusted to deliver, to innovate, and to drive next-generation solutions for tomorrow’s supply chain demands. Ready to make an impact? We proudly pursue top talent with a diverse and global set of experiences and backgrounds. We Are Looking For The RF Quality Inspector is responsible for communicating with suppliers as needed and handles the disposition and control of non-conforming products. Additionally, this individual will review and disposition all certification documentation to meet traceability requirements per drawing, AS standards, and Company Quality standards. They will perform First Articles for submission to customers and review and approval of First Articles from suppliers among other duties as assigned. What You'll Do (Responsibilities) • Conducts dimensional inspections per design record and documented AQL levels; Conducts visual inspections for obvious defects, • Review and disposition all certification documentation to meet traceability requirements per drawing, AS standards, and Company Quality standards, • Communicates with suppliers as needed, • Dispositions and control of non-conforming product, • Obtain and maintain Customer Designated Supplier Quality Representative Stamps (DSQR) for at least 2 customers, • Review and approval of First Articles from suppliers, • Perform First Articles for submission to customers, • Identify and communicate opportunities to increase inspector productivity and assist with RCCA activities pertaining to Inspection. Assist in internal, customer, and third-party audits, • 6S and general cleanliness of work area and warehouse What You Bring (Qualifications & Skills): • Requires High School diploma or equivalent, • 2-4 years of related work experience, • Previous aerospace inspection experience, • Experience in QA inspection methods and procedures, including First Article Inspect, • Strong leadership and problem-solving skills, with the ability to multitask in a fast-paced environment, • Strong analytical, organizational, and troubleshooting skills, • Knowledge of AS9120 requirements, • Experience in the usage of calipers, ring/pin gages, comparator, and Smart scope, • Proficient PC skills and use of Microsoft Office products (Outlook, Excel), • Advanced GD&T Skills – Optical Comparator, CMM, Layout, Vision Scope Systems, • Ability to manage multiple and competing priorities, • Embodies the FDH Core Values Special Requirements: • U.S. Citizen, U.S. Permanent Resident (Green Card holder) or asylee/refugee status as defined by 8 U.S.C. 1324b(a)(3) required., • ITAR requirement FDH Aero is an Equal Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Job Description Job Title: QA Inspector I Job Description As a QA Inspector I, you will be responsible for ensuring the quality and compliance of manufacturing processes in a pharmaceutical environment. You will play a crucial role in maintaining the integrity of the production lines by performing thorough inspections and documentation. Responsibilities • Perform room and equipment cleaning checks before commencing any activities., • Conduct daily rounds of the warehouse to ensure compliance., • Document cleaning activities in logbooks and checklists., • Physically release materials upon receiving and reviewing release reports from QA., • Verify that materials match incoming documents, release documents, and material labels., • Monitor and maintain the reject cage., • Perform daily verification of balances., • Monitor temperature and humidity according to SOP., • Maintain and file documents appropriately., • Adhere to company policies, safety requirements, cGMP, and SOPs., • Experience in quality assurance, line inspection, and document review., • Familiarity with line clearance in a manufacturing or production environment., • Experience with batch record review and quality inspection., • 1-5 years of QA experience, with a recent background in pharmaceuticals., • Ability to understand and adhere to GMP standards and regulations. The role is situated in a manufacturing environment within a pharmaceutical company. The facility, located in Central Islip, is a brand new setup where inspectors oversee the packaging lines, managing 1-3 lines simultaneously. There are three openings available: one in Central Islip and two in Hauppauge. The position operates on the 2nd shift from 3:00 PM to 11:30 PM, with potential variations based on business needs. This essential business offers holiday pay and overtime opportunities, ensuring continued operation during shutdowns. Job Type & Location This is a Permanent position based out of Central Islip, New York. Pay and Benefits The pay range for this position is $41600.00 - $49920.00/yr. benefits start day 1 and they are eligible for 2 weeks vacation, 56 hours sick and wellness add 2 days mental health days Workplace Type This is a fully onsite position in Central Islip,NY. Application Deadline This position is anticipated to close on Oct 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionDescription: Position Summary: The QA Packaging Inspector is responsible for inspecting documentation records, products, facilities and equipment before, during and after packaging runs. Responsibilities: Responsibilities include, but are not limited to: • Verification of line cleaning and line release approval on a timely basis, • Monitor packaging/inspection operations for conformance to specifications and procedures, • Sample of packaged product as required for QC Testing, Stability or as required by the packaging record, • Complete packaging logbooks which includes recording of required information neatly and accurately and verification that data entered by operations is neat, complete and accurate, • Perform and verify documentation for packaging qualification, • Maintenance of house standards, comparison of product for physical verification, • Communicate with production personnel which includes but not limited to the availability to perform line cleaning and line release approval, product and/or equipment related quality issues, • Review of packaging documentation, • Inspection of final finished, package prior to end of packaging run and before transfer to warehouse, • Notify QA management of any quality or safety concerns, • Knowledge of cGMPs related to US FDA manufacturing and packaging environments, • Compliance with applicable company policies such as cGMP and related SOPs, • Responsible for compliance with all rules and regulations pertaining to safety policies and for leading by example with the proper attitude toward safety and health help to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel., • High School or GED diploma required with college a plus, • Knowledge of and ability to perform basic math, • Knowledge of Microsoft Office Programs, • Excellent organizational skills and detail-oriented, • Required to reach with arms and use hands and fingers to handle or feel objects and tools, • Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs and ladders, • Work environment in production operations facilities include close proximity to heavy machinery with loud noises and pharmaceutical powders (dust)., • Potential to move between production operations sites/areas to complete job functions., • Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion., • Gowning as required by GMPs and/or SOPs $21.50 per hour

