- System One (Florham Park, NJ)
- …utilizing travel management software and working with a travel agency + Manage Contract Process and navigate internal and external clients (MSA's, SOW, CDA, ... Park: Hybrid ( Office presence is required at least 3 days per week) Contract : 12 months Overview This role will provide administrative support to Commercial Teams… more
- DuPont (Hemlock, MI)
- …for local Healthcare Industries Materials Site [HIMS] operations as well as contract manufacturers (globally); this involves providing direction & objectives to meet ... healthcare business; this involves working across the local operations and contract manufacturers. + Ensure the quality requirements for relevant quality standards… more
- System One (Cranbury, NJ)
- …in the production of solid oral dosage forms in a cGMP-regulated pharmaceutical environment. This role involves equipment setup, in- process testing, ... on 1st shift 7:00 am - 3:30pm), onsite Type: Contract To Hire Position Summary The Manufacturing Operator (2nd...thickness, and appearance, and adjust as necessary. + Perform in- process checks and document all results accurately and in… more
- Charles River Laboratories (Rockville, MD)
- …technical competency in the areas of the Biologics Industry eg, process development, cGMP manufacturing, process registration, analytical science, Quality ... River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination… more
- Catalent Pharma Solutions (Harmans, MD)
- …all Catalent Gene Therapy sites. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... with 6 - 8 years' experience within the biologic, pharmaceutical or medical device industry performing direct hands-on work...accommodation for any part of the application or hiring process due to a disability, you may submit your… more
- Curia (Camarillo, CA)
- …where our work has the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...Assurance and Regulatory Affairs. + Direct quality and compliance process improvements and goals for the site using current… more
- ThermoFisher Scientific (Middleton, WI)
- …other scientific discipline required 12+ years of relevant experience in a pharmaceutical or analytical testing laboratory that provides the knowledge, skills, and ... technical management, mentoring, and customer scientific interface for the CDMO ( Contract Development & Manufacturing Organization) sector within the GMP business.… more
- Charles River Laboratories (Memphis, TN)
- …equipment operation, and processes in accordance with cGMPs, Quality System, and process documents. * Conducts and/or schedules training for new employees including ... activities. * Provides assistance to management in the revision and/or writing of process documents to assure accuracy and completeness. This includes but is not… more
- ThermoFisher Scientific (Carlsbad, CA)
- …strong leadership, organizational expertise, and **_deep industry knowledge across the pharmaceutical , biotech, or medical device sectors_** , along with a proven ... Proposals & RFIs to Win Preferred Provider Opportunities:** Drive successful RFP/Proposals process to meet and exceed key account expectations; actively deliver RFP… more
- Kelly Services (San Mateo, CA)
- …**Pay:** $30-$35/hour **Start Date:** ASAP (with 2 weeks onboarding) **Employment Type** : Contract Employment - 1 year **About the Role** We're looking for a Supply ... Chain Specialist to support biotech and pharmaceutical supply chain operations. You'll work with teams across the US and headquarters to manage inventory, shipments,… more