- Kedplasma (Lubbock, TX)
- …developed and maintained. Operates within the scope of EU Good Practice Guidelines and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been made to make ... company standards and protocols to meet the regulatory requirements of the FDA , EMEA, Customer Specifications, and other regulatory bodies as required. + Maintains… more
- Kelly Services (Coppell, TX)
- …to effectively meet objectives. + Computer skills to include proficiency with Microsoft Office software . + Understanding of cGMP and FDA CFR 21 Parts 210/211. + ... testing, inspection, and production. + Interact with Regulatory bodies, such as the FDA , to ensure compliance. + Develop, review, and approve SOPs that meet and… more
- Veterans Affairs, Veterans Health Administration (Temple, TX)
- …compliance with all QC and QA requirements as per VHA policy, FDA /MQSA regulations, and ACR standards in mammography, digital breast tomosynthesis, breast ... the breast imaging section and representing the department at annual FDA /MQSA inspections. Working closely with the technologists, radiologists, clinicians, and… more
- Abbott (Plano, TX)
- …requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and experience with inspection sampling techniques. + Knowledge of FDA , GMP, and ISO 13485. + Good communication and...Word, Microsoft Excel, database entry, and use of statistical software packages. + Ability to work within a team… more
- Medtronic (Dallas, TX)
- …in the operating room, so healthcare/surgical setting experience + Familiarity with FDA product requirements and regulatory guidelines + Experience with robotics or ... understand schematics and engineering drawings + Familiar with the FDA 21 CFR, CGMP for Medical devices + Demonstrable...Microsoft Office products as well as ERP and CRM software packages (such as SAP, ServiceMax and SalesForce.com) +… more
- Charles River Laboratories (Houston, TX)
- …governing import/domestic as mandated by applicable regulatory agencies (ie: CDC, USDA, FDA , EPA, and US Fish & Wildlife). Effective written and verbal communication ... and meet deadlines. Proficiency in the use of standard software . Demonstrated ability to interact and communicate effectively in...drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to… more
- Kedplasma (Houston, TX)
- …Operates within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been made to make ... other Company standards and protocols to meet regulatory requirements of the FDA , EMEA, Customer Specifications, and other regulatory bodies, as required. . Ensures… more
- Fujifilm (Austin, TX)
- …Speech Recognition tools, as well as actual dictation functionality when Fuji Dictation software is utilized. + Maintains a clear understanding of FDA ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Lundbeck (Longview, TX)
- …and regulatory environment, including Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products. ... healthcare economy and industry practices. Accountability and adherence to corporate, FDA , and PDMA guidelines. **REQUIRED EDUCATION, EXPERIENCE and SKILLS:** +… more
- Bio-Techne (Austin, TX)
- …with all regulatory standards, systems, procedures, and practices. Includes ISO 13485, FDA QSR, MDSAP, IVDR, and other requirements relating to Quality Assurance ... Skills, and Abilities:** + Skilled in the use of software programs such as Microsoft Office and database management...+ Knowledge of cGMP, ISO 13485, MDSAP, IVDD/IVDR and FDA QSR preferred. **Why Join Bio-Techne:** **We offer competitive… more