Job Description QA INSPECTOR Join our Natural Organics Inc / Natures Plus Family! For more than 50 years, Natural Organics Inc. headquartered in Melville, NY has been the gold standard in natural vitamins and supplements. Marketing our products under the Natures Plus brand, we are committed to producing the finest, most effective formulations available. Our employees embody the true spirit of our Natures Plus brand. We have one goal... Bringing you high-quality products with the guaranteed potency you deserve! We are currently seeking an experienced QA Inspector. The position is responsible for daily support of the Packaging Lines and Receiving Dock. The Quality Assurance Inspector reports to the Quality Assurance Supervisor. Roles and Responsibilities: • Perform line clearances and releases, • Inspect Packaging lines to ensure correct components have been staged. Perform in-process checks for counts, labels, inner-seals etc., • Ensure all employees are adhering to current Good Manufacturing Practices (cGMPs)., • Perform inspections for incoming components and bulk products., • Assist with scanning and filing of Packaging Records and related documentation., • Provide input during the review and revision of Standard Operating Procedures. Knowledge of cGMP's and product release procedures a MUST. Strong verbal and written skills, along with computer literacy required. Some heavy lifting up to 50 lbs. could be involved at times. Benefits: • Competitive salary, • Medical, Dental, Life Insurance, Aflac, Short- and Long-Term Disability, • 401(k) with company match, • Generous paid time off days and holidays, • Opportunities for professional development and growth, • Discounted vitamins and supplements, • State-of-the-art relaxation room Job Posted by ApplicantPro

Job DescriptionDescription: Position Summary:The Inspector, QA Manufacturing has the primary responsibility of ensuring product quality is maintained through all phases of manufacturing in accordance with current good manufacturing practices. Responsibilities: Responsibilities include, but are not limited to: • Perform in-process monitoring (e.g. weight, thickness, hardness, disintegration, friability, etc.) of all manufacturing operations, • Perform duties using good documentation practices, • Collect in-process and finished product samples as required, • Support collection of microbiological samples per procedure as required, • Perform room inspections/clearances as required, • Perform Batch Record release of both Commercial and IP batch records, • Perform AQL sampling and inspections as required, • Identify and report any non-conformances/discrepancies to management if applicable, • Review general SOPs are being met by production, • Assist in employee training (initial and ongoing), • Support environmental monitoring activities (i.e. water sampling air sampling), • Provide additional QA technical support to Coating Department, • Review batch record documentation, • QMS form issuance as required to production, • Daily scale weight verification, • Maintain QA supplies, • Review and approve weekly pest control logs, • Sample transmittal to QC and Account Services, • Review grounds logbook for Maintenance, • Monthly audit of facility fire extinguishers, • High School or GED diploma required, • Ability to read, write, and communicate effectively., • Self-motivated with the ability to work in fast-paced environment and handle multiple tasks simultaneously., • Required to reach with arms and use hands and fingers to handle or feel objects and tools, • Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs and ladders, • Work environment in production operations facilities include close proximity to heavy machinery with loud noises and pharmaceutical powders (dust)., • Potential to move between production operations sites/areas to complete job functions., • Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion., • Gowning as required by GMPs and/or SOPs $21.50 per hour

