Quality Systems Analyst II

Job DescriptionJob Description

POSITION:  Quality Systems Analyst II

POSTING:    70113 (JNJNJP00070113)

LOCATION:   Titusville NJ (Onsite)

COMPENSATION:     $32 Per Hour, W2, OT payable at 1.5X, estimated annualized compensation of $64,000 based on 2000 working hours (50 weeks, 40 hours per week).  Actual hours worked will vary.  

The overall purpose of this position is to support quality activities for Commerical Quality including controlled substance requirements, quality complaints, change control, documentation, internal audit/ supplier audits. Adheres to environmental policy, procedures, and supports department environmental objectives.

Essential duties and responsibilities:
• Process Know Your Customer applications to purchase SPRAVATO®. (50%)
• Conduct routine data analysis for Suspicious Order Monitoring. (10%)
• Process day-to-day product quality complaint (PQC) in quality system including evaluating PQC, assigning investigation, conducting investigation, writing investigation summary. Proactively manage PQCs workflow with stakeholders to ensure all investigations are completed in a timely manner. (10%)
• Process day-to-day quality events and change control records in TrackWise/COMET system (10%)
• Coordinate documents and procedures in truVault system and any other document management system.(10%)
Coordinate internal and/or supplier audits including setting up logistic / preparation for the audits, drafting audit plan, supporting audit execution, coordinating audit response and CAPA with stakeholders, creating and documenting audit records in TrackWise system. Ensure all audit commitments are delivered on time (10%)
Required: BA/BS – Technical / Life Science
Desirable: MA/MS/MBA – Business / Technical /Life Science
Support Quality and Compliance Initiatives from Enterprise Quality and/or Global Business Quality

Essential Knowledge and Skills
Knowledge
• 5 years’ experience in the Pharmaceutical or related industry;
• Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP;
• Up-to-date knowledge of DEA regulations
• Experience working in the quality organization.
Skills
• Highly experienced in TrackWise/COMET system, generating query and report, and data analysis with excel spreadsheet
• Results-driven leader who commits to stretch goals and delivers results.
• Ability to build and nurture strong, positive relationships with business partners in IT, Manufacturing, Regulatory Affairs, Commercial and Quality functional groups.
Demonstrated understanding of regulatory requirements that impact Market Quality specifically, and client's more broadly. Experience in dealing with regulatory inspections and inspectional requirements

Core competencies required for this role:

• Credo Values
• Innovation
• Masters Complexity
• Customer/ Marketplace Focus
• Independent Partnering

Company DescriptionThe Mason-Grey Corporation provides engineering solutions and services to process industry clients in energy, metals, plastics, biotech, pharmaceutical, and other key process markets. Today Mason-Grey executes projects and provides services to the Fortune 500 and mid-tier companies from coast to coast. Mason-Grey employees live and work in support of our mission from Massachusetts to California. Mason-Grey is headquartered in Atlanta, Georgia.Company DescriptionThe Mason-Grey Corporation provides engineering solutions and services to process industry clients in energy, metals, plastics, biotech, pharmaceutical, and other key process markets. Today Mason-Grey executes projects and provides services to the Fortune 500 and mid-tier companies from coast to coast. Mason-Grey employees live and work in support of our mission from Massachusetts to California. Mason-Grey is headquartered in Atlanta, Georgia.