Quality Technician jobs in Greenwich, CT

Rich's, also known as Rich Products Corporation, is a family-owned food company dedicated to inspiring possibilities. From cakes and icings to pizza, appetizers and specialty toppings, our products are used in homes, restaurants and bakeries around the world. Beyond great food, our customers also gain insights to help them stay competitive, no matter their size. Our portfolio includes creative solutions geared at helping food industry professionals compete in foodservice, retail, in-store bakery, deli, and prepared foods, among others. Working in 100 locations globally, with annual sales exceeding $4 billion, Rich's is a global leader with a focus on everything that family makes possible. Rich's-Infinite Possibilities. One Family. Purpose Statement The QA Technician's purpose is to assure food safety through HACCP compliance monitoring, implementing corrective actions and reporting of deviations to the QA Manager. Shift hours will typically be from 730a-4p EST. Key Accountabilities and Outcomes * Document test results, communicate deviations with management and co-associates. * Review data and direct follow-up of product testing deviations and trends to meet customer requirements. * Conduct product and process capability studies as directed by QA Manager or designate. * Perform QA tasks including product sampling, line monitoring, auditing, lab testing and calibrations to ensure compliance to specifications. * Coordinate lab operation, raw material, finished product and audit analytical data and reports for process improvements. * Audit laboratory testing, analytical test methods and protocols for Compliance with Standard Operating Procedure and Quality Assurance Agreement. * Reviewing and approving deviation, investigations, and corrective and preventive action that is associated with analytical laboratories. * Review and audit of microbiological testing and sanitation cleaning inspection reports. * Place ingredients and finished goods on hold, as directed by the QA Manager/QA Team Leader. * Investigate the root cause of defects in raw and finished products and implement corrective actions. * Maintain and promote a quality culture through training * Maintain a well-organized and clean work area. * Maintain adequate inventory of supplies for lab Audit laboratory testing, analytical test methods and protocols for Compliance with Standard Operating Procedure and Quality Assurance Agreement * Coordinate timely hold and disposition of raw ingredients, packaging materials and finished product. * Utilize PLM, QDMS, SAP and Minitab in support of business processes. * Submit written reports on overall compliance, deviations and corrective actions implemented. * Understanding of Acidified Foods and compliance to all federal guidelines. Knowledge, Skills, and Experience * Bachelor's Degree in Food Science, chemistry or biology related field required. Related work experience preferred but not required. * Chemistry work related: Water activity., Free fatty acid testing; Viscosity, ; PH effect on Food; Brix, Concentration; Moisture analyses; allergen tests, Flour testing attributes, * Microbiology work related: Knowledge of pathogens and its growth characteristics as it relates to food manufacturing and the facility. Bacterial growth requirement; Bacterial identification; Growth morphology; Temperature growth requirement; Bacterial food source. * One year experience in commercial food processing preferred. * PC skills to include strong knowledge of Windows operating system, and applications to include Microsoft Word and Excel. * Knowledge of statistics and use of software packages. * Knowledge of Database systems preferred. * Ability to constructively deal with change and pressure. Willing to continue training/ education as necessary. * Ability to lift up to 50lbs. * Ability to operate powered equipment * Ability to use a full range of motion in both arms, hands, and legs. * Ability to taste. * Ability to operate normal laboratory equipment. * Must have understanding of microbiological contaminates. * Must have complete understanding of shortenings, sugars, starches, gums, and particulates. COMPENSATION In accordance with state law, the rate or range provided is Rich Products Corporation, its subsidiaries and affiliates ("Rich's"), reasonable estimate of the base compensation for this role. The actual amount may be higher or lower, based on non-discriminatory factors such as experience, knowledge, skills, abilities, shift differential, and location. Annual Range/Hourly Rate $30.00 - $35.00 Rich Products Corporation, its subsidiaries and affiliates ("Rich's"), are committed to a policy of Equal Employment Opportunity, standing up for fairness and maintaining a culture of belonging, to provide an exceptional experience for all. We will not discriminate against an applicant or employee on the basis of race, color, religion, sex, national origin, disability, military or veteran status, or any other Federal or State legally protected classes. The information collected by this application is solely to determine suitability for employment, verify identity, and maintain employment statistics on applicants. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is a change in the way things are normally done which will ensure an equal employment opportunity without imposing undue hardship on Rich's. Please contact Rich's Associate Experience Network at *************** if you need assistance completing this application or to otherwise participate in the application process. BRINGING YOUR BEST SELF TO WORK. As a family-owned company, caring for our associates-their whole selves-is a top priority. That's why we provide benefits and tools to help our people balance the integration of work and life: * Competitive compensation * Health & financial benefits * Paid time off * Parental leave * Family planning support * Flexible work policy * Associate resource groups * Volunteering & community impact opportunities * Holiday gatherings * In-house taste tests (we are a food company after all)! It's all part of how we support our family of associates. Because in the company of family, all things are possible. MEET RICH'S. Rich's, also known as Rich Products Corporation, is a family-owned food company dedicated to inspiring possibilities. From cakes and icings to pizza, appetizers and specialty toppings, our products are used in homes, restaurants and bakeries around the world. Beyond great food, our customers also gain insights to help them stay competitive, no matter their size. Our portfolio includes creative solutions geared at helping food industry professionals compete in foodservice, retail, in-store bakery, deli, and prepared foods, among others. Working in 100 locations globally, with annual sales exceeding $3.8 billion, Rich's is a global leader with a focus on everything that family makes possible. Rich's-Infinite Possibilities. One Family. Nearest Major Market: New York City Job Segment: PLM, Management

