Quality Technician Jobs in Clarkstown, NY

The Metal Manufacturing Q/A inspector is responsible for inspecting precision metal components and assemblies from production, confirming specifications, conducting visual and measurement tests, while utilizing various gauges and inspection equipment. Performs first article inspections, documents and records following QMS procedures. Is responsible for completing in process inspection reports and final inspection reports accurately and in a timely fashion. DUTIES AND RESPONSIBILITIES: Performs in-process, and final inspection of parts using measuring equipment such as micrometers and calipers while following established in-process inspection procedures Works from Engineering drawings and other established specifications Reads Blue Prints and inspects to ensure strict adherence to tolerances Produces In process and Final Inspection reports Inspects Incoming material Calibrates tools in inspection and for other machinists Inputs data into database, as required for calibration and rejection data Performs other related duties as assigned by management Completes in-process and other quality inspection paperwork to ensure that established processes are being followed and quality is ensured. SUPERVISORY RESPONSIBILITIES: This job has no supervisory responsibilities. QUALIFICATIONS: Ideally a BS from accredited school or Diploma from an accredited Technical School preferred; Minimum High School Diploma, GED or equivalent is required. Must be authorized to work in the US for any company. Minimum 5 Years quality assurance inspection experience in contract manufacturing. Must have basic GD&T knowledge. Working knowledge of ISO9001 / ISO13485 QMS requirements. Proficiency in using of mechanical inspection equipment; including micrometers, gages, calipers, CMM and other inspection measuring tools. Computer skills required: E2 MRP Systems; Microsoft Office Suite; Project Management Software; Ability to write and send E-mails to peers, reports, customers, and suppliers as needed Educated in ISO manufacturing requirements Educated in FDA manufacturing requirements Training requirements: Refer to employee orientation checklist F622-01. Ferry Machine Corporation is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. NO AGENCIES PLEASE!

Full time PROFESSIONAL Yonkers, NY Onsite Carter Lard Consulting is working with Leading Railcar Company Salary $80,000 - $95,000 Job Description: Leading Rail Car Company Responsible for implementing and maintaining the Quality Assurance program for the project assigned. Liaison for Quality Assurance group for the contracts assigned Develops Master Test and Inspection Plans, Project Quality Plan, First Article Inspection requirements/schedule and Quality Audit procedures(Qualification and Process audit) for the contracts assigned Attends Monthly Project Meetings with the necessary follow up and coordination. Submittal of Project Status report related to quality of project quality issues, bullet current problems, identify critical assignments, identify any long term corrective actions and status with project due dates Provide weekly reports to management to review the effectiveness of the quality assurance program. Analyze quality issues, prepare reports and interface with the customer on all Quality issues. Interface with customers, U.S. vendors, inter-office departments Manages the daily and long term project schedule for Quality in the production, acceptance, warranty, and modifications of the rail car. Coordinates customer schedules at manufacturing facility for weekly Resident Inspector meetings, documents, issues and follow up to action items. Interface with customers, U.S. vendors, inter-office departments, Oversees and ensures compliance to Customer technical specifications and terms and conditions. Performs periodic contract reviews Coordination and review/acceptance of procedures to support the quality program. Reviews records to ensure information is complete, accurate and compliant with all requirements. Tracks deviations in operating procedures and policies through established mechanisms. Reports errors, deficiencies, discrepancies and observations to management. Initiates standard operating procedures, quality inspection criteria and revisions as needed to support continuous improvement. Responds to and tracks responses to corrective actions for exception variances and post-production reports Assist management teams to ensure timely closure of audit findings and observations against the contract assigned. Assist in coordination for subcontractor activity from scheduling with customer to processing quality documents received from the subcontractors to support the project, Corrective action and improvements Reviews and reports on documentation for supplier and subcontractors (PSI, FAI, audit reports and vendor drawings, work reports within Quality Assurance or the Field. The Project Quality Engineer will have direct input into the Configuration Management planning, implementation, execution, and final delivery of product in relation to projects. Must be able to travel approximately 30% of assignment domestic / international Qualifications: Must have a Bachelor's Degree of Science in Engineering. (Master of Science in Engineering is plus) Minimum five (5) years' experience in support to manufacturing of Rail Cars or other Transportation products (i.e. buses or aircraft) at the prime or vendor level. Must have knowledge of Quality documents and Processes including but not limited to First Article Inspections, Source Inspections, FMEA and ISO 9001 Must have Excellent communication, problem solving and computer skills Must be able to organize, plan, schedule, conduct and coordinate workloads to meet established deadlines. Must be capable of working in both an office and field environment. Salary Range 80 to 95k

