's degree in life sciences, pharmacy, health sciences, or a related field. 2+ years of experience in regulatory affairs...
management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
most important research questions across clinical development, market access, and commercial use cases for our life sciences partners... (e.g., PhD, ScD, DrPH) in Biostatistics/Statistics, Data Science, Bioinformatics, Biological Sciences, Public Health, Math...
in a Validation/ Quality assurance / control role, preferably in the pharmaceutical /Life sciences industry preferred. Prior...Responsibilities: Create and support review of validation life cycle documents for Analytical Instrument...
in a Validation/ Quality assurance / control role, preferably in the pharmaceutical /Life sciences industry preferred....Responsibilities: Create and support review of validation life cycle documents for Analytical Instrument...
in a Validation/ Quality assurance / control role, preferably in the pharmaceutical /Life sciences industry preferred....Responsibilities: Create and support review of validation life cycle documents for Analytical. Instrument...
Document Review). Experience in electrical troubleshooting/electrical design. GXP or pharma/life sciences experience...
in a Validation/ Quality assurance / control role, preferably in the pharmaceutical /Life sciences industry preferred....Responsibilities: Create and support review of validation life cycle documents for Analytical Instrument...
for assisting in the full life cycle starting with detail design through commissioning, FAT/SAT, IQ/OQ/PQ and qualifications. 18... or similar field Fluent in controls on pressure vessels Good comms/ability to work cross-functionally Pharma/life science...
in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database...
Job Description: Our client is seeking an experienced Cleaning Sterilization Engineer to lead autoclave validation activities in a dynamic, regulated manufacturing environment. This role is highly hands-on, focusing on executing sterilizat...
Responsibilities: The Sr. Regulatory Affairs Specialist serves as the lead regulatory representative on project teams supporting product lifecycle management activities. Responsibilities include developing regulatory strategies, reviewin...
Responsibilities: Design, code, and test SAS programs used to generate CDISC SDTM & ADaM domains and tables, listings & figures outputs. Perform analyses defined in the statistical analysis plan as well as ad hoc analyses as requested. ...
Responsibilities: Execute validation activities across the full equipment lifecycle (FAT, SAT, Commissioning, DQ, IQ, OQ, PQ). Apply GAMP 5 methodology in a GMP-regulated environment. Support Greenfield project initiatives and equipment...