Quality control inspector jobs in Stamford, CT

Pay Range: $30-45 Must be a US Citizen or US Person (Greencard Holder) to apply. This is a W2 contract with a 4-month duration. Seeking a Quality Control Inspector for our client specializing in aerospace and defense products. Must have the ability to work autonomously as well as collaborate effectively with a team and be capable of maintaining precision in a fast-paced environment while meeting deadlines. Responsibilities: * Inspect material (incoming and in-process per J-STD, IPC, and NASA standards) * Minimal lifting (under 25 pounds) * Provide Quality control activities * Document non-conformances and report major quality issues to leadership * First Article inspection Qualifications to Apply: * Certified inspector in MIL/Aerospace workmanship: J-STD, IPC-6110, NASA * US Person or Citizenship * HS Diploma or GED required, advanced degrees desired. * Minimum 5 years of experience gained in a manufacturing environment. * Technically competent, able to read and interpret engineering drawings. Benefits provided: 401K, medical, dental, and vision, sick time as applicable to state law Butler America Aerospace, LLC. is an equal opportunity employer. Butler evaluates applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. The Butler America Aerospace, LLC. EEO Policy Statement and "Know Your Rights" Poster is available here: Applicant and Employee Notices. #zr Butler America Aerospace, LLC. is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process, please contact the Human Resources Department at accommodations@butler.com. #ZR

AMC Networks is home to many of the greatest stories and characters in TV and film and the premier destination for passionate and engaged fan communities around the world. We create and curate celebrated series and films across distinct brands and make them available to audiences everywhere. Our portfolio includes targeted streaming services AMC+, Acorn TV, Shudder, Sundance Now, ALLBLK and HIDIVE; cable networks AMC, BBC AMERICA, Independent Film Company, Sundance TV and We TV; and film distribution labels Independent Film Company and RLJE Films. The company also operates AMC Studios, our in-house studio, production, and distribution operation behind acclaimed and fan-favorite originals including The Walking Dead Universe and the Anne Rice Immortal Universe, and AMC Networks International, our international programming business. We are currently seeking a Quality Control Technician to join our Media Operations & Engineering team based in our Bethpage, NY office. JOB RESPONSIBILITIES * Responsible for the quality control evaluation of AMCN Broadcasting & Technologies client Network's program materials - both digitally delivered files and physical tapes. * Utilize and understand industry and departmental quality control procedures, guidelines, and department document database for proper and complete media evaluation. * Provide full and accurate metadata entries and reports of quality control assignments, giving great attention to detail and accuracy. * Maintain effective and productive communication channels with various AMCN B&T departments and colleagues, as they relate to scheduled work assignments and troubleshooting. * Understand and properly use all technical equipment related to work completion. * Report and document equipment issues and anomalies. Qualifications (Required & Preferred) * Bachelor's degree in relevant field major (i.e. Communications, TV Production, etc.) preferred. * At minimum, two years of relevant work experience in a broadcast television environment. * Excellent research, evaluation, and troubleshooting skills. * Outstanding communication skills, both verbal and written. * Comprehensive knowledge of time code, reference, frame rates, resolution, aspect ratios, audio formats (PCM) and types (surround/stereo), digital file formats. * Advanced knowledge of NTSC, PAL and HD video/audio broadcast standards and specifications. * General understanding of digital file codecs/wrappers and transcoding workflows. * Willingness to maintain flexible work schedule including nights, weekends, and holidays at management's discretion. * Strong analytic skills & critical thinking * Ability to absorb and retain information quickly * Excellent interpersonal skills. * High level of attention to detail. * Ability to interact and collaborate with all levels of management, co-workers and other departments. * Ability to quickly adapt to new technologies and workflows in a rapidly evolving environment. * Ideal candidate will be well versed in file based workflows. * Experience with the Evertz Mediator platform a plus. * Exposure to delivering digital files and elements to Electronic Sell Through platforms a plus. * Experience delivering media to VOD services a plus. The base compensation for this position is $52,000 to $55,000 commensurate with experience. AMC Networks additionally offers a comprehensive benefits package including Medical, Dental, Vision, Prescription Drug Coverage, 401k Plan, Wellness Program, Life Insurance, Tuition Reimbursement, Paid Time Off, Paid Parental Leave and Adoption Services, among other benefit plan options, subject to eligibility requirements. AMC Networks values the benefits achieved through in-office collaboration, but we provide our employees with the flexibility to work from home one day per week. The Company is committed to policy of nondiscrimination in its employment and personnel practices. Applicants are considered for all employment without regard to race, color, religious creed, religion, alienage, citizenship, gender, gender identity, national origin, ancestry, genetic predisposition or carrier status, age, marital status, familial status, military or veteran status, status as a victim of domestic violence, stalking or sexual assault, sexual orientation, disability or any other characteristic protected by federal, state or local law.

