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Senior Associate, Life Sciences, Regulatory Affairs

Boston, Massachusetts

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Senior Associate, Life Sciences, Regulatory Affairs

Requisition #: 51505

Practice Area: Advisory

Location: Chicago, IL; Boston, MA; Short Hills, NJ; New York, NY

The KPMG Advisory practice is currently our fastest growing practice. We are seeing tremendous client demand, and looking forward we don't anticipate that slowing down. In this ever-changing market environment, our professionals must be adaptable and thrive in a collaborative, team-driven culture. At KPMG, our people are our number one priority. With a wealth of learning and career development opportunities, a world-class training facility and leading market tools, we make sure our people continue to grow both professionally and personally. If you're looking for a firm with a strong team connection where you can be your whole self, have an impact, advance your skills, deepen your experiences, and have the flexibility and access to constantly find new areas of inspiration and expand your capabilities, then consider a career in Advisory.

KPMG is currently seeking a Senior Associate in Customer & Operations for our Consulting practice.

Responsibilities:

  • Deliver consulting projects for Life Sciences clients focused on process improvements or technology implementations in the Regulatory Affairs function
  • Perform analysis on regulatory-related processes, data, business requirements, operating models, IT systems
  • Support projects related to process transformation, operational improvements, and organizational redesign
  • Assist projects related to system implementations and/or digital solutions
  • Drive progress against project milestones to help ensure timely delivery of project deliverables
  • Provide input for engagement decisions, including work plan, timeline and project management

Qualifications:

  • Minimum of three years of work experience related to the Regulatory Affairs function within the pharmaceutical and/or medical device industry
  • Bachelor's degree in an appropriate field from an accredited college/university; Master's degree from an accredited college/university preferred
  • Experience with operational process improvement initiatives in pharmaceutical and/or medical device industry
  • Prior professional services or consulting experience preferred
  • Strong understanding of Regulatory Affairs related data and documents as well as experience with Regulatory Information Management (RIM) or Document Management systems preferred
  • Excellent foundational skills including strong analytical, written and verbal communication skills, MS Office expertise, impactful client presence, compelling facilitation and presentation skills

KPMG LLP (the U.S. member firm of KPMG International) offers a comprehensive compensation and benefits package. KPMG is an affirmative action-equal opportunity employer. KPMG complies with all applicable federal, state and local laws regarding recruitment and hiring. All qualified applicants are considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other category protected by applicable federal, state or local laws. The attached link contains further information regarding the firm's compliance with federal, state and local recruitment and hiring laws. No phone calls or agencies please.

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