KPMG Careers – Sr Associate, Quality Management

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:

• Perform analysis on QMS-related data, processes, business requirements, operating models
• Support projects related to process transformation, technology-enabled transformation, measurable improved operational performance, preparation for Quality mandates and organizational redesign
• Offer assistance with large system implementation projects for clients
• Support Quality System related projects including QMS implementation, Supplier Quality Audit, Remediation, CAPA, Deviations, Complaints Management etc. 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 team members

Qualification & Experience:

• Strong understanding of various Quality system regulations (21 CFR Part 820, QSReg) and standards including ISO13485 including Design Controls, Document Controls, Production and Process Controls, Corrective and Preventive Actions, Labeling and Packaging Controls, Records Management and Servicing
• Experience with any of the Quality Management Systems including Trackwise, Pilgrim, Master Control, Veeva and/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
• Applicants must be currently authorized to work in the United States without the need for visa sponsorship now or in the future
• Minimum of two years of work experience related to Quality Systems within the pharmaceutical, Biotech and/or medical device industry
• Bachelor’s degree in an appropriate field from an accredited college/university required; 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

Job Details:

Company: KPMG US

Vacancy Type:  Full Time

Job Location: Philadelphia, PA, US

Application Deadline: N/A

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