Quality Control Analyst Ii (Wednesday To Saturday, 3Pm - 1Am)
By Resilience At , East Norriton $72,000 - $91,500 a year
Review data, identify discrepancies, and escalate issues to management
Participate in method qualification/validation activities as necessary
Analyze, document, and report experimental data in accordance with Resilience requirements
Perform method transfer and qualification activities
2-5 years relevant life science experience
Experience in mammalian cell culture
Analyst 2 - Laboratory Quality Control (Contract)
By JnJ At , Raritan
Project management experience is preferred.
Benefits on offer for this contract position:
2+ years of QC laboratory experience
Truvault, TrackWise, eLIMS experience preferred.
Write and edit detailed SOPs, validation protocols/reports, forms, analytical and technical documents and reports from conception to utilization.
MS Office Application (Word, Excel, Powerpoint) required.
Analyst, Quality Control Analytics - Car-T
By Johnson & Johnson At , Raritan, Nj $60,000 - $96,600 a year
Minimum 2 years of relevant work experience
Knowledge and understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
Excellent written and verbal communication skills
Experience in a Quality Control setting
Experience within Biopharmaceutical or Pharmaceutical industry
Work experience in Cell and/or Gene Therapy or Biologics
Laboratory Quality Specialist Jobs
By Nucleus Healthcare At Armstrong, MO, United States
Comprehensive health and wellness benefits, including mental health support
Up to $111,426/ year based on experience
Monitor and perform supplier qualification, supplier monitoring processes, environmental control, and monitoring systems.
Becker Healthcare's 150 Top Places to Work
Affordable cost of living and housing
Paid-for tuition from the local top-rated university
Quality Control Lab Analyst I
By Pfizer At , Rocky Mount, Nc
Demonstrated proficiency in computerized systems (Experience and use of Laboratory Information Management System)
Manage own time, professional development, and accountable for own results.
Prioritize own workflow and assist in prioritizing the work flow of less-experienced colleagues.
Certification in assigned area, if applicable
Demonstrated analytical laboratory experience in a Good Manufacturing Practices {also cGMP} regulated environment
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS