Gamp Jobs in Tampa

Should have solid validation lead experience working forpharmaceutical companies as Val lead/SME. Should have Validation Lead and LIMS advisory experience to guidethe entire program/project teams. Should have great communication and coordination skillsbetween internal team an More...

Hope this email finds you in great spirits!! I believe you are a fantastic contact and would like to continue working for the below job Opening. Please send the resume to Job Location: North Carolina Raleigh: Remote ok (Yes / No) No Project Duration 12 Months Rate $60/hr Jo More...

Responsibilities: Provide CSV/CQV support to clients that manufacture GMP products on a consistent basis in conjunction with industry best practices. Help drive collaboration, exceeding expectations, and challenging the status quo. Develop CSV/CQV planning documents to manage CQV pro More...

Redwood City, CA Contract Duration: 12-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Manufacturing Technician in the Redwood City, CA. (100% onsite) Product: Spray drying technology of inhaled product. Typical day: Gowning up with plant provided More...

Responsibilities: 10+ years of Experience in Life Sciences, Computer System Validation Pharmacovigilance knowledge Must possess hands on experience and understanding of GAMP 5 Risk Based Validation Functional Risk Assessment GXP Assessment FR Part 11 Assessment Data Migration Qua More...

Redwood City, CA Contract Duration: 12-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Manufacturing Technician in the Redwood City, CA area. Supports production line by conducting routine tasks which may include setting up, taking down, cleani More...

Senior Validation Engineer Contract Woburn, Massachusetts The Senior Validation Engineer will support a diverse variety of Quality Control and Manufacturing instrumentation, including analytical and microbiological instruments, maintaining the validated state of the instruments fro More...

Purpose of the position Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Coordinate More...

Purpose of the position Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Coordinate wi More...

Job title: GXP-Validation Analyst; Location: Chicago/Nearshore CST time Purpose of the position Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facilities an More...

Project Scope and Brief Description: Responsible for ensuring all assigned laboratory equipment/software, IT systems and associated infrastructure, within the R&D GLP environment and cloud environments, is in a qualified, validated state. Responsible for leading management, creat More...

Project Scope and Brief Description: Responsible for ensuring all assigned laboratory equipment/software, IT systems and associated infrastructure, within the R&D GLP environment and cloud environments, is in a qualified, validated state. Responsible for leading management, creat More...

Project Scope and Brief Description: Responsible for ensuring all assigned laboratory equipment/software, IT systems and associated infrastructure, within the R&D GLP environment and cloud environments, is in a qualified, validated state. Responsible for leading management, creat More...

Project Scope and Brief Description: Responsible for ensuring all assigned laboratory equipment/software, IT systems and associated infrastructure, within the R&D GLP environment and cloud environments, is in a qualified, validated state. Responsible for leading management, creat More...