Job DescriptionDescription: Position Summary: The QA Packaging Inspector is responsible for inspecting documentation records, products, facilities and equipment before, during and after packaging runs. Responsibilities: Responsibilities include, but are not limited to: • Verification of line cleaning and line release approval on a timely basis, • Monitor packaging/inspection operations for conformance to specifications and procedures, • Sample of packaged product as required for QC Testing, Stability or as required by the packaging record, • Complete packaging logbooks which includes recording of required information neatly and accurately and verification that data entered by operations is neat, complete and accurate, • Perform and verify documentation for packaging qualification, • Maintenance of house standards, comparison of product for physical verification, • Communicate with production personnel which includes but not limited to the availability to perform line cleaning and line release approval, product and/or equipment related quality issues, • Review of packaging documentation, • Inspection of final finished, package prior to end of packaging run and before transfer to warehouse, • Notify QA management of any quality or safety concerns, • Knowledge of cGMPs related to US FDA manufacturing and packaging environments, • Compliance with applicable company policies such as cGMP and related SOPs, • Responsible for compliance with all rules and regulations pertaining to safety policies and for leading by example with the proper attitude toward safety and health help to ensure that all department operations are performed with the utmost regard for the safety and health for all personnel., • Other responsibilities as assigned by Senior management Requirements: Education and Experience: • High School or GED diploma required with college a plus, • Knowledge of and ability to perform basic math, • Knowledge of Microsoft Office Programs, • Excellent organizational skills and detail-oriented, • Required to reach with arms and use hands and fingers to handle or feel objects and tools, • Required to stoop, kneel, crouch, stand, bend, sit, talk, hear, climb stairs and ladders, • Work environment in production operations facilities include close proximity to heavy machinery with loud noises and pharmaceutical powders (dust)., • Potential to move between production operations sites/areas to complete job functions., • Employee work hours/schedule and/or shift are subject to change based on business needs and Management discretion., • Gowning as required by GMPs and/or SOPs $21.50 per hour

Job Title: QA Inspector Location: Hauppauge & Central Islip, NY Job Type: Full-Time Department: Quality Assurance About the Company We are a leading generic pharmaceutical manufacturing company with state-of-the-art facilities in Hauppauge and Central Islip, NY. We are committed to producing high-quality medicines that meet regulatory standards and improve patient lives. We are currently expanding our teams across multiple departments, including Warehouse, Packaging, Manufacturing, QA Document Control, and more. Position Summary The QA Inspector is responsible for ensuring that products, processes, and documentation comply with current Good Manufacturing Practices (cGMP), company policies, and regulatory requirements. This role involves in-process checks, batch record review, and oversight of production activities to maintain the highest level of quality and compliance. Key Responsibilities • Perform in-process inspections in manufacturing, packaging, and warehouse areas to ensure compliance with cGMP., • Review batch records, logbooks, and supporting documentation for accuracy and completeness., • Verify line clearance, equipment cleanliness, and readiness prior to manufacturing and packaging operations., • Conduct sampling of raw materials, in-process materials, and finished products as per SOPs., • Monitor adherence to Standard Operating Procedures (SOPs), regulatory requirements, and internal quality policies., • Document deviations, non-conformances, and report findings to QA management., • Support investigations, CAPAs, and change controls as required., • Ensure compliance with safety, sanitation, and quality standards throughout the facility., • Provide guidance to production teams to maintain compliance during daily operations., • Collaborate with cross-functional departments to resolve quality-related issues. Qualifications • Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, or related discipline preferred., • Minimum of 1–3 years QA experience in pharmaceutical manufacturing (OSD, sterile, or packaging)., • Strong knowledge of cGMP, FDA, and regulatory guidelines., • Experience with documentation review and in-process quality inspections., • Excellent attention to detail, organizational, and communication skills., • Ability to work independently and collaboratively in a fast-paced environment. Skills & Competencies • Knowledge of pharmaceutical production processes (Manufacturing, Packaging, Warehouse)., • Strong documentation and record-keeping abilities., • Problem-solving and decision-making skills., • Familiarity with QA Document Control processes., • Ability to multitask and manage priorities. What We Offer • Competitive base salary, • Comprehensive benefits package (Medical, Dental, Vision, 401(k) with match), • Paid Time Off (PTO), Holidays, and Sick Leave, • Professional growth opportunities in a fast-growing pharmaceutical company Equal Opportunity Employer: We value diversity and are committed to creating an inclusive environment for all employees.

