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
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
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
Quality Control Manager We are looking for a Quality Control Manager to join our Lombard, IL team! This is an opportunity to join a metal surface treatment technology facility with an established industrial company that is
Date Posted:2026-08-18 Country:United States of America Location:US-CA-REMOTE Position Role Type:Remote U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance
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
Logistics at full potential. At GXO, we’re constantly looking for talented individuals at all levels who can deliver the caliber of service our company requires. You know that a positive work environment creates happy employees, which
POSITION: Quality System Engineer LOCATION: Jupiter, FL STATUS: Salary-exempt JOB SUMMARY The position is responsible for ensuring that business processes within PSM are properly implemented, maintained and improved under a Quality Management System (QMS) which complies with
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
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
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
Document Control Analyst In coordination with internal groups, the Document Control Analyst manages documentation of engineering changes in product development, production, and validates data accuracy, integrity of documentation systems, and optimum manufacturing process. To ensure all
Quality Control Leadership Position This leadership position is responsible for planning, coordinating, maintaining, directing, overseeing and continuous improvement of the companys quality control function and maintaining and improving our quality management system to assure that the
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
Quality Manager 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