The Quality Engineer is a working member of the Quality team whose primary responsibilities are listed below. They will report to the Quality Manager and ensure that Arcmed is compliant with its own standardized processes and procedures. Promote quality across the entire company by raising awareness and driving improvements. Essential duties and responsibilities: Oversee CAPA, work with Manufacturing, Operations and Engineering to assist with containment, root cause analysis, corrective action, and preventive action. Conduct effectivity checks for CAPAs. Return Material Authorizations, supports RMA requests from customers, tracks, and trends RMA data for Management Review, they will assist with RMA investigations as needed and provide feedback to the customer. As well as complaint handling. Monitor and measure Key Performance Indicators (KPIs) and present findings during Management Review Conduct training to internal procedures. Non conformances and Material Review Board (MRB), disposition non conformances, disposition discrepancy material reports, manage MRB process as needed, tracks and trends nonconformance and MRB data. Represent Quality in product development teams/projects. Work with various Engineering groups or QA Manager to develop and execute plans including quality plan, risk management, Process Failure Mode and Effects Analysis (PFMEA), control plans, production part approval process (PPAP), part qualification checklist (PQC) Design verification and process validation (IQ, OQ, PQ) Process capability (cpk). Understand statistics and how it impacts statistical control over process. Lead Supplier Corrective Actions Requests (SCARs) - containment, root cause analysis, corrective action, and preventive action. Ability to interpret Geometric Dimensioning and Tolerancing (GD&T) Work as directed by manager. Qualifications: Bachelor's degree in an Engineering discipline. Knowledge of ISO 9001, ISO 13485 and other recognized international quality system standards. Read, analyze, and interpret technical procedures and regulations. Write technical reports, business correspondence, technical procedures, as well as administrative procedures. Interpret and inspect to GD&T Present proposals, data, and issues to Arcmed personnel at all levels. Independently determine and develop an approach to a wide range of issues and problems. Solutions must be thorough, practical, and consistent with organization objectives. Represent the department in frequent cross-functional interactions and possible customer, subcontractor, or vendor contacts. Provide solutions to difficult technical issues associated with specific projects. Determine and develop technical solutions to a wide range of difficult problems. Experience with Epicor a plus. Microsoft: Word; Teams; Visio; OneNote, PowerPoint, Outlook Ability to operate media equipment such as tablets, smartphones, and other electronic equipment. Ability to work with general office equipment. Ability to work with and understand databases a must and the ability to learn technical skills. Physical requirements: Shall have essential physical skills; be able to run, squat, stoop/bend, kneel, climb stairs, be able to lift at least 50 pounds (or ¼ own body weight). Shall have adequate vision, reading, writing, and documentation skills, and hearing to perform the essential functions of the job. Shall be able to visually differentiate colors. Will be engaged in speaking, sitting, walking, driving, listening, and in communicating both orally and in writing while performing his or her duties. Must be able to listen and respond to questions and instructions. About Arcmed Arcmed partners with the world's top Diagnostic and Analytical OEMs, Engineers, and Scientists to improve human health. We provide technology and supply chain solutions for the design and manufacture of precise fluid handling components for diagnostic and analytical instruments. Our product portfolio offers configurable fluidic components and engineered systems used for precise reagent and sample handling in instrumentation for OEMs in the In-Vitro Diagnostic (IVD), Next Generation Sequencing (NGS), and analytical chemistry markets. Arcmed offers labware and chromatography components to scientific laboratories in drug discovery and downstream biotech development workflows. We are recognized as a leader in helping engineers, scientists, and doctors to solve the world's toughest diagnostic and analytical challenges. Our Values We always act with intention and drive to achieve our purpose. Teamwork, collaboration, and diverse opinions make us stronger. We are unafraid to make timely decisions, and we empower our people to make decisions, execute them and move forward. We value people that take the initiative and hold themselves accountable. Challenging the status quo helps us grow. Look for and call out improvements. The qualifications, physical demands, and work environment described herein are representative of those an employee will encounter and must meet to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. Arcmed is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This document does not create an employment contract, implied or otherwise, other than an "at will" relationship . The above noted job description is not intended to describe, in detail, the variety of tasks that may be assigned but rather to give the incumbent a general sense of the responsibilities and expectations of his/her position. As the nature of business demands change, so, too, may the essential functions of this position.

