- ELECTRICAL COMPONENTS INTERNATIONALHOLDINGS COMPANY (Norwood, MA)
- …part of the effectiveness of the (QMS) Quality Management System Ensure conformance to ISO 9001 and ISO 13485 regulatory and legal requirements Adhere to ... Range $80000.00 - $90000.00 Salary/year Job Category QA - Quality Control Description ECI is seeking a Quality...QMS meetings on a regular basis as required by ISO standards Educate and provide Training to all employees… more
- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …devices or pharmaceutical industries is desirable. Must be familiar with 21CFR820 and ISO 13485 requirements. Hands on experience with these requirements is ... School Salary Range $25.00 - $25.00 Hourly Description Job Title : Inspector, Quality Control Supervisor /Manager Title: Staff Engineer, Quality (Production… more
- Elucent Medical, Inc. (Eden Prairie, MN)
- …Qualifications Education and Experience: HS diploma and minimum 2 years relevant medical device/ ISO 13485 experience or 2 yr degree. Knowledge and experience ... safe work area. Completes all other duties as assigned by supervisor . Develop and write quality systems procedures as requested by supervisor . Provides… more
- ThermoFisher Scientific (Middletown, VA)
- …thorough Manufacturing Quality Control (MQC) and Incoming Quality Assurance (IQA) Supervisor to join our ISO 13485 -certified facility. As the ... (MQC) and Incoming Quality Assurance (IQA) departments, ensuring adherence to ISO 13485 standards and regulatory requirements. + Develop and implement … more
- West Pharmaceutical Services (Tempe, AZ)
- …/ Validation Activities, Metrology/Manufacturing background and Risk Management preferred. + Experience with quality systems such as ISO 13485 and 21 CFR ... Quality Auditor Supervisor Requisition ID: 71230...(FDA) 21 CFR 820 and International Organization for Standardization ( ISO ) ISO 13485 . + Familiarity… more
- Terumo Medical Corporation (Caguas, PR)
- Quality Supervisor 2nd. Shift Date: Oct...CFR 820, Medical Device Directive, Canadian Device Regulation, and ISO 13485 . + Must have excellent audit ... ID: 5200 Location: Caguas, PR, PR Company: Terumo Puerto Rico, LLC Department: Quality - TPR Terumo Medical Corporation (TMC) develops, manufactures, and markets a… more
- Integra LifeSciences (Plainsboro, NJ)
- …Clean Room gowning. + Batch manufacturing experience. + Demonstrated knowledge of FDA regulations, ISO 9001, ISO 13485 , and other National and International ... and making headway to help improve outcomes. **SUMMARY DESCRIPTION** The Supervisor , Packaging Operations is responsible for the skin packaging production activities… more
- West Pharmaceutical Services (St. Petersburg, FL)
- …+ Experience in FDA regulated environment, pertinent to 21 CFR Part 211 or ISO 13485 preferred. **Preferred Knowledge, Skills and Abilities** + Must be familiar ... Quality Control Supervisor Requisition ID: 71495...within the inventory management/ERP system + Ensures compliance with quality system documents, cGMPs, ISO standards and… more
- Abbott (Plano, TX)
- …internal, domestic and international quality regulations, US 21 CFR 820 (QSR), ISO 13485 , etc Identify risk areas within your group and develop strategies ... provide interventional pain therapy to patients throughout the pain continuum. As a Supervisor Quality Assurance, main responsibility will include ensuring the … more
- Integra LifeSciences (Plainsboro, NJ)
- …Clean Room gowning. + Batch manufacturing experience. + Demonstrated knowledge of FDA regulations, ISO 9001, ISO 13485 , and other National and International ... to advance patient outcomes and set new standards of care. The ** Supervisor , Automated Medical Operations** is responsible for the medical dispersion production… more
- Integra LifeSciences (Plainsboro, NJ)
- …onsite. Must have working knowledge of US Food and Drug Administration regulations, ISO 13485 , and other applicable regulatory agencies. **ESSENTIAL DUTIES AND ... treatment pathways to advance patient outcomes and set new standards of care. The ** Quality Control Inspector Supervisor ** will be overseeing the quality … more
- Teleflex (Olive Branch, MS)
- …of work experience in Quality and/or experience in a regulated * Knowledge of Quality Systems Requirements ( ISO 13485 , CFR 820 & LATAM) * Knowledgeable ... facility and supervision of personnel * Previous experience overseeing a team, quality supervisor experience is preferred * People management skills, conflict… more
- Curia (Rensselaer, NY)
- Supervisor , Quality Control - Onsite position in...in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 Physical requirements The physical ... Rensselaer, NY - 12 Hour Nights The Quality Control Supervisor is responsible for overseeing routine and non-routine analytical chemistry assays of raw… more
- GRAIL (Durham, NC)
- …**LDT to FDA-regulated IVD environment** , ensuring compliance with **21 CFR Part 820, ISO 13485 , and Part 11** requirements. + Establish and enforce **formal ... or organization through a **regulatory transition** (eg, LDT to FDA-approved IVD, ISO 13485 implementation). + Basic understanding of **IT infrastructure and… more
- MPE Inc. (Sturtevant, WI)
- …activities in metal fabrication + Ensure all manufacturing processes comply with FDA, ISO 13485 , and other relevant medical device industry regulations. + ... Production Supervisor At MPE we are dedicated to making...of fabrication techniques and processes + Familiarity with FDA, ISO 13485 , and other relevant regulatory standards.… more
- GN Hearing (Bloomington, MN)
- …+ Leadership experience across multi-functional teams + Experience working in a regulated environment ( ISO 13485 :2016, ISO 9001, FDA QSR) + Experience with ... of their respective Division Operations Area. As an Operations Supervisor , you will set expectations and provide feedback to...will be responsible for maintaining and improving the overall quality and KPIs of your teams' area through continuous… more
- Medtronic (Brooklyn Center, MN)
- …the following: FDA Quality System Regulations, current Good Manufacturing Practices (cGMP), ISO 13485 , ISO 9001 standards or equivalent. **Physical Job ... **A Day in the Life** As a Senior Engineering Supervisor within Manufacturing Operations at Medtronic, you have a...Medtronic, you have a leading role in ensuring the quality , efficiency, and reliability of equipment and processes utilized… more
- Medtronic (Plymouth, MN)
- …the following: FDA Quality System Regulations, current Good Manufacturing Practices (cGMP), ISO 13485 , ISO 9001 standards or equivalent. **Physical Job ... in the Life** We are seeking a proactive and leadership oriented Operations Supervisor to support 1st shift clean room assembly operations at Plymouth Nathan Lane.… more
- Integra LifeSciences (Plainsboro, NJ)
- …and procedures. Must have working knowledge of US Food and Drug Administration regulations, ISO 9001, ISO 13485 , the European Medical Device Directive, ... patient outcomes and set new standards of care. The **Product Release Supervisor ** provides technical and supervisory leadership and mentoring to Product Release… more
- ThermoFisher Scientific (Meriden, CT)
- …Bachelor's or Associate's degree + Experience in medical, pharmaceutical, or food manufacturing (cGMP, ISO 13485 ) + Ability to drive and inspire change and lead ... as needed** **The Impact You'll Make in this Role** The Production Supervisor ensures manufacturing operations prioritize safety, quality , efficiency, and… more