The Quality Inspector will complete visual inspection of printed card assemblies and sub-assemblies. They will review paperwork, complete computer entry, read and interpret drawings and documents. They will interface with production line and visiting customers. They will also work in clean room environments. Required Skills Good written and verbal communication skills. Problem solving and analytical skills a plus. Keen attention to detail. Basic computer and math skills to measure specifications. Ability to use measuring devices such as gauges, meters, calipers and computers. Experience with workmanship specifications JSTD-001 and IPC-610 certifications required MIL-STD 38534, MIL-STD 38535 preferred EOE/Disability/Veteran This position is onsite We offer a comprehensive benefit package including: Health Insurance, Dental and Vision, Life Insurance, Short and Long-Term Disability. Flexible spending option and 401K. We also offer paid time off including: Vacation, Sick and Paid Holidays

I have an awesome QC Reference Tech role available near S Floral Park, New York State! Details - Full-time and permanent - Shift: Days or Evenings - Opportunities for growth - Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc) - Pay: $44-$52/hr Requirements - College degree - NYS license - ASCP cert - Prior experience Click apply or email your resume to leah@ka-recruiting.com/call or text 617-746-2751! You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min. REF#LM2491

Principal Responsibilities Capable of reading and understanding complex drawings. Ability to use a variety of complex inspection gages and equipment. Performs visual and dimensional inspection of various mechanical components and assemblies to close tolerances. Identifies defects in surface, dimensional, visual and non-conformities (material, documentation and workmanship) to blue prints and Heim quality standards. Reports non-conformance of materials or unusual conditions to Quality management. Familiarity with Quality System(s) - ISO 9001, AS9100, etc. Coordinates and performs inspection processes and accepts product as a Designated Supplier Quality Representative for customers. Interacts with customers during source inspection. Completes paperwork. Reviews and interprets customer specifications. Maintains and updates delegation/regulatory documentation. Verifies material and process certifications for compliance with customer/regulatory requirements. Passes customer required Delegation Program Tests to achieve and maintain delegation approval. Inspects and accepts product under the FAA: PMA/TSO program as a Designated Manufacturing Inspection Representative. Prepares and signs FAA Airworthiness Approval Tags. Initiates and completes Fist Article Inspection Reports and other relevant quality reports. Maintains records, data and logs as necessary. Investigates and analyzes Quality issues and brings departments together to resolve problems. Provides written documentation and reports. Follows work procedures. Provides support to achieve short-term and long-term department / company goals. Provides leadership/training as needed. Ensures that production schedules and customer requirements are met. Maintains clean and safe work environment. Follows safety and environmental procedures and regulations. Reports safety incidents to supervisor. Makes recommendations for improvements to work processes and procedures. Contributes to 6 S programs in work area. Provides a high level of service to all internal and external customers. Contributes to positive teamwork environment. Performs other duties as assigned. Participates in training/learning other positions. Accomplishes related results as needed. Qualifications An AS degree in Industrial Technology or equivalent work experience of 6-8 years in a manufacturing environment, preferably in an aerospace manufacturing environment. “A” level Inspector or equivalent experience is required or any combination of knowledge, skill and experience to the satisfaction of the manager. Knowledge, Skills and Abilities Analytical Thinking Attention to Detail, thoroughness and accuracy Blueprint Reading Inspection Mechanical Ability Measurement and Test Equipment Communication (Speaking, Questioning, Listening) Computer (Word, Excel, Access) Customer focus Decision Making Dependability Initiative Interpreting Customer Requirements Organization Problem Solving Results Oriented Team Oriented Writing, documentation Knowledge Essential to the Position Customer requirements Inspection Techniques - Read and Interpret specifications Other: Travel: 25% Requires Certificates / Licenses: Customer Requirements / Quality Delegation Programs FAA

