Director Life Sciences Regulatory Affairs and Labeling
Company: KPMG
Location: Dallas
Posted on: April 23, 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.Required
Keywords: KPMG, Allen , Director Life Sciences Regulatory Affairs and Labeling, Executive , Dallas, Texas
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