QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Knowledge of:

• Supply chain planning, scheduling, master data and procurement processes
• GMP and GXP
• Audit processes including CAPA
• Change control system and processes as change owner
• Improving processes
• Pharmaceutical industry
• Validation and Qualification

Skills:

• Facilitation and presentation
• Strong analytical problem-solving
• Strong technical writing
• Strong project management
• Good decision-making skills
• Change management
• Handling multiple responsibilities, priorities, tasks, and projects simultaneously.
• Working under time pressure, and effectively in a team matrix environment.
• Good organizational, detail-oriented & accurate, analytical.
• Effective verbal and written communication (writing and presentations).
• Good negotiation skills

Ability to:

• Influence staff and effect change outside of area of responsibility
• Initiate and lead cross-functional teams to resolve complex issues
• Deliver results
• Assume increasing levels of responsibility.
• Work autonomously
• Work under pressure

• Doctorate degree OR Master’s degree and 2 years of Project Management experience OR 
• Bachelor’s degree and 4 years of Project Management experience
• Fluent English and Spanish (verbal and written)

• Candidates should send resume in Word or PDF format.
• Willing to work as Independent Contractor.