Director Life Sciences Regulatory Affairs and Labeling
Company: KPMG
Location: Houston
Posted on: April 22, 2025
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Job Description:
KPMG Advisory practice is currently our fastest growing
practice. We are seeing tremendous client demand, and looking
forward we do not 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 Director
Life Sciences Regulatory Affairs & Labeling in Customer &
Operations for our practice. Responsibilities:* Lead consulting
projects for Life Sciences clients focused on process improvements
or technology/data related implementations in Regulatory Affairs,
Labeling and adjacent functions* Run fast-paced client engagements
for on-time and quality delivery of work products; be responsible
for overall engagement planning, budgeting, staffing, financial
management, deliverables and management of engagement team members*
Structure and perform analysis on regulatory related process, data,
business requirements, operating models, IT systems etc* Lead
client engagements in optimizing Regulatory Affairs and adjacent
functions by leveraging emerging technologies including Data
Analytics, AI/ML and GenAI among others* Provide domain expertise
in regulated data models specific to Pharmaceutical and Medical
Device companies as required by various regulatory agencies
including but not limited to US FDA, EU, UK MHRA, TGA, Health
Canada, India, China* Assist life sciences companies in designing
and implementing various regulated data requirements including but
not limited to IDMP, UDI and EUDAMED* Lead and support go-to-market
efforts, new business development and on-going revenue management
including representing KPMG thought leadership at conferences, in
publications and other growthAdditional Responsibilities:* Serve as
a Performance Management Leader (PML) for the staff and mentor team
members for their career growth, actively participate in staff
recruitment and retention activitiesQualifications:* Minimum ten
years of Regulatory experience in consulting and/or industry roles
in the Regulatory Affairs or Labeling domain within the Life
Science industry (Pharmaceutical, Medical Device, BioTech and
Clinical Research Organization) with prior professional services or
consulting preferred* Bachelors degree from an accredited
college/university, preferably in Biology, Chemistry, Pharmacy,
Biochemistry, Biomedical Engineering, or related field; graduate
degree in a Healthcare or Life Sciences discipline such as MA, MSc,
MPH, PhD or MD, or a Masters degree in Business or Healthcare
Administration from an accredited college/university is highly
preferred* Experienced with common industry software solutions in
the Regulatory and Labeling domains (e.g., Veeva, Rimsys, Loftware,
Esko, etc.)* Experience in regulatory pathways for pharmaceutical
and/or medical device product approvals and changes across multiple
regulatory jurisdictions globally with UDI and EUDAMED regulations
preferred* Experience implementing Regulatory Information
Management (RIM), Labeling and/or Document Management systems*
Ability to travel as necessary* Applicants must be currently
authorized to work in the United States without the need for visa
sponsorship now or in the future
KPMG complies with all local/state regulations regarding displaying
salary ranges. If required, the ranges displayed below or via the
URL below are specifically for those potential hires who will work
in the location(s) listed. Any offered salary is determined based
on relevant factors such as applicant's skills, job
responsibilities, prior relevant experience, certain degrees and
certifications and market considerations. In addition, the firm is
proud to offer a comprehensive, competitive benefits package, with
options designed to help you make the best decisions for yourself,
your family, and your lifestyle. Available benefits are based on
eligibility. Our Total Rewards package includes a variety of
medical and dental plans, vision coverage, disability and life
insurance, 401(k) plans, and a robust suite of personal well-being
benefits to support your mental health. Depending on job
classification, standard work hours, and years of service, KPMG
provides Personal Time Off per fiscal year. Additionally, each year
the firm publishes a calendar of holidays to be observed during the
year and provides two firmwide breaks each year where employees
will not be required to use Personal Time Off; one is at year end
and the other is around the July 4th holiday. Additional details
about our benefits can be found towards the bottom of our KPMG US
Careers site at "".
Follow this link to obtain salary ranges by city outside of CA:
California Salary Range: $167700 - $310900 KPMG LLP (the U.S.
member firm of KPMG International) offers a comprehensive
compensation and benefits package. KPMG is an 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, age, sex, sexual orientation, gender identity,
national origin, citizenship status, disability, protected veteran
status, or any other category protected by applicable federal,
state or local laws. The contains further information regarding the
firm's compliance with federal, state and local recruitment and
hiring laws. No phone calls or agencies please.KPMG does not
currently require partners or employees to be fully vaccinated or
test negative for COVID-19 in order to go to KPMG offices, client
sites or KPMG events, except when mandated by federal, state or
local law. In some circumstances, clients also may require proof of
vaccination or testing (e.g., to go to the client site). KPMG
recruits on a rolling basis. Candidates are considered as they
apply, until the opportunity is filled. Candidates are encouraged
to apply expeditiously to any role(s) for which they are qualified
that is also of interest to them.Los Angeles County applicants:
Material job duties for this position are listed above. Criminal
history may have a direct, adverse, and negative relationship with
some of the material job duties of this position. These include the
duties and responsibilities listed above, as well as the abilities
to adhere to company policies, exercise sound judgment, effectively
manage stress and work safely and respectfully with others, exhibit
trustworthiness, and safeguard business operations and company
reputation. Pursuant to the California Fair Chance Act, Los Angeles
County Fair Chance Ordinance for Employers, Fair Chance Initiative
for Hiring Ordinance, and San Francisco Fair Chance Ordinance, we
will consider for employment qualified applicants with arrest and
conviction records.
Keywords: KPMG, Houston , Director Life Sciences Regulatory Affairs and Labeling, Executive , Houston, Texas
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