Dreaming big is in our DNA. It's who we are as a company. It's our culture. It's our heritage. And more than ever, it's our future. A future where we're always looking forward. Always serving up new ways to meet life's moments. A future where we keep dreaming bigger. We look for people with passion, talent, and curiosity, and provide them with the teammates, resources and opportunities to unleash their full potential. The power we create together - when we combine your strengths with ours - is unstoppable. Are you ready to join a team that dreams as big as you do? This position is at our Metal Container Corporation SALARY: $27.00 per hour for first 8 hours; next 4.25 hours paid at 1.5 rate of $40.50 per hour. * SIGN ON BONUS of $10,000* SHIFT: 12.25 hour shifts 3 days on/3 days off. Rotate day/night shift every six weeks COMPANY: Michelob ULTRA. Cutwater Spirits. Budweiser. Kona Brewing Co. Stella Artois. Bud Light. That's right, over 100 of America's most loved brands, to be exact. But there's so much more to us than our top-notch portfolio of beers, seltzers, and more. We are powered by a 19,000-strong team that shares our passion to create a future with more cheers. We look for people with talent, curiosity, and commitment and provide the teammates, resources and opportunities to unleash their full potential. The power we create together - when we combine your strengths with ours - is unstoppable. Are you ready to join a team that dreams as big as you do? ROLE SUMMARY: If you are passionate about maintenance and troubleshooting while working in a fast-paced environment, Anheuser Busch could be your next stop in fulfilling your career. If you are looking for a new challenge, come join our team today! JOB RESPONSIBILITIES: * Work in a high-speed manufacturing environment * Troubleshoot, maintain, and repair manufacturing equipment with a focus on safety, quality, teamwork, and efficiency * Perform quality, maintenance, and housekeeping checks and record numerical results in various computer system programs * Analyze process data to make decisions on equipment maintenance and process improvement activities * Adhere to plant safety and sanitation requirements; complete assigned work safely and efficiently per the Standard Operating Procedures (SOP's) * Assist with process improvement initiatives utilizing Lean methodology including root cause analysis, process flow maps, etc. * Clearly document and communicate maintenance and quality events using computer reporting systems * Cross-training opportunities available to maximize your earnings and expand your technical knowledge JOB QUALIFICATIONS: * High School Diploma or GED required * Mechanical troubleshooting/maintenance experience required. Successful candidates typically have three or more years of experience in the below: * Proficient knowledge of precision measurements and pneumatic and hydraulic systems * Excellent troubleshooting skills, ability to identify a problem and use analytical skills to identify the root cause and implement sustainable solutions * Knowledge of safety policies and procedures required (e.g. lock out /tag out, confined space entry, etc.) * High-speed manufacturing or packaging facility experience * Strong interpersonal and communication skills * The ability to work effectively in a team environment with people of varying skills and backgrounds * Must be able to continuously stand, bend, and twist. Must be able to lift items up to 50 pounds * Computer skills required WHY ANHEUSER-BUSCH: Anheuser-Busch has always dreamed big. It's who we are as a company. It's our culture. It's our heritage. But more than ever, it's our future. A future where we're always looking forward. Always serving up new ways to meet life's moments. Even when they're hard. A future where we keep dreaming bigger. Together. To reimagine what a beer company can be. And what Anheuser-Busch can do. Where we provide more opportunity for our people, lift up our neighbors, and make a meaningful difference in the world. This future is our purpose. A future that everyone can celebrate, and everyone can share in. A future with more cheers. BENEFITS: * Relocation benefits, if applicable * Sign on bonus available * Health benefits including Medical, Dental, Vision, Wellness and Tax-Advantaged Savings and Spending Accounts * Life Insurance and Disability Income Protection * Generous Parental Leave and FMLA policies * 401(k) Retirement Savings options with a company matching contribution * Chance to work in a fast-paced environment among a company of owners * Free Beer! #AC-NWBRGH

The Role As a Production Tech, you'll be an essential part of the process of turning raw cannabis flower into our beautiful line of medicated products. Under the guidance of the management team, you will produce, package, and handle products, perform inventory duties, adhere to compliance requirements, and keep safety as your top priority while working daily in our facility. Here at GTI, we are looking for true team players who are the perfect hybrid between precision and energy. Responsibilities * Deliver on production goals, while focused on safety and quality * Produce product per recipes and SOP's, maintaining high quality standards * Package product into proper containers with proper labeling to ensure compliance with state regulations * Ensure all standards for processing procedures and laboratory protocols are followed * Compliance with local and state regulations * Adherence to quality control methods throughout entire process * Documentation of manufacturing methods are created and maintained * Electronically convert packaged products in the state traceability system * Manage time efficiently to meet goals while consistently producing quality product * Practice good housekeeping habits throughout the facility with focus and personal contributions towards a clean and organized assigned work area at the end of the assigned shift * Exhibit competency in basic organizational skills, communication skills and Windows based operating software * Use independent judgment regarding product processing, keeping quality and goals in mind * Help create a positive environment by having a positive attitude and by being self-motivated * Other duties as assigned Qualifications * High School Education or GED graduate; some college or college graduate preferred * 1-2 years' experience in manufacturing, food processing, warehousing, and/or inventory preferred * Equivalent combinations of education and experience may be considered * Must be able to work well in a group and independently; demonstrate self-motivation and initiative * Must be able to adapt quickly to changes in policy, procedure, and technique * Employee must exhibit personal hygiene and follow the health guidelines set forth by GTI * Ability to listen well and communicate effectively with various audiences * Ability to perform monotonous tasks with great efficiency without losing qualities * Must be able to follow basic instructions and accept constructive criticism Additional Requirements * Must have a valid driver's license or State ID card * Must be a minimum of 21 years of age * Must pass all required background checks * Must be and remain compliant with all legal and company regulations for working in the industry * Must be approved by the Cannabis Compliance Board to receive an Agent Card Working Conditions * While performing the duties of this job, the employee is regularly required to perform reaching, grasping, bending, stooping, talking, hearing, seeing and repetitive motions. * Must be able to sit and/or stand for extended periods of time while maintaining focus. * PHYSICAL DEMANDS: Must be able to lift, carry, and balance up to 50 pounds AND must be able to do so with extreme care and caution when working with product. * Work involves daily exposure to allergens (such as cannabis, tree nuts, and coconut oil). The pay range is competitive and based on experience, qualifications, and/or location of the role. Positions may be eligible for a discretionary annual incentive program driven by organization and individual performance. Green Thumb Pay Range $19.50-$20 USD

