Travel %.
Flexible Work Option.
The inspector will perform precision dimensional inspections using FARO systems and support shop floor inspection activities. System One is seeking a Certified FARO/NDE Inspector for a long-term onsite contract role.
b>Essential Duties and Responsibilities:
In this role, youll play a key part in maintaining Acero Precisions reputation for quality excellence by: Ensuring product accuracy and compliance through Monitor Reports and the our Data System. Demonstrated experience completing inspection reports, first article inspections, non-conformance documentation, calibration records, and production quality documentation.
However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. Depending on the size, complexity, and number of Definable Features of Work, this position manages the Project Quality Control Plan, ensures all contract requirements are being met, and supervises project Quality Control Inspectors.
p>Bonus/Incentive Pay : For hourly positions with incentive pay: Incentive pay may be available for certain job roles and may include piece rate incentives, weekly production bonuses, and trip rate bonuses. Compensation & Benefit Information: Hourly/Salary Pay Range: $50,000 - $100,000 annually dependent on experience* *pay range may be adjusted depending on cost of living .
p>With a strong focus on MEP/FP systems, building envelope performance, and water damage prevention, the QA/QC Manager serves as both a technical expert and trusted advisor, reinforcing IMC’s Plan-Do-Check-Act philosophy and culture of accountability and continuous improvement.
Position Summary: The Quality Control Supervisor is responsible for floor operations i.e., Quality Control, but is also a caretaker of sitewide adherence and continual improvement of company programmatic Quality Assurance policies and procedures. Qualifications: Strongly prefer education level of bachelors' degree (science or engineering preferred) with a minimum experience of as follows, Minimum 2 years of experience leading others.
p>Bonus/Incentive Pay : For hourly positions with incentive pay: Incentive pay may be available for certain job roles and may include piece rate incentives, weekly production bonuses, and trip rate bonuses. Compensation & Benefit Information: Hourly/Salary Pay Range: $50,000 - $100,000 annually dependent on experiencepay range may be adjusted depending on cost of living.
The ideal candidate will be comfortable performing inspections, interpreting blueprints and GD&T, supporting ISO compliance initiatives, and mentoring quality personnel in a fast-paced precision manufacturing environment. We are seeking a hands-on Quality Control Manager to lead inspection activities, support quality system compliance, and partner closely with manufacturing teams to ensure every product meets customer expectations.
Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). This position is accountable for building and developing a high-performing team through proactive coaching, structured mentoring, performance management, career-path development, and workforce planning to ensure the group is equipped to meet current and future business needs.
li>Specific vision abilities required for this job include: Close vision (clear vision at 20 inches or less); distance vision (clear vision at 20 feet or more); peripheral vision (ability to observe an area that can be seen up and down or to the left and right while eyes are fixed on a given point); depth perception (three-dimensional vision, ability to judge distances and spatial relationships); ability to adjust focus (ability to adjust the eye to bring an object into sharp focus). This role involves conducting regular inspections and audits of various airport services, including ground handling, maintenance, and passenger services.
To help spot these scams, remember that during our formal recruitment process, L3Harris will NOT (1) ask you for money; (2) offer to send you a check before doing any work; (3) require you to provide sensitive personal information early in the process or sensitive information about your previous employer; (4) send you emails from free commercial services (e.g. About L3Harris Technologies: L3Harris Technologies is an agile global aerospace and defense technology innovator, delivering end-to-end solutions that meet customers' mission-critical needs.
ul> The Scientist, Quality Control conducts routine and non-routine analysis, including but not limited to biochemical and chemical analysis of processes leading up to drug product according to established operating procedures.
div>Job Summary: This is an individual contributor position which works under regular supervision and is responsible for reviewing construction documents before sending to production and making corrections or edits based on client specifications.
Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. In addition to base salary, we also offer a comprehensive total rewards package, inclusive of annual incentive pay, a retirement savings plan, health care coverage, paid time off, recognition programs and a broad range of other benefits.
h5>HireNow Staffing is actively recruiting two seasoned, highly skilled Quality Control Managers - Machine Parts on behalf of a valued client partner in the precision manufacturing / medical device machining sector. https://www.careers-page.com/hirenow-staffing-inc/job/4R86989V.
