- Abbott (Pomona, CA)
- …federal and other regulations governing medical device assembly and design, eg GMP , QSR, ISO and CMDR. + Understanding of machine function, mechanical/electrical or ... software engineering. + Knowledge of Lab View, PLC and other specialty machine and vision software. + Able to work with a variety of people on multiple projects; Ability to work independently and in a team environment. + Organized and detail oriented +… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …development, validations and implementations. Experience must include time in a GMP environment. + Prior experience overseeing and working with external ... manufacturing and analytical sites + Expertise in chromatographic (HPLC, UPLC, GC) and spectroscopic (MS, UV/Vis, FTIR), and other analytical techniques. + Strong leadership, communication (written and verbal), and interpersonal skills, with the ability to… more
- ThermoFisher Scientific (Thousand Oaks, CA)
- …lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps ... hot/cold, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials **Job Description** Join Thermo Fisher Scientific Inc. as a… more
- Jacobs (Los Angeles, CA)
- …pre-design and pre-construction, building systems/components and technology, contract management ( gmp / lump sum), project delivery methods, team building and client ... relationship building * Strong working knowledge in vendor procurements, change order negotiation, budget and schedule management, operational governances, client satisfaction and management, * Develop project engineer's careers and development. Ideally,… more
- Aerotek (Cerritos, CA)
- …+ Ability to handle material, blend, and compound products. + Familiarity with GMP and FDA regulations. + Comfortable with manual labor and lifting heavy objects. ... **Additional Skills & Qualifications** + Previous experience in food manufacturing or pharmaceuticals. + Ability to read and follow recipes and work orders. + Comfortable working in an environment with strong flavors. + Ability to work with or without facial… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …preferred. + Minimum of 3 years of related experience in a pharmaceutical, GMP , or FDA regulated environment is required. + Demonstrated leadership skills with the ... ability to motivate, guide, train, coach and develop department personnel. + Comprehensive knowledge and understanding of cGMPs, FDA regulations, and industry guidelines. + Ability to work independently with minimum supervision. + Must be proactive, results… more
- Fujifilm (Irvine, CA)
- …Microsoft Suite, data. + General knowledge of project management. + Knowledge of GMP and GLP procedures + Attention to details with critical thinking and ... problem-solving skills, ability to follow instructions and SOP's, motivation in learning new knowledge and hands-on techniques, and awareness of basic lab etiquettes and hygiene is highly desirable + Bioreactor knowledge a plus + Ability to speak, write and… more
- Turner & Townsend (San Francisco, CA)
- …science and manufacturing facilities + Deep understanding of Good Manufacturing Practice ( GMP ), FDA, ISO, and other relevant standards. + Familiarity with cleanroom ... classifications, HVAC systems, and lab-specific infrastructure. + Experience with CQV (Commissioning, Qualification, and Validation) processes for life science facilities. + Ability to engage and align diverse stakeholders, including clients, regulators, and… more
- WuXi AppTec (San Diego, CA)
- …Experimental design and planning; Plan, execute, and document cGMP and non- GMP /GLP laboratory work supporting regulatory submissions; Assist with Scale up (multi-kg ... scale) tech transfers from Kilo Lab and Pilot Plant scales following cGMP compliant execution of API manufacturing processes; Research and recommend new methods and alternative synthetic sequence techniques to optimize existing processes (Process R&D); Perform… more
- Catalent Pharma Solutions (San Diego, CA)
- …auditor credentials are preferred + Experience and sound knowledge of GMP /GDP/GCP regulations, especially those related to comparator sourcing, wholesaler licensing, ... third party storage and distribution preferred + Prior experience in JDE and Trackwise systems preferred + Demonstrate project management skills with an ability to prioritize, plan, evaluate & execute deliverables for established tactical goals + Position is… more