- Aldevron (Fargo, ND)
- …for vital new discoveries worldwide. You will be a part of the Analytical Method Validation Team and report to the Sr. Manager of Analytical Method Validation ... experience in:Experience in technical writing and supporting investigations in a cGMP compliant Quality Control Laboratory setting.Experience working with… more
- Aldevron (Fargo, ND)
- …for vital new discoveries worldwide. You will be a part of the Analytical Method Validation Team and report to the Sr. Manager of Analytical Method Validation ... and improve human health.This position is part of the Quality and Regulatory Affairs Department located in Fargo, North...and will be responsible for representing the Analytical Method Validation team as a subject matter expert (SME) on… more
- Aldevron (Miami, FL)
- …Operational Quality Assurance team and report to the Sr. Manager , Operational QA, responsible for Developing and implementing labeling processes and procedures ... delivery of solutions that safeguard and improve human health.This position is part of Quality Assurance located in Fargo, ND and will be on site. At Aldevron, we… more
- Honeywell (Baton Rouge, LA)
- The Quality Assurance (QA) Manager oversees, implements, and maintains cGMP compliant systems and activities. Incumbent is also responsible for evaluating ... internal controls and maintenance of cGMP documentation for compliance with quality and regulatory standards. The GMP QA Manager also monitors Contract… more
- Element Materials Technology (Ann Arbor, MI)
- **Overview** Element Ann Arbor has an opportunity for a **Department Manager ( cGMP Testing)** to join our growing team in Michigan. In this role you will be a ... of conduct, and company policies and procedures. The **Department Manager ( cGMP Testing)** will provide leadership to...improvement. This is an exciting opportunity for an experienced Quality Control and cGMP Sample Analysis Leader… more
- Houston Methodist (Houston, TX)
- …and prioritize daily tasks **GROWTH/INNOVATION ESSENTIAL FUNCTIONS** + Participates with the Quality Assurance Manager and/or cGMP Core Director in ... defining quality policies. + Assists Quality Assurance Manager , cGMP Core...of biotechnology or pharmaceutical industry experience with exposure to cGMP manufacturing operations + Experience performing equipment validation… more
- Bristol Myers Squibb (Indianapolis, IN)
- …entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. The Sr. Manager , IT - GxP Computer Systems Validation & IT Process Lead is ... address process deficiencies. Work collaboratively with peers within various departments and Quality groups. + Provides validation subject matter expertise (SME)… more
- Eurofins (Philadelphia, PA)
- …areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Position Summary Eurofins BPT ... Sales Manager to join our team, focusing on facility validation and environmental monitoring solutions for the biopharmaceutical and medical device industries.… more
- Fujifilm (College Station, TX)
- …Computer cGMP regulations and practices pertaining to computer validation principles, manufacturing processes, quality systems, engineering design ... validation protocols and final reports and discrepancies for Quality Assurance. The QA Compliance Specialist III, QA ...and site SOPs to ensure regulatory compliance. **Reports to** Manager , QA Validation **Work Location** College Station,… more
- PCI Pharma Services (Rockford, IL)
- …**Location:** Rockford - Linden Road **Reports to:** **Senior Director of Quality , Biotech Center of Excellence** **FLSA Status:** Exempt **Summary of Objective:** ... The Director of Validation , Bio-Tech CoE is...Subject Matter Expert (SME), and assure that customer requirements, cGMP requirements, and all foreign and domestic regulations are… more
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