- Abbott (Alameda, CA)
- …processes and analytics. + Ensure compliance with QMS, EMS, GMP, FDA regulations, and company policies. **Required Qualifications** + Bachelor's Degree or ... equivalent combination of education and work experience **Preferred Qualifications** + MBA preferred + Professional certifications in Procurement or Supply Chain such as CPSM, CIPS, CPP, CPIM, or equivalent are highly desirable. + English proficiency required;… more
- Vitality Works Inc (Albuquerque, NM)
- …vitamin and nutraceutical supplements to help people get and stay well. While the FDA defines minimum quality, we strive for the highest level of quality. Vitality ... Works also operates in an environmentally sustainable way, recycling, composting, reducing energy and water consumption in a conscientious way. Our dedicated and passionate employees strive to produce amazing products in an uncompromising yet affordable way so… more
- Pacific Seafood (Doral, FL)
- …hazard analysis and Critical Control Points Program (HACCP) + Interpret and implement FDA , ODA regulations ensuring HACCP, SSOP, COOL Act standards are met. + ... Establish and maintain GFSI/BRC/SQF standards in order to meet audit requirements. + Interact with Regulatory Agencies and third-party auditors; monitor scheduled audits. + Develop and implement applicable training. + Remain current on all regulatory… more
- OhioHealth (Pickerington, OH)
- …of practices across the system; Ensures compliance with regulatory agencies including FDA , CAP, CLIA, TJC, OSHA, CMS; 10% Secures and retains staff of ... qualified personnel through recruitment, selection, training and motivating. Addresses personnel issue to maintain a productive and pleasant work environment; actively involved in staff development and identifying associates to mentor for succession planning… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …and software cybersecurity rules and regulations while working in an FDA /ISO-regulated environment + Excellent interpersonal and communication skills, with the ... ability to lead cross-functional teams **PREFERRED EDUCATION & EXPERIENCE:** + Professional certifications in materials management (eg, APICS - CPIM, CSCP) + Hands on experience in global logistics and/or reverse supply chain operations and/or other aspects of… more
- Globus Medical, Inc. (Audubon, PA)
- …several stages of development (ie existing portfolio, near-term launch, pending FDA approval and new products). Supports product lifecycle management, product ... roadmap, technique, new product training and product launch readiness with revenue goals in mind. **Essential Functions:** + Keeps a strong pulse on the market by attending trade shows, VIP surgeon events, spine surgeries and labs + Collaborates with upstream… more
- BD (Becton, Dickinson and Company) (Salt Lake City, UT)
- …solutions to complex problems + Knowledge of global medical device regulatory requirements ( FDA , Anvisa, NMPA, MDR) and quality standards (ISO, GB, JISC) + Complete ... understanding of medical device project management principles, theories & concepts + Experience with creating work breakdown structures, risk management, and integrated business plans + Thorough understanding of functional work streams in a phase gate process… more
- Beth Israel Lahey Health (Boston, MA)
- …a professional and timely manner, archiving records of correspondence per NIH, FDA , and/or other applicable Federal, State, and local regulations. + Develops ... program-specific performance measures to assess effectiveness and success of program components. Implements data collection processes and communicates performance through periodic reports to working and executive groups. + Has the authority to direct and… more
- Logan Health (Polson, MT)
- …state and federal regulatory practices to include, HQAA accreditation standards, FDA , DOT, HIPPA, Medicare/Medicaid; responsible for writing grants and overseeing ... all current grant reporting requirements, reports, data and other grant communications related to assigned area(s). + The above essential functions are representative of major duties of positions in this job classification. Specific duties and responsibilities… more
- Zimmer Biomet (Warsaw, IN)
- …related position. Must have 3 years of experience in the following: + FDA regulated industry experience; and + total engineering project experience including leading ... CAPA process use DMAIC methodology. Must have 2 years of experience with the following: + Apply statistical analysis for quality control/assurance and CAPA verification of effectiveness plan; + review and approve CAPA metrics and quality system records in a… more