Principal Quality Associate, Supplier Audits
Company: Disability Solutions
Location: Greenville
Posted on: February 5, 2025
Job Description:
Principal Quality Associate, Supplier AuditsPosition
SummaryCatalent's Greenville, N.C. facility specializes in
end-to-end turn-key solutions for oral solid dosage forms,
including integrated formulation development, analytical services,
commercial manufacturing, and packaging. This state-of-the-art
facility has had over $100M of investments in recent years and
features fit-for-scale capacity with potent handling capabilities,
ideal for orphan or targeted drug development. Catalent is
committed to a Patient First culture through excellence in quality
and--compliance, and to the safety of every patient, consumer and
Catalent employee.The Principal Quality Associate, Supplier Audits
requires the ability to perform and facilitate system-based audits
and risk assessments for Supplies Audits and Internal Quality
Systems. The Principal Quality Associate, Supplier Audits will
support non-commercial and commercial audits as well as the
Inspection Readiness Program.Catalent, Inc. is a leading global
contract development and manufacturing organization (CDMO) whose
mission is to develop, manufacture, and supply products that help
people live better and healthier lives. Catalent is dedicated to
delivering unparalleled service to pharma, biotech, and consumer
health customers, supporting product development, launch, and full
life-cycle supply. With time-tested experience in development
sciences, delivery technologies, and multi-modality manufacturing,
Catalent supports the acceleration of development programs and the
launch of more than a hundred new products every year. Powered by
thousands of scientists and technicians and the latest technology
platforms at more than 40 global sites, Catalent supplies billions
of doses of life-enhancing and life-saving treatments for patients
annually.The Role
- Conduct external supplier audits (Desktop, Virtual or On-Site)
per schedule, communicate findings and ensure CAPA plan is
appropriate to address the findings.
- Ensure the Supplier Audit Team members are properly qualified
and assign their roles and responsibilities; train staff to conduct
or assist with audits and risk assessments.
- Participate in Regulatory Inspections and assist Inspection
Readiness Team with inspection preparation, including walkthroughs
and gathering of documentation, per inspection agenda as
required.
- Assist with the generation of the Internal Audit Schedule,
preparation and execution of Internal Quality Audits of Catalent
systems / subsystems.
- Participate in process improvement projects and investigations,
as required.
- Ensure all work is performed and documented according to
approved standard operating procedures (SOPs), in general
compliance with cGMPs, and in a timely manner consistent with
agreed upon schedules.
- All other duties as assigned. The Candidate
- Bachelor's degree in a technical field with at least 6 years of
professional experience in the pharmaceutical industry, 3 of which
must have been in a Quality Auditing function or;
- Associate degree in a technical field with at least 7 years of
professional experience in the pharmaceutical industry, 4 of which
must have been in a Quality Auditing function or;
- In lieu of a technical field degree, at least 8 years of years
of professional experience in the pharmaceutical industry, 5 of
which must have been in a Quality Auditing function and completion
of formal auditing training may be substituted.
- At least 5 years of experience in a direct Quality role
required.
- Demonstrated knowledge of regulations and guidelines associated
with cGMPs for pharmaceutical industry.
- Knowledge of manufacturing and/or laboratory processes
required.
- ASQ CQA or equivalent certification preferred.
- Some exposure to hazardous chemicals and other active chemical
ingredients.
- Position requires the capacity to handle and manipulate objects
using hands and arm.Why You Should Join Catalent--
- Competitive medical benefits and 401K--
- 152 hours of PTO + 8 Paid Holidays--
- Dynamic, fast-paced work environment--
- Opportunity to work on Continuous Improvement
Processes--Catalent offers rewarding opportunities to further your
career!-- Join the global drug development and delivery leader and
help us bring over 7,000 life-saving and life-enhancing products to
patients around the world. Catalent is an exciting and growing
international company where employees work directly with pharma,
biopharma and consumer health companies of all sizes to advance new
medicines from early development to clinical trials and to the
market. Catalent produces more than 70 billion doses per year, and
each one will be used by someone who is counting on us. Join us in
making a difference.--personal initiative. dynamic pace. meaningful
work.Visit to explore career opportunities.Catalent is an Equal
Opportunity Employer, including disability and veterans.If you
require reasonable accommodation for any part of the application or
hiring process due to a disability, you may submit your request by
sending an email, and confirming your request for an accommodation
and include the job number, title and location to . This option is
reserved for individuals who require accommodation due to a
disability. Information received will be processed by a U.S.
Catalent employee and then routed to a local recruiter who will
provide assistance to ensure appropriate consideration in the
application or hiring process.--------Notice to Agency and Search
Firm Representatives: Catalent Pharma Solutions (Catalent) is not
accepting unsolicited resumes from agencies and/or search firms for
this job posting. Resumes submitted to any Catalent employee by a
third party agency and/or search firm without a valid written &
signed search agreement, will become the sole property of Catalent.
No fee will be paid if a candidate is hired for this position as a
result of an unsolicited agency or search firm referral. Thank
you.Important Security Notice to U.S. Job Seekers:Catalent NEVER
asks candidates to provide any type of payment, bank details,
photocopies of identification, social security number or other
highly sensitive personal information during the offer process, and
we NEVER do so via email or social media. If you receive any such
request, DO NOT respond- it is a fraudulent request. Please forward
such requests to spam@catalent.com for us to investigate with local
authorities.California Job Seekers can find our California Job
Applicant Notice .
Keywords: Disability Solutions, Durham , Principal Quality Associate, Supplier Audits, Accounting, Auditing , Greenville, North Carolina
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