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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 Immediate opening is available for full-time Mechanical Inspectors, 1st Class and 2nd Class for Production and Final Quality Inspection in Farmingdale. NY. Responsibilities include monitoring, measuring, and documenting the characteristics of products as compared to product requirements and prevent non-conforming product. This position will work with machined and fabricated metal products at various stages in our manufacturing processes including final Quality Inspection. We are seeking individuals with excellent interpersonal skills and operational expertise to join our production team. Essential Duties and Responsibilities include the following: • Monitor and measure the characteristics of products at appropriate stages of product realization., • Document and analyze the conformity of product to required specifications, • Cooperate with manufacturing to prevent non-conforming product and continuously improve processes. Supervisory Responsibilities: This job has no supervisory responsibilities. Balances team and individual responsibilities; Gives and welcomes feedback; Puts success of team above own interests. • Written Communication - Excellent command of the written English language; Writes clearly and informatively; Varies writing style to meet needs; comprehends and applies proper email etiquette; presents numerical data effectively; able to read and interpret complex written information (customer specification manuals, contracts, etc)., • Problem Solving -- identifies and resolves problems in a timely manner; gathers and analyzes information and data skillfully; develops alternative solutions; works well in group problem solving situations. Requirements Education and/or Experience: A high school diploma or equivalent. The preferred candidate will have: • Experience with Measuring and Testing Equipment including CMM equipment., • Ability to read and interpret part drawings, product specifications, and other related documentation. Must understand Geometric Dimensioning and Tolerances (GD&T) to product inspection Qualifications / Requirements: • Must be a detail-oriented, communicator, able to prioritize tasks and able to work under pressure with multiple deadlines., • Must be able to use all standard measuring instruments and CMM equipment., • While performing the duties of this Job, the employee is regularly required to sit; use hands to type, handle and feel. Employees must be able to communicate effectively through talking and listening. The employee is occasionally required to stand; walk, and reach, lift and carry objects weighing up to 25 lbs with hands and arms.

Job Description Schivo Medical, in Plainview , NY keeps the world’s most advanced CNC machining and precision manufacturing equipment running at peak performance. Our teams work with 5-axis mills, Swiss machines, EDM, lasers, and other high-end systems that produce critical components for medical and life science customers. We partner directly with leading OEMs and service providers, so every repair, calibration, and upgrade keep production moving and customers confident. Schivo is growing fast, with opportunities to build your skills across different technologies and move up or across into new roles. We are a team that values problem-solvers who can roll up their sleeves, think on their feet, and keep complex machines humming. Quality control inspector/ Operator Job Position Overview: Performs a variety Quality Control related tasks. Verifies components are produced to print and relate the results to appropriate personal. Prepares various paperwork. Inspect various inspection gages issued to production. Quality control inspector/ Operator Knowledge, Skills and Abilities: • Perform in-progress inspection for all machined components., • Review operator inspection reports and traveler information., • Submit reports to shift supervisor and communicate the results to machine operators., • Perform First Article Inspection for new parts (set ups), • Follows established departmental policies, procedures, and objectives, continuous quality improvement objectives, and safety, environmental, control standards., • Detail knowledge of inspection techniques, tools and methodology, • Working knowledge of GD &T, • Ability to read and interpret engineering drawings and blueprints, • Must possess the ability to use a wide variety of measuring devices to perform dimensional inspection of components produced., • Must be dependable and possess a willingness to learn new techniques., • Medical and Aerospace manufacturing experience with emphasis on FAIR, • Follow the quality standards of ISO-13485 Minimum Job Requirements & Education Associates or BS degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Or High school diploma or GED; at least 2 years of experience that is directly related to the duties and responsibilities specified in a ISO-certified company . Benefits: • 401(k), • 401(k)match, • Dental insurance, • Health insurance, • Vision insurance, • Generous Paid time off, • Employee referral program, • EAP Program, • Free coffee & tea daily Schivo Medical is an Equal Opportunity Employer. All qualified applicants will receive employment consideration without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

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 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 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 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 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.

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

The Quality Inspector is responsible for providing QA support to the manufacturing and packaging process. Minimum of 1 year experience in quality assurance in a manufacturing setting is required. Founded in 2011, Piping Rock Health Products has gone on to win Long Island's Top Workplaces Award 7 yea

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

We are committed to producing high-quality medicines that meet regulatory standards and improve patient lives. The QA Inspector is responsible for ensuring that products, processes, and documentation comply with current Good Manufacturing Practices (cGMP), company policies, and regulatory requiremen

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.

Participates in special projects related to quality issues; assists in recommendations and coordinating implementation of plan of corrective action; assists in preparing monthly variance reports for the leadership, physicians, and other hospital personnel as needed Presents patient specific issues a

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

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

Documents actions by completing production and quality forms.

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

Documents actions by completing production and quality forms.

Other duties include assist with processing returns and exchanges, adapt to shifting priorities and business needs, respond promptly to inquiries and resolve basic issues, maintain accurate records and documentation, manage daily responsibilities with a focus on quality and efficiency, along with co

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.

Position type: Contract Onsite Required: Experience as a Construction Inspector Responsibilities: Responsibilities of inspector in ensuring the work is conducted safely, to specified standards. Collection Network Construction Inspector. At-a-glance: Are you ready to build your career by joining an i

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

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

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

Other duties include coordinate tasks to ensure deadlines are met, gain knowledge of company offerings to better serve clients, manage daily responsibilities with a focus on quality and efficiency, adapt to shifting priorities and business needs, assist with processing returns and exchanges, along w

The Inspector II should be able to identify observed, measured or tested properties and provide accurate and appropriate notes and reports of such. Creighton Manning, a GAI Company is seeking a Construction Inspector II to join our team. Construction Inspector II should have basic knowledge and be a

Documents actions by completing production and quality forms.

The Inspector III can be responsible for the supervision of a small team of inspection staff. 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 ef

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.

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.

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.

Demonstrates accuracy and thoroughness; monitors own work to ensure quality. Presents objective evidence to Quality Control that tasks were completed to all specifications.

Publicly Traded US Company, NASDAQ (TTMI) - Top-5 Global Printed Circuit Board Manufacturer.RF") components and RF microwave/microelectronic assemblies, and quick-turn and technologically advanced printed circuit boards ("PCBs").TTM stands for time-to-market, representing how TTM's time-critical, on