Job DescriptionBenefits: 401(k) Health insurance Paid time off Special Testing Laboratories, a construction materials testing & inspection services company, is seeking a CWI Certified Structural Steel Inspector to provide scheduled steel inspection services on various construction job sites and steel shops. As an Inspector, you will work closely with project superintendents to inspect the different phases of steel construction and to identify any discrepancies as necessary. Inspections will include (but are not limited to) assessment and inspection of both field and shop welding, metal decking, bolting, light gauge, cold-form framing, shear studs, ultrasonic, and column plumb. As an inspector, you will also be required to provide daily inspection reports and work closely with office staff on scheduling and reporting. The ideal candidate should reside either in Connecticut or Westchester County, NY. Job Requirements: -AWS-CWI Certification or certification in progress -Minimum education of a high-school diploma, college a plus -Experience in the industry required -UT Certification a plus -OSHA Certification a plus -Good written and oral communication skills -Ability to work well with staff and clients in a professional manner -Ability to handle multiple tasks -A valid driver's license and have daily access to a reliable vehicle STL is an equal opportunity/affirmative action employer.

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, located in Plainview , NY, is a contract manufacturer that make medical components that enhance and save people lives. ***We are hiring a quality control inspector with knowledge in the manufacturing of medical and surgical tools*** Quality Control Inspector Job Overview: Quality Control related tasks such has verifying components that are produced to print and relate the results to appropriate personal. Quality Control Inspector Knowledge, Skills and Abilities Required: Perform in-progress inspection for all machined components. Operate CMM machines, Keyence and visions systems 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 Experience using measuring tools a plus 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 Knowledge of GD& T helpful Minimum Job Requirements & Education* Completed AAS degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis. Concentration on taking classes based in quality and metrology plus High school diploma or GED; at least 2 years of experience in a CNC Manufacturing environment Benefits:* 401(k) 401(Match) Dental insurance Health insurance Vision insurance Generous Paid time off EAP Program Employee referral ******Must be authorized to work in the United States********* 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 Principal Responsibilities Capable of reading and understanding complex drawings. Ability to use a variety of complex inspection gages and equipment. Performs visual and dimensional inspection of various mechanical components and assemblies to close tolerances. Identifies defects in surface, dimensional, visual and non-conformities (material, documentation and workmanship) to blue prints and Heim quality standards. Reports non-conformance of materials or unusual conditions to Quality management. Familiarity with Quality System(s) - ISO 9001, AS9100, etc. Coordinates and performs inspection processes and accepts product as a Designated Supplier Quality Representative for customers. Interacts with customers during source inspection. Completes paperwork. Reviews and interprets customer specifications. Maintains and updates delegation/regulatory documentation. Verifies material and process certifications for compliance with customer/regulatory requirements. Passes customer required Delegation Program Tests to achieve and maintain delegation approval. Inspects and accepts product under the FAA: PMA/TSO program as a Designated Manufacturing Inspection Representative. Prepares and signs FAA Airworthiness Approval Tags. Initiates and completes Fist Article Inspection Reports and other relevant quality reports. Maintains records, data and logs as necessary. Investigates and analyzes Quality issues and brings departments together to resolve problems. Provides written documentation and reports. Follows work procedures. Provides support to achieve short-term and long-term department / company goals. Provides leadership/training as needed. Ensures that production schedules and customer requirements are met. Maintains clean and safe work environment. Follows safety and environmental procedures and regulations. Reports safety incidents to supervisor. Makes recommendations for improvements to work processes and procedures. Contributes to 6 S programs in work area. Provides a high level of service to all internal and external customers. Contributes to positive teamwork environment. Performs other duties as assigned. Participates in training/learning other positions. Accomplishes related results as needed. Qualifications An AS degree in Industrial Technology or equivalent work experience of 6-8 years in a manufacturing environment, preferably in an aerospace manufacturing environment. “A” level Inspector or equivalent experience is required or any combination of knowledge, skill and experience to the satisfaction of the manager. Knowledge, Skills and Abilities Analytical Thinking Attention to Detail, thoroughness and accuracy Blueprint Reading Inspection Mechanical Ability Measurement and Test Equipment Communication (Speaking, Questioning, Listening) Computer (Word, Excel, Access) Customer focus Decision Making Dependability Initiative Interpreting Customer Requirements Organization Problem Solving Results Oriented Team Oriented Writing, documentation Knowledge Essential to the Position Customer requirements Inspection Techniques - Read and Interpret specifications Other: Travel: 25% Requires Certificates / Licenses: Customer Requirements / Quality Delegation Programs FAA

