- Actalent (Maplewood, MN)
- …degree. + Experience working with large animals. + Previous experience in an FDA -regulated environment. Job Type & Location This is a Contract to Hire position ... based out of Maplewood, MN. Pay and Benefits The pay range for this position is $21.00 - $26.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be… more
- Actalent (Hazelwood, MO)
- …+ Experience with pH meters, titration, and viscosity testing. + Knowledge of FDA regulations. + Experience in a laboratory setting within food manufacturing. + ... Understanding of SQF standards. Additional Skills & Qualifications + quality assurance, quality control, or laboratory work. + Ability to work in a fast-paced environment. + Capability to frequently stand and walk through a manufacturing environment. Work… more
- Abbott (St. Paul, MN)
- …+ Participate in design and requirements reviews. + Learn and apply FDA regulatory and ISO standard procedures. + Engage in process improvement initiatives ... and technical reviews. **Required Qualifications** + Bachelor's degree in Engineering (Electrical, Software, Mechanical, or Biomedical) or related field + 0-2 years Engineering experience + Basic understanding of system testing and development lifecycle. +… more
- Actalent (Branchburg, NJ)
- …production. + Carefully follow and accurately complete all procedures in accordance with FDA requirements, ensuring all documents are up to date. + Participate in ... cycle counts and review kit data to ensure product quality and consistency. + Assist Technical Services in troubleshooting any problems, facilitating sample and kit testing in response to customer complaints or requirements. + Interact with all other… more
- Weill Cornell Medical College (New York, NY)
- …**Knowledge, Skills and Abilities** + Knowledge in Food and Drug Administration ( FDA ) and Office for Human Research Protections (OHRP) regulations, and International ... Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines. + Excellent communication skills (both verbal and written). + Demonstrated strong communication and interpersonal skills; demonstrated ability to interact with multiple constituencies… more
- Kelly Services (Summit, NJ)
- …cross-functional projects. + Familiarity with regulatory requirements and guidelines (eg, FDA , ICH, ISO) related to analytical method development and validation. + ... Experience mentoring and training junior scientists is highly desirable. **What happens next** Once you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry-even if this position doesn't work out, you're… more
- Bristol Myers Squibb (Devens, MA)
- …in a regulated industry with 1+ year deviation experience. Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. + ... Demonstrated experience with electronic system and databases + Demonstrated experience in root cause analysis tools including but not limited to 5-WHY, Human error prevention, Ishikawa Diagram (Fishbone Analysis), Process Flow Diagram, etc. **BMSCART**… more
- Bristol Myers Squibb (Devens, MA)
- …requirements. **Knowledge, Skills, Abilities:** + Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing. + Must ... have the ability to work assigned shift (Day, Night, Weekends and/or Holidays). + Must be able to work in a cleanroom environment and perform aseptic processing + Must be comfortable being exposed to human blood components. + Must be able to be in close… more
- Catalent Pharma Solutions (Greenville, NC)
- …is required + Understanding safety and compliance standards (eg, OSHA, EPA, FDA , and EU regulations) and handling hazardous materials is beneficial + Demonstrated ... ability in project planning, scheduling, resource allocation, and cost estimation preferred + Some exposure to hazardous chemicals and other active chemical ingredients **Why You Should Work at Catalent** + Spearhead exciting and innovative projects +… more
- Balchem (Ogden, UT)
- …site power user for ERP & LIMS systems REQUIREMENTS: + Operated in an FDA regulated environment, ideally food or dietary supplement + 2+ years of experience in ... food, supplement, or related industry. + Effective project manager that knows how to prioritize and meet deadlines + Execution of CAPA and Customer Complaint system + Bachelor-s degree in relevant field or other relevant work experience + Project Management &… more