JT711 - SR. SPECIALIST QA

qualityconsultinggroup

Juncos (PR)

On-site

USD 90,000 - 130,000

Full time

14 days+
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Job summary

Quality Consulting Group, LLC is seeking a highly motivated QA professional to join our team in Puerto Rico & USA. You will approve validation protocols and reports, represent Quality on incident triage, and own site quality program procedures to ensure regulatory compliance.

You will also lead investigations, support NPI activities, and drive risk-based decision making across manufacturing and distribution processes with a strong emphasis on data integrity and GMP standards.

Qualifications

  • Bachelor's degree and 6 years of directly related experience.
  • Experience with validation, QA, and regulatory requirements.
  • Proficiency in GxP environments and data integrity.
  • Strong project management and QA leadership.

Responsibilities

  • Approve process validation protocols and reports for manufacturing processes.
  • Represent Quality on incident triage team.
  • Approve Environmental Characterization reports.
  • Release 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.

Skills

Facilities commissioning
Validation
Risk assessment
Data integrity
Change control
SOP
Documentation revision
Decision making
Risk management

Education

Bachelor's degree

Tools

KNEAT
CDOCS
SCADA
TRACKWISE
MAXIMO

Job description

QUALITY CONSULTING GROUP, a leader inthe 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 yearsof 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.

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