Global Quality Solutions Representative

GForce Life Sciences; United States; Remote; USD 65,000 - 80,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A growing pharmaceutical client is looking for a Global Quality Solutions Representative consultant with expertise in Pharma Quality processes and QMS systems. Responsibilities include analyzing business requirements, supporting QMS inquiries, and developing training. The consultant will work remotely with occasional travel to New Jersey, and benefits include medical, dental, vision, and 401(k).

Qualifications

• Minimum of 3 years of Pharma Quality-related processes experience required.
• Advanced analytical skills and understanding of drug development and regulatory processes.
• Knowledge of Computer System Validation.

Responsibilities

• Analyze business requirements and ensure compliance within TrackWise Digital.
• Lead meetings with Quality teams and act as primary support for QMS inquiries.
• Develop training materials and support innovation in Global Quality Operations.

Skills

Analytical skills

Knowledge of Pharma Quality Standards

Knowledge of GxP areas

Tools

TrackWise Digital

Excel

MS Project

SharePoint

PowerPoint

MS Teams

Job description

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Our mid-sized, growing pharmaceutical client is seeking a Global Quality Solutions Representative consultant. This position reports to the Associate Director of Global Quality.

General Duties / Expectations of Role:

• Analyze and translate business requirements into system configurations within TrackWise Digital to ensure compliance and meet user needs.
• Lead meetings with Quality teams to educate, align, and implement enhancements across global sites.
• Act as the primary support contact for QMS process inquiries and provide front-line business support.
• Assist in user acceptance testing (UAT), including system verification and documentation review (URS, FRS, workflows).
• Develop training materials and conduct sessions for new system enhancements.
• Manage user access to QMS and maintain data integrity through standardized data practices and master data management.
• Partner with Global Quality stakeholders to define and implement digital solutions that streamline processes.
• Support innovation and risk management projects relevant to Global Quality Operations.
• Lead dictionary maintenance and data quality improvement initiatives.
• Collaborate with IT to troubleshoot and resolve QMS-related issues.

Qualifications

• A minimum of 3 years of Pharma Quality-related processes and QMS systems experience is required (TrackWise Digital preferred).
• Knowledge of Pharma Quality Standards
• Advanced analytical skills and a general understanding of the drug development and regulatory process are required.
• Knowledge of GxP areas
• Knowledge of Computer System Validation
• Experience with software applications that will be regularly used (in particular: Excel, MS Project, SharePoint, PowerPoint, and MS Teams).

Term & Start

• 12+ -month contract – option to extend
• Start Date: 2 weeks from the offer
• 2 Video Interviews
• Remote Opportunity –potential travel to NJ – prefer East Coast
• Benefits included (Medical, Dental, Vision, 401k)

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance, Science, and Other

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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