JOB DESCRIPTION: The Receiving Quality Inspector shall be responsible for the following: Performing receiving inspection of raw material, hardware and consumable items Review of supplier-provided quality documentation (certificates, test results, etc.) Performance of mechanical inspection of purchased machined parts using hand-held measuring devices Performance of form, fit, function inspection of outside processed parts to design drawings/mylars of sheet metal parts Performance of hardness and continuity testing of outside processed heat treated parts Completion of inspection reports on company-provided formats Data entry in the organization's ERP system - Global Shop Assisting other inspectors in fulfillment of their job duties, as required Performance of any and all tasks in support of the organization's Quality Management System - as assigned by the Director of Quality or his designee

Hourly : 22.72 What do you get when you bring together a team of bright individuals and place them into an environment where “work” means making a difference in the lives of people across the globe? You get Sciolex Corporation, a fast-growing defense contractor focused on providing the U.S. Government a level of service that surpasses the epitome of excellence. Our core services include systems engineering technical advice, technical support, and administrative assistance. From our humble beginning as a small Service Disabled, Veteran Owned Small Business in Chantilly, VA, Sciolex Corporation is now the home for over 1,000 employees across the U.S. Over the past 19 years, Sciolex Corporation has constructed an environment that celebrates diversity and encourages a positive work/life balance, all while supporting government missions that our employees are proud to be a part of. When you work for Sciolex Corporation, you are working for a stable company that values you and is committed to ensuring you receive the utmost employee care. Responsibilities The Quality Control Inspector (QCI) supports the overall mission of the U.S. Citizenship and Immigration Services (USCIS) by facilitating the operations of a local Field Office. As a QCI, your responsibilities would include: Verifies compliance with work standards, SOPs, ROH, and other requirements documents, Pays particular attention to the timeliness and accuracy of work performed, Screens documents to determine accuracy of data contained in them and determines which need corrective action, Keeps various logs and uses random sampling to evaluate process efficiency, accuracy, and timeliness, Responsible for recognizing problems that might invalidate samples, investigating complaints, reviewing violations found by USCIS personnel, and preparing reports of findings and actions needed or taken, Recommends changes that will improve contract performance, Other duties as assigned. Qualifications & Physical Requirements High school diploma or equivalent Must be able to obtain a Public Trust/Suitability Clearance under the Department of Homeland Security from the United States Citizenship and Immigration Services Ability to read and understand proficiently in English Ability to lift and carry up to 45 lbs. or more in a physical environment Ability to perform tasks while bending, stooping, climbing, and reaching At Sciolex Corporation, our top priorities and most valuable resources are our employees, which is why we offer a competitive total compensation package. We are a proud Equal Opportunity Employer (EOE) who celebrates diversity in and out of our organization. Come see where your opportunities for success can flourish. NOTICE: Sciolex Corporation NEVER asks job applicants to issue any payment, service fees, or banking information to Sciolex Corporation or its recruiters as part of our application process. Before providing any personal information to outside parties, verify that the job you are applying for appears on our Careers site.