We are the leading provider of professional services to the middle market globally, our purpose is to instill confidence in a world of change, empowering our clients and people to realize their full potential. Our exceptional people are the key to our unrivaled, culture and talent experience and our ability to be compelling to our clients. You'll find an environment that inspires and empowers you to thrive both personally and professionally. There's no one like you and that's why there's nowhere like RSM. AUDIT ASSOCIATE At RSM, associates work with large and small companies in various industries. They develop strong working relationships with clients built on understanding their businesses and challenges. Associates work on multiple team engagements each year, including several pieces of any particular assignment - not just one part. Working in a mutually respectful team environment helps our associates perform at their best and integrate their career with their personal life. Examples of the candidate's responsibilities include: * Understanding clients' needs and expectations, their business and industry, accounting and control systems, employees, company values and industry-related GAAP and GAAS issues * Developing an understanding of the RSM audit approach and tools * Assessing risks and evaluating the client's internal control structure * Performing substantive tests and tests of internal controls to identify and resolve accounting or reporting issues * Drafting financial statements under prescribed formats Basic Qualifications: * Minimum B.A / B.S. degree or equivalent from an accredited university by the time employment commences * Accounting major * Travel to assigned client locations is required. Must have access to and ability to arrange for use of reliable modes of transportation to those locations * Ability to travel up to 25% * A minimum 3.0 GPA is preferred Preferred Qualifications: * Excellent written and verbal communication skills * Strong computer skills, including MS Office * Ability to work as an effective member of a team * Motivated to work in a fast-paced environment * Client focused * Ability to multitask At RSM, we offer a competitive benefits and compensation package for all our people. We offer flexibility in your schedule, empowering you to balance life's demands, while also maintaining your ability to serve clients. Learn more about our total rewards at ************************************************** All applicants will receive consideration for employment as RSM does not tolerate discrimination and/or harassment based on race; color; creed; sincerely held religious beliefs, practices or observances; sex (including pregnancy or disabilities related to nursing); gender; sexual orientation; HIV Status; national origin; ancestry; familial or marital status; age; physical or mental disability; citizenship; political affiliation; medical condition (including family and medical leave); domestic violence victim status; past, current or prospective service in the US uniformed service; US Military/Veteran status; pre-disposing genetic characteristics or any other characteristic protected under applicable federal, state or local law. Accommodation for applicants with disabilities is available upon request in connection with the recruitment process and/or employment/partnership. RSM is committed to providing equal opportunity and reasonable accommodation for people with disabilities. If you require a reasonable accommodation to complete an application, interview, or otherwise participate in the recruiting process, please call us at ************ or send us an email at *****************. RSM does not intend to hire entry level candidates who will require sponsorship now OR in the future (i.e. F-1 visa holders). If you are a recent U.S. college / university graduate possessing 1-2 years of progressive and relevant work experience in a same or similar role to the one for which you are applying, excluding internships, you may be eligible for hire as an experienced associate. RSM will consider for employment qualified applicants with arrest or conviction records in accordance with the requirements of applicable law, including but not limited to, the California Fair Chance Act, the Los Angeles Fair Chance Initiative for Hiring Ordinance, the Los Angeles County Fair Chance Ordinance for Employers, and the San Francisco Fair Chance Ordinance. For additional information regarding RSM's background check process, including information about job duties that necessitate the use of one or more types of background checks, click here. At RSM, an employee's pay at any point in their career is intended to reflect their experiences, performance, and skills for their current role. The salary range (or starting rate for interns and associates) for this role represents numerous factors considered in the hiring decisions including, but not limited to, education, skills, work experience, certifications, location, etc. As such, pay for the successful candidate(s) could fall anywhere within the stated range. Compensation Range: $74,800 - $89,250 Individuals selected for this role will be eligible for a discretionary bonus based on firm and individual performance.

This position will support all Quality Assurance activities related to maintain company and governmental food safety standard. This role will be required to perform tasks associated with GMPs, HACCP and continuous improvement programs. In addition, this person will work with management in various QA related projects. In the absence of the QC Technician, the QA Associate may temporarily fill in and assume responsibilities of QA Technician. This role offers responsibility, variety, and the satisfaction that your role makes a real impact on our success.

Title: Quality Assurance Associate Reports to: Quality Assurance Supervisor or Manager Department: Quality Responsibilities: Conducts Annual Drug (Product) Reviews and Device History Reviews. Maintains Regulatory Compliance documents and documents of external origin. Maintain Document Control (including Records Retention) Participates in internal and external audit process. Participates in Mock (product) recall audits. Maintain SOPs and Quality Forms as part of Document Control. Maintains records of customer-approvals documents as evidence of authenticity. Participate in QA Audits and draft reports of such audits. Effects changes to specification sheets as approved through change control requests. Support Change Control program and maintain evidence of product and process changes. Maintains SOP binders and updates such documents through approved CCs. Supports EWL Employee training and documentation. Maintains suppliers and vendors qualification program. Supports and maintains approvals of formulary, specifications and manufacturing records. Participates in Mock (product) recall audits. Maintains Records Retention for QA Dept. Initiates, Tracks, and authors Annual Drug Reviews (ADRs) for OTC and Annual Drug Reviews and Device History Reviews (DHRs). Assists in collating, reviewing, filing, maintaining of OTC bulk batch records, COAs, formula documents, etc. Tracks and Performs physical sample retain review for ADRs and DHRs. Tracks, Maintains, Closes requests for Change Control Notices (CC), Defective Material forms (DMF), and Deviations, Return Authorizations, Investigations, etc. Requirements Minimum of 2 years of diploma program or 4-year college degree. 2 to 3 years industry or related experience. Previous experience in Pharma, Cosmetics, food, medical device, or allied profession. Good Technical Writing ability. Excellent knowledge of Word, Excel, Access, and other Windows-based programs. Good record-keeping skills. Benefits Medical, Dental, and Vision Insurance Life Insurance 401k match