Conducts regular project site inspections to monitor progress and support project-assigned team members, steps in as needed to address and resolve issues and problems, and recommends modifications to the project plans, schedule, staffing, or budget as needed. Directly responsible for identifying, retaining and managing engineers, architects and consultants to perform 3rd party design reviews of project plans and specifications and their inspection teams in the field for final acceptance of projects.
Located in West Rockhill Township, PA, Naceville Quarry is strategically positioned to serve the growing Upper Bucks/Montgomery County region of PA. Beginning as a small family business a half century ago, we are now a dynamic group of vertically integrated companies that has been growing and prospering for over 50 years.
Beginning as a small family business a half century ago, we are now a dynamic group of vertically integrated companies that has been growing and prospering for over 50 years. The H&K Group, Inc. provides complete heavy civil contracting and construction materials solutions with safety, speed, quality, efficiency, and value.
What We Offer: We strive to provide a great company culture consisting of a variety of team building events: trivia nights, softball and volleyball leagues, mini golf tournaments, BBQ’s, happy hours, poker nights, catered weekly staff meetings, surfboard lending programs, and much more. We proudly serve Fortune 500 companies as well as independent owners and developers of all sizes, offering a comprehensive consulting experience that integrates expertise in design and permitting for commercial, industrial, and residential projects.
Tasks include but are not limited to analyze executed documents for accuracy and completeness, identify any closing errors or missing items on the E&O tracking report, be responsible and take ownership of E&O tracking report, perform a monthly review of E&O’s to ensure collateral is properly secured, and communicate with internal partners, Vendors and Client’s when additional information is required. The Commercial Quality Control Specialist supports risk mitigation and quality assurance by performing post-closing reviews of new, renewed, and modified Business Banking and Commercial loans.
Thorough and demonstrated understanding of Retail Lending Banking regulations including but not limited to Truth in Lending (Reg Z), National Flood Insurance requirements (NFIP), Biggert/Waters Act, RESPA, Fair Lending, Fair Credit Reporting Act and BSA as it relates to the Retail Lending Function. WSFS Bank will only consider candidates who are presently authorized to work for any employer in the United States and who will not require work visa sponsorship from WSFS Bank now or in the future in order to retain their authorization to work in the United States.
p>Qualifications for the Quality Control PCR Specialist include: • A minimum of 2 years' experience within quality control • Hands on experience conducting PCR testing within a GMP laboratory environment • Ability to conduct a deviation or OOS investigation • Technical writing experience preferred • Bachelor's degree in chemistry or related field. Keywords: Pharmaceutical, quality control, PCR, Elisa, SDS Page UV-Vis, Deviation, OOS, Investigations, Assay qualification, technical writing, FDA, manufacturing, Science, comprehensive benefits package, Health, Vision, Dental.
They will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping under appropriate conditions, for all the iCTC cell therapy asset. Required Education, Skills, and Knowledge:
UDC’s OLED ingredients are key parts of stunning, energy-efficient displays used in everything from smartwatches to phones, tablets, laptops, monitors, TVs and automobiles. Support the company’s Integrated Management System (IMS) and actively participate in internal and external audits, including ISO 9001, ISO14001 & ISO45001 audits.
This role is responsible for overseeing inspections, nonconformance investigations, CAPAs, MRBs, quality systems, and production quality initiatives. Our client is seeking a Quality Control Manager to lead quality operations within a precision medical device manufacturing environment.
p>This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. For more details, please visit : www.piramalpharmasolutions.com.
em> Maintain awareness of bank, regulatory, and industry changes and trends Responsibilities may also include contributing to CBB Risk Data Team projects or project implementation Perform other duties as assigned BASIC QUALIFICATIONS Seven to ten years of applicable experience Bachelor's degree or equivalent work experience PREFERRED SKILLS/EXPERIENCE SQL/SAS coding experience Five years of experience with bank systems Five years in a reporting, analytics, or technology environment Strong problem-solving, process facilitation, project management, and analytical skills Excellent interpersonal, written, and verbal communication skills Considerable knowledge of applicable laws, regulations, financial services, and regulatory trends that impact CBB Advanced understanding of CBB products, services, systems, and associated risks/controls, as well as supporting operational functions Python experience Advanced Excel computer skills and database knowledge Experience with SharePoint or TEAMS Comfortable working in a team environment with layers of required review/approval Ability to work in a fast-paced environment with large workloads If there's anything we can do to accommodate a disability during any portion of the application or hiring process, please refer to our disability accommodations for applicants. RESPONSIBILITIES Customer Remediation Support: The CBB Risk Data Team supports issue and business line management with research, data analysis, documentation and execution Credible Challenge: The CBB Risk Data Team accepts ownership of the data used within all CBB customer remediation events.
