Travel %.
Flexible Work Option.
This highly hands-on role supports a low-volume, high-precision manufacturing environment for advanced semiconductor-related capital equipment and plays a critical part in production readiness and overall product quality.
This role also performs data entries on paper batch records as well as SAP (ERP), Quarantine activities related to Client s (ER), cycle count, inventory management, Cross-functional communication across multiple departments etc. Responsible for, but not limited to, inspecting, and receiving human and porcine tissue, batch record review, cleaning, cycle count, product/tissue quarantine, media change and disposition activities.
strong>The ideal candidate will have experience in records management, document review, or administrative support within a Government or high-volume documentation setting. TeleSolv Consulting is seeking a detail-oriented Quality Control Specialist to support a Federal Government operation.
li>Experience supporting Government operations or high‑volume documentation environments.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
p>With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science.
Led today by their son Evan, David Yurman creates timeless, yet contemporary collections for women and men defined by inspiration, innovation, consummate craftsmanship and cable – the brand’s artistic signature. This role manages quality inspection teams, quality processes, vendor quality performance, and product validation programs across finished goods, components, repairs, and returned merchandise.
li>Document Control: Ensure that contractors are utilizing the latest revisions of design documents, maintaining accurate records of changes and updates throughout the project lifecycle.
Document Control: Ensure that contractors are utilizing the latest revisions of design documents, maintaining accurate records of changes and updates throughout the project lifecycle. Audit Reporting: Compile and report quality audit results and performance metrics to project management and stakeholders, highlighting areas of concern and recommending corrective actions where necessary.
li>Document Control: Ensure that contractors are utilizing the latest revisions of design documents, maintaining accurate records of changes and updates throughout the project lifecycle.
12+ years' experience of progressively more responsible laboratory management in a related scientific/technical discipline or equivalent combination of education and relevant experience in the pharmaceutical industry, related GMP environment, or equivalent. Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes.
Under the direction of the Quality Manager, the Quality Control Supervisor is responsible for leading and supervising a team of QC Inspectors performing inspection and disposition activities for makeup products, components, WIPs, and finished goods in accordance with cGMP requirements, company policies, and established specifications. Be a part of a portfolio of prestige beauty brands which includes Clé de Peau Beauté, Drunk Elephant, Dr. Dennis Gross Skincare, NARS, SHISEIDO and several prestige fragrance brands including Issey Miyake, Narciso Rodriguez and Tory Burch.
em>We are seeking an experienced Quality Assurance/Control Manager to oversee field operations, quality programs, inspections, and compliance activities for commercial and industrial energy efficiency projects throughout New Jersey. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from HEPCO, Inc and its affiliates, and contracted partners.
12+ years’ experience of progressively more responsible laboratory management in a related scientific/technical discipline or equivalent combination of education and relevant experience in the pharmaceutical industry, related GMP environment, or equivalent. Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes.
p>Sales Positions Only: For sales positions that are commission-based, the above range is an estimate of total potential commission-based compensation during an associate's first year, but UNFI offers an introductory period minimum of $680 per week. Actual Pay, where applicable, will depend on a number of factors, including, but not limited to, education, experience, training, and any requirements under applicable collective bargaining agreements.
p>Compensation: Senior Quality Control Specialist I (TA): $90,319.00 - $102,064.00 Senior Quality Control Specialist II (TA): $97,548.00 - $109,250.00 Senior Quality Control Specialist III (TA): $105,348.00 - $115,784.00 Senior Quality Control Specialist I (OA): $90,319.00 - $102,064.00 Senior Quality Control Specialist II (OA): $97,548.00 - $109,250.00 Senior Quality Control Specialist III (OA): $105,348.00 - $115,784.00.
Company networking opportunities with organized groups in the following topics: Network of Women, Black Professionals, LGBTQ+ Pride, Ability (Disabilities), Dynamic ((Neurodiversity), Women in Tech, OneEarth Champions, and more. This is a client-facing, player-coach role responsible for managing day-to-day operations across transaction monitoring, screening, and Travel Rule workflows.
li>Handle and report all substantive USPTO actions with input from Responsible Attorney, including preparing draft amendments/responses to official actions and notices to file missing parts, obtaining identified references, processing notices of allowance including attending to the Notice of Allowance Review Form in coordination with the Patent Prosecution Specialist and Patent Practitioner, addressing any inventorship/assignment issues, and preparing related paperwork (e.g., extensions, RCEs, corrected ADSs, name changes, maintenance fee addresses, etc.).
li>Collaborate with cross-functional teams including Analytical Sciences, Manufacturing, and Quality Assurance to ensure timely project delivery.
As an independent Brand Representative, you will act as a key liaison between the brand and retail store environments, conducting recurring in-store visits to perform audits, ensure product quality, and elevate the brand experience. Through innovative in-store retail technology solutions, we bring products to life inside retail environments, helping brands optimize performance and grow in today's dynamic retail landscape.
In this role, you will support daily Quality Control laboratory operations by assisting with sample management, inventory control, laboratory organization, and documentation while working in a regulated cGMP environment. Operating at the intersection of resources, critical infrastructure, and modernization of industries, RCM is a provider of services in Life Sciences, Data & Solutions (IT), Healthcare, Engineering, Aerospace & Defense, and Process & Industrial.
As Director, Quality Control you will be responsible for strategic leadership and oversight of the Quality Control (Analytical and Microbiology) function, including testing at contract labs for drug substance, drug product, and stability programs across commercial and development portfolios. Location: Parsippany, New Jersey Ferring Pharmaceuticals a privately owned, research-driven, specialty biopharmaceutical group committed to building families and helping people live better lives.
Candidates who successfully complete the program will be offered to join WuXi Biologics global network (not limited to the U.S. site) as management at levels ranging from Manager to Associate Director's. The Global Emerging Leaders Program (GELP) is a 2-year rotational leadership development program designed to cultivate future business and technical leaders within WuXi Biologics.
p>A growing dairy manufacturing operation is seeking a Quality Control Manager to take ownership of food safety and quality systems from the ground up. This is not a maintenance role — we are looking for someone who has built or significantly structured a QC/QA function, not just managed an existing one.
li>Minimum five years of quality experience is required with an Associate's degree, or one year of experience with a Bachelor's degree.
p>Ensure the systems are managed/maintained following system management/maintenance procedures within the analytical instrument/equipment life-cycle, including but not limited to user account management, system configuration and audit trail management. Daily maintenance of LIMS system and/or other computerized systems, including but not limited to static data configuration, functional requirements improvement and testing, problem handling, user training, etc., to meet the daily operation requirements of the system.
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.
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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.
li>5+ years of experience in quality control or analytical testing, with at least 3 years in a supervisory or management role. The Quality Control Lab Supervisor (QC Bulk Supervisor) is responsible for overseeing all QC laboratory and in-process.
Working under the guidance of senior Quality Assurance and QC engineers, you will document testing findings, contribute to the maintenance of test documentation, and collaborate directly with developers, analysts, and project teams. The person who fills this role will be required to work in a hybrid work environment adjacent to one of our offices in Oakland, CA; Orange, CA; New York, NY; Portland, OR; Boston, MA; or Chicago, IL.
Enable the timely completion of Quality System records associated with sample testing to improve reliability of test methods, facilitate change, and evaluate and prevent exceptions (change control, lab investigations, OOS, deviations, and CAPAs). Responsibilities (including, but not limited to): Design, implement, and continually improve Kiniksas Quality Control programs for commercial and late-stage clinical drug products, including combination products.
This role oversees method execution, data integrity, investigations, and continuous improvement while managing and developing a high‑performing QC team. Technical Expertise:
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