- Abbott (Portland, OR)
- …Qualifications** + Medical Device experience + Knowledge of medical device standards including FDA QSR, ISO 13485, ISO 14971, 21 CFR Part 11 and IEC 62304. ... + Experience implementing various product and process improvement methodologies (eg, Six Sigma and Lean Manufacturing) Apply Now (https://www.jobs.abbott/us/en) **Learn more about our health and wellness benefits, which provide the security to help you and… more
- Burlington (Edgewater Park, NJ)
- …will ensure the adherence to all company and government regulations around customs, FDA , CPSC, APHIS, C-TPAT, and similar. The Import Manager will also develop and ... implement import training materials and ensure their team is cross trained in all functions and aspects of the department. In addition; this person must provide solid leadership, coaching, direction, and must motivate the team to work together in the most… more
- SAIC (Silver Spring, MD)
- …and remote technical assistance for escalated issues beyond Tier 1 scope to FDA users at both sites, ensuring efficient operation of hardware, software, and ... peripheral devices. The ideal candidate would possess a Public Trust clearance and would serve as the primary escalation point for advanced troubleshooting and ensure seamless end-user support. **Core Competencies** + **Technical** Knowledge - Solid grasp of… more
- Cook Medical (Bloomington, IN)
- …of quality systems and engineering principles* Familiarity with ISO standards, FDA regulations, or GMP concepts preferred but not required* Excellent organizational ... skills* Ability to work with multiple persons and the multiple priorities that occur when each person has different needs* Proficiency with Microsoft Excel, Word, and PowerPoint Requisition ID2026-17786 Posting Date2 days ago(1/12/2026 2:46 PM) Job… more
- Edgewell Personal Care (Sidney, OH)
- …Ensure team members meet production rates, follow schedules, comply/enforce all Safety/OSHA/GMP/ FDA /GDP requirements, and ensure all components on the line meet ... current product quality standards and productivity levels + Maintain all documentation related to the performance of production lines (Production reports, Quality reports, and all other require paperwork, etc.) + Oversee all aspects of line maintenance; make… more
- Envista Holdings Corporation (Yorba Linda, CA)
- …of safety and hazardous material regulations + Knowledge retention of FDA Quality System requirements ("Good Manufacturing Practices") and ISO 9001 requirements ... after training + Basic CNC programming knowledge, enough to upload/download programs to machines **Critical Skills & Technical Know-how:** + Basic English proficiency at a High School level both in oral communications and reading comprehension + Ability to… more
- Lilly (Lebanon, IN)
- …of regulatory requirements in GMP (Good Manufacturing Practice), such as FDA regulations for pharmaceutical manufacturing. + Solid knowledge of Computer System ... Validation process. + Excellent problem-solving skills to address complex IT issues and implement effective solutions in a timely manner. + Strong customer service and communication skills to maintain high end-user satisfaction. + Proficiency in handling IT… more
- Boehringer Ingelheim (Indianapolis, IN)
- …based. + Performs all Company business in accordance with all regulations (eg, EEO, FDA , DEA, OSHA, PDMA, EPA, PhRMA, etc.) and Company policy and procedures. When ... violations are noted/observed they are to be immediately reported to management. Demonstrates high ethical and professional standards with all business contacts in order to maintain BIPI's excellent reputation within the medical and pharmaceutical community.… more
- Abbott (Altavista, VA)
- …equipment issues You'll be accountable for meeting our compliance standards including FDA , OSHA and Abbott policies and procedures. **Shift** This is for the ... night shift. Example of shift: **Shift Hours:** 6am to 6:30 pm, on a rotating basis. **Week One:** Mon - On / Tues - On / Weds - Off / Thurs - Off / Fri - On / Sat - On / Sun - On **Week Two:** Mon - Off / Tues - Off / Weds - On / Thurs - On / Fri - Off / Sat… more
- Nestle (Gaffney, SC)
- …at all times. Unauthorized deviations are strictly forbidden + Comply with all FDA rules, procedures, and work practices + Follow all Nestle and GMP procedures ... + Maintain confidential information on recipes + Report all deviations from the recipe _Operations:_ + Responsible for accurately and efficiently preparing all media to be used in the micro lab + Maintain inventories of all in-house prepared media used for… more