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NEW Senior Associate, Procurement and Operations - Regulatory Affairs

NJ - Short Hills

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The fastest growing Big Four professional services firm in the U.S., KPMG is known for being a great place to work and build a career. We provide audit, tax and advisory services for organizations in today’s most important industries. Our growth is driven by delivering real results for our clients. It’s also enabled by our culture, which encourages individual development, embraces an inclusive environment, rewards innovative excellence and supports our communities. With qualities like those, it’s no wonder we’re consistently ranked among the best companies to work for by Fortune Magazine, Consulting Magazine, Working Mother Magazine, Diversity Inc. and others. If you’re as passionate about your future as we are, join our team.

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

Responsibilities:

  • Support Regulatory Affairs transformation projects for Life Sciences clients
  • Drive progress against project milestones to help ensure timely delivery of project deliverables, review the work product of associates, and provide direction and training as necessary
  • Provide input into engagement decisions, including work plan and timeline, project management, resource allocation, and career development of staff members
  • Perform analysis on regulatory-related data, processes, business requirements, operating models, etc.
  • Execute process transformation, measurable improved operational performance, and organizational restructuring
  • Identify and communicate performance improvement opportunities for clients

Qualifications:

  • 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 a pharmaceutical and/or medical device industry; prior professional services or consulting experience preferred
  • Strong understanding of Regulatory Affairs related data and documents
  • Excellent foundational skills including strong analytical, written and verbal communication skills, MS Office expertise, impactful client presence, compelling facilitation and presentation skills
  • Travel may be up to 80-100%
  • Applicants must be currently authorized to work in the United States without the need for visa sponsorship now or in the future

KPMG offers a comprehensive compensation and benefits package. KPMG, an equal opportunity employer/disability/veteran. KPMG maintains a drug-free workplace. KPMG will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable local, state or federal law (including San Francisco Ordinance number 131192). No phone calls or agencies please.

Requisition# 65268

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