quality document control

Qualification HighlightsMust have + years working as an Industrial Pipe Fitter Fabricator.Must be able to read prints and illustrate thorough knowledge of pipe fitting procedures and skills.Must have good leadership and communication skills.Must be have experience on an industrial construction project.Physical RequirementsEmployee will be required to adhere...

   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 lifecycle partner to thousands of customers...

Company DescriptionMindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com. Job DescriptionJob Description: Quality Coordinator (Incoming Material Inspection)Hours: 7:30 am - 4:00 am; Monday – Friday (1st Shift)Position Responsibilities:•...

Job Description Job Description About Us: Panelmatic, Inc. was founded in 1957 in Youngstown, OH to serve manufacturing industries with the design and build of custom electrical, instrument, and pneumatic control panels. Our business has sufficiently grown over the years to support expansion for our clients. We have produced control packages for many of...

Requisition ID: 7266   Job Title: Manager, Quality Document Control   Job Country: United States (US)   Here at Avanos Medical, we passionately believe in three things: Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do; Making a difference in how we work and collaborate,...

DescriptionPosition Summary The Quality Document Control Specialist is responsible for maintaining organized, compliant, and audit-ready records and documents in a control system within a manufacturing environment. In this role, the Quality Document Control Specialist will collaborate with Quality, Engineering, Supply Chain and Production to control...

Quality Document Control Supervisor Quality Systems | Full-Time | Onsite Brighton, Michigan Biovire is advancing toward commercialization with a focus on innovation, operational excellence, and scalable GMP manufacturing. We are seeking a Quality Document Control Supervisor to lead and strengthen the document control activities that support pharmaceutical...

Location: ​Camarillo ​ / Hybrid: 4 days - Friday remote Our Team: ​​​At Semtech, our Quality Team is the heartbeat of our organization, ensuring that every customer request is met with precision and care. We pride ourselves on our deep understanding of industry regulations and our commitment to product compliance. Our team excels in...

DescriptionAbout Us:Panelmatic, Inc. was founded in 1957 in Youngstown, OH to serve manufacturing industries with the design and build of custom electrical, instrument, and pneumatic control panels. Our business has sufficiently grown over the years to support expansion for our clients. We have produced control packages for many of America's top corporations...

Job Overview We are seeking a proactive and detail-oriented Quality Compliance Document Control Coordinator to join our dynamic team. This position reports to the Quality Assurance Manager in the Quality Department. The purpose of this role is to ensure all documentation control systems are within GMP regulations to ensure the production of quality...

Job Description Job Description We are looking for a detail-oriented Office Assistant to support documentation and records coordination for a long-term contract opportunity in Haltom City, Texas. This onsite role focuses on preparing, reviewing, scanning, and organizing quality and delivery records to ensure complete and accurate final documentation. The...

Full-time Description Summary of PositionImplement and adhere to document control procedures, including version control, document approval, and archivingCreate and Edit Documents: Prepare, format, and edit documentation related to product development, quality assurance, and manufacturing processes.Coordinate Reviews: Facilitate the review and approval...

Avanos Medical seeks a Manager, Quality Document Control to lead our quality documentation program for innovative medical devices. In this role, you will oversee the creation, revision, and control of SOPs, work instructions, and quality records to meet FDA and ISO 13485 requirements. You will manage electronic document systems, change control, and...

Requisition ID: 7266 Job Title: Manager, Quality Document Control Job Country: United States (US) Here at Avanos Medical, we passionately believe in three things: Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do; Making a difference in how we work and collaborate,...

Quality Compliance & Document Control Specialist Location: Escondido, CA - Onsite Reports To: Quality Manager Pay Range: $75-95,000   Position Summary ARCH Medical Solutions is seeking a detail-oriented and proactive Quality Compliance & Document Control Specialist to support the maintenance, effectiveness, and compliance of our Quality Management System...

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods.   SUMMARY: The Quality Assurance Assistant – Document Control supports the Quality Assurance department by assisting with the issuance, routing, tracking, reconciliation, archival, and...

Shift: Mon-Fri First Shift , standard working hours Duration: 12 Months Pay range: $33.00 - $35.00 Hourly  Onsite Job Job Description: How will you make an impact? As a QMS & Document Control Specialist, you will support the effectiveness of the site Quality Management System (QMS) by ensuring controlled documents, change management processes, and...

Quality System Document Control AdministratorLocation: Santa Clara, CA 95054 (Onsite) | Job Type: ContractAbout the RoleJoin a dynamic, fast-paced team as a Quality System Document Control Administrator and play a critical role in ensuring our site remains compliant, audit-ready, and efficient. In this pivotal position, you will manage Quality Management...

A well-established pharmaceutical company in Miramar, FL is seeking an experienced and detail-oriented Quality Assurance (QA) Document Control Specialist to support its evening shift operations. This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual...

About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented...