'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...
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...
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....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...
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. ...
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: 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...