SBA Quality Control Specialist I We are looking for an SBA Quality Control Specialist to join our growing Post-close team. Through a dynamic, customer-centric model, this position will play a critical role in the proactive management of risk in the portfolio and in the participation of corresponding government loan programs. A successful candidate will possess the analytical thinking skills necessary to analyze and synthesize information to understand issues, identify options, and support sound decision making to contribute to the overall goals and objectives of Ready Capital. Essential Duties and Responsibilities: Provide a thorough review of documentation and compliance of SBA post closing loans for accuracy and completeness in accordance with Lender Policy and SBA SOP Guidelines Reviews include, but are not limited to: Credit memos, leases, real estate/asset/stock purchase agreements, corporate/entity documents, equity injection documents, ensuring borrowers financial data is current, review final estimates/budgets for construction projects and leasehold improvements, all insurances (flood, BPP, liability, hazard, life), real estate title commitments/policies, use of funds. Review Third-party reports and searches including, but not limited to: Appraisals, Valuations, Environmental, Background, Credit reports, CAIVRS, Clear Reports and OFAC. Review all post closing documentation, checking for dates, signatures, and 100% accuracy on all documentation Confirm all post closing items have been received Work closely and build professional relationships with Credit, Attorneys and Closing Departments to reconcile missing or incomplete loan-related documentation Present any deficient findings to the closer for both pre and post close reviews Respond to inquiries relating to exceptions from all levels of the organization Keep abreast of day to day policy and procedure and SBA SOP changes Qualifications for Success: 4 Year college degree or relevant industry experience preferred 4 or more years in banking, credit, finance, or lending related experience preferred SBA 7a lending experience preferred Experience in a compliance function preferred Able to demonstrate effective organization, critical thinking, and problem-solving skills Able to demonstrate initiative to accomplish work objectives Able to manage multiple tasks while meeting deadlines in a fast-paced work environment Able to work effectively in a team environment Able to prioritize and operate with a sense of urgency Strong verbal and written communication skills Requires knowledge of Microsoft Office Physical Demands: The physical demands of the position are typical of those found in a traditional office environment. Employees will not need to walk significant distances nor lift substantial weight. Employee will need to be able to remain seated at a desk for 8-9 hours in a typical workday. Conclusion: This is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position. 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, genetic information or any other characteristic protected by law.

Join the Zeiss team in White Plains, NY, as a Quality Assurance/Regulatory Affairs (QA/RA) Associate. You will support the Quality Department in meeting regulatory obligations (e.g.: FDA reporting, Rad. Health reporting) and the maintenance of the various activities related to sustaining an ISO 9001/13485 Quality Management System including document control, complaint & CAPA processing, and audit planning. This is a Hybrid (3/2) position, working in the office, and remotely. Job Functions: Administers complaint process, including review and logging of incoming complaints, preliminary investigation and follow-up to closure Assists process owners with development/review of Standard Operating Procedures for RMS and IQS Provides Regulatory support, including guidance, review and preparation of filings for initial, supplemental and annual CDRH reports (including, but not limited to RMS, IQS, XRM, SBE, and SMT) Maintains FDA establishment registrations, renewals and device listings Administers corporate document control process and updates QMS database Administers Corrective Action/ Preventive Action System Administers internal audit plan and scheduling Prepares graphs or charts of data and/or analyzes data Assist in internal and external audits Participates in preparation of Management Review data and presentations Other QA/regulatory duties and other duties as assigned Bachelors Degree with 2 years experience in an ISO certified or QSR compliant environment Working knowledge of FDA Quality System Regulation and CDRH reporting requirements Working knowledge of ISO requirements, specifically ISO 9001 or ISO 13485 Medical Devices ISO 9001 Auditor Certification a plus Effective verbal and written communication skills Strong Computer Skills (MS Word, Excel, PowerPoint, etc.) Ability to schedule and handle multi-tasking to meet deadlines Ability to interact positively and professionally at all levels of the organization Ability to work independently or as part of a team The annual salary range for this contingent position (temp - to - hire) is $65 - 70K. The salary offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, complexity/specialization/scarcity of talent. Your ZEISS Recruiting Team: Steve Warner

