MEI Pharma, Inc.
MEI Pharma (Nasdaq: MEIP) is a San Diego-based oncology company focused on the clinical development of novel therapies for cancer. Our portfolio of drug candidates includes Pracinostat, an oral HDAC inhibitor being developed in combination with...
Design and test formulations of drug compounds topical creams, ointments and solid dosage forms for ANDA products. Has an in-depth understanding of different drug formulations for oral and topical drug delivery, chemical...
Fate Therapeutics, Inc.
Fate Therapeutics has an immediate need for an experienced Senior Quality Associate. The successful candidate must thrive in a fast-paced team environment and have excellent communication, planning, and organizational skills, with the ability to...
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
• Review QC laboratory records to ensure accuracy and completeness
• Review stability study data
• Review analytical test method validation protocols, data and reports, as assigned
• Coordinate assigned...
Relypsa, Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of polymeric medicines for patients with conditions that are often overlooked and undertreated and can be addressed in the...
The Quality Assurance Auditor establishes and maintains systems to assure compliance regulatory and client requirements for all relevant GMP operations carried out within the organization. The person in this role will oversee...
Precision for Medicine
Direction of the Quality Systems:
Plan and direct resources and activities of the quality and compliance functions. Develop and maintain product and service quality audit programs and GMP audit programs for the Maryland operations.
Repligen is an bioprocessing organization which manufactures product following an ISO 9001:2008 Quality Management System. Repligen products are used in cGMP pharmaceutical and biotechnology applications, therefore the requirements for the Quality of...
Pharmatek Laboratories, Inc.
The Quality Assurance Associate, Document Control position is responsible for supporting quality systems to advance the development and manufacture of drug candidates, including document review and approval and support of GMP manufacturing.
We are looking for a CMC Director to oversee the chemistry, manufacturing, and controls of a compound for late phase clinical trials.
This position provides a phenomenal opportunity for a talented individual who seeks exposure and participation...