- Actalent (Summit Argo, IL)
- …beverage industry in QA/Food Safety/SQF Practitioner roles. + PCQI Certification. + Knowledge of FDA & GFSI (SQF, BRC, or FSSC) food safety and quality standards. + ... Experience working in an environment certified to a GFSI benchmarked standard. Additional Skills & Qualifications + ERP experience. + Ability to obtain or currently possess an SQF practitioner certification. + Internal audit certification or the ability to… more
- Northwell Health (New York, NY)
- …prescriptions into the workflow. Complies with Food and Drug Administration ( FDA ) mandates and self-imposed manufacturer restrictions on particular drugs, as ... applicable including Risk Evaluation and Mitigation Strategy (REMS) programs and manufacturer limited distribution drug requirements. Performs related duties, as required. Job Qualification High School Diploma or equivalent, required. Graduate of a recognized… more
- Penn Medicine (Wyndmoor, PA)
- …with all applicable federal, state, and local regulatory standards (ex TJC, DOH, FDA , HIPAA, HCFA, DPW, LCGME, SCGME, etc) + Flexible and readily adopts new ... processes and engages in practice operation changes. Credentials: + BLS/CPR, as a healthcare provider per the American Heart Association + MA Certification (Required within 90 days of hire ONLY if position is in PA) Education or Equivalent Experience: + HS… more
- GE HealthCare (Bellevue, WA)
- …Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485. Demonstrated expertise to effectively communicate ... within all levels of the organization around concepts of design controls, design verification and validation activities; production & process controls; Corrective & Preventive Action (CAPA), complaints & risk management. + Demonstrated collaboration,… more
- DEKA Research & Development (Manchester, NH)
- …and written communication skills Preferred skills and experience: + Knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device ... industry experience + Experience with research, development, and product testing + Experience writing procedures for others to follow + Experience with data and failure analysis + Broad measurement instrument knowledge About DEKA: One hour from the beach,… more
- Genentech (South San Francisco, CA)
- …The activities would include a systematic review of relevant literature, FDA /BLA/NDA documents, select databases, and/or internal data. + Participate in ... Model-Informed Drug Development (MIDD) by developing and applying mathematical models such as population pharmacokinetics/pharmacodynamics modeling, Physiologically-Based Pharmacokinetic (PBPK) modeling, Quantitative Systems Pharmacology (QSP) modeling, or… more
- Merck (West Point, PA)
- …Review, Documentations, Environmental Monitoring, Environmental Monitoring Systems, FDA Regulations, GMP Compliance, Immunochemistry, Interpersonal Relationships, IS ... Audit, Laboratory Operations, Laboratory Quality Control, Management Process, Problem Solving Therapy, Quality Inspections, Quality Operations {+ 5 more} **Preferred Skills:** Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)… more
- J&J Family of Companies (Horsham, PA)
- …Knowledge of the drug development process, including Good Clinical Practices (GCPs) and FDA Code of Federal Regulations + The ability to partner with stakeholders ... and influence decision-making across a matrix organization + Excellent analytical, problem solving, communication and presentation skills + Global business mindset + Ability to travel up to 10% of the time (Domestic/International) **Preferred:** + Experience… more
- ADM (Erlanger, KY)
- …including pasteurization, homogenization, carbonation, and aseptic techniques. + Familiarity with FDA food labeling regulations and nutritional claims, as well as ... TTB regulations related to alcoholic beverages. + Excellent project management and problem-solving skills; able to prioritize and drive multiple initiatives forward. + Competency in data analysis, experimental design, and technical reporting. + Strong… more
- Lilly (Concord, NC)
- …for training and benchmarking with other Lilly sites. + cGMP standards and FDA (or other industry) guidelines for production + HSE incident investigation, including ... multiple root cause analysis methods. + Facilitating employee safety teams, with the goal of turning over leadership to operations employees. + Managing a contractor safety program across a large footprint. + Implementation of electronic permit to work systems… more