Join the Zeiss team in White Plains, NY, as a Quality Assurance/Regulatory Affairs (QA/RA) Associate. You will support the Quality Department in meeting regulatory obligations (e.g.: FDA reporting, Rad. Health reporting) and the maintenance of the various activities related to sustaining an ISO 9001/13485 Quality Management System including document control, complaint & CAPA processing, and audit planning. This is a Hybrid (3/2) position, working in the office, and remotely. Job Functions: * Administers complaint process, including review and logging of incoming complaints, preliminary investigation and follow-up to closure * Assists process owners with development/review of Standard Operating Procedures for RMS and IQS * Provides Regulatory support, including guidance, review and preparation of filings for initial, supplemental and annual CDRH reports (including, but not limited to RMS, IQS, XRM, SBE, and SMT) * Maintains FDA establishment registrations, renewals and device listings * Administers corporate document control process and updates QMS database * Administers Corrective Action/ Preventive Action System * Administers internal audit plan and scheduling * Prepares graphs or charts of data and/or analyzes data * Assist in internal and external audits * Participates in preparation of Management Review data and presentations * Other QA/regulatory duties and other duties as assigned * Bachelors Degree with 2 years experience in an ISO certified or QSR compliant environment * Working knowledge of FDA Quality System Regulation and CDRH reporting requirements * Working knowledge of ISO requirements, specifically ISO 9001 or ISO 13485 Medical Devices * ISO 9001 Auditor Certification a plus * Effective verbal and written communication skills * Strong Computer Skills (MS Word, Excel, PowerPoint, etc.) * Ability to schedule and handle multi-tasking to meet deadlines * Ability to interact positively and professionally at all levels of the organization * Ability to work independently or as part of a team The annual salary range for this contingent position (temp - to - hire) is $65 - 70K. The salary offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, complexity/specialization/scarcity of talent. Your ZEISS Recruiting Team: Steve Warner

Join the Zeiss team in White Plains, NY, as a Quality Assurance/Regulatory Affairs (QA/RA) Associate. You will support the Quality Department in meeting regulatory obligations (e.g.: FDA reporting, Rad. Health reporting) and the maintenance of the various activities related to sustaining an ISO 9001/13485 Quality Management System including document control, complaint & CAPA processing, and audit planning. This is a Hybrid (3/2) position, working in the office, and remotely. Job Functions: Administers complaint process, including review and logging of incoming complaints, preliminary investigation and follow-up to closure Assists process owners with development/review of Standard Operating Procedures for RMS and IQS Provides Regulatory support, including guidance, review and preparation of filings for initial, supplemental and annual CDRH reports (including, but not limited to RMS, IQS, XRM, SBE, and SMT) Maintains FDA establishment registrations, renewals and device listings Administers corporate document control process and updates QMS database Administers Corrective Action/ Preventive Action System Administers internal audit plan and scheduling Prepares graphs or charts of data and/or analyzes data Assist in internal and external audits Participates in preparation of Management Review data and presentations Other QA/regulatory duties and other duties as assigned Bachelors Degree with 2 years experience in an ISO certified or QSR compliant environment Working knowledge of FDA Quality System Regulation and CDRH reporting requirements Working knowledge of ISO requirements, specifically ISO 9001 or ISO 13485 Medical Devices ISO 9001 Auditor Certification a plus Effective verbal and written communication skills Strong Computer Skills (MS Word, Excel, PowerPoint, etc.) Ability to schedule and handle multi-tasking to meet deadlines Ability to interact positively and professionally at all levels of the organization Ability to work independently or as part of a team The annual salary range for this contingent position (temp - to - hire) is $65 - 70K. The salary offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, complexity/specialization/scarcity of talent. Your ZEISS Recruiting Team: Steve Warner

We invite you to join Takasago, where you can be innovative and contribute to society through technology. The management of Takasago aims to create a company where each employee can experience a sense of fulfillment and happiness at a high level. Specifically, we strive to establish an environment where people from diverse backgrounds can work with joy and a sense of purpose, create a system that supports individual growth, and above all, implement management practices that enable employees to achieve a healthy work-life balance. Takasago is a major global leader and producer of flavors and fragrances providing innovative solutions in flavors, fragrances, aroma ingredients, and fine chemicals. Takasago is headquartered in Japan and operates in over 27 countries, with manufacturing facilities, research and development centers, and sales offices worldwide. Takasago ranked 8th overall and 1st in Asia on the Global Top Food Flavors and Fragrances Companie Essential Job Functions: Routine analytical testing of raw materials and finished product samples submitted by production and sample lab. Working knowledge and familiarity of QC analytical instruments such as HPLC, GC, flashpoint, specific gravity, refractive index and various color tests. Maintain documents, data archives, and tracking of samples. Ensure conformance to accepted quality standards. Review laboratory records for trends or inconsistencies. Take necessary corrective and preventive actions. Communicate between production and laboratory personnel to assure that the laboratory is prepared to support production in a timely and efficient manner. Follow all safety and corporate policies. This job description reflects management's assignment of essential functions; it does not prescribe or restrict the tasks that may be assigned. Ensure all processes and procedures related to inventory management are maintained and followed. Includes but not limited to inventory movements related to production regarding quantities consumed, and proper storage. Educational Qualifications: Bachelor's degree in related science field preferred Experience: Minimum of 2 yrs. experience in related flavor QC environment preferred. Good experience in sensory evaluation of raw materials and finished products. Ability to approve raw materials as well as compounds based on GC/analytical and sensory results. Knowledge of GC, flashpoint, specific gravity, refractive index and various color tests. Must be computer literate. Takasago's Employee Benefits and Perks: Takasago offers flexible work arrangements, tuition assistance, health benefits, employee discounts to various services and products, and life insurance 1.5 times your salary. When we think about employee success and financial security, we think long-term. Takasago provides robust retirement savings plans, as well as an employee assistance program. We hope you will join us and achieve professional growth and enrichment. EEO Statement Takasago provides equal opportunities and equal access to all individuals regardless of race or ethnicity, sex/gender (including pregnancy), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, civil union status, familial status, religion, national origin or citizenship, military service status, or any other category protected by law.