Safety Assurance/Regulatory Affairs Associate 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 Companies. We currently have an opportunity for a Safety Assurance/Regulatory Affairs Associate within the Fragrance division located in Rockleigh, NJ. Essential Job Functions: Conduct safety review of fragrance formulas according to industry, regulatory and customer requirements Provide assistance to perfumers on safety/regulatory requirements for fragrance creation. Prepare fragrance safety documents as per customer requests. Communicate with customers on safety and regulatory issues. Communicate with suppliers on requests for safety/regulatory information. Ensure maintenance and security of fragrance formulas. Ensures MSDS databases are maintained on chemicals used in the fragrance, aroma chemical and export divisions. Review new and updated MSDS's and industry information on fragrance division chemicals for health hazard statements. Maintain the safety information on fragrance division chemicals used in the creation of MSDS's for fragrance compounds. Prepare and maintain MSDS's for fragrance compounds, according to appropriate country regulations. Expert on the use and setup of The Wercs MSDS authoring software. Distribute MSDS's to Sales, customers, etc. Maintain the Health Hazard Communication SAP program for the fragrance division. Maintain the NJ Right to Know system for the fragrance division. Provide assistance on projects for Fragrance Safety Assurance Specialists/Manage Educational Qualifications: Bachelor's degree in a science (e.g. toxicology, biology, chemistry or related) Experience: 2 years of experience in regulatory or product safety preferred. Computer proficient; Windows, Microsoft Office. SAP knowledge desirable. 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 is dedicated to providing 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.

Principal Responsibilities Solve technical problems supporting production. Troubleshoot problem, identify and fix root cause to eliminate re-occurring issues affecting daily production. Implement continuous improvement ideas that support the management goals outlined yearly. Creating, updating, training on Standard Operating Procedures Manage technical projects to completion. This may include machine rebuilds, corrective actions, new product launches, machine repairs, lean activities, designing tooling, etc. Knowledge, Skills & Abilities Problem solving Communicate effectively Work well on teams. Computer skills (Microsoft Suite, Email, etc.) Understanding lean manufacturing principles Machine shop skills Bearing technology Grinding theory

The Assurance Experienced Associate will be responsible for preparing financial statements with disclosures, applying basic areas of GAAP as necessary and documenting, validating, testing, and assessing various control systems. This position may also be involved in reviews and agreed-upon procedure engagements. Job Duties: Control Environment: Applies knowledge and understanding of the collective effect of various factors on establishing or enhancing effectiveness, or mitigating the risks, of specific policies and procedures by: Identifying and considering all applicable policies, laws, rules, and regulations of the firm, regulators, or other authoritative bodies as part of engagement team Making constructive suggestions to improve client internal controls and accounting procedures Documenting and validating the operating effectiveness of the clients' internal control system GAAP: Applies knowledge and understanding of governing principles; applying these principles to client transactions; and documenting and communicating an understanding and application of these principles by: Providing support of conclusions with authoritative literature Drafting basic sets of financial statements with disclosures Researching intermediate areas of accounting and forming an initial opinion on the correct treatment independently GAAS: Applies knowledge and understanding of professional standards; application of the principles contained in professional standards; and the ability to document and communicate an understanding and application of professional standards on an engagement by: Developing and applying an intermediate knowledge of auditing theory, a sense of audit skepticism, and the use of BDO audit manuals Applying auditing theory to various client situations Documenting in line with BDO policy, identifying deviations and notifying more senior team members in order to obtain appropriate approvals Applying knowledge to identify instances where testing may be reduced or expanded and notifying more senior team members of the occurrence Contributing ideas/opinions to the engagement teams Methodology: Applies knowledge and application of BDO standards to guide effective and efficient delivery of quality services and products by: Completing all appropriate documentation of BDO work papers Ensuring assigned work is performed in accordance with BDO methodology and requirements Research: Applies methodology used to seek or maintain information from authoritative sources and to draw conclusions regarding a target issue based on the information by: Researching basic and intermediate accounting topics and forming an initial opinion on the treatment independently Other duties as required: Supervisory Responsibilities: N/A Qualifications, Knowledge, Skills and Abilities: Education: Bachelor's degree in Accounting, Finance, Economics or Statistics, required OR Bachelor's degree in other focus area and CPA certification, required Master's in Accountancy, preferred Experience: One (1) or more years of prior relevant audit experience and/or public accounting, private industry accounting or consulting/professional services experience, required License/Certifications: Eligible to sit for the CPA exams upon starting employment required and actively pursuing completion of the exams, required CPA, preferred Software: Proficient with the Microsoft Office Suite, preferred Experience with assurance applications and research tools, preferred Language: N/A Other Knowledge, Skills & Abilities: Basic understanding and experience planning and coordinating the stages to perform an audit of a basic public and/or private company Ability and willingness to travel, as needed Knowledge of internal accounting controls and professional standards and regulations (GAAP, GAAS, Sarbanes-Oxley, etc) Strong verbal and written communication skills with the ability to adapt style and messaging to effectively communicate with professionals at all levels both within the client organization and the firm Ability to successfully multi-task while working independently and within a group environment Solid analytical and diagnostic skills and ability to break down complex issues and implementing appropriate resolutions Ability to of work in a demanding, deadline driven environment with a focus on details and accuracy Solid project management skills Individual salaries that are offered to a candidate are determined after consideration of numerous factors including but not limited to the candidate's qualifications, experience, skills, and geography. California Range: $79,000 - $86,000 Colorado Range: $68,000 - $72,000 Illinois Range: $74,000 - $79,000 Maryland Range: $72,000 - $78,000 Minnesota Range: $67,000 - $72,000 NYC/Long Island/Westchester Range: $75,000 - $80,000 Washington Range: $70,000 - $80,000

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. The QC Inspector is responsible for performing hourly quality checks on packaging, ensuring compliance with cGMP guidelines. Key duties include verifying lot numbers and expiration dates, maintain accurate Batch Records, inspecting packaging components, and conducting equipment accuracy checks. The ideal candidate has knowledge of FDA/cGMP guidelines, basic math and writing skills, and strong communication abilities. Work Schedule: Monday-Friday 7:00 am - 3:15 pm JOB QUALIFICATIONS: 0 - 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 POSITION RESPONSIBILITIES: Perform hourly quality checks of work-in-progress (WIP) and finished goods packaging according to company pre-defined attributes Maintain outgoing packaging quality levels and assures compliance of cGMP's Verify lot number and expiration dates of finished packaging against the Certificate of Analysis and pick slip Perform verification that the packaging line clearance was properly carried out and releases the packaging line to Production Sign-off that the packaging line was properly prepared by initialing and dating the Equipment Use and Cleaning Log Make certain all pertinent information and required signatures are present on various Batch Record forms Pull and record “beginning”, “middle” and “end” packaging line retention samples Make certain all required documents are present in the Batch Record Perform kit inspection of staged components waiting to be packaged only as required Perform accuracy checks of the weigh scales, in-line scales, and leak detection equipment as needed Perform cap torque measurements as required Verify packaging specifications for customer packaging requirements PHYSICAL REQUIREMENTS: Must be able to lift 50 lbs. Must be able to stand for extended periods Must wear required personal protective equipment (PPE) at all times, including but not limited to: safety glasses, gloves, steel-toe shoes, hairnets, and hearing protection Hourly rate starting at $18.00/hour BENEFITS: PLD is a proud employer offering many corporate benefits, including: ⠁ Medical and Dental Benefits ⠁ Vision ⠁ 401K with employer match ⠁ Group Life Insurance ⠁ Flex Spending Accounts ⠁ Paid Time Off and Paid Holidays ⠁ Tuition Assistance ⠁ Corporate Discount Program ⠁ Opportunities to Flourish Within the Company PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. #HP1

