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Digital Quality Transformation - Senior Consultant - Life Sciences; QMS

Job in Raleigh, Wake County, North Carolina, 27601, USA
Listing for: Ernst & Young Oman
Full Time position
Listed on 2026-02-16
Job specializations:
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Digital Quality Transformation - Senior Consultant - Life Sciences (QMS)

Overview

Location:

Atlanta, Austin, Baltimore, Boston, Charlotte, Chicago, Cleveland, Dallas, Detroit, Pittsburgh, Hartford, Hoboken, Houston, McLean, New York, New York, Philadelphia, Stamford

At EY, we’re all in to shape your future with confidence.

We’ll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go. Join EY and help to build a better working world.

Our clients operate in a world where achieving high performance is just as important as the patients they serve. EY’s Life Sciences team advises clients in the Life Sciences sector on setting strategic decisions to address risks impacting their organization’s performance and impacting patient safety.

The opportunity

The Life Sciences Risk Consulting Services team focuses on biotechnology, pharmaceutical, medical device manufacturers, and the medical technology industry. You will be an integral part of this team helping clients identify, manage, and respond to risks while accelerating performance and maintaining growth. Our team advises clients on aligning risk and business objectives from strategy to execution, and improving coordination of risk activities across the organization for better outcomes.

This involves working with life sciences clients to develop business processes, and design and implement systems to effectively manage these areas governed by the FDA and similar regulatory bodies globally:

  • Quality Management Systems (including complaint management, CAPAs, deviations, change control, quality audit management, supplier quality management, etc.)
  • Regulatory Affairs (regulatory submissions, Health Registration Management, etc.)
  • Laboratory Information Management Systems
  • Computer Systems Validation (following a GxP system development lifecycle)

In addition, our team also works on projects with clients to manage these Quality business processes for supply chain, manufacturing, commercial operations and R&D. This includes analyzing various cGMP and 21 CFR Part 11 regulations in the Regulatory Compliance area to determine impact on risk exposure.

Your key responsibilities

Your time will be spent supporting client engagement teams to deliver projects in the life sciences domain, including:

  • Implementation of QMS, DMS, Safety, LIMS, and RIM systems (e.g. Veeva, Trackwise, EtQ Reliance, Argus, Calyx) in the roles of business process analyst, technical writer, project manager, computer systems validation, and other business / project roles associated with delivery and execution.
  • Implementation of validation lifecycle management systems (e.g. Val Genesis, Kneat)
  • Design and execution of QMS and Regulatory processes.
  • Performing computer systems validation activities as part of a service.
  • Performing Quality audits of client processes within the QMS area.

You will also be expected to work on teams to consistently deliver quality client services by demonstrating in-depth technical capabilities and professional knowledge, and maintaining long-term client relationships.

Full time employment, Travel required up to 40%.

Skills and attributes for success
  • Performing large-scale implementations with consistent high quality delivery
  • Driving high-quality work products within expected time frames and on budget
  • Ability to monitor progress, manage risk, and ensure key stakeholders are kept informed about progress and expected outcomes
  • Staying abreast of current industry trends relevant to the client’s business
  • Effectively working on teams with diverse skills and backgrounds
  • Fostering an innovative and inclusive team-oriented work environment
  • Demonstrating deep technical capabilities and professional knowledge
To qualify for the role you must have
  • A bachelor’s or master’s degree in Computer Science, Biomedical Engineering, Quality Engineering, Manufacturing or a related field and at least three years of related work experience.
  • 3+ years of Life Sciences work experience, including working with Life Science regulatory statutes, GxP business processes or system validations, risk management or compliance programs or integration of risk management functions.
Ideally, you’ll also have

Experience in implementing Veeva Vaults…

Position Requirements
10+ Years work experience
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