The 2nd Shift QC Inspector ensures product quality and compliance with FDA regulations and cGMP standards.This role involves performing in-process and final inspections of OTC lip balm, sunscreen, and hand sanitizer, as well as verifying packaging, labeling, and material integrity.The inspector docu

We are committed to producing high-quality medicines that meet regulatory standards and improve patient lives. This role involves in-process checks, batch record review, and oversight of production activities to maintain the highest level of quality and compliance. Monitor adherence to Standard Oper

Inspector; QA Manufacturing - Weekend (12:00PM - 12:30AM).Commerce+Drive+Hauppauge+NY+USA+11788).Position Summary:The Inspector, QA Manufacturing has the primary responsibility of ensuring product quality is maintained through all phases of manufacturing in accordance with current good manufacturing

Quality Assurance Inspector II - DPI. The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing or packaging in compliance with established specification.

Quality Inspector Job Duties: Inspects and approves incoming materials by confirming specifications, conducting visual and measurement tests, and rejecting and returning unacceptable materials. Docum

Ensure compliance with safety, sanitation, and quality standards throughout the facility. Collaborate with cross-functional departments to resolve quality-related issues. Experience with documentation review and in-process quality inspections.

East Syracuse, NY, we are seeking a Senior Quality Inspector, In-Process Inspection to:. Develop deviation reports and represent quality at the Material Review Board. Experienced in quality management systems and become a subject matter expert in the company management system.

Collaborate with cross-functional departments to resolve quality-related issues. Experience with documentation review and in-process quality inspections. We are committed to producing high-quality medicines that meet regulatory standards and improve patient lives.

Monitor adherence to Standard Operating Procedures (SOPs), regulatory requirements, and internal quality policies. Ensure compliance with safety, sanitation, and quality standards throughout the facility. Collaborate with cross-functional departments to resolve quality-related issues.

Manpower - JobID: 5773517 [Production Operator / Assembly Line Worker] As an Assembler at Manpower, you'll: Assemble products according to specifications; Inspect finished products for quality control; Operate machinery and tools to complete tasks; Follow safety protocols and guidelines at all times

Develop and monitor program goals and outcomes and provide quality improvement training for staff to facilitate achievement of goals. Knowledge of quality management issues. Participate in task groups and committees that work towards overall agency Quality improvement initiatives.

Purpose of the Position: To conduct Quality Improvement activities within the Department/division to help ensure the quality of care and services of the persons and families served at SCO Family of Services. Prepare quarterly and annual Internal Quality Monitoring reports capturing key program indic

This position is instrumental in enhancing and strengthening our manufacturing processes by executing on our internal manufacturing and quality processes and procedures and contributing to continuous improvement and optimization efforts. Upholding quality standards while meeting production quotas. P

Installer] - PT or FT / Easy Payments With Competitive Pay Rates / Flexible Scheduling / Access to Handy's Large Customer Base - As a Handy Pro Furniture Assembler you'll: Be responsible for for assembling a variety of furniture pieces in our customers' homes; Assemble a wide range of furniture item

Documents actions by completing production and quality forms.

