- Actalent (Farmington, CT)
- …analyses. + Prepare, dilute, and plate samples using standard ISO, BAM, USDA-FSIS, and FDA methods. + Record all necessary lab data on work orders and verify data ... accuracy before releasing client reports. + Communicate findings to senior staff and assist with client inquiries as needed. + Follow laboratory safety protocols, including PPE use and biosafety level requirements. + Maintain a clean, organized, and… more
- Actalent (Deerfield, IL)
- …and external stakeholders. + Maintain compliance with safety and regulatory standards (OSHA, FDA , USDA, etc.). + Train and direct part-time team members on SOPs and ... sensory protocols. Essential Skills + Bachelor's degree in food science or a related field (Master's a plus). + 5-7 years of sensory or consumer research experience, including panel leadership. + Strong statistical analysis skills for sensory methodologies. +… more
- J&J Family of Companies (Anasco, PR)
- …+ Demonstrated experience as a lead or supervisor is required. + Knowledge of FDA regulations is required. + Must be computer literate in Microsoft Office, E-Mail, ... word processing and spread sheets is required. + Knowledge in SAP is preferred. + Must be detailed oriented and have the ability to develop and meet deadlines, and be able to delegate and follow-up. + Strong verbal and written communication skills required as… more
- Integra LifeSciences (Cincinnati, OH)
- …ability to practically apply solutions to routine problems. + Understanding of FDA device manufacturing requirements. Salary Pay Range: $25.96 - $35.58 USD Hourly ... Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training **.** In addition to base pay, employees may be eligible for bonus,… more
- Actalent (Cambridge, MA)
- …small scale tissue culture processing is preferred. + Experience working in an FDA or ISO regulated environment. Work Environment Work in a cleanroom lab ... environment, under a hood for 8 hours daily to culture cells. Spend 6 hours on foot culturing cells and 2 hours on documentation. Collaborate with a team in a business casual setting. Initial training is Monday-Friday, transitioning to either… more
- J&J Family of Companies (Danvers, MA)
- …+ Ensure that Design Controls are compliant with IEC 62304. + Ensure that FDA and other regulatory knowledge and experience is applied to risk management, software ... development and testing. + Participate in software development sprint cycles by supporting the software development team through attending SCRUMs, design reviews, code reviews and providing feedback on software verification and validation deliverables. +… more
- Lilly (Indianapolis, IN)
- …problem-solving skills. + Experience with regulatory guidelines and standards (eg, GLP, FDA , EMA). Lilly is dedicated to helping individuals with disabilities to ... actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (… more
- Adecco US, Inc. (Ocala, FL)
- …of study participants. Essential Functions: * Conducts clinical studies according to FDA /GCP and ICH regulations and guidelines. * Provides medical care to patients, ... always ensuring patient safety comes first. * Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized. * Performs all defined study activities (ie, informed consent, screening, and protocol procedures which include but not… more
- Nestle (Fort Smith, AR)
- …work with external certification and regulatory parties as required such as USDA, FDA , Kosher, Halal and Organic programs + Develop, provide and facilitate Quality ... Training modules + Batch record and CCP reviews + Act as resource for business unit for In-Line Quality verifications and training + Quality liaison from business unit to material supplier as applicable + Back up for SSOP, Pre-Op and other inspections as… more
- CSL Plasma (Tulsa, OK)
- …donor disconnect. 2 In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin pheresis process. 3 Evaluates ... vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the… more