Job Description BASIC FUNCTIONS Entry level position. Performs basic counterfeit lab testing and visual inspection of various commodities including, but not limited to, electromechanical and electrical devices, electronic components, aircraft parts and hardware. This individual has the responsibility and authority to carry out assigned tasks. SPECIFIC DUTIES Visual and dimensional inspection of all product, including corresponding documentation received into CTG facility Ability to complete a full analysis on all EEE Devices within the Laboratory Ability to learn and subsequently operate all test equipment within the Laboratory Department Prepare and complete all necessary documentation (records) for reporting acceptance/rejection of items inspected and/or tested. Identify nonconformity to provide data to Quality Manager. Ability to communicate, document and report all nonconformity within internal system and direct supervisor. Ability to conduct work as assigned by senior management. Ensure daily tasks and priority inspections are completed ensuring all stock sales are completed for the day. Ability to understand industry traceability and documentation requirement as required for each industry Ability to evaluate and differentiate between various commodity types. Review and implement detailed inspection reports to provide all information regarding product testing and inspection Ability to use general inspection gages, Ex. Calipers, Micrometers, etc. Ability to understand and decipher basic blueprint, data sheet, technical sheet requirements. Must possess the ability to verify products fit, form and function by utilizing the appropriate gages to identify conformity. Ensure First Article Inspection requirements are done in accordance with AS9102 and customer requirements. For source conducted first article inspection, utilized tools, equipment as appropriate to conduct GD&T for inspection reports. Complete AS9102 or equivalent or customer source designated reports for all First Articles and Source Inspections. STANDARD REQUIREMENTS Comply with all requirements of International Standard ISO9001 and ISO27001, NIST 800-171, CMMC - Cyber Security and Informational Data Security Requirements. Aerospace Management System Standards AS9100, AS9120, IDEA-QMS-9090, ASA-100 and supporting construct standards AS6081, IDEA-STD-1010, AC7402-CAAP, CCAP-101, FAA AC00-56, ANSI/ESD S20.20. All employees shall commit and comply with the requirements of AS5553 for Counterfeit Electrical, Electronic and Electromechanical (EEE) Parts - Avoidance, Detection, Mitigation and Disposition practices. METRICS AND MEASURABLES Daily throughput (inspections/Lab steps completed) Quality Issue detections (Incoming NCM ) Outgoing Quality (customer Escapes) IDEA Certification and knowledge implementation Use of GD&T and FAI knowledge for timely FAIR completion Issue communication Daily 6S/ESD/FOD policies followed Ability to find datasheets/drawings information on CTG Systems Diversity of inspections (EC/EM/HA/Hardware/etc) Achieving CQI certification EDUCATION / EXPERIENCE / COMPENTENCY High School Diploma or equivalent 1 year of manufacturing or quality experience is a plus but not required Must be proficient in English, both written and verbal communication skills Good arithmetic skills are required Mechanical aptitude desired Working knowledge of measurement instruments: i.e., calipers, etc. Basic proficiency of Microsoft Excel and Word Must complete IDEA-ICE-3000 Certification within 6 months of hire. Able to pass internal testing and training to meet internal requirements Must demonstrate acceptable vision requirement.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: Quality Control (QC) Lab Technician- Sampling Associate FLSA Classification: Full-Time, Non-Exempt/Hourly Professional Work Location: Central Islip, NY Work Hours: General Shift: 9:00 AM - 5:30 PM (may vary based on business needs) Reports To: Quality Control Director Hourly Rate: $16.64 - $22.88 Purpose: The content and statements documented in this are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent of this is to be representative of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in accordance with the established performance expectations. Scope: The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role. Duties and Responsibilities The general duties and responsibilities of the Quality Control Lab Technician-Sampling associates include but are not limited to the following: Perform sample management for all incoming raw materials and Packing Materials , Ensure correct sampling techniques used for sampling to avoid contamination or mix-ups. Label samples accurately with batch details, ILMS numbers, and other identifiers. Maintain sampling records in logbooks and electronic systems. Follow Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP) during sampling. Adhere to safety and hygiene protocols in the sampling area. Store samples under specified conditions (temperature, humidity) to maintain integrity. Deliver samples to QC analysts for testing within defined timelines. Update all sample information in SAP as per company procedures. Communicate any deviations or abnormalities observed during sampling. Retain samples for reserve samples or additional studies (e.g., NDSRI evaluation) as per SOP. Track sampling tools and consumables. Ensure calibration and cleanliness of sampling equipment. Maintain qualification status for sampling activities. Participate in periodic training on updated SOPs and regulatory requirements. Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and standards and discarding as per company procedures. Complete data entry as required. Maintain lab consumables supply and placing orders as per requirement Assist in the shipment of the samples to contract labs as required Provide general housekeeping in the QC lab and any other functional activity as assigned by management. Other duties as assigned. Education and Experience: Minimum of High School Diploma or equivalent education credential (ex. GED) required. Proficient user of Microsoft Office Programs to include Word, Excel, Outlook, PowerPoint, and other lab-related systems. 2 years' work experience in a laboratory setting. Associates degree or higher in Chemistry, Laboratory Science, or related fields of study from an accredited institution. (Preferred) Bachelor's degree (BS or BA), physical sciences preferred Proficiently speak English as a first or second language Have excellent organization, learning and teaching skills required to work in teams Ability to understand and analyze complex data sets. Working knowledge of Microsoft Office programs and other scientific based software. Experience in oral solid dosage is a plus. Professional and Behavioral Competencies Hourly position. Full time Must be willing to work in a pharmaceutical sampling of Raw material and Packing Material Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. Must be willing to work some weekends based on business needs as required by management. Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors. No remote work available No employment sponsorship or work visas. Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift up to 35 pounds. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: Quality Control (QC) Lab Technician- Sampling Associate FLSA Classification: Full-Time, Non-Exempt/Hourly Professional Work Location: Central Islip, NY Work Hours: General Shift: 9:00 AM - 5:30 PM (may vary based on business needs) Reports To: Quality Control Director Hourly Rate: $16.64 - $22.88 Purpose: The content and statements documented in this are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent of this is to be representative of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position satisfactorily and in accordance with the established performance expectations. Scope: The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role. Duties and Responsibilities The general duties and responsibilities of the Quality Control Lab Technician-Sampling associates include but are not limited to the following: * Perform sample management for all incoming raw materials and Packing Materials , * Ensure correct sampling techniques used for sampling to avoid contamination or mix-ups. * Label samples accurately with batch details, ILMS numbers, and other identifiers. * Maintain sampling records in logbooks and electronic systems. * Follow Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP) during sampling. * Adhere to safety and hygiene protocols in the sampling area. * Store samples under specified conditions (temperature, humidity) to maintain integrity. * Deliver samples to QC analysts for testing within defined timelines. * Update all sample information in SAP as per company procedures. * Communicate any deviations or abnormalities observed during sampling. * Retain samples for reserve samples or additional studies (e.g., NDSRI evaluation) as per SOP. * Track sampling tools and consumables. * Ensure calibration and cleanliness of sampling equipment. * Maintain qualification status for sampling activities. * Participate in periodic training on updated SOPs and regulatory requirements. * Coordinate chemical and reference standard inventory in the lab, verifying the expired chemicals and standards and discarding as per company procedures. * Complete data entry as required. * Maintain lab consumables supply and placing orders as per requirement * Assist in the shipment of the samples to contract labs as required * Provide general housekeeping in the QC lab and any other functional activity as assigned by management. * Other duties as assigned. Education and Experience: * Minimum of High School Diploma or equivalent education credential (ex. GED) required. * Proficient user of Microsoft Office Programs to include Word, Excel, Outlook, PowerPoint, and other lab-related systems. * 2 years' work experience in a laboratory setting. * Associates degree or higher in Chemistry, Laboratory Science, or related fields of study from an accredited institution. (Preferred) * Bachelor's degree (BS or BA), physical sciences preferred * Proficiently speak English as a first or second language * Have excellent organization, learning and teaching skills required to work in teams * Ability to understand and analyze complex data sets. * Working knowledge of Microsoft Office programs and other scientific based software. * Experience in oral solid dosage is a plus. Professional and Behavioral Competencies * Hourly position. * Full time * Must be willing to work in a pharmaceutical sampling of Raw material and Packing Material * Must be willing and able to work any assigned shift ranging from first or second shift. * Work schedule may be Monday to Friday. * Must be willing to work some weekends based on business needs as required by management. * Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors. * No remote work available * No employment sponsorship or work visas. Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Long periods of standing up/walking during the working hours; ability to ascent/decent ladders; and able to lift up to 35 pounds. GLOBAL COMPANY Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