Installer] - PT or FT / Easy Payments With Competitive Pay Rates / Flexible Scheduling / Access to Handy's Large Customer Base - As a Handy Pro Furniture Assembler you'll: Be responsible for for assembling a variety of furniture pieces in our customers' homes; Assemble a wide range of furniture item

Make an impact in the role of Coca-Cola Quality Control Technician to follow safety procedures and company policies, provide excellent service to customers and team members, and gain knowledge of company offerings to better serve clients. Other duties include assist with processing returns and excha

Installer] - PT or FT / Easy Payments With Competitive Pay Rates / Flexible Scheduling / Access to Handy's Large Customer Base - As a Handy Pro Furniture Assembler you'll: Be responsible for for assembling a variety of furniture pieces in our customers' homes; Assemble a wide range of furniture item

Take the next step as our new Coca-Cola Quality Control Technician to perform daily responsibilities with dedication.

Installer] - PT or FT / Easy Payments With Competitive Pay Rates / Flexible Scheduling / Access to Handy's Large Customer Base - As a Handy Pro Furniture Assembler you'll: Be responsible for for assembling a variety of furniture pieces in our customers' homes; Assemble a wide range of furniture item

We have an opening for a talented Assembler to gain knowledge of company offerings to better serve clients, provide excellent service to customers and team members, and manage daily responsibilities with a focus on quality and efficiency.

Installer] - PT or FT / Easy Payments With Competitive Pay Rates / Flexible Scheduling / Access to Handy's Large Customer Base - As a Handy Pro Furniture Assembler you'll: Be responsible for for assembling a variety of furniture pieces in our customers' homes; Assemble a wide range of furniture item

We have an opening for a talented Coca-Cola Quality Control Technician to maintain accurate records and documentation, support the preparation and delivery of goods or services, and respond promptly to inquiries and resolve basic issues. Other duties include coordinate tasks to ensure deadlines are

Construction Inspector III is qualified to independently perform, test, inspect and record project operations with a high degree of complexity. The Inspector III must have demonstrated ability to perform effectively in the field and in the office with minimal supervision/oversight in all phases of c

Documents actions by completing production and quality forms.

Construction Inspector II should have basic knowledge and be able to inspect basic operations of earthwork, pavement, structural components and utilities. The Inspector II should be able to identify observed, measured or tested properties and provide accurate and appropriate notes and reports of suc

Make an impact in the role of Coca-Cola Quality Control Technician to follow safety procedures and company policies, provide excellent service to customers and team members, and gain knowledge of company offerings to better serve clients. Other duties include assist with processing returns and excha

Construction Inspector I should be able to follow technical instructions and learn typical construction inspection methods from more experienced construction inspectors. Creighton Manning, a GAI Company is seeking a Construction Inspector I to join our team.

Documents actions by completing production and quality forms.

Our Melville, NY office is seeking a Senior Construction Inspector to work on various roadway and bridge infrastructure projects in Nassau and Suffolk Counties. Prepare daily Inspector reports.

Help us succeed as our next Coca-Cola Quality Control Technician to inspect products for quality and compliance.

Our Melville, NY office is seeking Construction Inspectors to work on various roadway and bridge infrastructure projects in Nassau and Suffolk Counties. Prepare daily Inspector reports.

An exciting opportunity awaits for a Coca-Cola Quality Control Technician to inspect products for quality and compliance.

Production Assembler/Builder Since 2014, RW Gate Company has designed and manufactured the highest quality water control gates and related equipment used in water control systems. You will assemble component parts into high quality water control gates. Essential duties and Responsibilities: Com

Documents actions by completing production and quality forms.

Quality Assurance: Perform quality work checks, identify product defects, and record any identified defects for further analysis and correction. Safety and Cleanliness: Perform all work in accordance with quality standards and established safety procedures.

If job security and benefits are a priority to you, you'll want to interview with this awesome company for this excellent career opportunity! Our client has decades of secure government contracts to keep them busy and they really go above and beyond with their benefits package to include:.AND an add

Quality Assurance: Perform quality work checks, identify product defects, and record any identified defects for further analysis and correction. Safety and Cleanliness: Perform all work in accordance with quality standards and established safety procedures.