KPMG Careers – Manager for Life Sciences and Regulatory Affairs

Job Summary

KPMG US currently has a vacancy for those looking to work as a KPMG Careers – Manager for Life Sciences and Regulatory Affairs for Full Time at their offices in Short Hills, NJ, US. Applicants should be sure to read the job outline attentively if they intend to apply.

Job Title:	KPMG Careers – Manager for Life Sciences and Regulatory Affairs
Company Name:	KPMG US
Job Location:	Short Hills, NJ, US
Job Type:	Full Time
Job Category:	KPMG
Job Link Expiry:	2023-12-30
Posted on:	Jobinton.com

Job Details:

Job Description:

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.

Job Responsibilities:

• Structure and perform analysis on regulatory-related processes, data, business requirements, operating models, IT systems
• Facilitate engagement decisions, including work plan and timeline, project management, resource allocation, and career development of team members
• Lead consulting projects for Life Sciences clients focused on process improvements or technology implementations in the Regulatory Affairs function
• Oversee projects related to system implementations and/or digital solutions
• Manage projects related to process transformation, operational improvements, and organizational redesign
• Provide oversight of client and KPMG work teams throughout the project lifecycle and help ensure timely execution of project deliverables

Job Requirements:

• Prior professional services or consulting experience preferred
• Experience with Regulatory Information Management (RIM) or Document Management systems preferred as well as experience serving on an implementation team for a RIM or Document Management system preferred
• Strong understanding of Regulatory Affairs related data and documents

Qualification & Experience:

• Bachelor’s degree in an appropriate field from an accredited college/university; Master’s degree from an accredited college/university preferred
• Minimum of five years of work experience related to the Regulatory Affairs function within the pharmaceutical and/or medical device industry
• Experience with operational process improvement initiatives in pharmaceutical and/or medical device industry

Job Details:

Company: KPMG US

Vacancy Type: Full Time

Job Location: Short Hills, NJ, US

Application Deadline: N/A

Apply Here

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