The Quality INSEPCTOR position will be responsible for inspection of all incoming raw materials and finished products. Tasks will require use of calipers, micrometers, gauges, optical comparator, drawing comparisons and other inspection tools - candidate MUST have experience with relevant equiptment. Report, analyze and trend quality data (i.e. non-conforming material and inspection results). Work directly with suppliers to address quality concerns and assess performance. Responsible for specific quality programs as assigned, other related responsibilities as follows: Ensures company standard practices and cGMP procedures are followed. Issue Batch Records to production and Finished Good inspection records to Operations Maintains SOP binders and updates such through approved Change Controls. Participate in internal and external audit process Inspect and evaluate all incoming components and labeling Inspection and testing of finished goods Authorize release of Quarantined components for production use Responsible for calibration schedules for testing and production equipment PROVIDE SALARY HISTORY TO BE CONSIDERED Qualifications Relevant quality experience along with cGMP and 2 years experience preferred. Experience with FDA compliance regulations a plus Additional Information To be considered you MUST provide the following: Current resume Full Salary History Salary & Benefits : Salary will be based on experience Medical Benefits package available Schedule - F/T Monday to Friday 7:30 to 4:00 pm PLEASE NO RECRUITERS OR SOLICITATIONS! All your information will be kept confidential according to EEO guidelines.