Full-time Description A Quality Control Technician II is responsible for ensuring that products and services meet the established standards set by the company. Duties include maintaining strong overall quality control of products made by the company adhering to reliability, performance, and customer expectation. Performs incoming inspections of raw materials, customer supplied raw materials, returned goods and special components. Performs finished good inspections. Performs start-up and in process inspections. Monitors specific areas of production as directed by the Quality Control Supervisor. Makes measurements and records data as per inspection forms or job cards. Performs testing and records data for statistical process control (SPC) during manufacturing, (when required). Communicates with Quality Control Supervisor any occurrences of non-conforming product, out of control process or any other items of concern. Communicates with Manufacturing Engineers any occurrences of tests failing engineering limits or any other items of concern. Performs computer set up for label printing programs on cutting lines. Assists Engineering as needed for experimental testing. Enters finished goods inspection data into BMS as appropriate. Any other duties as assigned by supervisor. Requirements Excellent organizational skills and attention to detail. Must have good documentation practice. A proven understanding of part workmanship. Ability to handle numbers required. Strong interpersonal skills. Ability to use micrometer, computers, testing equipment and electronic balance is essential. Experience using Excel is preferred. Ability to speak, read, and write in English. Education & Experience High school diploma or equivalent. Working Conditions While performing the duties of this job, the employee occasionally works near moving mechanical parts and is occasionally exposed to wet and/or humid conditions, ambient air, fumes, or airborne particles. The noise level in the work environment is usually moderate. Physical Requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Candidate must be able to perform the physical responsibilities of the job utilizing arms, hands, and fingers to perform complex functions of manufacturing parts and performing other duties of the job, e.g., standing, sitting, walking throughout the facility and stairs, bending, squatting, and kneeling, etc. Ability to lift items weighing up to 15 lbs. We're proud to be an equal opportunity employer. This means we actively pursue ways to celebrate our differences and don't discriminate based on an individual's race (including traits historically associated with race, such as hair texture, hair type, and protective hairstyles including braids, locks, and twists), creed, national origin, nationality, religion, ancestry, age (40 or over), sex (including pregnancy), familial status, marital status, civil union or domestic partnership status, affectional or sexual orientation, gender identity or expression, mental or physical disability (including perceived disability, AIDS, and HIV status), atypical hereditary cellular or blood trait, genetic information, because of liability for service in military, status as a smoker or non-smoker, status as a registered medical marijuana user, or any unlawful criterion existing under applicable federal, state, or local laws. If you need assistance or an accommodation due to a disability, contact us at **********************.

Inspection Metrologist with Specialty in CT Inspection Capabilities Expertise performing tolerance verification on CT Scan point clouds from components with complex geometry Must be proficient with Calypso and/or Volume Graphic Software Proven ability to correctly interpret drawings and geometric dimensions and tolerances.

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.

