Specialist Qa Jobs

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!

Specialist QA with experience in regulated industries to perform the following duties and responsibilities in support of Quality Assurance program.

Duties and Responsibilities:

• Perform oversight of the process and procedures/GMP tasks
• Participate in triage process
• Compliance review of batch record elements (e.g., MPs, MSRs) and identification of discrepancies
• Trackwise system queries, deviations
• Perform sampling plans for all manufactured products
• Batch record review
• Participate in internal plant audits
• Work with operations to resolve basic compliance discrepancies
• SAP transactions

• Availability to work 3rd shift
• Fully Bilingual in (English and Spanish) (Written and Oral)
• Bilingual (Spanish/English) (Oral/Written)
• Enhanced skills in leading, influencing and negotiating with the ability to interact with regulatory agencies and evaluate compliance issues.
• Computer Literacy
• Doctorate or Master's degree and 3 years of directly related experience or Bachelor's degree and 5 years of directly related experience or Associate's degree and 10 years of directly related experience
• Microsoft Office spreadsheet and application skills and presentation knowledge
• Technical writing
• Strong organizational skills, including ability to follow assignments through to completion.

All your information will be kept confidential according to EEO guidelines.