Job Description LNK International, Inc. is one of the nation's largest manufacturers of solid and liquid dose, over the counter (OTC) pharmaceuticals. For over 40 years, we have built a reputation for delivering the highest quality products, outstanding service and product innovation. What sets LNK apart? We believe it is our employees. There is a commitment to quality in every department at LNK. As a member of our QA department you will be working with dedicated professionals who support and interact with all areas of the company. Our full time employees enjoy competitive benefits including: 401(k) with generous employer match Health Insurance Dental Insurance Paid holidays Paid vacation Shift: Day Shift Responsibilities Provides support with all day-to-day operations of a Product Complaint Department. The ability to handle multiple complex projects and operational tasks while maintaining attention to detail. Under general supervision, responds to and documents complaints/inquiries received from the public and/or vendors. Documents product complaint information on an intake form, employing good documentation practices; initiates an electronic Drug Product Complaint Assessment Form. Researches and collects documents required to support and address a complaint file (label, tablet imprint, info about other medications, etc.) Prepares letters and Fed Ex envelopes to retrieve customer complaint samples. Communicates with consumers regarding product complaints. Requests, receives and tracks retention samples & batch records needed for evaluating customer complaints. Maintains a complaint/trending database and a visual tracking complaint dashboard. Prepares year-to-date statistics of all Complaint Department activities. Performs related duties and special projects as needed (e.g. product labels, monthly folders, etc.) Education/Experience An Associate's Degree or one (1) year of quality assurance experience, or an equivalent combination of education and experience may be substituted. Basic English language, spelling, grammar and punctuation a must. Experience in a professional office environment with Customer Service, including telephone interaction with customers in response to customer inquiries. Knowledge of Current Good Manufacturing Practices & Food and Drug Administration regulations and requirements a plus. Effective verbal and written communication skills Strong knowledge of Microsoft Office Suite products such as Word, Excel and Outlook Strong organizational skills and the ability to multi-task Positive, enthusiastic attitude, self-motivated, and possess excellent interpersonal skills The salary listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as permitted by law. LNK provides equal employment opportunities to all applicants and prohibits discrimination of any type on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and pregnancy-related conditions), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information or any other characteristic protected by applicable federal, state or local laws. Job Posted by ApplicantPro

Overview About LamothermicLamothermic is a second-generation, family-run investment casting foundry known for producing high-quality steel parts with a focus on customer service, technical excellence, and continuous improvement. We serve a wide range of industries with precision-engineered cast components, and we are looking for a hands-on leader to take our CNC operations to the next level The Quality Technician is responsible for supporting all aspects of product and process quality to ensure wax patterns and metal castings meet internal specifications and customer requirements. This position involves performing routine inspections, maintaining quality documentation, and assisting in corrective actions, with a strong focus on dimensional and visual inspection. Knowledge of nondestructive testing (NDT) methods is highly desirable. We offer many perks: Attendance Bonus - Earn up to an extra 50 hours/year 8 paid holidays per year 2 weeks paid vacation after one year Medical/dental packages - 1 employer sponsored pkg at 75% savings 401k program after one year employment Prescription safety eyewear paid by company Reimbursement for steel toe shoes Entry-level candidates are strongly encouraged to apply. On-the-job training is available and preferred, making this an excellent opportunity to grow your skills while contributing to a dynamic team within a manufacturing environment. Compensation up to $25 an hour, commensurate with experience. Qualifications High school diploma or GED required; associate degree or technical training in a related field is a plus. Minimum 2 years of experience in quality control or inspection in a manufacturing environment, preferably metal casting or aerospace. Strong attention to detail and problem-solving skills. Basic understanding of geometric dimensioning and tolerancing (GD&T). Proficient in MS Office (Word, Excel, Outlook). Ability to lift up to 50 lbs. and stand for extended periods. Preferred Skills & Experience but not required: NDT Level II certification or experience in Magnetic Particle Testing (MT), Penetrant Testing (PT), and Radiographic Testing (RT) per SNT-TC-1A or NAS 410 (preferred but not required) . Experience with investment casting processes is a strong plus. Knowledge of quality standards such as ISO 9001, AS9100, or relevant industry-specific standards. Familiarity with CR/DR radiography and reading X-ray images is a bonus. Responsibilities Perform in-process and final inspections of wax patterns, steel and bronze castings. Verify product conformity using measuring instruments (e.g., calipers, micrometers, gauges). Interpret blueprints, engineering drawings, and customer specifications. Maintain accurate inspection records, nonconformance reports (NCRs), and inspection logs. Assist in developing and reviewing work instructions and inspection criteria. Support the disposition and follow-up of nonconforming material. Collaborate with production, engineering, and quality departments to resolve quality issues. Contribute to continuous improvement efforts (e.g., 5S, root cause analysis, corrective/preventive actions). Company Website **************************** Company Profile Careers - Lamothermic Corp. Are you looking to work for a continuously developing company, where the culture is focused on teamwork and development? Look no further. Working at Lamothermic, you will join a team whose goal is simple - employ the best people, technology, processes and materials to provide our customers with quality investment castings. Lamothermic is your premier supplier of precision investment castings - quality first, every time. Our commitment to superior quality combined with our best in class engineering and advanced automation means that our customers get the best castings for their needs.

