Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices,
Description The Senior Quality Management System & Document Control Specialist is responsible for administering and maintaining the companys QMS & Document Control systems to ensure the integrity, accuracy, accessibility, and compliance of controlled documentation throughout its lifecycle.
Quality Compliance Specialist Skydio is the leading US drone company and the world leader in autonomous flight, the key technology for the future of drones and aerial mobility. The Skydio team combines deep expertise in artificial
As the largest pureplay adhesives company in the world, H.B. Fuller’s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2024
Job Title: Quality Document Control Company: Loenbro, LLC Business Unit/Department: Quality Control Location: Westminster, CO / On-site Reports to: Director of Quality Employment Type: Full-Time FLSA Classification: Exempt About Loenbro Loenbro is a trusted, long-term construction
Portfolio Business: Huber Engineered Materials J.M. Huber Corporation is one of the largest privately held, family-owned companies in the United States. Established in 1883, we are a diversified, global supplier of specialty and commodity chemicals, hydrocolloid
Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day,
Job Summary: The Manufacturing Industrial Engineer is a senior individual contributor responsible for analyzing, designing, and continuously improving the end-to-end production flow across the mechanical assembly facility. Reporting directly to the Executive Vice President, this role
Job Overview: The Quality Assurance Manager will be directly responsible for ensuring that products meet certain thresholds of acceptability. Will plan, direct or coordinate quality assurance programs and formulates quality control policies. Responsible for maintaining a
Description Come build quality on purpose. Balanced Body builds Pilates equipment the way a master craftsman builds anything — nothing leaves the shop until its right. Every reformer, tower, and accessory that leaves our Sacramento facility
Director, Quality Systems & Restricted Material Compliance FormFactor, Inc. is a leading provider of essential test and measurement technologies along the full semiconductor product life cycle from characterization, modeling, reliability, and design de-bug, to qualification and
Engineering Manager Full-time | Permanent Salaried | $137k - $171k We are not currently working with third party agencies on this role. About Us: Vander-Bend is a U.S.-based manufacturer dedicated to building the precision infrastructure that
Assembly Operator Assembly Operators are responsible for the assembly of medical components, subassemblies, products, or systems. Every team member is responsible for maintaining housekeeping and organization of the work area as well as following CathX Medical
Date Posted: 2026-07-27 Country: United States of America Location: US-PR-SANTA ISABEL-B4 ~ Felicia Industrial Park - St B4 ~ BLDG 4 Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is
CPC Scientific is a globally recognized and leading CDMO specializing in synthetic peptide and oligonucleotide production, with one of the largest research peptide facilities in the world. CPC Scientific works directly with leaders in the biotechnology
GeneFab is seeking an experienced and highly motivated Sr. Manager/Manager, Manufacturing to lead and oversee cGMP manufacturing operations for our Cell and Gene Therapy CDMO. This position carries direct responsibility for managing day-to-day manufacturing activities, building
Objective This senior technical position within Henry Schein engineering is based on-site at the Lompoc, California manufacturing site and serves as the principal technical authority for mechanical and electro‑mechanical engineering at the site. The role requires
Quality Engineer Primary Duties & Responsibilities Develop, implement, and monitor quality control plans for both Ion Implantation and Disk Refurbishment Lead root cause analysis (e.g., 8D, FMEA, CAR processes) Drive corrective action and preventive actions with
Job Opportunity At Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products
Job Title Facility Manager Job Description This position is responsible for all facility matters and EH&S requirements. This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS). Responsibilities