QA Compliance Specialist 2

Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused,Practices safety awareness at all times. Monitor compliance metrics and prepare management reports through trending and visual KPI management.

Job Title: QA Compliance Specialist
Location: Portsmouth, NH
Duration: 6 Months

Job Description:

• Lead gap assessments of local Quality Management System procedures against Group Quality Procedures and Corporate Standards.
• Coordinate updates to local SOPs, work instructions, and controlled documents.
• Track implementation and drive completion to defined timelines.
• Partner with process owners and SMEs to establish and implement compliant solutions.
• Support Change Control, CAPA, Deviations, and Quality Risk Management activities.
• Support internal audits and regulatory inspections.
• Monitor compliance metrics and prepare management reports through trending and visual KPI management.
• Develop and Provide training and guidance on new or revised quality procedures.
• Drive continuous improvement and harmonization of Quality System processes.

Education:
Bachelors Degree

Skills:
Bachelor’s Degree or equivalent experience. Preferred area of study:  Scientific related field
·        3-5 or more years in GMP environment. Minimum 0-3 years in Quality Assurance or similar discipline. Biotechnology manufacturing background is preferred
·        Knowledge of cGMP and regulations
·        Project Management Experience: Presentation, Customer Liaison, Meeting facilitation
·        Demonstrates flexibility to adapt to changing business priorities.  .
·        Demonstrate ability for effective Planning, Organizing and Controlling competency.
·        Demonstrate sound decision making, considering broad scope of factors.
·        Able to manage multiple priorities and achieve results.
·        Good ability to complete assignments under tight timelines, and work under pressure.
·        Demonstrates knowledge on continuous improvement within the adherence to standardized procedures & cGMP compliance.
·        Experience with Trackwise, SAP, Document management system preferred.
·        Detail-oriented
·        Self-motivated
·        Displays a clear willingness to listen to others.
Self-starter, solid written and verbal communication, good attention to detail, works effectively individually and with teams, positive attitude, customer focused,Practices safety awareness at all times.
 

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