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Digital Quality Transformation - Manager - Life Sciences

Digital Quality Transformation - Manager - Life Sciences

Pennsylvania StaffingPhiladelphia, PA, US
5 days ago
Job type
  • Full-time
Job description

Digital Quality Transformation - Manager - Life Sciences (QMS)

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

  • Overseeing and directing the implementation of QMS, DMS, Safety, LIMS, and RIM systems (such as Veeva, Trackwise, EtQ Reliance, Argus, Calyx), ensuring effective collaboration across business process analysis, technical documentation, project management, computer systems validation, and other delivery and execution functions.
  • Leading teams in the implementation of validation lifecycle management systems (including ValGenesis and Kneat), setting strategic direction and ensuring successful project delivery.
  • Managing the design and execution of QMS and Regulatory processes, providing guidance and oversight to project teams to achieve compliance and operational excellence.
  • Supervising the performance of computer systems validation activities, allocating resources, and ensuring adherence to industry standards as part of client service delivery.
  • Coordinating and overseeing Quality audits of client processes within the QMS domain, ensuring comprehensive evaluation and actionable reporting.
  • You will also be expected to lead teams in consistently delivering high-quality client services by leveraging your extensive technical expertise and professional knowledge. In addition, you will be responsible for nurturing and maintaining long-term client relationships, ensuring a strategic and collaborative approach to project delivery.

    Skills and attributes for success include :

  • Performing large-scale implementations with consistent high quality delivery
  • Driving high-quality work products within expected timeframes 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 5 years of related work experience.
  • 5+ 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 (Quality, Clinical, Regulatory, Safety), LIMS, and / or Validation Lifecycle Management Systems
  • Travel required up to 40%.
  • We are interested in passionate leaders with strong delivery capability, and a strong desire to stay on top of trends in the life sciences industry. If you have a strong passion for helping businesses drive measurable value while serving patients, then this role is for you.

    We offer a comprehensive compensation and benefits package where you'll be rewarded based on your performance and recognized for the value you bring to the business. The base salary range for this job in all geographic locations in the US is $114,800 to $210,600. The base salary range for New York City Metro Area, Washington State and California (excluding Sacramento) is $137,900 to $239,300. Individual salaries within those ranges are determined through a wide variety of factors including but not limited to education, experience, knowledge, skills and geography. In addition, our Total Rewards package includes medical and dental coverage, pension and 401(k) plans, and a wide range of paid time off options.

    Join us in our team-led and leader-enabled hybrid model. Our expectation is for most people in external, client serving roles to work together in person 40-60% of the time over the course of an engagement, project or year. Under our flexible vacation policy, you'll decide how much vacation time you need based on your own personal circumstances. You'll also be granted time off for designated EY Paid Holidays, Winter / Summer breaks, Personal / Family Care, and other leaves of absence when needed to support your physical, financial, and emotional well-being.

    Are you ready to shape your future with confidence? Apply today. EY accepts applications for this position on an on-going basis. For those living in California, please click here for additional information. EY focuses on high-ethical standards and integrity among its employees and expects all candidates to demonstrate these qualities. EY is committed to providing reasonable accommodation to qualified individuals with disabilities including veterans with disabilities. If you have a disability and either need assistance applying online or need to request an accommodation during any part of the application process, please call 1-800-EY-HELP3, select Option 2 for candidate related inquiries, then select Option 1 for candidate queries and finally select Option 2 for candidates with an inquiry which will route you to EY's Talent Shared Services Team (TSS) or email the TSS at ssc.customersupport@ey.com.

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