Long known as "The Professional's Source", B&H is recognized by savvy consumers worldwide for its honest, knowledgeable guidance, expert tips and articles… and always-great prices. At over 50 years old and counting, B&H has built a reputation as the trusted resource for photography and videography enthusiasts via its NYC SuperStore and its award-winning website.
Job Description: The Centralized Governance & Control - Remediation Quality Assurance Testing team performs in-flight Assurance Testing Activities throughout the Issue Remediation Lifecycle to ensure Management Action Plans (MAPs) are designed to sufficiently mitigate and manage risk drivers of the issues and operate effectively. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition.
By applying for this job, you agree to receive calls, Al-generated calls, text messages, or emails from Synerfac Technical Staffing and our contracted partners. Under the direction of the Quality manager, they will be asked to help with the inspection, testing and production of goods starting with raw materials.
Our products include the popular La Yogurt and Sabor Latino yogurt, Tree Ripe juices, Earth Wise juice beverages, Ssips and Sabor Latino drinks and nectars, and Ssips aseptic drink boxes, all using cutting-edge technologies and only the freshest, highest quality ingredients.
li>Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. The Bioassays and Potency Analysis group strives to deliver creative medicines to patients through performance of bioassay, potency and impurities testing activities within a GxP-compliant QC laboratory to support pre-clinical studies and clinical development for biological products manufactured in a GMP production facility.
Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
Oldcastle Infrastructure, a CRH company, is the leading provider of utility infrastructure solutions for the water, energy, and communications markets throughout North America. ACI / PCI Certification preferred, or required to pass ACI Concrete Field Testing within 3 months and maintain certification.
This hands-on position is responsible for maintaining sample organization, assisting with testing preparation, ensuring accurate documentation, and helping to uphold cleanliness and efficiency within the lab and production environment. - Cross-train on basic QC tasks to provide coverage as needed, including data entry, sample preparation for viscosity testing, bake tests, & outbound product quality checks.
p>This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. The QC Supervisor is responsible and accountable for achieving targets/key metrics, and investigations within the laboratory, as well as scheduling the testing for finished product and stability samples, and coordination of activities within the lab.
This position is responsible for performing in-process environmental monitoring of cGMP manufacturing suites, conducting finished product safety testing including endotoxin and sterility assays, and assisting with stability program testing to evaluate product performance over time. The Quality Control Microbiology Associate will support the safety, quality, and compliance of drug products through the execution of routine microbiological testing and monitoring activities.
div class="col col-xs-7 description" id="job-description"> The Quality Control Technician inspects work performed by client employees, internal employees, or client subcontractors. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. **Your Skills and Experience** Education + Minimum: BS/MS in applicable discipline + Preferred: Biochemistry, Biology Experience + Minimum: 1 year in the (Bio)pharmaceutical industry with bioassays/potency assays + Preferred: 2–3 years in the (Bio)pharmaceutical industry with bioassays/potency assays **Also Good to Have** Physical Requirements: + Ability to lift 25 pounds .
p>The Quality Control Raw Materials and Stability Associate will support the quality control function through coordination, documentation, and data review activities for raw materials and stability programs in accordance with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements. The associate will coordinate raw material testing with contract testing laboratories (CTLs), review and summarize externally generated data to support material release, and assist in the qualification of critical ancillary materials and excipients used in GMP manufacturing.
li>This position requires consistent wearing of a lab coat, safety glasses, gloves, long pants, and closed-toe shoes; with additional specific PPE depending on the chemicals or materials handled, which could include respirators, hearing protection, or specialized gloves for hazardous substances. Responsible for testing raw materials, in-process materials, finished goods as well as auditing the manufacturing process for proper weights, container marking, labeling and overall aesthetics of finished goods.
The Quality Control Analytical Associate is a dual-function role responsible for performing analytical testing in a GMP laboratory environment while also supporting inventory control and sample management activities. Perform routine and non-routine analytical testing of in-process samples, and finished products in accordance with approved SOPs.
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