Full-time Description About Generant: Initially founded in the early 1930's, Generant designs and manufactures valves and pressure regulators for a wide variety of industries with a strong position in the Industrial Gases and Cryogenics, Medical Gases and Equipment, Energy, and Chemicals markets. Generant is 100% employee-owned and is headquartered in Butler, NJ where most valve and regulator products are manufactured. Job Summary: The primary function of the 3rd SHIFT Quality Control inspector is to help assure the quality of finished goods and conformance to product requirements. This is accomplished by inspecting parts, checking calibration status of measurement devices, and documenting inspections and nonconformance. Essential Functions: Conduct First Article Inspection and in-process inspections of products to ensure compliance with quality standards and specifications. Data Entry into Quality Databases (Inspections, DMR Tracking, etc.) - QC 2000 Interpret mechanical drawings. Communicate product and material nonconformances to management. Identify and report any deviations from quality standards to the appropriate personnel. Collaborate with production teams to resolve quality issues and implement corrective actions. Conduct root cause analysis and implement preventive measures to minimize defects and improve product quality. Maintain accurate records of inspections, test results, and quality documentation. Assist in the development and implementation of quality control procedures and processes. Perform other assignments as required by the QC Manager for example, but not limited to: In-Process Inspection, Final Inspection, Raw Material Inspection - Bar Stock, Incoming Inspection - Purchased Parts, Calibration of Metrology Tools, and Outside Process Inspection Requirements Qualifications: Education/Experience/Skills: -High School Diploma or equivalent -Experience as a quality control inspector with a minimum of 2+ years experience in a manufacturing environment -Able to read and interpret engineering drawings -Must have a complete knowledge of metrology equipment and their uses including micrometers, calipers, indicators, depth micrometers, gauge pins, thread gauges and optical comparators -Strong knowledge of Statistical Process Control (SPC) techniques and tools -Familiarity with quality control standards and regulations -Must be able to work in a fast-paced environment -Excellent attention to detail and analytical skills -Ability to work independently and as part of a team Language Skills: -Fluent in English (Good Verbal and Written Communication Skills) Mathematical Skills: -Basic Math Skills (measuring, use of calculator) Reasoning Ability: -Ability to carryout detailed, but uninvolved written and verbal instructions Physical Demands: -Must frequently lift up to 25 pounds and occasionally lift up to 75 pounds -When performing the duties of this job, the employee is regularly required to sit, use hands to finger or handle or feel objects and tools or controls and talk or hear -Employee is frequently required to reach with hands and arms -Employee is occasionally required to stand, walk, stoop, kneel, crouch, or crawl -Specific vision abilities require close vision, distant vision, color vision, peripheral vision, depth perception and the ability to adjust focus. Work Environment: -Inspector works near moving mechanical parts and is occasionally exposed to vibration -Noise level is usually moderate for a manufacturing plant -Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Benefits: Medical, Dental, Vision, Employee Stock Ownership Plan (ESOP), 401k, Life and AD&D Insurance Please note that this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Goodwill NYNJ Ecommerce Quality Control - Full Time Position To receive merchandise and sort & separate items based on quality standards for listing. • Receive incoming totes from stores & record seal information as directed. • Research items online for matching descriptions and value by using different market places. • Accept and reject items based on quality standards. • Use provided manifesting software to print SKUs and safely apply them to a variety of items. • Comply with production expectation. • May need to lift up to 50lbs. • Additional duties as required. • Minimum high school diploma. • Ability to read and write English. • Basic computer & internet research skills. • Ability to deal with change and work in a dynamic environment. • Able to work under minimal supervision and process the expected number totes per day. • Able to work as part of a team involved in the quality control of items for Goodwill's E-Commerce (Online) department. Duties will be performed in an industrial warehouse environment. This job requires you to stand/move for long periods of time. Covid-19 Update - In alignment with New York City's decision to lift the private employer vaccination requirements, effective November 1, 2022, Retail Employees in NYC are now exempt from submitting vaccination proof and/or no longer required of submitting proof of weekly PCR/Antigen(Rapid) testing if they have requested medical/ religious accommodation. Retail stores in NJ and Upstate continue to be exempt as per New Jersey and New York State Guidelines.

We invite you to join Takasago, where you can be innovative and contribute to society through technology. The management of Takasago aims to create a company where each employee can experience a sense of fulfillment and happiness at a high level. Specifically, we strive to establish an environment where people from diverse backgrounds can work with joy and a sense of purpose, create a system that supports individual growth, and above all, implement management practices that enable employees to achieve a healthy work-life balance. Takasago is a major global leader and producer of flavors and fragrances providing innovative solutions in flavors, fragrances, aroma ingredients, and fine chemicals. Takasago is headquartered in Japan and operates in over 27 countries, with manufacturing facilities, research and development centers, and sales offices worldwide. Takasago ranked 8th overall and 1st in Asia on the Global Top Food Flavors and Fragrances Companie Essential Job Functions: Routine analytical testing of raw materials and finished product samples submitted by production and sample lab. Working knowledge and familiarity of QC analytical instruments such as HPLC, GC, flashpoint, specific gravity, refractive index and various color tests. Maintain documents, data archives, and tracking of samples. Ensure conformance to accepted quality standards. Review laboratory records for trends or inconsistencies. Take necessary corrective and preventive actions. Communicate between production and laboratory personnel to assure that the laboratory is prepared to support production in a timely and efficient manner. Follow all safety and corporate policies. This job description reflects management's assignment of essential functions; it does not prescribe or restrict the tasks that may be assigned. Ensure all processes and procedures related to inventory management are maintained and followed. Includes but not limited to inventory movements related to production regarding quantities consumed, and proper storage. Educational Qualifications: Bachelor's degree in related science field preferred Experience: Minimum of 2 yrs. experience in related flavor QC environment preferred. Good experience in sensory evaluation of raw materials and finished products. Ability to approve raw materials as well as compounds based on GC/analytical and sensory results. Knowledge of GC, flashpoint, specific gravity, refractive index and various color tests. Must be computer literate. Takasago's Employee Benefits and Perks : Takasago offers flexible work arrangements, tuition assistance, health benefits, employee discounts to various services and products, and life insurance 1.5 times your salary. When we think about employee success and financial security, we think long-term. Takasago provides robust retirement savings plans, as well as an employee assistance program. We hope you will join us and achieve professional growth and enrichment. EEO Statement Takasago provides equal opportunities and equal access to all individuals regardless of race or ethnicity, sex/gender (including pregnancy), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, civil union status, familial status, religion, national origin or citizenship, military service status, or any other category protected by law.