Job DescriptionDescription: RK Pharma Inc, a US based company with subsidiaries in India, is seeking a Quality Assurance Sr. Associate to assist our associate director of QA with leading our Quality Assurance Team as we scale towards commercial manufacturing in the next upcoming months. As a company focused on the development, manufacturing and sale of high quality and affordable generic pharmaceutical products worldwide we are looking for sharp, driven, self-directed individuals to help us grow our mid-stage start-up team. This position will focus heavily on building and managing our QA team, providing feedback, and sharing industry standards as well as assisting the Associate Director of QA with the day-to-day management of the team. This position is in Pearl River, New York, and is required to be onsite. Requirements: If this sounds interesting to you, it’s probably because up to this point you have: Bachelor’s or master’s degree or foreign equivalent in Chemistry or other related field. 6+ years of experience in Quality Control or Quality Assurance Assisted in the management of anywhere from 6-15 people. Knowledge of Laboratory Instruments such as HPLC, GC, UV/Vis, IR, Particle Counter. Provided guidance and mentorship to your team around standards cGMP, and QMS Functions. Experience and knowledge of compliance requirements and cGMP and keep precise records. Experience with injectables or generic pharmaceutical manufacturing. The main responsibilities for this position are: Manage the workflow of the team on a day-to-day basis. Provide feedback and management of the team. Ensuring proper staffing for batches on a day-to-day basis. Maintain precises documentation for the team as well holding to all compliance and cGMP standards. Participate in Internal & External Audits Review and approve SOPs and QMS documents If this sounds like something that is of interest to you, please do not hesitate to apply to start a conversation. We look forward to getting to know more about you and the skills you can bring to a company like RK Pharma Inc.

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.

Job Description Radienz Living is a leading North American manufacturer of home and personal care products, such as unit dose laundry and dish products, facial wipes, and baby wipes. With manufacturing plants and warehouses in Mt. Prospect, IL and Long Island, NY, the company provides customers with private-label solutions and contract manufacturing services for products found in retail and institutional markets. Radienz Living is driven by a commitment to innovation, trust, reliability, and sustainability—delivering products that support a cleaner way of living and help create a more radiant world. Over the past two years, the company has undergone a remarkable transformation, strategically focusing on two core product lines: Unit Dose products—where it stands as the undisputed leader in Private Label and Contract Manufacturing—and Personal Care Wipes, proudly producing wipes for the nation’s #1 beauty care brand. Supporting this growth, the company has established robust quality systems, earned multiple GMP certifications, and built in-house FDA/EPA-compliant laboratories for microbiology, quality control, chemistry, and R&D. Background: Under the direction of the Quality Supervisor, the Quality Technician is responsible for ensuring products are being produced in a manner that meets all cGMP and Product Specification criteria. The Quality Technician provides real time review of in-process test data and batch documentation to limit the need for later review or rework. Responsibilities: Conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks. Consistently reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices, company SOP’s and cGMP’s. Discusses errors and reviews production logbooks for accuracy and compliance. Collects data and supports release of batch records. Complies with company policies and procedures and maintains exceptional work attendance. Responsible for conducting duties in compliance with safety rules, applicable SOPs, and cGMP guidelines. Conduct regular quality line audits of in-process and finished goods against pre-defined characteristics to validate that all process and product requirements have been satisfied. Document audit results on the appropriate QA paperwork making notes about out-of-spec conditions found or other observations of interest. Perform Leak test on in-process material to ensure that product meets intended performance requirements. Perform Lot Code validations. perform Control Weight validations at a determined frequency. Monitor the performance of metal detection equipment, as applicable. Investigate production related QA problems and make recommendations. Visual verification of raw material and packaging material to validate material is in spec to artwork and functionality requirements and is used for its intended purpose on the correct product. Execute the plant non-conforming materials procedure when out-of-specification conditions are observed. Help individuals performing activities affecting Fit and Function of the product to understand why something is not right when process and/or product nonconformance’s are identified. Notify supervisor of unusual problems, delays, and/or safety issues. Performs other duties as assigned by Quality Management. Flexibility to work some weekends to support production schedule is required. Qualifications: High School Diploma or General Education Degree (GED) required. Quality Operations experience is required. Working knowledge of Microsoft Word, Excel, and Outlook is preferred High attention to detail to required. Understanding of basic measurement concepts, such as length, width, height, weight, and average. Must be able to communicate, respond to verbal and written instructions in English. Knowledge and experience working in a Manufacturing environment. Ability and willingness to follow directions. Ability to effectively troubleshoot problems and recognize when to escalate issues to manager. Pay Range: $19.00 – $22.00 per hour. Compensation will be based on the candidate’s experience. Schedule: Monday - Friday; 4:30pm - 1:00 am. Shift: 2nd shift Schedule: Monday - Friday; 4:30pm - 1:00 am.