Open Scientific provides contract staffing and direct hire recruitment services for the scientific, engineering, laboratory and manufacturing sectors. Job Description Quality Inspector A large labeling company is looking for Quality Inspectors. The labeling company works with large companies nationwide to provide labels for their products. The Quality Inspectors ensure the overall excellence of products or goods manufactured. They are the “last line of defense” to ensure the product is in excellent condition for the customers. Successful people in this role has great attention to detail. This is perfect for someone looking for long term work and growth. Requirements: · 1 - 2 years' experience in related field · Knowledge of FDA/cGMP guidelines · Basic writing and math skills · Strong verbal communication skills · Fluent in English, Spanish a plus · Must be able to stand on feet all day Location: Hauppauge Pay Rate: $12-$15 per hour 1st and 2nd shift available Benefits: Sick days, Vacation, 401k, Medical, Dental and much more Additional Information All your information will be kept confidential according to EEO guidelines.

As a leader and innovator in the snack food industry for over 50 years, J&J Snack Foods provides branded snack foods to foodservice and retail supermarket outlets across the U.S. Its products include such icons as SUPERPRETZEL, ICEE, and Dippin' Dots along with other key brands like LUIGI'S Real Italian Ice, The Funnel Cake Factory Funnel Cakes, and Hola Churros. J&J also has a strong presence in bakery providing cakes, cookies, and pies to some of the largest grocery and convenience retailers in industry. Our company continues to deliver record sales led by a talented team and a commitment to “Fun Served Here”. POSITION SUMMARY: The Technician I, FSQA-Bakery is a contributing member of the team-oriented FSQA process, including responsibility for protecting the food by conducting food safety and quality sampling, testing, and completing required documentation to meet J&J Snacks Foods requirements. ESSENTIAL FUNCTIONS: The Technician I, FSQA-Bakery conducts food safety and quality assurance procedures to ensure J&J Snacks Foods is in compliance with expectations for food safety and quality. Understanding of and demonstrates J&J Snack Foods core values and acts with integrity, takes ownership in their work, proactively identifies the needs of our customers, generates creative and new ideas, and promotes an environment where our people and foods are safe. Understanding of the Food Safety and Quality Objectives and Global Food Safety and Quality Policy. Verifies all applicable J&J Snacks Foods expectations are met. Ensure that our foods meet J&J Snacks Foods standards and specifications. Participate in Pre-operational inspections with a cross-functional team. Physical bakery inspections, such as GMP and Hygiene, Food Safety, Foreign material, etc. Understanding and identification of non-conforming raw materials, semi-finished and finished foods. Communicate any human, food, or equipment safety concerns to Supervision immediately. Support the Hazard Analysis & Risk-Based Preventive Controls Food Safety Team in the participation of an effective Food Safety plan focused on the elimination of biological, chemical, physical, and economically motivated hazards from our foods. Conduct sampling, testing, and documentation of the J&J Snacks Foods procedures and records. Understanding and verification of 21 CFR 117 Subpart B Current Good Manufacturing Practices (cGMPs), Prerequisite and Preventive Control Programs and Critical Control Points (HACCP). Trained in and verification of Net Weight Policy and MAV limits. Verification of lot traceability, how packaging and raw ingredients are coded, coding of finished foods, and recipe verification against the manufacturing specification. Verification and understanding of Document Control and Record Completion Procedures. Verification and understanding of J&J Snacks Foods (i.e., GMP, Hygiene and Personnel Practices Program, Allergen Control and Preventive Control Program, Non- conformance Program). Performs other duties as assigned or required. COMPETENCIES: Effective work ethic Ability to operate scales, metal detection and imaging devices (if applicable), ovens and other instrumentation and measuring devices. Education, Technical Qualifications, Experience and Competencies Proficiency Level Required High School Diploma Reading, Writing and Math Skills Proficient computer skills including experience MS Outlook & Excel Must be able to work in a fast-paced environment and must also effectively manage and execute changes. Position requires ability to act as a member of a highly functioning team. Effective communication, writing, analytical, and critical thinking skills. Preferred Some college science courses or experience in the food industry. 1-2 years related experience. US Hourly Pay Range $18.50 - $20 USD Disclaimer: This position description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the team member. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. EEO Statement: J&J Snack Foods Corp.is an equal opportunity employer and prohibits discriminatory employment actions against, and treatment of, employees and applicants for employment based on actual or perceived Federal, State and local laws that prohibit employment discrimination on the basis of race, color, age, national origin, ethnicity, alienage, religion or creed, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability or veteran's status, sex offenses, prior record of arrest or conviction, genetic information or predisposing genetic characteristic, status as a victim or witness of domestic violence, sex offenses or stalking and unemployment status.

Hamilton Connections is seeking candidates for a quality control inspector operating at a manufacturing company in Danbury, CT. The quality control inspector is responsible for testing, evaluating and documenting the quality of manufactured products. The hours are 3:30 p.m.-12 a.m., Monday-Friday. The job pays $28-$32 an hour, depending on experience. Job Responsibilities: Perform first piece, final and first article inspections of products to inspect for damage and/or defects Use measuring tools like calipers, micrometers and gages to inspect products Measure products for accuracy according to blueprint specifications Maintain accurate documentation and reporting Other duties as assigned Job Requirements: 5 or more years of quality control experience, including first piece, final and first article inspections Experience with precision measuring instruments, including calipers, micrometers, height gages, plug gages and thread gages Able to read blueprints Coordinate Measuring Machines (CMM), vision system and/or optical comparator experience Geometric Dimensioning and Tolerancing (GD&T) experience Familiar with ISO procedures a plus Organized, responsible and self-driven High school diploma or equivalent Able to pass pre-employment screenings

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.