Analytical Lab Director Jobs
By CannabizTeam - Executive Search and Staffing At Baltimore, MD, United States
Complies with and supports continuous improvement of the ISO 17025 accredited laboratory Quality Management System.
Performs labeling and logging of samples using the Laboratory Information Management System (LIMS).
Processes, organizes and summarizes data and computerized results of analysis through the Laboratory Information Management System (LIMS)
If necessary provide remedial training or continuing education to improve skills.
Experience with ISO 17025, GMP, GLP, or similar certification process
PRIOR CANNABIS LAB TESTING EXPERIENCE IS REQUIRED ***
Manager, Qc Analytical Jobs
By BioSpace At Baltimore, MD, United States
Iii. Minimum Education, Experience, Skills
Responsible for generating management review metrics and KPIs.
Provides mentoring and Conducts Performance Management of direct reports.
Performs managerial duties, as assigned, in support of QC operations such as resource management, routine data and investigation review.
Must possess skills and knowledge of implementing and managing a compliant stability program.
Manage the Biochemistry Group operations in support of production by ensuring the timely execution of QC testing.
Analyst Iii, Qc Analytical- Limited Term Hire
By BioSpace At Baltimore, MD, United States
Skills and knowledge in immunological and ligand-based test methods such as ELISA, Western Blot and SDS-PAGE testing is also desirable.
Experience in executing phase appropriate method qualifications and validations.
Excellent written and verbal communication skills including ability to write reports for method verification/qualification/validation.
Provides technical expertise for method development, optimization, verification, qualification and validation.
Assists in equipment and instrument qualification, calibration, and preventive maintenance, as assigned.
Advanced knowledge of cGMPs, safety and data integrity as relevant to a QC laboratory.
Qc Analytical Lab Ops Specialist I
By Kite Pharma At , Frederick, Md $65,960 - $85,360 a year
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).
Author or revise SOPs, qualification/validation protocols and reports.
AA Degree and 2+ years’ experience in biotechnology or related field and Quality Control experience OR
High School Degree and 3+ years’ experience in biotechnology or related field and Quality Control experience
Deep knowledge of GMP, SOPs and quality control processes.
Deep written and verbal communication skills.