Job Description Schivo Medical is a contract manufacturer on Long Island. We produce machined parts such medical devices, surgical tools, and firearms. We are hiring a quality technician, perfect for someone who would like a career in quality Inspection working closely with the CNC operations . Come work in an environmentally clean facility with great team players that support and guide you through your daily work schedules. We are a company that is committed to helping you build a fulfilling and rewarding career. ***Recent Graduates welcome**** Position Overview: Quality Technician is responsible for load and unloading components onto CMM fixtures for inspection. Analyze reports and provide data to the production team. Maintain equipment as necessary. Assist with a variety of Quality Control related tasks. Follow written and oral instructions Maintaining good housekeeping practice Review work center for maintenance compliance. Maintain correct time reporting and accurate entries on applicable manufacturing documentation. Comply with company quality and safety requirements Attention to detail Required Education and Experience: AAS or Bachelor’s degree in Mechanical, manufacturing engineering or relatable industry Will accept a high school graduate with 2 years’ experience working in this industry. Benefits: Employee referral 401(k) 401(k) matching Dental insurance Vision insurance Employee assistance program Health insurance Paid time off Referral program 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.

Kit QC Inspector- Farmingdale NY- onsite ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Kit QC Inspector- Farmingdale, NY onsite The role: To ensure the quality and correctness of all visit kits distributed to investigator sites. Inspect all visit kits according to SOP prior to packing and transfer to the shipping department. Perform quality control of all visit kits as required by the SOP. Ensure all errors are corrected & logged appropriately. Inform the QC supervisor of any issues or delays. Achieve daily/weekly departmental Quota assigned. Perform additional responsibilities as requested by Management To be successful you will need: 2 to 3 years of QC experience Skills - Detail oriented, excellent organizational skills, Commutations skills and the ability to deal well with stress. Basic computer skills including knowledge in MS Outlook, of MS Word, Excel and typing skills. High School or Equivalent (Required) Hourly Rate range: Up to 23.50 hour Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Visit our careers site to read more about the benefits ICON offers. #LI-FL1 What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Salary range: - Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance. Are you a current ICON Employee? Please click here to apply

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.

