- Catalent (Philadelphia, PA)
- …is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for ... Philadelphia area is Catalent's global Center of Excellence for Clinical Supply Packaging . Catalent offers GMP secondary packaging and clinical labeling services… more
- Bristol Myers Squibb (Bowdre, IL)
- …and laboratory investigation management:** + Act as Deviation Owner or lead investigator for QC incoming packaging deviations. + Work cross-functionally with ... is part of the Sample Management & Incoming testing Packaging team, in Quality Control department, at BMS Boudry....You will play a critical role in leading method development and verification/validation related to raw materials as well… more
- Lilly (Concord, NC)
- …with or understanding of:** + Working within or directly supporting pharmaceutical , food, packaging , or applicable manufacturing departments + Highly ... will house warehousing & logistics, parenteral operations, medical device assembly, and packaging , QC laboratories, and support teams to produce medicines for an… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for ... is Catalent's global Center of Excellence for Clinical Supply Packaging . Catalent offers GMP secondary packaging and...+ Assist in ensuring the quality and identity of pharmaceutical products during all aspects of the incoming, distribution,… more
- Merck (Boston, MA)
- …and Study Management (CSSM), Regulatory, Chemistry, Manufacturing and Controls (CMC), Pharmaceutical Sciences, Formulation Development , and Global Development ... supply needs per project and providing the signal for sourcing, manufacturing, packaging , and distribution for our company's development products and non-company… more
- ICON Clinical Research (Rocky Mount, NC)
- …medicine, we advance clinical research providing outsourced services to pharmaceutical , biotechnology, medical device and government and public health organisations. ... all that we do, we help to accelerate the development of drugs and devices that save lives and...procedure necessary for the protocol as ordered by the investigator . + Attending investigator meetings, site initiation… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …Responsibilities:** + Manages direct reports including performance evaluations and professional development . + Oversees third party vendors as well as develops and ... required clinical documents for submission to regulatory authorities (eg, protocols, investigator brochures, clinical study reports), as necessary. + Manages overall… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …**Primary responsibilities for role:** + Develops and manages clinical development program plans (eg, strategies, budgets, timelines). + Provides clinical ... clinical data prior to submission to regulatory authorities (eg, protocols, investigator brochures, clinical study reports). + Manages clinical timelines, budgets,… more
- Merck (West Point, PA)
- …and project team meetings to provide a broad perspective on the drug development process in the pharmaceutical industry. Required Education and Experience: + ... trials run in-house, 400+ outsourced or run by partners, and 300+ company Investigator Initiated Studies (IIS) clinical trials. GCS is accountable for the planning,… more
