Job Description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities

• Approve process validation protocols and reports for mfg. processes.
• Represent Quality on incident triage team.
• Approve Environmental Characterization reports.
• Release of sanitary utility systems.
• Approve planned incidents.
• Represent QA on NPI team.
• Lead investigations.
• Own site quality program procedures.
• Designee for QA manager on local CCRB.
• Project management skills.
• Strong knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation, and processes development.

Qualifications

• Bachelor's degree and 6 years of directly related experience
• Facilities and Utilities Commissioning and Qualification,
• Computer System Validation,
•  Equipment validation,
•  Risk Assessments,
•  KNEAT,CDOCS, SCADA, TRACKWISE,MAXIMO
•  Good Documentation Practices, Data Integrity
•  Change Controls,
•  Standard Operation Procedure
•  Syringe/Vials Inspection Process
•  Documents revision and approval
• o Strong knowledge in Decision Making Techniques
• o Risk Management applicable procedures, quality standards, and regulatory requirements.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.