Quality Assurance Associate IIIAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT & Human Resources disciplines in New Jersey. The Quality Assurance Associate III is responsible for performing Quality Assurance activities within minimal supervision of daily tasks in support of Quality Systems and/or client procedures including but not limited to document management, issuance, review and approval of batch records, SOPs, Qualification and Validation Reports; review of QC data; perform material releases and final product releases; review of Deviations as well as assists Quality management with department needs. He/she exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. This role manages internal and external audits which may include interaction with Health Authorities and clients Interfaces directly with client and cross functional teams Provides resolutions pertaining to quality for project related issues Independently prioritize, schedule, and manage multiple projects and resources (team) Ensures the safe release of cellular products in accordance with company and/or client procedures and requirements. Ensure and promote compliance with applicable CGMP and GTP regulations and company and client SOPs Able to provide input based on knowledge and experience on quality systems and procedures and CGMP/GTP issues. Author and review relevant SOPs, validation and other documents. Responsible for the timely issuance, review and approval of QC certificates, closure of Batch Records, and deviation reports. Responsible for the completion of all client requirements related to cellular product and/or material releases. Master Batch Record Control, distribution and label verification Perform line clearance activities as required. Assignment and maintenance of product Lot numbers as applicable. Perform internal documentation audits as assigned. Materials management nonconformance disposition and release activity as applicable. Responsible for accurate deviation reporting as applicable and tracking/trending follow up actions to closures Evaluate and investigate deviation reports and initiate and coordinate corrective and preventive actions. Track and trend relevant quality metrics including environmental monitoring data. Provide Quality Assurance related support to various departments. Interface with suppliers and in-house production personnel to ensure effective corrective and preventive actions are implemented for recurring product/process discrepancies. Electronic Document Control activities as assigned. Provide training to personnel as assigned by supervisor. Travel may be required. REQUIREMENTS BS in biological sciences or other relevant field of study 5 years + experience in QA in a life sciences company company with a strong focus in the manufacturing and/or testing of biologics. Working knowledge and technical understanding of aseptic manufacture of biologics Understanding of quality system applications Experience in both clinical and commercial manufacturing is preferred. Experience in authoring, reviewing, and /or approving cGMP/cGTP related documents (validation/qualification reports, SOPS. Etc. Experience in organizing teams for effective and timely completion of projects. Understanding of quality system applications, including the use of electronic applications for training, deviations, CAPA management, etc. Experience participating in or hosting health authority inspections and/or client audits. Computer skills (Microsoft Office, Outlook) Detail-oriented and organized Analytical and problem-solving skills Good written and oral communication skills Ability to multi-task and be adaptable Flexible and able to adapt to company growth and evolving responsibilities Ability to work independently and with a team Strong Project Management and organization skills Must have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays and as required by the company May be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, etc. Please note 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.

Job DescriptionQuality Inspector – Trumbull, CT Pay: $19/hour Schedule: Monday–Friday, 7:00 AM – 3:30 PM Seeking a detail-oriented Quality Inspector to ensure crate production meets required standards through inspections and documentation.Responsibilities: Crate Inspections – Perform measurements and visual checks to confirm specifications. Process Improvements – Identify issues, recommend solutions, and assist with audits. Collaboration – Communicate errors and quality concerns to the production team. What You’ll Need: Blueprint reading experience. Ability to use measuring tools and track data in MS Office. Bilingual in Spanish is a plus! #LSCTJOBS

Safety Assurance/Regulatory Affairs Associate 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 Companies. We currently have an opportunity for a Safety Assurance/Regulatory Affairs Associate within the Fragrance division located in Rockleigh, NJ. Essential Job Functions: Conduct safety review of fragrance formulas according to industry, regulatory and customer requirements Provide assistance to perfumers on safety/regulatory requirements for fragrance creation. Prepare fragrance safety documents as per customer requests. Communicate with customers on safety and regulatory issues. Communicate with suppliers on requests for safety/regulatory information. Ensure maintenance and security of fragrance formulas. Ensures MSDS databases are maintained on chemicals used in the fragrance, aroma chemical and export divisions. Review new and updated MSDS's and industry information on fragrance division chemicals for health hazard statements. Maintain the safety information on fragrance division chemicals used in the creation of MSDS's for fragrance compounds. Prepare and maintain MSDS's for fragrance compounds, according to appropriate country regulations. Expert on the use and setup of The Wercs MSDS authoring software. Distribute MSDS's to Sales, customers, etc. Maintain the Health Hazard Communication SAP program for the fragrance division. Maintain the NJ Right to Know system for the fragrance division. Provide assistance on projects for Fragrance Safety Assurance Specialists/Manage Educational Qualifications: Bachelor's degree in a science (e.g. toxicology, biology, chemistry or related) Experience: 2 years of experience in regulatory or product safety preferred. Computer proficient; Windows, Microsoft Office. SAP knowledge desirable. 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 is dedicated to providing 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.

Overview About LamothermicLamothermic is a second-generation, family-run investment casting foundry known for producing high-quality steel parts with a focus on customer service, technical excellence, and continuous improvement. We serve a wide range of industries with precision-engineered cast components, and we are looking for a hands-on leader to take our CNC operations to the next level The Quality Technician is responsible for supporting all aspects of product and process quality to ensure wax patterns and metal castings meet internal specifications and customer requirements. This position involves performing routine inspections, maintaining quality documentation, and assisting in corrective actions, with a strong focus on dimensional and visual inspection. Knowledge of nondestructive testing (NDT) methods is highly desirable. We offer many perks: Attendance Bonus - Earn up to an extra 50 hours/year 8 paid holidays per year 2 weeks paid vacation after one year Medical/dental packages - 1 employer sponsored pkg at 75% savings 401k program after one year employment Prescription safety eyewear paid by company Reimbursement for steel toe shoes Entry-level candidates are strongly encouraged to apply. On-the-job training is available and preferred, making this an excellent opportunity to grow your skills while contributing to a dynamic team within a manufacturing environment. Compensation up to $25 an hour, commensurate with experience. Responsibilities Perform in-process and final inspections of wax patterns, steel and bronze castings. Verify product conformity using measuring instruments (e.g., calipers, micrometers, gauges). Interpret blueprints, engineering drawings, and customer specifications. Maintain accurate inspection records, nonconformance reports (NCRs), and inspection logs. Assist in developing and reviewing work instructions and inspection criteria. Support the disposition and follow-up of nonconforming material. Collaborate with production, engineering, and quality departments to resolve quality issues. Contribute to continuous improvement efforts (e.g., 5S, root cause analysis, corrective/preventive actions). Qualifications High school diploma or GED required; associate degree or technical training in a related field is a plus. Minimum 2 years of experience in quality control or inspection in a manufacturing environment, preferably metal casting or aerospace. Strong attention to detail and problem-solving skills. Basic understanding of geometric dimensioning and tolerancing (GD&T). Proficient in MS Office (Word, Excel, Outlook). Ability to lift up to 50 lbs. and stand for extended periods. Preferred Skills & Experience but not required: NDT Level II certification or experience in Magnetic Particle Testing (MT), Penetrant Testing (PT), and Radiographic Testing (RT) per SNT-TC-1A or NAS 410 (preferred but not required) . Experience with investment casting processes is a strong plus. Knowledge of quality standards such as ISO 9001, AS9100, or relevant industry-specific standards. Familiarity with CR/DR radiography and reading X-ray images is a bonus. Company Website **************************** Company Profile Careers - Lamothermic Corp. Are you looking to work for a continuously developing company, where the culture is focused on teamwork and development? Look no further. Working at Lamothermic, you will join a team whose goal is simple - employ the best people, technology, processes and materials to provide our customers with quality investment castings. Lamothermic is your premier supplier of precision investment castings - quality first, every time. Our commitment to superior quality combined with our best in class engineering and advanced automation means that our customers get the best castings for their needs.

Job Description BASIC FUNCTIONS Mid-level position. Performs 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 Prepare and complete all necessary documentation (records) for reporting acceptance/rejection of items inspected and/or tested. Ability to complete a full analysis on all EEE Devices within the Laboratory Ability to operate all test equipment within the Laboratory Department 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 Compile, review data and complete test reports IAW CTG Standards 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. Comply with all requirements of the AS9120, ISO 9001, ASA-100, and IDEA QMS 9090 Quality Management System and criteria of CCAP-101, AS6081, AC7402 and ANSI/ESD-S20.20 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 with a minimum of 2 years’ experience performing in-process and final inspection preferably in a machining, automotive or aerospace business Must be proficient in English, both written and verbal communication skills Good arithmetic skills are required Mechanical aptitude desired Ability to correctly use and interpret basic measuring tools including weight gauge, micrometer, caliper scale (linear), gauge blocks, thread gauges, and comparative standards Basic proficiency of Microsoft Excel and Word Independent; can work with limited supervision and direction Must complete IDEA-ICE-3000 Certification within 6 months of hire. Able to pass internal testing and training to meet internal requirements ASQ CQI certified or must completed certification within 1 year of accepting position Strong Electronics inspection knowledge preferred Must demonstrate acceptable vision requirement.

Quality Inspector – Trumbull, CT? Pay: $19/hour ? Schedule: Monday–Friday, 7:00 AM – 3:30 PM Seeking a detail-oriented Quality Inspector to ensure crate production meets required standards through inspections and documentation.Responsibilities: ? Crate Inspections – Perform measurements and visual checks to confirm specifications. ? Process Improvements – Identify issues, recommend solutions, and assist with audits. ? Collaboration – Communicate errors and quality concerns to the production team. What You’ll Need:?? Blueprint reading experience. ?? Ability to use measuring tools and track data in MS Office. ?? Bilingual in Spanish is a plus! #LSCTJOBS